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,1,1555,1],[1556,1,1557,1],[1558,1,1559,1],[1560,1,1561,1],[1562,1,1563,1],[1564,1,1565,1],[1569,1,1569,13],[1571,1,1572,1],[1573,1,1574,1],[1575,1,1576,1],[1577,1,1578,1],[1579,1,1580,1],[1581,1,1582,1],[1583,1,1584,1],[1585,1,1586,1],[1590,1,1590,13],[1592,1,1593,1],[1594,1,1595,1],[1596,1,1597,1],[1598,1,1599,1],[1600,1,1601,1],[1602,1,1603,1],[1604,1,1605,1],[1606,1,1607,1],[1611,1,1611,13],[1613,1,1614,1],[1615,1,1616,1],[1617,1,1618,1],[1619,1,1620,1],[1621,1,1622,1],[1623,1,1624,1],[1625,1,1626,1],[1627,1,1628,1],[1632,1,1632,13],[1634,1,1635,1],[1636,1,1637,1],[1638,1,1639,1],[1640,1,1641,1],[1642,1,1643,1],[1644,1,1645,1],[1646,1,1647,1],[1648,1,1649,1],[1653,1,1653,13],[1655,1,1656,1],[1657,1,1658,1],[1659,1,1660,1],[1661,1,1662,1],[1663,1,1664,1],[1665,1,1666,1],[1667,1,1668,1],[1669,1,1670,1],[1674,1,1674,13],[1676,1,1677,1],[1678,1,1679,1],[1680,1,1681,1],[1682,1,1683,1],[1684,1,1685,1],[1686,1,1687,1],[1688,1,1689,1],[1690,1,1691,1],[1695,1,1695,13],[1697,1,1698,1],[1699,1,1700,1],[1701,1,1702,1],[1703,1,1704,1],[1705,1,1706,1],[1707,1,1708,1],[1709,1,1710,1],[1711,1,1712,1],[1716,1,1716,13],[1718,1,1719,1],[1720,1,1721,1],[1722,1,1723,1],[1724,1,1725,1],[1726,1,1727,1],[1728,1,1729,1],[1730,1,1731,1],[1732,1,1733,1],[1737,1,1737,13],[1739,1,1740,1],[1741,1,1742,1],[1743,1,1744,1],[1745,1,1746,1],[1747,1,1748,1],[1749,1,1750,1],[1751,1,1752,1],[1753,1,1754,1],[1758,1,1758,13],[1760,1,1761,1],[1762,1,1763,1],[1764,1,1765,1],[1766,1,1767,1],[1768,1,1769,1],[1770,1,1771,1],[1772,1,1773,1],[1774,1,1775,1],[1779,1,1779,13],[1781,1,1782,1],[1783,1,1784,1],[1785,1,1786,1],[1787,1,1788,1],[1789,1,1790,1],[1791,1,1792,1],[1793,1,1794,1],[1795,1,1796,1],[1800,1,1800,13],[1802,1,1803,1],[1804,1,1805,1],[1806,1,1807,1],[1808,1,1809,1],[1810,1,1811,1],[1812,1,1813,1],[1814,1,1815,1],[1816,1,1817,1],[1821,1,1821,13],[1823,1,1824,1],[1825,1,1826,1],[1827,1,1828,1],[1829,1,1830,1],[1831,1,1832,1],[1833,1,1834,1],[1835,1,1836,1],[1837,1,1838,1],[1842,1,1842,13],[1844,1,1845,1],[1846,1,1847,1],[1848,1,1849,1],[1850,1,1851,1],[1852,1,1853,1],[1854,1,1855,1],[1856,1,1857,1],[1858,1,1859,1],[1863,1,1863,13],[1865,1,1866,1],[1867,1,1868,1],[1869,1,1870,1],[1871,1,1872,1],[1873,1,1874,1],[1875,1,1876,1],[1877,1,1878,1],[1879,1,1880,1],[1884,1,1884,13],[1886,1,1887,1],[1888,1,1889,1],[1890,1,1891,1],[1892,1,1893,1],[1894,1,1895,1],[1896,1,1897,1],[1898,1,1899,1],[1900,1,1901,1],[1905,1,1905,13],[1907,1,1908,1],[1909,1,1910,1],[1911,1,1912,1],[1913,1,1914,1],[1915,1,1916,1],[1917,1,1918,1],[1919,1,1920,1],[1921,1,1922,1],[1926,1,1926,13],[1928,1,1929,1],[1930,1,1931,1],[1932,1,1933,1],[1934,1,1935,1],[1936,1,1937,1],[1938,1,1939,1],[1940,1,1941,1],[1942,1,1943,1],[1947,1,1947,13],[1949,1,1950,1],[1951,1,1952,1],[1953,1,1954,1],[1955,1,1956,1],[1957,1,1958,1],[1959,1,1960,1],[1961,1,1962,1],[1963,1,1964,1],[1968,1,1968,13],[1970,1,1971,1],[1972,1,1973,1],[1974,1,1975,1],[1976,1,1977,1],[1978,1,1979,1],[1980,1,1981,1],[1982,1,1983,1],[1984,1,1985,1],[1989,1,1989,13],[1991,1,1992,1],[1993,1,1994,1],[1995,1,1996,1],[1997,1,1998,1],[1999,1,2000,1],[2001,1,2002,1],[2003,1,2004,1],[2005,1,2006,1],[2010,1,2010,13],[2012,1,2013,1],[2014,1,2015,1],[2016,1,2017,1],[2018,1,2019,1],[2020,1,2021,1],[2022,1,2023,1],[2024,1,2025,1],[2026,1,2027,1],[2031,1,2031,13],[2033,1,2034,1],[2035,1,2036,1],[2037,1,2038,1],[2039,1,2040,1],[2041,1,2042,1],[2043,1,2044,1],[2045,1,2046,1],[2047,1,2048,1],[2052,1,2052,13],[2054,1,2055,1],[2056,1,2057,1],[2058,1,2059,1],[2060,1,2061,1],[2062,1,2063,1],[2064,1,2065,1],[2066,1,2067,1],[2068,1,2069,1],[2073,1,2073,13],[2075,1,2076,1],[2077,1,2078,1],[2079,1,2080,1],[2081,1,2082,1],[2083,1,2084,1],[2085,1,2086,1],[2087,1,2088,1],[2089,1,2090,1],[2094,1,2094,13],[2096,1,2097,1],[2098,1,2099,1],[2100,1,2101,1],[2102,1,2103,1],[2104,1,2105,1],[2106,1,2107,1],[2108,1,2109,1],[2110,1,2111,1],[2115,1,2115,13],[2117,1,2118,1],[2119,1,2120,1],[2121,1,2122,1],[2123,1,2124,1],[2125,1,2126,1],[2127,1,2128,1],[2129,1,2130,1],[2131,1,2132,1],[2136,1,2136,13],[2138,1,2139,1],[2140,1,2141,1],[2142,1,2143,1],[2144,1,2145,1],[2146,1,2147,1],[2148,1,2149,1],[2150,1,2151,1],[2152,1,2153,1],[2157,1,2157,13],[2159,1,2160,1],[2161,1,2162,1],[2163,1,2164,1],[2165,1,2166,1],[2167,1,2168,1],[2169,1,2170,1],[2171,1,2172,1],[2173,1,2174,1],[2178,1,2178,13],[2180,1,2181,1],[2182,1,2183,1],[2184,1,2185,1],[2186,1,2187,1],[2188,1,2189,1],[2190,1,2191,1],[2192,1,2193,1],[2194,1,2195,1],[2199,1,2199,13],[2201,1,2202,1],[2203,1,2204,1],[2205,1,2206,1],[2207,1,2208,1],[2209,1,2210,1],[2211,1,2212,1],[2213,1,2214,1],[2215,1,2216,1],[2220,1,2220,13],[2222,1,2223,1],[2224,1,2225,1],[2226,1,2227,1],[2228,1,2229,1],[2230,1,2231,1],[2232,1,2233,1],[2234,1,2235,1],[2241,1,2241,13],[2262,1,2262,13],[2283,1,2283,13],[2304,1,2304,13],[2325,1,2325,13],[2346,1,2346,13],[2367,1,2367,13],[2388,1,2388,13],[2409,1,2409,13],[2430,1,2430,13],[2451,1,2451,13],[2472,1,2472,13],[2493,1,2493,13],[2514,1,2514,13],[2535,1,2535,13],[2556,1,2556,13],[2577,1,2577,13],[2598,1,2598,13],[2619,1,2619,13],[2640,1,2640,13],[2661,1,2661,13],[2682,1,2682,13],[2703,1,2703,13],[2724,1,2724,13],[2745,1,2745,13],[2766,1,2766,13],[2787,1,2787,13],[2808,1,2808,13],[2829,1,2829,13]],"merged_total":3671,"flags":["merged_cut"]}
[{"$nulls":3},"Bioactive Compound Library-I (96-well)-L1700"]
[null,"For more information on Selleck library service, please contact us via +1-832-582-8158 or library@selleckchem.com"]
[]
[null,"Product Details:"]
[null,"Description",null,"A unique collection of 10524 compounds"]
[null,"Container",null,"96  Well"]
[null,"Stability",null,"12 months | ﹣20°C | in DMSO"]
[{"$nulls":3},"24 months | ﹣80°C | in DMSO"]
[null,"Shipping",null,"Blue ice or Dry ice"]
[null,"Formulation",null,"Solubility ≥10 mM pre-dissolved in 10 mM solution and solubility between 2 mM and 10 mM pre-dissolved in 2 mM solution"]
[{"$nulls":3},"In 10 mM DMSO : Plate layout L1700-01~107, 120~135;    In 10 mM Water: Plate layout L1700-108~114;"]
[{"$nulls":3},"In 2 mM DMSO : Plate layout L1700-115~117;    In 2 mM Water  : Plate layout L1700-118"]
[{"$nulls":3},"In 2mg/ml DMSO: Plate layout L1700-119"]
[]
[]
[null,"Plate layout: L1700-01"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S1002","S1011","S1022","S1035","S1047","S1060","S1070","S1082","S1092","S1101","Empty"]
[{"$nulls":3},"ABT-737","Afatinib (BIBW2992)","Ridaforolimus (Deforolimus, MK-8669)","Pazopanib HCl (GW786034 HCl)","Vorinostat (SAHA)","Olaparib (AZD2281)","PHA-665752","Vismodegib (GDC-0449)","KU-55933 (ATM Kinase Inhibitor)","Vatalanib (PTK787) 2HCl"]
[null,"b","Empty","S1003","S1012","S1025","S1036","S1048","S1061","S1071","S1084","S1093","S1102","Empty"]
[{"$nulls":3},"Linifanib (ABT-869)","BMS-536924","Gefitinib (ZD1839)","Mirdametinib (PD0325901)","Tozasertib","Nutlin-3","HA14-1","Brivanib (BMS-540215)","GSK1904529A","U0126-EtOH"]
[null,"c","Empty","S1004","S1013","S1026","S1038","S1049","S1064","S1072","S1085","S1094","S1103","Empty"]
[{"$nulls":3},"Veliparib (ABT-888)","Bortezomib (PS-341)","Imatinib (STI571) Mesylate","PI-103","Y-27632 2HCl","Masitinib (AB1010)","ZSTK474","Belinostat (PXD101)","PF-04217903","ZM 447439"]
[null,"d","Empty","S1005","S1014","S1028","S1039","S1052","S1065","S1075","S1087","S1095","S1104","Empty"]
[{"$nulls":3},"Axitinib (AG 013736)","Bosutinib (SKI-606)","Lapatinib (GW-572016) Ditosylate","Rapamycin (AY-22989)","Elesclomol (STA-4783)","Pictilisib (GDC-0941)","SB216763","Iniparib (BSI-201)","Dacinostat (LAQ824)","GDC-0879"]
[null,"e","Empty","S1006","S1017","S1029","S1040","S1053","S1066","S1076","S1088","S1096","S1105","Empty"]
[{"$nulls":3},"Saracatinib (AZD0530)","Cediranib (AZD2171)","Lenalidomide (CC-5013)","Sorafenib (BAY 43-9006) tosylate","Entinostat (MS-275)","SL-327","Adezmapimod (SB203580)","NVP-ADW742","Quisinostat (JNJ-26481585) 2HCl","LY294002"]
[null,"f","Empty","S1007","S1018","S1030","S1041","S1055","S1067","S1077","S1089","S1097","S1106","Empty"]
[{"$nulls":3},"Roxadustat (FG-4592)","Dovitinib (TKI-258)","Panobinostat (LBH589)","STF-62247","Enzastaurin (LY317615)","SB431542","SB202190 (FHPI)","Refametinib (RDEA119)","BTZ043 Racemate","OSU-03012 (AR-12)"]
[null,"g","Empty","S1008","S1020","S1032","S1042","S1056","S1068","S1078","S1090","S1098","S1107","Empty"]
[{"$nulls":3},"Selumetinib (AZD6244)","PD184352 (CI-1040)","Motesanib Diphosphate (AMG-706)","Sunitinib (SU11248) malate","AC480 (BMS-599626)","Crizotinib (PF-02341066)","MK-2206 2HCl","Abexinostat (PCI-24781)","Rucaparib (AG-014699) phosphate","Danusertib (PHA-739358)"]
[null,"h","Empty","S1010","S1021","S1033","S1044","S1057","S1069","S1080","S1091","S1100","S1109","Empty"]
[{"$nulls":3},"Nintedanib (BIBF 1120)","Dasatinib (BMS-354825)","Nilotinib (AMN-107)","Temsirolimus (CCI-779)","Obatoclax Mesylate (GX15-070)","Luminespib (NVP-AUY922)","SU11274","Linsitinib (OSI-906)","MLN8054","BI 2536"]
[]
[]
[]
[null,"Plate layout: L1700-02"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S1110","S1121","S1137","S1148","S1158","S1169","S1178","S1189","S1197","S1208","Empty"]
[{"$nulls":3},"Varespladib (LY315920)","TW-37","Malotilate","Docetaxel (RP56976)","MK-8245","TGX-221","Regorafenib (BAY 73-4506)","Aprepitant (MK-0869)","Finasteride","Doxorubicin (Adriamycin) HCl"]
[null,"b","Empty","S1111","S1122","S1138","S1150","S1159","S1170","S1179","S1190","S1199","S1209","Empty"]
[{"$nulls":3},"Foretinib (GSK1363089)","Mocetinostat (MGCD0103)","Brivanib Alaninate (BMS-582664)","Paclitaxel (NSC 125973)","Ganetespib (STA-9090)","WZ3146","WZ8040","Bicalutamide (ICI-176334)","Cladribine (RWJ 26251)","Fluorouracil (5-Fluorouracil, 5-FU)"]
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[{"$nulls":3},"GSK690693","BMS-754807","Tanespimycin (17-AAG)","PLX-4720","Pretomanid (PA-824)","CYC116","XAV-939","Fulvestrant (ICI-182780)","Decitabine (NSC 127716)","Methotrexate (CL-14377)"]
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[{"$nulls":3},"JNJ-38877605","SRT1720 HCl","Alvespimycin (17-DMAG) HCl","Roscovitine (CYC202)","Onalespib (AT13387)","Serdemetan (JNJ-26854165)","ENMD-2076","Raltitrexed","Dimesna","Bendamustine (SDX105) HCl"]
[null,"e","Empty","S1115","S1130","S1143","S1154","S1164","S1173","S1183","S1193","S1202","S1213","Empty"]
[{"$nulls":3},"Odanacatib (MK-0822)","Sepantronium Bromide","AG-490 (Tyrphostin B42)","SNS-314","Lenvatinib (E7080)","WZ4002","Danoprevir (ITMN-191)","Thalidomide (K17)","Dutasteride","Nelarabine"]
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[{"$nulls":3},"Triciribine (NSC 154020)","3-Aminobenzamide","Ivacaftor (VX-770)","S3I-201","ABT-751 (E7010)","BIIB021","Ritonavir (ABT-538)","CUDC-101","Melatonin (NSC 113928)","Bleomycin (NSC125066) sulfate"]
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[{"$nulls":3},"Cabozantinib (BMS-907351)","Alisertib (MLN8237)","SNS-032 (BMS-387032)","Capecitabine (RO 09-1978)","CP-724714","Plinabulin (NPI-2358)","BIBR 1532","Orteronel","Bisoprolol fumarate","PFI-1 (PF-6405761)"]
[null,"h","Empty","S1120","S1134","S1147","S1157","S1168","S1177","S1188","S1196","S1207","S1218","Empty"]
[{"$nulls":3},"Everolimus (RAD001)","AT9283","Barasertib (AZD1152-HQPA)","Delanzomib (CEP-18770)","Valproic Acid (NSC 93819) sodium salt","PD98059","Anastrozole (ZD-1033)","Exemestane (FCE 24304)","Tivozanib (AV-951)","Clofarabine"]
[]
[]
[]
[null,"Plate layout: L1700-03"]
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[null,"a","Empty","S1219","S1229","S1241","S1252","S1262","S1276","S1287","S1299","S1324","S1336","Empty"]
[{"$nulls":3},"YM201636","Fludarabine Phosphate","Vincristine (NSC-67574) sulfate","Entecavir Hydrate","Avagacestat (BMS-708163)","Adapalene","Bumetanide","Floxuridine (NSC 27640)","Doxazosin Mesylate","Fluvoxamine (DU-23000) maleate"]
[null,"b","Empty","S1220","S1230","S1243","S1255","S1263","S1278","S1289","S1300","S1326","S1340","Empty"]
[{"$nulls":3},"OSI-930","Flavopiridol (L86-8275)","Agomelatine (S20098)","Nepafenac","Laduviglusib (CHIR-99021)","Altretamine","Carmofur","Tegafur (FT-207)","Edaravone","Gatifloxacin"]
[null,"c","Empty","S1221","S1231","S1244","S1256","S1264","S1280","S1290","S1302","S1328","S1342","Empty"]
[{"$nulls":3},"Dacarbazine (NSC-45388)","Topotecan (NSC609699) HCl","Amuvatinib (MP-470)","Rufinamide","PD173074","Amisulpride","Celastrol (NSC 70931)","Ifosfamide (NSC109724)","Etodolac","Genistein (NPI 031L)"]
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[{"$nulls":3},"Dexrazoxane HCl (ICRF-187)","2-Methoxyestradiol (2-MeOE2)","Latrepirdine 2HCl","Posaconazole (SCH 56592)","WYE-354","Aniracetam","Cetirizine DiHCl","Megestrol Acetate","Felbamate","Ginkgolide B"]
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[{"$nulls":3},"Epirubicin (IMI 28) HCl","AG-1024","Leflunomide (HWA486)","Prasugrel","Vemurafenib (PLX4032)","Artemisinin","Chelerythrine Chloride (NSC 646662)","Mercaptopurine (6-MP)","Fluconazole (UK 49858)","Glimepiride"]
[null,"f","Empty","S1225","S1235","S1249","S1259","S1271","S1283","S1293","S1315","S1332","S1351","Empty"]
[{"$nulls":3},"Etoposide (VP-16)","Letrozole (CGS 20267)","JNJ-7706621","Ramelteon","Acarbose","Asenapine maleate","Cilnidipine (FRC-8653)","Ki16425","Flumazenil (RO 15-1788)","Ivermectin (MK-933)"]
[null,"g","Empty","S1226","S1237","S1250","S1260","S1274","S1284","S1294","S1319","S1333","S1352","Empty"]
[{"$nulls":3},"KU-0063794","Temozolomide (CCRG 81045)","Enzalutamide (MDV3100)","Cinacalcet (AMG-073) HCl","BX-795","Benazepril HCl","Cilostazol (OPC-13013)","Costunolide","Fluoxetine (Lilly 110140) HCl","TG100-115"]
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[{"$nulls":3},"Raloxifene HCl","Tamoxifen (ICI 46474)","Dienogest","Celecoxib (SC 58635)","BX-912","Budesonide","Epothilone A","Dexamethasone (MK-125)","Flupirtine maleate","Lansoprazole"]
[]
[]
[]
[null,"Plate layout: L1700-04"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
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[{"$nulls":3},"Levetiracetam (UCB-L059)","BMS-707035","Ruxolitinib (INCB018424)","Omeprazole","Stavudine (d4T)","Alfuzosin HCl","Tamsulosin hydrochloride","Zonisamide","Neflamapimod (VX-745)","Safinamide Mesylate"]
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[{"$nulls":3},"Lidocaine","Amonafide","Isotretinoin","Ondansetron HCl","Tenofovir (GS 1278) Disoproxil Fumarate","Clopidogrel (SR-25990C) Bisulfate","Tizanidine HCl","Aurora A Inhibitor I (TC-S 7010)","Thiazovivin","GSK429286A"]
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[{"$nulls":3},"Loratadine (SCH29851)","Acitretin","Lopinavir (ABT-378)","Oxcarbazepine","Tenofovir","Droxinostat","Topiramate","Ispinesib (SB-715992)","SP600125","Pimasertib (AS-703026)"]
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[{"$nulls":3},"Losartan Potassium (DuP 753)","Bafetinib (INNO-406)","Meropenem","Pelitinib (EKB-569)","Tigecycline (GAR-936)","Ranolazine 2HCl","Tranilast (SB 252218)","Tipifarnib (R115777)","AZD6482","SB525334"]
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[{"$nulls":3},"MGCD-265 analog","Daptomycin (LY146032)","Mianserin HCl","Pirarubicin (NSC-333054)","Trilostane","Repaglinide","Venlafaxine HCl","PHA-680632","Moxifloxacin (BAY12-8039) HCl","Lomibuvir (VX-222)"]
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[{"$nulls":3},"Rigosertib (ON-01910)","Doripenem Hydrate","Mosapride Citrate","Pizotifen Malate","Vecuronium Bromide","Rolipram (ZK-62711)","Voriconazole (UK-109496)","Cilomilast","Doxercalciferol","Zosuquidar (LY335979) 3HCl"]
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[{"$nulls":3},"Ki8751","Gestodene","Nafamostat mesilate (FUT-175)","Resveratrol (SRT501)","Bimatoprost","Sildenafil Citrate","Zileuton (A-64077)","Zibotentan (ZD4054)","Alfacalcidol","Daclatasvir (BMS-790052)"]
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[{"$nulls":3},"Patupilone (Epothilone B)","Drospirenone","Naftopidil DiHCl","Rocuronium Bromide","Linezolid (PNU-100766)","Sumatriptan Succinate","Ziprasidone HCl","Atazanavir (BMS-232632) Sulfate","Orantinib (SU6668)","Iloperidone"]
[]
[]
[]
[null,"Plate layout: L1700-05"]
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[{"$nulls":3},"MC1568","Pralatrexate (NSC 754230)","Tadalafil (IC351)","LY2811376","Vadimezan (ASA404)","Nebivolol hydrochloride (R-65824)","Lumacaftor (VX-809)","Sulfasalazine (NSC 667219)","Reserpine","Metolazone"]
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[{"$nulls":3},"HMN-214","Cefaclor","Cyclosporine","Hesperadin","Telaprevir (VX-950)","Pimobendan","Pomalidomide (CC-4047)","Tie2 kinase inhibitor","Furosemide (NSC 269420)","Cefoperazone"]
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[{"$nulls":3},"AEE788 (NVP-AEE788)","Betamethasone","Pracinostat (SB939)","BIX 02188","Saxagliptin (BMS-477118)","Delafloxacin (ABT-492)","PD318088","Candesartan (CV-11974)","Olmesartan Medoxomil","Silodosin"]
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[{"$nulls":3},"PHA-793887","Mycophenolate mofetil (RS-61443)","Natamycin","BIX 02189","Selisistat (EX 527)","AZD8055","Tazarotene","H 89 2HCl","Cefdinir","Riluzole (PK 26124)"]
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[{"$nulls":3},"Naratriptan HCl","Dyphylline","Voxtalisib (XL765) Analogue","AZD7762","AM1241","PHT-427","KU-60019","TWS119","Clotrimazole","Sulfameter"]
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[{"$nulls":3},"PIK-93","Aztreonam","AT7519","R406 (free base)","SB408124","KRN 633","BS-181 HCl","Bestatin (NK421)","Rizatriptan Benzoate","Prilocaine"]
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[{"$nulls":3},"Ponatinib (AP24534)","Alprostadil","Adavosertib (MK-1775)","Org 27569","Febuxostat","AT7867","Fasudil (HA-1077) HCl","Apixaban (BMS 562247-01)","Pyridostigmine Bromide","Darunavir Ethanolate"]
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[{"$nulls":3},"Fludarabine (NSC 118218)","Lactulose","Quizartinib (AC220)","CP-673451","Dapagliflozin (BMS-512148)","BMS-777607","Doramapimod (BIRB 796)","Semagacestat (LY450139)","Methimazole","Prednisone (NSC-10023)"]
[]
[]
[]
[null,"Plate layout: L1700-06"]
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[{"$nulls":3},"Ethinyl Estradiol","Erythromycin","Ketoprofen","Ezetimibe (SCH-58235)","Aminophylline","Sulfanilamide","Desonide","Piroxicam","Indomethacin (NSC-77541)","Mesna"]
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[{"$nulls":3},"Naproxen Sodium","Amphotericin B","Ketorolac","Enalaprilat Dihydrate","Lubiprostone","Betamethasone Dipropionate","Didanosine","Gemcitabine (LY-188011)","Terbinafine","Methocarbamol"]
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[{"$nulls":3},"Nitazoxanide (NSC 697855)","Ibuprofen (NSC 256857)","Adenosine","Dofetilide","Amorolfine HCl","Meprednisone","Divalproex Sodium","Glipizide","Levonorgestrel","Prednisolone (NSC-9900)"]
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[{"$nulls":3},"Triamcinolone Acetonide","Amprenavir (VX-478)","Zolmitriptan","Isradipine","Chloramphenicol","Betamethasone Valerate","Emtricitabine (BW 1592)","Glyburide (Glibenclamide)","Gemfibrozil","Telmisartan"]
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[{"$nulls":3},"Orlistat (Ro 18-0647)","Albendazole (SKF-62979)","Telbivudine","Estrone","Flurbiprofen","Praziquantel","Progesterone (NSC 9704)","Fomepizole","Indapamide","Thiabendazole"]
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[{"$nulls":3},"Allopurinol","Chlorothiazide","Monobenzone","Flucytosine","Disulfiram (NSC 190940)","Busulfan (NSC-750)","Lamivudine (BCH-189)","Adefovir Dipivoxil (GS 0840)","Mitotane","Guaifenesin"]
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[{"$nulls":3},"Allopurinol Sodium","Ursodiol","Tretinoin (NSC 122758)","Trichlormethiazide","Mesalamine (5-ASA)","Carbamazepine","Estradiol","Zalcitabine","Methylprednisolone (NSC-19987)","Rifabutin (LM427)"]
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[{"$nulls":3},"Zafirlukast (ICI-204219)","Nitrofural","Phenylbutazone","Loteprednol etabonate","Ipratropium Bromide","Hydrocortisone (NSC 10483)","Deferasirox (ICL-670)","Azathioprine","Meloxicam","Nevirapine (NSC 641530)"]
[]
[]
[]
[null,"Plate layout: L1700-07"]
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[{"$nulls":3},"Esomeprazole magnesium","Rifapentine","Oxytetracycline (Terramycin)","Verteporfin (CL 318952)","Ranolazine","Amlodipine Besylate","Oxfendazole","Chenodeoxycholic Acid","Dienestrol","Protionamide"]
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[{"$nulls":3},"Nicotinic Acid","Suprofen","Thioguanine (NSC 752)","Teniposide","Ranitidine Hydrochloride","Chlorpheniramine Maleate","Carvedilol","Cimetidine","Diethylstilbestrol","Idoxuridine"]
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[{"$nulls":3},"Nimodipine","Pyrazinamide","Thiotepa","Tetrabenazine (Xenazine)","AICAR (Acadesine)","Clofibrate","Atracurium Besylate","Clemastine (HS-592) fumarate","Diltiazem HCl","Sparfloxacin"]
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[{"$nulls":3},"Nisoldipine","Quetiapine (ICI-204636) fumarate","Toremifene Citrate (NK 622)","Rifaximin","Acetylcholine Chloride","Fenoprofen Calcium","Butoconazole nitrate","Curcumin","Diphenhydramine HCl","Felodipine"]
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[{"$nulls":3},"Octocrylene","Rifampin (NSC-113926)","Ethionamide","Bacitracin Zinc","Acipimox","Erdosteine","Azithromycin (CP-62993)","Daidzein","Dapoxetine HCl","Deflazacort"]
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[{"$nulls":3},"Oxybutynin","Cefditoren Pivoxil","Trifluridine (NSC 75520)","Simvastatin (MK 733)","Aciclovir (BW 248U)","Betaxolol HCl","Albendazole Oxide","Bifonazole","Valaciclovir HCl","Nizatidine"]
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[{"$nulls":3},"Enoxacin","Sulfadiazine","Azacitidine (5-Azacytidine)","Ramipril","Nifedipine (BAY-a-1040)","Proparacaine HCl","Chloroxine","Pefloxacin Mesylate","Ganciclovir (BW 759)","Carbidopa"]
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[{"$nulls":3},"Pitavastatin (NK-104) calcium","Chlorprothixene","Vidarabine","Fenofibrate (NSC-281319)","Amiloride (MK-870) HCl","Pranlukast","Lomustine","Metoprolol Tartrate","Roxatidine Acetate HCl","Valsartan (CGP-48933)"]
[]
[]
[]
[null,"Plate layout: L1700-08"]
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[{"$nulls":3},"Dipyridamole (NSC 515776)","Amlodipine","Sulfisoxazole","Levofloxacin","Tolfenamic Acid","Cyclocytidine HCl","Capsaicin(Vanilloid)","Pramipexole 2HCl Monohydrate","Formoterol Hemifumarate","Fenticonazole Nitrate"]
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[{"$nulls":3},"Hydroxyurea (NSC-32065)","Metronidazole","Crystal Violet","Enalapril Maleate","Pranoprofen","Meglumine","Fluticasone propionate","PCI-34051","Chlormezanone","Rebamipide"]
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[{"$nulls":3},"Potassium Iodide","Flutamide","Haloperidol","Menadione (NSC 4170)","Sulphadimethoxine","Aripiprazole","Lacidipine","PF-573228","Ketotifen Fumarate","Aspartame"]
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[{"$nulls":3},"Tropisetron HCl","Fluvastatin (XU-62-320) Sodium","Phenindione","Metformin HCl","Rimantadine","Methscopolamine","Elvitegravir (JTK-303)","BMS-265246","Urapidil HCl","Candesartan Cilexetil"]
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[{"$nulls":3},"Nicotinamide (NSC 13128)","Tioconazole","Alibendol","Methoxsalen","Primidone","Amiodarone (NSC 85442) HCl","Maraviroc (UK-427857)","Suplatast Tosylate","Ginkgolide A","Phentolamine Mesylate"]
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[{"$nulls":3},"Vitamin B12","Tropicamide","Triamcinolone","Miconazole Nitrate","Nefiracetam","Adenine HCl","Raltegravir (MK-0518)","Mirtazapine","Diclazuril","Nimesulide"]
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[{"$nulls":3},"Diclofenac Sodium","Pregnenolone","Nystatin (Fungicidin)","Sulfamethizole","Nicorandil","Mometasone furoate","Pyrimethamine","Benidipine HCl","Uridine","Dyclonine HCl"]
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[{"$nulls":3},"Avobenzone","Sulfamethoxazole","Isoniazid","Sulbactam","Tamoxifen (ICI 46474) Citrate","Propylthiouracil","Sulindac","ENMD-2076 L-(+)-Tartaric acid","Flunarizine 2HCl","Cyproterone Acetate"]
[]
[]
[]
[null,"Plate layout: L1700-09"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S2043","S2055","S2065","S2077","S2086","S2099","S2111","S2124","S2149","S2160","Empty"]
[{"$nulls":3},"Memantine HCl","Gimeracil","Lafutidine","Atorvastatin Calcium","Ivabradine HCl","Temocapril HCl","Lapatinib (GW-572016)","Xylose","GSK1292263","Almorexant HCl"]
[null,"b","Empty","S2044","S2057","S2066","S2078","S2087","S2101","S2113","S2125","S2151","S2161","Empty"]
[{"$nulls":3},"Cyproheptadine HCl","Cyclophosphamide (NSC-26271) Monohydrate","Moxonidine","Famotidine","Rivastigmine Tartrate","Gabexate Mesylate","Cisatracurium Besylate","Mestranol","Sonidegib (NVP-LDE225)","RAF265 (CHIR-265)"]
[null,"c","Empty","S2045","S2058","S2067","S2079","S2090","S2102","S2114","S2126","S2153","S2162","Empty"]
[{"$nulls":3},"Doxifluridine","Tolnaftate","Ozagrel HCl","Moexipril HCl","Dexmedetomidine HCl","Rasagiline Mesylate","Dronedarone HCl","Naftopidil","CGS 21680 HCl","AZD1480"]
[null,"d","Empty","S2046","S2059","S2069","S2080","S2091","S2103","S2116","S2127","S2154","S2163","Empty"]
[{"$nulls":3},"Pioglitazone HCl","Terazosin HCl Dihydrate","Argatroban (MCI-9038)","Clevidipine Butyrate","Betaxolol","Naltrexone HCl","Conivaptan HCl","S-(+)-Rolipram","Dabigatran (BIBR-1048) etexilate","PF-4708671"]
[null,"e","Empty","S2051","S2060","S2071","S2082","S2092","S2104","S2118","S2128","S2155","S2167","Empty"]
[{"$nulls":3},"Captopril","Bromhexine HCl","Prulifloxacin (NM441)","Adiphenine HCl","Detomidine HCl","Levosulpiride","Ibutilide Fumarate","Bazedoxifene (WAY-140424) HCl","LY2608204","Bazedoxifene (TSE-424) acetate"]
[null,"f","Empty","S2052","S2061","S2072","S2083","S2096","S2105","S2119","S2130","S2156","S2168","Empty"]
[{"$nulls":3},"Oxytetracycline Dihydrate","Lovastatin (MK-803)","Seratrodast(AA-2414)","Procaterol HCl","Almotriptan Malate","Pantoprazole","Probucol","Atropine sulfate monohydrate","LY2886721","PD128907 HCl"]
[null,"g","Empty","S2053","S2062","S2074","S2084","S2097","S2108","S2120","S2131","S2158","S2169","Empty"]
[{"$nulls":3},"Cytidine","Tiopronin","Mecarbinate","Duloxetine HCl","Ambrisentan","Flunixin Meglumin","Arbidol HCl","Roflumilast (B9302-107)","KW-2449","Rosuvastatin (ZD4522) calcium"]
[null,"h","Empty","S2054","S2064","S2075","S2085","S2098","S2109","S2123","S2134","S2159","S2170","Empty"]
[{"$nulls":3},"Orphenadrine Citrate","Balofloxacin","Rosiglitazone (BRL-49653) HCl","Trimebutine","Bexarotene (LGD1069)","Imidapril HCl","Dextrose","AZD8330","Tebipenem Pivoxil","Givinostat (ITF2357)"]
[]
[]
[]
[null,"Plate layout: L1700-10"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S2173","S2185","S2197","S2215","S2225","S2235","S2252","S2262","S2270","S2284","Empty"]
[{"$nulls":3},"Telotristat Etiprate (LX 1606 Hippurate)","Allitinib tosylate","A-966492","DAPT (GSI-IX)","TAME","Volasertib (BI 6727)","(+)-Usniacin","Apigenin (LY 080400)","Bergenin","Colchicine (NSC 757)"]
[null,"b","Empty","S2177","S2186","S2198","S2216","S2226","S2238","S2253","S2263","S2271","S2285","Empty"]
[{"$nulls":3},"Dichlorphenamide","SB505124","SGI-1776 free base","Mubritinib (TAK 165)","Idelalisib","Palomid 529 (P529)","3-Indolebutyric acid (IBA)","Arbutin","Berberine chloride (NSC 646666)","Cryptotanshinone"]
[null,"c","Empty","S2178","S2187","S2199","S2217","S2227","S2243","S2254","S2264","S2276","S2286","Empty"]
[{"$nulls":3},"AG-14361","Avasimibe (CI-1011)","Aliskiren Hemifumarate","Irinotecan (CPT-11) HCl Trihydrate","PIK-294","Degrasyn (WP1130)","4-Demethylepipodophyllotoxin(NSC-122819,VM-26)","Artemether","Bilobalide","Cyclosporin A (NSC 290193)"]
[null,"d","Empty","S2179","S2188","S2201","S2218","S2228","S2244","S2256","S2265","S2277","S2287","Empty"]
[{"$nulls":3},"Gandotinib (LY2784544)","Phenprocoumon","BMS-794833","Torkinib (PP242)","Belnacasan (VX-765)","AR-42","4-Methylumbelliferone (4-MU)","Artesunate (WR-256283)","Caffeic Acid","Cytisine"]
[null,"e","Empty","S2180","S2192","S2202","S2219","S2229","S2246","S2258","S2266","S2280","S2289","Empty"]
[{"$nulls":3},"Ixazomib (MLN2238)","Sapitinib (AZD8931)","NVP-BHG712","Momelotinib (CYT387)","Eltrombopag (SB497115) Olamine","Abiraterone Acetate (CB7630)","Esculin","Asiatic Acid","Chlorogenic Acid","Daidzin"]
[null,"f","Empty","S2181","S2193","S2205","S2220","S2230","S2247","S2259","S2267","S2281","S2290","Empty"]
[{"$nulls":3},"Ixazomib Citrate (MLN9708) Analogue","GSK461364","OSI-420","SB590885","Galunisertib (LY2157299)","Buparlisib (BKM120)","Aloe-emodin","Azomycin","Chrysin","Dihydroartemisinin (DHA)"]
[null,"g","Empty","S2182","S2194","S2207","S2222","S2231","S2248","S2260","S2268","S2282","S2293","Empty"]
[{"$nulls":3},"SB743921 HCl","R406","PIK-293","PF-3716556","Telatinib","Silmitasertib (CX-4945)","Amygdalin","Baicalein","Cinchonidine","DL-Carnitine HCl"]
[null,"h","Empty","S2183","S2195","S2214","S2224","S2233","S2250","S2261","S2269","S2283","S2295","Empty"]
[{"$nulls":3},"Infigratinib (BGJ398)","Lexibulin (CYT997)","AZ 960","UK 383367","Esomeprazole sodium","(-)-Epigallocatechin Gallate","Andrographolide","Baicalin (NSC-661431)","Cinchonine(LA40221)","Emodin"]
[]
[]
[]
[null,"Plate layout: L1700-11"]
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[null,"a","Empty","S2296","S2305","S2314","S2323","S2333","S2342","S2351","S2363","S2373","S2381","Empty"]
[{"$nulls":3},"Enoxolone","Grape Seed Extract","Kaempferol (NSC 407289)","Methyl-Hesperidin","Nobiletin (NSC 76751)","Phloretin (RJC 02792)","Salicin","Tangeretin","Yohimbine HCl","D-Mannitol"]
[null,"b","Empty","S2298","S2306","S2316","S2325","S2334","S2343","S2354","S2364","S2374","S2382","Empty"]
[{"$nulls":3},"Fisetin","Gynostemma Extract","Kinetin","Morin Hydrate","Oleanolic Acid","Phlorizin","Sclareol","Tanshinone I","5-hydroxytryptophan (5-HTP)","Evodiamine"]
[null,"c","Empty","S2299","S2308","S2317","S2326","S2335","S2344","S2355","S2365","S2375","S2383","Empty"]
[{"$nulls":3},"Formononetin","Hesperetin","L-(+)-Rhamnose Monohydrate","Myricetin","Oridonin (NSC-250682)","Piperine","Sclareolide","Tanshinone IIA","Aloin","Gastrodin"]
[null,"d","Empty","S2300","S2309","S2318","S2327","S2336","S2346","S2356","S2366","S2376","S2384","Empty"]
[{"$nulls":3},"Ferulic Acid","Hesperidin","Lappaconitine","Myricitrin","Orotic acid (6-Carboxyuracil)","Puerarin","Shikimic Acid","Taxifolin (Dihydroquercetin)","Ammonium Glycyrrhizinate","Hematoxylin"]
[null,"e","Empty","S2301","S2310","S2319","S2328","S2337","S2347","S2357","S2369","S2377","S2385","Empty"]
[{"$nulls":3},"Genistin (Genistoside)","Honokiol (NSC 293100)","Limonin","Nalidixic acid","Osthole","Quercetin Dihydrate","Silibinin (NSC 651520)","Troxerutin","Biochanin A","Hordenine"]
[null,"f","Empty","S2302","S2311","S2320","S2329","S2338","S2348","S2358","S2370","S2378","S2386","Empty"]
[{"$nulls":3},"Glycyrrhizin (NSC 167409)","Hyodeoxycholic acid (HDCA)","Luteolin","Naringin","Oxymatrine","Rotenone (Barbasco)","Silymarin","Ursolic Acid","Butylscopolamine Bromide","Indirubin (NSC 105327)"]
[null,"g","Empty","S2303","S2312","S2321","S2331","S2339","S2349","S2359","S2371","S2379","S2387","Empty"]
[{"$nulls":3},"Gossypol Acetate","Icariin","Magnolol","Neohesperidin Dihydrochalcone (Nhdc)","Paeonol","Rutaecarpine","Sinomenine","Vanillylacetone","Dioscin","Lappaconite HBr"]
[null,"h","Empty","S2304","S2313","S2322","S2332","S2341","S2350","S2362","S2372","S2380","S2388","Empty"]
[{"$nulls":3},"Gramine","Indole-3-carbinol","(+)-Matrine","Neohesperidin","(-)-Parthenolide","Rutin","Synephrine","Xanthone","Diosmetin","L-carnitine"]
[]
[]
[]
[null,"Plate layout: L1700-12"]
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[{"$nulls":3},"Naringin Dihydrochalcone","Dihydromyricetin","Cephalomannine","(S)-10-Hydroxycamptothecin","Gambogic Acid","Clindamycin HCl","Fluocinolone Acetonide","Milrinone","Olopatadine HCl","Ribavirin (ICN-1229)"]
[null,"b","Empty","S2390","S2400","S2409","S2425","S2449","S2458","S2471","S2485","S2496","S2505","Empty"]
[{"$nulls":3},"Polydatin","Rheic Acid","10-Deacetylbaccatin-III","Apocynin (NSC 2146)","Colforsin","Clonidine HCl","Gallamine Triethiodide","Mitoxantrone (NSC-301739) 2HCl","Ozagrel","Rosiglitazone (BRL-49653) maleate"]
[null,"c","Empty","S2391","S2401","S2410","S2437","S2450","S2459","S2473","S2486","S2497","S2506","Empty"]
[{"$nulls":3},"Quercetin (NSC 9221)","Sodium Danshensu","Paeoniflorin (NSC 178886)","Rotundine","Equol","Clozapine","Hexestrol","Moroxydine HCl","Pancuronium dibromide","Roxithromycin"]
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[{"$nulls":3},"Sesamin","Tetrandrine (NSC-77037)","Geniposide","Synephrine HCl","Amantadine HCl","Pramipexole","Imatinib (STI571)","Mycophenolic acid","Phenoxybenzamine HCl","Scopolamine (LSM-4015) HBr"]
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[{"$nulls":3},"Sorbitol","Isoliquiritigenin","Genipin","Guanosine","Amfebutamone (Bupropion) HCl","Domperidone","Lincomycin HCl","Nateglinide","Propafenone HCl","Sotalol HCl"]
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[{"$nulls":3},"Naringenin","Sophocarpine","Geniposidic acid","Inosine","Bupivacaine HCl","Estriol","Loperamide HCl","Nitrendipine","Pyrantel Pamoate","Spectinomycin 2HCl"]
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[{"$nulls":3},"Salidroside","Chrysophanic Acid","Astragaloside A","Tolbutamide (HLS 831)","Bethanechol chloride","Famciclovir","Manidipine","Novobiocin Sodium (NSC 2382)","Quinine HCl Dihydrate","Sulfadoxine"]
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[{"$nulls":3},"Palmatine chloride","Curcumol","Ipriflavone (Osteofix)","Levosimendan","Chlorpromazine HCl","Fenbendazole","Manidipine 2HCl","Olanzapine","Racecadotril","Tenoxicam"]
[]
[]
[]
[null,"Plate layout: L1700-13"]
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[{"$nulls":3},"Vardenafil HCl Trihydrate","Ciclopirox","Secnidazole","5-Aminolevulinic acid HCl","Amoxicillin Sodium","Phenacetin","Pioglitazone (AD-4833)","Idebenone","Clorsulon","OSI-027"]
[null,"b","Empty","S2516","S2529","S2541","S2554","S2566","S2579","S2593","S2606","S2614","S2625","Empty"]
[{"$nulls":3},"Xylazine HCl","Dopamine HCl","Clomipramine HCl","Daphnetin","Isoprenaline (NCI-C55630) HCl","Zidovudine","Tolvaptan","Mifepristone (RU486)","Arecoline HBr","Fostamatinib (R788)"]
[null,"c","Empty","S2517","S2531","S2543","S2555","S2567","S2581","S2594","S2607","S2615","S2626","Empty"]
[{"$nulls":3},"Maprotiline HCl","Asaraldehyde","Ceftiofur HCl","Clarithromycin","Medroxyprogesterone acetate (NSC-26386)","Quinapril HCl","Pramiracetam","Buflomedil HCl","Noradrenaline bitartrate monohydrate","Rabusertib (LY2603618)"]
[null,"d","Empty","S2519","S2532","S2545","S2556","S2569","S2583","S2596","S2608","S2617","S2627","Empty"]
[{"$nulls":3},"Naphazoline HCl","L-Ascorbyl 6-palmitate","Scopine","Rosiglitazone (BRL 49653)","Phenylephrine (NCI-C55641) HCl","Thiamphenicol","Clindamycin palmitate HCl","Fluocinonide","TAK-733","Tubastatin A HCl"]
[null,"e","Empty","S2521","S2533","S2547","S2557","S2570","S2584","S2599","S2609","S2619","S2629","Empty"]
[{"$nulls":3},"Epinephrine bitartrate","Ritodrine HCl","Tiotropium Bromide hydrate","Terbinafine HCl","Prednisolone Acetate","Clobetasol propionate","L-Thyroxine","Inulin","MG132","PNU-120596"]
[null,"f","Empty","S2524","S2534","S2549","S2559","S2573","S2585","S2601","S2610","S2621","S2630","Empty"]
[{"$nulls":3},"Phenytoin Sodium","Isoconazole nitrate","Trospium chloride","Cortisone acetate","Tetracaine HCl","Brompheniramine hydrogen maleate","Gliclazide","Lonidamine (AF-1890)","AZD5438","GW3965 HCl"]
[null,"g","Empty","S2525","S2535","S2551","S2561","S2574","S2586","S2602","S2611","S2622","S2631","Empty"]
[{"$nulls":3},"Phenytoin","Econazole nitrate","Sulbactam sodium","Clomifene citrate","Tetracycline HCl","Dimethyl Fumarate","Acemetacin","Ethisterone","PP121","URB597"]
[null,"h","Empty","S2526","S2536","S2552","S2564","S2576","S2589","S2603","S2612","S2623","S2632","Empty"]
[{"$nulls":3},"Alizarin","Miconazole","Azelastine HCl","Cloxacillin Sodium","Xylometazoline HCl","Miglitol","Tioxolone","Ribitol","Omecamtiv mecarbil (CK-1827452)","BMS-378806"]
[]
[]
[]
[null,"Plate layout: L1700-14"]
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[{"$nulls":3},"NPS-2143","MK-0752","A-674563","AS-604850","ADX-47273","RS-127445","TAK-901","SB415286","PF-04691502","HER2-Inhibitor-1"]
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[{"$nulls":3},"Rebastinib (DCC-2036)","WYE-125132 (WYE-132)","AS-252424","CAY10505","BMY 7378 Dihydrochloride","CH5132799","AMG-900","Crenolanib (CP-868596)","CHIR-98014","Tivantinib (ARQ 197)"]
[null,"c","Empty","S2635","S2662","S2672","S2683","S2692","S2700","S2720","S2731","S2746","S2754","Empty"]
[{"$nulls":3},"CCT128930","Foscenvivint (ICG-001)","PF-00562271 Besylate","CHIR-124","TG101209","Tirbanibulin","ZM 336372","AZ 3146","AZ 628","Xevinapant (AT406)"]
[null,"d","Empty","S2636","S2663","S2673","S2685","S2693","S2703","S2721","S2736","S2747","S2755","Empty"]
[{"$nulls":3},"A66","WAY-100635 Maleate","Trametinib (GSK1120212)","KW-2478","Resminostat","GSK1838705A","Nilvadipine","Fedratinib (TG101348)","AMG-458","Varlitinib"]
[null,"e","Empty","S2637","S2664","S2674","S2686","S2694","S2711","S2722","S2738","S2748","S2757","Empty"]
[{"$nulls":3},"Fasiglifam(TAK-875) Hemihydrate","Clinofibrate","A922500","NVP-BSK805 2HCl","Turofexorate Isopropyl (XL335)","Dibenzazepine (YO-01027)","JTC-801","PAC-1","Anacetrapib (MK-0859)","Evofosfamide (TH-302)"]
[null,"f","Empty","S2639","S2665","S2677","S2687","S2695","S2713","S2726","S2740","S2749","S2759","Empty"]
[{"$nulls":3},"SNX-2112 (PF-04928473)","Ciprofibrate","BRL-15572 Dihydrochloride","Mardepodect (PF-2545920)","Nepicastat (SYN-117) HCl","Geldanamycin (NSC 122750)","PH-797804","GSK1070916","BGT226 (NVP-BGT226) maleate","Fimepinostat (CUDC-907)"]
[null,"g","Empty","S2656","S2666","S2679","S2688","S2696","S2714","S2727","S2741","S2750","S2760","Empty"]
[{"$nulls":3},"PF-04929113 (SNX-5422)","PF-3845","Flavopiridol (L86-8275) HCl","R547","Apitolisib (GDC-0980)","LY411575","Dacomitinib (PF-00299804)","Niraparib (MK-4827)","GW788388","Canagliflozin (JNJ 28431754)"]
[null,"h","Empty","S2658","S2667","S2680","S2689","S2697","S2717","S2728","S2742","S2751","S2761","Empty"]
[{"$nulls":3},"Omipalisib (GSK2126458)","Dolutegravir (GSK1349572)","Ibrutinib (PCI-32765)","WAY-600","A-769662","CP-91149","AG-1478 (Tyrphostin AG-1478)","PHA-767491 HCl","Milciclib (PHA-848125)","NVP-BVU972"]
[]
[]
[]
[null,"Plate layout: L1700-15"]
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[{"$nulls":3},"Alectinib (CH5424802)","Nocodazole (R17934)","Vistusertib (AZD2014)","Sofosbuvir (GS-7977)","CEP-33779","Tyrphostin AG 879","TPCA-1","Cathepsin Inhibitor 1","(-)-Dizocilpine (MK 801) Maleate","VUF 10166"]
[null,"b","Empty","S2765","S2776","S2784","S2795","S2807","S2817","S2825","S2849","S2858","S2866","Empty"]
[{"$nulls":3},"MK-2048","Devimistat (CPI-613)","TAK-285","VU 0357121","Dabrafenib (GSK2118436)","Torin 2","ML133 HCl","SB269970 HCl","StemRegenin 1 (SR1)","U-104"]
[null,"c","Empty","S2768","S2777","S2785","S2796","S2808","S2818","S2828","S2851","S2859","S2867","Empty"]
[{"$nulls":3},"Dinaciclib (SCH727965)","PF-5274857","A-803467","WP1066","Ipatasertib (GDC-0068)","Tacedinaline (CI994)","JNJ-1661010","Baricitinib (INCB028050)","Golvatinib (E7050)","WHI-P154"]
[null,"d","Empty","S2769","S2778","S2787","S2797","S2809","S2819","S2830","S2852","S2860","S2868","Empty"]
[{"$nulls":3},"Dovitinib (TKI-258) Dilactic Acid","GW842166X","Laquinimod","Lonafarnib (SCH66336)","MPEP","AM251","Clindamycin","BRL-54443","IEM 1754 2HBr","Alogliptin (SYR-322) benzoate"]
[null,"e","Empty","S2770","S2779","S2789","S2799","S2811","S2820","S2840","S2853","S2861","S2871","Empty"]
[{"$nulls":3},"MK-5108 (VX-689)","M344","Tofacitinib (CP-690550)","Daporinad","Sapanisertib (MLN0128)","TAE226 (NVP-TAE226)","Apalutamide (ARN-509)","Carfilzomib (PR-171)","CTEP (RO4956371)","T0070907"]
[null,"f","Empty","S2772","S2780","S2790","S2801","S2812","S2821","S2842","S2854","S2862","S2872","Empty"]
[{"$nulls":3},"Dalcetrapib (JTT-705)","I-BET151 (GSK1210151A)","Istradefylline","AZD4547","(R)-(-)-Gossypol acetic acid","RG108","SAR131675","BML-190","VU 0364770","GW5074"]
[null,"g","Empty","S2773","S2781","S2791","S2803","S2813","S2822","S2843","S2855","S2863","S2874","Empty"]
[{"$nulls":3},"SB705498","RITA (NSC 652287)","Sotrastaurin (AEB071)","Galeterone","Ciproxifan Maleate","OC000459","BI-D1870","MRS 2578","Nodinitib-1","Camostat Mesilate"]
[null,"h","Empty","S2774","S2782","S2792","S2804","S2814","S2823","S2845","S2856","S2864","S2875","Empty"]
[{"$nulls":3},"MK-2461","GW4064","Torcetrapib","Sirtinol","Alpelisib (BYL719)","Tideglusib (NP031112)","Semaxanib (SU5416)","SB 271046 hydrochloride","IMD 0354","Prucalopride"]
[]
[]
[]
[null,"Plate layout: L1700-16"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S2876","S2894","S2902","S2912","S2922","S2930","S3015","S3025","S3036","S3052","Empty"]
[{"$nulls":3},"(+)-Dizocilpine (MK 801) Maleate","SB742457","S-Ruxolitinib (INCB018424)","WZ811","Icotinib (BPI-2009H)","Pifithrin-μ","Amoxicillin","PMSF","Pravastatin sodium","Rupatadine Fumarate"]
[null,"b","Empty","S2882","S2895","S2903","S2913","S2923","S3000","S3017","S3026","S3037","S3053","Empty"]
[{"$nulls":3},"IKK-16 (IKK Inhibitor VII)","Tyrphostin 9","Lumiracoxib","BAY 11-7082","Salubrinal","Carbazochrome sodium sulfonate (AC-17)","Aspirin (NSC 27223)","Piceatannol","Bepotastine Besilate","Azelnidipine"]
[null,"c","Empty","S2883","S2896","S2904","S2914","S2924","S3001","S3018","S3027","S3038","S3054","Empty"]
[{"$nulls":3},"4-Aminohippuric Acid","ZM 323881 HCl","PF-477736","Dapivirine (TMC120)","Laduviglusib (CHIR-99021) HCl","Clevudine","Niflumic acid","Fenoprofen calcium hydrate","Fosaprepitant dimeglumine salt","Alverine Citrate"]
[null,"d","Empty","S2884","S2897","S2905","S2915","S2925","S3002","S3019","S3030","S3043","S3057","Empty"]
[{"$nulls":3},"Acesulfame Potassium","ZM 306416","JNJ-7777120","GW9662","Evacetrapib (LY2484595)","Rivaroxaban (BAY 59-7939)","Ciclopirox ethanolamine","Niclosamide (BAY2353)","Rofecoxib","Azilsartan Medoxomil"]
[null,"e","Empty","S2885","S2898","S2906","S2916","S2926","S3003","S3021","S3031","S3045","S3060","Empty"]
[{"$nulls":3},"A-205804","MLN0905","Ki16198","ML161 (Parmodulin 2)","TDZD-8","Prostaglandin E2 (PGE2)","Rimonabant (SR141716)","Linagliptin (BI-1356)","Cinepazide maleate","Medetomidine HCl"]
[null,"f","Empty","S2890","S2899","S2907","S2918","S2927","S3005","S3022","S3032","S3046","S3061","Empty"]
[{"$nulls":3},"PF-562271","GNF-2","Pirfenidone (S-7701)","HC-030031","Apoptosis Activator 2","Paroxetine HCl","Cabazitaxel (XRP6258)","Bindarit (AF 2838)","Azilsartan","Epinephrine HCl"]
[null,"g","Empty","S2891","S2900","S2910","S2919","S2928","S3008","S3023","S3033","S3047","S3062","Empty"]
[{"$nulls":3},"GW441756","Cobicistat (GS-9350)","Tempol","IOX2","TAK-715","Zaltoprofen","Bufexamac","Vildagliptin (LAF-237)","Otilonium Bromide","Diclofenac Potassium"]
[null,"h","Empty","S2892","S2901","S2911","S2921","S2929","S3012","S3024","S3035","S3051","S3063","Empty"]
[{"$nulls":3},"VU 0361737","CCG 50014","Go 6983","PF-4981517","Pifithrin-α (PFTα) HBr","Pazopanib","Lamotrigine","Daunorubicin (RP 13057) HCl","Bosentan Hydrate","Diclofenac Diethylamine"]
[]
[]
[]
[null,"Plate layout: L1700-17"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3066","S3080","S3114","S3132","S3150","S3163","S3179","S3193","S3208","S3610","Empty"]
[{"$nulls":3},"Naloxone HCl","Etravirine (TMC125)","Vitamin C","Sulfamerazine","Articaine HCl","Benztropine mesylate","Carbenicillin disodium","Ticarcillin sodium","Fexofenadine HCl","Cordycepin"]
[null,"b","Empty","S3067","S3081","S3116","S3133","S3151","S3167","S3180","S3195","S3212","S3611","Empty"]
[{"$nulls":3},"Chlorhexidine 2HCl","Ulipristal Acetate (CDB 2914)","Sulfathiazole","Sulfamethazine","Gliquidone","Altrenogest","Eletriptan HBr","Azlocillin sodium salt","Moclobemide (Ro 111163)","(+)-Fangchinoline"]
[null,"c","Empty","S3070","S3083","S3117","S3137","S3153","S3170","S3181","S3196","S3600","S3612","Empty"]
[{"$nulls":3},"Piracetam","Indacaterol Maleate","Oxybutynin hydrochloride","Sodium salicylate","Levalbuterol tartrate","Ampicillin sodium","Flumequine","Azacyclonol","Schisandrin B (Sch B)","Rosmarinic acid"]
[null,"d","Empty","S3071","S3100","S3120","S3138","S3154","S3172","S3183","S3199","S3603","S3613","Empty"]
[{"$nulls":3},"Vanillin","2-Thiouracil","Doxepin HCl","Methylthiouracil","Butenafine HCl","Anagrelide HCl","Amitriptyline HCl","Reboxetine mesylate","Betulinic acid","Scoparone"]
[null,"e","Empty","S3074","S3104","S3121","S3140","S3155","S3173","S3185","S3200","S3604","S3615","Empty"]
[{"$nulls":3},"Chlorthalidone","Moguisteine","Ornidazole","Milnacipran HCl","Mepivacaine HCl","Antipyrine","Adrenalone HCl","Triflusal","Triptolide (PG490)","Dehydrocostus Lactone"]
[null,"f","Empty","S3077","S3105","S3124","S3144","S3160","S3175","S3186","S3201","S3606","S3616","Empty"]
[{"$nulls":3},"Tazobactam","Nadifloxacin","Dexamethasone Acetate","Darifenacin HBr","Ethynodiol diacetate","Atomoxetine HCl","Azatadine dimaleate","Trifluoperazine 2HCl","Fangchinoline","Asiaticoside"]
[null,"g","Empty","S3078","S3106","S3129","S3147","S3161","S3176","S3189","Empty","S3608","S3617","Empty"]
[{"$nulls":3},"Beclomethasone dipropionate","Pidotimod","Trimethoprim","Entacapone","Sertaconazole nitrate","Betahistine 2HCl","Ropinirole HCl",null,"Demethylzeylasteral (T-96)","(20S)-Protopanaxatriol"]
[null,"h","Empty","S3079","S3113","S3130","S3149","S3162","S3178","S3190","S3207","S3609","S3618","Empty"]
[{"$nulls":3},"Atovaquone","Pyridoxine HCl","Biotin (Vitamin B7)","Estradiol valerate","Tylosin tartrate","Brinzolamide","N6-methyladenosine (m6A)","Iopromide","Berbamine dihydrochloride","Acetylspiramycin (ASPM)"]
[]
[]
[]
[null,"Plate layout: L1700-18"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3621","S3629","S3640","S3652","S3660","S3672","S3680","S3689","S3697","S3705","Empty"]
[{"$nulls":3},"Pazufloxacin mesylate","Syringic acid","Methoxyphenamine Hydrochloride","3-Nitropropionic acid","Uniconazole (S 3307D)","Cefonicid sodium","NLRP3 Inflammasome Inhibitor I","Ethidium bromide","Mafenide hydrochloride","Chlorobutanol"]
[null,"b","Empty","S3622","S3630","S3641","S3653","S3661","S3673","S3681","S3690","S3698","S3706","Empty"]
[{"$nulls":3},"Diammonium Glycyrrhizinate","Methyl Vanillate","Osalmid","Spermidine trihydrochloride","2-Methoxy-1,4-naphthoquinone","Sulfaphenazole","Vitamin E Acetate","Pargyline hydrochloride","Nortriptyline hydrochloride","Sarpogrelate hydrochloride"]
[null,"c","Empty","S3623","S3633","S3643","S3654","S3663","S3674","S3682","S3691","S3699","S3707","Empty"]
[{"$nulls":3},"Ceftibuten dihydrate","Pyrrolidinedithiocarbamate ammonium","Amitraz","Tauroursodeoxycholic Acid (TUDCA)","Afloqualone","Levamlodipine","Ethyl 3-Aminobenzoate methanesulfonate","4-Chlorosalicylic acid","2,3-Butanedione-2-monoxime","Ethopabate"]
[null,"d","Empty","S3624","S3634","S3644","S3655","S3665","S3675","S3683","S3692","S3700","S3708","Empty"]
[{"$nulls":3},"Quinolinic acid","6-Hydroxyflavone (6-HF)","Sulfamonomethoxine","Cefepime Dihydrochloride Monohydrate","Trolox","Umbelliferone","Methylmalonate","N-Ethylmaleimide (NEM)","DHBP dibromide","Sulfachloropyridazine"]
[null,"e","Empty","S3625","S3635","S3645","S3656","S3666","S3676","S3684","S3693","S3701","S3709","Empty"]
[{"$nulls":3},"Tyramine","Medroxyprogesterone","Kitasamycin","Piribedil","Ilaprazole","Carbendazim","Methacholine chloride","2,6-Dihydroxypurine","Benactyzine hydrochloride","Furagin"]
[null,"f","Empty","S3626","S3637","S3647","S3657","S3668","S3677","S3686","S3694","S3702","S3711","Empty"]
[{"$nulls":3},"Sesamol","Cefpirome sulfate","Mafenide Acetate","Promestriene","Thymopentin","Cinnamic acid","Thioisonicotinamide","Glucosamine hydrochloride","Dihydrothymine","Carbasalate Calcium"]
[null,"g","Empty","S3627","S3638","S3648","S3658","S3669","S3678","S3687","S3695","S3703","S3712","Empty"]
[{"$nulls":3},"Tryptamine","Cefamandole nafate","Amlexanox (AA-673)","O6-Benzylguanine","Carmustine","PTP Inhibitor II","Urea","Cystamine dihydrochloride","Phenethyl alcohol","Tulathromycin A"]
[null,"h","Empty","S3628","S3639","S3651","S3659","S3671","S3679","S3688","S3696","S3704","S3713","Empty"]
[{"$nulls":3},"BHQ","Tacrine hydrochloride hydrate","4-Amino-5-imidazolecarboxamide","Fludrocortisone acetate","Quinestrol","Flavanone","2,4-Diamino-6-hydroxypyrimidine","PTP Inhibitor I","4-Methylbenzylidene camphor","Moxidectin"]
[]
[]
[]
[null,"Plate layout: L1700-19"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3714","S3726","S3735","S3750","S3763","S3774","S3782","S3790","S3800","S3809","Empty"]
[{"$nulls":3},"Lifitegrast","Selexipag","Umeclidinium bromide","Sodium benzoate","Cinnamaldehyde","Dehydroandrographolide Succinate Potasium Salt","Neomangiferin","Methyl gallate","Lycorine hydrochloride","Imperatorin"]
[null,"b","Empty","S3716","S3727","S3738","S3751","S3764","S3775","S3783","S3791","S3802","S3810","Empty"]
[{"$nulls":3},"Flibanserin","Vilanterol Trifenate","Travoprost","Quinidine hemisulfate hydrate","Isoferulic Acid","Ligustrazine hydrochloride","Echinacoside","Succinic acid","Trigonelline Hydrochloride","Scutellarin"]
[null,"c","Empty","S3719","S3728","S3739","S3754","S3765","S3776","S3784","S3792","S3803","S3811","Empty"]
[{"$nulls":3},"Topiroxostat","Grazoprevir","Calcipotriene","4-Hydroxybenzoic acid","Picroside II","Sophoricoside","Obacunone (AI3-37934)","Guggulsterone E&Z","Angelic acid","Ginsenoside Re"]
[null,"d","Empty","S3720","S3729","S3741","S3756","S3766","S3777","S3785","S3794","S3804","S3812","Empty"]
[{"$nulls":3},"Elafibranor","Iron sucrose","Benznidazole","Methyl salicylate","Tanshinone IIA sulfonate sodium","Gentiopicroside","Notoginsenoside R1","Palmitic acid","Alpha-Mangostin","Monocrotaline"]
[null,"e","Empty","S3722","S3730","S3742","S3757","S3769","S3778","S3786","S3795","S3805","S3813","Empty"]
[{"$nulls":3},"Isavuconazole","Metaxalone","Cholic acid","2'-Deoxyinosine","Palmatine","Patchouli alcohol","Glabridin","Phloretic acid","Stevioside","Bakuchiol"]
[null,"f","Empty","S3723","S3731","S3745","S3758","S3771","S3779","S3787","S3796","S3806","S3814","Empty"]
[{"$nulls":3},"Ramosetron Hydrochloride","Tipiracil hydrochloride","Balsalazide disodium","Sinomenine hydrochloride","Stachydrine","cis-Anethole","Picroside I","Rebaudioside A","Angelic anhydride","Tubeimoside I"]
[null,"g","Empty","S3724","S3732","S3746","S3759","S3772","S3780","S3788","S3797","S3807","S3815","Empty"]
[{"$nulls":3},"Velpatasvir","Avibactam sodium","Lumefantrine","Norcantharidin","5-Hydroxymethylfurfural","Secoisolariciresinol diglucoside","Carvacrol","Helicide","Dehydroandrographolide","Mogroside V"]
[null,"h","Empty","S3725","S3733","S3747","S3762","S3773","S3781","S3789","S3799","S3808","S3816","Empty"]
[{"$nulls":3},"ELR-510444","Boceprevir","Levothyroxine sodium","Methylnonylketone","Tyrosol","Ginkgolide C","Tiglic acid","Gentisic acid","Mangiferin","Dehydroevodiamine"]
[]
[]
[]
[null,"Plate layout: L1700-20"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3817","S3826","S3836","S3844","S3854","S3863","S3871","S3879","S3887","S3897","Empty"]
[{"$nulls":3},"Harmine hydrochloride","Hydroxytyrosol","6-Gingerol","Rosavin","Tetrahydropalmatine hydrochloride","Methyl EudesMate","Muscone","Kaempferide","α-L-Rhamnose monohydrate","(-)-Arctigenin"]
[null,"b","Empty","S3818","S3827","S3837","S3846","S3855","S3864","S3872","S3880","S3888","S3898","Empty"]
[{"$nulls":3},"Tectoridin","Royal jelly acid","Echinocystic acid","Eupatilin","Ethyl ferulate","Dulcitol","Guaiacol","Schisantherin A","3,4',5-Trimethoxy-trans-stilbene","Hydroxy Camptothecine"]
[null,"c","Empty","S3819","S3828","S3838","S3847","S3856","S3865","S3873","S3881","S3889","S3899","Empty"]
[{"$nulls":3},"Decursinol angelate","Orcinol glucoside","Carnosic acid","Panaxatriol","Allantoin","Taurochenodeoxycholic acid","Methyl 4-hydroxycinnamate","Scopoletin","Arteether","Hederagenin"]
[null,"d","Empty","S3820","S3829","S3839","S3848","S3857","S3866","S3874","S3882","S3892","S3900","Empty"]
[{"$nulls":3},"Dehydroevodiamine hydrochloride","Isoalantolactone","1-Deoxynojirimycin","Hydroxytyrosol Acetate","4-Hydroxybenzyl alcohol","Galanthamine","Curcumenol","Brassinolide","Isopsoralen","Betulonic acid"]
[null,"e","Empty","S3822","S3832","S3840","S3849","S3858","S3867","S3875","S3883","S3893","S3901","Empty"]
[{"$nulls":3},"Schisandrin A","Euphorbiasteroid","Baohuoside I","D-Galactose","Lawsone","(E)-Cardamonin","Alpinetin","Protopine","Bornyl acetate","Astragaloside IV"]
[null,"f","Empty","S3823","S3833","S3841","S3850","S3859","S3868","S3876","S3884","S3894","S3902","Empty"]
[{"$nulls":3},"Schizandrol A","Amentoflavone","Eleutheroside B","Glucosamine sulfate","Vanillyl Alcohol","Harmine","Indigo","Jatrorrhizine","Cycloastragenol","Ursonic acid"]
[null,"g","Empty","S3824","S3834","S3842","S3851","S3860","S3869","S3877","S3885","S3895","S3903","Empty"]
[{"$nulls":3},"Quercitrin","Astaxanthin","Isoquercitrin","Camphor","Allicin","Methyl protocatechuate","Lysionotin","Pyrogallol","Sophoridine","Lycorine"]
[null,"h","Empty","S3825","S3835","S3843","S3853","S3862","S3870","S3878","S3886","S3896","S3904","Empty"]
[{"$nulls":3},"Glycitin","Loganin","Madecassoside","Perillyl alcohol","Gallic acid trimethyl ether","D-Pinitol","Bavachinin","Quinic acid","(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine","Isoimperatorin"]
[]
[]
[]
[null,"Plate layout: L1700-21"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3905","S3914","S3922","S3930","S3938","S3949","S3960","S3971","S3981","S3990","Empty"]
[{"$nulls":3},"Iso-Steviol","α-Hederin","(-)-epigallocatechin","Liquiritin","Bisdemethoxycurcumin (BDMC)","N-Sulfo-glucosamine sodium salt","Higenamine hydrochloride","Fusidine","Sinapinic Acid","Trans-Anethole"]
[null,"b","Empty","S3906","S3915","S3923","S3931","S3939","S3950","S3962","S3974","S3982","S3991","Empty"]
[{"$nulls":3},"Astragalus polyphenols","Gracillin","Ginsenoside Rg1","Ginsenoside Rd","4'-Methoxyresveratrol","Maltitol","Dihydroactinidiolide","(+)-Catechin hydrate","Batyl alcohol","Ketoisophorone"]
[null,"c","Empty","S3907","S3916","S3924","S3932","S3940","S3951","S3965","S3975","S3983","S3992","Empty"]
[{"$nulls":3},"Bulleyaconi cine A","Macranthoidin B","Ginsenoside Rb1","Astilbin","3'-Hydroxypterostilbene","Tannic acid","Vanillyl Butyl Ether","Protocatechuic acid","Caryophyllene oxide","D-(+)-Trehalose dihydrate"]
[null,"d","Empty","S3908","S3917","S3925","S3933","S3941","S3952","S3966","S3976","S3984","S3993","Empty"]
[{"$nulls":3},"4'-Demethylpodophyllotoxin","Tetrahydrocurcumin","(-)-Epicatechin gallate","10-deacetyl-paclitaxel","Pinocembrin","3,4-Dihydroxybenzaldehyde","Nifuratel","Acetylvanillin","Nordihydroguaiaretic acid (NDGA)","Ethyl Vanillate"]
[null,"e","Empty","S3909","S3918","S3926","S3934","S3942","S3956","S3967","S3977","S3985","S3994","Empty"]
[{"$nulls":3},"Catalpol","4',7-Dimethoxy-5-Hydroxyflavone","Forsythin","Acetyl Resveratrol","Cardamonin","Tetramethylpyrazine","Flavone","(-)-Borneol","Methyl 4-hydroxybenzoate","Methyl Cholate"]
[null,"f","Empty","S3910","S3919","S3927","S3935","S3944","S3957","S3968","S3978","S3986","S3995","Empty"]
[{"$nulls":3},"4',7-Dimethoxyisoflavone","Hederacoside C","Swertiamarin","Nonivamide","Valproic acid (VPA)","Gamma-Oryzanol","Histamine","5-Phenyl-2,4-pentadienoic acid","L-Arabinose","Guaiazulene"]
[null,"g","Empty","S3911","S3920","S3928","S3936","S3945","S3958","S3969","S3979","S3987","S3996","Empty"]
[{"$nulls":3},"Veratramine","7β-Hydroxylathyrol","Baccatin Ⅲ","7-Hydroxycarbostyril","L-Cycloserine","3,5-Diiodotyrosine Dihydrate","Veratric acid","Zinc Undecylenate","L-Tryptophan","Thioctic acid"]
[null,"h","Empty","S3912","S3921","S3929","S3937","S3947","S3959","S3970","S3980","S3988","S3997","Empty"]
[{"$nulls":3},"Cephalotaxine","Lathyrol","Liquiritigenin","Pterostilbene","Hydroumbellic acid","(+)-Borneol","Vindoline","Pyridoxine","Theophylline-7-acetic acid","Oxaceprol"]
[]
[]
[]
[null,"Plate layout: L1700-22"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S3998","S4009","S4019","S4031","S4043","S4051","S4061","S4073","S4082","S4091","Empty"]
[{"$nulls":3},"(+)-α-Lipoic acid","Mirabegron","Avanafil","Aclidinium Bromide","Tetrahydrozoline HCl","Nabumetone","Levobupivacaine HCl","Sodium 4-Aminosalicylate","Spiramycin","Ifenprodil Tartrate"]
[null,"b","Empty","S3999","S4010","S4020","S4034","S4044","S4053","S4062","S4075","S4083","S4092","Empty"]
[{"$nulls":3},"α-santonin","Acebutolol HCl","Sodium Picosulfate","Diphemanil Methylsulfate","Toltrazuril","Sertraline HCl","Ronidazole","Zinc Pyrithione","Vitamin A Acetate","Pramoxine HCl"]
[null,"c","Empty","S4000","S4011","S4021","S4037","S4045","S4054","S4064","S4076","S4084","S4095","Empty"]
[{"$nulls":3},"Pergolide Mesylate","Ampiroxicam","Tolcapone","Doxapram HCl","Pheniramine Maleate","Spironolactone","Escitalopram Oxalate","Propranolol HCl","Lomerizine 2HCl","Difluprednate"]
[null,"d","Empty","S4001","S4012","S4022","S4038","S4046","S4056","S4065","S4077","S4085","S4096","Empty"]
[{"$nulls":3},"Cabozantinib malate","Desloratadine","Probenecid","Dibucaine HCl","Estradiol Cypionate","Retapamulin","Guanabenz Acetate","Mequinol","Levobetaxolol HCl","Droperidol"]
[null,"e","Empty","S4002","S4014","S4023","S4039","S4047","S4057","S4068","S4078","S4086","S4098","Empty"]
[{"$nulls":3},"Sitagliptin phosphate monohydrate","Hyoscyamine","Procaine HCl","Methazolamide","Bisacodyl","Methyclothiazide","Tinidazole","Mefenamic Acid","Loxapine Succinate","Halcinonide"]
[null,"f","Empty","S4003","S4015","S4024","S4040","S4048","S4058","S4070","S4079","S4088","S4099","Empty"]
[{"$nulls":3},"Lithocholic acid","Cyclamic  acid","Homatropine Methylbromide","Norethindrone","Carbimazole","Ropivacaine HCl","Guanidine HCl","Ticagrelor","Flumethasone","Dexlansoprazole"]
[null,"g","Empty","S4004","S4017","S4025","S4041","S4049","S4059","S4071","S4080","S4089","S4100","Empty"]
[{"$nulls":3},"Ethambutol 2HCl","Allylthiourea","Homatropine Bromide","Olsalazine Sodium","Valdecoxib","Sodium Nitroprusside Dihydrate","Griseofulvin","Triamterene","Halobetasol Propionate","Esmolol HCl"]
[null,"h","Empty","S4007","S4018","S4026","S4042","S4050","S4060","S4072","S4081","S4090","S4101","Empty"]
[{"$nulls":3},"Pentamidine isethionate","Sennoside B","Hydroxyzine 2HCl","Nafcillin Sodium","Valganciclovir HCl","Erythromycin Ethylsuccinate","Decamethonium Bromide","Sulfacetamide Sodium","Fenspiride HCl","Voglibose"]
[]
[]
[]
[null,"Plate layout: L1700-23"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4102","S4113","S4124","S4139","S4155","S4166","S4176","S4186","S4195","S4204","Empty"]
[{"$nulls":3},"Eprosartan Mesylate","Desvenlafaxine","Tolazoline HCl","Cyclizine 2HCl","Chlorzoxazone","Chlorpropamide","Trometamol","Domiphen Bromide","Broxyquinoline","Isosorbide"]
[null,"b","Empty","S4104","S4114","S4125","S4141","S4159","S4167","S4177","S4187","S4196","S4205","Empty"]
[{"$nulls":3},"Diminazene Aceturate","Triclabendazole","Sodium Phenylbutyrate","Dinitolmide","Bezafibrate","Cyromazine","Uracil","Salicylanilide","Ethacridine lactate monohydrate","Dibenzothiophene"]
[null,"c","Empty","S4105","S4116","S4128","S4143","S4160","S4169","S4178","S4188","S4197","S4206","Empty"]
[{"$nulls":3},"Closantel Sodium","Isovaleramide","Troxipide","Pentoxyverine Citrate","Penicillin G Sodium","Teriflunomide","Climbazole","Sasapyrine","Bemegride","Cysteamine HCl"]
[null,"d","Empty","S4106","S4118","S4131","S4147","S4161","S4170","S4179","S4189","S4198","S4207","Empty"]
[{"$nulls":3},"Closantel","Histamine 2HCl","Levodropropizine","Azithromycin Dihydrate","Benzoic Acid","Coumarin","Mezlocillin Sodium","Cyclandelate","Aminothiazole","Clofibric Acid"]
[null,"e","Empty","S4107","S4119","S4132","S4148","S4162","S4171","S4181","S4190","S4200","S4208","Empty"]
[{"$nulls":3},"Clofazimine","Pefloxacin Mesylate Dihydrate","Deoxyarbutin","Ampicillin Trihydrate","Benzethonium Chloride","Choline Chloride","Nicardipine HCl","Cinchophen","Tolperisone HCl","Chromocarb"]
[null,"f","Empty","S4110","S4120","S4135","S4149","S4163","S4172","S4182","S4191","S4201","S4210","Empty"]
[{"$nulls":3},"Estradiol Benzoate","Sulconazole Nitrate","Clorprenaline HCl","Amfenac Sodium Monohydrate","Doxycycline Hyclate (WC2031)","Cetylpyridinium Chloride","Nifuroxazide","Betamipron","Florfenicol","Benzocaine"]
[null,"g","Empty","S4111","S4122","S4136","S4151","S4164","S4173","S4184","S4192","S4202","S4212","Empty"]
[{"$nulls":3},"Dicloxacillin Sodium","Tilmicosin","Carprofen","Penfluridol","Doxofylline","1-Hexadecanol","Penciclovir","Chlorquinaldol","Verapamil (CP-16533-1) HCl","Tenatoprazole"]
[null,"h","Empty","S4112","S4123","S4138","S4152","S4165","S4175","S4185","S4194","S4203","S4213","Empty"]
[{"$nulls":3},"Desvenlafaxine Succinate hydrate","Timolol Maleate","Dropropizine","Ethamsylate","Benzydamine HCl","Sulfaguanidine","Tiratricol","Azaguanine-8","Furaltadone HCl","Dirithromycin"]
[]
[]
[]
[null,"Plate layout: L1700-24"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4214","S4225","S4235","S4246","S4256","S4265","S4278","S4286","S4296","S4308","Empty"]
[{"$nulls":3},"Sucralose","Mexiletine HCl","Phenazopyridine HCl","Tranylcypromine (2-PCPA) HCl","Buspirone HCl","Nicaraven","Carteolol HCl","Anidulafungin (LY303366)","Salmeterol Xinafoate","Benzthiazide"]
[null,"b","Empty","S4216","S4227","S4237","S4247","S4257","S4266","S4279","S4288","S4297","S4309","Empty"]
[{"$nulls":3},"Valnemulin HCl","Fidaxomicin","Primaquine Diphosphate","Prucalopride Succinate","Alizapride HCl","Brimonidine Tartrate","Demeclocycline HCl","Chloroambucil","Mupirocin","Bromocriptine Mesylate"]
[null,"c","Empty","S4217","S4228","S4238","S4248","S4258","S4267","S4280","S4289","S4299","S4312","Empty"]
[{"$nulls":3},"Liothyronine Sodium","Fluorometholone Acetate","Cepharanthine","Bromfenac Sodium","Luliconazole","Diacerein","Meclofenoxate (Centrophenoxine) HCl","Metoclopramide HCl","Dicoumarol","Carbadox"]
[null,"d","Empty","S4219","S4229","S4239","S4249","S4259","S4268","S4281","S4291","S4301","S4315","Empty"]
[{"$nulls":3},"Azaperone","Oxybuprocaine HCl","Bergapten","Flopropione","Vilazodone HCl","Flufenamic acid","Tasimelteon","Labetalol HCl","(R)-(+)-Atenolol HCl","Clinafoxacin HCl"]
[null,"e","Empty","S4221","S4230","S4240","S4250","S4260","S4269","S4282","S4292","S4303","S4316","Empty"]
[{"$nulls":3},"Benzbromarone","Oxaprozin","Doxylamine Succinate","Sulfamethoxypyridazine","Tamibarotene","Vinorelbine ditartrate (KW-2307)","Nelfinavir (AG 1343) Mesylate","Diphenidol HCl","9-Aminoacridine","Clopamide"]
[null,"f","Empty","S4222","S4231","S4242","S4251","S4261","S4270","S4283","S4293","S4304","S4317","Empty"]
[{"$nulls":3},"Piperacillin Sodium","Pilocarpine HCl","Cetrimonium Bromide (CTAB)","Phenothiazine","EUK 134","Oxiracetam","Cyclobenzaprine HCl","Promethazine HCl","Anisindione","Clorgyline HCl"]
[null,"g","Empty","S4223","S4232","S4243","S4253","S4263","S4274","S4284","S4294","S4305","S4319","Empty"]
[{"$nulls":3},"Mevastatin","Nithiamide","Deoxycorticosterone acetate","Epinastine HCl","Efaproxiral Sodium","Rotigotine","Chloroprocaine HCl","Procainamide HCl","Anisotropine Methylbromide","Dibenzepine HCl"]
[null,"h","Empty","S4224","S4233","S4244","S4255","S4264","S4277","S4285","S4295","S4307","S4320","Empty"]
[{"$nulls":3},"Erythritol","Zoxazolamine","Serotonin HCl","Quinacrine 2HCl","Etofibrate","Bambuterol HCl","Ospemifene","Meclofenamate Sodium","Auranofin","Dimaprit 2HCl"]
[]
[]
[]
[null,"Plate layout: L1700-25"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4322","S4335","S4349","S4365","S4380","S4393","S4408","S4502","S4510","S4520","Empty"]
[{"$nulls":3},"Disopyramide Phosphate","Metaproterenol Sulfate","Procyclidine HCl","Phthalylsulfacetamide","Nomifensine Maleate","Cephapirin Sodium","Procodazole","Eltrombopag","4-Aminobenzoic acid","2-Aminoheptane"]
[null,"b","Empty","S4326","S4336","S4351","S4366","S4381","S4394","S4409","S4503","S4511","S4521","Empty"]
[{"$nulls":3},"Ethoxzolamide","Metaraminol Bitartrate","Ractopamine HCl","Pinacidil","Proadifen HCl","Clofoctol","Quipazine Maleate","Calcium D-Panthotenate","6-Benzylaminopurine","DEET"]
[null,"c","Empty","S4329","S4338","S4353","S4367","S4382","S4396","S4412","S4504","S4512","S4522","Empty"]
[{"$nulls":3},"Hemicholinium Bromide","Methoxamine HCl","Terfenadine","Suxibuzone","Pyrilamine Maleate","Digoxigenin","DL-Mevalonic Acid Lactone","6-Mercaptopurine (6-MP) Monohydrate","Aceglutamide","Dehydroacetic acid"]
[null,"d","Empty","S4330","S4339","S4354","S4368","S4385","S4398","S4414","S4505","S4514","S4524","Empty"]
[{"$nulls":3},"Isoetharine Mesylate","Meticrane","Thiostrepton","Carbenoxolone Sodium","Fosfomycin Tromethamine","Isoxicam","Sodium 4-aminohippurate","Vinblastine (NSC-49842) sulfate","Acetylleucine","2-Ethoxybenzamide"]
[null,"e","Empty","S4331","S4342","S4357","S4373","S4387","S4401","S4415","S4506","S4515","S4525","Empty"]
[{"$nulls":3},"Meclocycline Sulfosalicylate","Nialamide","Tacrine HCl","Dicyclomine HCl","Bendroflumethiazide","Nifenazone","Misoprostol","Acetazolamide","Ademetionine disulfate tosylate","Ethylparaben"]
[null,"f","Empty","S4332","S4343","S4358","S4375","S4388","S4402","S4416","S4507","S4516","S4526","Empty"]
[{"$nulls":3},"Medrysone","Oxethazaine","Pimozide","Mepenzolate Bromide","Bentiromide","Oxeladin Citrate","Trimipramine Maleate","17-Hydroxyprogesterone","(+)-Camphor","Fenbufen"]
[null,"g","Empty","S4333","S4344","S4361","S4376","S4389","S4404","S4420","S4508","S4517","S4527","Empty"]
[{"$nulls":3},"Mepiroxol","Oxprenolol HCl","Cinoxacin","Aceclidine HCl","Bephenium Hydroxynaphthoate","Pasiniazid","Mefloquine HCl","2,2,2-Tribromoethanol","Cefotaxime sodium","Fenofibric acid"]
[null,"h","Empty","S4334","S4345","S4362","S4377","S4391","S4406","S4422","S4509","S4518","S4528","Empty"]
[{"$nulls":3},"Mesoridazine Besylate","Pentoxifylline","Glafenine HCl","Imipramine HCl","Camylofin Chlorhydrate","Pindolol","Nitenpyram","4-Aminoantipyrine","Chloroxylenol","Furazolidone"]
[]
[]
[]
[null,"Plate layout: L1700-26"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4529","S4541","S4552","S4562","S4571","S4587","S4596","S4607","S4623","S4631","Empty"]
[{"$nulls":3},"Idramantone","Triclosan","Bithionol","Dehydrocholic acid","Hexylresorcinol","Pentylenetetrazol","Cefixime","2,2′-Dihydroxy-4-methoxybenzophenone","Methylbenactyzine Bromide","Prochlorperazine dimaleate salt"]
[null,"b","Empty","S4530","S4542","S4553","S4563","S4576","S4588","S4597","S4609","S4624","S4633","Empty"]
[{"$nulls":3},"i-Inositol","Trihexyphenidyl hydrochloride","Bronopol","Diatrizoic acid","Sulfabenzamide","Docusate Sodium","Lercanidipine hydrochloride","Diflunisal","5,5-Dimethyloxazolidine-2,4-dione","Isosorbide Mononitrate"]
[null,"c","Empty","S4532","S4543","S4554","S4564","S4577","S4589","S4599","S4610","S4625","S4634","Empty"]
[{"$nulls":3},"Iopamidol","Trimetazidine dihydrochloride","Bucetin","Diethylcarbamazine citrate","Terpin hydrate","Amodiaquine dihydrochloride dihydrate","Benzyl benzoate","Mebendazole","Alcaftadine","Sodium sulfadiazine"]
[null,"d","Empty","S4534","S4544","S4555","S4565","S4578","S4590","S4600","S4612","S4626","S4635","Empty"]
[{"$nulls":3},"6-Acetamidohexanoic acid","Urethane","Carsalam","Diiodohydroxyquinoline","Tyloxapol","Dithranol","Benzyl alcohol","Dapson","Ethosuximide","Cyproheptadine hydrochloride sesquihydrate"]
[null,"e","Empty","S4535","S4546","S4556","S4566","S4581","S4591","S4601","S4618","S4627","S4636","Empty"]
[{"$nulls":3},"Methylene Blue","Xylitol","Carzenide","DL-Panthenol","Triacetin","Nitroxoline","Clioquinol","Fenoldopam mesylate","TTNPB (Arotinoid Acid)","Teneligliptin hydrobromide"]
[null,"f","Empty","S4536","S4547","S4558","S4568","S4583","S4593","S4602","S4619","S4628","S4637","Empty"]
[{"$nulls":3},"Nitrofurantoin","8-Hydroxyquinoline","Citiolone","Ethylvanillin","Butamben","Chlormadinone acetate","Acetohydroxamic acid","Itopride hydrochloride","(+/-)-Sulfinpyrazone","Prasugrel Hydrochloride"]
[null,"g","Empty","S4538","S4548","S4559","S4569","S4584","S4594","S4603","S4620","S4629","S4638","Empty"]
[{"$nulls":3},"Pantoprazole sodium","Aminoguanidine hydrochloride","Cloxiquine","Fluphenazine dihydrochloride","Butylparaben","Cephalothin sodium","Gallic acid","Cefuroxime sodium","Chlorotrianisene","Desogestrel"]
[null,"h","Empty","S4539","S4550","S4561","S4570","S4585","S4595","S4604","S4622","S4630","S4640","Empty"]
[{"$nulls":3},"Salicylic acid","Azelaic acid","Danthron","Halothane","Succinylsulfathiazole","Cefazolin Sodium","Levofloxacin hydrate","3,4-Diaminopyridine","Diazoxide","Lesinurad"]
[]
[]
[]
[null,"Plate layout: L1700-27"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4641","S4655","S4664","S4676","S4689","S4698","S4711","S4720","S4732","S4742","Empty"]
[{"$nulls":3},"Tedizolid Phosphate","Sulpiride","Molsidomine","Gluconolactone","Deoxycholic acid","Vitamin K1","Esculetin","Cefotaxime","MPTP hydrochloride","Rebaudioside C"]
[null,"b","Empty","S4646","S4656","S4665","S4678","S4690","S4699","S4712","S4722","S4733","S4743","Empty"]
[{"$nulls":3},"Ciclesonide","Parecoxib","Rabeprazole sodium","Povidone iodine","Escin","Etretinate","Diethylmaleate","(+)-Catechin","Retigabine","Wogonin"]
[null,"c","Empty","S4647","S4657","S4666","S4679","S4691","S4701","S4714","S4723","S4734","S4744","Empty"]
[{"$nulls":3},"Cefmenoxime hydrochloride","Eslicarbazepine Acetate","Sivelestat sodium tetrahydrate","Terazosin HCl","Oxybenzone","2-Deoxy-D-glucose (2-DG)","(-)-Menthol","(-)Epicatechin","Retigabine 2HCl","Anethole trithione"]
[null,"d","Empty","S4648","S4658","S4667","S4682","S4692","S4706","S4715","S4725","S4735","S4746","Empty"]
[{"$nulls":3},"Dantrolene sodium hemiheptahydrate","Hydroquinidine","Lidocaine hydrochloride","Loxoprofen","Succimer","Eugenol","Benzamide","Benzenesulfonamide","Salvianolic acid B","(20S)-Protopanaxadiol"]
[null,"e","Empty","S4649","S4660","S4669","S4683","S4693","S4707","S4716","S4726","S4736","S4747","Empty"]
[{"$nulls":3},"Atipamezole hydrochloride","Glycopyrrolate","Benzocaine hydrochloride","Sildenafil Mesylate","Guanfacine Hydrochloride","Oleic Acid","Evans Blue","Lauric Acid","Trapidil","Jervine"]
[null,"f","Empty","S4650","S4661","S4672","S4685","S4695","S4708","S4717","S4727","S4737","S4748","Empty"]
[{"$nulls":3},"Atipamezole","Tiagabine hydrochloride","Dimenhydrinate","Efavirenz","D panthenol","Palmitoylethanolamide","Isatin","Cinnarizine","Psoralen","Ondansetron Hydrochloride Dihydrate"]
[null,"g","Empty","S4651","S4662","S4673","S4686","S4696","S4709","S4718","S4728","S4738","S4749","Empty"]
[{"$nulls":3},"Etoricoxib","Atazanavir","Etonogestrel","Vitamin E","CarbinoxaMine Maleate","Latanoprost","Acetylcholine iodide","3,3'-Diindolylmethane","Arctiin","Citalopram HBr"]
[null,"h","Empty","S4652","S4663","S4674","S4687","S4697","S4710","S4719","S4731","S4739","S4750","Empty"]
[{"$nulls":3},"Sulisobenzone","Fusidate Sodium","Hydroxyprogesterone caproate","Rivastigmine","Saxagliptin hydrate","Picolinamide","Kynurenic acid","Perphenazine","Oxyresveratrol","Sulfacetamide sodium salt hydrate"]
[]
[]
[]
[null,"Plate layout: L1700-28"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4751","S4762","S4771","S4781","S4790","S4804","S4816","S4834","S4844","S4852","Empty"]
[{"$nulls":3},"Cisapride hydrate","2,4-Dihydroxyacetophenone","β-thujaplicin","Xanthoxyline","3-Hydroxyflavone","1-Naphthyl acetate","Diatrizoate sodium","Propantheline bromide","Cefcapene Pivoxil Hydrochloride","Gadopentetate Dimeglumine"]
[null,"b","Empty","S4752","S4763","S4772","S4782","S4792","S4805","S4817","S4835","S4845","S4853","Empty"]
[{"$nulls":3},"Corticosterone (NSC-9705)","4-Hydroxychalcone","alpha-Asarone","5-methoxyflavone","N-Acetylneuraminic acid","Carboxine","Atenolol","Aceclofenac","Rabeprazole","Ecabet sodium"]
[null,"c","Empty","S4753","S4764","S4774","S4783","S4793","S4806","S4819","S4836","S4846","S4854","Empty"]
[{"$nulls":3},"Ganoderic acid A","Melezitose","Xanthurenic Acid","Benzyl isothiocyanate","Cedryl acetate","Potassium 1-Naphthaleneacetate","Saccharin","Nilutamide","Meropenem Trihydrate","Bedaquiline fumarate"]
[null,"d","Empty","S4754","S4765","S4775","S4784","S4797","S4807","S4820","S4837","S4847","S4856","Empty"]
[{"$nulls":3},"Betulin","Syringaldehyde","Cortodoxone","Phloracetophenone","Nicergoline","Uracil 1-β-D-arabinofuranoside","Diastase","Ibudilast","Faropenem Sodium","Iproniazid"]
[null,"e","Empty","S4758","S4766","S4777","S4785","S4799","S4809","S4830","S4838","S4848","S4858","Empty"]
[{"$nulls":3},"Crocin","Gibberellic acid","Plumbagin","Nicotinamide N-oxide","Indole-3-acetic acid","3-Indolepropionic acid","Maltose","Acotiamide hydrochloride","Dalbavancin","Tryptophol"]
[null,"f","Empty","S4759","S4767","S4778","S4787","S4801","S4812","S4831","S4839","S4849","S4859","Empty"]
[{"$nulls":3},"p-Coumaric Acid","7-Hydroxy-3,4-dihydrocarbostyril","o-Veratraldehyde","Methyl syringate","6-Chloropurine","Ceftizoxime","Piperonyl butoxide","Mosapride","Levocetirizine Dihydrochloride","TriacetonaMine"]
[null,"g","Empty","S4760","S4768","S4779","S4788","S4802","S4813","S4832","S4841","S4850","S4860","Empty"]
[{"$nulls":3},"(2-Hydroxypropyl)-β-cyclodextrin (HP-β-CD)","Melibiose","Menadiol Diacetate","L-α-Phosphatidylcholine","6-Methylcoumarin","Cefuroxime axetil","Tolmetin","Laurocapram","Flucloxacillin sodium","Indole-3-carboxylic acid"]
[null,"h","Empty","S4761","S4769","S4780","S4789","S4803","S4815","S4833","S4843","S4851","S4861","Empty"]
[{"$nulls":3},"Thymoquinone","L-5-Hydroxytryptophan","7-Methoxy-4-methylcoumarin","5-Acetylsalicylic acid","Thymidine (NSC 21548)","L-Cysteine HCl","Cefoxitin sodium","Potassium acetate","Tafluprost","Oxindole"]
[]
[]
[]
[null,"Plate layout: L1700-29"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4862","S4871","S4880","S4890","S4899","S4921","S4938","S4952","S4961","S4973","Empty"]
[{"$nulls":3},"Squalene","Pyridoxal 5-phosphate monohydrate","Cefathiamidine","Bifendate","Sulfogaiacol","MNS (3,4-Methylenedioxy-β-nitrostyrene)","Cedrol","Fumaric acid","3,4,5-Trimethoxycinnamic acid","Iminostilbene"]
[null,"b","Empty","S4864","S4872","S4881","S4891","S4900","S4926","S4939","S4953","S4963","S4975","Empty"]
[{"$nulls":3},"2-Furoic acid","Titanium tetrafluoride","Calcium Dobesilate","1-Aminohydantoin Hydrochloride","Tenovin-6","(R)-Nepicastat HCl","cis-Aconitic acid","Usnic acid","Purpurin","Fimasartan"]
[null,"c","Empty","S4865","S4873","S4882","S4892","S4901","S4927","S4940","S4955","S4964","S4976","Empty"]
[{"$nulls":3},"Cefetamet pivoxil hydrochloride","Dicyclanil","Resorantel","Phenibut","JNK-IN-8","Cyclen","Maltol","Acetosyringone","Lactobionic acid","Sulfalene (SMPZ)"]
[null,"d","Empty","S4866","S4874","S4883","S4893","S4902","S4931","S4941","S4956","S4965","S4977","Empty"]
[{"$nulls":3},"Nicarbazin","Cefazedone","Lynestrenol","Cytosine","QNZ (EVP4593)","Propiverine hydrochloride","Farnesol","Benzamidine HCl","Helecin","Efonidipine"]
[null,"e","Empty","S4867","S4875","S4884","S4894","S4904","S4932","S4942","S4957","S4966","S4978","Empty"]
[{"$nulls":3},"Propacetamol hydrochloride","Cephapirin Benzathine","Trans-Zeatin","D-Glucurone","JZL184","Proxyphylline","4-Hydroxy-3,5-dimethoxybenzyl alcohol","Linalool","4-Methylesculetin","Azathramycin"]
[null,"f","Empty","S4868","S4876","S4885","S4896","S4907","S4935","S4943","S4958","S4969","S4980","Empty"]
[{"$nulls":3},"Xanthinol Nicotinate","Robenidine Hydrochloride","Taurolidine","Elagolix Sodium","SC-514","Asunaprevir (BMS-650032)","Isovanillin","Glycocholic acid","Tropine","Anamorelin"]
[null,"g","Empty","S4869","S4877","S4886","S4897","S4908","S4936","S4946","S4959","S4970","S4981","Empty"]
[{"$nulls":3},"Sulfamethoxazole sodium","Eperisone hydrochloride","Menbutone","Nortropine Hydrochloride","SN-38","Antiarol","2,3-Dihydroxybenzoic acid","Skatole","Nerol","Cyclogalegenol"]
[null,"h","Empty","S4870","S4878","S4889","S4898","S4920","S4937","S4949","S4960","S4971","S4982","Empty"]
[{"$nulls":3},"Cefodizime Sodium","Neticonazole Hydrochloride","Perospirone hydrochloride","Sulfalozine sodium","b-AP15","4'-Hydroxychalcone","Nonanoic acid","Jasmone","Buparvaquone","2,2':5',2''-Terthiophene"]
[]
[]
[]
[null,"Plate layout: L1700-30"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S4983","S4994","S5003","S5013","S5025","S5038","S5047","S5059","S5070","S5079","Empty"]
[{"$nulls":3},"Sorbic acid","Methylcobalamin","Tacrolimus (FK506)","Ioversol","Efinaconazole","Valethamate Bromide","Methyl α-D-mannopyranoside","Pixantrone Maleate","Mupirocin calcium","Sitagliptin"]
[null,"b","Empty","S4984","S4995","S5004","S5014","S5027","S5040","S5049","S5060","S5071","S5081","Empty"]
[{"$nulls":3},"2,2'-Cyclouridine","Nicotinic acid N-oxide","Pimecrolimus","Crisaborole (AN2728)","Mebeverine Hydrochloride","Tiamulin","Thiocolchicoside","Metadoxine","Duloxetine","Ceforanide"]
[null,"c","Empty","S4985","S4996","S5005","S5015","S5029","S5041","S5052","S5062","S5073","S5082","Empty"]
[{"$nulls":3},"Dimethyl 4-Hydroxyisophthalate","Tavaborole (AN-2690)","Cefotiam hydrochloride","Simeprevir (TMC435)","Etofylline","Difloxacin hydrochloride","Granisetron","Daclatasvir Dihydrochloride","Donepezil","Vitamin K2"]
[null,"d","Empty","S4988","S4997","S5006","S5016","S5030","S5042","S5053","S5063","S5074","S5083","Empty"]
[{"$nulls":3},"Tiamulin fumarate","4-Butylresorcinol","Teprenone","Isoprinosine","Dihydralazine sulphate","Bevantolol hydrochloride","Imazalil","Trelagliptin succinate","Argatroban Monohydrate","Lentinan"]
[null,"e","Empty","S4989","S4998","S5007","S5017","S5032","S5043","S5054","S5065","S5075","S5084","Empty"]
[{"$nulls":3},"AOA hemihydrochloride","2-Aminobenzenesulfonamide","Delamanid","Oxyclozanide","Mephenesin","Benorylate","Rifamycin sodium salt","Ganciclovir sodium","Acotiamide","Carbazochrome"]
[null,"f","Empty","S4990","S4999","S5009","S5019","S5033","S5044","S5055","S5066","S5076","S5085","Empty"]
[{"$nulls":3},"TBHQ","Avermectin B1","Brivudine","Indobufen","Terconazole","Isoxepac","Milbemycin Oxime","Pramipexole dihydrochloride","Xipamide","Azamethiphos"]
[null,"g","Empty","S4991","S5001","S5010","S5020","S5034","S5045","S5056","S5067","S5077","S5086","Empty"]
[{"$nulls":3},"Valpromide","Tofacitinib (CP-690550) Citrate","Indometacin Sodium","Tilorone dihydrochloride","Melitracen hydrochloride","Nomilin","Dinoprost tromethamine","Losartan","Regorafenib (BAY-734506) Monohydrate","p-Anisaldehyde"]
[null,"h","Empty","S4992","S5002","S5012","S5023","S5037","S5046","S5058","S5069","S5078","S5088","Empty"]
[{"$nulls":3},"Nanofin","Fingolimod (FTY720) HCl","Octenidine Dihydrochloride","Nadolol","Phenazine methosulfate","Clonixin","Revaprazan Hydrochloride","Dabrafenib Mesylate","Osimertinib mesylate","Labetalone hydrochloride"]
[]
[]
[]
[null,"Plate layout: L1700-31"]
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[{"$nulls":3},"4-Isopropylbenzaldehyde","Tabersonine hydrochloride","7-Ethylcamptothecin","Aleuritic Acid","Citral","1,3,5-Trimethylpyrazole","alpha-Naphthoflavone","Benzyl cinnamate","Naproxen","Nilotinib hydrochloride"]
[null,"b","Empty","S5090","S5102","S5112","S5127","S5139","S5148","S5159","S5168","S5178","S5206","Empty"]
[{"$nulls":3},"4-Isopropylbenzyl Alcohol","stachyose tetrahydrate","alpha-Arbutin","Spiculisporic Acid","Methyl Dihydrojasmonate","2-Methylenebutyrolactone","Doxycycline","Anthraquinone","4-Hydroxy-2,5-dimethyl-3(2H)furanone","Benzylpenicillin potassium"]
[null,"c","Empty","S5091","S5104","S5113","S5128","S5141","S5151","S5160","S5169","S5179","S5208","Empty"]
[{"$nulls":3},"Geranyl acetate","Tea polyphenol","Propyl gallate","Orsellinic acid ethyl ester","Pyrithioxin","Gypenoside","4-Methoxysalicylic acid","2,6-Dihydroxyanthraquinone","Ropivacaine Mesilate","Ciprofloxacin hydrochloride hydrate"]
[null,"d","Empty","S5092","S5105","S5114","S5130","S5142","S5153","S5162","S5171","S5182","S5209","Empty"]
[{"$nulls":3},"Febantel","Proanthocyanidins","Hydroquinine","Taurocholic acid sodium salt hydrate","D-(+)-Melezitose","Tetrahydroberberine","Isovanillic acid","Atrazine","GSK4112","Enoxacin Sesquihydrate"]
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[{"$nulls":3},"Rafoxanide","Lanolin","Doramectin","Casanthranol","Citropten","Tetrahydropiperine","7-Methoxycoumarin","2'-Hydroxy-4'-methylacetophenone","Diaveridine","Sulfamethazine Sodium Salt"]
[null,"f","Empty","S5094","S5108","S5120","S5133","S5144","S5155","S5164","S5174","S5201","S5211","Empty"]
[{"$nulls":3},"Maduramycin Ammonium","Tylosin","Elemicin","Sodium erythorbate","Neferine","Raffinose","Chlorotetracycline","Kojic acid","Acetylisovaleryltylosin Tartrate","4-Aminosalicylic acid"]
[null,"g","Empty","S5096","S5109","S5121","S5134","S5145","S5156","S5165","S5175","S5202","S5212","Empty"]
[{"$nulls":3},"SulfadiMethoxine sodium","Ademetionine","Phytol","D(-)-Arabinose","Protoporphyrin IX","4-Methoxysalicylaldehyde","Solvent Red 23","(-)-Ambroxide","Quinocetone","Imidazolidinyl Urea"]
[null,"h","Empty","S5100","S5110","S5122","S5135","S5146","S5157","S5166","S5176","S5203","S5213","Empty"]
[{"$nulls":3},"Pralidoxime Iodide","Safflower Yellow","Abietic Acid","Hydroferulic acid","3-Methylpyrazole","Thymol","Benzoyleneurea","Fructose","Sulbutiamine","Piroctone Olamine"]
[]
[]
[]
[null,"Plate layout: L1700-32"]
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[{"$nulls":3},"Imidocarb dipropionate","Isosorbide dinitrate","Lenvatinib (E7080) Mesylate","Cisapride (R 51619)","TBB","Tedizolid (TR-700)","Estropipate","Amoxicillin trihydrate","PSI-6206 (GS-331007)","PRT4165"]
[null,"b","Empty","S5215","S5230","S5241","S5254","S5266","S5279","S5289","S5299","S5308","S5316","Empty"]
[{"$nulls":3},"Abacavir (1592U89)","Elubiol","Lapatinib ditosylate monohydrate","Dasatinib hydrochloride","Stiripentol","Fendiline hydrochloride","Ceftezole","Tosufloxacin p-Toluenesulfonate Hydrate","7-(Diethylamino)coumarin-3-carboxylic acid","NU2058"]
[null,"c","Empty","S5217","S5233","S5242","S5255","S5268","S5281","S5291","S5301","S5309","S5317","Empty"]
[{"$nulls":3},"Arformoterol Tartrate","Fenretinide (NSC 374551)","Cediranib Maleate","Nicardipine","Solithromycin","Dapiprazole Hydrochloride","sulfaisodimidine","Carglumic Acid","Propyphenazone (4-Isopropylantipyrine)","UK 5099"]
[null,"d","Empty","S5221","S5234","S5243","S5256","S5269","S5282","S5292","S5302","S5310","S5318","Empty"]
[{"$nulls":3},"Diludine","Nintedanib Ethanesulfonate Salt","Ruxolitinib Phosphate","Benproperine phosphate","J147","Lactitol monohydrate","Diazolidinyl urea","6-Methoxy-2-naphthoic acid","4,4'-Dimethoxybenzil","Acacetin"]
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[{"$nulls":3},"Coluracetam","β-Estradiol 17-Acetate","Raltegravir potassium","Doxapram","Suloctidil","TMB-PS","Nimustine Hydrochloride","Afalanine (N-Acetyl-DL-phenylalanine)","Pyridoxal phosphate","Imepitoin"]
[null,"f","Empty","S5224","S5237","S5246","S5258","S5273","S5284","S5294","S5304","S5312","S5320","Empty"]
[{"$nulls":3},"Adrafinil","Dihydroartemisinic acid","Entecavir","Revefenacin","Canrenone","Adenosine 5'-monophosphate monohydrate","Cephalotin acid","2-Acetylphenothiazine (ML171)","Urolithin A","Octinoxate"]
[null,"g","Empty","S5227","S5238","S5247","S5261","S5274","S5285","S5295","S5305","S5313","S5321","Empty"]
[{"$nulls":3},"Erythromycin thiocyanate","Solifenacin (YM905)","Selamectin","Ufenamate","GS967","RU58841","Lincomycin Hydrochloride Monohydrate","Bromisoval","SC66","Y15"]
[null,"h","Empty","S5228","S5239","S5250","S5262","S5277","S5286","S5297","S5306","S5314","S5322","Empty"]
[{"$nulls":3},"Minoxidil sulphate","Paroxetine mesylate","Darunavir","UNC-926","INCB032304","Ramatroban","Vidarabine monohydrate","Forchlorfenuron (CPPU)","HTHQ (1-O-Hexyl-2,3,5-trimethylhydroquinone)","Sodium gualenate"]
[]
[]
[]
[null,"Plate layout: L1700-33"]
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[{"$nulls":3},"Nitisinone","Corey Lactone Diol","2-Phenylethylamine","Safinamide","Fipronil","γ-Decalactone","Imidafenacin","Cyclofenil","Tegaserod Maleate","Chloramphenicol sodium succinate"]
[null,"b","Empty","S5326","S5337","S5348","S5358","S5367","S5376","S5386","S5394","S5402","S5411","Empty"]
[{"$nulls":3},"Dolasetron","Rauwolscine hydrochloride","Pherocon (4-(4-Acetoxyphenyl)-2-butanone)","Regadenoson","Ethyl Oleate","Decyl aldehyde","7-Dehydrocholesterol","Tizoxanide","Dasabuvir (ABT-333)","Sultamicillin"]
[null,"c","Empty","S5327","S5339","S5349","S5359","S5368","S5377","S5387","S5395","S5403","S5413","Empty"]
[{"$nulls":3},"Meisoindigo","4-Allylanisole","Ethyl chrysanthemumate","Butoconazole","Lactitol","Dibutyl phthalate","D-Tagatose","Phenolphthalein","Ombitasvir (ABT-267)","Ertugliflozin"]
[null,"d","Empty","S5328","S5341","S5350","S5360","S5369","S5378","S5388","S5396","S5404","S5414","Empty"]
[{"$nulls":3},"Gamithromycin","Metroprolol succinate","Cefpodoxime proxetil","Diflorasone","Ethoxyquin","Dimethyl phthalate","Betrixaban","4'-Hydroxypropiophenone","Paritaprevir (ABT-450)","Diflucortolone valerate"]
[null,"e","Empty","S5329","S5342","S5351","S5361","S5370","S5379","S5389","S5397","S5405","S5416","Empty"]
[{"$nulls":3},"FAAH-IN-2","Dihydrojasmone","Cefmetazole sodium","Bendazac","10-Hydroxydecanoic acid","Fenchyl Alcohol","Betrixaban maleate","Chlorhexidine","Propylparaben","Metyrapone"]
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[{"$nulls":3},"Ceftezole sodium","Vanillic acid","Cefminox Sodium","Pikamilone","Ajmaline","7-Hydroxyflavone","N-(Hytroxymethy)micotinamide","Nefazodone hydrochloride","Sultamicillin Tosylate","Parecoxib Sodium"]
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[{"$nulls":3},"Cefquinome sulfate","(+/-)-nerolidol","Cefpiramide sodium","DY131","Methyl Aminolevulinate Hydrochloride","Behenic Acid","α-Boswellic acid","Chlorprothixene hydrochloride","Squalane","1,4-Cineole"]
[null,"h","Empty","S5333","S5346","S5356","S5365","S5373","S5383","S5392","S5400","S5409","S5420","Empty"]
[{"$nulls":3},"Sulbenicillin Sodium","2-Phenylethylamine hydrochloride","Ceftiofur","Alogliptin","Pseudolaric Acid B","Erucic acid","Mepivacaine","3-chloro-5-hydroxybenzoic Acid","Chelidamic acid hydrate","Clindamycin alcoholate"]
[]
[]
[]
[null,"Plate layout: L1700-34"]
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[{"$nulls":3},"Fluoroquinolonic Acid","Dibenamine Hydrochloride","1-Naphthyl phosphate potassium salt","Ferulic acid methyl ester","Aucubin","Asarinin","Gefarnate","Desipramine Hydrochloride","Salbutamol","2’-deoxyuridine"]
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[{"$nulls":3},"Trimethyloctadecylammonium bromide","AS057278","BSTFA-TMCS","Sanguinarine chloride","Vitexin-2-O-rhaMnoside","Bavachin","Dantrolene sodium","Fluorometholone","Iopanoic acid","Trimebutine maleate"]
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[{"$nulls":3},"4-Chloro-2-(trifluoroacetyl)aniline hydrochloride","Quinacrine Dihydrochloride Dihydrate","4-Bromo-3-hydroxybenzoic acid","Hyperoside","Cimicifugoside","Monotropein","Cloperastine hydrochloride","Cefoperazone sodium","Betahistine mesylate","DMNB"]
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[{"$nulls":3},"Carbaryl","2-Hydroxycaprylic acid","AMI-1 (free acid)","Saikosaponin D","5-O-Methylvisammioside","Nafronyl oxalate salt","Clidinium Bromide","Fluorescein","Amodiaquine hydrochloride","Ethyl (triphenylphosphoranylidene) acetate"]
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[{"$nulls":3},"Phenylglyoxal hydrate","4,4'-DDE","2-Chloro-1-(4-fluorobenzyl)benzimidazole","Akebia saponin D","Curcurbitacin IIA","Pivmecillinam hydrochloride","Molindone hydrochloride","Disopyramide","Hydrocortisone acetate","Lanthanum(III) chloride heptahydrate"]
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[{"$nulls":3},"Bromopyruvic acid","Biphenyl-4-sulfonyl chloride","Triprolidine Hydrochloride","Isobavachalcone","Psoralidin","Dibenzoyl Thiamine","Prilocaine hydrochloride","Lomefloxacin","Ilaprazole sodium","Penicillin G Procaine"]
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[{"$nulls":3},"Promazine hydrochloride","5-Bromoindole","3-Methoxybenzamide","Curculigoside","Morroniside","Novaluron","Tribenzagan Hydrochloride","Econazole","O-Acetyl-L-carnitine hydrochloride","Fenamic acid"]
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[{"$nulls":3},"Metoprolol","Berberine Sulfate","Sofalcone","Verbascoside","Saikosaponin A","Rolapitant","Rimantadine Hydrochloride","Atropine sulfate","Ropivacaine","4-Methylsalicylic acid"]
[]
[]
[]
[null,"Plate layout: L1700-35"]
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[{"$nulls":3},"Phenidone","Doripenem","7-Nitroindazole","Amenamevir","Midecamycin","Tocofersolan","Olmesartan","(1S)-(-)-α-Pinene","Sulfamide","Betahistine"]
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[{"$nulls":3},"Eosin Y Disodium","Erythromycin estolate","1, 10-Phenanthroline monohydrate","Kasugamycin hydrochloride","Ethacrynic Acid","Arachidic acid","Cytarabine hydrochloride","(1R)-(-)-Menthyl acetate","4,4'-Bis(4-aminophenoxy)biphenyl","NSI-189"]
[null,"c","Empty","S5522","S5535","S5544","S5554","S5562","S5573","S5583","S5599","S5609","S5621","Empty"]
[{"$nulls":3},"H-Cys(Trt)-OH","Moxifloxacin","D-Ribose","Lanatoside C","2-Hydroxybenzyl alcohol","Tilmicosin phosphate","Cinnamyl acetate","Sodium cholate","Chicago Sky Blue 6B","Cilastatin"]
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[{"$nulls":3},"SodiuM Metatungstate","Tizanidine","Sulfacetamide","Pamabrom","Thioridazine hydrochloride","Benzoic aldehyde","Citronellal","Flavokawain A","Indole-3-acetamide","Prohydrojasmon"]
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[{"$nulls":3},"Salmeterol","Tropisetron","Hydroxylammonium chloride","(-)-Sparteine Sulfate","Xylazine","2-Benzoxazolinone","3-Hydroxycinnamic acid","Gallocyanine","2-Thiohydantoin","Bedaquiline"]
[null,"f","Empty","S5528","S5539","S5548","S5557","S5565","S5576","S5592","S5603","S5614","S5625","Empty"]
[{"$nulls":3},"Acetophenone","Olprinone","7-Hydroxy-4-chromone","Aklomide","Triflupromazine hydrochloride","Benzyl acetate","Vitamin A","5-Bromocytosine","(+)-Longifolene","Ammonium lactate"]
[null,"g","Empty","S5529","S5540","S5550","S5558","S5566","S5579","S5594","S5604","S5616","S5626","Empty"]
[{"$nulls":3},"Galangin","Landiolol hydrochloride","Ethyl gallate","D-Pantothenate Sodium","Dapagliflozin propanediol monohydrate","Chelidonic acid","(-)-(S)-α-terpineol","Diphenylamine Hydrochloride","4-Methylcatechol","Benzalkonium chloride"]
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[{"$nulls":3},"Geraniol","Dimetridazole","6-Paradol","(+/-)-tetrahydropalmatine","Trimethadione","Arabic gum","3-Carene","Tos-Arg-OMe HCl","Hippuric acid","Amsacrine hydrochloride"]
[]
[]
[]
[null,"Plate layout: L1700-36"]
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[{"$nulls":3},"Methyl furan-2-carboxylate","Hydroxyzine pamoate","Omeprazole Sodium","Fruquintinib (HMPL-013)","Dolasetron Mesylate","Tropolone (NSC 89303)","Phthalylsulfathiazole","Deracoxib","Glecaprevir","Fosfosal"]
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[{"$nulls":3},"Cefotiam Hexetil Hydrochloride","Dexrazoxane","Emedastine","Chlorindione","(-)-Verbenone","Triacanthine","Alvimopan dihydrate (LY246736 dihydrate)","Pravastatin","Oxantel Pamoate","Alimemazine Tartrate"]
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[{"$nulls":3},"Cefozopran hydrochloride","Elbasvir","Tiaprofenic acid","Isoxsuprine hydrochloride","Methyl linolenate","Terpinyl Acetate","Fenipentol","lurasidone","Carvedilol EP IMpurity E","Glyceryl tridecanoate"]
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[{"$nulls":3},"Ethyl caffeate","Indigo carmine","Ranitidine","Chloropyramine hydrochloride","Isoproterenol sulfate dihydrate","Mexenone","Carvedilol Phosphate","Atorvastatin","Dichlorophen","Sebacic acid"]
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[{"$nulls":3},"Rhodamine B","Indacaterol","Minaprine dihydrochloride","Hydroxyhexamide","Lapachol","Levomilnacipran Hydrochloride","Myclobutanil","Abemaciclib (LY2835219)","Pempidine","Stearic acid"]
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[{"$nulls":3},"Homovanillic acid","Venlafaxine","Orphenadrine Hydrochloride","Mivacurium chloride","Desoximetasone","JNJ0966","Raceanisodamine","Acetohexamide","Triiodothyronine","Midodrine hydrochloride"]
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[{"$nulls":3},"Emedastine Difumarate","Diphenylpyraline hydrochloride","Drofenine Hydrochloride","Zearalenone","Tryptanthrin","Isopropamide Iodide","Norgestrel","Acrivastine","Tetryzoline","Midodrine"]
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[{"$nulls":3},"Iguratimod","Ertapenem sodium","Moxisylyte hydrochloride","trans-Zeatin-riboside","Tropinone","Ketorolac tromethamine salt","Ambroxol","Ceftizoxime sodium","Delapril Hydrochloride","Benzathine penicilline"]
[]
[]
[]
[null,"Plate layout: L1700-37"]
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[{"$nulls":3},"Diclofenac Epolamine","4′-Deoxyphlorizin","Isoeugenol","Sodium Dehydrocholate","SR1078","Vancomycin","Alda 1","UF010","MRE-269 (ACT-333679)","L-Xylose"]
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[{"$nulls":3},"Nebivolol","Chlorpromazine","2-Methoxycinnamic acid","Alfuzosin","Proflavine","Dronedarone","Alprenolol hydrochloride","Kevetrin hydrochloride","Linoleic acid","Furfuryl acetate"]
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[{"$nulls":3},"Palonosetron","DL-Norepinephrine hydrochloride","Methyl linoleate","Aliskiren","Esmolol","Cyclic Pifithrin-α hydrobromide","Alrestatin","Choline Fenofibrate","Butyl benzyl phthalate","Pyrrole-2-carboxylic acid"]
[null,"d","Empty","S5741","S5752","S5760","S5768","S5779","S5792","S5804","S5814","S5823","S5833","Empty"]
[{"$nulls":3},"Quetiapine","Abametapir","6-Chloro-7-hydroxy-4-methylcoumarin","Fenoterol hydrobromide","Trimetazidine","CID 2011756","N-Acetylcysteine amide","cariporide","L-Pyroglutamic acid","Methyl Nonadecanoate"]
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[{"$nulls":3},"Deferoxamine mesylate (Ba 33112)","Setipiprant (ACT-129968)","Citric acid","Fenoterol","Prazosin","Motesanib (AMG-706)","Allopregnanolone","WAY-316606","Cinnamyl alcohol","p-Coumaric acid ethyl ester"]
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[{"$nulls":3},"γ-Linolenic acid","Baricitinib phosphate","Methyl Oleate","Sulforaphane","Raloxifene","Glycochenodeoxycholic acid","Cilostamide","Pyrvinium","Monobutyl phthalate","3-(4-Hydroxyphenyl)-1-propanol"]
[null,"g","Empty","S5744","S5755","S5763","S5772","S5782","S5795","S5807","S5817","S5827","S5836","Empty"]
[{"$nulls":3},"Spiramycin I","Methyl Eugenol","D-Mannose","AS-8351","Doxazosin","Rasagiline","HMN-176","GSK0660","Citronellyl acetate","IBMX"]
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[{"$nulls":3},"Morantel tartrate","Methyl Stearate","YM 90709","CY-09","Montelukast","Vanoxerine dihydrochloride","Relugolix","acalisib (GS-9820)","Monomyristin","BRL-50481"]
[]
[]
[]
[null,"Plate layout: L1700-38"]
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[{"$nulls":3},"SDMA","Ethacrynate Sodium","Lercanidipine","D-Carnitine hydrochloride","Suberohydroxamic acid","GSK 5959","Olodaterol hydrochloride","K 858","Argireline","Imidazole"]
[null,"b","Empty","S5839","S5848","S5862","S5885","S5906","S5917","S5926","S5935","S5948","S6007","Empty"]
[{"$nulls":3},"L-Kynurenine","Frovatriptan Succinate","Metoclopramide","Rabeprazole Related Compound E","2,4-Pyridinedicarboxylic acid","Solcitinib","Pitolisant hydrochloride","Alvimopan","Amodiaquine","Bisphenol A"]
[null,"c","Empty","S5840","S5851","S5863","S5886","S5907","S5918","S5927","S5936","S5950","S6008","Empty"]
[{"$nulls":3},"Palifosfamide","4'-Methoxychalcone","Metronidazole Benzoate","Hodostin","5-Methyl-2'-deoxycytidine","CAY10602","Proguanil","Cefazolin","Fingolimod","p-Hydroxybenzaldehyde"]
[null,"d","Empty","S5841","S5853","S5868","S5887","S5909","S5919","S5928","S5938","S5951","S6009","Empty"]
[{"$nulls":3},"DKM 2-93","2'-Hydroxy-2-methoxychalcone","DL-Menthol","Khellin","Anagliptin","KHS101 hydrochloride","Zerumbone","Benazepril","Cefoxitin","1-Phenyl-1,2-propanedione"]
[null,"e","Empty","S5842","S5854","S5869","S5900","S5911","S5920","S5929","S5939","S5952","S6010","Empty"]
[{"$nulls":3},"Cabergoline","Xylometazoline","Cortisone","Edrophonium chloride","Bictegravir","CA-5f","4-Octyl Itaconate","Bendamustine (SDX105)","Baloxavir marboxil","Sodium L-lactate"]
[null,"f","Empty","S5843","S5857","S5871","S5901","S5913","S5921","S5930","S5940","S6002","S6011","Empty"]
[{"$nulls":3},"Cinitapride Hydrogen Tartrate","Trazodone","Trans-Tranilast","Canagliflozin hemihydrate","Cambinol","Cyclopentolate Hydrochloride","PNU 282987 HCl","Bepotastine","Disufenton sodium","Acetamide"]
[null,"g","Empty","S5845","S5858","S5872","S5903","S5914","S5923","S5931","S5943","S6003","S6012","Empty"]
[{"$nulls":3},"Chalcone","Vilazodone","Estradiol dipropionate","JANEX-1","AK 7","Celiprolol hydrochloride","BQCA","Bromhexine","Ataluren (PTC124)","Methyloxalacetic acid diethyl ester"]
[null,"h","Empty","S5846","S5859","S5873","S5904","S5915","S5924","S5932","S5944","S6005","S6014","Empty"]
[{"$nulls":3},"Apocarotenal","Sancycline","Scopolamine HBr trihydrate","WHI-P97","OAC2","Olanexidine Hydrochloride semihydrate","BIA 10-2474","Butenafine","VX-702","Isonicotinic acid"]
[]
[]
[]
[null,"Plate layout: L1700-39"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6015","S6029","S6040","S6049","S6059","S6072","S6089","S6099","S6113","S6124","Empty"]
[{"$nulls":3},"Benzylcetyldimethylammonium chloride hydrate","4-Methyl-n-octanoic Acid","2,3-Butanediol (mixture of isomers)","(+)-(S)-Carvone","cis-3-Hexen-1-ol","Monomethyl glutarate","3-Methylvaleric acid","2-Methylheptanoic Acid","Tridecanoic acid","3-Hydroxyisovaleric acid"]
[null,"b","Empty","S6018","S6030","S6041","S6050","S6063","S6073","S6091","S6101","S6114","S6125","Empty"]
[{"$nulls":3},"2,3,4-Trihydroxybenzoic acid","3-(3-Methoxyphenyl)propionic acid","Dibutyl sebacate","1,3-Dimethyluracil","1,11-Undecanedicarboxylic acid","Diclofenac acid","Glycodeoxycholic acid sodium salt","Solvent Blue 35","D-Arabitol","Glycerol trilinoleate"]
[null,"c","Empty","S6020","S6031","S6042","S6051","S6065","S6074","S6092","S6104","S6115","S6127","Empty"]
[{"$nulls":3},"Potassium thioacetate","2,6-Dihydroxybenzoic acid","Trimethylamine N-oxide dihydrate","Phenyl-ac-Gly-OH","Congo Red","3-(3-Hydroxyphenyl)propionic Acid","cis,cis-Muconic acid","(±)-α-Tocopherol","Pyridoxal 5′-phosphate hydrate","5-Hydroxymethyluracil"]
[null,"d","Empty","S6022","S6032","S6043","S6052","S6066","S6076","S6094","S6105","S6118","S6131","Empty"]
[{"$nulls":3},"Cyclohexaneacetic acid","2-Aminobenzenesulfonic acid","3-Indoleacetonitrile","Saccharin sodium salt hydrate","Methyl 4-aminobutyrate HCl","Phenylacetylglutamine","Imidazole-4(5)-acetic Acid Hydrochloride","trans-3-Indoleacrylic acid","Terpinen-4-ol","2-Oxo-3-phenylpropanoic acid"]
[null,"e","Empty","S6024","S6033","S6045","S6053","S6067","S6079","S6095","S6107","S6119","S6132","Empty"]
[{"$nulls":3},"Ethyl acetoacetate","Azo Rubine","L-Arabinitol","Phenylglyoxylic acid","2,4-dichlorobenzyl alcohol","2-Methylhexanoic acid","Quinoline-4-carboxylic acid","1-Furfurylpyrrole","2-Hydroxybutyric acid","All trans-Retinal"]
[null,"f","Empty","S6025","S6035","S6046","S6055","S6068","S6081","S6096","S6110","S6121","S6136","Empty"]
[{"$nulls":3},"3-Methoxybenzoic acid","2-Naphthol","(S)-Leucic acid","(S)-(−)-Limonene","Doxycycline monohydrate","5-Hydroxymethyl-2-furancarboxylic acid","5-Phenylvaleric Acid","2-Methylpentanedioic acid","Maltotriose","(±)-α-Bisabolol"]
[null,"g","Empty","S6027","S6037","S6047","S6057","S6069","S6083","S6097","S6111","S6122","S6138","Empty"]
[{"$nulls":3},"D-(−)-Pantolactone","Methyl p-tert-butylphenylacetate","Lactose","2-Ethylbutyric Acid","trans-4-Hydroxycyclohexanecarboxylic Acid","DL-Dopa","3-Furoic acid","L-Hydroorotic acid","Cyclohexanecarboxamide","5-Methylcytidine"]
[null,"h","Empty","S6028","S6039","S6048","S6058","S6071","S6088","S6098","S6112","S6123","S6139","Empty"]
[{"$nulls":3},"α-D-Glucose anhydrous","4-Ethyloctanoic acid","3-Oxopentanedioic acid","β-Caryophyllene","3,5-Dimethoxyphenol","6-(Dimethylamino)purine","2-Hydroxy-3-methylbutanoic acid","Oxalacetic acid","DL-Benzylsuccinic acid","Piperonyl acetone"]
[]
[]
[]
[null,"Plate layout: L1700-40"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6140","S6155","S6164","S6173","S6185","S6204","S6217","S6229","S6243","S6254","Empty"]
[{"$nulls":3},"16-Dehydroprogesterone","L-Tryptophanamide Hydrochloride","(-)-Citronellal","Amylmetacresol","Arachidonic acid","Allyl Methyl Sulfide","o-Toluic acid","Lauryl gallate","Ethyl pyruvate","Hydrocinnamic acid"]
[null,"b","Empty","S6143","S6156","S6165","S6175","S6187","S6205","S6218","S6231","S6245","S6256","Empty"]
[{"$nulls":3},"Ureidopropionic acid","5-Methyluridine","Erythrosine B","1,5,5-Trimethylhydantoin","N-(5-Aminopentyl)acetamide","N-Acetyl-L-methionine","Sodium lauryl sulfate","Methyl nicotinate","N-Acetylglutamic acid","Isocytosine"]
[null,"c","Empty","S6144","S6157","S6167","S6178","S6188","S6207","S6219","S6232","S6247","S6257","Empty"]
[{"$nulls":3},"O-Acetylserine","Benzyldimethylstearylammonium Chloride Hydrate","2-Methyl-4-pentenoic Acid","DL-6,8-Thioctamide","p-Toluenesulfonic acid monohydrate","Levulinic acid","β-Alanine methyl ester hydrochloride","Methylamine hydrochloride","Senecioic acid","N-Acetylglucosamine"]
[null,"d","Empty","S6146","S6158","S6168","S6180","S6189","S6208","S6220","S6233","S6249","S6258","Empty"]
[{"$nulls":3},"Glycoursodeoxycholic acid","Acid orange 7","trans-trans-Muconic acid","L-Gulose","Acid Yellow 36","Diethyl malonate","Octanedioic acid","Tartaric acid","Picolinic acid (PCL 016)","1,2-Propanediol"]
[null,"e","Empty","S6147","S6159","S6169","S6181","S6190","S6209","S6221","S6234","S6250","S6259","Empty"]
[{"$nulls":3},"Hexadecanedioic acid","Food Yellow 3","3-Methyladipic acid","N-Isovaleroylglycine","Isethionic acid sodium salt","Diethyl succinate","Methyl cinnamate","Pentadecanoic acid","L-Lactic acid","Ureidosuccinic acid"]
[null,"f","Empty","S6148","S6160","S6170","S6182","S6191","S6210","S6223","S6235","S6251","S6260","Empty"]
[{"$nulls":3},"3-Methyl-2-oxobutanoic acid","3,5-Dihydroxybenzoic acid","Benzyldodecyldimethylammonium Chloride Dihydrate","L-Gulono-1,4-lactone","Sudan I","Ethanolamine hydrochloride","Triethyl citrate","Sodium dehydroacetate","Terephthalic acid","(S)-(−)-α-Methylbenzylamine"]
[null,"g","Empty","S6150","S6162","S6171","S6183","S6197","S6215","S6225","S6237","S6252","S6261","Empty"]
[{"$nulls":3},"Farnesyl Acetate (mixture of isomers)","2-Octenoic acid","trans-β-Hydromuconic acid","2-Hydroxy-2-methylbutanoic acid","Dimethylamine hydrochloride","Phthalic acid","10-Undecen-1-ol","2-Ketoglutaric acid","3-Hydroxypicolinic acid","2-Acetylpyrazine"]
[null,"h","Empty","S6152","S6163","S6172","S6184","S6202","S6216","S6228","S6241","S6253","S6262","Empty"]
[{"$nulls":3},"Acid Red 27","Traumatic acid","Brucine sulfate heptahydrate","N-Methylhydantoin","Butylated hydroxytoluene","1-Methylpyrrolidine","Indole-2-carboxylic acid","β-D-Glucose pentaacetate","H-D-Trp-OH","Ammonium formate"]
[]
[]
[]
[null,"Plate layout: L1700-41"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6263","S6274","S6284","S6295","S6308","S6320","S6335","S6348","S6403","S6412","Empty"]
[{"$nulls":3},"Glycerol Tributyrate","2-Methyltetrahydrofuran-3-one","Tetraethylammonium bromide","2-Methoxybenzoic acid","4-Ethylphenol","2,5-Furandicarboxylic acid","Ethyl maltol","(+)-Delta-Tocopherol","Chloramine-T","Altiratinib"]
[null,"b","Empty","S6264","S6275","S6285","S6296","S6309","S6321","S6338","S6349","S6404","S6413","Empty"]
[{"$nulls":3},"Rutin hydrate","(−)-β-Pinene","6-Hydroxynicotinic acid","Octanoic acid","Methylguanidine HCl","2-Phenylpropionic acid","3,4-Dihydroxyhydrocinnamic acid","NADH Disodium Salt Hydrate","Salicylamide","fexaramine"]
[null,"c","Empty","S6265","S6278","S6286","S6297","S6310","S6323","S6339","S6354","S6405","S6414","Empty"]
[{"$nulls":3},"γ-caprolactone","4-Methylvaleric acid","Tricarballylic acid","4-Hydroxy-3-methylbenzoic acid","N-(2-Acetamido)-2-Iminodiacetic acid","2,6-Dimethoxybenzoic acid","Black PN","Ac-Arg-OH","Octisalate","Apilimod (STA-5326)"]
[null,"d","Empty","S6267","S6279","S6287","S6298","S6311","S6324","S6341","S6355","S6407","S6415","Empty"]
[{"$nulls":3},"Dodecanedioic acid","Cyclohexanecarboxylic Acid","3-Methylbutanoic acid","2,5-Dimethyl-2,3-dihydrofuran-3-one","Dimethyl Trisulfide","5-Methoxytryptamine","3-(Methylthio)propionic acid","Glycochenodeoxycholic acid sodium salt","Tulobuterol hydrochloride","Azeliragon (TTP488)"]
[null,"e","Empty","S6268","S6280","S6288","S6299","S6314","S6326","S6342","S6356","S6408","S6416","Empty"]
[{"$nulls":3},"4-Pentenoic acid","Methyl 3-indolyacetate","Chlorhexidine diacetate","Methyl cyclohexanecarboxylate","Bis(2-methyl-3-furyl)disulphide","D-3-Phenyllactic acid","Glycerol Tri-n-octanoate","2-Methylsuccinic acid","Hexetidine","JNJ 31020028"]
[null,"f","Empty","S6269","S6281","S6292","S6300","S6316","S6327","S6343","S6357","S6409","S6417","Empty"]
[{"$nulls":3},"Leucomalachite green","Sodium Thiocyanate","(S)-2-Hydroxysuccinic acid","1,4-Dichlorobenzene","N-Acetyl-L-tyrosine","trans-2-Methyl-2-pentenoic Acid","D-Glucuronic acid","1,5-Diaminopentane dihydrochloride","Zucapsaicin","GK921"]
[null,"g","Empty","S6271","S6282","S6293","S6303","S6317","S6329","S6344","S6400","S6410","S6418","Empty"]
[{"$nulls":3},"(S)-2-Hydroxy-3-phenylpropanoic acid","1-Methyl-2-pyrrolidone","2,4-Dihydroxybenzoic acid","trans-2-Hexenal","2-Picolinic acid methyl ester","2-Oxobutanoic acid","Tetradecanedioic acid","Glucosamine","Clemizole","PF 429242"]
[null,"h","Empty","S6272","S6283","S6294","S6307","S6319","S6333","S6346","S6402","S6411","S6419","Empty"]
[{"$nulls":3},"Glycolic acid","3,3-Dimethylglutaric acid","1,3,5-Trimethoxybenzene","2-Methyllactic acid","5-Methoxysalicylic acid","Undecanedioic acid","L-(+)-Arabinose","2-Aminoethanethiol","Nimorazole","Omilancor (BT-11)"]
[]
[]
[]
[null,"Plate layout: L1700-42"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6420","S6429","S6440","S6451","S6461","S6471","S6487","S6499","S6509","S6520","Empty"]
[{"$nulls":3},"AGI 1067","Coniferyl alcohol","Halazone","Salifungin","Permethrin","Lucanthone","fluticasone furoate","PF-6260933","AG 494","WHI-P180"]
[null,"b","Empty","S6421","S6430","S6441","S6452","S6462","S6472","S6492","S6500","S6510","S6521","Empty"]
[{"$nulls":3},"Diroximel Fumarate","Nervonic acid","Riboflavin Tetrabutyrate","Delavirdine mesylate","Amezinium (methylsulfate)","Tinoridine hydrochloride","Doravirine (MK-1439)","KX1-004","Iso-H7 dihydrochloride","WHI-P258"]
[null,"c","Empty","S6422","S6431","S6442","S6453","S6464","S6473","S6493","S6501","S6511","S6522","Empty"]
[{"$nulls":3},"Lazabemide","Damascenone","Chlorphenesin","Bicyclol","Ftaxilide","Pinaverium bromide","n-Butylidenephthalide","NVP 231","RIPA-56","ST 271"]
[null,"d","Empty","S6423","S6432","S6443","S6454","S6465","S6476","S6494","S6503","S6512","S6523","Empty"]
[{"$nulls":3},"Tildipirosin","Cevimeline HCl hemihydrate","Chromium picolinate","Docosahexaenoic Acid","Tafamidis","Eicosapentaenoic Acid","CCCP","LX2343","Defensamide (MHP)","RG14620"]
[null,"e","Empty","S6424","S6433","S6444","S6455","S6467","S6478","S6495","S6505","S6513","S6524","Empty"]
[{"$nulls":3},"TAS-301","Udenafil","Triclocarban","Clebopride malate","Fosfluconazole","Fipexide hydrochloride","6-Bromo-2-hydroxy-3-methoxybenzaldehyde","X-376","HG-14-10-04","NSC 42834"]
[null,"f","Empty","S6425","S6435","S6447","S6456","S6468","S6479","S6496","S6506","S6516","S6525","Empty"]
[{"$nulls":3},"JNJ 63533054","Mequitazine","Carazolol","Glycyrrhetinic acid","Trandolapril","Isohomovanillic acid","Genz-123346 free base","Compound 401","GNE-477","AG 555"]
[null,"g","Empty","S6426","S6438","S6448","S6457","S6469","S6481","S6497","S6507","S6518","S6527","Empty"]
[{"$nulls":3},"Hesperidin methylchalcone","Ufiprazole","Ibuprofen piconol","Flurbiprofen Axetil","Thonzylamine","3beta-hydroxy-delta5-cholenic acid","SMI-16a","KN-92 phosphate","Desmethylanethol trithione","Kobe2602"]
[null,"h","Empty","S6427","S6439","S6450","S6459","S6470","S6484","S6498","S6508","S6519","S6529","Empty"]
[{"$nulls":3},"AZ876","Talniflumate","Apronal","Nifurtimox","Fluralaner","uridine triacetate","T56-LIMKi","Mitapivat","R112","NIH-12848"]
[]
[]
[]
[null,"Plate layout: L1700-43"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6532","S6545","S6566","S6577","S6608","S7003","S7016","S7036","S7050","S7070","Empty"]
[{"$nulls":3},"kb-NB77-78","BI-4464","NSC23005 Sodium","PKC-theta inhibitor","AL082D06","AZD2932","VS-5584 (SB2343)","XL019","AZ20","GSK J4 HCl (GSKJ4 HCl)"]
[null,"b","Empty","S6533","S6550","S6567","S6578","S6609","S7006","S7018","S7037","S7051","S7071","Empty"]
[{"$nulls":3},"Briciclib","URB602","Src Inhibitor 1","Longdaysin","JZL195","BAY-61-3606","CZC24832","Wnt-C59 (C59)","CGI1746","(+)-Bicuculline"]
[null,"c","Empty","S6536","S6554","S6569","S6585","S6610","S7007","S7024","S7038","S7057","S7072","Empty"]
[{"$nulls":3},"TTP 22","ML365","VUF10460","Triethylenetetramine Dihydrochloride","GSK2981278","Binimetinib (MEK162)","Stattic","Epoxomicin (BU-4061T)","LY2874455","NMDA (N-Methyl-D-aspartic acid)"]
[null,"d","Empty","S6537","S6555","S6571","S6587","S6611","S7008","S7025","S7039","S7059","S7076","Empty"]
[{"$nulls":3},"CVT-313","AZD2098","BQR695","Clobetasone butyrate","Cyclothiazide","PP2","Embelin","PD168393","Tezacaftor (VX-661)","T0901317"]
[null,"e","Empty","S6538","S6557","S6573","S6588","S6612","S7009","S7028","S7040","S7060","S7077","Empty"]
[{"$nulls":3},"B-Raf IN 1","ML355","MD2-IN-1","Methylprednisolone hemisuccinate","Betazole Dihydrochloride","LCL161","Duvelisib (IPI-145)","AZD3514","PP1","Cilengitide trifluoroacetate"]
[null,"f","Empty","S6541","S6561","S6574","S6590","S6613","S7010","S7029","S7041","S7063","S7079","Empty"]
[{"$nulls":3},"MTX-211","4-IBP","KDU691","Hydrocortisone butyrate","Vanillylmandelic acid","GDC-0152","AZD2461","CX-6258 HCl","LY2090314","SGC 0946"]
[null,"g","Empty","S6543","S6562","S6575","S6601","S6614","S7014","S7030","S7046","S7065","S7080","Empty"]
[{"$nulls":3},"ZD-4190","KKL-35","C-176","(±)-Equol","Fursultiamine","Merestinib (LY2801653)","RG-7112","Brefeldin A","MK-8745","RN486"]
[null,"h","Empty","S6544","S6565","S6576","S6605","S7000","S7015","S7033","S7049","S7067","S7083","Empty"]
[{"$nulls":3},"SR-3029","JK184","BW-A78U","AR7","AP26113-analog (ALK-IN-1)","Birinapant (TL32711)","GSK2656157","Oprozomib (ONX 0912)","Tepotinib (EMD 1214063)","Ceritinib (LDK378)"]
[]
[]
[]
[null,"Plate layout: L1700-44"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S7086","S7096","S7110","S7124","S7134","S7143","S7153","S7163","S7176","S7193","Empty"]
[{"$nulls":3},"IWR-1-endo","KY02111","(+)-JQ1","SC144","IU1","LGK-974","10058-F4","Dyngo-4a","SKI II","1-Azakenpaullone"]
[null,"b","Empty","S7087","S7097","S7111","S7125","S7135","S7144","S7155","S7165","S7177","S7194","Empty"]
[{"$nulls":3},"GSK2334470","HSP990 (NVP-HSP990)","IDO-IN-2","KPT-185","LDN-57444","BMS-911543","Batimastat (BB-94)","UNC1999","PF-543 hydrochloride","Olverembatinib dimesylate (HQP1351)"]
[null,"c","Empty","S7088","S7098","S7113","S7126","S7136","S7145","S7156","S7167","S7179","S7195","Empty"]
[{"$nulls":3},"UNC1215","PD123319","Zebularine (NSC 309132)","Marinopyrrole A (Maritoclax)","CGK 733","AZD1080","Marimastat (BB-2516)","SSR128129E","Siponimod (BAF312)","RKI-1447"]
[null,"d","Empty","S7090","S7099","S7114","S7127","S7137","S7146","S7157","S7169","S7182","S7198","Empty"]
[{"$nulls":3},"GSK923295","(-)-Blebbistatin","NU6027","TIC10 Analogue","GLPG0634 analogue","DMH1","Ilomastat","Crenigacestat (LY3039478)","JTE 013","BIO"]
[null,"e","Empty","S7091","S7102","S7115","S7129","S7138","S7147","S7158","S7170","S7185","S7199","Empty"]
[{"$nulls":3},"Zotarolimus (ABT-578)","Berzosertib (VE-822)","AMG-517","PYR-41","BMS-833923","LDN-212854","Abemaciclib mesylate (LY2835219)","Avutometinib","AGI-5198","DBeQ"]
[null,"f","Empty","S7092","S7103","S7119","S7130","S7139","S7148","S7160","S7171","S7188","S7205","Empty"]
[{"$nulls":3},"SANT-1","Taselisib (GDC 0032)","Go6976","PR-619","CFTRinh-172","ML347","Glasdegib (PF-04449913)","Setanaxib (GKT137831)","CID755673","Idasanutlin (RG-7388)"]
[null,"g","Empty","S7093","S7104","S7121","S7132","S7140","S7149","S7161","S7173","S7189","S7206","Empty"]
[{"$nulls":3},"IPA-3","AZD1208","Tovorafenib (MLN2480)","P5091 (P005091)","TCID","NSC 319726","Motolimod (VTX-2337)","Spebrutinib (CC-292)","Molibresib (I-BET-762)","CNX-2006"]
[null,"h","Empty","S7094","S7106","S7122","S7133","S7142","S7152","S7162","S7174","S7192","S7207","Empty"]
[{"$nulls":3},"PF-3758309","AZD3463","XL888","P22077","NSC697923","C646","Mdivi-1","Opaganib (ABC294640)","PF-04620110","Bisindolylmaleimide IX (Ro 31-8220 Mesylate)"]
[]
[]
[]
[null,"Plate layout: L1700-45"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S7208","S7223","S7238","S7255","S7265","S7278","S7291","S7300","S7310","S7320","Empty"]
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[{"$nulls":3},"CC-115","BMS-1 (PD-1/PD-L1 inhibitor 1)","Tiplaxtinin (PAI-039)","SR9243","O4I1","ETC-1002","PLX8394","FG-2216","Tenovin-1","AG-18"]
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[{"$nulls":3},"Empagliflozin (BI 10773)","Apremilast (CC-10004)","GW2580","ASP3026","UNC0638","Mirin","NSC59984","MK571","GNF-7","GDC-0326"]
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[]
[]
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[{"$nulls":3},"Ro 61-8048","NSC87877","umbralisib (TGR-1202)","Hydroxyfasudil (HA-1100) HCl","MK-886","RK-33","GSK6853","(±)-Shikonin","NQDI-1","SR-12813"]
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[{"$nulls":3},"VO-Ohpic trihydrate","FPS-ZM1","ML264","BAY 1217389","SB366791","HPI-4 (Ciliobrevin A)","SRT2183","CCF642","Selonsertib (GS-4997)","Azoramide"]
[]
[]
[]
[null,"Plate layout: L1700-53"]
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[{"$nulls":3},"Leukadherin-1","MLR-1023","Eganelisib (IPI-549)","PT2385","CRT0066101 dihydrochloride","YM-58483 (BTP2)","KRIBB11","R-IMPP","Monastrol","VPS34 inhibitor 1 (Compound 19)"]
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[{"$nulls":3},"ATI-2341","Samotolisib (LY3023414)","XMU-MP-1","Lirametostat (CPI-1205)","GSK2193874","ML390","MX69","10074-G5","LW 6","UK-371804 HCl"]
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[{"$nulls":3},"5-Iodotubercidin","ZK756326 2HCl","1400W 2HCl","WNK463","Lys05","ML-7 HCl","RRx-001","PNU-74654","KPT 9274 ( ATG-019)","Salermide"]
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[{"$nulls":3},"Alantolactone","KYA1797K","SGC2085","Tucatinib","AZD9496","Eltanexor (KPT-8602)","KG-501 (2-naphthol-AS-E-phosphate)","NS-398 (NS398)","8-OH-DPAT (8-Hydroxy-DPAT)","GSK'872 (GSK2399872A)"]
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[{"$nulls":3},"7,8-Dihydroxyflavone","CeMMEC1 HCl","ONO-7300243","NMS-P118","Rbin-1","Mivebresib (ABBV-075)","Naquotinib(ASP8273)","B02","ZINC00881524 (ROCK inhibitor)","CCG-203971"]
[]
[]
[]
[null,"Plate layout: L1700-54"]
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[{"$nulls":3},"LLY-284","WT161","GSK2256098","Btk inhibitor 2","IRAK4-IN-2","EAD1","Pamiparib (BGB-290)","Adenosine Dialdehyde (ADOX)","3-TYP","GNF-6231"]
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[{"$nulls":3},"SRT3025 HCl","EED226","GDC-0575 (ARRY-575)","Asciminib (ABL001)","Verubecestat (MK-8931)","PRN1371","Tirofiban Hydrochloride","Derazantinib(ARQ-087)","Linrodostat (BMS-986205)","IWP-O1"]
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[{"$nulls":3},"CBL0137 HCl","TMP195","SR-18292","AZ31","Omarigliptin (MK-3102)","COTI-2","Autophinib","Vorasidenib (AG-881)","Chk2 Inhibitor II (BML-277)","iCRT3"]
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[{"$nulls":3},"GSK2982772","Fisogatinib (BLU-554)","Temuterkib (LY3214996)","IDO inhibitor 1","Tucidinostat (Chidamide)","Serabelisib (TAK-117)","LYN-1604","α-cyano-4-hydroxycinnamic acid(α-CHCA)","Ipragliflozin (ASP1941)","ACY-738"]
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[{"$nulls":3},"GSK180736A (GSK180736)","Belizatinib (TSR-011)","Ritlecitinib (PF-06651600)","Tofogliflozin(CSG 452)","RXDX-106 (CEP-40783)","Repotrectinib (TPX-0005)","S 38093","Sodium dichloroacetate (DCA)","Diphenyleneiodonium chloride (DPI)","BTSA1"]
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[{"$nulls":3},"PD-166866 (PD166866)","A-317491","Voxelotor (GBT440)","Seletalisib (UCB-5857)","Sitravatinib (MGCD516)","SF2523","C188-9","NCT-503","Necrostatin 2 racemate (Nec-1s)","ex229 (compound 991)"]
[]
[]
[]
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[{"$nulls":3},"kira6","ONC212","PHTPP","GLPG1837","PDGFR inhibitor 1","BI-3812","H3B-5942","XRK3F2","Abrocitinib (PF-04965842)","Evobrutinib (M-2951)"]
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[{"$nulls":3},"GI254023X","H3B-6527","Abequolixron (RGX-104)","SNS-314 Mesylate","ABBV-744","Verinurad (RDEA3170)","BAY-8002","Ripretinib (DCC-2618)","Tinostamustine(EDO-S101)","UPGL00004"]
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[{"$nulls":3},"CA3 (CIL56)","Glumetinib (SCC244)","RAF709","TP0427736 HCl","A-804598","Bimiralisib (PQR309)","MBQ-167","S55746","Lanifibranor (IVA-337)","AZD3229"]
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[{"$nulls":3},"PTC-028","Cu-CPT22","ML204","MK-8353 (SCH900353)","Anlotinib (AL3818) dihydrochloride","PLX51107","NGI-1 (ML414)","Iberdomide (CC220)","IDF-11774","GSK'547"]
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[{"$nulls":3},"Takinib (EDHS-206)","BTK inhibitor 1 (Compound 27)","Selective PI3Kδ Inhibitor 1 (compound 7n)","iCRT14","Atuveciclib (BAY-1143572)","Avitinib (AC0010)","leniolisib (CDZ 173)","Adavivint (SM04690)","LY 3200882","CH7057288"]
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[{"$nulls":3},"Pemrametostat (GSK3326595)","AZD1390","CID16020046","UM-164","PK11000","SKLB-23bb","INCB054329","dBET6","TH34","SSE15206"]
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[{"$nulls":3},"Elimusertib (BAY-1895344) hydrochloride","Selective JAK3 inhibitor 1","ML221","Nemtabrutinib (ARQ 531)","AZ32","PHY34","Alofanib (RPT835)","ZL0420","HS-1371","ML385"]
[]
[]
[]
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[{"$nulls":3},"UAMC-3203","SPHINX31","BAY-218","Letermovir (AIC246)","23-Hydroxybetulinic acid","20S-Ginsenoside Rh2","Calycosin","Leonurine Hydrochloride","Gallocatechin gallate","Trillin"]
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[{"$nulls":3},"ULK-101","LIT-927","compound 3i (666-15)","7,8-Dihydroxy-4-methylcoumarin","Bevirimat","Hastatoside","Albiflorin","(+)-Gallocatechin","4'-O-Glucosylvitexin","Jatrorrhizine chloride"]
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[{"$nulls":3},"FDL169","Almonertinib (HS-10296)","JNJ-38877618(OMO-1)","Malic acid","Paulownin","Gambogenic acid","Maslinic acid","Parishin A","Nystose","Isoxanthohumol"]
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[{"$nulls":3},"CC-90003","V-9302","BMS-1166","L-Fucose","Columbianadin","Sanguinarine","Corosolic acid","Asperuloside","Hydroxy safflor yellow A","Nootkatone"]
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[{"$nulls":3},"MK-3903","GSK3179106","ZT-12-037-01","(R)-(-)-Mandelic acid","Luteoloside","Incensole acetate","Wedelolactone","Auraptene","Harringtonine","Sweroside"]
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[{"$nulls":3},"Brepocitinib (PF-06700841)","ABX-1431","Bentamapimod (AS602801)","Perillartine","Dihydrotanshinone I","Isochlorogenic acid C","6-Shogaol","Salvianolic acid A","Trilobatin","Lithospermoside"]
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[{"$nulls":3},"PFK158","BAY-293","Omadacycline tosylate","2'-deoxyguanosine","(20R)Ginsenoside Rg3","Isovitexin","Triptophenolide","Tuberostemonine","Songorine","Mulberroside A"]
[]
[]
[]
[null,"Plate layout: L1700-57"]
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[{"$nulls":3},"Plantamajoside","Calycosin-7-O-beta-D-glucoside","Alisol B Acetate","Timosaponin A3","Scutellarein","Harpagide","Berbamine","Epiberberine","Griffonilide","Sinapine thiocyanate"]
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[{"$nulls":3},"Epigoitrin","Magnoflorine","Dehydrodiisoeugenol","1-Kestose","Irigenin","Chicoric acid","Sparteine","Betulinicaldehyde","Columbin","Catharanthine hemitartrate"]
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[{"$nulls":3},"Anhydroicaritin","Corilagin","Orientin","Kaempferitrin","Tectorigenin","Spinosin","Ammonium Glycyrrhizate","Chelidonine","Periplogenin","Tussilagone"]
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[{"$nulls":3},"Manninotriose","10-Gingerol","Fraxinellone","Ononin","Apigetrin","Artemisic acid","Anwuligan","Aurantio-obtusin","Engeletin","Periplocin"]
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[{"$nulls":3},"Rhapontin","Norisoboldine","Ingenol","Polyphyllin I","Schizandrol B","Neochlorogenic acid","Peiminine","Ziyu-glycoside I","Phellodendrine","Crebanine"]
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[{"$nulls":3},"Rhoifolin","Nardosinone","Ginsenoside CK","Wogonoside","Carnosol","Erianin","Benzoylpaeoniflorin","Rubimaillin","Sec-O-Glucosylhamaudol","Forsythoside B"]
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[{"$nulls":3},"Corynoline","Pogostone","Eleutheroside E","Beta-Asarone","20(S)-Ginsenoside Rh1","5-Methyl-7-methoxyisoflavone","Daurisoline","Rhapontigenin","Xanthotoxol","Nitidine Chloride"]
[]
[]
[]
[null,"Plate layout: L1700-58"]
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[{"$nulls":3},"Liensinine perchlorate","Levistilide A","Huperzine B","Schisandrin C","Isocorynoxeine","Oxypeucedanin","Nodakenin","Alisol A","Astragalin","Verbenalin"]
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[{"$nulls":3},"Magnoflorine chloride","Oroxylin A","Stylopine hydrochloride","Linderane","Isofraxidin","Corydaline","3-n-Butylphathlide","Euphorbia factor L3","Isopimpinellin","Polyphyllin VI"]
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[{"$nulls":3},"Oroxin A","Hydroxygenkwanin","Ferulaldehyde","Vaccarin","Polygalaxanthone III","Coixol","7-Epitaxol","Demethoxycurcumin","Dictamnine","Saikosaponin B2"]
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[{"$nulls":3},"Oroxin B","Hydroprotopine","Dipotassium glycyrrhizinate","Schisanhenol","Narirutin","Skimmin","Epimedin A","Isochlorogenic acid A","Isoliquiritin","Shanzhiside methyl ester"]
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[{"$nulls":3},"Aristolochic acid A","Eriocitrin","Talatisamine","Imperialine","Protosappanin B","Isoscopoletin","Koumine","Aristolone","Dauricine","Micheliolide"]
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[{"$nulls":3},"Toddalolactone","Melamine","Santalol","Schaftoside","Phellodendrine chloride","Isobavachin","Isochlorogenic acid B","Aloesin","Kirenol","Isorhychophylline"]
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[{"$nulls":3},"Maltotetraose","Complanatuside","Steviolbioside","α-Cyperone","Securinine","(+)-Isocorynoline","Isoguanosine","Neobavaisoflavone","Corylin","Germacrone"]
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[{"$nulls":3},"Calceolarioside B","Phytolaccagenin","Sinensetin","Polygalic acid","Isosilybin","Lithospermic acid","Alisol B","Genkwanin","Ginsenoside F1","Cyanidin-3-O-glucoside chloride"]
[]
[]
[]
[null,"Plate layout: L1700-59"]
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[{"$nulls":3},"Atractylenolide III","Neodiosmin","Gibberellins A4/A7","Sequoyitol","2,4'-Dihydroxybenzophenone","6-Hydroxycoumarin","2'-Hydroxyacetophenone","Methyl palmitate","1,2,3,4,6-O-Pentagalloylglucose","Angoroside C"]
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[{"$nulls":3},"Atractylenolide II","Alnustone","Ethyl Coumarin-3-carboxylate","1-Indanone","7,8-Dihydroxy-4-phenylcoumarin","5'-Adenylic acid","Benzylacetone","Sophocarpine Monohydrate","Rhynchophylline","Beta-Elemonic acid"]
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[{"$nulls":3},"Praeruptorin A","Scopolamine","Ethyl vanillin acetate","Allitol","Phenylacetaldehyde","ADP","Eugenyl acetate","Maackiain","3,6'-Disinapoyl sucrose","Kavain"]
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[{"$nulls":3},"Forsythoside A","Carboprost","Octyl gallate","D-(+)-Trehalose Anhydrous","Anthraquinone-2-carboxylic Acid","Xanthosine","4',5-Dihydroxyflavone","Praeruptorin B","(20R)-Protopanaxadiol","Euphorbia factor L1"]
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[{"$nulls":3},"(20R)-Ginsenoside Rh1","5,6,7-Trimethoxyflavone","S-(-)-Cotinine","D-(+)-Raffinose pentahydrate","4-Hydroxyquinazoline","1-Iodoadamantane","Dihydrocoumarin","(4S)-4-Hydroxy-L-isoleucine","Ecliptasaponin A","Liensinine"]
[null,"f","Empty","S9319","S9329","S9340","S9350","S9361","S9372","S9380","S9395","S9404","S9412","Empty"]
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[{"$nulls":3},"Efetaal","6-Hydroxy-4-methylcoumarin","3,4-Dimethoxycinnamic acid","2'-Deoxyadenosine monohydrate","1-Naphthaleneacetic acid","Neryl acetate","5-Methyl furfural","Alliin","Sesamoside","Yangonin"]
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[{"$nulls":3},"Topotecan","7-Hydroxy-4-methyl-8-nitrocoumarin","1,4-Naphthoquinone","Oxalic acid","Coumarin 151","2',5'-Dihydroxyacetophenone","Thymine","Crassicauline A","Sauchinone","Cyasterone"]
[]
[]
[]
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[{"$nulls":3},"Demethylnobiletin","Dehydrocorydalin","Naringenin chalcone","Urocanic acid","Ethotoin","Nuzhenide","Darutoside","Madecassic acid","Rotundic acid","Evodine"]
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[{"$nulls":3},"Liensinine diperchlorate","Secoxyloganin","Schisantherin B","2-Undecanol","Methenamine Hippurate","Dendrobine","Lobetyolin","(−)-Norepinephrine","Farrerol","Indinavir Sulfate"]
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[]
[]
[]
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[{"$nulls":3},"Vadadustat","Adelmidrol","RCGD423","IRAK-1-4 Inhibitor I","BMS309403","Belotecan (CKD-602) hydrochloride","Ciforadenant (CPI-444)","YHO-13177","MK1064","JD-5037"]
[]
[]
[]
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[{"$nulls":3},"MN 64","ML364","Talabostat (PT-100)","AZD7648","PLX5622","3-O-Acetyl-11-keto-β-boswellic acid (AKBA)","Eriodictyol","Peimine","momordin-Ic","SKLB4771 (FLT3-IN-1)"]
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[{"$nulls":3},"DB07268","ASP-9521","Navarixin (SCH-527123)","Orludodstat (BAY 2402234)","Imidazole ketone erastin (PUN30119)","Cimifugin","Harpagoside","Fargesin","LTI-291","CZC-25146"]
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[{"$nulls":3},"Inauhzin","CP 640186","zipalertinib","Mavacamten (MYK-461)","FF-10101","Dihydrocapsaicin","Pneumocandin B0","Triptonide","BI-1347","ISCK03"]
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[]
[]
[]
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[{"$nulls":3},"WDR5-0103","Frentizole","CPI-1189","SU5408","SRI-011381","Sparsentan (PS-433540, RE-021)","Yoda1","BAY1125976","G150","Solamargine"]
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[{"$nulls":3},"Sphingosine","Eprobemide","Fabomotizole hydrochloride","NKL 22","VAS2870","FT113","L-779450","CM272","Olutasidenib (FT-2102)","Pinoresinol diglucoside"]
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[{"$nulls":3},"AIM-100","PF-04457845","VTP-27999 TFA","SAR7334","2-Aminoethyl Diphenylborinate (2-APB)","STING inhibitor C-178","IOX4","ODM-203","Ginsenoside F2","Didymin"]
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[{"$nulls":3},"BIBF-0775","Tirapazamine","Fexinidazole","Bardoxolone","ETC-206 (AUM 001)","MC-Val-Cit-PAB","SIS17","Firsocostat (GS-0976)","ligustroflavone","Linarin"]
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[{"$nulls":3},"PF 4800567","Isopropyl myristate","4-IPP","E7046 (ER-886406)","Rimegepant (BMS-927711)","GPNA (L-γ-Glutamyl-p-nitroanilide)","Fmoc-Val-Cit-PAB","USP25/28 inhibitor AZ1","Chikusetsusaponin IVa","Toosendanin"]
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[{"$nulls":3},"Indoprofen","Pranidipine","SIB 1757","G15 (GRB-G15)","AST-487 (NVP-AST487)","Cytosporone B","TOFA (5-(Tetradecyloxy)-2-furoic acid)","UBCS039","Punicalagin","BI-409306"]
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[]
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[]
[]
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[]
[]
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[{"$nulls":3},"GSK369796 Dihydrochloride","BMS303141","Treprostinil sodium","Indibulin","Butyl isobutyl phthalate","Isuzinaxib (APX-115 free base)","Allosecurinin","Vindesine sulfate","Uridine 5'-diphosphoglucose disodium salt","L-Fucitol"]
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[]
[]
[]
[null,"Plate layout: L1700-67"]
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[{"$nulls":3},"Resibufogenin","Corypalmine","Rebaudioside D","Acetylcorynoline","Kaempferol-3-O-neohesperidoside","Rosamultin","Hosenkoside A","Galangin 3-methyl ether","LM22B-10","ML-9 HCl"]
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[{"$nulls":3},"H3B-120","Plantagoside","Agarotetrol","Hypericin","Rebaudioside M","Gardenoside","β,β-dimethyl-acryl-alkannin","TPI-1","1-BCP","ONC206"]
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[]
[]
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[{"$nulls":3},"Thioflavin T","PIN1 inhibitor API-1","MDL-28170","BAY 1251152","BI-3406","DCLK1-IN-1","IM156","NEO2734","GSK137647A","BD-1047 dihydrobromide"]
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[{"$nulls":3},"SRT-1460","MCP110","VH298","FB23-2","SB290157 trifluoroacetate","NVP-2","ABTL-0812","Remibrutinib (LOU064)","YKL 06-061","NQ301"]
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[]
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[{"$nulls":3},"Mitochonic acid 5","FL-411","7-Methoxyisoflavone","Dooku1","DL-Tartaric acid","N-Acetyl-DL-methionine","Itaconic acid","Pyridoxal hydrochloride","2-Amino-1-phenylethanol","Amiloxate"]
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[{"$nulls":3},"RA-9","Histone Acetyltransferase Inhibitor II","Staurosporine (AM-2282)","NP-G2-044","Isophorone","(±)-Methyl Jasmonate","5,6-Dimethylbenzimidazole","3-Methyl-2-buten-1-ol","Maleimide","2'-Deoxyadenosine 5'-monophosphate"]
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[{"$nulls":3},"MLS000532223","Irinotecan (CPT-11)","Adenine","HA-100 dihydrochloride","Acetic acid octyl ester","12-Hydroxydodecanoic acid","N-Acetylglycine","N-Formylglycine","Pyruvic acid","2'-Deoxycytidine 5'-monophosphate"]
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[{"$nulls":3},"4',5,7-Trimethoxyflavone","CPTH2",null,"N-Acetyl-5-hydroxytryptamine","Methyl isoeugenol","trans-Aconitic acid","δ-Valerolactone","Sodium 2-hydroxybutanoate","Pimelic acid","D-(+)-Galacturonic acid monohydrate"]
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[{"$nulls":3},"TBOPP","Amarogentin","BCI","4-Methyl-2-oxovaleric acid","Malonic acid","Glyoxylic acid monohydrate","D-Pyroglutamic acid","N-Acetyl-D-galactosamine","3-Hydroxybenzaldehyde","Diethyl phosphate"]
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[]
[]
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[{"$nulls":3},"2-Methylpentanoic acid","Nicotinuric acid","(2R,3R)-(-)-2,3-Butanediol","Methyl β-D-Galactopyranoside","4-Acetamidobutyric acid","Oxiglutatione","N-Acetyl-L-phenylalanine","Trypan Blue","D-Luciferin sodium salt","Perhexiline maleate"]
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[{"$nulls":3},"6-Hydroxyindole","2-Hydroxycaproic acid","Glycolaldehyde dimer","Serotonin creatinine sulfate monohydrate","Bis(2-ethylhexyl) phthalate","Ceftaroline Fosamil","3-Hydroxybenzyl alcohol","MSAB","GNF351","TPEN"]
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[{"$nulls":3},"5-Hydroxy-1-tetralone","Sodium 2-(1H-indol-3-yl)acetate","Heptadecanoic acid","3-Methylglutaric acid","(3-Carboxypropyl)trimethylammonium chloride","Apatinib","1-Hydroxy-2-naphthoic acid","Rapastinel (GLYX-13)","AMG-9810","APTO-253"]
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[{"$nulls":3},"cis-3-Hexenyl hexanoate","L-Cysteic acid monohydrate","L-Histidinol dihydrochloride","O-Acetyl-L-serine hydrochloride","D-Gulonic acid γ-lactone","Hemin","Quinaldic acid","DOTAP chloride","Lanreotide","S-Adenosyl-L-homocysteine (SAH)"]
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[{"$nulls":3},"N-Acetyl-L-arginine dihydrate","N-Formyl-L-methionine","D-(-)-Lyxose","Tricosanoic acid","(S)-(-)-1-Phenylethanol","Pyriproxyfen","3-Hydroxybenzoic acid","Vacuolin-1","PRE-084 hydrochloride","PT2399"]
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[{"$nulls":3},"Levoglucosan","(L)-Dehydroascorbic acid","3-(2-Hydroxyphenyl)propionic acid","Lithium acetoacetate","Monoethyl malonic acid","Indole","GNE-493","SEA0400","Insulin (human)","Epibrassinolide"]
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[{"$nulls":3},"(R)-3-Hydroxybutanoic acid","Maleamic acid","Palmitoleic acid","Phosphonoacetic acid","3-Methoxytyramine hydrochloride","2-Hydroxypyridine","ML213","Dorzagliatin","β-Elemene","2-NBDG"]
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[]
[]
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[{"$nulls":3},"Prim-o-glucosylcimifugin","Neoandrographolide","Ginsenoside Rk1","Decursin","Methylprotodioscin","Tubeimoside II","CBR-5884","FDI-6","Fluzoparib (SHR-3162)","BAR501"]
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[]
[]
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[{"$nulls":3},"SPI-112","DSP Crosslinker","AKR1C1-IN-1","Crotamiton","cis-Resveratrol","Metarrestin (ML246)","CEBPα inducer 1","Triolein","Pimethixene maleate","Tenofovir alafenamide fumarate"]
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[{"$nulls":3},"Gap 26","Azide-PEG5-Tos","RP-64477","Liranaftate","Mitochondrial Fusion Promoter M1","Lefamulin acetate (Xenleta)","Spermidine","Rhodamine 6G","Phenol Red sodium salt","Ertugliflozin L-pyroglutamic acid"]
[]
[]
[]
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[{"$nulls":3},"Ledipasvir acetone","Dimercaprol","Tetraethylammonium chloride","Homosalate","Enasidenib Mesylate","Ciprofloxacin hydrochloride","Ribociclib succinate","Promethazine","Pantoprazole sodium hydrate","Propafenone"]
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[{"$nulls":3},"GSK4716","TC-E 5003","LCH-7749944","PFM01","(R)-(-)-Ibuprofen","H-1152 dihydrochloride","SHP099","TCPOBOP","Bavdegalutamide (ARV-110)","Centrinone (LCR-263)"]
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[{"$nulls":3},"Diarylpropionitrile (DPN)","HLY78","C75","KA2507","SJ-172550","Mericitabine","Raclopride","β-Anhydroicaritin","Aurora kinase Inhibitor II","SEN12333"]
[]
[]
[]
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[{"$nulls":3},"Hepln-13","Zapnometinib (PD0184264)","RTICBM-189","7BIO","SP-8356","Flecainide","Arecaidine hydrochloride","(R)-CR8 trihydrochloride","Gemifloxacin mesylate","Silydianin"]
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[{"$nulls":3},"(E/Z)-GSK-3β inhibitor 1","L002 (NSC764414)","Robinetin","N-Caffeoyl O-methyltyramine","Firocoxib (ML 1785713)","Metipranolol","Methyl methanesulfonate","ADAMTS-5 Inhibitor","Nomegestrol Acetate","Neotuberostemonine"]
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[{"$nulls":3},"WQ 1","JP1302","Pyrintegrin","MRT-81","Senicapoc (ICA-17043)","Prednicarbate","TC-067533","γ-Terpinene","1-[(4R,5R)-4,5-Dihydroxy-L-ornithine]echinocandin B hydrochloride (1:1)","Z944"]
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[{"$nulls":3},"DUBs-IN-2","AA38-3","Adarotene","MP-A08","Metrizoic acid","TMS","AWL-II-38.3","2-Hydroxyisocaproic acid","AA147","o-3M3FBS"]
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[{"$nulls":3},"YK 3-237","(R)-Avanafil","GW 610","Calmidazolium chloride","chinifur","IRAK-4 protein kinase inhibitor 2","Lodenafil","Trans-ferulic acid","Opoponax oil","Paprotrain"]
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[{"$nulls":3},"Vercirnon","SGC-SMARCA-BRDVIII","Alkyne tyramide","CNQX","Flugestone 17-acetate","WAY-340935","AX 20017","7-Methylcoumarin","Coumalic acid","MNITMT"]
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[{"$nulls":3},"AS1949490","Dansylcadaverine (Monodansyl cadaverine)","BMS-986122","Stafia-1","sappanone A","WAY-303290","Cedirogant","Deacetylasperulosidic acid","Dihydrouracil","BAZ1A-IN-1"]
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[{"$nulls":3},"BI6015","ARN-19702","CUDA","C-021","Norgestimate","WAY-309060","Ibiglustat succinate","Esaxerenone (CS-3150)","Guvacoline hydrochloride","MRT 10"]
[]
[]
[]
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[{"$nulls":3},"SM-7368","SW-106065","BI-6C9","Levamlodipine Besylate","MS7972","Rebamipide mofetil","ERG240","SBP-3264","TC-DAPK 6","CHD1Li 6.11"]
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[{"$nulls":3},"YS-49","G5-7","Timapiprant Sodium","Mitonafide","IGS-1.76","Mebicar","NAV-2729","Phen-DC3 Trifluoromethanesulfonate","K145","VY-3-135"]
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[{"$nulls":3},"N-Desmethyltamoxifen","MID-1","CXD101","Nitrocaramiphen hydrochloride","Segesterone acetate","MP07-66","JR14a","HG106","AFN-1252","BOS-318"]
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[{"$nulls":3},"ALLO-2","COH-SR4","Masitinib mesylate","Compound 10w","BVDV IN-1","ZX-29","PEAQX","MiTMAB","CHR-6494","SIRT7 inhibitor 97491"]
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[{"$nulls":3},"PfDHODH-IN-2","NF-κB-IN-1","Rilpivirine Hydrochloride","O-Demethyl-Gefitinib","NBD-556","RO5186582","UNC6934","5-amino-2,4-dimethylpyridine (5A-DMP)","SKLB-197","JR-AB2-011"]
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[{"$nulls":3},"SC-58125","WAY-383487","Oritavancin Diphosphate","7,8-Dimethoxy-4H-chromen-4-one","IMD-0560","PFE-360","TRULI","DNPH1i(N6-benzyladenosine)","CQ31","AGX51"]
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[{"$nulls":3},"ILK-IN-3","WAY-119064","OX02983","CID-1517823","BIA","Upamostat (WX-671)","Piperazine Erastin","ODM-207","GSK2033","LMT-28"]
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[{"$nulls":3},"PTGR2-IN-1","VU 0365114","AST-1306","Raf inhibitor 2","Iu1-248","Aficamten (CK-274)","MINA53 inhibitor (Compound 10)","CTB","GA-017","CAY10444"]
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[]
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[{"$nulls":3},"tetrathiomolybdate","NF-56-EJ40","AZD-9574","Valepotriate","KY-05009","α-Linolenic acid","WAY-297848","WAY-327157","Tris(2-chloroethyl) phosphate","HA-100"]
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[{"$nulls":3},"R162","p-Nitrobenzyl mesylate","PHD-1-IN-1","Dotinurad","2′-O-(2-Methoxyethyl)guanosine","JNJ-10198409","WAY-301398","WAY-345989","H-Leu-Leu-OMe Hydrochloride","AZ1495"]
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[{"$nulls":3},"SBI-425","Deschloroclozapine","N-piperidine Ibrutinib hydrochloride","Tandospirone","GNE-3511","STK16-IN-1","ZINC05007751","STK414603","EDC hydrochloride","RIPK1-IN-7"]
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[{"$nulls":3},"V-0219","Dimethyl itaconate","1-Naphthyl PP1 hydrochloride","Azosemide","(E)-Akt inhibitor-IV","1A-116","Doxorubicin","WAY-639418","N-Ethyl-N-(2-hydroxy-3-sulfopropyl)-3-toluidine","Raf inhibitor 1"]
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[{"$nulls":3},"FHD-286","Kisspeptin-10 (human)","DMU-212","Glutaminase C-IN-1","SAR407899 hydrochloride","T-1101 tosylate","WAY-388264-A","N-(p-Coumaroyl) Serotonin","M2N12","DMAT"]
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[{"$nulls":3},"TES-1025","WAY-272077","IBT6A","N-Desmethyltamoxifen hydrochloride","PKR-IN-2","TBAP-001","WAY-297342","SKF-86002","trans-Chalcone","Pamoic acid disodium"]
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[{"$nulls":3},"UC2288","WAY-620645","Mutated EGFR-IN-1","CAN508","ML-098","A-3 hydrochloride","WAY-624704","Colcemid","CGP60474","Chitosan oligosaccharide"]
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[{"$nulls":3},"WAY-309236-A","WAY-297407","SU3327","PI-273","Thalidomide-5-NH2-CH2-COOH","WAY-608241","WAY-358871","Norharmane","TL02-59","BT2"]
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[]
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[{"$nulls":3},"Cridanimod","TCPP","PS47","TPPU","Epitalon","Autocamtide 2, amide","Box5","Bemcentinib (R428)","Rocaglamide","Avapritinib (BLU-285)"]
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[{"$nulls":3},"RPI-1","Tris(2-ethylhexyl) phosphate","GRK5-IN-2","ORM-15341","diprotin A","Epsilon-V1-2","Disitertide(P144)","Procyanidin B2","Leptomycin B","Withaferin A"]
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[{"$nulls":3},"Ursodeoxycholic acid sodium","Tris(2-butoxyethyl) phosphate","Hematein","Carbetocin Acetate","Gastrin Tetrapeptide","Angstrom6","tat-nr2b9c","TC-H 106","MI-503","AZD4573"]
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[{"$nulls":3},"Icilin","Neutral Red Solution","Alkannin","BAM (8-22)","HIV Peptide T","LSKL, Inhibitor of Thrombospondin (TSP-1)","CYN154806","Oleandrin (PBI-05204)","Upadacitinib (ABT-494)","MC180295"]
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[{"$nulls":3},"Methoprene","Tridecafluorohexane-1-sulfonic acid potassium salt","LCS-1","Alamandine","Oglufanide","Pep2m, myristoylated (TFA)","Cafestol","Talazoparib (BMN 673)","ARV-825","Branebrutinib (BMS-986195)"]
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[{"$nulls":3},"Iodonitrotetrazolium chloride","3-Amino-9-ethylcarbazole","1,5-Anhydro-D-glucitol","Bremelanotide Acetate","PKG inhibitor peptide","Sakamototide substrate peptide (TFA)","Heterophyllin B","Pinometostat (EPZ5676)","AZD-5153 6-hydroxy-2-naphthoic acid","TAS0728"]
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[{"$nulls":3},"3,3'-Diaminobenzidine tetrahydrochloride","Coomassie Blue R-250","M7583","Etelcalcetide HCl","PKI 14-22 amide,myristoylated","pm26TGF-β1 peptide (TFA)","Calcifediol","SCH772984","BMS-986142","Deucravacitinib (BMS-986165)"]
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[{"$nulls":3},"11-Mercaptoundecanoic acid","Antimalarial agent 1","FBPase-1 inhibitor-1","Dasiglucagon","Malantide","CDK7/9 tide","Neoruscogenin","Encorafenib (LGX818)","Fenebrutinib (GDC-0853)","MAK683"]
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[]
[]
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[{"$nulls":3},"AstragalosideⅠ","Tetramethylcurcumin","AB-423","Eptapirone","COH000","LY2562175","Sulfo-SMCC sodium","Brr2 Inhibitor C9","AT-001","Vicriviroc Malate"]
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[{"$nulls":3},"Jujuboside A","EGCG Octaacetate","UCB9608","MD2-TLR4-IN-1","1-Methyl-7-nitroisatoic anhydride (1M7)","Etalocib","Propargyl-PEG4-NHS ester","MDR-652","Salvianolic acid C","AG-13958"]
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[{"$nulls":3},"UNC6852","IAXO-102","CAY10593 (VU0155069)","AZD-7325","Volinanserin","SAR-20347","α-Conotoxin GI","SP-13786","NVP-AEW541","Apatinib (YN968D1) mesylate"]
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[{"$nulls":3},"Caerulein (FI-6934)","BTdCPU","D-I03","XMD-17-51","NB 598","ASP7663","Tegatrabetan (BC-2059)","PF-06446846","T16Ainh-A01","Tubacin"]
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[{"$nulls":3},"Hypaconitine","HT-2157","Gefitinib-based PROTAC 3","CTX-0294885","Smurf1-IN-A01","SCH-23390 hydrochloride","AG 556","G-1","Cyclophosphamide","Podophyllotoxin (Podofilox)"]
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[{"$nulls":3},"Quercetagetin","Ingliforib","1V209 (TLR7 agonist T7)","GSK467","Pulrodemstat (CC-90011) besylate","ZK824859","eCF506","Laninamivir Octanoate","Tosedostat (CHR2797)","9-amino-CPT (9-Aminocamptothecin)"]
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[{"$nulls":3},"Deslanoside","PF-06869206","PH-002","DLin-KC2-DMA","(1E)-CFI-400437 dihydrochloride","Manogepix (E1210)","Spastazoline","L-765314","RO4929097","AV-412 free base"]
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[{"$nulls":3},"Guvacine hydrochloride","Nidufexor (LMB-763)","Asapiprant","AMZ30","KAN0438757","SU14813","Danicopan (ACH-4471)","ASTX-029","GABAA receptor agent 1","Wortmannin (KY 12420)"]
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[]
[]
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[{"$nulls":3},"Lixivaptan (VPA-985)","Tegobuvir","AZ10606120 dihydrochloride","CVT-11127","PF-05221304","SN50","CC-671","PD146176","Resatorvid (TAK-242)","Phorbol 12-myristate 13-acetate (PMA)"]
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[{"$nulls":3},"ML359","NEDD8 inhibitor M22","2OH-BNPP1","PCNA-I1","Fasnall","PF-05175157","JAK Inhibitor I (Pyridone 6)","Foxy-5","Ravoxertinib (GDC-0994)","A-1155463 Dihydrochloride"]
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[{"$nulls":3},"BRD9539","CYM50308","AZD7507","PNPP","PBTZ169","(R)-GNE-140","3-deazaadenosine","Dianhydrogalactitol (VAL-083)","MHY-1685","A-1331852"]
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[{"$nulls":3},"CarboxyaMidotriazole orotate","PH-064","N-desMethyl EnzalutaMide","Iodixanol","Liarozole dihydrochloride","C25-140","MRX-2843","TD-165","SAR405","Lifirafenib (BGB-283)"]
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[{"$nulls":3},"CU-T12-9","AQX-016A","TVB-3166","NS1643","CCG215022","D-Lin-MC3-DMA (MC3)","OSU-T315","Guadecitabine (SGI-110)","R-268712","Ixabepilone (BMS-247550)"]
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[{"$nulls":3},"Romidepsin","Vicriviroc maleate","Z433927330","2-Phenylimidazole","BAY-545","Eliprodil (SL-820715)","MF-438","Z-VAD-FMK","MLN120B","Brusatol"]
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[{"$nulls":3},"Azumolene","(S,R,S)-AHPC-PEG4-NH2 hydrochloride","iGOT1-01","AST5902  trimesylate","VcMMAE","NVR 3-778","Epertinib hydrochloride","AZ505","Telacebec (Q203)","CCT251545"]
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[{"$nulls":3},"RBPJ Inhibitor-1 (RIN1)","NLX-101","VPC-80051","ER-000444793","NVS-ZP7-4","GSK805","GEN-6776","Pevonedistat (MLN4924)","1-Methoxy PMS","GW7647"]
[]
[]
[]
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[{"$nulls":3},"Lersivirine (UK-453061)","NVS-PAK1-1","Zimlovisertib (PF-06650833)","ARS-1620","LY3295668","Cintirorgon (LYC-55716)","BI-4020","Camizestrant (AZD9833)","Gypenoside XLIX","BMS-P5"]
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[{"$nulls":3},"Nutlin-3a","TAK-243 (MLN7243)","ARV-771","AZD0364 (ATG-017)","A1874","YKL-5-124","Simurosertib","BI-2852","SB 265610","LY3143921 hydrate"]
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[{"$nulls":3},"Midostaurin (PKC412)","ND646","Galicaftor (ABBV-2222)","Pralsetinib (BLU-667)","Subasumstat (TAK-981)","UNBS5162","Valemetostat (DS-3201)","CD38 inhibitor 1 (compound 78c)","Valrubicin","PROTAC SGK3 degrader-1"]
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[{"$nulls":3},"GSK1016790A","NCB-0846","TVB-3664","RMC-4550","Sotorasib (AMG510)","DS-1001b (DS 1001)","VTP50469","T-5224","Etrumadenant (AB928)","Ropsacitinib (PF-06826647)"]
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[{"$nulls":3},"ICI-118551 Hydrochloride","SPD304","Elenbecestat","Imaradenant (AZD4635)","GB1107","Adagrasib (MRTX849)","BAY-985","XL177A","ACBI1","BMS-986158"]
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[{"$nulls":3},"Salinomycin (from Streptomyces albus)","AP20187","Selitrectinib (LOXO-195)","Samuraciclib hydrochloride (ICEC0942 hydrochloride)","TAS4464","MK-8719","Mizagliflozin (KWA 0711)","PRI-724","LDC7559","Finerenone"]
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[{"$nulls":3},"INCB3344","JNJ-47965567","GNE-781","A-485","Elexacaftor (VX-445)","BAY-885","Suramin sodium salt","TNO155","Elacestrant (RAD1901) Dihydrochloride","Rimiducid (AP1903)"]
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[{"$nulls":3},"PF-3644022","Edicotinib(JNJ-40346527)","Tolinapant (ASTX660)","VU661013","GSK3368715 (EPZ019997) 3HCl","MLT-748","Sotorasib (AMG510) racemate","Exatecan Mesylate","BRD0705","Ac-YVAD-cmk"]
[]
[]
[]
[null,"Plate layout: L1700-89"]
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[{"$nulls":3},"Ac-FLTD-CMK","KB-0742 Dihydrochloride","Evatanepag","XL092","CVT-10216","Chiauranib","Bemnifosbuvir Hemisulfate (AT-527)","TP-064","Ensitrelvir fumarate","MRTX0902"]
[null,"b","Empty","S9825","S9944","E0077","E0145","E0357","E0636","E1037","E1091","E1134","E1184","Empty"]
[{"$nulls":3},"Pirtobrutinib (LOXO-305)","PRN1008","Simufilam","LOX-IN-3 Dihydrochloride","Eliapixant","GSK-1520489A","ZZW-115","Relacorilant","ABR-238901","CFT7455"]
[null,"c","Empty","S9829","S9970","E0082","E0146","E0369","E0742","E1066","E1098","E1139","E1191","Empty"]
[{"$nulls":3},"BVT-948","APG-2575 (lisaftoclax)","R59949","PF-9363 (CTx-648)","Endovion (NS 3728)","Melengestrol Acetate","SN-011 (GUN35901)","MF-094","DX3-213B","GDC-1971"]
[null,"d","Empty","S9858","S9975","E0102","E0164","E0447","E0818","E1069","E1103","E1149","E1204","Empty"]
[{"$nulls":3},"Lufotrelvir (PF-07304814)","ASN007","I-191","Antazoline Phosphate","SM-102","Quinupristin","M2912","AU-15330","BAY-179","NVP-DKY709"]
[null,"e","Empty","S9866","E0002","E0114","E0184","E0488","E0940","E1074","E1111","E1167","E1205","Empty"]
[{"$nulls":3},"Nirmatrelvir (PF-07321332)","CGP-37157","Dilmapimod (SB-681323)","2-Mercaptobenzothiazole","BC-LI-0186","Propyl pyrazole triol (PPT)","MM3122","VV116","X1 compound","BAY 2666605"]
[null,"f","Empty","S9867","E0014","E0116","E0250","E0494","E0946","E1078","E1112","E1174","E1208","Empty"]
[{"$nulls":3},"LY-3475070","BIBO 3304 Trifluoroacetate","PF-06446846 hydrochloride","Artemitin","NI-42","MAP4K4-IN-3","Emvododstat (PTC299)","GS-621763","NK01-63","NPX800"]
[null,"g","Empty","S9889","E0034","E0121","E0301","E0496","E1000","E1079","E1113","E1179","E1212","Empty"]
[{"$nulls":3},"dCBP-1","CyPPA","Parsaclisib (INCB050465)","Necrostatin-34 (Nec-34)","ZLc002","Zn-C3","GNE-9815","GSK215","EZM0414","CC-99282"]
[null,"h","Empty","S9898","E0041","E0132","E0326","E0499","E1007","E1086","E1125","E1180","E1213","Empty"]
[{"$nulls":3},"Proxalutamide (GT0918)","Tolebrutinib (SAR442168)","NCGC00244536","S18-000003","4SC-203","BRD0639","KT-531","A-443654","Sovilnesib","MCC-7840"]
[]
[]
[]
[null,"Plate layout: L1700-90"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E1239","E1277","E2375","E2399","E2649","E2694","E2813","E2836","P1032","P1208","Empty"]
[{"$nulls":3},"Apararenone","TH10785","PI3K/mTOR Inhibitor-2","Falnidamol","Afatinib impurity 11","D-Saccharic acid 1,4-lactone monohydrate","SR 11237","ALK inhibitor 1","CCK Octapeptide (Sincalide)","PMX 205"]
[null,"b","Empty","E1244","E2136","E2379","E2401","E2652","E2805","E2815","E2837","P1069","P1234","Empty"]
[{"$nulls":3},"FINO2","WAY-299775","ASK1-IN-2","SPP-86","Kira8","WAY-320461","Lalistat 2","Zabedosertib","Ganirelix acetate (Antagon)","Apamin"]
[null,"c","Empty","E1245","E2178","E2380","E2404","E2653","E2806","E2819","E2839","P1106","S5975","Empty"]
[{"$nulls":3},"Ro5-3335","IM-54","GNE 2861","NVP-LCQ195","JNK-IN-7","WAY-323096","PF-04802367","Bisindolylmaleimide VIII (acetate)","D-JNKI-1","Calcein"]
[null,"d","Empty","E1247","E2227","E2382","E2406","E2655","E2807","E2821","E2843","P1109","E4044","Empty"]
[{"$nulls":3},"SR95531","GLN-1062","(Rac)-IBT6A","Paltusotine","Terevalefim","WAY-641966","RGB-286638 free base","Poseltinib","Linaclotide","N-Acetyl-L-aspartic acid"]
[null,"e","Empty","E1257","E2361","E2387","E2438","E2656","E2808","E2822","E2848","P1129","E4048","Empty"]
[{"$nulls":3},"(R,S)-3,5-DHPG Hydrochloride","KR-33494","FLT3-IN-2","Ginsenoside Rg3","R1530","WAY-296817","GSK2983559 active metabolite","Afoxolaner","Substance P TFA","Phenyl acetate"]
[null,"f","Empty","E1258","E2366","E2394","E2484","E2658","E2809","E2823","E2852","P1144","E4049","Empty"]
[{"$nulls":3},"Pridopidine","IHMT-PI3Kδ-372","TGFβRI-IN-3","Hydrastine","FN-1501","WAY-328168","PIK-108","BC-1471","Antide","Taurodeoxycholate (sodium salt)"]
[null,"g","Empty","E1259","E2370","E2397","E2515","E2665","E2810","E2834","E2853","P1150","E4054","Empty"]
[{"$nulls":3},"DNQX","CDK-IN-2","hVEGF-IN-1","JT010","Tafenoquine","WAY-328178","Hck-IN-1","GSK626616","Saralasin Acetate","Ethylmalonic acid"]
[null,"h","Empty","E1275","E2372","E2398","E2629","E2667","E2811","E2835","P1005","P1151","E4062","Empty"]
[{"$nulls":3},"FR054","p38-α MAPK-IN-1","STAT5-IN-2","Vimseltinib","IPI-9119","WAY-328133","NVP-BHG712 isomer","Abarelix Acetate","Difelikefalin","(−)-Myrtenal"]
[]
[]
[]
[null,"Plate layout: L1700-91"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E4065","E4085","E4099","E4115","E4131","E4149","E4176","E4193","E4215","E4231","Empty"]
[{"$nulls":3},"Caprylic/Capric Triglyceride","4-Methoxycinnamic acid","1,3-Dithiane","Isomaltose","Methyl laurate","5-Methoxyindole-3-acetic acid","Methyl palmitoleate","2-(2-Methylbenzamido)acetic acid","Ac-DL-Trp-OH","3-(3,4,5-Trimethoxyphenyl)propanoic acid"]
[null,"b","Empty","E4066","E4086","E4100","E4116","E4132","E4152","E4177","E4194","E4216","E4234","Empty"]
[{"$nulls":3},"Dicaprylyl carbonate","p-Anisic acid","Coumaran","Isoeugenol acetate","Methyl tridecanoate","Acridone","2′-O-Methyluridine","β-Ionone","2-Hydroxycinnamic acid","1-Octanol"]
[null,"c","Empty","E4072","E4089","E4103","E4117","E4133","E4153","E4178","E4195","E4217","E4235","Empty"]
[{"$nulls":3},"1-Linoleoyl Glycerol","3,4-Dimethoxyphenol","Pyridoxylamine (dihydrochloride)","Methyl propyl disulfide","Methyl myristate","Methyl 3-phenylpropanoate","N-Acetyl-L-tryptophan","Methyl anisate","Adenine monohydrochloride hemihydrate","1-Hexanol"]
[null,"d","Empty","E4074","E4090","E4105","E4118","E4134","E4163","E4179","E4197","E4218","E4236","Empty"]
[{"$nulls":3},"p-Toluic acid","Isoborneol","Quinizarin","(-)-Menthone","Methyl pentadecanoate","2-Tridecanone","2-Hydroxyanthraquinone","Diallyl disulfide","L-Cysteine (hydrochloride hydrate)","ω-Pentadecalactone"]
[null,"e","Empty","E4077","E4091","E4106","E4119","E4135","E4168","E4182","E4202","E4219","E4241","Empty"]
[{"$nulls":3},"Methyl indole-3-carboxylate","3-O-Methylgallic acid","α-Angelica lactone","7-Methoxyflavone","Methyl heptadecanoate","Sulcatone","Ethyl 3-hydroxybutyrate","4-Hydroxybenzyl cyanide","Carveol","Tropic acid"]
[null,"f","Empty","E4080","E4092","E4110","E4125","E4137","E4171","E4187","E4207","E4220","E4254","Empty"]
[{"$nulls":3},"Pharmatose DCL 14","Ricinoleic acid","Myrcene","3-Hydroxy-2-methylpyridine","1-Pentadecanol","2,3,5-Trimethylpyrazine","2-Acetylpyrrole","2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid hydrate","3,4-Dimethylbenzoic acid","Methyl octanoate"]
[null,"g","Empty","E4082","E4093","E4112","E4129","E4141","E4172","E4191","E4209","E4229","E4259","Empty"]
[{"$nulls":3},"2'-Deoxycytidine","DL-Mannitol","Menthol","4-Hydroxybenzylamine","Octadecanedioic acid","trans-Cyclohexane-1,2-diol","trans,trans-2,4-Decadienal","4-Methylbiphenyl","N4-Acetylcytidine","Ethyl cinnamate"]
[null,"h","Empty","E4083","E2662","E4114","E4130","E4147","E4175","E4192","E4213","E4230","E4265","Empty"]
[{"$nulls":3},"D-arabinose","4-Hydroxycoumarin","Arabinose","Methyl undecanoate","Indole-3-carboxaldehyde","(±)-Naringenin","1-Hydroxypyrene","DL-3-Phenyllactic acid","α-Terpinene","Pyrimidine"]
[]
[]
[]
[null,"Plate layout: L1700-92"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E4272","E4289","E4300","E4314","E4322","E4330","E4343","E4354","E4373","E4381","Empty"]
[{"$nulls":3},"Dimethyl sulfone","2-Amino-5-nitrothiazole","Dicyclo hexyl Phthalate","2-Methoxypyrazine","(E)-3,4,5-Trimethoxycinnamic acid","5'-Deoxy-5-fluorocytidine","ISOBUTYRALDEHYDE OXIME","Phenylethyl isothiocyanate","Gibberllin A7","(+)-Fenchone"]
[null,"b","Empty","E4279","E4290","E4306","E4315","E4323","E4331","E4344","E4355","E4374","E4382","Empty"]
[{"$nulls":3},"N,N-Bis(2-hydroxyethyl)-p-phenylenediami","Methyl acetylsalicylate","PALATINOSE","6-Methoxyflavone","Atraric acid","6-Aminonicotinic acid","Thiaproline","Methylsyringol","Zinc Orotate","2-Isopropyl Thioxanthone"]
[null,"c","Empty","E4281","E4291","E4307","E4316","E4324","E4332","E4347","E4356","E4375","E4383","Empty"]
[{"$nulls":3},"Undecanoic gamma-lactone","DL-Pyroglutamic acid","1,4-Anthraquinone","ETHYL OCTANOATE","1,3-BUTANEDIOL","N-Benzylmethylamine","Methyl (E)-ferulate","Pseudotropine","Menthofuran","Hexyl hexanoate"]
[null,"d","Empty","E4282","E4292","E4308","E4317","E4325","E4335","E4348","E4357","E4376","E4385","Empty"]
[{"$nulls":3},"guaiacylpropionic acid","(-)-TERPINEN-4-OL","N-phenethylbenzamide","Ethyl salicylate","2-Fluoroadenosine","ATMP","Phlorizin dihydrate","3-Acetylcoumarin","Kresoxim-Methyl","1-piperoylpiperidine"]
[null,"e","Empty","E4283","E4293","E4309","E4318","E4326","E4336","E4349","E4358","E4377","E4386","Empty"]
[{"$nulls":3},"2-Hydroxybenzothiazole","Tetrahydrofurfuryl Alcohol","Amylopectin","3,5-Diiodo-L-tyrosine dihydrate","2,4-Dihydroxypyridine","2-Hydroxychalcone","Methylarbutin","7-Methoxy-1-tetralone","Cyclopentadecanone","α-Lipoic Acid"]
[null,"f","Empty","E4284","E4294","E4311","E4319","E4327","E4337","E4351","E4359","E4378","E4387","Empty"]
[{"$nulls":3},"Phenyl-β-D-glucopyranoside","(-)-CAMPHOR","Potassium 7-hydroxy-1-naphthalenesulfona","N-PENTADECANE","2-Acetylthiazole","8-Bromoguanosine","m-Coumaric acid","Methyl L-pyroglutamate","Terpineol","4-Methylcinnamic acid"]
[null,"g","Empty","E4285","E4297","E4295","E4320","E4328","E4338","E4352","E4369","E4379","E4391","Empty"]
[{"$nulls":3},"Pyrolin","3,4-(Methylenedioxy)cinnamic acid","Butyl isothiocyanate","Tectoquinone","5-Bromouracil","N-BENZYLFORMAMIDE","Br-Mmc","Oxalic acid dihydrate","Erythorbic Acid","Methyl benzoin"]
[null,"h","Empty","E4286","E4298","E4313","E4321","E4329","E4340","E4353","E4370","E4380","E4393","Empty"]
[{"$nulls":3},"Bromothymol Blue","(-)-Carvone","gamma-Nonanolactone","3-Methoxysalicylaldehyde","Gallic aldehyde","2,6-Dimethylbenzoquinone","Ampicillin","Glycocholic acid hydrate","Isobornyl acetate","2-tert-Butyl-1,4-benzoquinone"]
[]
[]
[]
[null,"Plate layout: L1700-93"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E4394","E4402","E4422","E4480","E4501","E4521","E4537","E4546","E4493","E4563","Empty"]
[{"$nulls":3},"(S)-N-Glycidylphthalimide","Benzofuroxan","DL-Adrenaline Hydrochloride","Sulfentrazone","3,6-Dihydroxyflavone","(S)-3-Hydroxybutanoic acid","(±)-Catechin hydrate","D-(+)-ALLOSE","1-Methylxanthine","7-Ethoxy-4-Methylcoumarin"]
[null,"b","Empty","E4395","E4403","E4423","E4483","E4435","E4526","E4538","E4547","E4488","E4564","Empty"]
[{"$nulls":3},"Methyl 2,4-dihydroxybenzoate","[(2-Methoxyphenoxy)Methyl]Oxirane","Bronidox","(-)-Bornyl acetate","4-Hydroxy-6-methylcoumarin","3-Methoxyflavone","Aegeline","4-Ethoxycoumarin","Zeatin","4-Methyl-6-Methoxycoumarin"]
[null,"c","Empty","E4396","E4404","E4424","E4484","E4507","E4527","E4539","E4548","E4479","E4566","Empty"]
[{"$nulls":3},"Methyl DL-mandelate","2-Amino-3-hydroxypyridine","2,4-Dichlorophenoxyacetic acid","Deltamethrin","7-Ethoxycoumarin","1,3-Dimethyluric acid","4-Hydroxymandelic acid","D-(+)-Fucose","Pseudouridine","Xanthosine dihydrate"]
[null,"d","Empty","E4397","E4405","E4434","E4490","E4508","E4529","E4540","E4550","S7830","E4568","Empty"]
[{"$nulls":3},"ETHYL 3,5-DIHYDROXYBENZOATE","D(+)-LACTIDE","Phenylephrine","Cys-Gly","GLYCODEOXYCHOLIC ACID","DL-O-Tyrosine","Halosulfuron-methyl","3-Hydroxycoumarin","Coenzyme A","meso-Tartaric acid monohydrate"]
[null,"e","Empty","E4398","E4407","E4029","E4492","E4513","E4530","E4542","E4555","E4558","E4569","Empty"]
[{"$nulls":3},"N4-Benzoyl-2′-deoxycytidine","Thiobarbituric acid","Tyramine hydrochloride","Damascone","6-Methylflavone","γ-Linolenic Acid Methyl Ester","D-chiro-Inositol","7-Hydroxyisoflavone","Musk ketone","d-Neomenthol"]
[null,"f","Empty","E4399","E4408","E4440","E4494","E1552","E4532","E4543","E4556","E4559","E4570","Empty"]
[{"$nulls":3},"16a,17a-Epoxy-4-Pregnen-3,20-Dione","Phenyl salicylate","Piperitone","Se-Methylselenocysteine","Oleoylethanolamide","Indoxyl sulfate potassium salt","4,7-Dihydroxycoumarin","Coumarin 7","2-​Methoxy-​4-​vinylphenol","2-Hydroxyflavanone"]
[null,"g","Empty","E4400","E4409","E2164","E4496","E4518","E4534","E4544","E4557","E4560","E4572","Empty"]
[{"$nulls":3},"4-METHOXYCHALCONE","4-(4-Methoxyphenyl)-2-butanone","Citric acid hydrate","Cinnamoylglycine","Oxypurinol","Safranal","DL-Glyceraldehyde","Sinapaldehyde","Carminic acid","5,7-Dihydroxy-4-phenylcoumarin"]
[null,"h","Empty","E4401","E4421","E4516","E4498","E4520","E4535","E4545","E4499","E4561","E4573","Empty"]
[{"$nulls":3},"2-Amino-2-dichlorobenzophenone","Testosterone acetate","L-Sophoridine","4'-Methoxyflavone","Phenazine-1-carboxylic acid","D(+)-Glucuronic acid sodium salt monohydrate","5-Hydroxyflavone","Levomenol","D-Menthol","4-Hydroxyflavanone"]
[]
[]
[]
[null,"Plate layout: L1700-94"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E4574","E4051","E4068","E4079","E4102","E4127","E4150","E4167","E4186","E4201","Empty"]
[{"$nulls":3},"2-Hydroxy Hippuric Acid","(R)-Leucic acid","5-Methyl-2-thiophenecarboxaldehyde","Benzyl salicylate","2,2,2-Trichloroethanol","2-Amino-5-phenylpyridine","H-Tyr-OMe","2,6-Dimethylquinoline","2-Methylcyclopentane-1,3-dione","Phthalide"]
[null,"b","Empty","E4575","E4053","E4069","E4081","E4109","E4128","E4151","E4170","E4188","E4203","Empty"]
[{"$nulls":3},"Phytosphingosine","2-Hexylthiophene","cis-Isolimonenol","1,2-Dimethoxybenzene","rel-α-Vitamin E","4-Methoxyphenethyl alcohol","3-Furanmethanol","1,2,4-Trihydroxybenzene","2,3-Pentanedione","(R)-3-Hydroxybutanoic acid (sodium)"]
[null,"c","Empty","E4576","E4056","E4070","E4084","E4113","E4140","E4154","E4173","E4189","E4205","Empty"]
[{"$nulls":3},"Graveoline","(R,R)-(+)-Hydrobenzoin","Piperonylic acid","Gallic acid (hydrate)","Oleamide","2,6-Dimethylhydroquinone","Dimethylmalonic acid","2-Methylcyclohexanone","3-Methyl-2-cyclopenten-1-one","2-Heptanol"]
[null,"d","Empty","S6135","E4057","E4071","E4088","E4120","E4142","E4155","E4174","E4190","E4206","Empty"]
[{"$nulls":3},"Cholesterol 3-Sulfate Sodium Salt","2-O-Methylcytosine","Ac-β-Ala-OH","(E)-3,4-Dimethoxycinnamic acid","2-Amino-4-methoxyphenol","Linoleyl alcohol","2(5H)-Furanone","2-Methylthiophene","4-Isopropylbenzoic acid","1-Aminopropan-2-ol"]
[null,"e","Empty","E4043","E4058","E4073","E4095","E4121","E4143","E4159","E4181","E4196","E4208","Empty"]
[{"$nulls":3},"DL-Homocysteine thiolactone (hydrochloride)","Xylan","3-Furaldehyde","Nonanal","3,5-Dimethoxybenzoic acid","Methyl 5-hydroxypyridine-2-carboxylate","Dibenzyl disulfide","Benzylideneacetone","Acetylvaline","δ-Decalactone"]
[null,"f","Empty","E4045","E4059","E4075","E4096","E4123","E4145","E4161","E4183","E4198","E4210","Empty"]
[{"$nulls":3},"2-Hydroxymethyltetrahydropyran","Lignin","m-Tolualdehyde","1-Hydroxyanthraquinone","4-Carboxypyrazole","Phenylpropiolic acid","Dibutyl maleate","3-Methylcatechol","2,2-Dimethylsuccinic acid","2-Hydroxy-6-methoxybenzoic acid"]
[null,"g","Empty","E4046","E4064","E4076","E4098","E4124","E4146","E4162","E4184","E4199","E4212","Empty"]
[{"$nulls":3},"(S)-(−)-Perillyl alcohol","Ethyl nonanoate","(S)-(+)-1,2-Propanediol","5-Hydroxyindole","1,3-Dimethylpyrazole","1,2-Cyclohexanedione","Dibenzoylmethane","4-Methylanisole","1,4-Dimethoxybenzene","2-Isobutyl-3-methoxypyrazine"]
[null,"h","Empty","E4050","E4067","E4078","E4101","E4126","E4148","E4164","E4185","E4200","E4214","Empty"]
[{"$nulls":3},"Hygric acid","4-Hydroxymethylpyrazole","α-Cyclodextrin","Pyrrole-2-carboxaldehyde","Methyl isovanillate","4-Methyl-1-pentanol","Diethyl fumarate","2-Thiophenecarboxaldehyde","6-Methylnicotinamide","1-Naphthalenemethanol"]
[]
[]
[]
[null,"Plate layout: L1700-95"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E4222","E4237","E4248","E4261","E4271","E4302","E4368","E4414","E4429","E4458","Empty"]
[{"$nulls":3},"(Ethoxymethyl)benzene","2-Methylbenzoxazole","2-Aminoimidazole","Phenoxyacetic acid","1-Naphthol","2-Ethyl-6-methylphenol","alpha-lactose monohydrate","Octyl acetate","1-Methylguanidine hydrochloride","3-Octanol"]
[null,"b","Empty","E4223","E4238","E4249","E4262","E4273","E4094","E4388","E4415","E4433","E4460","Empty"]
[{"$nulls":3},"1,3-Propanediol","2,4,6-Trimethylphenol","4-Nitrocatechol","1-Dodecanol","Hydroxyacetone","3-Pentanol","D-Sorbitol","Dimethyl malonate","(E，Z)-10-hydroxydec-2-enoic acid","trans,trans-Farnesol"]
[null,"c","Empty","E4224","E4239","E4250","E4263","E4274","E4362","E4389","E4416","E4437","E4461","Empty"]
[{"$nulls":3},"2,5-Furandimethanol","2-Ethylpyrazine","2-Methylpyrazine","1,3-Dihydroxyacetone","2,6-Dibromophenol","N-Demethylricinine","L-Cysteine (hydrochloride)","Stearamide","(E/Z)-Squalene","1-Decanol"]
[null,"d","Empty","E4225","E4240","E4251","E4266","E4275","E4363","E4392","E4417","E4438","E4462","Empty"]
[{"$nulls":3},"(S)-2-Hydroxybutanoic acid","3,5-Di-tert-butylphenol","(E)-Cinnamamide","2,4,5-Trimethoxybenzoic acid","β-Aminopropionitrile","L-Cystine (dihydrochloride)","DPPC","1-Heptadecanol","trans-Nerolidol","1-Tetradecanol"]
[null,"e","Empty","E4226","E4242","E4252","E4267","E4277","E4364","E4410","E4419","E4442","E2419","Empty"]
[{"$nulls":3},"7-Ketolithocholic acid","(±)-Dihydroactinidiolide","(E)-3-(4-Methoxyphenyl)acrylic acid","Methoxyacetic acid","2-Acetonaphthone","Leelamine (hydrochloride)","Methyl citrate","Ethyl linoleate","1,4-Dihydro-4-oxoquinoline-2-carboxylic acid","2-Deoxyadenosine"]
[null,"f","Empty","E4228","E4244","E4253","E4268","E4278","E4365","E4411","E4425","E4455","E4482","Empty"]
[{"$nulls":3},"Meconine","Tetradecyl acetate","5-Methyl-2-furanmethanol","Monomethyl phthalate","(R)-(-)-1,2-Propanediol","4-Methoxycinnamaldehyde","α-Hexylcinnamaldehyde","4-tert-Octylphenol","Monolaurin","3-Pyridineacetic acid"]
[null,"g","Empty","E4232","E4246","E4255","E4269","E4301","E4366","E4412","E4426","E4456","E4485","Empty"]
[{"$nulls":3},"Ethoxyacetic acid","2-Methylquinazolin-4-ol","Tridecane","6-Methyluracil","2,6-Dimethylpyrazine","Lysozyme from chicken egg white","1-Phenylethane-1,2-diol","Glucosamine (sulfate)","Hordenine HCL","L-Perillaldehyde"]
[null,"h","Empty","E4233","E4247","E4257","E4270","E4097","E4367","E4413","E4427","E4457","E4495","Empty"]
[{"$nulls":3},"N,N'-Dimethylthiourea","DL-Pantolactone","Vanillylamine","3-Hydroxypyridine","2,4,6-Trihydroxybenzoic acid","Boc-D-Tyr-OH","Methyl 2,6-dihydroxybenzoate","Ginkgolide K","a-L-Rhamnopyranose","12-Ethyl-9-hydroxycamptothecin"]
[]
[]
[]
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[{"$nulls":3},"Thymopentin Acetate","2'-O-Methyladenosine","(±)-Evodiamine","N-hydroxymethyl succinimide","MF-766","Heclin","Lac-Phe","DPH","Usp22i-S02","E-7386"]
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[{"$nulls":3},"Quininic acid","8-Hydroxy-2'-deoxyguanosine","D-Allose","NS3623","LIT-001 trifluoroacetate","K6PC-5","MDL-800","N-Formyl-Met-Leu-Phe (fMLP)","SU056","NF-κΒ activator 1"]
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[{"$nulls":3},"(-)-Camphoric acid","3-Hydroxy-4-aminopyridine","4-Methylumbelliferyl-β-D-xylopyranoside","Evocalcet","Opnurasib (JDQ-443)","CBR-470-1","TH1760","TDI-011536","EG-011","AZD1656"]
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[{"$nulls":3},"Palmitoylglycine","H-Val-Tyr-OH","Parthenolide","Dubs-IN-1","EG00229","CIA1","MK-0159","Digitonin","wiskostatin","PD173212"]
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[{"$nulls":3},"Validamycin A","L-Uridine","Tylosin Phosphate","NK-252","KI696","Blebbistatin","BGB 15025","GS-4224","SD49-7","JKE-1674"]
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[{"$nulls":3},"Trimethylamine N-oxide","Ononetin","β-Naphthoflavone","LDC195943 (IMT1)","SR-0813","5-Ethynyluridine","SJ6986","CWI1-2 hydrochloride","HPPE","NX-2127"]
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[{"$nulls":3},"2-Hydroxypalmitic acid","Cyclo(Ala-Gly)","4,6-O-Ethylidene-α-D-glucose","LDC203974 (IMT1B)","KSQ-4279","Ibotenic acid","RBN013209","TP-1454","Sebetralstat","BI 1015550"]
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[{"$nulls":3},"Aloin(mixture of A&B)","Tropone","GSK3987","ELN441958","JQAD1","Chroman 1","DPCPX","K-975","HS94","Cp2-SO4"]
[]
[]
[]
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[{"$nulls":3},"KP-457","A2ti-1","IDE397 (GSK-4362676)","Soyasaponin Bb","Laropiprant","Suc-Ala-Ala-Pro-Phe-pNA","Poly(vinyl alcohol)","Ovalbumin (257-264) chicken","2,2-Diphenyl-1-picrylhydrazyl","Pifithrin-β"]
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[{"$nulls":3},"ISA-2011B","Nesuparib","Deutenzalutamide","SR 2640 hydrochloride","Sofpironium bromide","LY3000328","DIRECT RED 80","Sudan Black B","A-1155463","Norepinephrine hydrochloride"]
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[{"$nulls":3},"Eeyarestatin I","MRT-2359","TRC102 (methoxyamine hydrochloride)","(+/-)-Naringenin","Levobunolol(l-Bunolol) hydrochloride","MS023 hydrochloride","Tetrazolium Red","ABTS","SI-2 Hydrochloride","TMRM Perchlorate"]
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[{"$nulls":3},"SP 600125, negative control","Mps1-IN-6 (Compound 9)","TRYPTAMINE HYDROCHLORIDE","Cy7","pemafibrate","Dxd","1-Thioglycerol","5-Chloro-2'-deoxyuridine","MOMIPP","Recilisib"]
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[{"$nulls":3},"GW806742X","T1-44","PK68","Sodium tetradecyl sulfate","dextrothyroxine sodium","3,4-Dichlorophenyl isothiocyanate","1-PHENYL-2-THIOUREA","3-Aminopropyltriethoxysilane","Methyl cellulose (Viscosity:100000mPa.s)","β-Amyloid (25-35)"]
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[{"$nulls":3},"Rilematovir","TPH104m","YLF-466D","Naloxegol Oxalate","iothalamate sodium","MG132 SSS","bisBenzimide H 33258 Trihydrochloride","Diethyl Pyrocarbonate","Didox","D-Desthiobiotin"]
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[{"$nulls":3},"Fluspirilene","A2ti-2","Taurodeoxycholic acid sodium hydrate","Trovafloxacin Mesylate","Lapyrium chloride","(-)-Isoproterenol hydrochloride","Fast Green FCF","Formamide","Bromophenol Blue","2-Chloroacetamide"]
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[{"$nulls":3},"Tuvusertib","MSU-42011","Allocholic acid","Clocortolone Pivalate","methylnaltrexone bromide","Sodium Pyruvate","5,6-Dichlorobenzimidazole 1-beta-D-ribofuranoside","BCIP","MES","MES hydrate"]
[]
[]
[]
[null,"Plate layout: L1700-98"]
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[{"$nulls":3},"Ethyl methanesulfonate","Zinc sulfate heptahydrate","Ruthenium Red","DL-beta-Hydroxybutyric acid sodium salt","Calcium chloride dihydrate","6-Maleimidohexanoic acid N-hydroxysuccinimide ester","APS6-45","GS-6207","DEG-35","Zasocitinib"]
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[{"$nulls":3},"N-Dodecyl beta-D-maltoside","Gramicidin","Formamide deionized","Safranin O","Polyethylenimine","SLC13A5-IN-1","Filanesib hydrochloride","INCB086550","Lirafugratinib","ART812"]
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[{"$nulls":3},"Toluidine Blue O","Influenza Hemagglutinin (HA) Peptide","Xylene Cyanol FF","Sodium DL-lactate solution","1-Oleoyl-rac-glycerol","BLT-1","AR-C155858","CB-5339","Tinengotinib","PRGL493"]
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[{"$nulls":3},"D-(+)-Malic acid","TMRE","(+)-Biotin N-hydroxysuccinimide ester","L-3,4-Dihydroxyphenylalanine methyl ester hydrochloride","N-p-Tosyl-L-phenylalanine chloromethyl ketone","SC-26196","25-Hydroxycholesterol","Enpatoran Hydrochloride","BDTX-1535","AZD0095"]
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[{"$nulls":3},"Carmine","4-AMino-1-phenylpyrazolo[3,4-d]pyriMidine","Acetylthiocholine iodide","4-Methylumbelliferyl beta-D-glucopyranoside","5'-Deoxy-5'-(methylthio)adenosine","KCC-07","Olcegepant","ART558","DJ4","ARV-766"]
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[{"$nulls":3},"Norepinephrine tartrate","IFN alpha-IFNAR-IN-1 hydrochloride","Dimethyl pimelimidate dihydrochloride","Melanin","4-Nitrophenyl beta-D-glucopyranoside","Dobutamine HCl","CA-170 (AUPM-170)","Fezolinetant","PF-07220060 (CDK4/6-IN-6)","FSEN1"]
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[{"$nulls":3},"4-Nitrophenyl-2-acetamido-2-deoxy-β-D-glucopyranoside","GSK-7975A","Sodium pyrophosphate decahydrate","4-Nitrophenyl alpha-D-glucopyranoside","BAR502","UVI 3003","AB680","ZAP-180013","Zilurgisertib fumarate","EN450"]
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[{"$nulls":3},"Triethylenediamine","Sulfosuccinimidyl oleate sodium","N,N'-Methylenebisacrylamide","4-Methylumbelliferyl N-acetyl-beta-D-glucosaminide","HA130","KPLH1130","FX11","PCLX-001 (DDD86481)","M3541","garsorasib (D-1553 )"]
[]
[]
[]
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[{"$nulls":3},"UCL-TRO-1938","Fluorofurimazine","PRT543","SR9011","Reversan","Etrasimod(APD334)","ONO-AE3-208","S-Nitrosoglutathione","Temozolomide Acid","Zandelisib"]
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[{"$nulls":3},"AOH1996","MV1035","Adaptaquin","Pimicotinib","VX-561(CTP-656, Deutivacaftor)","Cirtuvivint","Poly-D-lysine hydrobromide","3-Benzoylpropionic acid","Clavulanic acid","MK-28"]
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[{"$nulls":3},"VT103","Exarafenib","LY2880070","JW74","UNC5293","Propiolactone","8-Cyclopentyl-1,3-dimethylxanthine","S-(5'-Adenosyl)-L-methionine p-toluenesulfonate salt","Infigratinib Phosphate","Cariprazine hydrochloride"]
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[{"$nulls":3},"VT107","Opevesostat (ODM208)","C1632","Itacnosertib (TP-0184)","Protokylol hydrochloride","Cefotetan disodium salt","Ficoll(R) 400","Coenzyme Q1","Lumateperone","INDY"]
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[{"$nulls":3},"Lotiglipron","CD532","BAY 2965501","PBIT","Fasoracetam (NS 105)","MEHP","Cyclic AMP sodium","N6-Cyclopentyladenosine","Acetrizoic acid","Zeocin (Phleomycin D1, zeomycin)"]
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[{"$nulls":3},"ACT001(DMAMCL)","CTPB","Fialuridine","OD36","2,4-Thiazolidinedione","PI4KIIIbeta-IN-10","5,5-Dimethyl-1-pyrroline N-oxide","DL-Thiorphan","MYCMI-6","TEN-010 (RG6146,Ro-6870810,(S)-JQ-35)"]
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[{"$nulls":3},"Avotaciclib trihydrochloride","AS601245","FM19G11","PK11007","Alexidine dihydrochloride","PF-04957325","CSRM617 hydrochloride","Hexythiazox","CD437(AHPN)","Acriflavine"]
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[{"$nulls":3},"TC-S 7009","Gamcemetinib (CC-99677)","B022","MST-312","N6F11","Capadenoson","3,3-Dimethyl-1-butanol","Saquinavir Mesylate","TTK21","TAS-119"]
[]
[]
[]
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[{"$nulls":3},"RMC-4630","DEG-77","Zamaporvint (RXC004)","ALKBH5 inhibitor 2 (Cpd 20m)","Solutol HS-15","AG-120 (racemic)","Tubeimoside III","9-Methoxycamptothecin","Isoastragaloside I","Nepetin"]
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[{"$nulls":3},"UNC 3230","LY3537982 (KRAS G12C inhibitor 19)","Tulmimetostat","Gold(III) chloride trihydrate","3-(Trimethoxysilyl)propyl methacrylate","Azvudine","Chrysoeriol","7-(α-L-Rhamnopyranosyloxy)-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-4H-1-benzopyran-4-one","Isoastragaloside II","Parishin C"]
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[{"$nulls":3},"Pyrilutamide(KX-826)","Palovarotene","Bezuclastinib","Bax inhibitor peptide V5","Nonaethylene glycol Monododecyl ether","Dimethindene maleate","Rhodionin","Tetrahydromagnolol","Ethoxysanguinarine","Tricin"]
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[{"$nulls":3},"POMHEX","ITF3756","ZEN-3694","Lysipressin Acetate","Lactate","Idarubicin HCl","Apiopaeonoside","N-Nornuciferine","Isodeoxyelephantopin","Asperulosidic Acid"]
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[{"$nulls":3},"Sirpiglenastat","BI-2865","icFSP1","Pasireotide","Mal-PEG6-NHS ester","Opicapone","Platycodin D3","3-Hydroxymorindone","Heteroclitin G","Fraxinol"]
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[{"$nulls":3},"Ubrogepant","EP4-IN-1","2,4-dihydroxybenzaldehyde","Poly(2-hydroxyethyl methacrylate)","Sildenafil","Degarelix acetate","Ganoderic acid B","COLUMBIANETIN ACETATE","Prunetin","6,7,8-TRIMETHOXYCOUMARIN"]
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[{"$nulls":3},"Mavorixafor","I-138","Pyronin Y","Sodium propionate","Eprinomectin","Minoxidil","6'-O-beta-D-Glucosylgentiopicroside","Sibiricose A6","Polyporusterone A","DESMETHYLBELLIDIFOLIN"]
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[{"$nulls":3},"Zidesamtinib","IK-930","Phenylarsine oxide","MMRi62","Acetaminophen","Dihydrochelerythrine","7-O-Methylmangiferin","Demethylwedelolactone","Polyporusterone B","11-KETO-BETA-BOSWELLIC ACID"]
[]
[]
[]
[null,"Plate layout: L1700-101"]
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[{"$nulls":3},"2\"-O-Galloylhyperin","Usaramine","Ginsenoside Rf","Coptisine Sulfate","(-​)​-Maackiain","Swertisin","Kurarinone","Mogroside III","Loureirin C","1-[2-Hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one"]
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[{"$nulls":3},"Isovitexin","6'''-Feruloylspinosin","(+)-Magnoflorine iodide","Ophiopogonin D'","Pinosylvin","Avicularin","Saikosaponin F","Aristolactam I","7-Methoxyrosmanol","Diphyllin"]
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[{"$nulls":3},"20(R)-Ginsenoside Rg2","Eudesmin","APIIN","9'''-Methyl salvianolate B","Procyanidin B3","Dihydrokaempferol","Angeloylgomisin H","8-​Prenylnaringenin","Tenuifoliside B","Hederacolchiside A1"]
[null,"d","Empty","E0673","E0690","E0751","E0770","E0903","E0913","E0924","E0980","E2011","E2039","Empty"]
[{"$nulls":3},"Isoschaftoside","Blumeatin","Dihydrosanguinarine","GAULTHERIN","Vicenin 2","Gamabufotalin","EPICATECHIN-(4BETA->8:2BETA-O-7) CATECHIN","Saikosaponin B1","Heteroclitin D","Alisol C 23-acetate"]
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[{"$nulls":3},"Alisol A 24-acetate","Afzelin","Paederosidic acid","Tirucallol","Sesamolin","Methylophiopogonanone A","Agnuside","Pseudolaric acid B β-D-glucoside","Palmaturbine","Aloe-emodin-8-O-β-D-glucopyranoside"]
[null,"f","Empty","E0677","E0695","E0754","E0772","E0907","E0917","E0927","E0992","E2016","E2041","Empty"]
[{"$nulls":3},"Vicine","Byakangelicin","GL3","Vicenin 3","Tilianin","Deoxyshikonin","Saikosaponin B3","Triglochinic acid","Prosapogenin A","Androsin"]
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[{"$nulls":3},"Notoginsenoside Fc","Methyl gypsogenin-3-O-glucuronide","Deapioplatycodin D","Rhodojaponin III","Bellidifolin","Oroxylin A-7-O-glucuronide","Saikosaponin B4","(E)-3,4-Dihydroxybenzylideneacetone, 97%","Dihydromethysticin","Astragaloside III"]
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[{"$nulls":3},"Gomisin D","Arteannuin","ranaconitine","Rhodojaponin II","Deoxyelephantopin","Ginsenoside Rk3","3'-Methoxypuerarin","Methyl rosmarinate","Diosmetin-7-O-β-D-glucopyranoside","Atractyloside A"]
[]
[]
[]
[null,"Plate layout: L1700-102"]
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[{"$nulls":3},"Bayogenin","Methylnissolin","Parishin E","Persicogenin","Rosmanol","CIMIGENOL 3-O-BETA-D-XYLOPYRANOSIDE","Sarracenin","Hydroxy-β-sanshool","5-hydroxy-7,8-dimethoxyflavone","Methylsticin"]
[null,"b","Empty","E2048","E2058","E2085","E2095","E2110","E2127","E2174","E2197","E2211","E2222","Empty"]
[{"$nulls":3},"Oxyberberine","3-Isomangostin","Plantainoside D","Poricoic acid B","Norwogonin","Yibeissine","5,6-dehydrokawain","Epoxymicheliolide","Oxyimperatorin","Noricaritin"]
[null,"c","Empty","E2049","E2060","E2086","E2096","E2111","E2128","E2175","E2198","E2212","E2223","Empty"]
[{"$nulls":3},"β-Boswellic acid","Vitexin-4''-O-glucoside","Rhein 8-Glucoside","Toddaculin","Dehydrotumulosic acid","Corylifol A","Evolitrine","Bruceine A","Chrysin-7-O-glucuronide","Ponicidin"]
[null,"d","Empty","E2050","E2062","E2087","E2097","E2112","E2129","E2184","E2204","E2215","E2224","Empty"]
[{"$nulls":3},"beta-Mangostin","Mosloflavone","Physcion 8-O-β-D-glucopyranoside","Furanodienone","Tetradehydropodophyllotoxin","THEAFLAVIN 3'-O-GALLATE","Suberosin","4-Ethylresorcinol","(E)-Flavokawain A","Prunin"]
[null,"e","Empty","E2051","E2063","E2088","E2098","E2113","E2165","E2190","E2205","E2216","E2229","Empty"]
[{"$nulls":3},"Bilobetin","8-Deoxygartanin","Chrysophanol 8-O-glucoside","Geissoschizine methyl ether","Pinostrobin","Bancroftinone","Dehydroeffusol","Panasenoside","Methyl caffeate","Chrysosplenetin"]
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[{"$nulls":3},"Byakangelicol","Aconine","Emodin-1-O-β-D-glucopyranoside","Platycoside E","Mulberrin","Sinapyl alcohol","(±)-Pinocembrin","Carboxyatractyloside dipotassium","Ethyl 3,4-dihydroxybenzoate","Coniferyl ferulate"]
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[{"$nulls":3},"3,29-Dibenzoyl rarounitriol","Desacetylcinobufagin","Euphol","Nordihydrocapsaicin","Nepodin","4-Methoxyfuro[2,3-b]quinolin-8-ol",null,"Silychristin","PROCYANIDIN A2","Cirsimaritin"]
[null,"h","Empty","E2056","E2074","E2091","E2105","E2120","E2171","E2195","E2209","E2219","E2236","Empty"]
[{"$nulls":3},"Flaconitine","Telocinobufagin","Miltirone","Loureirin D","cephaeline hydrochloride","Senkyunolide H","Hydroxy-α-sanshool","Hirsuteine","Isosakuranin","Yunaconitine"]
[]
[]
[]
[null,"Plate layout: L1700-103"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E2239","E2254","E2290","E2312","E2324","E2333","E2348","E2409","E2418","E2445","Empty"]
[{"$nulls":3},"Methylophiopogonanone B","Gomisin N","Kadsurin","Pseudolaric Acid C","[10]-Shogaol","Paeonolide","IKarisoside A","Rosin","Sanggenon D","Thonningianin A"]
[null,"b","Empty","E2240","E2257","E2295","E2315","E2325","E2334","E2349","E2410","E2421","E2447","Empty"]
[{"$nulls":3},"Kukoamine A","Fructo-oligosaccharide DP8/GF7","3-O-Caffeoylquinic acid methyl ester","Tubuloside B","[8]-Shogaol","Pinoresinol","Kuwanon H","Curculigoside B","Negletein","Guaijaverin"]
[null,"c","Empty","E2241","E2264","E2297","E2316","E2326","E2335","E2350","E2412","E2422","E2450","Empty"]
[{"$nulls":3},"Dehydronuciferine","7-Hydroxyflavanone","Siamenoside I","Glomeratose A","Leucoside","Dactylorhin A","Kakkalide","5,​7,​3'-​Trihydroxy-​6,​4',​5'-​trimethoxyflavone","Glaucine","AESCIN IB(SH)"]
[null,"d","Empty","E2245","E2271","E2300","E2317","E2327","E2336","E2351","E2413","E2423","E2452","Empty"]
[{"$nulls":3},"(-)-Zuonin A","(25R)-Spirost-4-ene-3,12-dione","8-Epidiosbulbin E acetate","Deapi-platycodin D3","AESCIN IA(SH)","Shancigusin I","Tenacissoside G","Nuezhenidic acid","Protogracillin","Platycodin D2"]
[null,"e","Empty","E2246","E2273","E2303","E2318","E2329","E2337","E2352","E2414","E2424","E2453","Empty"]
[{"$nulls":3},"5,7,3',4'-Tetramethoxyflavone","Isolinderalactone","Fructo-​oligosaccharide DP7/GF6","Tripterifordin","Gardenin B","Entadamide-A-β-D-glucopyranoside","Forsythoside I","Sibiricaxanthone B","Kuwanon G","Rosiridin"]
[null,"f","Empty","E2247","E2276","E2306","E2319","E2330","E2340","E2353","E2415","E2426","E2457","Empty"]
[{"$nulls":3},"Dimethyl lithospermate B","Epiberberine chloride","Celosin H","Mirificin","Aristolochic acid D","Feretoside","Forsythoside H","Aristolochic acid B","Cistanoside A","Quercetin 3-gentiobioside"]
[null,"g","Empty","E2248","E2282","E2310","E2322","E2331","E2342","E2405","E2416","E2436","E2462","Empty"]
[{"$nulls":3},"Eupalinolide B","Shanziside","Obtusin","Dehydrocorydaline nitrate","Aristolochic acid C","Iristectorigenin A","vexibinol","Piceatannol 3'-O-glucoside","Ciwujianoside B","Tsugaric acid A"]
[null,"h","Empty","E2249","E2283","E2311","E2323","E2332","E2347","E2408","E2417","E2440","E2465","Empty"]
[{"$nulls":3},"Mogrol","8-Epideoxyloganic acid","Chrysoobtusin","Bavachalcone","Notoginsenoside Fa","Kinsenoside","Rosarin","Gomisin J","Pseudoginsenoside RT5","Agaric acid"]
[]
[]
[]
[null,"Plate layout: L1700-104"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E2468","E2534","E2559","E2596","E2624","E2730","E2796","E5010","E5054","E5096","Empty"]
[{"$nulls":3},"Decursinol","inulicin","N-Benzylpentadecanamide","N-​Benzyllinolenamide","Podophyllotoxone","Isoforskolin","GINSENOSIDE F3","3-HYDROXY-3-METHYLGLUTARIC ACID","Guan-fu base A","Sphondin"]
[null,"b","Empty","E2470","E2537","E2562","E2600","E2625","E2736","E2798","E5012","E5056","E5097","Empty"]
[{"$nulls":3},"Glycycoumarin","N-trans-Feruloyltyramine","14-Deoxyandrographolide","Hirsutine","Garcinone C","Pinostilbene","Gomisin G","2'-Deoxyguanosine monohydrate","4-Allylpyrocatechol","Tribuloside"]
[null,"c","Empty","E2477","E2538","E2570","E2606","E2628","E2737","E2799","E5022","E5071","E5111","Empty"]
[{"$nulls":3},"Cephaeline","LAUROLITSINE","Evocarpine","N-(3-Methoxybenzyl)Palmitamide","Neoliquiritin","Theaflavin-3-gallate","Hederasaponin B","1-Caffeoylquinic acid","3-ACETYL-BETA-BOSWELLIC ACID","Isoforsythiaside"]
[null,"d","Empty","E2478","E2539","E2574","E2607","E2709","E2753","E2801","E5028","E5077","E5112","Empty"]
[{"$nulls":3},"Neoeriocitrin","Irisolidone","Coniferin","8-Epiloganic acid","Halofuginone hydrobromide","Polyphyllin H","Indaconitine","Isoescin IB","AcetylciMigenol-3-O-α-L-arabinopyranside","Sternbin"]
[null,"e","Empty","E2479","E2544","E2575","E2610","E2715","E2781","E2802","E5034","E5078","E5113","Empty"]
[{"$nulls":3},"Kaempferol 3-O-gentiobioside","Lotusine hydroxide","6-Demethoxytangeretin","Vomicine","Polygalaxanthone XI","Kahweol","Iridin","(3S)-3β-Butyl-1,3,4,5-tetrahydroisobenzofuran-1-one","Forsythoside E","Acanthoside B"]
[null,"f","Empty","E2526","E2549","E2578","E2617","E2716","E2791","E2804","E5042","E5087","E5114","Empty"]
[{"$nulls":3},"Phenethyl ferulate","Licarin B","12-O-Methylcarnosic acid","Naringenin triacetate","Cirsimarin","Cynaropicrin","(3beta,4beta,16alpha,21beta,22alpha)-28-(Acetyloxy)-16,22,23-trihydroxy-21-[[(2E)-2-methyl-1-oxo-2-buten-1-yl]oxy]olean-12-en-3-yl O-beta-D-glucopyranosyl-(1-2)-O-[beta-D-glucopyranosyl-(1-4)]-beta-D-glucopyranosiduronic acid","Notoginsenoside Ft1","N-Benzyllinoleamide","Ursolic acid acetate"]
[null,"g","Empty","E2528","E2554","E2586","E2619","E2725","E2794","E5004","E5047","E5089","E5117","Empty"]
[{"$nulls":3},"Phellopterin","N-FeruloyloctopaMine","Chebulic acid","Regaloside A","LARIXYL ACETATE","Garcinone D","magnessium lithospermate B","Phenol, 4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy-","Eupatorin","Bruceine E"]
[null,"h","Empty","E2532","E2557","E2588","E2621","E2728","E2795","E5008","E5049","E5094","E5118","Empty"]
[{"$nulls":3},"Continentalic acid","Prudomestin","dichotomitin","N-(3-Methoxybenzyl)stearamide","Nevadensin","Gartanin","13-Acetyl-9-dihydrobaccatin III","TOTAROL","Erythrodiol","Grosvenorine"]
[]
[]
[]
[null,"Plate layout: L1700-105"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","E5121","E5158","E5178","E5194","E5217","E5265","E5328","E5368","E5416","E5430","Empty"]
[{"$nulls":3},"Ombuoside","Soyasapogenol B","γ-Tocopherol","Carvacrol methyl ether","4-Hydroxy-5-methylfuran-3(2H)-one","(Rac)-Norcantharidin","Baicalin methyl ester","Tetrahydroharmine","Effusol","8-Deacetylyunaconitine"]
[null,"b","Empty","E5122","E5160","E5179","E5197","E5230","E5267","E5334","E5369","E5417","E5435","Empty"]
[{"$nulls":3},"Obtucarbamate A","Gypenoside XLVI","11-Methoxyyangonin","Crocetin","Catechin 7-O-β-D-glucopyranoside","Sanggenon C","Neosmitilbin","Protosappanin A","Liriopesides B","β-D-glucopyranosyl-[α-L-rhamnopyranosyl-(1→3)-βD-glucuronopyranosyl-(1→3)]-3β-hydroxyolean-12-ene28-oate"]
[null,"c","Empty","E5125","E5162","E5182","E5204","E5234","E5268","E5335","E5372","E5418","E5444","Empty"]
[{"$nulls":3},"Meranzin","Pinocembrin-7-O-β-D-glucopyranoside","Prosaikogenin D","Pennogenin","Kaempferol 3-O-sophoroside","Mulberroside C","Beta-Eudesmol","Piperlonguminine","Timosaponin A1","Mesaconine"]
[null,"d","Empty","E5126","E5163","E5183","E5206","E5241","E5273","E5341","E5374","E5421","E5448","Empty"]
[{"$nulls":3},"Juglanin","Glucovanillin","Flavanomarein","Neogambogic acid","Neoisoastilbin","Eupalinolide A","Voacamine","7-Epi 10-desacetyl paclitaxel","Crocin III","Raddeanoside R8"]
[null,"e","Empty","E5136","E5164","E5184","E5207","E5242","E5292","E5346","E5380","E5422","E5449","Empty"]
[{"$nulls":3},"Arnidiol","Iristectorin A","(-)-(E)-Guggulsterone","Macranthoside B","Celosin I","Nigakinone","(-)-Epipodophyllotoxin","Quercimeritrin","Mogroside IIe","Taurolithocholic acid sodium salt"]
[null,"f","Empty","E5140","E5168","E5186","E5208","E5247","E5306","E5347","E5386","E5423","E5453","Empty"]
[{"$nulls":3},"Yadanziolide A","Glycyrrhetic acid 3-O-β-D-glucuronide","4'-O-Methylpyridoxine","1β-Hydroxybaccatin I","Tetrahydropalmatine","Demethylsuberosin","4-O-Methyl honokiol","Shikonin","Iristectorin B","Lasiokaurin"]
[null,"g","Empty","E5144","E5175","E5189","E5215","E5261","E5309","E5357","E5397","E5425","E5454","Empty"]
[{"$nulls":3},"Nepitrin","7-Prenyloxycoumarin","Andrograpanin","Pro-xylane","Rubiadin","Iristectorigenin B","Orthosphenic acid","Puerarin 6''-O-Xyloside","DiosMetin 7-O-β-D-Glucuronide","Vicenin-1"]
[null,"h","Empty","E5150","E5176","E5192","E5216","E5263","E5316","E5362","E5403","E5427","E5455","Empty"]
[{"$nulls":3},"α-Terpineol","3',​4',​5',​5,​7-​Pentamethoxyflavone","Paraxanthine","SodiuM new houttuyfonate","(-)-Gallocatechin","Ilexsaponin A","Maltoheptaose","Swertianolin","Clitorin","Hesperetin 7-O-glucoside"]
[]
[]
[]
[null,"Plate layout: L1700-106"]
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[null,"a","Empty","E5464","E5498","E5556","E5577","E5590","E5602","E5624","E5661","E5720","E5747","Empty"]
[{"$nulls":3},"(+)-Bornyl acetate","Taurochenodeoxycholic acid sodium","Britannin","Cauloside F","Arborine","Granilin","Spirostan-3-ol","3,5-O-Dicaffeoylquinic acid","Isocurcumenol","Euphorbia factor L7b"]
[null,"b","Empty","E5471","E5508","E5557","E5579","E5593","E5604","E5628","E5670","E5721","E5749","Empty"]
[{"$nulls":3},"L-Hyoscyamine sulfate","Pyromeconic acid","Noreugenin","Asatone","Acetylalkannin","28-Homobrassinolide","Ricinine","Silybin","Orcinol gentiobioside","Gentianose"]
[null,"c","Empty","E5477","E5523","E5559","E5583","E5594","E5608","E5629","E5689","E5723","E5757","Empty"]
[{"$nulls":3},"Qingyangshengenin A","(5R,6E)-5-Hydroxy-1,7-diphenyl-6-hepten-3-one","Loganetin","18α-Glycyrrhizic acid","Angoline","6-Hydroxyluteolin 7-glucoside","Decaffeoylacteoside","Ethyl linolenate","Anemarrhenasaponin I","7-Hydroxyaristolochic acid A"]
[null,"d","Empty","E5483","E5525","E5561","E5584","E5595","E5609","E5630","E5697","E5726","S0336","Empty"]
[{"$nulls":3},"Isorhamnetin-3-O-glucoside","Beta-Acetoxyisovalerylshikonin","Dihydropinosylvin","Scutellarin methyl ester","Isookanin","Stachyose hydrate","Rupestonic acid","Polygalasaponin V","Euphorbia Factor L2","Eurycomanone"]
[null,"e","Empty","E5484","E5526","E5562","E5585","E5596","E5614","E5631","E5705","E5728","S0703","Empty"]
[{"$nulls":3},"20(R)-Protopanaxatriol","Ecliptasaponin D","Eriodictyol-7-O-glucoside","Mogroside III-E","Regaloside B","Kaempferol 3-O-β-D-galactopyranoside","Catharanthine Sulfate","Rhodiosin","Terrestrosin D","DELTALINE"]
[null,"f","Empty","E5491","E5528","E5565","E5586","E5599","E5616","E5632","E5706","E5741","S0704","Empty"]
[{"$nulls":3},"Notoginsenoside R2","N-trans-p-coumaroyloctopamine","Morellic acid","(R,R)-Secoisolariciresinol diglucoside","Euphorbia factor L7a","Silybin B","Neocnidilide","Adynerin","Lactiflorin","Delsoline"]
[null,"g","Empty","E5493","E5530","E5570","E5588","E5600","E5617","E5633","E5709","E5742","S0903","Empty"]
[{"$nulls":3},"Euphornin","Ipecoside","Quercetagitrin","25-O-Methylalisol A","Malabaricone C","Theaflavin 3,3'-digallate","Reptoside","Karanjin","Marein","Mogroside IV"]
[null,"h","Empty","E5494","E5542","E5574","E5589","E5601","E5621","E5636","E5712","E5744","S0905","Empty"]
[{"$nulls":3},"Clinodiside A","Gypenoside A","Saponin C, from Liriope muscari","Isoasatone A","Cimicifugoside H-1","Eriocalyxin B","Glycohyodeoxycholic acid","Oxypeucedanin hydrate","Complanatoside B","(-)-Syringaresnol-4-O-β-D-apiofuranosyl-(1→2)-β-D-glucopyranoside"]
[]
[]
[]
[null,"Plate layout: L1700-107"]
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[{"$nulls":3},"Peimisine","Epimedin A1","Oxypaeoniflorin","Alismoxide","11-oxo-mogroside V","Osthenol","Defactinib (VS-6063)"]
[null,"b","Empty","S0908","S0930","S0946","S0960","S0971","S5870","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"β,β-Dimethylacrylshikonin","6-Demethoxylnobiletin","Theaflavin","Psoralenoside","Kakuol","Paederosidic acid methyl ester"]
[null,"c","Empty","S0909","S0932","S0948","S0961","S0972","S5889","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"D-Tetrahydropalmatine","Baimaside","Allocryptopine","Isopsoralenoside","Incensole","N-Methylnuciferine"]
[null,"d","Empty","S0910","S0933","S0952","S0962","S0974","S5890","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Bufotalin","Melittoside","Benzoylhypaconine","Methylnissolin-3-O-glucoside","Sulforaphene","Epibetulinic acid"]
[null,"e","Empty","S0912","S0934","S0954","S0963","S0975","S6372","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Oxysophoridine","Xylotetraose","Picroside III","2'-Acetylacteoside","araloside A","Meranzin hydrate"]
[null,"f","Empty","S0914","S0935","S0955","S0964","S4275","S8688","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"(±)-Decursinol","isomangiferin","Roburic acid","Liquiritin apioside","Bergamottin","Fucoxanthin"]
[null,"g","Empty","S0919","S0937","S0956","S0965","S4916","S9191","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Tubuloside A","3-Dehydrotrametenolic acid","Pinoresinol 4-O-β-D-glucopyranoside","Aloeresin D","Cyanidin Chloride","Loganic acid"]
[null,"h","Empty","S0927","S0940","S0957","S0966","S5470","S9495","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Tenuifoliside C","Edpetiline","Fuziline","SCIADOPITYSIN","(Z)-Ligustilide","Flavokawain C"]
[]
[]
[]
[null,"Plate layout: L1700-108"]
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[{"$nulls":3},"Perifosine (KRX-0401)","Biapenem","Cidofovir","Etidronate","Sodium butyrate","Chondroitin sulfate","Lomefloxacin HCl","Hygromycin B","Amikacin disulfate","L-Arginine HCl (L-Arg)"]
[null,"b","Empty","S1116","S1375","S1518","S1875","S2000","S2420","S2560","S3007","S3072","S3211","Empty"]
[{"$nulls":3},"Palbociclib (PD-0332991) HCl","Dorzolamide HCl","Ibuprofen Lysine","Tranexamic Acid","Sodium orthovanadate","Aloperine","Amiloride HCl dihydrate","Zanamivir","(R)-baclofen","Thiamine HCl (Vitamin B1)"]
[null,"c","Empty","S1135","S1384","S1579","S1893","S2008","S2462","S2563","S3013","S3073","S3620","Empty"]
[{"$nulls":3},"Pemetrexed (LY-231514) disodium","Mizoribine","Palbociclib (PD0332991) Isethionate","D-glutamine","Taurine","Donepezil HCl","Oxacillin sodium monohydrate","Plerixafor (AMD3100) 8HCl","Caspofungin (MK-0991) Acetate","β-Glycerophosphate sodium salt hydrate"]
[null,"d","Empty","S1149","S1395","S1624","S1939","S2048","S2490","S2568","S3028","S3102","S3631","Empty"]
[{"$nulls":3},"Gemcitabine (LY-188011) HCl","Polymyxin B sulphate","Alendronate sodium trihydrate","Levamisole hydrochloride","Clindamycin Phosphate","Neostigmine Bromide","Neomycin sulfate","Geneticin (G418 Sulfate)","Creatinine","(S)-Methylisothiourea sulfate"]
[null,"e","Empty","S1311","S1399","S1648","S1984","S2076","S2507","S2572","S3048","S3122","S3642","Empty"]
[{"$nulls":3},"Pamidronate Disodium","Teicoplanin","Cytarabine (U-19920A)","Ticlopidine HCl","Lisinopril dihydrate","Salbutamol Sulfate","Streptomycin sulfate","Solifenacin succinate","Amikacin hydrate","Cesium chloride"]
[null,"f","Empty","S1338","S1440","S1749","S1985","S2129","S2514","S2575","S3050","S3146","S3649","Empty"]
[{"$nulls":3},"Gabapentin HCl","Varenicline Tartrate (CP 526555-18)","L-Glutamine","ATP disodium","Fudosteine","Tobramycin","Vancomycin HCl","Palonosetron HCl","Tripelennamine HCl","Ceftazidime"]
[null,"g","Empty","S1339","S1494","S1751","S1995","S2133","S2518","S2877","S3056","S3148","S3650","Empty"]
[{"$nulls":3},"Galanthamine HBr","Ralimetinib (LY2228820) dimesylate","Gadodiamide Hydrate","Procarbazine HCl","Gabapentin","NAD+","L-NAME HCl","Miltefosine","Ibandronate sodium monohydrate","Penicillin V potassium salt"]
[null,"h","Empty","S1345","S1506","S1853","S1998","S2315","S2527","S2879","S3058","S3165","S3662","Empty"]
[{"$nulls":3},"Granisetron HCl","Perindopril Erbumine","Penicillamine","D-Cycloserine","Kanamycin sulfate","Methacycline HCl","AMD3465 hexahydrobromide","Danofloxacin Mesylate","Abacavir sulfate","Pirenzepine dihydrochloride"]
[]
[]
[]
[null,"Plate layout: L1700-109"]
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[null,"a","Empty","S3667","S3861","S4028","S4117","S4158","S4254","S4392","S4606","S4740","S4827","Empty"]
[{"$nulls":3},"Imipenem","Sodium Demethylcantharidate","Dexamethasone Sodium Phosphate","Histamine Phosphate","Ceftriaxone disodium salt hemi (heptahydrate)","Apramycin Sulfate","Potassium Canrenoate","Glutathione","Sodium ferulate","Manganese chloride"]
[null,"b","Empty","S3737","S3953","S4029","S4121","S4174","S4271","S4430","S4653","S4741","S4828","Empty"]
[{"$nulls":3},"Cangrelor Tetrasodium","L-Lysine hydrochloride","Colistin Sulfate","Succinylcholine Chloride Dihydrate","Sodium Gluconate","Isepamicin Sulphate","Hydroxychloroquine Sulfate (NSC 4375)","L-Ornithine hydrochloride","Danshensu","Sodium carbonate"]
[null,"c","Empty","S3748","S3963","S4030","S4127","S4180","S4287","S4523","S4671","S4770","S4950","Empty"]
[{"$nulls":3},"Acamprosate Calcium","DL-Glutamine","Gentamicin Sulfate","Terbutaline Sulfate","Nefopam HCl","Micafungin (FK 463) Sodium","Dihydrostreptomycin sulfate","Cefradine","Creatine phosphate disodium salt","L(+)-Asparagine monohydrate"]
[null,"d","Empty","S3752","S3973","S4052","S4130","S4183","S4298","S4540","S4700","S4786","S4951","Empty"]
[{"$nulls":3},"isoleucine","L-SelenoMethionine","Netilmicin Sulfate","Mildronate","Paromomycin Sulfate","Amifostine trihydrate","Sisomicin sulfate","4-Aminobutyric acid (GABA)","S-Methyl-L-cysteine","L-Threonine"]
[null,"e","Empty","S3753","S3989","S4069","S4137","S4215","S4311","S4567","S4702","S4791","S4972","Empty"]
[{"$nulls":3},"L-Leucine","L-​Histidine","Hexamethonium Dibromide","Eprazinone 2HCl","Ribostamycin Sulfate","Calcium Gluceptate","Eprodisate disodium","Sarcosine","S-allyl-L-cysteine","Choline Glycerophosphate"]
[null,"f","Empty","S3793","S4008","S4093","S4144","S4234","S4314","S4575","S4703","S4810","S4993","Empty"]
[{"$nulls":3},"Phytic acid","Pemirolast potassium","Bismuth Subcitrate Potassium","Amprolium HCl","Capreomycin Sulfate","Ceftazidime Pentahydrate","Pralidoxime chloride","Choline bitartrate","Glycylglycine","Timonacic"]
[null,"g","Empty","S3798","S4013","S4094","S4146","S4236","S4328","S4582","S4704","S4811","S5048","Empty"]
[{"$nulls":3},"L-Citrulline","Sodium Monofluorophosphate","Tetramisole HCl","Bacitracin","Proflavine Hemisulfate","Guanethidine Sulfate","Eflornithine (MDL-71782) hydrochloride hydrate","D-(+)-Cellobiose","VitaMin U","Fosfomycin Disodium"]
[null,"h","Empty","S3852","S4027","S4108","S4157","S4245","S4360","S4592","S4721","S4821","S5051","Empty"]
[{"$nulls":3},"L-Theanine","Flavoxate HCl","Clodronate Disodium","Chloroquine diphosphate","Sodium ascorbate","Tolmetin Sodium","Captisol (SBE-β-CD)","L-Glutamic acid monosodium salt","Glycine","Pipemidic acid"]
[]
[]
[]
[null,"Plate layout: L1700-110"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S5097","S5226","S5362","S5518","S5584","S5632","S5746","S6044","S6103","S6134","Empty"]
[{"$nulls":3},"Methotrexate disodium","L-carnosine","Citicoline","D-Glucose 6-phosphate disodium salt","Citronellol","L-aspartic Acid","pentetate calcium trisodium hydrate","H-Tyr(3-I)-OH","Inosine 5′-triphosphate trisodium salt","3-Aminoisobutyric acid"]
[null,"b","Empty","S5107","S5252","S5374","S5524","S5588","S5633","S5801","S6054","S6106","S6137","Empty"]
[{"$nulls":3},"Riboflavin phosphate sodium","Ozagrel sodium","5'-Cytidylic acid","Spermine Tetrahydrochloride","Creatine","L-methionine","Ala-Gln","Glycyl-L-leucine","3-Chloro-L-tyrosine","4-Guanidinobutanoic acid"]
[null,"c","Empty","S5115","S5259","S5384","S5526","S5591","S5634","S5820","S6056","S6109","S6141","Empty"]
[{"$nulls":3},"Sodium L-ascorbyl-2-phosphate","β-Nicotinamide Mononucleotide","UTP Trisodium Salt","β-Alanine","Ectoine","L-arginine","L-Hydroxyproline","N-Methylsarcosine","H-HoArg-OH","Anserine"]
[null,"d","Empty","S5124","S5267","S5412","S5533","S5612","S5635","S5866","S6061","S6116","S6142","Empty"]
[{"$nulls":3},"DL-Citrulline","Nylidrin Hydrochloride","Loxoprofen Sodium","Tobramycin sulfate","Isonipecotic acid","L-cysteine","Gastrodenol","DL-m-Tyrosine","N-Acetylornithine","3-Amino-4-methylpentanoic acid"]
[null,"e","Empty","S5131","S5296","S5431","S5545","S5628","S5660","S5867","S6064","S6120","S6153","Empty"]
[{"$nulls":3},"Homotaurine","Cephradine monohydrate","L-Homoarginine hydrochloride","DL-Serine","L-Valine","Clodronate disodium tetrahydrate","Bendazac L-lysine","Acid Yellow 23","Glycyl-L-valine","L-Leucyl-L-alanine Hydrate"]
[null,"f","Empty","S5136","S5338","S5433","S5549","S5629","S5674","S6016","S6075","S6128","S6176","Empty"]
[{"$nulls":3},"Calcium folinate","L(-)-Sorbose","Sodium succinate","DL-Arginine","L-Proline","Lodoxamide Tromethamine","D-Proline","Nepsilon-Acetyl-L-lysine","L-Homocitrulline","Scyllo-Inositol"]
[null,"g","Empty","S5137","S5340","S5468","S5571","S5630","S5706","S6021","S6082","S6129","S6201","Empty"]
[{"$nulls":3},"O-Phospho-L-serine","3-Aminopropionitrile fumarate","Kaempferol-3-O-glucorhamnoside","L-Asparagine","L-lysine","Edetate Trisodium","5-Methylcytosine","8-Aminooctanoic acid","Aminomalonic acid","Malachite green"]
[null,"h","Empty","S5220","S5344","S5496","S5572","S5631","S5721","S6023","S6102","S6133","S6203","Empty"]
[{"$nulls":3},"D-Pantethine","1,4-Diaminobutane dihydrochloride","Guanethidine Monosulfate","Azetidine-2-carboxylic acid","L-Alanine","Edetate calcium disodium","Creatine monohydrate","Thiamine pyrophosphate hydrochloride","H-Gly-Pro-OH","H-Abu-OH"]
[]
[]
[]
[null,"Plate layout: L1700-111"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S6222","S6306","S6460","S7419","S7901","S8674","P1011","P1084","S2441","S0189","Empty"]
[{"$nulls":3},"Ethyl potassium malonate","Guanosine 5'-monophosphate disodium salt","Sugammadex (sodium)","Blasticidin S HCl","Ac-DEVD-CHO","GO-203","Eptifibatide Acetate","Desmopressin Acetate","Estramustine phosphate sodium","PMPA tetrasodium salt"]
[null,"b","Empty","S6224","S6312","S6480","S7507","S8008","S9062","P1017","P1085","S3948","S3203","Empty"]
[{"$nulls":3},"(R)-Serine","L-Threonic acid Calcium Salt","Triphosphopyridine nucleotide disodium salt","LDN-193189 2HCl","RGD (Arg-Gly-Asp) Peptides","4-Hydroxyisoleucine","Octreotide (SMS 201-995) acetate","Angiotensin II human Acetate","Spermine","D-Alanine"]
[null,"c","Empty","S6230","S6315","S6483","S7537","S8199","S9344","P1025","P1087","S2433","S6871","Empty"]
[{"$nulls":3},"Methyl 3-aminopyrazine-2-carboxylate","Sodium phytate hydrate","O-Phosphoethanolamine","LB-100","Ruxotemitide (LTX 315)","DL-Methionine","Atosiban Acetate","Carperitide Acetate","DL-Buthionine-Sulfoximine","Sodium oxamate"]
[null,"d","Empty","S6266","S6322","S6488","S7547","S8442","S9345","P1029","S1671","S2435","S6894","Empty"]
[{"$nulls":3},"(S)-Glutamic acid","Pipecolic acid","Gadoxetate sodium","XL413 (BMS-863233)","TAK-659","Disodium 5'-Inosinate","Oxytocin (Syntocinon)","(6-)ε-​Aminocaproic acid","Sodium stibogluconate","BCH"]
[null,"e","Empty","S6270","S6325","S6592","S7548","S8454","S9353","P1030","S3076","S6831","S8620","Empty"]
[{"$nulls":3},"2-Aminoisobutyric acid","Adenosine 5′-diphosphate sodium salt","Diquafosol Tetrasodium","Rilmenidine Phosphate","ATN-161 (Ac-PHSCN-NH2)","L-serine","Salmon Calcitonin Acetate","Foscarnet Sodium","HEPES","6-Diazo-5-oxo-L-norleucine"]
[null,"f","Empty","S6276","S6330","S7204","S7785","S8501","S9365","P1034","S4519","S7764","S9665","Empty"]
[{"$nulls":3},"Bicine","D(-)-2-Aminobutyric acid","Fosbretabulin (Combretastatin A4 Phosphate (CA4P)) Disodium","Pemetrexed Disodium Hydrate","Adaptavir (DAPTA)","Disodium uridine-5'-monophosphate","Terlipressin Acetate","Citric acid trilithium salt tetrahydrate","WST-8","Motixafortide (BL-8040)"]
[null,"g","Empty","S6290","S6334","S7306","S7809","S8549","S9367","P1039","S5865","S8670","P1088","Empty"]
[{"$nulls":3},"D-Fructose-1,6-diphosphate trisodium salt octahydrate","DL-Norvaline","Dorsomorphin (Compound C) 2HCl","MCC950 Sodium (CP-456773 Sodium)","AUNP-12","Adenosine disodium triphosphate hydrate","Somatostatin Acetate","Hyaluronic acid","Vipivotide tetraxetan (PSMA-617)","Lanreotide acetate"]
[null,"h","Empty","S6302","S6445","S7362","S7873","S8651","P1004","P1049","S4986","S4933","S1325","Empty"]
[{"$nulls":3},"L(-)-Pipecolinic acid","Chlorophyllin (sodium copper salt)","AZD5582","Disodium (R)-2-Hydroxyglutarate","bpV (HOpic)","Bivalirudin Trifluoroacetate","GHRP-2","Latamoxef sodium","Lithium carbonate","L-2-Hydroxyglutaric acid disodium"]
[]
[]
[]
[null,"Plate layout: L1700-112"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S2988","S3084","S3327","S3368","P1201","S4443","S5260","S6077","S9489","E0375","Empty"]
[{"$nulls":3},"DL-5-Hydroxylysine hydrochloride","Guanosine 5'-triphosphate trisodium salt","Disodium 5'-inosinate monohydrate","Uridine-5'-diphosphate disodium salt","LL37 (Human cathelicidin)","Piperazine adipate","ATP","Cytidine 5′-triphosphate (disodium salt)","Sodium citrate","Ammonium ferric citrate"]
[null,"b","Empty","S2991","S3096","S3331","S8414","P1202","S4494","S5330","S2967","S0430","P1104","Empty"]
[{"$nulls":3},"Thiamine monophosphate chloride dihydrate","L-Histidine monohydrochloride monohydrate","2-Aminoethylphosphonic acid","PACAP 1-27","TMPyP4 tosylate","Methionine","Amikacin Sulfate Salt","XE991 dihydrochloride","MELK-8a Dihydrochloride","Glatiramer acetate"]
[null,"c","Empty","S2992","S3118","S3335","S8415","P1204","S4513","S5956","S5962","S9820","P1210","Empty"]
[{"$nulls":3},"Sodium mesoxalate monohydrate","L-Homoserine","Phospho(enol)pyruvic acid monopotassium salt","PACAP 1-38","Myelin Oligodendrocyte Glycoprotein 35-55, mouse, rat","RGD peptide (GRGDNP)","Dexamethasone phosphate disodium","DL-Penicillamine","Angiotensin (1-7)","11R-VIVIT TFA"]
[null,"d","Empty","S2993","S3119","S3345","S9664","S1314","S4857","S5964","S5976","E0029","S6289","Empty"]
[{"$nulls":3},"D-Saccharic acid potassium salt","1-Aminocyclopropanecarboxylic acid","Nα-Acetyl-L-lysine","Colivelin","Zoledronic acid (ZOL 446)","L-Ornithine","Gatifloxacin hydrochloride","Sulforhodamine B sodium salt","Hexa-D-arginine","Gentamicin"]
[null,"e","Empty","S2994","S3142","S3346","S9666","S2961","S4879","S5968","S6090","E0134","S6872","Empty"]
[{"$nulls":3},"DL-Homocysteine","Potassium sorbate","1-Methylnicotinamide chloride","DX600","GC7 Sulfate","Tenofovir hydrate","Kasugamycin hydrochloride hydrate","JFD01307SC","L-Albizziin","Merbromin"]
[null,"f","Empty","S2996","S3221","S3349","S9728","S3351","S5000","S6446","S6991","E0152","E0510","Empty"]
[{"$nulls":3},"L-DAB HBR","Thymidine 5'-monophosphate disodium salt","Phosphocholine chloride calcium salt tetrahydrate","BSO (L-Buthionine-(S,R)-sulfoximine)","Sodium phenylpyruvate","Gadodiamide","Sodium citrate dihydrate","Sodium Acetate","L(+)-Monosodium glutamate monohydrate","Cidofovir hydrate"]
[null,"g","Empty","S3040","S3266","S3354","P1033","S3497","S5022","S9794","S6992","E0351","E0511","Empty"]
[{"$nulls":3},"Isocitric acid trisodium salt","L-Anserine nitrate salt","DL-2,3-Diaminopropionic acid monohydrochloride","Teriparatide Acetate","Gadobutrol","Varenicline Hydrochloride","Melittin","Calcium chloride","NSC232003","Framycetin sulphate"]
[null,"h","Empty","S3049","S3326","S3367","P1047","S4383","S5198","S9803","S7920","E0353","E0525","Empty"]
[{"$nulls":3},"Calcium 2-hydroxy-4-(methylthio)butanoate","Phytic acid dipotassium salt","cis-4-Hydroxy-D-proline","Felypressin Acetate","Bekanamycin","Sodium Etidronate","Elamipretide (MTP-131)","L-NMMA acetate","Potassium oxonate","Colistin"]
[]
[]
[]
[null,"Plate layout: L1700-113"]
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[null,"a","Empty","E0532","E2688","S3406","S8522","P1019","P1148","E4204","E4341","E4567","E4221","Empty"]
[{"$nulls":3},"Menotropin","Glufosinate-ammonium","LDN-192960","Compstatin","Cetrorelix Acetate","BPC157","5-Aminovaleric acid","DL-Leucine","D-Isoleucine","DL-Asparagine"]
[null,"b","Empty","E0654","E2691","S3734","S8554","P1020","E4052","E4227","E4342","E4047","E4243","Empty"]
[{"$nulls":3},"D-Arginine","BAPTA tetrapotassium salt","Albiglutide Fragment","Super-TDU","Argipressin acetate","D-Ornithine (hydrochloride)","D-Cysteine","Phosphocreatine disodium salt hydrate","Laminaran","DL-Glutamic acid"]
[null,"c","Empty","E0705","E2692","S3736","S8595","P1027","E4063","E4245","E4346","E4104","E4390","Empty"]
[{"$nulls":3},"Flavin Adenine Dinucleotide Disodium","L-Ascorbic acid 2-phosphate sesquimagnesium salt","Fondaparinux Sodium (Org 31540)","Tat-beclin 1 (Tat-BECN1)","Melanotan II","β-Glycerophosphate (disodium salt hydrate)","L-Azetidine-2-carboxylic acid","Creatine phosphate disodium salt tetrahydrate","DL-Lysine","Aspartic acid (calcium)"]
[null,"d","Empty","E2403","E2701","S8164","S9725","E0149","E4144","E4258","E4350","E4107","E4428","Empty"]
[{"$nulls":3},"ζ-Stat (NSC37044)","Sodium phosphate monobasic monohydrate","YAP-TEAD Inhibitor 1 (Peptide 17)","Balixafortide (POL6326)","Papain","H-Val-Ala-OH","L-Norleucine","D-Glutamic acid","DL-Threonine","(S)-2-(Methylamino)-3-phenylpropanoic acid"]
[null,"e","Empty","E2435","E2830","S8187","E0016","S6482","E4156","E4264","E4481","E4108","E4430","Empty"]
[{"$nulls":3},"Perindopril L-Arginine","Cyclocreatine","ReACp53","Tertiapin-Q","Fosphenytoin (disodium)","L-Allothreonine","D-Leucine","(S)-Spinacine","L-Aspartic aicd (sodium)","fish sperm DNA"]
[null,"f","Empty","E2635","P1137","S8197","E0518","S5961","E4157","E4287","E4487","E4111","E4431","Empty"]
[{"$nulls":3},"Bicinchoninic acid disodium salt","Thymulin","APTSTAT3-9R","Polyinosinic acid-polycytidylic acid","Prednisolone disodium phosphate","Hydroxycitric acid (tripotassium hydrate)","3-Aminobutanoic acid","L-allo-Isoleucine","Phytic acid (dodecasodium salt hydrate)","D-Fructose-1,6-Diphosphate"]
[null,"g","Empty","E2638","P1213","S8416","E1223","E0178","E4165","E4288","E4491","E4122","E4504","Empty"]
[{"$nulls":3},"Tricine","gp91ds-tat","PACAP 6-38","RGX-202","Cysteamine bitartrate","L-Methionine sulfoxide","DL-Valine","α-D-Glucose 1-phosphate disodium salt hy","D-Allothreonine","Phenylalanylalanine"]
[null,"h","Empty","E2681","S0833","S8505","E2035","P1155","E4166","E4339","E4549","E4169","E4509","Empty"]
[{"$nulls":3},"Sodium acrylate","EIDD-1931","LY2510924","Larazotide","CREBtide","Methionine sulfoxide","4-Hydroxy-L-phenylglycine","D-Glucose 6-phosphate sodium salt","Imidazol-1-yl-acetic acid","L-Prolylglycine"]
[]
[]
[]
[null,"Plate layout: L1700-114"]
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[{"$nulls":3},"Copper tripeptide","Ammonium sulfate","Trilaciclib dihydrochloride","Secologanoside","Neonuezhenide"]
[null,"b","Empty","E1723","E1689","S2542","E5185","E5685","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"NSC16168","NADPH tetrasodium salt","Phenformin (NSC-756501) HCl","Stachyose","Carboxyatractyloside tripotassium"]
[null,"c","Empty","E0162","E4037","E2228","E5190","E5734","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Cupric sulfate","L-Canavanine sulfate","DisodiuM trans-crocetinate","2'-Fucosyllactose","Fructo-​oligosaccharide DP10/GF9"]
[null,"d","Empty","E1246","E4448","E2256","E5300","E5740","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"D-AP5","EGTA tetrasodium","Fructo-oligosaccharide DP9/GF8","Arecaidine","Quercetin-3-O-D-glucosyl]-(1-2)-L-rhamnoside"]
[null,"e","Empty","E2759","S1872","E2309","E5428","S0929","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"L-(+)-Ergothioneine","Amino-PEG1-C2-acid","Glucoraphanin","Macrozamin","Kukoamine B"]
[null,"f","Empty","E2909","E2895","E5043","E5450","S9207","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"L-Ascorbic acid 2-phosphate sesquimagnesium salt hydrate","Sodium Bicarbonate","[(1aS,1bα,5aα,6aβ)-1a,1b,2,5a,6,6a-Hexahydro-6α-hydroxy-1aβ-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2α-yl]6-O-α-D-galactopyranosyl-β-D-glucopyranoside","Taurohyodeoxycholic acid","Gypenoside XVII"]
[null,"g","Empty","E2979","E4470","E5046","E5457","Empty","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"DL-AP5 (2-APV)","Potassium Chloride","3-FUCOSYLLACTOSE","β-Gentiobiose"]
[null,"h","Empty","E4002","E4420","E5166","E5545","Empty","Empty","Empty","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"Potassium D-gluconate","NADP sodium salt","1,4-b-D-Xylopentaose","α-Lactose"]
[]
[]
[]
[null,"Plate layout: L1700-115"]
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[{"$nulls":3},"Canertinib (CI-1033)","Imiquimod (R-837)","Marbofloxacin","Eplerenone (CGP 30083)","Lornoxicam","Diosmin","NU7441 (KU-57788)","TG100713","Cefadroxil hydrate","Clopidol"]
[null,"b","Empty","S1023","S1288","S1507","S1724","S2110","S2395","S2684","S2893","S3721","S4156","Empty"]
[{"$nulls":3},"Erlotinib (OSI-774) HCl","Camptothecin (NSC-100880)","Irbesartan","Paliperidone","Vinpocetine","Rheochrysidin","Pidnarulex (CX-5461)","NU7026","Bilastine","Chlortetracycline HCl (NSC 13252)"]
[null,"c","Empty","S1043","S1327","S1509","S1837","S2150","S2424","S2704","S2920","S3770","S4218","Empty"]
[{"$nulls":3},"Tandutinib (MLN518)","Ellagic acid","Norfloxacin","Flubendazole","Neratinib (HKI-272)","Hypoxanthine","LY2109761","Mozavaptan","Sodium Aescinate","Amoxapine"]
[null,"d","Empty","S1046","S1353","S1519","S1851","S2152","S2476","S2735","S3041","S3801","S4262","Empty"]
[{"$nulls":3},"Vandetanib (ZD6474)","Ketoconazole (R 41400)","CCT129202","Oxibendazole","Sitafloxacin Hydrate","Itraconazole (R 51211)","MK-8776 (SCH 900776)","Droxidopa","Sodium Houttuyfonate","Ebastine"]
[null,"e","Empty","S1108","S1360","S1615","S1929","S2157","S2530","S2744","S3042","S3821","S4605","Empty"]
[{"$nulls":3},"TAE684 (NVP-TAE684)","GSK1059615","Risperidone","Irsogladine","Taladegib (LY2940680)","7-Aminocephalosporanic acid","CCT137690","Purmorphamine","Nuciferine","Folic acid"]
[null,"f","Empty","S1112","S1371","S1617","S1977","S2206","S2582","S2788","S3059","S3891","S4642","Empty"]
[{"$nulls":3},"SGX-523","Cefoselis Sulfate","Sulfapyridine","Sarafloxacin HCl","Fostamatinib (R788) disodium","Trazodone HCl","Capmatinib (INCB28060)","Enrofloxacin","Vincamine","Dolutegravir Sodium"]
[null,"g","Empty","S1118","S1424","S1642","S1986","S2232","S2597","S2805","S3064","S4033","S4654","Empty"]
[{"$nulls":3},"XL147 analogue","Prazosin HCl","Methyldopa","Meclizine 2HCl","Ketanserin","Oseltamivir Phosphate","LY364947","Ambroxol HCl","Sennoside A","Netupitant"]
[null,"h","Empty","S1205","S1463","S1698","S2035","S2251","S2628","S2827","S3614","S4126","S4930","Empty"]
[{"$nulls":3},"PIK-75 HCl","Ofloxacin","Torsemide","Epalrestat (ONO-2235)","(-)-Huperzine A (HupA)","Gedatolisib (PKI-587)","Torin 1","Lupeol","Retinyl (Vitamin A) Palmitate","Cetilistat"]
[]
[]
[]
[null,"Plate layout: L1700-116"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
[null,"a","Empty","S5018","S5427","S5902","S7004","S7342","S7819","S8527","S9081","S5031","S3304","Empty"]
[{"$nulls":3},"Mebhydrolin napadisylate","Alloxazine","1,2,3,4,5,6-Hexabromocyclohexane","EPZ005687","UNC2250","BLU9931","ROC-325","Anemoside B4","Sulfaquinoxaline sodium","Stylopine"]
[null,"b","Empty","S5035","S5499","S5908","S7035","S7400","S7840","S8548","S9209","S1502","S6345","Empty"]
[{"$nulls":3},"6-Aminopenicillanic acid","Amantadine","Garenoxacin","XL388","ISRIB (trans-isomer)","Dorsomorphin (Compound C)","Roblitinib (FGF401)","Tritetradecanoin","Cephalexin","3-Nitro-L-tyrosine"]
[null,"c","Empty","S5116","S5516","S6001","S7061","S7485","S7842","S8568","S9246","S9430","S0063","Empty"]
[{"$nulls":3},"Bilibubin","Ellagic Acid hydrate","pomaglumetad (LY404039)","GSK126","CCT007093","LY3009120","G1T38","Tiliroside","Tomatidine Hydrochloride","RG3039"]
[null,"d","Empty","S5123","S5577","S6606","S7085","S7518","S7846","S8724","S9257","S8875","S0147","Empty"]
[{"$nulls":3},"Dihydrocholesterol","6-Biopterin","CDD3505","IWP-2","Voreloxin (SNS-595) hydrochloride","Dubermatinib(TP-0903)","Lazertinib","Acetylshikonin","MKC8866","KKL-10"]
[null,"e","Empty","S5170","S5601","S6618","S7105","Empty","S8012","S9011","S9551","S0280","S6949","Empty"]
[{"$nulls":3},"Coumarin 6","Balofloxacin Dihydrate","JNJ-42153605","BAM7",null,"Otenabant (CP-945598) HCl","Hederacoside D","Uvaol","Madrasin","OTX008"]
[null,"f","Empty","S5232","S5611","S6632","S7128","S7698","S8113","S9016","S5098","S0399","S4482","Empty"]
[{"$nulls":3},"Alectinib (CH5424802) hydrochloride","2-cyano-Pyrimidine","Mirogabalin (DS-5565)","Tazemetostat (EPZ-6438)","LY2584702","BI-9564","Dipsacoside B","Gefitinib hydrochloride","SJB2-043","Palbociclib"]
[null,"g","Empty","S5249","S5677","S6642","S7164","S7756","S8138","S9067","S2213","S3206","S9054","Empty"]
[{"$nulls":3},"Coptisine chloride","Xanthopterin Hydrate","Branaplam (LMI070)","GSK343","Indoximod (NLG-8189）","Molidustat (BAY 85-3934)","Pseudoprotodioscin","AMG-47a","5a-Pregnane-3,20-dione","Pectolinarin"]
[null,"h","Empty","S5272","S5712","S6719","S7221","S7790","S8229","S9079","S8927","S3299","S0293","Empty"]
[{"$nulls":3},"Toceranib phosphate","Zofenopril calcium","E6446 dihydrochloride","Vesatolimod (GS-9620)","A-1210477","Brigatinib (AP26113)","Ginsenoside Rb2","GSK2983559 (compound 3)","Demethyleneberberine","MSX-130"]
[]
[]
[]
[null,"Plate layout: L1700-117"]
[null,null,1,2,3,4,5,6,7,8,9,10,11,12]
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[{"$nulls":3},"Potassium guaiacolsulfonate hemihydrate","W-84 Dibromide","ARRY-382","HS-276","1-Hydroxyoctadecane","cis-4-Hydroxy-L-proline","CHIR-090","Taraxasterol","Gitogenin"]
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[]
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[{"$nulls":3},"Polidocanol"]
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[{"$nulls":3},"WAY-638575","WAY-638778","WAY-638934","WAY-639117",null,"WAY-639715","WAY-639907","WAY-640257","WAY-640582","WAY-640879"]
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[{"$nulls":3},"WAY-638584","WAY-638832","WAY-638944","WAY-639228-A","WAY-639446","WAY-639717","WAY-639917","WAY-640327","WAY-640666","WAY-640898"]
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[null,"Plate layout: L1700-134"]
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[{"$nulls":3},"WAY-641910","WAY-655810","WAY-656416","WAY-656903","WAY-657206","WAY-657667","WAY-658494","WAY-658876","WAY-659512","WAY-659977"]
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[{"$nulls":3},"WAY-642555","WAY-655834","WAY-656494","WAY-657003","WAY-657273","WAY-658118","WAY-658650","WAY-658979","WAY-659611","WAY-660211"]
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[{"$nulls":3},"WAY-642938","WAY-655953","WAY-656520","WAY-657021","WAY-657541","WAY-658230","WAY-658674","WAY-659053","WAY-659677","WAY-660313"]
[null,"f","Empty","P3126","P3134","P3142","P3150","P3158","P3166","P3174","P3182","Empty","P3198","Empty"]
[{"$nulls":3},"WAY-643053","WAY-656018","WAY-656522","WAY-657095","WAY-657568","WAY-658261","WAY-658675","WAY-659095",null,"WAY-660319"]
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[null,"h","Empty","P3128","P3136","P3144","P3152","P3160","P3168","P3176","P3184","P3192","P3200","Empty"]
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[null,"Plate layout: L1700-135"]
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[{"$nulls":4},"WAY-661156","WAY-662041","WL-312474","WYE-175819","WYE-176204-A","WYE-176272"]
[null,"b","Empty","P3202","P3210","P3218","P3226","P3234","P3242","P3250","Empty","Empty","Empty","Empty"]
[{"$nulls":3},"WAY-660764","WAY-661688","WAY-662152","WL-389539","WYE-175827","WYE-176234","WYE-176392"]
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[{"$nulls":3},"WAY-660770","WAY-661708","WAY-662162","WY-507","WYE-175839","WYE-176235","WYE-179397"]
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{"sheet":"L1700-Bioactive-10524 cpds","index":1,"n_rows":10525,"n_cols":23,"rows_kept":2250,"cut":true,"bounds":{"rows_first":1000,"rows_last":250,"rows_between":1000,"halvings":1}}
["Cat","Name","Plate Location","Rack Number","Formulation","Target","Pathway","Information","M.w.","CAS Number","DMSO (mg/mL)Max Solubility","DMSO (mM)Max Solubility","Water (mg/mL)Max Solubility","Water (mM)Max Solubility","URL","Formula","Form","Synonyms","SMILES","ALogP","HBA_Count","HBD_Count","RotatableBond"]
["S1002","ABT-737","a2","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,Bcl-2,Mitophagy","Apoptosis","ABT-737 is a BH3 mimetic inhibitor of Bcl-xL, Bcl-2 and Bcl-w with EC50 of 78.7 nM, 30.3 nM and 197.8 nM in cell-free assays, respectively; no inhibition observed against Mcl-1, Bcl-B or Bfl-1. ABT-737 induces mitochondrial pathway apoptosis and mitophagy. Phase 2.",813.43,"852808-04-9",{"v":100,"d":"100.00"},122.94,"<1","N/A","http://selleckchem.com/products/ABT-737.html","C42H45ClN6O5S2","free base","N/A","CN(C)CCC(CSC1=CC=CC=C1)NC2=CC=C(C=C2[N+]([O-])=O)[S](=O)(=O)NC(=O)C3=CC=C(C=C3)N4CCN(CC4)CC5=C(C=CC=C5)C6=CC=C(Cl)C=C6",8.198,3,2,16]
["S1003","Linifanib (ABT-869)","b2","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,CSF-1R,FLT3,PDGFR,VEGFR","Protein Tyrosine Kinase","Linifanib (ABT-869, AL39324, RG3635) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR, CSF-1R, Flt-1/3 and PDGFRβ with IC50 of 4 nM, 3 nM, 3 nM/4 nM and 66 nM respectively, mostly effective in mutant kinase-dependent cancer cells (i.e. FLT3). Linifanib (ABT-869) induces autophagy and apoptosis. Phase 3.",375.41,"796967-16-3",{"v":75,"d":"75.00"},199.78,"<1","N/A","http://selleckchem.com/products/ABT-869.html","C21H18FN5O","free base","AL39324,RG3635","CC1=CC(=C(F)C=C1)NC(=O)NC2=CC=C(C=C2)C3=C4C(=N[NH]C4=CC=C3)N",4.169,2,4,3]
["S1004","Veliparib (ABT-888)","c2","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,PARP","DNA Damage/DNA Repair","Veliparib (ABT-888, NSC 737664) is a potent inhibitor of PARP1 and PARP2 with Ki of 5.2 nM and 2.9 nM in cell-free assays, respectively. It is inactive to SIRT2. Veliparib increases autophagy and apoptosis. Phase 3.",244.29,"912444-00-9",{"v":17,"d":"17.00"},69.59,"<1","N/A","http://selleckchem.com/products/ABT-888.html","C13H16N4O","free base","NSC 737664","CC1(CCCN1)C2=NC3=C(C=CC=C3[NH]2)C(N)=O",0.986,2,3,2]
["S1005","Axitinib (AG 013736)","d2","L1700-01","in 10mM DMSO","c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Axitinib (AG 013736) is a multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFRβ and c-Kit with IC50 of 0.1 nM, 0.2 nM, 0.1-0.3 nM, 1.6 nM and 1.7 nM in Porcine aorta endothelial cells, respectively.",386.47,"319460-85-0",{"v":35,"d":"35.00"},90.56,"<1","N/A","http://selleckchem.com/products/Axitinib.html","C22H18N4OS","free base","AG 013736","CNC(=O)C1=CC=CC=C1SC2=CC3=C(C=C2)C(=N[NH]3)\\C=C\\C4=CC=CC=N4",4.492,3,2,5]
["S1006","Saracatinib (AZD0530)","e2","L1700-01","in 10mM DMSO","Autophagy,EGFR,Src","Angiogenesis","Saracatinib (AZD0530) is a potent Src inhibitor with IC50 of 2.7 nM in cell-free assays, and potent to c-Yes, Fyn, Lyn, Blk, Fgr and Lck; less active for Abl and EGFR (L858R and L861Q). Saracatinib induces autophagy. Phase 2/3.",542.03,"379231-04-6",{"v":35,"d":"35.00"},64.57,"<1","N/A","http://selleckchem.com/products/AZD0530.html","C27H32ClN5O5","free base","N/A","CN1CCN(CCOC2=CC(=C3C(=NC=NC3=C2)NC4=C(Cl)C=CC5=C4OCO5)OC6CCOCC6)CC1",3.814,7,1,8]
["S1007","Roxadustat (FG-4592)","f2","L1700-01","in 10mM DMSO","Ferroptosis,HIF","Angiogenesis","Roxadustat (FG-4592) is an HIF-α prolyl hydroxylase inhibitor in a cell-free assay, stabilizes HIF-2 and induces EPO production. Roxadustat potentiates RSL3 induced ferroptosis. Phase 3.",352.34,"808118-40-3",{"v":70,"d":"70.00"},198.67,"<1","N/A","http://selleckchem.com/products/fg-4592.html","C19H16N2O5","free base","ASP1517","CC1=NC(=C(O)C2=C1C=C(OC3=CC=CC=C3)C=C2)C(=O)NCC(O)=O",2.306,4,2,5]
["S1008","Selumetinib (AZD6244)","g2","L1700-01","in 10mM DMSO","Apoptosis related,MEK","MAPK","Selumetinib (AZD6244, ARRY-142886) is a potent, highly selective MEK inhibitor with IC50 of 14 nM for MEK1 and Kd value of 530 nM for MEK2. It  also inhibits ERK1/2 phosphorylation with IC50 of 10 nM, no inhibition to p38α, MKK6, EGFR, ErbB2, ERK2, B-Raf, etc. Selumetinib suppresses cell proliferation, migration and trigger apoptosis. Phase 3.",457.68,"606143-52-6",{"v":91,"d":"91.00"},198.83,"<1","N/A","http://selleckchem.com/products/AZD6244.html","C17H15BrClFN4O3","free base","ARRY-142886","C[N]1C=NC2=C(F)C(=C(C=C12)C(=O)NOCCO)NC3=CC=C(Br)C=C3Cl",3.234,3,3,6]
["S1010","Nintedanib (BIBF 1120)","h2","L1700-01","in 10mM DMSO","FGFR,PDGFR,Src,VEGFR","Protein Tyrosine Kinase","Nintedanib (BIBF 1120, Intedanib, Vargatef, Ofev) is a potent triple angiokinase inhibitor for VEGFR1/2/3, FGFR1/2/3 and PDGFRα/β with IC50 of 34 nM/13 nM/13 nM, 69 nM/37 nM/108 nM and 59 nM/65 nM in cell-free assays. Phase 3.",539.62,"656247-17-5",{"v":6,"d":"6.00"},11.12,"<1","N/A","http://selleckchem.com/products/BIBF1120.html","C31H33N5O4","free base","Intedanib, Vargatef, Ofev","COC(=O)C1=CC=C\\2C(=C1)NC(=O)C2=C(NC3=CC=C(C=C3)N(C)C(=O)CN4CCN(C)CC4)/C5=CC=CC=C5",2.965,4,2,8]
["S1011","Afatinib (BIBW2992)","a3","L1700-01","in 10mM DMSO","Autophagy,EGFR,HER2","Protein Tyrosine Kinase","Afatinib (BIBW2992) inhibits EGFR/ErbB irreversibly in vitro with IC50 of 0.5, 0.4, 10, 14, 1 nM for EGFRwt, EGFR L858R , EGFR L858R/T790M ErbB2 (HER2) and ErbB4 (HER4), respectively. Afatinib induces autophagy.",485.94,"850140-72-6",{"v":97,"d":"97.00"},199.61,"<1","N/A","http://selleckchem.com/products/BIBW2992.html","C24H25ClFN5O3","Free Base","BIBW2992","CN(C)C/C=C/C(=O)NC1=CC2=C(NC3=CC=C(F)C(=C3)Cl)N=CN=C2C=C1OC4CCOC4",3.917,5,2,8]
["S1012","BMS-536924","b3","L1700-01","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","BMS-536924 (CS-0117) is an ATP-competitive IGF-1R/IR inhibitor with IC50 of 100 nM/73 nM, modest activity for Mek, Fak, and Lck with very little activity for Akt1, MAPK1/2.",479.96,"468740-43-4",{"v":96,"d":"96.00"},200.02,"<1","N/A","http://selleckchem.com/products/BMS-536924.html","C25H26ClN5O3","free base","CS-0117","CC1=C2N=C([NH]C2=CC(=C1)N3CCOCC3)C4=C(NCC(O)C5=CC=CC(=C5)Cl)C=CNC4=O",2.385,3,4,6]
["S1013","Bortezomib (PS-341)","c3","L1700-01","in 10mM DMSO","Autophagy,Cathepsin B,Cysteine Protease,ERK,NF-κB,Proteasome","Proteases","Bortezomib (PS-341, Velcade, LDP-341, MLM341, NSC 681239) is a potent 20S proteasome inhibitor with Ki of 0.6 nM. It exhibits favorable selectivity towards tumor cells over normal cells. Bortezomib (PS-341) inhibits NF-κB and induces ERK phosphorylation to suppress cathepsin B and inhibit the catalytic process of autophagy in ovarian cancer and other solid tumors.",384.24,"179324-69-7",{"v":76,"d":"76.00"},197.79,"<1","N/A","http://selleckchem.com/products/Bortezomib.html","C19H25BN4O4","Free Base","Velcade, LDP-341, MLM341, NSC 681239,PS-341","CC(C)CC(NC(=O)C(CC1=CC=CC=C1)NC(=O)C2=NC=CN=C2)B(O)O",2.183,4,2,9]
["S1014","Bosutinib (SKI-606)","d3","L1700-01","in 10mM DMSO","Autophagy,Bcr-Abl,ERK,S6 Kinase,Src,STAT","Angiogenesis","Bosutinib (SKI-606) is a novel, dual Src/Abl inhibitor with IC50 of 1.2 nM and 1 nM in cell-free assays, respectively. Bosutinib also effectively decreases the activity of PI3K/AKT/mTOR, MAPK/ERK and JAK/STAT3 signaling pathways by blocking the phosphorylation levels of p-ERK, p-S6, and p-STAT3. Bosutinib promotes autophagy.",530.45,"380843-75-4",{"v":100,"d":"100.00"},188.52,"<1","N/A","http://selleckchem.com/products/Bosutinib.html","C26H29Cl2N5O3","free base","SKI-606","COC1=C(Cl)C=C(Cl)C(=C1)NC2=C(C=NC3=CC(=C(OC)C=C23)OCCCN4CCN(C)CC4)C#N",4.883,4,1,9]
["S1017","Cediranib (AZD2171)","e3","L1700-01","in 10mM DMSO","Autophagy,c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Cediranib (AZD2171, NSC-732208) is a highly potent VEGFR(KDR) inhibitor with IC50 of <1 nM, also inhibits Flt1/4 with IC50 of 5 nM/≤3 nM, similar activity against c-Kit and PDGFRβ, 36-, 110-fold and >1000-fold selective more for VEGFR than PDGFR-α, CSF-1R and Flt3 in HUVEC cells. Cediranib (AZD2171) induces autophagic vacuole accumulation. Phase 3.",450.51,"288383-20-0",{"v":90,"d":"90.00"},199.77,"<1","N/A","http://selleckchem.com/products/Cediranib.html","C25H27FN4O3","free base","NSC-732208","COC1=C(OCCCN2CCCC2)C=C3N=CN=C(OC4=C(F)C5=C([NH]C(=C5)C)C=C4)C3=C1",4.761,5,1,8]
["S1018","Dovitinib (TKI-258)","f3","L1700-01","in 10mM DMSO","c-Kit,FGFR,FLT3,PDGFR,VEGFR","Angiogenesis","Dovitinib (TKI258, CHIR258) is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit) with IC50 of 1 nM/2 nM, also potent to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs with IC50 of 8-13 nM, less potent to InsR, EGFR, c-Met, EphA2, Tie2, IGF-1R and HER2 in cell-free assays. Phase 4.",392.43,"405169-16-6",{"v":30,"d":"30.00"},76.45,"<1","N/A","http://selleckchem.com/products/CHIR-258.html","C21H21FN6O","Citrate","CHIR-258","CN1CCN(CC1)C2=CC3=C(C=C2)N=C([NH]3)C4=C(N)C5=C(NC4=O)C=CC=C5F",1.781,2,3,2]
["S1020","PD184352 (CI-1040)","g3","L1700-01","in 10mM DMSO","Apoptosis related,MEK","MAPK","PD184352 (CI-1040) is an ATP non-competitive MEK1/2 inhibitor with IC50 of 17 nM in cell-based assays, 100-fold more selective for MEK1/2 than MEK5. PD184352 (CI-1040) selectively induces apoptosis.",478.67,"212631-79-3",{"v":96,"d":"96.00"},200.56,"<1","N/A","http://selleckchem.com/products/CI-1040-(PD184352).html","C17H14ClF2IN2O2","free base","N/A","FC1=CC=C(C(=O)NOCC2CC2)C(=C1F)NC3=CC=C(I)C=C3Cl",4.907,2,2,6]
["S1021","Dasatinib (BMS-354825)","h3","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,Bcr-Abl,c-Kit,Src","Angiogenesis","Dasatinib (BMS-354825) is a novel, potent and multi-targeted inhibitor that targets Abl, Src and c-Kit, with IC50 of <1 nM, 0.8 nM and 79 nM in cell-free assays, respectively. Dasatinib induces autophagy and apoptosis with anti-tumor activity.",488.01,"302962-49-8",{"v":98,"d":"98.00"},200.82,"<1","N/A","http://selleckchem.com/products/Dasatinib.html","C22H26ClN7O2S","free base","BMS-354825","CC1=NC(=CC(=N1)N2CCN(CCO)CC2)NC3=NC=C(S3)C(=O)NC4=C(Cl)C=CC=C4C",3.439,4,3,7]
["S1022","Ridaforolimus (Deforolimus, MK-8669)","a4","L1700-01","in 10mM DMSO","FKBP,mTOR","PI3K/Akt/mTOR","Ridaforolimus (Deforolimus, MK-8669, AP23573) is a selective mTOR inhibitor with IC50 of 0.2 nM in HT-1080 cell line; while not classified as a prodrug, mTOR inhibition and FKBP12 binding is similar to rapamycin. Phase 3.",990.21,"572924-54-0",{"v":198,"d":"198.00"},199.96,"<1","N/A","http://selleckchem.com/products/Deforolimus.html","C53H84NO14P","free base","AP23573","COC1CC(CCC1O[P](C)(C)=O)CC(C)C2CC(=O)C(C)\\C=C(C)\\C(O)C(OC)C(=O)C(C)CC(C)/C=C/C=C/C=C(C)/C(CC3CCC(C)C(O)(O3)C(=O)C(=O)N4CCCCC4C(=O)O2)OC",6.303,12,1,8]
["S1025","Gefitinib (ZD1839)","b4","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,EGFR","Protein Tyrosine Kinase","Gefitinib (ZD-1839, Iressa) is an EGFR inhibitor for Tyr1173, Tyr992, Tyr1173 and Tyr992 in the NR6wtEGFR and NR6W cells with IC50 of 37 nM, 37nM, 26 nM and 57 nM, respectively. Gefitinib promotes autophagy and apoptosis of lung cancer cells via blockade of the PI3K/AKT/mTOR pathway.",{"v":446.9,"d":"446.90"},"184475-35-2",{"v":89,"d":"89.00"},199.15,"<1","N/A","http://selleckchem.com/products/Gefitinib.html","C22H24ClFN4O3","free base","Iressa,ZD1839","COC1=C(OCCCN2CCOCC2)C=C3C(=NC=NC3=C1)NC4=CC=C(F)C(=C4)Cl",4.203,5,1,8]
["S1026","Imatinib (STI571) Mesylate","c4","L1700-01","in 10mM DMSO","Autophagy,Bcr-Abl,c-Kit,PDGFR","Protein Tyrosine Kinase","Imatinib (STI571, CGP057148B, Gleevec) Mesylate is an orally bioavailability mesylate salt of Imatinib, which is a multi-target inhibitor of v-Abl, c-Kit and PDGFR with IC50 of 0.6 μM, 0.1 μM and 0.1 μM in cell-free or cell-based assays, respectively. Imatinib Mesylate (STI571) induces autophagy.",589.71,"220127-57-1",{"v":118,"d":"118.00"},{"v":200.1,"d":"200.10"},{"v":118,"d":"118.00"},{"v":200.1,"d":"200.10"},"http://selleckchem.com/products/Imatinib-Mesylate.html","C29H31N7O.CH4SO3","Mesylate","Gleevec, Glivec, CGP-57148B,STI571","CN1CCN(CC1)CC2=CC=C(C=C2)C(=O)NC3=CC=C(C)C(=C3)NC4=NC=CC(=N4)C5=CC=CN=C5.C[S](O)(=O)=O",3.806,4,2,7]
["S1028","Lapatinib (GW-572016) Ditosylate","d4","L1700-01","in 10mM DMSO","EGFR,HER2","Protein Tyrosine Kinase","Lapatinib (GW-572016) Ditosylate is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM in cell-free assays, respectively.",925.46,"388082-77-7",{"v":100,"d":"100.00"},108.05,"<1","N/A","http://selleckchem.com/products/Lapatinib-Ditosylate.html","C29H26ClFN4O4S.2C7H8O3S","Ditosylat","GW-572016","CC1=CC=C(C=C1)[S](O)(=O)=O.CC2=CC=C(C=C2)[S](O)(=O)=O.C[S](=O)(=O)CCNCC3=CC=C(O3)C4=CC=C5N=CN=C(NC6=CC=C(OCC7=CC=CC(=C7)F)C(=C6)Cl)C5=C4",9.339,6,2,13]
["S1029","Lenalidomide (CC-5013)","e4","L1700-01","in 10mM DMSO","Apoptosis related,Caspase,E3 Ligase ,E3 ligase Ligand,TNF-alpha,VEGFR","Ubiquitin","Lenalidomide (CC-5013) is a TNF-α secretion inhibitor with IC50 of 13 nM in PBMCs. Lenalidomide (CC-5013) is a ligand of ubiquitin E3 ligase cereblon (CRBN), and it causes selective ubiquitination and degradation of two lymphoid transcription factors, IKZF1 and IKZF3, by the CRBN-CRL4 ubiquitin ligase. Lenalidomide promotes cleaved caspase-3 expression and inhibit VEGF expression and induces apoptosis.",259.26,"191732-72-6",{"v":52,"d":"52.00"},200.57,"<1","N/A","https://www.selleckchem.com/products/lenalidomide-s1029.html","C13H13N3O3","free base","CC-5013","NC1=C2CN(C3CCC(=O)NC3=O)C(=O)C2=CC=C1",-0.515,3,2,1]
["S1030","Panobinostat (LBH589)","f4","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,HDAC,HIV Protease","Epigenetics","Panobinostat (LBH589, NVP-LBH589) is a novel broad-spectrum HDAC inhibitor with IC50 of 5 nM in a cell-free assay. Panobinostat (LBH589) induces autophagy and apoptosis. Panobinostat effectively disrupts HIV latency in vivo. Phase 3.",349.43,"404950-80-7",{"v":69,"d":"69.00"},197.46,"<1","N/A","http://selleckchem.com/products/LBH-589.html","C21H23N3O2","Free Base","NVP-LBH589","CC1=C(CCNCC2=CC=C(\\C=C\\C(=O)NO)C=C2)C3=C([NH]1)C=CC=C3",3.194,1,3,7]
["S1032","Motesanib Diphosphate (AMG-706)","g4","L1700-01","in 10mM DMSO","c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Motesanib Diphosphate (AMG-706) is a potent ATP-competitive inhibitor of VEGFR1/2/3 with IC50 of 2 nM/3 nM/6 nM, respectively; similar activity against Kit (c-Kit), ~10-fold more selective for VEGFR than PDGFR and Ret. Phase 3.",569.44,"857876-30-3",{"v":100,"d":"100.00"},175.61,{"v":19,"d":"19.00"},33.37,"http://selleckchem.com/products/Motesanib-Diphosphate.html","C22H23N5O.2H3PO4","Diphosphate","N/A","CC1(C)CNC2=CC(=CC=C12)NC(=O)C3=C(NCC4=CC=NC=C4)N=CC=C3.O[P](O)(O)=O.O[P](O)(O)=O",1.783,3,3,5]
["S1033","Nilotinib (AMN-107)","h4","L1700-01","in 10mM DMSO","AMPK,Autophagy,Bcr-Abl","Angiogenesis","Nilotinib (AMN-107) is a selective Bcr-Abl inhibitor with IC50 less than 30 nM in Murine myeloid progenitor cells. Nilotinib induces autophagy through AMPK activition.",529.52,"641571-10-0",{"v":27,"d":"27.00"},50.99,"<1","N/A","http://selleckchem.com/products/Nilotinib.html","C28H22F3N7O","free base","AMN-107","CC1=C[N](C=N1)C2=CC(=CC(=C2)C(F)(F)F)NC(=O)C3=CC=C(C)C(=C3)NC4=NC=CC(=N4)C5=CN=CC=C5",5.084,5,2,7]
["S1035","Pazopanib HCl (GW786034 HCl)","a5","L1700-01","in 10mM DMSO","Autophagy,c-Kit,CSF-1R,FGFR,PDGFR,VEGFR","Protein Tyrosine Kinase","Pazopanib HCl (GW786034 HCl) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit and c-Fms with IC50 of 10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM and 146 nM in cell-free assays, respectively. Pazopanib induces autophagic Type II cell death.",473.98,"635702-64-6",{"v":17,"d":"17.00"},35.87,"<1","N/A","http://selleckchem.com/products/Pazopanib-Hydrochloride.html","C21H23N7O2S.HCl","Hydrochloride","GW786034 HCl","Cl.C[N]1N=C2C=C(C=CC2=C1C)N(C)C3=NC(=NC=C3)NC4=CC=C(C)C(=C4)[S](N)(=O)=O",4.123,5,2,5]
["S1036","Mirdametinib (PD0325901)","b5","L1700-01","in 10mM DMSO","MEK","MAPK","Mirdametinib (PD0325901) is a selective and non ATP-competitive MEK inhibitor with IC50 of 0.33 nM in cell-free assays, roughly 500-fold more potent than CI-1040 on phosphorylation of ERK1 and ERK2. Phase 2.",482.19,"391210-10-9",{"v":96,"d":"96.00"},199.09,"<1","N/A","http://selleckchem.com/products/PD-0325901.html","C16H14F3IN2O4","free base","N/A","OCC(O)CONC(=O)C1=C(NC2=CC=C(I)C=C2F)C(=C(F)C=C1)F",2.578,2,4,7]
["S1038","PI-103","c5","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,DNA-PK,mTOR,PI3K","PI3K/Akt/mTOR","PI-103 is a multi-targeted PI3K inhibitor for p110α/β/δ/γ with IC50 of 2 nM/3 nM/3 nM/15 nM in cell-free assays, less potent to mTOR/DNA-PK with IC50 of 30 nM/23 nM. PI-103 induces apoptosis in murine T-cell Lymphoma.",348.36,"371935-74-9",{"v":24,"d":"24.00"},68.89,"<1","N/A","http://selleckchem.com/products/PI-103.html","C19H16N4O3","free base","N/A","OC1=CC(=CC=C1)C2=NC3=C(OC4=C3C=CC=N4)C(=N2)N5CCOCC5",2.798,5,1,2]
["S1039","Rapamycin (AY-22989)","d5","L1700-01","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Autophagy,mTOR","PI3K/Akt/mTOR","Rapamycin (AY-22989, Rapamune, Sirolimus, NSC-2260804,AY-22989) is a specific mTOR inhibitor with IC50 of ~0.1 nM HEK293 cells.",914.18,"53123-88-9",{"v":20,"d":"20.00"},21.88,"<1","N/A","http://selleckchem.com/products/Rapamycin.html","C51H79NO13","free base","Rapamune, Sirolimus, NSC-2260804,AY-22989","COC1CC(CCC1O)CC(C)C2CC(=O)C(C)\\C=C(/C)C(O)C(OC)C(=O)C(C)CC(C)/C=C/C=C/C=C(C)/C(CC3CCC(C)C(O)(O3)C(=O)C(=O)N4CCCCC4C(=O)O2)OC",6.295,10,2,6]
["S1040","Sorafenib (BAY 43-9006) tosylate","e5","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,c-Kit,Ferroptosis,FGFR,FLT3,PDGFR,Raf,VEGFR","MAPK","Sorafenib tosylate (BAY 43-9006 tosylate,NSC-724772 tosylate)  is a multikinase inhibitor of Raf-1 and B-Raf with IC50 of 6 nM and 22 nM in cell-free assays, respectively. Sorafenib Tosylate inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and c-KIT with IC50 of 90 nM, 20 nM, 57 nM, 59 nM and 68 nM, respectively. Sorafenib Tosylate induces autophagy and apoptosis and activates ferroptosis with anti-tumor activity.",637.03,"475207-59-1",{"v":127,"d":"127.00"},199.36,0.01,0.02,"http://selleckchem.com/products/Sorafenib-Tosylate.html","C21H16ClF3N4O3.C7H8O3S","Tosylate","BAY 43-9006 tosylate,NSC-724772 tosylate","CNC(=O)C1=CC(=CC=N1)OC2=CC=C(NC(=O)NC3=CC=C(Cl)C(=C3)C(F)(F)F)C=C2.CC4=CC=C(C=C4)[S](O)(=O)=O",5.824,4,3,7]
["S1041","STF-62247","f5","L1700-01","in 10mM DMSO","Autophagy","Autophagy","STF-62247 is a molecule targeting VHL-deficient renal cell carcinoma that induces autophagy. STF-62247 shows selective toxicity and growth inhibition of renal cells lacking VHL; 25-fold greater sensitivity observed for cells with VHL deficiency compared to wild-type (VHL+).",267.35,"315702-99-9",{"v":53,"d":"53.00"},198.24,"<1","N/A","http://selleckchem.com/products/STF-62247.html","C15H13N3S","free base","N/A","CC1=CC(=CC=C1)NC2=NC(=CS2)C3=CC=NC=C3",3.659,2,1,3]
["S1042","Sunitinib (SU11248) malate","g5","L1700-01","in 10mM DMSO","Apoptosis related,c-Kit,IRE1,Mitophagy,PDGFR,VEGFR","Protein Tyrosine Kinase","Sunitinib (SU11248) malate is a multi-targeted RTK inhibitor targeting VEGFR2 (Flk-1) and PDGFRβ with IC50 of 80 nM and 2 nM in cell-free assays, and also inhibits c-Kit. Sunitinib Malate effectively inhibits autophosphorylation of Ire1α. Sunitinib Malate increases both death receptor and mitochondrial-dependent apoptosis.",532.56,"341031-54-7",{"v":15,"d":"15.00"},28.17,"<1","N/A","http://selleckchem.com/products/Sunitinib-Malate-(Sutent).html","C22H27FN4O2.C4H6O5","Malate","N/A","CCN(CC)CCNC(=O)C1=C(C)[NH]C(=C1C)/C=C/2C(=O)NC3=CC=C(F)C=C23.OC(CC(O)=O)C(O)=O",-1.049,4,4,10]
["S1044","Temsirolimus (CCI-779)","h5","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,mTOR","PI3K/Akt/mTOR","Temsirolimus (CCI-779, NSC 683864) is a specific mTOR inhibitor with IC50 of 1.76 μM in a cell-free assay. Temsirolimus induces autophagy and apoptosis.",1030.29,"162635-04-3",{"v":67,"d":"67.00"},65.03,"<1","N/A","http://selleckchem.com/products/Temsirolimus.html","C56H87NO16","free base","NSC 683864,CCI-779","COC1CC(CCC1OC(=O)C(C)(CO)CO)CC(C)C2CC(=O)C(C)\\C=C(C)\\C(O)C(OC)C(=O)C(C)CC(C)/C=C/C=C/C=C(C)/C(CC3CCC(C)C(O)(O3)C(=O)C(=O)N4CCCCC4C(=O)O2)OC",6.039,12,3,11]
["S1047","Vorinostat (SAHA)","a6","L1700-01","in 10mM DMSO","Autophagy,HDAC,HPV","Epigenetics","Vorinostat (SAHA,MK0683, Suberoylanilide hydroxamic acid, Zolinza) is an HDAC inhibitor with IC50 of ~10 nM in a cell-free assay. Vorinostat abrogates productive HPV-18 DNA amplification.",{"v":264.3,"d":"264.30"},"149647-78-9",{"v":52,"d":"52.00"},196.75,"<1","N/A","http://selleckchem.com/products/Vorinostat-saha.html","C14H20N2O3","free base","SAHA,MK0683, Suberoylanilide hydroxamic acid, Zolinza","ONC(=O)CCCCCCC(=O)NC1=CC=CC=C1",2.005,2,2,8]
["S1048","Tozasertib","b6","L1700-01","in 10mM DMSO","Aurora Kinase,Autophagy,Bcr-Abl,FLT3","Cell Cycle","Tozasertib (VX-680, MK-0457) is a pan-Aurora inhibitor, mostly against Aurora A with Kiapp of 0.6 nM in a cell-free assay, less potent towards Aurora B/Aurora C and 100-fold more selective for Aurora A than 55 other kinases. The only exceptions are Fms-related tyrosine kinase-3 (FLT-3) and BCR-ABL tyrosine kinase, which are inhibited by the Tozasertib with both Ki of 30 nM. Tozasertib induces apoptosis and autophagy. Phase 2.",464.59,"639089-54-6",{"v":93,"d":"93.00"},200.18,"<1","N/A","http://selleckchem.com/products/VX-680(MK-0457).html","C23H28N8OS","free base","VX-680, MK-0457","CN1CCN(CC1)C2=NC(=NC(=C2)NC3=N[NH]C(=C3)C)SC4=CC=C(NC(=O)C5CC5)C=C4",4.445,4,3,7]
["S1049","Y-27632 2HCl","c6","L1700-01","in 10mM DMSO","Autophagy,ROCK","Cell Cycle","Y-27632 2HCl is a selective ROCK1 and ROCK2 inhibitor with a Ki of 140 nM and 300nM in a cell-free assay, exhibits >200-fold selectivity over other kinases, including PKC, cAMP-dependent protein kinase, MLCK and PAK.",320.26,"129830-38-2",{"v":64,"d":"64.00"},199.84,{"v":14,"d":"14.00"},43.71,"http://selleckchem.com/products/Y-27632.html","C14H21N3O.2HCl","Dihydrochloride","N/A","Cl.Cl.CC(N)C1CCC(CC1)C(=O)NC2=CC=NC=C2",1.871,2,2,3]
["S1052","Elesclomol (STA-4783)","d6","L1700-01","in 10mM DMSO","Apoptosis related,HSP (HSP90)","Cytoskeletal Signaling","Elesclomol (STA-4783) is a novel potent oxidative stress inducer that elicits pro-apoptosis events among tumor cells. Phase 3.Elesclomol specifically binds ferredoxin 1 (FDX1) α2/α3 helices and β5 strand and inhibits FDX1-mediated Fe-S cluster biosynthesis.",{"v":400.5,"d":"400.50"},"488832-69-5",{"v":80,"d":"80.00"},199.75,"<1","N/A","http://selleckchem.com/products/Elesclomol.html","C19H20N4O2S2","free base","N/A","CN(NC(=O)CC(=O)NN(C)C(=S)C1=CC=CC=C1)C(=S)C2=CC=CC=C2",2.885,2,2,8]
["S1053","Entinostat (MS-275)","e6","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,HDAC","Epigenetics","Entinostat (MS-275, SNDX-275) strongly inhibits HDAC1 and HDAC3 with IC50 of 0.51 μM and 1.7 μM in cell-free assays, compared with HDACs 4, 6, 8, and 10. Entinostat induces autophagy and apoptosis. Phase 3.",376.41,"209783-80-2",{"v":75,"d":"75.00"},199.25,"<1","N/A","http://selleckchem.com/products/MS-275.html","C21H20N4O3","free base","SNDX-275","NC1=CC=CC=C1NC(=O)C2=CC=C(CNC(=O)OCC3=CN=CC=C3)C=C2",2.071,4,3,7]
["S1055","Enzastaurin (LY317615)","f6","L1700-01","in 10mM DMSO","PKC","TGF-beta/Smad","Enzastaurin (LY317615) is a potent PKCβ selective inhibitor with IC50 of 6 nM in cell-free assays, 6- to 20-fold selectivity against PKCα, PKCγ and PKCε. Phase 3.",515.61,"170364-57-5",{"v":30,"d":"30.00"},58.18,"<1","N/A","http://selleckchem.com/products/Enzastaurin.html","C32H29N5O2","free base","N/A","C[N]1C=C(C2=CC=CC=C12)C3=C(C(=O)NC3=O)C4=C[N](C5CCN(CC5)CC6=NC=CC=C6)C7=CC=CC=C47",{"v":4.32,"d":"4.320"},3,1,5]
["S1056","AC480 (BMS-599626)","g6","L1700-01","in 10mM DMSO","EGFR,HER2","Protein Tyrosine Kinase","AC480 (BMS-599626) is a selective and efficacious inhibitor of HER1 and HER2 with IC50 of 20 nM and 30 nM, ~8-fold less potent to HER4, >100-fold to VEGFR2, c-Kit, Lck, MET etc. Phase 1.",530.55,"714971-09-2",{"v":113,"d":"113.00"},212.99,"<1","N/A","http://selleckchem.com/products/BMS-599626.html","C27H27FN8O3","free base","N/A","CC1=C2[N](C=C1NC(=O)OCC3COCCN3)N=CN=C2NC4=CC5=C(C=C4)[N](CC6=CC=CC(=C6)F)N=C5",3.726,6,3,8]
["S1057","Obatoclax Mesylate (GX15-070)","h6","L1700-01","in 10mM DMSO","Autophagy,Bcl-2","Apoptosis","Obatoclax Mesylate (GX15-070) is an antagonist of Bcl-2 with Ki of 0.22 μM in a cell-free assay, can assist in overcoming MCL-1 mediated resistance to apoptosis.",413.49,"803712-79-0",{"v":83,"d":"83.00"},200.73,"<1","N/A","http://selleckchem.com/products/Obatoclax-Mesylate.html","C20H19N3O.CH4O3S","Mesylate","N/A","COC\\1=CC(=NC1=C\\C2=C(C)C=C(C)[NH]2)C3=CC4=CC=CC=C4[NH]3.C[S](O)(=O)=O",3.757,2,2,3]
["S1060","Olaparib (AZD2281)","a7","L1700-01","in 10mM DMSO","Autophagy,Mitophagy,PARP","DNA Damage/DNA Repair","Olaparib (AZD2281, KU0059436) is a selective inhibitor of PARP1/2 with IC50 of 5 nM/1 nM in cell-free assays, 300-times less effective against tankyrase-1. Olaparib induces significant autophagy that is associated with mitophagy in cells with BRCA mutations.",434.46,"763113-22-0",{"v":86,"d":"86.00"},197.95,"N/A","N/A","http://selleckchem.com/products/AZD2281(Olaparib).html","C24H23FN4O3","free base","Ku-0059436","FC1=C(C=C(CC2=NNC(=O)C3=C2C=CC=C3)C=C1)C(=O)N4CCN(CC4)C(=O)C5CC5",2.127,4,1,4]
["S1061","Nutlin-3","b7","L1700-01","in 10mM DMSO","E3 Ligase ,MDM2/MDMX","Apoptosis","Nutlin-3 is a potent and selective Mdm2 (RING finger-dependent ubiquitin protein ligase for itself and p53) antagonist with IC50 of 90 nM in a cell-free assay; stabilizes p73 in p53-deficient cells.",{"v":581.5,"d":"581.50"},"890090-75-2",{"v":100,"d":"100.00"},171.97,"<1","N/A","http://selleckchem.com/products/Nutlin-3.html","C30H30Cl2N4O4","free base","N/A","COC1=CC(=C(C=C1)C2=NC(C(N2C(=O)N3CCNC(=O)C3)C4=CC=C(Cl)C=C4)C5=CC=C(Cl)C=C5)OC(C)C",5.434,5,1,6]
["S1064","Masitinib (AB1010)","c7","L1700-01","in 10mM DMSO","c-Kit,PDGFR","Protein Tyrosine Kinase","Masitinib is a novel inhibitor for Kit (c-Kit) and PDGFRα/β with IC50 of 200 nM and 540 nM/800 nM, weak inhibition to ABL and c-Fms. Phase 3.",498.64,"790299-79-5",{"v":100,"d":"100.00"},200.55,"<1","N/A","http://selleckchem.com/products/Masitinib-(AB1010).html","C28H30N6OS","free base","N/A","CN1CCN(CC1)CC2=CC=C(C=C2)C(=O)NC3=CC(=C(C)C=C3)NC4=NC(=CS4)C5=CC=CN=C5",4.475,3,2,7]
["S1065","Pictilisib (GDC-0941)","d7","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,PI3K","PI3K/Akt/mTOR","Pictilisib (GDC-0941, RG7321) is a potent inhibitor of PI3Kα/δ with IC50 of 3 nM in cell-free assays, with modest selectivity against p110β (11-fold) and p110γ (25-fold). Pictilisib (GDC-0941) induces autophagy and apoptosis. Phase 2.",513.64,"957054-30-7",{"v":44,"d":"44.00"},85.66,"<1","N/A","http://selleckchem.com/products/GDC-0941.html","C23H27N7O3S2","free base","RG7321","C[S](=O)(=O)N1CCN(CC1)CC2=CC3=NC(=NC(=C3S2)N4CCOCC4)C5=CC=CC6=C5C=N[NH]6",2.153,6,1,5]
["S1066","SL-327","e7","L1700-01","in 10mM DMSO","MEK","MAPK","SL327 is a selective inhibitor for MEK1/2 with IC50 of 0.18 μM/ 0.22 μM, no activity towards Erk1, MKK3, MKK4, c-JUN, PKC, PKA, or CamKII;capable of transport through the blood-brain barrier.",335.35,"305350-87-2",{"v":67,"d":"67.00"},199.79,"<1","N/A","http://selleckchem.com/products/SL327.html","C16H12F3N3S","free base","N/A","NC(\\SC1=CC=C(N)C=C1)=C(C#N)/C2=C(C=CC=C2)C(F)(F)F",3.705,0,2,4]
["S1067","SB431542","f7","L1700-01","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","SB431542 is a potent and selective inhibitor of ALK5 with IC50 of 94 nM in a cell-free assay, 100-fold more selective for ALK5 than p38 MAPK and other kinases.",384.39,"301836-41-9",{"v":76,"d":"76.00"},197.72,"<1","N/A","http://selleckchem.com/products/SB-431542.html","C22H16N4O3","free base","N/A","NC(=O)C1=CC=C(C=C1)C2=NC(=C([NH]2)C3=NC=CC=C3)C4=CC5=C(OCO5)C=C4",3.447,5,2,4]
["S1068","Crizotinib (PF-02341066)","g7","L1700-01","in 10mM DMSO","ALK,Autophagy,c-Met,ROS1","Protein Tyrosine Kinase","Crizotinib (PF-02341066) is a potent inhibitor of c-Met and ALK with IC50 of 11 nM and 24 nM in cell-based assays, respectively. It is also a potent ROS1 inhibitor with Ki value less than 0.025 nM. Crizotinib induces autophagy through inhibition of the STAT3 pathway in multiple lung cancer cell lines.",450.34,"877399-52-5",{"v":9,"d":"9.00"},19.98,"<1","N/A","http://selleckchem.com/products/PF-2341066.html","C21H22Cl2FN5O","free base","PF-02341066","CC(OC1=C(N)N=CC(=C1)C2=C[N](N=C2)C3CCNCC3)C4=C(Cl)C=CC(=C4Cl)F",3.693,3,2,5]
["S1069","Luminespib (NVP-AUY922)","h7","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,HSP (HSP90),IGF-1R","Cytoskeletal Signaling","Luminespib (AUY-922, NVP-AUY922, VER-52296) is a highly potent HSP90 inhibitor for HSP90α/β with IC50 of 13 nM /21 nM in cell-free assays, weaker potency against the HSP90 family members GRP94 and TRAP-1, exhibits the tightest binding of any small-molecule HSP90 ligand. Luminespib (AUY-922, NVP-AUY922) effectively downregulates and destabilizes the IGF-1Rβ protein and results in growth inhibition, autophagy and apoptosis. Phase 2.",465.54,"747412-49-3",{"v":93,"d":"93.00"},199.77,"<1","N/A","http://selleckchem.com/products/NVP-AUY922.html","C26H31N3O5","free base","AUY-922, VER-52296","CCNC(=O)C1=NOC(=C1C2=CC=C(CN3CCOCC3)C=C2)C4=CC(=C(O)C=C4O)C(C)C",4.069,4,3,7]
["S1070","PHA-665752","a8","L1700-01","in 10mM DMSO","c-Met","Protein Tyrosine Kinase","PHA-665752 is a potent, selective and ATP-competitive c-Met inhibitor with IC50 of 9 nM in cell-free assays,  >50-fold selectivity for c-Met than RTKs or STKs.",641.61,"477575-56-7",{"v":128,"d":"128.00"},{"v":199.5,"d":"199.50"},"<1","N/A","http://selleckchem.com/products/PHA-665752.html","C32H34Cl2N4O4S","free base","N/A","CC1=C(C(=C([NH]1)/C=C/2C(=O)NC3=C2C=C(C=C3)[S](=O)(=O)CC4=C(Cl)C=CC=C4Cl)C)C(=O)N5CCCC5CN6CCCC6",5.689,4,2,7]
["S1071","HA14-1","b8","L1700-01","in 10mM DMSO","Bcl-2","Apoptosis","HA14-1 is a non-peptidic ligand of a Bcl-2 surface pocket with IC50 of ~9 μM.",409.23,"65673-63-4",{"v":82,"d":"82.00"},200.38,"<1","N/A","http://selleckchem.com/products/HA14-1.html","C17H17BrN2O5","free base","N/A","CCOC(=O)C(C#N)C1C2=CC(=CC=C2OC(=C1C(=O)OCC)N)Br",2.511,5,1,7]
["S1072","ZSTK474","c8","L1700-01","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","ZSTK474 inhibits class I PI3K isoforms with IC50 of 37 nM in a cell-free assay, mostly PI3Kδ. Phase1/2.",417.41,"475110-96-4",{"v":21,"d":"21.00"},50.31,"<1","N/A","http://selleckchem.com/products/ZSTK474.html","C19H21F2N7O2","free base","N/A","FC(F)C1=NC2=C(C=CC=C2)[N]1C3=NC(=NC(=N3)N4CCOCC4)N5CCOCC5",3.366,6,0,4]
["S1075","SB216763","d8","L1700-01","in 10mM DMSO","Autophagy,GSK-3","PI3K/Akt/mTOR","SB216763 is a potent and selective GSK-3 inhibitor with IC50 of 34.3 nM for GSK-3α and equally effective at inhibiting human GSK-3β. SB216763 activates autophagy.",371.22,"280744-09-4",{"v":23,"d":"23.00"},61.96,"<1","N/A","http://selleckchem.com/products/SB-216763.html","C19H12N2O2Cl2","free base","N/A","C[N]1C=C(C2=C1C=CC=C2)C3=C(C(=O)NC3=O)C4=CC=C(Cl)C=C4Cl",4.391,2,1,2]
["S1076","Adezmapimod (SB203580)","e8","L1700-01","in 10mM DMSO","Mitophagy,p38 MAPK","MAPK","Adezmapimod (SB203580, RWJ 64809, PB 203580) is a p38 MAPK inhibitor with IC50 of 0.3-0.5 μM in THP-1 cells, 10-fold less sensitive to SAPK3(106T) and SAPK4(106T) and blocks PKB phosphorylation with IC50 of 3-5 μM. SB203580 induces mitophagy and autophagy.",377.43,"152121-47-6",{"v":43,"d":"43.00"},113.93,"<1","N/A","http://selleckchem.com/products/SB-203580.html","C21H16FN3OS","Free Base","RWJ 64809, PB 203580","C[S](=O)C1=CC=C(C=C1)C2=NC(=C([NH]2)C3=CC=NC=C3)C4=CC=C(F)C=C4",3.883,3,1,4]
["S1077","SB202190 (FHPI)","f8","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,Ferroptosis,p38 MAPK","MAPK","SB202190 (FHPI) is a potent p38 MAPK inhibitor targeting p38α/β with IC50 of 50 nM/100 nM in cell-free assays, sometimes used instead of SB 203580 to investigate potential roles for SAPK2a/p38 in vivo. SB202190 inhibits endothelial cell apoptosis via induction of autophagy and heme oxygenase-1. SB202190 significantly suppresses Erastin‐dependent ferroptosis.",331.34,"152121-30-7",{"v":66,"d":"66.00"},199.19,"<1","N/A","http://selleckchem.com/products/SB-202190.html","C20H14N3OF","free base","N/A","OC1=CC=C(C=C1)C2=NC(=C([NH]2)C3=CC=NC=C3)C4=CC=C(F)C=C4",4.211,2,2,3]
["S1078","MK-2206 2HCl","g8","L1700-01","in 10mM DMSO","Akt,Apoptosis related,Autophagy","PI3K/Akt/mTOR","MK-2206 2HCl is a highly selective inhibitor of Akt1/2/3 with IC50 of 8 nM/12 nM/65 nM in cell-free assays, respectively; no inhibitory activities against 250 other protein kinases observed. MK-2206 2HCl induces autophagy and apoptosis in cancer cells. Phase 2.",480.39,"1032350-13-2",{"v":14,"d":"14.00"},29.14,"<1","N/A","http://selleckchem.com/products/MK-2206.html","C25H21N5O.2HCl","Dihydrochloride","N/A","Cl.Cl.NC1(CCC1)C2=CC=C(C=C2)C3=C(C=C4C(=N3)C=CN5C(=O)NN=C45)C6=CC=CC=C6",4.183,3,2,3]
["S1080","SU11274","h8","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,c-Met","Protein Tyrosine Kinase","SU11274 (PKI-SU11274) is a selective Met (c-Met) inhibitor with IC50 of 10 nM in cell-free assays, no effects on PGDFRβ, EGFR or Tie2. SU11274 induces autophagy, apoptosis and cell cycle arrest.",568.09,"658084-23-2",{"v":92,"d":"92.00"},161.95,"<1","N/A","http://selleckchem.com/products/SU11274.html","C28H30CIN5O4S","free base","PKI-SU11274","CN1CCN(CC1)C(=O)C2=C(C)[NH]C(=C2C)/C=C/3C(=O)NC4=C3C=C(C=C4)[S](=O)(=O)N(C)C5=CC(=CC=C5)Cl",3.477,4,2,5]
["S1082","Vismodegib (GDC-0449)","a9","L1700-01","in 10mM DMSO","Hedgehog/Smoothened","Stem Cells & Wnt","Vismodegib (GDC-0449) is a potent, novel and specific hedgehog inhibitor with IC50 of 3 nM and also inhibits P-gp with IC50 of 3.0 μM in a cell-free assay.",{"v":421.3,"d":"421.30"},"879085-55-9",{"v":84,"d":"84.00"},199.38,"<1","N/A","http://selleckchem.com/products/GDC-0449.html","C19H14Cl2N2O3S","free base","GDC-0449","C[S](=O)(=O)C1=CC=C(C(=C1)Cl)C(=O)NC2=CC(=C(Cl)C=C2)C3=NC=CC=C3",4.265,4,1,4]
["S1084","Brivanib (BMS-540215)","b9","L1700-01","in 10mM DMSO","FGFR,VEGFR","Protein Tyrosine Kinase","Brivanib is an ATP-competitive inhibitor against VEGFR2 with IC50 of 25 nM, moderate potency against VEGFR-1 and FGFR-1, but >240-fold against PDGFR-β. Phase 3.",370.38,"649735-46-6",{"v":74,"d":"74.00"},199.79,"<1","N/A","http://selleckchem.com/products/Brivanib.html","C19H19FN4O3","free base","N/A","CC(O)COC1=C[N]2N=CN=C(OC3=C(F)C4=C([NH]C(=C4)C)C=C3)C2=C1C",3.481,4,2,5]
["S1085","Belinostat (PXD101)","c9","L1700-01","in 10mM DMSO","Autophagy,HDAC","Epigenetics","Belinostat (PXD101, NSC726630, PX-105684) is a novel HDAC inhibitor with IC50 of 27 nM in a cell-free assay, with activity demonstrated in cisplatin-resistant tumors. Belinostat (PXD101) induces autophagy.",318.35,"866323-14-0",{"v":64,"d":"64.00"},201.04,"<1","N/A","http://selleckchem.com/products/Belinostat.html","C15H14N2O4S","free base","PXD101,NSC726630, PX-105684","ONC(=O)/C=C/C1=CC(=CC=C1)[S](=O)(=O)NC2=CC=CC=C2",{"v":1.8,"d":"1.800"},3,2,5]
["S1087","Iniparib (BSI-201)","d9","L1700-01","in 10mM DMSO","PARP","DNA Damage/DNA Repair","Iniparib (BSI-201, NSC-746045, IND-71677) is a PARP1 inhibitor with demonstrated effectiveness in triple-negative breast cancer (TNBC). Phase 3.",292.03,"160003-66-7",{"v":58,"d":"58.00"},198.61,"<1","N/A","http://selleckchem.com/products/BSI-201.html","C7H5IN2O3","free base","NSC-746045, IND-71677","NC(=O)C1=CC(=C(I)C=C1)[N+]([O-])=O",1.304,1,1,2]
["S1088","NVP-ADW742","e9","L1700-01","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","NVP-ADW742 (GSK 552602A) is an IGF-1R inhibitor with IC50 of 0.17 μM, >16-fold more potent against IGF-1R than InsR;  little activity to HER2, PDGFR, VEGFR-2, Bcr-Abl and c-Kit.",453.58,"475488-23-4",{"v":10,"d":"10.00"},22.05,"<1","N/A","http://selleckchem.com/products/NVP-ADW742.html","C28H31N5O","Free Base","GSK 552602A, ADW742","NC1=NC=NC2=C1C(=C[N]2C3CC(C3)CN4CCCC4)C5=CC(=CC=C5)OCC6=CC=CC=C6",4.806,3,1,7]
["S1089","Refametinib (RDEA119)","f9","L1700-01","in 10mM DMSO","MEK","MAPK","Refametinib (RDEA119, Bay 86-9766) is a potent, ATP non-competitive and highly selective inhibitor of MEK1 and MEK2 with IC50 of 19 nM and 47 nM, respectively.",572.34,"923032-37-5",{"v":100,"d":"100.00"},174.72,"<1","N/A","http://selleckchem.com/products/refametinib-rdea119-bay86-9766.html","C19H20F3IN2O5S","free base","Bay 86-9766","COC1=C(N[S](=O)(=O)C2(CC2)CC(O)CO)C(=C(F)C(=C1)F)NC3=CC=C(I)C=C3F",2.827,3,4,9]
["S1090","Abexinostat (PCI-24781)","g9","L1700-01","in 10mM DMSO","HDAC","Cytoskeletal Signaling","Abexinostat (PCI-24781, CRA-024781) is a novel pan-HDAC inhibitor mostly targeting HDAC1 with Ki of 7 nM, modest potent to HDACs 2, 3, 6, and 10 and greater than 40-fold selectivity against HDAC8. Phase 1/2.",397.42,"783355-60-2",{"v":80,"d":"80.00"},{"v":201.3,"d":"201.30"},"<1","N/A","http://selleckchem.com/products/PCI-24781.html","C21H23N3O5","free base","CRA-024781","CN(C)CC1=C(OC2=CC=CC=C12)C(=O)NCCOC3=CC=C(C=C3)C(=O)NO",2.353,4,2,8]
["S1091","Linsitinib (OSI-906)","h9","L1700-01","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","Linsitinib (OSI-906) is a selective inhibitor of IGF-1R with IC50 of 35 nM in cell-free assays; modestly potent to InsR with IC50 of 75 nM, and no activity towards Abl, ALK, BTK, EGFR, FGFR1/2, PKA etc. Phase 3.",421.49,"867160-71-2",{"v":84,"d":"84.00"},199.29,"<1","N/A","http://selleckchem.com/products/OSI-906.html","C26H23N5O","free base","N/A","CC1(O)CC(C1)C2=NC(=C3[N]2C=CN=C3N)C4=CC=C5C=CC(=NC5=C4)C6=CC=CC=C6",3.757,3,1,3]
["S1092","KU-55933 (ATM Kinase Inhibitor)","a10","L1700-01","in 10mM DMSO","ATM/ATR,Autophagy,ULK","DNA Damage/DNA Repair","KU-55933 (ATM Kinase Inhibitor) is a potent and specific ATM inhibitor with IC50/Ki of 12.9 nM/2.2 nM in cell-free assays, and is highly selective for ATM as compared to DNA-PK, PI3K/PI4K, ATR and mTOR. KU‑55933 (ATM Kinase Inhibitor) inhibits the activation of autophagy‑initiating kinase ULK1 and results in a significant decrease of autophagy.",395.49,"587871-26-9",{"v":33,"d":"33.00"},83.44,"<1","N/A","http://selleckchem.com/products/KU-55933.html","C21H17NO3S2","free base","N/A","O=C1C=C(OC(=C1)C2=CC=CC3=C2SC4=CC=CC=C4S3)N5CCOCC5",4.393,3,0,2]
["S1093","GSK1904529A","b10","L1700-01","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","GSK1904529A (GSK 4529) is a selective inhibitor of IGF-1R and IR with IC50 of 27 nM and 25 nM in cell-free assays, >100-fold more selective for IGF-1R/InsR than Akt1/2, Aurora A/B,B-Raf, CDK2, EGFR etc.",851.96,"1089283-49-7",{"v":124,"d":"124.00"},145.55,"<1","N/A","http://selleckchem.com/products/GSK1904529A.html","C44H47F2N9O5S","free base","GSK 4529","CCC1=CC(=C(OC)C=C1N2CCC(CC2)N3CCN(CC3)[S](C)(=O)=O)NC4=NC(=CC=N4)C5=C(N=C6C=CC=C[N]56)C7=CC(=C(OC)C=C7)C(=O)NC8=C(F)C=CC=C8F",6.571,8,2,12]
["S1094","PF-04217903","c10","L1700-01","in 10mM DMSO","c-Met","Protein Tyrosine Kinase","PF-04217903 is a selective ATP-competitive c-Met inhibitor with IC50 of 4.8 nM in A549 cell line, susceptible to oncogenic mutations (no activity to Y1230C mutant). Phase 1.",372.38,"956905-27-4",{"v":5,"d":"5.00"},13.43,"<1","N/A","http://selleckchem.com/products/PF-04217903.html","C19H16N8O","free base","N/A","OCC[N]1C=C(C=N1)C2=NC3=C(N=C2)N=N[N]3CC4=CC5=CC=CN=C5C=C4",1.561,6,1,5]
["S1095","Dacinostat (LAQ824)","d10","L1700-01","in 10mM DMSO","HDAC,p21","Epigenetics","Dacinostat (LAQ824, NVP-LAQ824) is a novel HDAC inhibitor with IC50 of 32 nM and is known to activate the p21 promoter.",379.46,"404951-53-7",{"v":76,"d":"76.00"},200.29,"<1","N/A","http://selleckchem.com/products/LAQ824(NVP-LAQ824).html","C22H25N3O3","free base","NVP-LAQ824","OCCN(CCC1=C[NH]C2=C1C=CC=C2)CC3=CC=C(\\C=C\\C(=O)NO)C=C3",3.045,1,3,9]
["S1096","Quisinostat (JNJ-26481585) 2HCl","e10","L1700-01","in 10mM DMSO","HDAC","Epigenetics","Quisinostat (JNJ-26481585) 2HCl is a novel second-generation HDAC inhibitor with highest potency for HDAC1 with IC50 of 0.11 nM in a cell-free assay, modest potent to HDACs 2, 4, 10, and 11; greater than 30-fold selectivity against HDACs 3, 5, 8, and 9 and lowest potency to HDACs 6 and 7. Phase 2.",467.39,"875320-31-3",{"v":79,"d":"79.00"},169.02,"<1","N/A","http://selleckchem.com/products/JNJ-26481585.html","C21H28Cl2N6O2","Dihydrochloride","N/A","Cl.Cl.C[N]1C=C(CNCC2CCN(CC2)C3=NC=C(C=N3)C(=O)NO)C4=CC=CC=C14",2.749,3,2,6]
["S1097","BTZ043 Racemate","f10","L1700-01","in 10mM DMSO","Bacterial","Microbiology","BTZ043 racemate is a decaprenylphosphoryl-β-D-ribose 2'-epimerase (DprE1) inhibitor acting as a new antimycobacterial agent that kill Mycobacterium tuberculosis.",431.39,"957217-65-1",{"v":22,"d":"22.00"},{"v":51,"d":"51.00"},"<1","N/A","http://selleckchem.com/products/BTZ043.html","C17H16F3N3O5S","free base","N/A","CC1COC2(CCN(CC2)C3=NC(=O)C4=CC(=CC(=C4S3)[N+]([O-])=O)C(F)(F)F)O1",3.515,4,0,3]
["S1098","Rucaparib (AG-014699) phosphate","g10","L1700-01","in 10mM DMSO","PARP","DNA Damage/DNA Repair","Rucaparib (AG-014699, PF-01367338) is an inhibitor of PARP with Ki of 1.4 nM for PARP1 in a cell-free assay, also showing binding affinity to eight other PARP domains. Phase 3.",421.36,"459868-92-9",{"v":84,"d":"84.00"},199.35,"<1","N/A","http://selleckchem.com/products/AG-014699.html","C19H18FN3O.H3PO4","Phosphate","PF-01367338","CNCC1=CC=C(C=C1)C2=C3CCNC(=O)C4=CC(=CC(=C34)[NH]2)F.O[P](O)(O)=O",{"v":2.49,"d":"2.490"},1,3,3]
["S1100","MLN8054","h10","L1700-01","in 10mM DMSO","Aurora Kinase","Cell Cycle","MLN8054 is a potent and selective inhibitor of Aurora A with IC50 of 4 nM in Sf9 insect cell. It is more than 40-fold selective for Aurora A than Aurora B. Phase 1.",476.86,"869363-13-3",{"v":95,"d":"95.00"},199.22,"<1","N/A","http://selleckchem.com/products/MLN8054.html","C25H15ClF2N4O2","free base","N/A","OC(=O)C1=CC=C(NC2=NC3=C(CN=C(C4=CC(=CC=C34)Cl)C5=C(F)C=CC=C5F)C=N2)C=C1",6.192,4,1,4]
["S1101","Vatalanib (PTK787) 2HCl","a11","L1700-01","in 10mM DMSO","VEGFR","Protein Tyrosine Kinase","Vatalanib 2HCl (PTK787, ZK 222584, cpg-79787) is an inhibitor of VEGFR2/KDR with IC50 of 37 nM in a cell-free assay, less potent against VEGFR1/Flt-1, 18-fold against VEGFR3/Flt-4. Phase 3.",419.73,"212141-51-0",{"v":85,"d":"85.00"},202.51,{"v":10,"d":"10.00"},23.82,"http://selleckchem.com/products/Vatalanib,Dihydrochloride-Salt.html","C20H15ClN4.2HCl","Dihydrochloride","ZK 222584 (cpg-79787) 2HCl","Cl.Cl.ClC1=CC=C(NC2=NN=C(CC3=CC=NC=C3)C4=CC=CC=C24)C=C1",5.469,3,1,4]
["S1102","U0126-EtOH","b11","L1700-01","in 10mM DMSO","Antiviral,Autophagy,MEK,Mitophagy","MAPK","U0126-EtOH is a highly selective inhibitor of MEK1/2 with IC50 of 0.07 μM/0.06 μM in cell-free assays, 100-fold higher affinity for ΔN3-S218E/S222D MEK than PD98059. U0126 inhibits autophagy and mitophagy with antiviral activity.",426.56,"1173097-76-1",{"v":85,"d":"85.00"},199.27,"<1","N/A","http://selleckchem.com/products/U0126.html","C18H16N6S2.C2H6O","Ethanolate","N/A","CCO.N\\C(SC1=CC=CC=C1N)=C(C#N)\\C(C#N)=C(N)/SC2=CC=CC=C2N",2.169,0,5,5]
["S1103","ZM 447439","c11","L1700-01","in 10mM DMSO","Aurora Kinase","Cell Cycle","ZM 447439 is a selective and ATP-competitive inhibitor for Aurora A and Aurora B with IC50 of 110 nM and 130 nM, respectively. It is more than 8-fold selective for Aurora A/B than MEK1, Src, Lck and has little effect against CDK1/2/4, Plk1, Chk1, etc.",513.59,"331771-20-1",{"v":103,"d":"103.00"},200.55,"<1","N/A","http://selleckchem.com/products/ZM-447439.html","C29H31N5O4","free base","N/A","COC1=C(OCCCN2CCOCC2)C=C3N=CN=C(NC4=CC=C(NC(=O)C5=CC=CC=C5)C=C4)C3=C1",4.118,6,2,10]
["S1104","GDC-0879","d11","L1700-01","in 10mM DMSO","Raf","MAPK","GDC-0879 (AR-00341677) is a novel, potent, and selective B-Raf inhibitor with IC50 of 0.13 nM in A375 and Colo205 cells with activity against c-Raf as well; no inhibition known to other protein kinases.",334.37,"905281-76-7",{"v":66,"d":"66.00"},197.39,"<1","N/A","http://selleckchem.com/products/GDC-0879.html","C19H18N4O2","free base","AR-00341677","OCC[N]1C=C(C2=CC=C\\3C(=C2)CCC3=N\\O)C(=N1)C4=CC=NC=C4",2.387,3,1,4]
["S1105","LY294002","e11","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,Casein Kinase,DNA-PK,PI3K","PI3K/Akt/mTOR","LY294002 (SF 1101, NSC 697286) is the first synthetic molecule known to inhibit PI3Kα/δ/β with IC50 of 0.5 μM/0.57 μM/0.97 μM, respectively; more stable in solution than Wortmannin, and also blocks autophagosome formation. It not only binds to class I PI3Ks and other PI3K-related kinases, but also to novel targets seemingly unrelated to the PI3K family. LY294002 also inhibits CK2 with IC50 of 98 nM. LY294002 is a non-specific DNA-PKcs inhibitor and activates autophagy and apoptosis.",307.34,"154447-36-6",{"v":36,"d":"36.00"},117.13,"<1","N/A","http://selleckchem.com/products/LY294002.html","C19H17NO3","free base","SF 1101, NSC 697286","O=C1C=C(OC2=C(C=CC=C12)C3=CC=CC=C3)N4CCOCC4",3.342,3,0,2]
["S1106","OSU-03012 (AR-12)","f11","L1700-01","in 10mM DMSO","PDPK1","PI3K/Akt/mTOR","OSU-03012 (AR-12) is a potent inhibitor of recombinant PDK-1(phosphoinositide-dependent kinase 1) with IC50 of 5 μM in a cell-free assay and 2-fold increase in potency over OSU-02067.",460.45,"742112-33-0",{"v":11,"d":"11.00"},23.89,"<1","N/A","http://selleckchem.com/products/OSU-03012.html","C26H19F3N4O","free base","N/A","NCC(=O)NC1=CC=C(C=C1)[N]2N=C(C=C2C3=CC4=C(C=C3)C5=C(C=CC=C5)C=C4)C(F)(F)F",5.212,2,2,5]
["S1107","Danusertib (PHA-739358)","g11","L1700-01","in 10mM DMSO","Apoptosis related,Aurora Kinase,Autophagy,Bcr-Abl,c-RET,FGFR,Trk receptor","Cell Cycle","Danusertib (PHA-739358) is an Aurora kinase inhibitor for Aurora A/B/C with IC50 of 13 nM/79 nM/61 nM in cell-free assays, modestly potent to Abl, TrkA, c-RET and FGFR1, and less potent to Lck, VEGFR2/3, c-Kit, CDK2, etc. Danusertib induces apoptosis, cell cycle arrest, and autophagy. Phase 2.",474.55,"827318-97-8",{"v":95,"d":"95.00"},200.19,"<1","N/A","http://selleckchem.com/products/PHA-739358(Danusertib).html","C26H30N6O3","free base","N/A","COC(C(=O)N1CC2=C(C1)C(=N[NH]2)NC(=O)C3=CC=C(C=C3)N4CCN(C)CC4)C5=CC=CC=C5",2.337,4,2,6]
["S1109","BI 2536","h11","L1700-01","in 10mM DMSO","Apoptosis related,Autophagy,Epigenetic Reader Domain,Myc,PLK","Cell Cycle","BI-2536 is a potent Plk1 inhibitor with IC50 of 0.83 nM in a cell-free assay. BI-2536 inhibits Bromodomain 4 (BRD4) with Kd of 37 nM and potently suppresses c-Myc expression. BI-2536 induces apoptosis and attenuates autophagy. Phase 2.",521.66,"755038-02-9",{"v":21,"d":"21.00"},40.26,"<1","N/A","http://selleckchem.com/products/BI-2536.html","C28H39N7O3","free base","N/A","CCC1N(C2CCCC2)C3=NC(=NC=C3N(C)C1=O)NC4=CC=C(C=C4OC)C(=O)NC5CCN(C)CC5",3.548,5,2,7]
["S1110","Varespladib (LY315920)","a2","L1700-02","in 10mM DMSO","Phospholipase (e.g. PLA)","Metabolism","Varespladib (LY315920) is a potent and selective human non-pancreatic secretory phospholipase A2 (hnsPLA) inhibitor with IC50 of 7 nM. Phase 3.",380.39,"172732-68-2",{"v":76,"d":"76.00"},199.79,"<1","N/A","http://selleckchem.com/products/LY315920(Varespladib).html","C21H20N2O5","free base","N/A","CCC1=C(C(=O)C(N)=O)C2=C(C=CC=C2OCC(O)=O)[N]1CC3=CC=CC=C3",3.078,4,1,8]
["S1111","Foretinib (GSK1363089)","b2","L1700-02","in 10mM DMSO","c-Kit,c-Met,FLT3,PDGFR,VEGFR","Protein Tyrosine Kinase","Foretinib (GSK1363089, EXEL-2880, XL-880, GSK089) is an ATP-competitive inhibitor of HGFR and VEGFR, mostly for Met (c-Met) and KDR with IC50 of 0.4 nM and 0.9 nM in cell-free assays. Less potent against Ron, Flt-1/3/4, Kit (c-Kit), PDGFRα/β and Tie-2, and little activity to FGFR1 and EGFR. Phase 2.",632.65,"849217-64-7",{"v":100,"d":"100.00"},158.07,"<1","N/A","http://selleckchem.com/products/XL880(GSK1363089,EXEL-2880).html","C34H34F2N4O6","free base","EXEL-2880, XL-880, GSK089","COC1=CC2=C(C=C1OCCCN3CCOCC3)N=CC=C2OC4=C(F)C=C(NC(=O)C5(CC5)C(=O)NC6=CC=C(F)C=C6)C=C4",4.437,7,2,12]
["S1113","GSK690693","c2","L1700-02","in 10mM DMSO","Akt,AMPK,Autophagy,DAPK,PKA,PKC,STING,ULK","PI3K/Akt/mTOR","GSK690693 is a pan-Akt inhibitor targeting Akt1/2/3 with IC50 of 2 nM/13 nM/9 nM in cell-free assays, also sensitive to the AGC kinase family: PKA, PrkX and PKC isozymes. GSK690693 also potently inhibits AMPK and DAPK3 from the CAMK family with IC50 of 50 nM and 81 nM, respectively. GSK690693 affects Unc-51-like autophagy activating kinase 1 (ULK1) activity, robustly inhibits STING-dependent IRF3 activation. Phase 1.",425.48,"937174-76-0",{"v":39,"d":"39.00"},91.66,"<1","N/A","http://selleckchem.com/products/GSK690693.html","C21H27N7O3","free base","N/A","CC[N]1C(=NC2=C1C(=CN=C2C#CC(C)(C)O)OCC3CCCNC3)C4=NON=C4N",1.839,6,2,7]
["S1114","JNJ-38877605","d2","L1700-02","in 10mM DMSO","c-Met","Protein Tyrosine Kinase","JNJ-38877605 is an ATP-competitive inhibitor of c-Met with IC50 of 4 nM, 600-fold selective for c-Met than 200 other tyrosine and serine-threonine kinases. Phase 1.",377.35,"943540-75-8",{"v":37,"d":"37.00"},98.05,"<1","N/A","http://selleckchem.com/products/JNJ-38877605.html","C19H13F2N7","free base","N/A","C[N]1C=C(C=N1)C2=N[N]3C(=NN=C3C(F)(F)C4=CC5=C(C=C4)N=CC=C5)C=C2",3.052,5,0,3]
["S1115","Odanacatib (MK-0822)","e2","L1700-02","in 10mM DMSO","Cysteine Protease","Proteases","Odanacatib (MK 0822) is a potent, selective, and neutral inhibitor of cathepsin K (human/rabbit) with IC50 of 0.2 nM/1 nM, and demonstrated high selectivity versus off-target cathepsin B, L, S. Phase 3.",525.56,"603139-19-1",{"v":100,"d":"100.00"},190.27,"<1","N/A","http://selleckchem.com/products/Odanacatib-(MK0822).html","C25H27F4N3O3S","free base","N/A","CC(C)(F)CC(NC(C1=CC=C(C=C1)C2=CC=C(C=C2)[S](C)(=O)=O)C(F)(F)F)C(=O)NC3(CC3)C#N",3.978,3,2,10]
["S1117","Triciribine (NSC 154020)","f2","L1700-02","in 10mM DMSO","Akt,DNA/RNA Synthesis,HIV","PI3K/Akt/mTOR","Triciribine (NSC 154020, VD-0002, vqd-002, API-2, TCN) is a DNA synthesis inhibitor, also inhibits Akt in PC3 cell line and HIV-1 in CEM-SS, H9, H9IIIB, U1 cells with IC50 of 130 nM and 20 nM, respectively; does not inhibit PI3K/PDK1; 5000-fold less active in cells lacking adenosine kinase. Phase 1/2.",{"v":320.3,"d":"320.30"},"35943-35-2",{"v":64,"d":"64.00"},199.81,"<1","N/A","http://selleckchem.com/products/Triciribine.html","C13H16N6O4","free base","VD-0002, vqd-002, API-2, TCN","CN1N=C(N)C2=C[N](C3OC(CO)C(O)C3O)C4=C2C1=NC=N4",-1.119,4,4,2]
["S1119","Cabozantinib (BMS-907351)","g2","L1700-02","in 10mM DMSO","Apoptosis related,Axl,c-Met,VEGFR","Protein Tyrosine Kinase","Cabozantinib (XL184, BMS-907351) is a potent VEGFR2 inhibitor with IC50 of 0.035 nM and also inhibits c-Met, Ret, Kit, Flt-1/3/4, Tie2, and AXL with IC50 of 1.3 nM, 4 nM, 4.6 nM, 12 nM/11.3 nM/6 nM, 14.3 nM and 7 nM in cell-free assays, respectively. Cabozantinib induces PUMA-dependent apoptosis in colon cancer cells via AKT/GSK-3β/NF-κB signaling pathway.",501.51,"849217-68-1",{"v":100,"d":"100.00"},{"v":199.4,"d":"199.40"},"<1","N/A","http://selleckchem.com/products/XL184.html","C28H24FN3O5","Free Base","XL184,BMS-907351","COC1=CC2=C(C=C1OC)C(=CC=N2)OC3=CC=C(NC(=O)C4(CC4)C(=O)NC5=CC=C(F)C=C5)C=C3",4.342,6,2,8]
["S1120","Everolimus (RAD001)","h2","L1700-02","in 10mM DMSO","Apoptosis related,Autophagy,FKBP,mTOR","PI3K/Akt/mTOR","Everolimus (RAD001, SDZ-RAD, Afinitor) is an mTOR inhibitor of FKBP12 with IC50 of 1.6-2.4 nM in a cell-free assay. Everolimus induces cell apoptosis and autophagy and inhibits tumor cells proliferation.",958.22,"159351-69-6",{"v":100,"d":"100.00"},104.36,"<1","N/A","http://selleckchem.com/products/Everolimus(RAD001).html","C53H83NO14","free base","RAD001,SDZ-RAD, Afinitor","COC1CC(CCC1OCCO)CC(C)C2CC(=O)C(C)\\C=C(C)\\C(O)C(OC)C(=O)C(C)CC(C)/C=C/C=C/C=C(C)/C(CC3CCC(C)C(O)(O3)C(=O)C(=O)N4CCCCC4C(=O)O2)OC",6.164,11,2,9]
["S1121","TW-37","a3","L1700-02","in 10mM DMSO","Bcl-2","Apoptosis","TW-37 is a novel nonpeptide inhibitor to recombinant Bcl-2, Bcl-xL and Mcl-1 with Ki of 0.29 μM, 1.11 μM and 0.26 μM in cell-free assays, respectively.",{"v":573.7,"d":"573.70"},"877877-35-5",{"v":115,"d":"115.00"},200.45,"<1","N/A","http://selleckchem.com/products/TW-37.html","C33H35NO6S","free base","N/A","CC(C)C1=CC=CC=C1CC2=CC(=C(O)C(=C2O)O)C(=O)NC3=CC=C(C=C3)[S](=O)(=O)C4=C(C=CC=C4)C(C)(C)C",{"v":7.56,"d":"7.560"},3,4,8]
["S1122","Mocetinostat (MGCD0103)","b3","L1700-02","in 10mM DMSO","Apoptosis related,Autophagy,HDAC","Epigenetics","Mocetinostat (MGCD0103, MG0103) is a potent HDAC inhibitor with most potency for HDAC1 with IC50 of 0.15 μM in a cell-free assay, 2- to 10- fold selectivity against HDAC2, 3, and 11, and no activity to HDAC4, 5, 6, 7, and 8. Mocetinostat (MGCD0103) induces apoptosis and autophagy. Phase 2.",396.44,"726169-73-9",{"v":13,"d":"13.00"},32.79,"<1","N/A","http://selleckchem.com/products/MGCD0103(Mocetinostat).html","C23H20N6O","free base","MG0103","NC1=CC=CC=C1NC(=O)C2=CC=C(CNC3=NC=CC(=N3)C4=CC=CN=C4)C=C2",2.798,4,3,6]
["S1124","BMS-754807","c3","L1700-02","in 10mM DMSO","c-Met,IGF-1R,RON,Trk receptor","Protein Tyrosine Kinase","BMS-754807 is a potent and reversible inhibitor of IGF-1R/InsR with IC50 of 1.8 nM/1.7 nM in cell-free assays, less potent to Met (c-Met), Aurora A/B, TrkA/B and Ron, and shows little activity to Flt3, Lck, MK2, PKA, PKC etc. Phase 2.",461.49,"1001350-96-4",{"v":92,"d":"92.00"},199.35,"<1","N/A","http://selleckchem.com/products/BMS-754807.html","C23H24FN9O","free base","N/A","CC1(CCCN1C2=N[N]3C=CC=C3C(=N2)NC4=N[NH]C(=C4)C5CC5)C(=O)NC6=CC=C(F)N=C6",4.069,5,3,6]
["S1129","SRT1720 HCl","d3","L1700-02","in 10mM DMSO","Autophagy,Sirtuin","Epigenetics","SRT1720 HCl is a selective SIRT1 activator with EC50 of 0.16 μM in a cell-free assay, but is >230-fold less potent for SIRT2 and SIRT3. SRT1720 induces autophagy.",506.02,"1001645-58-4",{"v":38,"d":"38.00"},{"v":75.1,"d":"75.10"},"<1","N/A","http://selleckchem.com/products/SRT1720.html","C25H23N7OS.HCl","Hydrochloride","N/A","Cl.O=C(NC1=CC=CC=C1C2=C[N]3C(=CSC3=N2)CN4CCNCC4)C5=NC6=CC=CC=C6N=C5",3.018,4,2,5]
["S1130","Sepantronium Bromide","e3","L1700-02","in 10mM DMSO","Autophagy,IAP,Survivin","Apoptosis","Sepantronium Bromide(YM155) is a potent survivin suppressant by inhibiting Survivin promoter activity with IC50 of 0.54 nM in HeLa-SURP-luc and CHO-SV40-luc cells; does not significantly inhibit SV40 promoter activity, but is observed to slightly inhibit the interaction of Survivin with XIAP. YM155 down-regulates survivin and XIAP, modulates autophagy and induces autophagy-dependent DNA damage in breast cancer cells. Phase 2.",443.29,"781661-94-7",{"v":55,"d":"55.00"},124.07,{"v":89,"d":"89.00"},200.77,"http://selleckchem.com/products/YM155.html","C20H19BrN4O3","Bromide","YM155","[Br-].COCC[N]1C(=[N+](CC2=CN=CC=N2)C3=C1C(=O)C4=C(C=CC=C4)C3=O)C",-0.733,5,0,5]
["S1132","3-Aminobenzamide","f3","L1700-02","in 10mM DMSO","Apoptosis related,PARP","DNA Damage/DNA Repair","3-Aminobenzamide (3-ABA , 3-Amino Benzamide, 3-AB) is a potent inhibitor of Poly(ADP-ribose)polymerase (PARP) and inhibits cell apoptosis after SCI (Spinal Cord Injury) in caspase-independent way.",136.15,"3544-24-9",{"v":27,"d":"27.00"},198.31,"<1","N/A","https://www.selleckchem.com/products/3-aminobenzamide.html","C7H8N2O","free base","3-ABA , 3-amino Benzamide, 3-AB","NC(=O)C1=CC(=CC=C1)N",0.085,1,2,1]
["S1133","Alisertib (MLN8237)","g3","L1700-02","in 10mM DMSO","Apoptosis related,Aurora Kinase,Autophagy","Cell Cycle","Alisertib (MLN8237) is a selective Aurora A inhibitor with IC50 of 1.2 nM in a cell-free assay. It has >200-fold higher selectivity for Aurora A than Aurora B. Alisertib induces cell cycle arrest, apoptosis and autophagy. Phase 3.",518.92,"1028486-01-2",{"v":27,"d":"27.00"},52.03,"<1","N/A","http://selleckchem.com/products/MLN8237.html","C27H20ClFN4O4","free base","N/A","COC1=C(C(=CC=C1)F)C2=NCC3=C(N=C(NC4=CC(=C(C=C4)C(O)=O)OC)N=C3)C5=C2C=C(Cl)C=C5",5.954,6,1,6]
["S1134","AT9283","h3","L1700-02","in 10mM DMSO","Aurora Kinase,Bcr-Abl,JAK","JAK/STAT","AT9283 is a potent JAK2/3 inhibitor with IC50 of 1.2 nM/1.1 nM in cell-free assays; also potent to Aurora A/B, Abl1(T315I).",381.43,"896466-04-9",{"v":76,"d":"76.00"},199.25,"<1","N/A","http://selleckchem.com/products/AT9283.html","C19H23N7O2","free base","N/A","O=C(NC1CC1)NC2=C[NH]N=C2C3=NC4=CC(=CC=C4[NH]3)CN5CCOCC5",{"v":1.51,"d":"1.510"},4,4,5]
["S1137","Malotilate","a4","L1700-02","in 10mM DMSO","Lipoxygenase","Metabolism","Malotilate (NKK105) is a drug used for the treatment of liver cirrhosis. Malotilate is a liver protein metabolism improved compound, which selectively inhibit the 5-lipoxygenase.",288.38,"59937-28-9",{"v":58,"d":"58.00"},201.12,"<1","N/A","http://selleckchem.com/products/Malotilate.html","C12H16O4S2","free base","NKK105","CC(C)OC(=O)C(C(=O)OC(C)C)=C1SC=CS1",2.363,4,0,6]
["S1138","Brivanib Alaninate (BMS-582664)","b4","L1700-02","in 10mM DMSO","FGFR,VEGFR","Protein Tyrosine Kinase","Brivanib alaninate (BMS-582664) is the prodrug of BMS-540215, an ATP-competitive inhibitor against VEGFR2 with IC50 of 25 nM.",441.46,"649735-63-7",{"v":88,"d":"88.00"},199.34,"<1","N/A","http://selleckchem.com/products/Brivanib-alaninate.html","C22H24FN5O4","Alaninate","N/A","CC(N)C(=O)OC(C)COC1=C[N]2N=CN=C(OC3=C(F)C4=C([NH]C(=C4)C)C=C3)C2=C1C",3.383,6,2,8]
["S1141","Tanespimycin (17-AAG)","c4","L1700-02","in 10mM DMSO","Apoptosis related,Autophagy,HSP (HSP90),Mitophagy","Cytoskeletal Signaling","Tanespimycin (17-AAG, CP127374, NSC-330507, KOS 953) is a potent HSP90 inhibitor with IC50 of 5 nM in a cell-free assay, having a 100-fold higher binding affinity for HSP90 derived from tumour cells than HSP90 from normal cells. Tanespimycin (17-AAG) induces apoptosis, necrosis, autophagy and mitophagy. Phase 3.",585.69,"75747-14-7",{"v":100,"d":"100.00"},170.74,"<1","N/A","http://selleckchem.com/products/17-AAG(Geldanamycin).html","C31H43N3O8","free base","CP127374, NSC-330507, KOS 953","COC1CC(C)CC2=C(NCC=C)C(=O)C=C(NC(=O)C(=C\\C=C/C(OC)C(OC(N)=O)/C(=C/C(C)C1O)C)\\C)C2=O",2.524,7,4,7]
["S1142","Alvespimycin (17-DMAG) HCl","d4","L1700-02","in 10mM DMSO","HSP (HSP90)","Cytoskeletal Signaling","Alvespimycin (17-DMAG, NSC 707545, BMS 826476, KOS 1022) HCl is a potent HSP90 inhibitor with IC50 of 62 nM in a cell-free assay.",653.21,"467214-21-7",{"v":131,"d":"131.00"},200.55,"<1","N/A","http://selleckchem.com/products/17-DMAG,Hydrochloride-Salt.html","C32H48N4O8.HCl","Hydrochloride","NSC 707545,BMS 826476 HCl,KOS 1022","Cl.COC1CC(C)CC2=C(NCCN(C)C)C(=O)C=C(NC(=O)C(=C\\C=C/C(OC)C(OC(N)=O)/C(=C/C(C)C1O)C)\\C)C2=O",2.428,7,4,8]
["S1143","AG-490 (Tyrphostin B42)","e4","L1700-02","in 10mM DMSO","EGFR,JAK","Protein Tyrosine Kinase","AG-490 (Tyrphostin B42, Zinc02557947) is an inhibitor of EGFR with IC50 of 0.1 μM in cell-free assays, 135-fold more selective for EGFR versus ErbB2, also inhibits JAK2 with no activity to Lck, Lyn, Btk, Syk and Src.",{"v":294.3,"d":"294.30"},"133550-30-8",{"v":58,"d":"58.00"},197.08,"<1","N/A","http://selleckchem.com/products/AG-490.html","C17H14N2O3","free base","Zinc02557947","OC1=C(O)C=C(C=C1)\\C=C(C#N)\\C(=O)NCC2=CC=CC=C2",2.444,1,3,4]
["S1144","Ivacaftor (VX-770)","f4","L1700-02","in 10mM DMSO","CFTR","Transmembrane Transporters","Ivacaftor (VX-770) is a selective potentiator of CFTR targeting G551D-CFTR and F508del-CFTR with EC50 of 100 nM and 25 nM in fisher rat thyroid cells, respectively.",392.49,"873054-44-5",{"v":78,"d":"78.00"},198.73,"<1","N/A","http://selleckchem.com/products/VX-770.html","C24H28N2O3","free base","VX-770","CC(C)(C)C1=CC(=C(NC(=O)C2=CNC3=C(C=CC=C3)C2=O)C=C1O)C(C)(C)C",4.516,2,3,4]
["S1145","SNS-032 (BMS-387032)","g4","L1700-02","in 10mM DMSO","Apoptosis related,CDK","Cell Cycle","SNS-032 (BMS-387032) has firstly been described as a selective inhibitor of CDK2 with IC50 of 48 nM in cell-free assays and is 10- and 20-fold selective over CDK1/CDK4. It is also found to be sensitive to CDK7/9 with IC50 of 62 nM/4 nM, with little effect on CDK6. SNS-032 (BMS-387032) induces apoptosis.",380.53,"345627-80-7",{"v":76,"d":"76.00"},199.72,"<1","N/A","http://selleckchem.com/products/SNS-032.html","C17H24N4O2S2","free base","N/A","CC(C)(C)C1=CN=C(CSC2=CN=C(NC(=O)C3CCNCC3)S2)O1",{"v":2.07,"d":"2.070"},4,2,6]
["S1147","Barasertib (AZD1152-HQPA)","h4","L1700-02","in 10mM DMSO","Aurora Kinase","Cell Cycle","Defosbarasertib (AZD1152-HQPA, AZD2811, INH-34, Barasertib-HQPA) is a highly selective Aurora B inhibitor with IC50 of 0.37 nM in a cell-free assay, ~3700 fold more selective for Aurora B over Aurora A. Phase 1.",507.56,"722544-51-6",{"v":102,"d":"102.00"},200.96,"<1","N/A","http://selleckchem.com/products/AZD1152-HQPA.html","C26H30FN7O3","free base","AZD2811, INH-34, Barasertib-HQPA , Defosbarasertib","CCN(CCO)CCCOC1=CC=C2C(=NC=NC2=C1)NC3=CC(=N[NH]3)CC(=O)NC4=CC=CC(=C4)F",3.493,5,4,13]
["S1148","Docetaxel (RP56976)","a5","L1700-02","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Docetaxel (RP56976, NSC 628503), an analog of paclitaxel, is an inhibitor of depolymerisation of microtubules by binding to stabilized microtubules.",807.88,"114977-28-5",{"v":100,"d":"100.00"},123.78,"<1","N/A","http://selleckchem.com/products/Docetaxel(Taxotere).html","C43H53NO14","Free Base","NSC 628503,RP56976","CC(=O)OC12COC1CC(O)C3(C)C2C(OC(=O)C4=CC=CC=C4)C5(O)CC(OC(=O)C(O)C(NC(=O)OC(C)(C)C)C6=CC=CC=C6)C(=C(C(O)C3=O)C5(C)C)C",2.586,10,4,13]
["S1150","Paclitaxel (NSC 125973)","b5","L1700-02","in 10mM DMSO","ADC Cytotoxin,Antineoplastic and Immunosuppressive Antibiotics,Autophagy,Microtubule Associated","Cytoskeletal Signaling","Paclitaxel (NSC 125973, PTX, Taxol, Onxal, Abraxane) is a microtubule polymer stabilizer with IC50 of 0.1 pM in human endothelial cells.",853.91,"33069-62-4",{"v":171,"d":"171.00"},200.26,"<1","N/A","http://selleckchem.com/products/Paclitaxel(Taxol).html","C47H51NO14","free base","PTX, Taxol, Onxal, Abraxane,NSC 125973","CC(=O)OC1C(=O)C2(C)C(O)CC3OCC3(OC(C)=O)C2C(OC(=O)C4=CC=CC=C4)C5(O)CC(OC(=O)C(O)C(NC(=O)C6=CC=CC=C6)C7=CC=CC=C7)C(=C1C5(C)C)C",3.055,11,3,14]
["S1152","PLX-4720","c5","L1700-02","in 10mM DMSO","Raf","MAPK","PLX4720 is a potent and selective inhibitor of B-RafV600E with IC50 of 13 nM in a cell-free assay, equally potent to c-Raf-1(Y340D and Y341D mutations), 10-fold selectivity for B-RafV600E than wild-type B-Raf.",413.83,"918505-84-7",{"v":83,"d":"83.00"},200.57,"<1","N/A","http://selleckchem.com/products/PLX-4720.html","C17H14ClF2N3O3S","free base","N/A","CCC[S](=O)(=O)NC1=CC=C(F)C(=C1F)C(=O)C2=C[NH]C3=NC=C(Cl)C=C23",3.435,4,2,6]
["S1153","Roscovitine (CYC202)","d5","L1700-02","in 10mM DMSO","CDK","Cell Cycle","Roscovitine (CYC202, Seliciclib, R-roscovitine) is a potent and selective CDK inhibitor for Cdc2, CDK2 and CDK5 with IC50 of 0.65 μM, 0.7 μM and 0.16 μM in cell-free assays. It shows little effect on CDK4/6. Phase 2.",354.45,"186692-46-6",{"v":71,"d":"71.00"},200.31,"<1","N/A","http://selleckchem.com/products/Roscovitine.html","C19H26N6O","free base","Seliciclib, R-roscovitine","CCC(CO)NC1=NC(=C2N=C[N](C(C)C)C2=N1)NCC3=CC=CC=C3",{"v":3.32,"d":"3.320"},3,3,8]
["S1154","SNS-314","e5","L1700-02","in 10mM DMSO","Aurora Kinase","Cell Cycle","SNS-314 is a potent and selective inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 9 nM, 31 nM, and 3 nM, respectively. It is less potent to Trk A/B, Flt4, Fms, Axl, c-Raf and DDR2. Phase 1.",430.93,"1057249-41-8",{"v":105,"d":"105.00"},243.66,{"v":6,"d":"6.00"},13.92,"http://selleckchem.com/products/sns-314-mesylate.html","C18H15ClN6OS2","Mesylate","N/A","C[S](O)(=O)=O.ClC1=CC=CC(=C1)NC(=O)NC2=NC=C(CCNC3=NC=NC4=C3SC=C4)S2",3.539,4,3,6]
["S1155","S3I-201","f5","L1700-02","in 10mM DMSO","STAT","JAK/STAT","S3I-201 (NSC 74859) shows potent inhibition of STAT3 DNA-binding activity with IC50 of 86 μM in cell-free assays, and low activity towards STAT1 and STAT5.",365.36,"501919-59-1",{"v":73,"d":"73.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://selleckchem.com/products/S31-201.html","C16H15NO7S","free base","NSC 74859","CC1=CC=C(C=C1)[S](=O)(=O)OCC(=O)NC2=CC=C(C(O)=O)C(=C2)O",1.712,3,2,6]
["S1156","Capecitabine (RO 09-1978)","g5","L1700-02","in 10mM DMSO","Apoptosis related,DNA/RNA Synthesis","DNA Damage/DNA Repair","Capecitabine (RO 09-1978) is a tumor-selective fluoropyrimidine carbamate, which achieves higher intratumoral 5-FU level with lower toxicity than 5-FU. Capecitabine treatment of HCT-15 cells causes condensation of DNA and induces apoptosis.",359.35,"154361-50-9",{"v":72,"d":"72.00"},200.36,{"v":6,"d":"6.00"},{"v":16.7,"d":"16.70"},"http://selleckchem.com/products/Capecitabine(Xeloda).html","C15H22FN3O6","free base","RO 09-1978","CCCCCOC(=O)NC1=NC(=O)N(C=C1F)C2OC(C)C(O)C2O",{"v":0.82,"d":"0.820"},5,3,7]
["S1157","Delanzomib (CEP-18770)","h5","L1700-02","in 10mM DMSO","Proteasome","Proteases","Delanzomib (CEP-18770) is an orally active inhibitor of the chymotrypsin-like activity of proteasome with IC50 of 3.8 nM, with only marginal inhibition of the tryptic and peptidylglutamyl activities of the proteosome. Phase 1/2.",413.28,"847499-27-8",{"v":83,"d":"83.00"},200.83,"<1","N/A","http://selleckchem.com/products/cep-18770.html","C21H28BN3O5","free base","N/A","CC(C)C(CNC(=O)C(NC(=O)C1=NC(=CC=C1)C2=CC=CC=C2)C(C)O)B(O)O",2.646,3,3,9]
["S1158","MK-8245","a6","L1700-02","in 10mM DMSO","SCD","Metabolism","MK-8245 is an liver-targeting inhibitor of stearoyl-CoA desaturase (SCD) with IC50 of 1 nM for human SCD1 and 3 nM for both rat SCD1 and mouse SCD1, with anti-diabetic and anti-dyslipidemic efficacy. Phase 2.",467.25,"1030612-90-8",{"v":93,"d":"93.00"},199.04,"<1","N/A","http://selleckchem.com/products/mk-8245.html","C17H16BrFN6O4","free base","N/A","OC(=O)C[N]1N=NC(=N1)C2=CC(=NO2)N3CCC(CC3)OC4=CC(=CC=C4Br)F",2.991,7,0,6]
["S1159","Ganetespib (STA-9090)","b6","L1700-02","in 10mM DMSO","Apoptosis related,HSP (HSP90)","Cytoskeletal Signaling","Ganetespib (STA-9090) is an HSP90 inhibitor with IC50 of 4 nM in OSA 8 cells, induces apoptosis of OSA cells while normal osteoblasts are not affected; active metabolite of STA-1474. Phase 3.",{"v":364.4,"d":"364.40"},"888216-25-9",{"v":40,"d":"40.00"},109.77,"<1","N/A","http://selleckchem.com/products/ganetespib-sta-9090.html","C20H20N4O3","free base","N/A","CC(C)C1=C(O)C=C(O)C(=C1)C2=NNC(=O)N2C3=CC4=C(C=C3)[N](C)C=C4",3.866,2,3,3]
["S1162","Pretomanid (PA-824)","c6","L1700-02","in 10mM DMSO","Bacterial","Microbiology","PA-824 is an anti-tuberculosis drug for tuberculosis with MIC less than 2.8 μM.Phase 2.",359.26,"187235-37-6",{"v":72,"d":"72.00"},200.41,"<1","N/A","http://selleckchem.com/products/pa-824.html","C14H12F3N3O5","free base","N/A","[O-][N+](=O)C1=C[N]2CC(COC2=N1)OCC3=CC=C(OC(F)(F)F)C=C3",4.301,4,0,6]
["S1163","Onalespib (AT13387)","d6","L1700-02","in 10mM DMSO","HSP (HSP90)","Cytoskeletal Signaling","Onalespib (AT13387) is a selective potent Hsp90 inhibitor with IC50 of 18 nM in A375 cells, displays a long duration of anti-tumor activity. Phase 2.",409.52,"912999-49-6",{"v":25,"d":"25.00"},61.05,"<1","N/A","http://selleckchem.com/products/at13387.html","C24H31N3O3","free base","N/A","CC(C)C1=C(O)C=C(O)C(=C1)C(=O)N2CC3=C(C2)C=C(CN4CCN(C)CC4)C=C3",3.322,1,2,4]
["S1164","Lenvatinib (E7080)","e6","L1700-02","in 10mM DMSO","c-Kit,c-RET,FGFR,PDGFR,VEGFR","Protein Tyrosine Kinase","Lenvatinib (E7080) is a multi-target inhibitor, mostly for VEGFR2(KDR)/VEGFR3(Flt-4) with IC50 of 4 nM/5.2 nM, less potent against VEGFR1/Flt-1, ~10-fold more selective for VEGFR2/3 against FGFR1, PDGFRα/β in cell-free assays. Lenvatinib (E7080) also inhibits FGFR1-4, PDGFR, Kit (c-Kit), RET (c-RET), and shows potent antitumor activities. Phase 3.",426.85,"417716-92-8",{"v":40,"d":"40.00"},93.71,"<1","N/A","http://selleckchem.com/products/E7080.html","C21H19ClN4O4","free base","N/A","COC1=C(C=C2C(=CC=NC2=C1)OC3=CC(=C(NC(=O)NC4CC4)C=C3)Cl)C(N)=O",2.832,5,3,6]
["S1165","ABT-751 (E7010)","f6","L1700-02","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","ABT-751 (E7010) binds to the colchicine site on β-tubulin and inhibits polymerization of microtubules, not a substrate for the MDR transporter and is active against cell lines resistant to vincristine, doxorubicin, and cisplatin. Phase 1/2.",371.41,"141430-65-1",{"v":74,"d":"74.00"},199.24,"<1","N/A","http://selleckchem.com/products/ABT-751.html","C18H17N3O4S","free base","N/A","COC1=CC=C(C=C1)[S](=O)(=O)NC2=C(NC3=CC=C(O)C=C3)N=CC=C2",2.997,4,3,6]
["S1167","CP-724714","g6","L1700-02","in 10mM DMSO","EGFR,HER2","Protein Tyrosine Kinase","CP-724714 is a potent, selective inhibitor of HER2/ErbB2 with IC50 of 10 nM, >640-fold selectivity against EGFR, InsR, IRG-1R, PDGFR, VEGFR2, Abl, Src, c-Met etc in cell-free assays. Phase 2.",469.53,"537705-08-1",{"v":94,"d":"94.00"},{"v":200.2,"d":"200.20"},"<1","N/A","http://selleckchem.com/products/CP-724714.html","C27H27N5O3","free base","N/A","COCC(=O)NC/C=C/C1=CC=C2N=CN=C(NC3=CC=C(OC4=CC=C(C)N=C4)C(=C3)C)C2=C1",3.987,6,2,9]
["S1168","Valproic Acid (NSC 93819) sodium salt","h6","L1700-02","in 10mM DMSO","Autophagy,GABA Receptor,HDAC,Mitophagy,Notch,PGC-1α","Neuronal Signaling","Valproic Acid sodium salt (NSC 93819, Sodium valproate) is a HDAC inhibitor by selectively inducing proteasomal degradation of HDAC2, used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches. Valproic acid induces Notch1 signaling in small cell lung cancer (SCLC) cells. Valproic acid is under investigation for treatment of HIV and various cancers. Valproic acid (VPA) induces autophagy and mitophagy by upregulation of BNIP3 and mitochondrial biogenesis by upregulating PGC-1α.",166.19,"1069-66-5",{"v":33,"d":"33.00"},198.57,{"v":33,"d":"33.00"},198.57,"http://selleckchem.com/products/Sodium-valproate.html","C8H15NaO2","Sodium salt","Sodium valproate,NSC 93819,2-Propylpentanoic Acid","CCCC(CCC)C(=O)O[Na]",1.275,0,0,5]
["S1169","TGX-221","a7","L1700-02","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","TGX-221 is a p110β-specific inhibitor with IC50 of 5 nM in a cell-free assay, 1000-fold more selective for p110β than p110α.",364.44,"663619-89-4",{"v":12,"d":"12.00"},32.93,"<1","N/A","http://selleckchem.com/products/TGX-221.html","C21H24N4O2","free base","N/A","CC(NC1=CC=CC=C1)C2=CC(=CN3C(=O)C=C(N=C23)N4CCOCC4)C",2.373,3,1,4]
["S1170","WZ3146","b7","L1700-02","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","WZ3146 is a mutant-selective irreversible inhibitor of EGFR(L858R) and EGFR(E746_A750) with IC50 of 2 nM and 2 nM; does not inhibit ERBB2 phosphorylation (T798I).",464.95,"1214265-56-1",{"v":93,"d":"93.00"},200.02,"<1","N/A","http://selleckchem.com/products/WZ3146.html","C24H25ClN6O2","free base","N/A","CN1CCN(CC1)C2=CC=C(NC3=NC=C(Cl)C(=N3)OC4=CC(=CC=C4)NC(=O)C=C)C=C2",4.823,4,2,7]
["S1171","CYC116","c7","L1700-02","in 10mM DMSO","Aurora Kinase,VEGFR","Cell Cycle","CYC116 is a potent inhibitor of Aurora A/B with Ki of 8.0 nM/9.2 nM, is less potent to VEGFR2 (Ki of 44 nM), with 50-fold greater potency than CDKs, not active against PKA, Akt/PKB, PKC, no effect on GSK-3α/β, CK2, Plk1 and SAPK2A. Phase 1.",368.46,"693228-63-6",{"v":24,"d":"24.00"},65.14,"<1","N/A","http://selleckchem.com/products/CYC116.html","C18H20N6OS","free base","N/A","CC1=C(SC(=N1)N)C2=NC(=NC=C2)NC3=CC=C(C=C3)N4CCOCC4",2.743,4,2,4]
["S1172","Serdemetan (JNJ-26854165)","d7","L1700-02","in 10mM DMSO","E3 Ligase ,p53","Apoptosis","Serdemetan (JNJ-26854165) acts as a HDM2 ubiquitin ligase antagonist and also induces early apoptosis in p53 wild-type cells, inhibits cellular proliferation followed by delayed apoptosis in the absence of functional p53. Phase 1.",328.41,"881202-45-5",{"v":66,"d":"66.00"},200.97,"<1","N/A","http://selleckchem.com/products/JNJ-26854165.html","C21H20N4","free base","N/A","C(CC1=C[NH]C2=CC=CC=C12)NC3=CC=C(NC4=CC=NC=C4)C=C3",4.236,1,3,6]
["S1173","WZ4002","e7","L1700-02","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","WZ4002 is a novel, mutant-selective EGFR inhibitor for EGFR(L858R)/(T790M) with IC50 of 2 nM/8 nM in BaF3 cell line; does not inhibit ERBB2 phosphorylation (T798I).",494.18,"1213269-23-8",{"v":13,"d":"13.00"},26.31,"<1","N/A","http://selleckchem.com/products/WZ4002.html","C25H27ClN6O3","free base","N/A","COC1=C(NC2=NC=C(Cl)C(=N2)OC3=CC(=CC=C3)NC(=O)C=C)C=CC(=C1)N4CCN(C)CC4",4.807,5,2,8]
["S1175","BIIB021","f7","L1700-02","in 10mM DMSO","HSP (HSP90)","Cytoskeletal Signaling","BIIB021 (CNF2024) is an orally available, fully synthetic small-molecule inhibitor of HSP90 with Ki and EC50 of 1.7 nM and 38 nM, respectively. Phase 2.",318.76,"848695-25-0",{"v":64,"d":"64.00"},200.78,"<1","N/A","http://selleckchem.com/products/BIIB021.html","C14H15ClN6O","free base","CNF2024","COC1=C(C)C=NC(=C1C)C[N]2C=NC3=C(Cl)N=C(N)N=C23",2.223,5,1,3]
["S1176","Plinabulin (NPI-2358)","g7","L1700-02","in 10mM DMSO","Microtubule Associated,VDA","Angiogenesis","Plinabulin (NPI-2358) is a vascular disrupting agent (VDA) against tubulin-depolymerizing with IC50 of 9.8~18 nM in tumor cells. Phase 1/2.",336.39,"714272-27-2",{"v":54,"d":"54.00"},160.53,"<1","N/A","http://selleckchem.com/products/NPI-2358.html","C19H20N4O2","free base","N/A","CC(C)(C)C1=C(/C=C/2NC(=O)C(/NC2=O)=C/C3=CC=CC=C3)N=C[NH]1",1.921,3,3,3]
["S1177","PD98059","h7","L1700-02","in 10mM DMSO","AhR,MEK","MAPK","PD98059 is a non-ATP competitive MEK inhibitor with IC50 of 2 μM in a cell-free assay, specifically inhibits MEK-1-mediated activation of MAPK; does not directly inhibit ERK1 or ERK2. PD98059 is a ligand for the aryl hydrocarbon receptor (AHR) and functions as an AHR antagonist.",267.28,"167869-21-8",{"v":14,"d":"14.00"},52.38,"<1","N/A","http://selleckchem.com/products/PD-98059.html","C16H13NO3","free base","N/A","COC1=C(N)C(=CC=C1)C2=CC(=O)C3=CC=CC=C3O2",2.373,3,1,2]
["S1178","Regorafenib (BAY 73-4506)","a8","L1700-02","in 10mM DMSO","Autophagy,c-Kit,c-RET,PDGFR,Raf,VEGFR","Protein Tyrosine Kinase","Regorafenib (BAY 73-4506,Fluoro-Sorafenib, Resihance, Stivarga) is a multi-target inhibitor for VEGFR1, VEGFR2, VEGFR3, PDGFRβ, Kit (c-Kit), RET (c-RET) and Raf-1 with IC50 of 13 nM/4.2 nM/46 nM, 22 nM, 7 nM, 1.5 nM and 2.5 nM in cell-free assays, respectively. Regorafenib induces autophagy.",482.82,"755037-03-7",{"v":97,"d":"97.00"},{"v":200.9,"d":"200.90"},"<1","N/A","http://selleckchem.com/products/BAY-73-4506.html","C21H15ClF4N4O3","free base","Fluoro-Sorafenib, Resihance, Stivarga,BAY 73-4506","CNC(=O)C1=CC(=CC=N1)OC2=CC(=C(NC(=O)NC3=CC=C(Cl)C(=C3)C(F)(F)F)C=C2)F",4.381,4,3,6]
["S1179","WZ8040","b8","L1700-02","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","WZ8040 is a novel mutant-selective irreversible EGFRT790M inhibitor, does not inhibit ERBB2 phosphorylation (T798I).",481.01,"1214265-57-2",{"v":96,"d":"96.00"},199.58,"<1","N/A","http://selleckchem.com/products/WZ8040.html","C24H25ClN6OS","free base","N/A","CN1CCN(CC1)C2=CC=C(NC3=NC=C(Cl)C(=N3)SC4=CC(=CC=C4)NC(=O)C=C)C=C2",5.381,3,2,7]
["S1180","XAV-939","c8","L1700-02","in 10mM DMSO","PARP,Wnt/beta-catenin","Stem Cells & Wnt","XAV-939 (NVP-XAV939) selectively inhibits Wnt/β-catenin-mediated transcription through tankyrase1/2 inhibition with IC50 of 11 nM/4 nM in cell-free assays, regulates axin levels and does not affect CRE, NF-κB or TGF-β.",312.31,"284028-89-3",{"v":12,"d":"12.00"},38.42,"<1","N/A","http://selleckchem.com/products/XAV-939.html","C14H11F3N2OS","free base","NVP-XAV939","OC1=C2CSCCC2=NC(=N1)C3=CC=C(C=C3)C(F)(F)F",3.676,2,1,2]
["S1181","ENMD-2076","d8","L1700-02","in 10mM DMSO","Apoptosis related,Aurora Kinase,CSF-1R,FGFR,FLT3,PDGFR,Src,VEGFR","Angiogenesis","ENMD-2076 has selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.86 nM, 25-fold selective for Aurora A than over Aurora B and less potent to RET, SRC, NTRK1/TRKA, CSF1R/FMS, VEGFR2/KDR, FGFR and PDGFRα. ENMD-2076 inhibits the growth of a wide range of human solid tumor and hematopoietic cancer cell lines with IC50 from 0.025 to 0.7 μM, which induces apoptosis and G2/M phase arrest. Phase 2.",375.47,"934353-76-1",{"v":105,"d":"105.00"},279.65,{"v":1,"d":"1.00"},2.66,"http://selleckchem.com/products/enmd-2076.html","C21H25N7","Tartaric Acid","N/A","CN1CCN(CC1)C2=CC(=NC(=N2)\\C=C\\C3=CC=CC=C3)NC4=N[NH]C(=C4)C",4.015,3,2,5]
["S1183","Danoprevir (ITMN-191)","e8","L1700-02","in 10mM DMSO","COVID-19,HCV Protease","Proteases","Danoprevir (ITMN-191, RG7227) is a peptidomimetic inhibitor of the NS3/4A protease of hepatitis C virus (HCV) with IC50 of 0.2-3.5 nM, inhibition effect for HCV genotypes 1A/1B/4/5/6 is ~10-fold higher than 2B/3A. Phase 2.",731.83,"850876-88-9",{"v":144,"d":"144.00"},196.77,"<1","N/A","http://selleckchem.com/products/Danoprevir.html","C35H46FN5O9S","free base","RG7227","CC(C)(C)OC(=O)NC1CCCCC\\C=C/C2CC2(NC(=O)C3CC(CN3C1=O)OC(=O)N4CC5=C(C4)C(=CC=C5)F)C(=O)N[S](=O)(=O)C6CC6",2.922,9,3,8]
["S1185","Ritonavir (ABT-538)","f8","L1700-02","in 10mM DMSO","Apoptosis related,COVID-19,HIV Protease,P450 (e.g. CYP17)","Proteases","Ritonavir (ABT-538, A 84538, RTV, Norvir, Norvir Softgel) is a Cytochrome P450 3A and Protease Inhibitor; Also inhibits Cytochrome P450 2D6, P-Glycoprotein and induces Cytochrome P450 2C19, Cytochrome P450 1A2, Cytochrome P450 2C9, Cytochrome P450 2B6 and UDP Glucuronosyltransferases. Ritonavir induces apoptosis.",720.94,"155213-67-5",{"v":100,"d":"100.00"},138.71,"<1","N/A","http://selleckchem.com/products/Ritonavir.html","C37H48N6O5S2","free base","ABT-538,A 84538, RTV, Norvir, Norvir Softgel","CC(C)C(NC(=O)N(C)CC1=CSC(=N1)C(C)C)C(=O)NC(CC(O)C(CC2=CC=CC=C2)NC(=O)OCC3=CN=CS3)CC4=CC=CC=C4",4.978,6,4,18]
["S1186","BIBR 1532","g8","L1700-02","in 10mM DMSO","Apoptosis related,Telomerase","DNA Damage/DNA Repair","BIBR 1532 is a potent, selective, non-competitive telomerase inhibitor with IC50 of 100 nM in a cell-free assay. No inhibition of DNA and RNA polymerases, including HIV reverse transcriptase are observed at concentrations vastly exceeding the IC50 for telomerase. BIBR 1532 induces apoptosis in cancer cells.",331.36,"321674-73-1",{"v":66,"d":"66.00"},199.18,"<1","N/A","http://selleckchem.com/products/BIBR1532.html","C21H17NO3","free base","N/A","CC(=C\\C(=O)NC1=C(C=CC=C1)C(O)=O)/C2=CC3=CC=CC=C3C=C2",4.067,2,1,4]
["S1188","Anastrozole (ZD-1033)","h8","L1700-02","in 10mM DMSO","Aromatase","Endocrinology & Hormones","Anastrozole (Arimidex,ZD-1033) is a third-generation nonsteroidal selective aromatase inhibitor. It may offer greater selectivity compared with other aromatase inhibitors, being without any intrinsic endocrine effects and with no apparent effect on the synthesis of adrenal steroids.",293.37,"120511-73-1",{"v":59,"d":"59.00"},201.11,"<1","N/A","http://selleckchem.com/products/Anastrozole.html","C17H19N5","free base","Arimidex,ZD-1033","CC(C)(C#N)C1=CC(=CC(=C1)C[N]2C=NC=N2)C(C)(C)C#N",2.965,2,0,4]
["S1189","Aprepitant (MK-0869)","a9","L1700-02","in 10mM DMSO","CSF-1R,HIV,Interleukins,Neurokinin Receptor,TNF-alpha","Neuronal Signaling","Aprepitant (MK-0869, L-754030, Emend) is a potent and selective neurokinin-1 receptor antagonist with IC50 of 0.1 nM. Aprepitant reduces levels of pro-inflammatory cytokines including G-CSF, IL-6, IL-8 and TNFα. Aprepitant inhibits HIV infection of human macrophages.",534.43,"170729-80-3",{"v":107,"d":"107.00"},200.21,"<1","N/A","http://selleckchem.com/products/Aprepitant.html","C23H21F7N4O3","free base","MK-0869, L-754030, Emend","CC(OC1OCCN(CC2=NNC(=O)N2)C1C3=CC=C(F)C=C3)C4=CC(=CC(=C4)C(F)(F)F)C(F)(F)F",4.635,4,2,8]
["S1190","Bicalutamide (ICI-176334)","b9","L1700-02","in 10mM DMSO","Androgen Receptor,Autophagy","Endocrinology & Hormones","Bicalutamide (ICI-176334) is an androgen receptor (AR) antagonist with IC50 of 0.16 μM in LNCaP/AR(cs)cell line. Bicalutamide promotes autophagy.",430.37,"90357-06-5",{"v":86,"d":"86.00"},199.83,"<1","N/A","http://selleckchem.com/products/Bicalutamide(Casodex).html","C18H14F4N2O4S","free base","ICI-176334","CC(O)(C[S](=O)(=O)C1=CC=C(F)C=C1)C(=O)NC2=CC=C(C#N)C(=C2)C(F)(F)F",2.926,3,1,6]
["S1191","Fulvestrant (ICI-182780)","c9","L1700-02","in 10mM DMSO","Apoptosis related,Autophagy,Estrogen/progestogen Receptor","Endocrinology & Hormones","Fulvestrant (ICI-182780, ZD 9238, ZM 182780) is an estrogen receptor (ER) antagonist with IC50 of 0.94 nM in a cell-free assay. Fulvestrant also induces autophagy and apoptosis and has antitumor activity.",606.77,"129453-61-8",{"v":100,"d":"100.00"},164.81,"<1","N/A","http://selleckchem.com/products/Fulvestrant.html","C32H47F5O3S","free base","ICI-182780, ZD 9238, ZM 182780","CC12CCC3C(C(CCCCCCCCC[S](=O)CCCC(F)(F)C(F)(F)F)CC4=C3C=CC(=C4)O)C1CCC2O",8.437,1,2,15]
["S1192","Raltitrexed","d9","L1700-02","in 10mM DMSO","DNA/RNA Synthesis,Thymidylate Synthase","DNA Damage/DNA Repair","Raltitrexed (ZD-1694) is a thymidylate synthase inhibitor with an IC50 of 9 nM for the inhibition of L1210 cell growth.",458.49,"112887-68-0",{"v":91,"d":"91.00"},198.48,"<1","N/A","http://selleckchem.com/products/Raltitrexed.html","C21H22N4O6S","free base","ZD-1694, ICI-D1694, D1694","CN(CC1=CC2=C(C=C1)N=C(C)NC2=O)C3=CC=C(S3)C(=O)NC(CCC(O)=O)C(O)=O",1.528,5,2,9]
["S1193","Thalidomide (K17)","e9","L1700-02","in 10mM DMSO","E3 Ligase ,E3 ligase Ligand,TNF-alpha","Ubiquitin","Thalidomide (K17) was introduced as a sedative drug, immunomodulatory agent and also is investigated for treating symptoms of many cancers. Thalidomide inhibits cereblon (CRBN), a part of the cullin-4 E3 ubiquitin ligase complex CUL4-RBX1-DDB1.",258.23,"50-35-1",{"v":51,"d":"51.00"},{"v":197.5,"d":"197.50"},"<1","N/A","http://selleckchem.com/products/Thalidomide.html","C13H10N2O4","free base","K17","O=C1CCC(N2C(=O)C3=C(C=CC=C3)C2=O)C(=O)N1",0.097,4,1,1]
["S1194","CUDC-101","f9","L1700-02","in 10mM DMSO","EGFR,HDAC,HER2","Epigenetics","CUDC-101 is a potent multi-targeted inhibitor against HDAC, EGFR and HER2 with IC50 of 4.4 nM, 2.4 nM, and 15.7 nM, and inhibits class I/II HDACs, but not class III, Sir-type HDACs. Phase 1.",434.49,"1012054-59-9",{"v":20,"d":"20.00"},46.03,"<1","N/A","http://selleckchem.com/products/CUDC-101.html","C24H26N4O4","free base","N/A","COC1=CC2=C(C=C1OCCCCCCC(=O)NO)C(=NC=N2)NC3=CC(=CC=C3)C#C",5.376,5,2,11]
["S1195","Orteronel","g9","L1700-02","in 10mM DMSO","Androgen Receptor,P450 (e.g. CYP17)","Metabolism","Orteronel(TAK-700) is a potent and highly selective human 17,20-lyase inhibitor with IC50 of 38 nM, exhibits >1000-fold selectivity over other CYPs (e.g. 11-hydroxylase and CYP3A4). TAK-700 (Orteronel) is an androgen biosynthesis inhibitor. Phase 3.",307.35,"426219-18-3",{"v":61,"d":"61.00"},198.47,"<1","N/A","http://selleckchem.com/products/TAK-700.html","C18H17N3O2","free base","TAK-700","CNC(=O)C1=CC=C2C=C(C=CC2=C1)C3(O)CC[N]4C=NC=C34",1.075,2,1,2]
["S1196","Exemestane (FCE 24304)","h9","L1700-02","in 10mM DMSO","Aromatase","Endocrinology & Hormones","Exemestane (Aromasin,FCE24304, PNU155971,EXE) is an aromatase inhibitor, inhibits human placental and rat ovarian aromatase with IC50 of 30 nM and 40 nM, respectively.",{"v":296.4,"d":"296.40"},"107868-30-4",{"v":54,"d":"54.00"},182.19,"<1","N/A","http://selleckchem.com/products/Exemestane.html","C20H24O2","free base","Aromasin,FCE24304, PNU155971,EXE","CC12CCC3C(CC(=C)C4=CC(=O)C=CC34C)C1CCC2=O",3.606,2,0,0]
["S1197","Finasteride","a10","L1700-02","in 10mM DMSO","5-alpha Reductase","Endocrinology & Hormones","Finasteride (MK-906) is a potent, reversible inhibitor of the rat type 1 5 alpha-reductase with Ki of 10.2 nM, used in the treatment of benign prostatic hyperplasia (BPH) and male pattern baldness (MPB).",372.54,"98319-26-7",{"v":75,"d":"75.00"},201.32,"<1","N/A","http://selleckchem.com/products/Finasteride.html","C23H36N2O2","free base","MK-906","CC(C)(C)NC(=O)C1CCC2C3CCC4NC(=O)C=CC4(C)C3CCC12C",3.174,2,2,2]
["S1199","Cladribine (RWJ 26251)","b10","L1700-02","in 10mM DMSO","Adenosine Deaminase,DNA/RNA Synthesis","Neuronal Signaling","Cladribine (RWJ 26251, Leustatin, 2-CdA, 2-chlorodeoxyadenosine, 2-Chloro-2′-deoxyadenosine, CldAdo, Jk 6251, NSC 105014) is an adenosine deaminase inhibitor for U266, RPMI8226, and MM1.S cells with IC50 of approximately 2.43 μM, 0.75 μM, and 0.18 μM, respectively.",285.69,"4291-63-8",{"v":57,"d":"57.00"},199.52,"<1","N/A","http://selleckchem.com/products/Cladribine.html","C10H12ClN5O3","free base","Leustatin,2-CdA,2-Chloro-2′-deoxyadenosine,CldAdo,Jk 6251,NSC 105014,RWJ 26251","NC1=NC(=NC2=C1N=C[N]2C3CC(O)C(CO)O3)Cl",-0.259,4,3,2]
["S1200","Decitabine (NSC 127716)","c10","L1700-02","in 10mM DMSO","Apoptosis related,DNA Methyltransferase,Nucleoside Analog/Antimetabolite","Epigenetics","Decitabine (Deoxycytidine, Dacogen, 5-aza-2'-deoxycytidine, 5-AZA-dC, 5-aza-CdR,NSC 127716) is a DNA methyltransferase inhibitor, incorporating into DNA and resulting in hypomethylation of DNA and intra-S-phase arrest of DNA replication. It is used to treat myelodysplastic syndrome (MDS). Decitabine induces cell cycle arrest and apoptosis in various cancer cell lines.",228.21,"2353-33-5",{"v":45,"d":"45.00"},197.19,{"v":10,"d":"10.00"},43.82,"http://selleckchem.com/products/Decitabine.html","C8H12N4O4","free base","Deoxycytidine, Dacogen, 5-aza-2'-deoxycytidine, 5-AZA-dC, 5-aza-CdR,NSC 127716","NC1=NC(=O)N(C=N1)C2CC(O)C(CO)O2",-1.093,4,3,2]
["S1201","Dimesna","d10","L1700-02","in 10mM DMSO","Others","Others","Dimesna (BNP-7787) is an uroprotective agent used to decrease urotoxicity.",326.34,"16208-51-8",{"v":65,"d":"65.00"},199.18,{"v":65,"d":"65.00"},199.18,"http://selleckchem.com/products/Dimesna.html","C4H8Na2O6S4","Disodium salt","BNP-7787","[Na+].[Na+].[O-][S](=O)(=O)CCSSCC[S]([O-])(=O)=O",-4.295,0,0,7]
["S1202","Dutasteride","e10","L1700-02","in 10mM DMSO","5-alpha Reductase","Endocrinology & Hormones","Dutasteride (GI198745, GG-745) is a dual 5-α reductase inhibitor that inhibits conversion of testosterone to dihydrotestosterone (DHT).",528.53,"164656-23-9",{"v":62,"d":"62.00"},117.31,"<1","N/A","http://selleckchem.com/products/Dutasteride.html","C27H30F6N2O2","free base","GI198745, GG-745","CC12CCC3C(CCC4NC(=O)C=CC34C)C1CCC2C(=O)NC5=CC(=CC=C5C(F)(F)F)C(F)(F)F",5.703,2,2,4]
["S1204","Melatonin (NSC 113928)","f10","L1700-02","in 10mM DMSO","Apoptosis related,ATF/CREB & c-Fos/c-Jun,Autophagy,COX,Mitophagy,MT Receptor","GPCR & G Protein","Melatonin (NSC 113928, NSC 56423, N-Acetyl-5-methoxytryptamine,MT) is a MT receptor agonist, used as a dietary supplement. Melatonin is a selective ATF-6 inhibitor and downregulates COX-2. Melatonin enhances mitophagy and regulates the homeostasis of apoptosis and autophagy.",232.28,"73-31-4",{"v":47,"d":"47.00"},202.34,"<1","N/A","http://selleckchem.com/products/Melatonin.html","C13H16N2O2","free base","NSC 56423, N-Acetyl-5-methoxytryptamine,NSC 113928,MT","COC1=CC2=C([NH]C=C2CCNC(C)=O)C=C1",1.555,2,2,4]
["S1206","Bisoprolol fumarate","g10","L1700-02","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Bisoprolol fumarate (EMD33512) is a selective type β1 adrenergic receptor blocker.",441.52,"104344-23-2",{"v":88,"d":"88.00"},199.31,{"v":88,"d":"88.00"},199.31,"http://selleckchem.com/products/Bisoprolol-Fumarate.html","C22H35NO8","fumarate","EMD33512","CC(C)NCC(O)COC1=CC=C(COCCOC(C)C)C=C1.OC(=O)\\C=C\\C(O)=O",-0.635,5,2,14]
["S1207","Tivozanib (AV-951)","h10","L1700-02","in 10mM DMSO","c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Tivozanib (AV-951, KRN-951) is a potent and selective VEGFR inhibitor for VEGFR1/2/3 with IC50 of 30 nM/6.5 nM/15 nM, and also inhibits PDGFR and c-Kit, low activity observed against FGFR-1, Flt3, c-Met, EGFR and IGF-1R. Phase 3.",454.86,"475108-18-0",{"v":20,"d":"20.00"},43.97,"<1","N/A","http://selleckchem.com/products/AV-951.html","C22H19ClN4O5","free base","KRN-951","COC1=CC2=C(C=C1OC)C(=CC=N2)OC3=CC=C(NC(=O)NC4=NOC(=C4)C)C(=C3)Cl",4.039,7,2,6]
["S1208","Doxorubicin (Adriamycin) HCl","a11","L1700-02","in 10mM DMSO","ADC Cytotoxin,AMPK,Antibiotics,Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,HIV,Mitophagy,Topoisomerase","DNA Damage/DNA Repair","Doxorubicin (Adriamycin, NSC 123127, DOX, Hydroxydaunorubicin) HCl is an antibiotic agent that inhibits DNA topoisomerase II and induces DNA damage, mitophagy and apoptosis in tumor cells. Doxorubicin reduces basal phosphorylation of AMPK. Doxorubicin is used in the concomitant treatment of HIV-infected patients but is found to be at high risk of HBV reactivation.",579.98,"25316-40-9",{"v":100,"d":"100.00"},172.42,{"v":20,"d":"20.00"},34.48,"http://selleckchem.com/products/Adriamycin.html","C27H29NO11.HCl","Hydrochloride","NSC 123127, DOX, Doxorubicin hydrochloride, Hydroxydaunorubicin HCl,Adriamycin HCl","Cl.COC1=C2C(=O)C3=C(C(=C4CC(O)(CC(OC5CC(N)C(O)C(C)O5)C4=C3O)C(=O)CO)O)C(=O)C2=CC=C1",0.338,6,5,5]
["S1209","Fluorouracil (5-Fluorouracil, 5-FU)","b11","L1700-02","in 10mM DMSO","Apoptosis related,DNA/RNA Synthesis,HIV,Nucleoside Analog/Antimetabolite,Thymidylate Synthase","DNA Damage/DNA Repair","Fluorouracil (5-Fluorouracil, 5-FU, NSC 19893) is a DNA/RNA synthesis inhibitor, which interrupts nucleotide synthetic by inhibiting thymidylate synthase (TS) in tumor cells. Fluorouracil induces apoptosis and can be used in the treatment of HIV.",130.08,"51-21-8",{"v":26,"d":"26.00"},199.88,"<1","N/A","http://selleckchem.com/products/Adrucil(Fluorouracil).html","C4H3FN2O2","free base","NSC 19893,5-Fluorouracil, 5-FU","FC1=CNC(=O)NC1=O",-1.102,2,2,0]
["S1210","Methotrexate (CL-14377)","c11","L1700-02","in 10mM DMSO","ADC Cytotoxin,DHFR","Metabolism","Methotrexate (CL14377, MTX, NCI-C04671, Amethopterin, WR19039, abitrexate), analog of folic acid, is a nonspecific inhibitor of the dihydrofolate reductase(DHFR) of bacteria and cancerous cells as well as normal cells. It forms an inactive ternary complex with DHFR and NADPH. Methotrexate (MTX) induces apoptosis.",454.44,"59-05-2",{"v":90,"d":"90.00"},198.05,"<1","N/A","http://selleckchem.com/products/Abitrexate.html","C20H22N8O5","free base","NCI-C04671, Amethopterin, CL14377, WR19039, abitrexate","CN(CC1=NC2=C(N)N=C(N)N=C2N=C1)C3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O",0.114,7,3,9]
["S1212","Bendamustine (SDX105) HCl","d11","L1700-02","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Bendamustine (SDX-105, Cytostasane) HCl is a DNA-damaging agent with IC50 of 50 μM in cell-free assay.",394.72,"3543-75-7",{"v":78,"d":"78.00"},197.61,{"v":2,"d":"2.00"},5.07,"http://selleckchem.com/products/Bendamustine-Hydrochloride.html","C16H21Cl2N3O2.HCl","Hydrochloride","Cytostasane HCl","Cl.C[N]1C(=NC2=CC(=CC=C12)N(CCCl)CCCl)CCCC(O)=O",3.988,2,0,9]
["S1213","Nelarabine","e11","L1700-02","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Nelarabine (506U78,Arranon) is a purine nucleoside analog and DNA synthesis inhibitor with IC50 from 0.067-2.15 μM in tumor cells.",297.27,"121032-29-9",{"v":60,"d":"60.00"},201.84,{"v":3,"d":"3.00"},10.09,"http://selleckchem.com/products/Arranon.html","C11H15N5O5","free base","506U78,Arranon","COC1=NC(=NC2=C1N=C[N]2C3OC(CO)C(O)C3O)N",-1.376,5,4,3]
["S1214","Bleomycin (NSC125066) sulfate","f11","L1700-02","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,DNA/RNA Synthesis,Selection Antibiotics for Transfected Cell","DNA Damage/DNA Repair","Bleomycin Sulfate (Blenoxane,NSC125066) is a glycopeptide antibiotic and an anticancer agent for squamous cell carcinomas (SCC) with IC50 of 4 nM in UT-SCC-19A cells.",1512.62,"9041-93-4",{"v":100,"d":"100.00"},{"v":66,"d":"66.00"},"N/A","N/A","http://www.selleckchem.com/products/Bleomycin-sulfate.html","C55H85N17O25S4","Sulfate","Blenoxane,NSC125066","CC(O)C(NC(=O)C(C)C(O)C(C)NC(=O)C(NC(=O)C1=C(C)C(=NC(=N1)C(CC(N)=O)NCC(N)C(N)=O)N)C(OC2OC(CO)C(O)C(O)C2OC3OC(CO)C(O)C(OC(N)=O)C3O)C4=C[NH]C=N4)C(=O)NCCC5=NC(=CS5)C6=NC(=CS6)C(=O)NCCC[S+](C)C.O[S]([O-])(=O)=O","N/A","N/A","N/A","N/A"]
["S1216","PFI-1 (PF-6405761)","g11","L1700-02","in 10mM DMSO","Epigenetic Reader Domain","Epigenetics","PFI-1 (PF-6405761) is a highly selective BET (bromodomain-containing protein) inhibitor for BRD4 with IC50 of 0.22 μM and for BRD2 with IC50 of 98 nM in a cell-free assay.",347.39,"1403764-72-6",{"v":69,"d":"69.00"},198.62,"<1","N/A","http://selleckchem.com/products/pfl-1.html","C16H17N3O4S","free base","N/A","COC1=C(C=CC=C1)[S](=O)(=O)NC2=CC=C3NC(=O)N(C)CC3=C2",1.376,4,2,4]
["S1218","Clofarabine","h11","L1700-02","in 10mM DMSO","Apoptosis related,Autophagy,DNA/RNA Synthesis,RNR","DNA Damage/DNA Repair","Clofarabine (Clolar) inhibits the enzymatic activities of ribonucleotide reductase (RNR) (IC50 = 65 nM) and DNA polymerase. Clofarabine induces autophagy and apoptosis.",303.68,"123318-82-1",{"v":60,"d":"60.00"},197.58,"<1","N/A","http://selleckchem.com/products/Clofarabine.html","C10H11ClFN5O3","free base","Clolar","NC1=C2N=C[N](C3OC(CO)C(O)C3F)C2=NC(=N1)Cl",-0.085,4,3,2]
["S1219","YM201636","a2","L1700-03","in 10mM DMSO","Autophagy,PI3K,PIKfyve","PI3K/Akt/mTOR","YM201636 is a selective PIKfyve inhibitor with IC50 of 33 nM, less potent to p110α and insensitive to Fabl (yeast orthologue). YM-201636 suppresses the growth of liver cancer via the induction of autophagy.",467.48,"371942-69-7",{"v":35,"d":"35.00"},74.87,"<1","N/A","http://selleckchem.com/products/ym201636.html","C25H21N7O3","free base","N/A","NC1=CC=C(C=N1)C(=O)NC2=CC=CC(=C2)C3=NC(=C4OC5=NC=CC=C5C4=N3)N6CCOCC6",2.467,7,2,4]
["S1220","OSI-930","b2","L1700-03","in 10mM DMSO","c-Kit,CSF-1R,VEGFR","Protein Tyrosine Kinase","OSI-930 is a potent inhibitor of Kit (c-Kit), KDR and CSF-1R with IC50 of 80 nM, 9 nM and 15 nM, respectively; also potent to Flt-1, c-Raf and Lck and low activity against PDGFRα/β, Flt-3 and Abl. Phase 1.",443.44,"728033-96-3",{"v":89,"d":"89.00"},{"v":200.7,"d":"200.70"},"<1","N/A","http://selleckchem.com/products/OSI-930.html","C22H16F3N3O2S","free base","N/A","FC(F)(F)OC1=CC=C(NC(=O)C2=C(NCC3=CC=NC4=CC=CC=C34)C=CS2)C=C1",6.266,3,2,7]
["S1221","Dacarbazine (NSC-45388)","c2","L1700-03","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,DNA/RNA Synthesis","DNA Damage/DNA Repair","Dacarbazine (NSC-45388, DTIC-Dome, Imidazole Carboxamide) is a triazene derivative with antineoplastic activity. Dacarbazine alkylates and cross-links DNA during all phases of the cell cycle, resulting in disruption of DNA function, cell cycle arrest, and apoptosis; used in the treatment of various cancers.",182.18,"4342-03-4",{"v":12,"d":"12.00"},65.87,{"v":2,"d":"2.00"},10.98,"http://selleckchem.com/products/Dacarbazine.html","C6H10N6O","free base","DTIC-Dome, Imidazole Carboxamide,NSC-45388","CN(C)N=NC1=C(N=C[NH]1)C(N)=O",-0.344,4,2,3]
["S1222","Dexrazoxane HCl (ICRF-187)","d2","L1700-03","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Dexrazoxane HCl (ADR-529,Totect, ICRF-187, Zinecard, Cardioxane) is an intracellular iron chelator, which decreases the formation of superoxide radicals, used as a cardioprotective agent; also an inhibitor of topoisomerase II",304.73,"149003-01-0",{"v":60,"d":"60.00"},{"v":196.9,"d":"196.90"},{"v":60,"d":"60.00"},{"v":196.9,"d":"196.90"},"http://selleckchem.com/products/Dexrazoxane-Hydrochloride.html","C11H16N4O4.HCl","Hydrochloride","ADR-529,Totect, ICRF-187, Zinecard, Cardioxane","Cl.CC(CN1CC(=O)NC(=O)C1)N2CC(=O)NC(=O)C2",-1.722,4,2,3]
["S1223","Epirubicin (IMI 28) HCl","e2","L1700-03","in 10mM DMSO","Apoptosis related,Topoisomerase","DNA Damage/DNA Repair","Epirubicin HCl (Ellence, Pharmorubicin, Epirubicin Ebewe,IMI 28, NSC 256942, 4'-epidoxorubicin,Epirubicin hydrochloride), a semisynthetic L-arabino derivative of doxorubicin, is an antineoplastic agent by inhibiting Topoisomerase. Epirubicin induces apoptosis.",579.98,"56390-09-1",{"v":100,"d":"100.00"},172.42,{"v":100,"d":"100.00"},172.42,"http://selleckchem.com/products/Ellence.html","C27H29NO11.HCl","Hydrochloride","Ellence, Pharmorubicin, Epirubicin Ebewe,IMI 28, NSC 256942, 4'-epidoxorubicin,Epirubicin hydrochloride","Cl.COC1=C2C(=O)C3=C(C(=C4CC(O)(CC(OC5CC(N)C(O)C(C)O5)C4=C3O)C(=O)CO)O)C(=O)C2=CC=C1",0.338,6,5,5]
["S1225","Etoposide (VP-16)","f2","L1700-03","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,Autophagy,Mitophagy,Topoisomerase","DNA Damage/DNA Repair","Etoposide (VP-16213,Vepesid,VP-16) is a semisynthetic derivative of podophyllotoxin, which inhibits DNA synthesis via topoisomerase II  inhibition activity. Etoposide induces autophagy, mitophagy and apoptosis.",588.56,"33419-42-0",{"v":100,"d":"100.00"},169.91,"<1","N/A","http://selleckchem.com/products/Etopophos.html","C29H32O13","free base","VP-16213,Vepesid,VP-16","COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(OC4OC5COC(C)OC5C(O)C4O)C6=C2C=C7OCOC7=C6",0.935,10,3,5]
["S1226","KU-0063794","g2","L1700-03","in 10mM DMSO","mTOR","PI3K/Akt/mTOR","KU-0063794 is a potent and highly specific dual-mTOR inhibitor of mTORC1 and mTORC2 with IC50 of ~10 nM in cell-free assays; no effect on PI3Ks.",465.54,"938440-64-3",{"v":16,"d":"16.00"},34.37,"<1","N/A","http://selleckchem.com/products/KU-0063794.html","C25H31N5O4","free base","N/A","COC1=C(CO)C=C(C=C1)C2=NC3=NC(=NC(=C3C=C2)N4CCOCC4)N5CC(C)OC(C)C5",3.274,6,1,5]
["S1227","Raloxifene HCl","h2","L1700-03","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Raloxifene (LY156758, Keoxifene) HCl is a selective and orally active estrogen receptor modulator (SERM), which inhibits human cytosolic aldehyde oxidase-catalyzed phthalazine oxidation activity with IC50 of 5.7 nM.",510.04,"82640-04-8",{"v":100,"d":"100.00"},196.06,"<1","N/A","http://selleckchem.com/products/Evista.html","C28H27NO4S.HCl","Hydrochloride","LY156758 (Keoxifene) HCl","Cl.OC1=CC=C(C=C1)C2=C(C(=O)C3=CC=C(OCCN4CCCCC4)C=C3)C5=C(S2)C=C(O)C=C5",6.843,2,2,7]
["S1229","Fludarabine Phosphate","a3","L1700-03","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Fludarabine Phosphate (F-ara-A, NSC 312887) is an analogue of adenosine and deoxyadenosine, which is able to compete with dATP for incorporation into DNA and inhibit DNA synthesis.",365.21,"75607-67-9",{"v":73,"d":"73.00"},199.88,{"v":2,"d":"2.00"},5.48,"http://selleckchem.com/products/Fludara.html","C10H13FN5O7P","Phosphate","F-ara-A (NSC 312887) Phosphate","NC1=NC(=NC2=C1N=C[N]2C3OC(CO[P](O)(O)=O)C(O)C3O)F",-1.384,5,3,4]
["S1230","Flavopiridol (L86-8275)","b3","L1700-03","in 10mM DMSO","Autophagy,CDK,HIV","Cell Cycle","Flavopiridol (L86-8275, Alvocidib, NSC 649890, HMR-1275) competes with ATP to inhibit CDKs including CDK1, CDK2, CDK4, CDK6, and CDK9 with IC50 values in the 20-100 nM range. It is more selective for CDK1, 2, 4, 6, 9 versus CDK7. Flavopiridol is initially found to inhibit EGFR and PKA. Flavopiridol induces autophagy and ER stress. Flavopiridol blocks HIV-1 replication. Phase 1/2.",401.84,"146426-40-6",{"v":15,"d":"15.00"},37.33,"<1","N/A","http://selleckchem.com/products/Flavopiridol.html","C21H20ClNO5","Free Base","NSC 649890 HCl, HMR-1275, Alvocidib","CN1CCC(C(O)C1)C2=C3OC(=CC(=O)C3=C(O)C=C2O)C4=C(Cl)C=CC=C4",3.108,2,3,2]
["S1231","Topotecan (NSC609699) HCl","c3","L1700-03","in 10mM DMSO","Apoptosis related,Autophagy,Topoisomerase","DNA Damage/DNA Repair","Topotecan HCl (Nogitecan HCl, SKFS 104864A,Hycamtin, NSC 609699) is a topoisomerase I inhibitor for MCF-7 Luc cells and DU-145 Luc cells with IC50 of 13 nM and 2 nM in cell-free assays, respectively. Topotecan HCl induces autophagy and apoptosis.",457.91,"119413-54-6",{"v":91,"d":"91.00"},198.73,{"v":91,"d":"91.00"},198.73,"http://selleckchem.com/products/Topotecan-Hydrochloride.html","C23H23N3O5.HCl","Hydrochloride","Nogitecan HCl, SKFS 104864A,Hycamtin, NSC 609699","Cl.CCC1(O)C(=O)OCC2=C1C=C3N(CC4=C3N=C5C=CC(=C(CN(C)C)C5=C4)O)C2=O",1.959,4,1,3]
["S1233","2-Methoxyestradiol (2-MeOE2)","d3","L1700-03","in 10mM DMSO","Apoptosis related,Autophagy,HIF,Microtubule Associated","Angiogenesis","2-Methoxyestradiol (2-MeOE2, NSC 659853, 2-ME2) depolymerizes microtubules and blocks HIF-1α nuclear accumulation and HIF-transcriptional activity. 2-Methoxyestradiol induces both autophagy and apoptosis in various carcinogenic cell lines.",302.41,"362-07-2",{"v":60,"d":"60.00"},198.41,"<1","N/A","http://selleckchem.com/products/2-Methoxyestradiol(2ME2).html","C19H26O3","free base","NSC 659853, 2-ME2","COC1=C(O)C=C2CCC3C(CCC4(C)C(O)CCC34)C2=C1",3.821,1,2,1]
["S1234","AG-1024","e3","L1700-03","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","AG-1024 (Tyrphostin, AGS 200) inhibits IGF-1R autophosphorylation with IC50 of 7 μM, is less potent to IR with IC50 of 57 μM and specifically distinguishes between InsR and IGF-1R (as compared to other tyrphostins).",305.17,"65678-07-1",{"v":61,"d":"61.00"},199.89,"<1","N/A","http://selleckchem.com/products/ag-1024-tyrphostin.html","C14H13BrN2O","free base","Tyrphostin, AGS 200","CC(C)(C)C1=C(O)C(=CC(=C1)C=C(C#N)C#N)Br",3.922,0,1,2]
["S1235","Letrozole (CGS 20267)","f3","L1700-03","in 10mM DMSO","Aromatase,Autophagy","Endocrinology & Hormones","Letrozole (CGS 20267,Femara, Piroxicam) is a third generation inhibitor of aromatase with IC50 of 0.07-20 nM in cell-free assays.It has no effect on the plasma levels of 17α-OH progesterone, thyroid-stimulating hormone (TSH), luteinizing hormone (LH), follicle-stimulating hormone (FSH), or androstenedione and does not affect normal urine electrolyte excretion or thyroid function in clinical studies. Letrozole induces autophagy.",{"v":285.3,"d":"285.30"},"112809-51-5",{"v":57,"d":"57.00"},199.79,"<1","N/A","http://selleckchem.com/products/Letrozole.html","C17H11N5","free base","CGS 20267,Femara, Piroxicam","N#CC1=CC=C(C=C1)C([N]2C=NC=N2)C3=CC=C(C=C3)C#N",2.749,2,0,3]
["S1237","Temozolomide (CCRG 81045)","g3","L1700-03","in 10mM DMSO","Apoptosis related,Autophagy,DNA/RNA Synthesis","DNA Damage/DNA Repair","Temozolomide (NSC 362856,TMZ,CCRG 81045,Methazolastone,Temodar,Temodal) is a monofunctional SN-1 alkylating agent that can modify nitrogen atoms in the DNA ring and the extracyclic oxygen group, chemically converted to MTIC and degrades to methyldiazonium cation, which transfers methyl groups to DNA at physiologic pH. A DNA damage inducer in L-1210 and L-1210/BCNU cells. Temozolomide induces apoptosis and exhibits antitumor activity.",194.15,"85622-93-1",{"v":38,"d":"38.00"},195.72,"<1","N/A","http://selleckchem.com/products/Methazolastone.html","C6H6N6O2","free base","NSC 362856,TMZ,CCRG 81045,Methazolastone,Temodar,Temodal","CN1N=NC2=C(N=C[N]2C1=O)C(N)=O",0.052,5,1,1]
["S1238","Tamoxifen (ICI 46474)","h3","L1700-03","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,ATPase,Autophagy,Estrogen/progestogen Receptor,HSP (HSP90)","Angiogenesis","Tamoxifen (ICI 46474, (Z)-Tamoxifen, trans-Tamoxifen) is a selective estrogen receptor modulator (SERM). Tamoxifen enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen induces apoptosis.",371.51,"10540-29-1",{"v":74,"d":"74.00"},199.19,"<1","N/A","http://selleckchem.com/products/Nolvadex.html","C26H29NO","Free Base","ICI 46474, (Z)-Tamoxifen, trans-Tamoxifen","CC/C(C1=CC=CC=C1)=C(C2=CC=CC=C2)/C3=CC=C(OCCN(C)C)C=C3.OC(=O)CC(O)(CC(O)=O)C(O)=O",1.966,4,0,13]
["S1241","Vincristine (NSC-67574) sulfate","a4","L1700-03","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,Autophagy,Microtubule Associated","Cytoskeletal Signaling","Vincristine sulfate (NSC-67574, Leurocristine, Oncovin, 22-Oxovincaleukoblastine) is an inhibitor of polymerization of microtubules by binding to tubulin with IC50 of 32 μM in a cell-free assay. Vincristine sulfate induces apoptosis.",923.04,"2068-78-2",{"v":100,"d":"100.00"},108.34,{"v":60,"d":"60.00"},{"v":65,"d":"65.00"},"http://selleckchem.com/products/Vincristine-Sulfate.html","C46H58N4O14S","free base","Leurocristine, Oncovin, NSC-67574, 22-Oxovincaleukoblastine","CCC1(O)CC2CN(CCC3=C([NH]C4=C3C=CC=C4)C(C2)(C(=O)OC)C5=CC6=C(C=C5OC)N(C=O)C7C(O)(C(OC(C)=O)C8(CC)C=CCN9CCC67C89)C(=O)OC)C1.O[S](O)(=O)=O",3.365,8,1,10]
["S1243","Agomelatine (S20098)","b4","L1700-03","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Agomelatine (Valdoxan, Melitor, Thymanax,S20098) is classified as a norepinephrine-dopamine disinhibitor (NDDI) due to its antagonism of the 5-HT2C receptor.",{"v":243.3,"d":"243.30"},"138112-76-2",{"v":48,"d":"48.00"},197.29,"<1","N/A","http://selleckchem.com/products/Agomelatine.html","C15H17NO2","free base","Valdoxan, Melitor, Thymanax,S20098","COC1=CC2=C(CCNC(C)=O)C=CC=C2C=C1",{"v":2.17,"d":"2.170"},2,1,4]
["S1244","Amuvatinib (MP-470)","c4","L1700-03","in 10mM DMSO","Apoptosis related,c-Kit,c-Met,c-RET,FLT3,PDGFR,RAD51","Protein Tyrosine Kinase","Amuvatinib (MP-470, HPK 56) is a potent and multi-targeted inhibitor of c-Kit, PDGFRα and Flt3 with IC50 of 10 nM, 40 nM and 81 nM, respectively. Amuvatinib suppresses c-MET and c-RET. Amuvatinib is also active as a DNA repair protein Rad51 inhibitor with antineoplastic activity. Phase 2.",447.51,"850879-09-3",{"v":32,"d":"32.00"},71.51,"<1","N/A","http://selleckchem.com/products/MP-470.html","C23H21N5O3S","free base","HPK 56","S=C(NCC1=CC=C2OCOC2=C1)N3CCN(CC3)C4=NC=NC5=C4OC6=CC=CC=C56",4.867,5,1,5]
["S1245","Latrepirdine 2HCl","d4","L1700-03","in 10mM DMSO","5-HT Receptor,GluR,Histamine Receptor","Neuronal Signaling","Latrepirdine is an orally active,and neuroactive antagonist of multiple drug targets, including histamine receptors, GluR, and 5-HT receptors, used as an antihistamine drug.",392.37,"97657-92-6",{"v":24,"d":"24.00"},61.17,"<1","N/A","http://selleckchem.com/products/Dimebon.html","C21H25N3.2HCl","Dihydrochloride","N/A","Cl.Cl.CN1CCC2=C(C1)C3=C(C=CC(=C3)C)[N]2CCC4=CC=C(C)N=C4",4.769,1,0,3]
["S1247","Leflunomide (HWA486)","e4","L1700-03","in 10mM DMSO","AhR,Dehydrogenase","Metabolism","Leflunomide (HWA486, RS-34821, SU101, Arava) is a pyrimidine synthesis and protein tyrosine kinase inhibitor belonging to the DMARD, used as an immunosuppressant agent. The active metabolite of Leflunomide is A77 1726, which inhibits dihydroorotate dehydrogenase (DHODH). Leflunomide is also an agonist of the AhR.",270.21,"75706-12-6",{"v":54,"d":"54.00"},199.84,"<1","N/A","http://selleckchem.com/products/Leflunomide.html","C12H9F3N2O2","free base","HWA486, RS-34821, SU101, Arava","CC1=C(C=NO1)C(=O)NC2=CC=C(C=C2)C(F)(F)F",2.156,3,1,3]
["S1249","JNJ-7706621","f4","L1700-03","in 10mM DMSO","Aurora Kinase,CDK","Cell Cycle","JNJ-7706621 is a pan-CDK inhibitor with the highest potency on CDK1/2 with IC50 of 9 nM/4 nM and showing >6-fold selectivity for CDK1/2 than CDK3/4/6 in cell-free assays. It also potently inhibits Aurora A/B and has no activity on Plk1 and Wee1.",394.36,"443797-96-4",{"v":79,"d":"79.00"},200.32,"<1","N/A","http://selleckchem.com/products/JNJ-7706621.html","C15H12F2N6O3S","free base","N/A","NC1=NC(=N[N]1C(=O)C2=C(F)C=CC=C2F)NC3=CC=C(C=C3)[S](N)(=O)=O",2.226,5,3,4]
["S1250","Enzalutamide (MDV3100)","g4","L1700-03","in 10mM DMSO","Androgen Receptor,Autophagy","Endocrinology & Hormones","Enzalutamide (MDV3100) is an androgen-receptor (AR) antagonist with IC50 of 36 nM in LNCaP cells. Enzalutamide is shown to increase autophagy.",464.44,"915087-33-1",{"v":92,"d":"92.00"},198.09,"<1","N/A","http://selleckchem.com/products/MDV3100.html","C21H16F4N4O2S","free base","MDV3100","CNC(=O)C1=C(F)C=C(C=C1)N2C(=S)N(C(=O)C2(C)C)C3=CC=C(C#N)C(=C3)C(F)(F)F",4.954,2,1,4]
["S1251","Dienogest","h4","L1700-03","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Dienogest (STS 557) is an orally active synthetic progesterone, used for contraception and the treatment of endometriosis.",311.42,"65928-58-7",{"v":62,"d":"62.00"},199.09,"<1","N/A","http://selleckchem.com/products/Dienogest.html","C20H25NO2","free base","STS 557","CC12CCC3=C4CCC(=O)C=C4CCC3C1CCC2(O)CC#N",3.046,1,0,1]
["S1252","Entecavir Hydrate","a5","L1700-03","in 10mM DMSO","Reverse Transcriptase","Microbiology","Entecavir Hydrate (ETV, Baraclude,BMS200475 Hydrate,SQ34676 Hydrate), a new deoxyguanine nucleoside analogue, is a selective inhibitor of the replication of the hepatitis B virus (HBV).",295.29,"209216-23-9",{"v":59,"d":"59.00"},{"v":199.8,"d":"199.80"},"<1","N/A","https://www.selleckchem.com/products/s1252-entecavir.html","C12H15N5O3.H2O","Hydrate","ETV, Baraclude,BMS200475 Hydrate,SQ34676 Hydrate","O.NC1=NC(=O)C2=C(N1)[N](C=N2)C3CC(O)C(CO)C3=C",-1.611,3,4,2]
["S1255","Nepafenac","b5","L1700-03","in 10mM DMSO","COX","Neuronal Signaling","Nepafenac (AHR 9434, AL 6515) is a prodrug of amfenac that acts as an inhibitor of COX-1 and COX-2 activity, used in the treatment of pain and inflammation associated with cataract surgery.",254.28,"78281-72-8",{"v":50,"d":"50.00"},196.63,"<1","N/A","http://selleckchem.com/products/Nepafenac.html","C15H14N2O2","free base","AHR 9434, AL 6515","NC(=O)CC1=CC=CC(=C1N)C(=O)C2=CC=CC=C2",1.524,2,2,4]
["S1256","Rufinamide","c5","L1700-03","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Rufinamide (CGP 33101,E 2080,RUF 331,Banzel) is a voltage-gated sodium channel blocker, used an anticonvulsant medication.",238.19,"106308-44-5",{"v":18,"d":"18.00"},75.57,"<1","N/A","http://selleckchem.com/products/Rufinamide.html","C10H8F2N4O","free base","CGP 33101,E 2080,RUF 331,Banzel","NC(=O)C1=C[N](CC2=C(F)C=CC=C2F)N=N1",1.437,3,1,3]
["S1257","Posaconazole (SCH 56592)","d5","L1700-03","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Posaconazole (SCH 56592,POS,Noxafil) is an inhibitor primarily of CYP3A4, but it does not inhibit the activity of other CYP enzymes; Also an inhibitor of sterol C14ɑ demethylase inhibitor with IC50 of 0.25 μM. Posaconazole has a median terminal elimination half-life of 15-35 hours.",700.78,"171228-49-2",{"v":100,"d":"100.00"},{"v":142.7,"d":"142.70"},"<1","N/A","http://selleckchem.com/products/Posaconazole.html","C37H42F2N8O4","free base","SCH 56592,POS,Noxafil","CCC(C(C)O)N1N=CN(C1=O)C2=CC=C(C=C2)N3CCN(CC3)C4=CC=C(OCC5COC(C5)(C[N]6C=NC=N6)C7=CC=C(F)C=C7F)C=C4",5.096,6,1,12]
["S1258","Prasugrel","e5","L1700-03","in 10mM DMSO","P2 Receptor","Neuronal Signaling","Prasugrel (Effient, Efient, Prasita,CS-747, LY640315,PCR 4099) is a thienopyridine ADP receptor (P2Y12) antagonist, used for the reduction of thrombotic cardiovascular events.",373.44,"150322-43-3",{"v":30,"d":"30.00"},80.33,"<1","N/A","http://selleckchem.com/products/Prasugrel.html","C20H20FNO3S","Free Base","Effient, Efient, Prasita,CS-747, LY640315,PCR 4099","CC(=O)OC1=CC2=C(CCN(C2)C(C(=O)C3CC3)C4=CC=CC=C4F)S1",3.801,3,0,6]
["S1259","Ramelteon","f5","L1700-03","in 10mM DMSO","MT Receptor","GPCR & G Protein","Ramelteon (TAK-375) is a novel melatonin receptor agonist for human MT1 and MT2 receptors and chick forebrain melatonin receptors with Ki of 14 pM, 112 pM and 23.1 pM, respectively.",259.34,"196597-26-9",{"v":52,"d":"52.00"},200.51,"<1","N/A","http://selleckchem.com/products/Ramelteon.html","C16H21NO2","free base","TAK-375","CCC(=O)NCCC1CCC2=CC=C3OCCC3=C12",2.826,2,1,4]
["S1260","Cinacalcet (AMG-073) HCl","g5","L1700-03","in 10mM DMSO","CaSR","GPCR & G Protein","Cinacalcet (Mimpara, Sensipar,AMG-073) HCl represents a new class of compounds for the treatment of hyperparathyroidism.",393.87,"364782-34-3",{"v":79,"d":"79.00"},200.57,"<1","N/A","http://selleckchem.com/products/Cinacalcet-hydrochloride.html","C22H22F3N.HCl","Hydrochloride","Mimpara, Sensipar,AMG-073","Cl.CC(NCCCC1=CC(=CC=C1)C(F)(F)F)C2=CC=CC3=C2C=CC=C3",6.338,0,1,7]
["S1261","Celecoxib (SC 58635)","h5","L1700-03","in 10mM DMSO","COX","Neuronal Signaling","Celecoxib (Celebrex, Celebra,SC 58635) is a selective COX-2 inhibitor with IC50 of 40 nM in Sf9 cells.",381.37,"169590-42-5",{"v":76,"d":"76.00"},199.28,"<1","N/A","http://selleckchem.com/products/Celecoxib.html","C17H14F3N3O2S","free base","Celebrex, Celebra,SC 58635","CC1=CC=C(C=C1)C2=CC(=N[N]2C3=CC=C(C=C3)[S](N)(=O)=O)C(F)(F)F",4.428,3,1,4]
["S1262","Avagacestat (BMS-708163)","a6","L1700-03","in 10mM DMSO","Beta Amyloid,Notch,Secretase","Proteases","Avagacestat (BMS-708163) is a potent, selective, orally bioavailable γ-secretase inhibitor of Aβ40 and Aβ42 with IC50 of 0.3 nM and 0.27 nM, demonstrating a 193-fold selectivity against Notch. Phase 2.",520.88,"1146699-66-2",{"v":104,"d":"104.00"},199.66,"<1","N/A","http://selleckchem.com/products/BMS-708163.html","C20H17ClF4N4O4S","free base","N/A","NC(=O)C(CCC(F)(F)F)N(CC1=C(F)C=C(C=C1)C2=NOC=N2)[S](=O)(=O)C3=CC=C(Cl)C=C3",3.364,6,1,10]
["S1263","Laduviglusib (CHIR-99021)","b6","L1700-03","in 10mM DMSO","Autophagy,GSK-3,Wnt/beta-catenin","PI3K/Akt/mTOR","Laduviglusib (CHIR-99021, CT99021) is a GSK-3α and GSK-3β inhibitor with IC50 of 10 nM and 6.7 nM, respectively. CHIR99201 does not exhibit cross-reactivity against cyclin-dependent kinases (CDKs) and shows a 350-fold selectivity toward GSK-3β compared to CDKs. CHIR99021 functions as a Wnt/β-catenin activator and induces autophagy.",465.34,"252917-06-9",{"v":10,"d":"10.00"},21.49,"<1","N/A","http://selleckchem.com/products/CHIR-99021.html","C22H18Cl2N8","free base","CT99021","CC1=C[NH]C(=N1)C2=CN=C(NCCNC3=CC=C(C=N3)C#N)N=C2C4=CC=C(Cl)C=C4Cl",4.476,4,3,7]
["S1264","PD173074","c6","L1700-03","in 10mM DMSO","Apoptosis related,FGFR,VEGFR","Angiogenesis","PD173074 is a potent FGFR1 inhibitor with IC50 of ~25 nM and also inhibits VEGFR2 with IC50 of 100-200 nM in cell-free assays, ~1000-fold selective for FGFR1 than PDGFR and c-Src. PD173074 reduces proliferation and promotes apoptosis in gastric cancer cells.",523.67,"219580-11-7",{"v":100,"d":"100.00"},190.96,"<1","N/A","http://selleckchem.com/products/PD-173074.html","C28H41N7O3","free base","N/A","CCN(CC)CCCCNC1=NC=C2C=C(C(=NC2=N1)NC(=O)NC(C)(C)C)C3=CC(=CC(=C3)OC)OC",4.313,6,3,13]
["S1266","WYE-354","d6","L1700-03","in 10mM DMSO","mTOR","PI3K/Akt/mTOR","WYE-354 is a potent, specific and ATP-competitive inhibitor of mTOR with IC50 of 5 nM, blocks mTORC1/P-S6K(T389) and mTORC2/P-AKT(S473) not P-AKT(T308), selective for mTOR than PI3Kα (>100-fold) and PI3Kγ (>500-fold).",495.53,"1062169-56-5",{"v":99,"d":"99.00"},199.79,"<1","N/A","http://selleckchem.com/products/WYE-354.html","C24H29N7O5","free base","N/A","COC(=O)NC1=CC=C(C=C1)C2=NC3=C(C=N[N]3C4CCN(CC4)C(=O)OC)C(=N2)N5CCOCC5",1.886,8,1,6]
["S1267","Vemurafenib (PLX4032)","e6","L1700-03","in 10mM DMSO","Autophagy,Raf","MAPK","Vemurafenib (PLX4032, RG7204, RO5185426) is a novel and potent inhibitor of B-RafV600E with IC50 of 31 nM in cell-free assay. 10-fold selective for B-RafV600E over wild-type B-Raf in enzymatic assays and the cellular selectivity can exceed 100-fold. Vemurafenib (PLX4032, RG7204) induces autophagy.",489.92,"918504-65-1",{"v":97,"d":"97.00"},197.99,"<1","N/A","http://selleckchem.com/products/PLX-4032.html","C23H18ClF2N3O3S","free base","RG7204, RO5185426,PLX4032","CCC[S](=O)(=O)NC1=CC=C(F)C(=C1F)C(=O)C2=C[NH]C3=NC=C(C=C23)C4=CC=C(Cl)C=C4",4.953,4,2,7]
["S1271","Acarbose","f6","L1700-03","in 10mM DMSO","Carbohydrate Metabolism","Metabolism","Acarbose(BAY g 5421,Prandase, Precose, Glucobay, Bay-g 5421) is an inhibitor of intestinal alpha-glucosidase, used to treat type 2 diabetes mellitus.",{"v":645.6,"d":"645.60"},"56180-94-0",{"v":100,"d":"100.00"},154.89,{"v":100,"d":"100.00"},154.89,"http://selleckchem.com/products/Acarbose.html","C25H43NO18","free base","BAY g 5421,Prandase, Precose, Glucobay, Bay-g 5421","CC1OC(OC2C(O)C(O)C(OC2CO)OC3C(O)C(O)C(O)OC3CO)C(O)C(O)C1NC4C=C(CO)C(O)C(O)C4O",-6.839,5,13,9]
["S1274","BX-795","g6","L1700-03","in 10mM DMSO","Autophagy,IκB/IKK,PDPK1,TBK1","PI3K/Akt/mTOR","BX-795 is a potent and specific PDK1 inhibitor with IC50 of 6 nM, 140- and 1600-fold more selective for PDK1 than PKA and PKC in cell-free assays, respectively. Meanwhile, in comparison to GSK3β more than 100-fold selectivity observed for PDK1. BX-795 modulates autophagy via inhibiting ULK1. BX-795 also is a potent TBK1 inhibitor that blocks both TBK1 and IKKε with IC 50 values of 6 nM and 41 nM, respectively.",591.47,"702675-74-9",{"v":100,"d":"100.00"},169.07,"<1","N/A","http://selleckchem.com/products/bx-795.html","C23H26IN7O2S","free base","N/A","IC1=CN=C(NC2=CC(=CC=C2)NC(=O)N3CCCC3)N=C1NCCCNC(=O)C4=CC=CS4",3.704,4,4,9]
["S1275","BX-912","h6","L1700-03","in 10mM DMSO","PDK","PI3K/Akt/mTOR","BX912 is a potent and specific PDK1 inhibitor with IC50 of 12 nM, 9- and 105- fold greater selectivity for PDK1 than PKA and PKC in cell-free assays, respectively. In comparison to GSK3β, selectivity for PDK1 is 600-fold.",471.35,"702674-56-4",{"v":94,"d":"94.00"},199.43,"<1","N/A","http://selleckchem.com/products/bx-912.html","C20H23BrN8O","free base","N/A","BrC1=CN=C(NC2=CC(=CC=C2)NC(=O)N3CCCC3)N=C1NCCC4=CN=C[NH]4",2.798,4,4,7]
["S1276","Adapalene","a7","L1700-03","in 10mM DMSO","Retinoid Receptor","Metabolism","Adapalene (CD-271) is a dual RAR and RXR agonist, used in the treatment of acne.",412.52,"106685-40-9",{"v":8,"d":"8.00"},19.39,"<1","N/A","http://selleckchem.com/products/Adapalene.html","C28H28O3","free base","CD-271","COC1=C(C=C(C=C1)C2=CC3=C(C=C2)C=C(C=C3)C(O)=O)[C]45CC6[CH2][CH](C[CH]([CH2]6)C4)C5",6.279,2,0,4]
["S1278","Altretamine","b7","L1700-03","in 10mM DMSO","DNA alkylator","DNA Damage/DNA Repair","Altretamine (Hexamethylmelamine, NSC13875, ENT50852) is an anti-neoplastic agent.",210.28,"645-05-6",{"v":15,"d":"15.00"},71.33,"<1","N/A","http://selleckchem.com/products/Altretamine.html","C9H18N6","free base","Hexamethylmelamine, NSC13875, ENT50852","CN(C)C1=NC(=NC(=N1)N(C)C)N(C)C",1.995,3,0,3]
["S1280","Amisulpride","c7","L1700-03","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Amisulpride (DAN-2163) is an atypical antipsychotic used to treat psychosis in schizophrenia and episodes of mania in bipolar disorder.",369.48,"71675-85-9",{"v":73,"d":"73.00"},197.57,"<1","N/A","http://selleckchem.com/products/Amisulpride.html","C17H27N3O4S","free base","DAN-2163","CCN1CCCC1CNC(=O)C2=CC(=C(N)C=C2OC)[S](=O)(=O)CC",1.127,4,2,7]
["S1281","Aniracetam","d7","L1700-03","in 10mM DMSO","AMPA Receptor-kainate Receptor-NMDA Receptor","Neuronal Signaling","Aniracetam (RO 13-5057) is a nootropics and neuroprotective drug.",219.24,"72432-10-1",{"v":44,"d":"44.00"},200.69,"<1","N/A","http://selleckchem.com/products/Aniracetam.html","C12H13NO3","free base","RO 13-5057","COC1=CC=C(C=C1)C(=O)N2CCCC2=O",1.267,3,0,2]
["S1282","Artemisinin","e7","L1700-03","in 10mM DMSO","ADC Cytotoxin,Anti-infection","Microbiology","Artemisinin (Qinghaosu,Artemisinine,Coartem,NSC 369397) is a sesquiterpene endoperoxide which is a potent antimalarial agent.",282.33,"63968-64-9",{"v":57,"d":"57.00"},201.89,"<1","N/A","http://selleckchem.com/products/Artemisinin.html","C15H22O5","free base","Qinghaosu,Artemisinine,Coartem,NSC 369397","CC1CCC2C(C)C(=O)OC3OC4(C)CCC1C23OO4",1.998,5,0,0]
["S1283","Asenapine maleate","f7","L1700-03","in 10mM DMSO","5-HT Receptor,Adrenergic Receptor","Neuronal Signaling","Asenapine maleate (Org 5222) is a high-affinity antagonist of serotonin, norepinephrine, dopamine and histamine receptors, used for the treatment of schizophrenia and acute mania associated with bipolar disorder.",401.84,"85650-56-2",{"v":80,"d":"80.00"},199.08,"<1","N/A","http://selleckchem.com/products/Asenapine.html","C17H16ClNO.C4H4O4","Maleate","Org 5222","CN1CC2C(C1)C3=C(OC4=C2C=CC=C4)C=CC(=C3)Cl.OC(=O)\\C=C/C(O)=O",0.883,3,0,2]
["S1284","Benazepril HCl","g7","L1700-03","in 10mM DMSO","RAAS","Endocrinology & Hormones","Benazepril HCl (CGS 14824A) is a novel angiotensin I converting enzyme inhibitor, used primarily in treatment of hypertension.",460.95,"86541-74-4",{"v":92,"d":"92.00"},199.59,{"v":19,"d":"19.00"},41.22,"http://selleckchem.com/products/Benazepril-hydrochloride.html","C24H28N2O5.HCl","Hydrochloride","CGS 14824A HCl","Cl.CCOC(=O)C(CCC1=CC=CC=C1)NC2CCC3=C(C=CC=C3)N(CC(O)=O)C2=O",1.003,4,1,10]
["S1286","Budesonide","h7","L1700-03","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Budesonide(Labazenit) is a glucocorticoid steroid for the treatment of asthma, non-infectious rhinitis.",430.53,"51333-22-3",{"v":86,"d":"86.00"},199.75,"<1","N/A","http://selleckchem.com/products/Budesonide.html","C25H34O6","free base","Labazenit","CCCC1OC2CC3C4CCC5=CC(=O)C=CC5(C)C4C(O)CC3(C)C2(O1)C(=O)CO",2.198,4,2,4]
["S1287","Bumetanide","a8","L1700-03","in 10mM DMSO","NKCC","Transmembrane Transporters","Bumetanide (Bumex) is a loop diuretic of the sulfamyl category to treat heart failure. Bumetanide is a selective Na+-K+-Cl- cotransporter 1 (NKCC1) inhibitor, weakly inhibits NKCC2, with IC50s of 0.68 and 4.0 μM for hNKCC1A and hNKCC2A, respectively.",364.42,"28395-03-1",{"v":73,"d":"73.00"},200.32,"<1","N/A","http://selleckchem.com/products/Bumetanide.html","C17H20N2O5S","free base","N/A","CCCCNC1=C(OC2=CC=CC=C2)C(=CC(=C1)C(O)=O)[S](N)(=O)=O",2.862,4,2,8]
["S1289","Carmofur","b8","L1700-03","in 10mM DMSO","COVID-19,DNA/RNA Synthesis","DNA Damage/DNA Repair","Carmofur (HCFU) is a highly potent acid ceramidase inhibitor, used in the treatment of breast and colorectal cancer.",257.26,"61422-45-5",{"v":52,"d":"52.00"},202.13,"<1","N/A","http://selleckchem.com/products/Carmofur.html","C11H16FN3O3","free base","HCFU","CCCCCCNC(=O)N1C=C(F)C(=O)NC1=O",1.125,3,2,5]
["S1290","Celastrol (NSC 70931)","c8","L1700-03","in 10mM DMSO","Apoptosis related,Autophagy,Mitophagy,Proteasome","Proteases","Celastrol (NSC 70931, Tripterine) is a potent proteasome inhibitor for the chymotrypsin-like activity of a purified 20S proteasome with IC50 of 2.5 μM. Celastrol induces apoptosis and autophagy via the ROS/JNK signaling pathway. Celastrol inhibits dopaminergic neuronal death of Parkinson's disease through activating mitophagy.",450.61,"34157-83-0",{"v":90,"d":"90.00"},199.73,"<1","N/A","http://selleckchem.com/products/Celastrol.html","C29H38O4","free base","Tripterine","CC1=C(O)C(=O)C=C2C1=CC=C3C2(C)CCC4(C)C5CC(C)(CCC5(C)CCC34C)C(O)=O",5.475,2,1,1]
["S1291","Cetirizine DiHCl","d8","L1700-03","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Cetirizine DiHCl (Zyrtec, Reactine,UCB P071) is an antihistamine.",461.81,"83881-52-1",{"v":92,"d":"92.00"},199.22,{"v":92,"d":"92.00"},199.22,"http://selleckchem.com/products/Cetirizine-Dihydrochloride.html","C21H25ClN2O3.2HCl","Dihydrochloride","Zyrtec, Reactine,UCB P071","Cl.Cl.OC(=O)COCCN1CCN(CC1)C(C2=CC=CC=C2)C3=CC=C(Cl)C=C3",1.217,2,0,8]
["S1292","Chelerythrine Chloride (NSC 646662)","e8","L1700-03","in 10mM DMSO","PKC","TGF-beta/Smad","Chelerythrine Chloride (NSC 646662, Broussonpapyrine) is a potent, selective antagonist of PKC with IC50 of 0.66 μM.",384.83,"3895-92-9",{"v":4,"d":"4.00"},10.39,"<1","N/A","http://www.selleck.cn/products/Chelerythrine-chloride.html","C21H18NO4.HCl","Chloride","Broussonpapyrine chloride","Cl.COC1=CC=C2C(=C1OC)C=[N+](C)C3=C2C=CC4=C3C=C5OCOC5=C4",4.568,4,0,2]
["S1293","Cilnidipine (FRC-8653)","f8","L1700-03","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Cilnidipine (FRC-8653) is a unique L-type and N-type calcium channel blocker, used for high blood pressure treatment.",492.52,"132203-70-4",{"v":99,"d":"99.00"},201.01,"<1","N/A","http://selleckchem.com/products/Cilnidipine.html","C27H28N2O7","free base","FRC-8653","COCCOC(=O)C1=C(C)NC(=C(C1C2=CC(=CC=C2)[N+]([O-])=O)C(=O)OC\\C=C\\C3=CC=CC=C3)C",3.686,5,1,12]
["S1294","Cilostazol (OPC-13013)","g8","L1700-03","in 10mM DMSO","PDE","Metabolism","Cilostazol (Pletal,OPC-13013) is a potent cyclic nucleotide phosphodiesterase type 3 (PDE3) inhibitor with IC50 of 0.2 μM and inhibitor of adenosine uptake.",369.46,"73963-72-1",{"v":74,"d":"74.00"},200.29,"<1","N/A","http://selleckchem.com/products/Cilostazol.html","C20H27N5O2","free base","Pletal,OPC-13013","O=C1CCC2=C(N1)C=CC(=C2)OCCCCC3=NN=N[N]3C4CCCCC4",{"v":3.23,"d":"3.230"},5,1,7]
["S1297","Epothilone A","h8","L1700-03","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Epothilone A is a paclitaxel-like microtubule-stabilizing agent with EC0.01 of 2 μM.",493.66,"152044-53-6",{"v":99,"d":"99.00"},200.54,"<1","N/A","http://selleckchem.com/products/Epothilone-A.html","C26H39NO6S","free base","N/A","CC1CCCC2OC2CC(OC(=O)CC(O)C(C)(C)C(=O)C(C)C1O)\\C(C)=C\\C3=CSC(=N3)C",3.574,5,2,2]
["S1299","Floxuridine (NSC 27640)","a9","L1700-03","in 10mM DMSO","Apoptosis related,CMV,DNA/RNA Synthesis","DNA Damage/DNA Repair","Floxuridine (NSC 27640, Deoxyfluorouridine, FUDR) is a prodrug that is rapidly catabolized to 5-fluorouracil in vivo. Floxuridine is used to treat various cancers, particularly metastases to the liver. Floxuridine inhibits Poly(ADP-Ribose) polymerase and induces DNA damage and apoptosis. Floxuridine has antiviral effects against HSV and CMV.",246.19,"50-91-9",{"v":49,"d":"49.00"},199.03,{"v":49,"d":"49.00"},199.03,"http://selleckchem.com/products/Floxuridine.html","C9H11FN2O5","free base","Deoxyfluorouridine, FUDR,NSC 27640","OCC1OC(CC1O)N2C=C(F)C(=O)NC2=O",-1.775,3,3,2]
["S1300","Tegafur (FT-207)","b9","L1700-03","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Tegafur (NSC 148958,Fluorafur,FT-207) is a substance being used in the treatment of some types of cancer.",200.17,"17902-23-7",{"v":40,"d":"40.00"},199.83,{"v":8,"d":"8.00"},39.97,"http://selleckchem.com/products/Ftorafur.html","C8H9FN2O3","free base","NSC 148958,Fluorafur,FT-207","FC1=CN(C2CCCO2)C(=O)NC1=O",-0.625,3,1,1]
["S1302","Ifosfamide (NSC109724)","c9","L1700-03","in 10mM DMSO","DNA alkylator,DNA/RNA Synthesis","DNA Damage/DNA Repair","Ifosfamide (Mitoxana, Ifex,Isophosphamide,NSC109724) is a nitrogen mustard alkylating agent used in the treatment of cancer.",261.09,"3778-73-2",{"v":52,"d":"52.00"},199.17,{"v":52,"d":"52.00"},199.17,"http://selleckchem.com/products/Ifosfamide.html","C7H15Cl2N2O2P","free base","Mitoxana, Ifex,Isophosphamide,NSC109724","ClCCN[P]1(=O)OCCCN1CCCl",0.144,2,1,5]
["S1304","Megestrol Acetate","d9","L1700-03","in 10mM DMSO","Androgen Receptor,Estrogen/progestogen Receptor","Endocrinology & Hormones","Megestrol acetate (BDH1298, SC10363) is a synthetic progestogen, used to treat breast cancer and loss of appetite.",384.51,"595-33-5",{"v":33,"d":"33.00"},85.82,"<1","N/A","http://selleckchem.com/products/Megestrol-Acetate.html","C24H32O4","free base","BDH1298, SC10363","CC(=O)OC1(CCC2C3C=C(C)C4=CC(=O)CCC4(C)C3CCC12C)C(C)=O",3.505,4,0,3]
["S1305","Mercaptopurine (6-MP)","e9","L1700-03","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Mercaptopurine(6-MP) is a widely used antileukemic agent and immunosuppressive drug that inhibits de novo purine synthesis through incorporation of thiopurine methyltransferase metabolites into DNA and RNA.",152.18,"50-44-2",{"v":30,"d":"30.00"},197.13,"<1","N/A","http://selleckchem.com/products/Mercaptopurine.html","C5H4N4S","free base","6-MP","S=C1N=CNC2=C1[NH]C=N2",0.367,2,2,0]
["S1315","Ki16425","f9","L1700-03","in 10mM DMSO","LPA Receptor","GPCR & G Protein","Ki16425 is a competitive, potent and reversible antagonist to LPA1, LPA2 and LPA3 with Ki of 0.34 μM, 6.5 μM and 0.93 μM in RH7777 cell lines, respectively, shows no activity at LPA4, LPA5, LPA6.",474.96,"355025-24-0",{"v":94,"d":"94.00"},197.91,"<1","N/A","http://selleckchem.com/products/Ki16425.html","C23H23ClN2O5S","free base","N/A","CC(OC(=O)NC1=C(ON=C1C)C2=CC=C(CSCCC(O)=O)C=C2)C3=C(Cl)C=CC=C3",5.043,5,1,10]
["S1319","Costunolide","g9","L1700-03","in 10mM DMSO","Telomerase","DNA Damage/DNA Repair","Costunolide (NSC 106404), a natural sesquiterpene compound with multiple biological activities; inhibits FPTase with IC50 of 20 μM, also inhibits telomerase with IC50 of 65-90 μM.",232.32,"553-21-9",{"v":47,"d":"47.00"},202.31,"<1","N/A","http://selleckchem.com/products/Costunolide.html","C15H20O2","free base","NSC 106404","CC/1=C\\CC\\C(=C\\C2OC(=O)C(=C)C2CC1)C",4.022,2,0,0]
["S1322","Dexamethasone (MK-125)","h9","L1700-03","in 10mM DMSO","Autophagy,Complement System,COVID-19,Glucocorticoid Receptor,IL Receptor,Mitophagy","Immunology & Inflammation","Dexamethasone (MK-125, NSC 34521, Hexadecadrol, Prednisolone F) is a potent synthetic member of the glucocorticoid class of steroid drugs, and an interleukin receptor modulator that has anti-inflammatory and immunosuppressant effects. Dexamethasone induces autophagy and mitophagy. Dexamethasone is tested in hospitalized patients with COVID-19 and is found to have benefits for critically ill patients.",392.46,"50-02-2",{"v":79,"d":"79.00"},201.29,"<1","N/A","http://selleckchem.com/products/Dexamethasone.html","C22H29FO5","free base","NSC 34521, Hexadecadrol, Prednisolone F,MK-125","CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO",1.708,2,2,2]
["S1324","Doxazosin Mesylate","a10","L1700-03","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Doxazosin, a quinazoline-derivative, selectively antagonizes postsynaptic α1-adrenergic receptors, used in the treatment of high blood pressure and urinary retention associated with benign prostatic hyperplasia.",547.58,"77883-43-3",{"v":15,"d":"15.00"},27.39,"<1","N/A","http://selleckchem.com/products/Doxazosin-mesylate.html","C23H25N5O5.CH4O3S","Mesylate","N/A","COC1=C(OC)C=C2C(=NC(=NC2=C1)N3CCN(CC3)C(=O)C4COC5=C(O4)C=CC=C5)N.C[S](O)(=O)=O",2.071,7,1,4]
["S1326","Edaravone","b10","L1700-03","in 10mM DMSO","Antioxidant","ER stress & UPR","Edaravone (MCI-186) is a novel potent free radical scavenger that has been clinically used to reduce the neuronal damage following ischemic stroke.",{"v":174.2,"d":"174.20"},"89-25-8",{"v":35,"d":"35.00"},200.92,"<1","N/A","http://selleckchem.com/products/Edaravone.html","C10H10N2O","free base","MCI-186","CC1=NN(C(=O)C1)C2=CC=CC=C2",1.123,2,0,1]
["S1328","Etodolac","c10","L1700-03","in 10mM DMSO","COX","Neuronal Signaling","Etodolac(AY-24236) is a nonsteroidal anti-inflammatory drug (NSAID) and a COX inhibitor, used for the treatment of inflammation and pain.",287.35,"41340-25-4",{"v":58,"d":"58.00"},201.84,"<1","N/A","http://selleckchem.com/products/Etodolac.html","C17H21NO3","free base","AY-24236","CCC1=CC=CC2=C1[NH]C3=C2CCOC3(CC)CC(O)=O",3.723,2,1,4]
["S1330","Felbamate","d10","L1700-03","in 10mM DMSO","NMDAR","Neuronal Signaling","Felbamate (Felbatol, ADD-03055,W-554) is an anticonvulsant drug used in the treatment of epilepsy; NMDAR antagonist.",238.24,"25451-15-4",{"v":48,"d":"48.00"},201.48,"<1","N/A","http://selleckchem.com/products/Felbamate.html","C11H14N2O4","free base","Felbatol, ADD-03055,W-554","NC(=O)OCC(COC(N)=O)C1=CC=CC=C1",0.984,4,2,7]
["S1331","Fluconazole (UK 49858)","e10","L1700-03","in 10mM DMSO","Fungal,P450 (e.g. CYP17)","Metabolism","Fluconazole (Diflucan, Trican, Alfumet,UK 49858) is a fungal lanosterol 14 alpha-demethylase inhibitor, which thereby prevents the formation of ergosterol,used in the treatment and prevention of superficial and systemic fungal infections.",306.27,"86386-73-4",{"v":61,"d":"61.00"},199.17,"<1","N/A","http://selleckchem.com/products/Fluconazole.html","C13H12F2N6O","free base","Diflucan, Trican, Alfumet,UK 49858","OC(C[N]1C=NC=N1)(C[N]2C=NC=N2)C3=C(F)C=C(F)C=C3",{"v":0.75,"d":"0.750"},4,0,5]
["S1332","Flumazenil (RO 15-1788)","f10","L1700-03","in 10mM DMSO","GABA Receptor","Neuronal Signaling","Flumazenil (RO 15-1788) is a competitive GABAA receptor antagonist, used in the treatment of benzodiazepine overdoses.",303.29,"78755-81-4",{"v":5,"d":"5.00"},16.49,"<1","N/A","http://selleckchem.com/products/Flumazenil.html","C15H14FN3O3","free base","RO 15-1788","CCOC(=O)C1=C2CN(C)C(=O)C3=CC(=CC=C3[N]2C=N1)F",1.583,4,0,3]
["S1333","Fluoxetine (Lilly 110140) HCl","g10","L1700-03","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Fluoxetine HCl (Prozac, Sarafem,LY-110140) is a selective serotonin-reuptake inhibitor (SSRI) at the neuronal membrane, used in the treatment of depression.",345.79,"56296-78-7",{"v":69,"d":"69.00"},199.54,{"v":4,"d":"4.00"},11.57,"http://selleckchem.com/products/Fluoxetine-hydrochloride.html","C17H18F3NO.HCl","Hydrochloride","Prozac, Sarafem,LY-110140","Cl.CNCCC(OC1=CC=C(C=C1)C(F)(F)F)C2=CC=CC=C2",4.415,1,1,7]
["S1334","Flupirtine maleate","h10","L1700-03","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Flupirtine maleate is the salt form of Flupirtine, which is a centrally acting non-opioid analgesia, is a selective neuronal potassium channel opener that also has NMDA receptor antagonist properties.",420.39,"75507-68-5",{"v":84,"d":"84.00"},199.81,"<1","N/A","http://selleckchem.com/products/Flupirtine-maleate.html","C15H17FN4O2.C4H4O4","Maleate","N/A","CCOC(=O)NC1=C(N)N=C(NCC2=CC=C(F)C=C2)C=C1.OC(=O)\\C=C\\C(O)=O",{"v":2.76,"d":"2.760"},5,3,8]
["S1336","Fluvoxamine (DU-23000) maleate","a11","L1700-03","in 10mM DMSO","Serotonin Transporter","Neuronal Signaling","Fluvoxamine maleate (DU-23000, MK-264) is a selective serotonin (5-HT) reuptake inhibitor (SSRI), used in the treatment of obsessive-compulsive disorder.",434.41,"61718-82-9",{"v":87,"d":"87.00"},200.27,"<1","N/A","http://selleckchem.com/products/Fluvoxamine-maleate.html","C19H25F3N2O6","Maleate","MK-264,DU-23000 maleate","COCCCCC(=N\\OCCN)/C1=CC=C(C=C1)C(F)(F)F.OC(=O)\\C=C/C(O)=O",0.111,5,1,12]
["S1340","Gatifloxacin","b11","L1700-03","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Gatifloxacin (AM-1155, CG5501, BMS-206584) is an antibiotic of the fourth-generation fluoroquinolone family, and inhibits the bacterial enzymes DNA gyrase and topoisomerase IV.",375.39,"112811-59-3",{"v":7,"d":"7.00"},18.65,"<1","N/A","http://selleckchem.com/products/Gatifloxacin.html","C19H22FN3O4","free base","AM-1155, CG5501, BMS-206584","COC1=C2N(C=C(C(O)=O)C(=O)C2=CC(=C1N3CCNC(C)C3)F)C4CC4",-0.909,3,1,4]
["S1342","Genistein (NPI 031L)","c11","L1700-03","in 10mM DMSO","EGFR,Topoisomerase","Protein Tyrosine Kinase","Genistein (NPI 031L), a phytoestrogen found in soy products, is a highly specific inhibitor of protein tyrosine kinase (PTK)  which blocks the mitogenic effect mediated by EGF on NIH-3T3 cells with IC50 of 12μM or by insulin with IC50 of 19 μM.",270.24,"446-72-0",{"v":54,"d":"54.00"},199.82,"<1","N/A","http://selleckchem.com/products/Genistein.html","C15H10O5","free base","NPI 031L","OC1=CC=C(C=C1)C2=COC3=C(C(=CC(=C3)O)O)C2=O",{"v":2.14,"d":"2.140"},2,3,1]
["S1343","Ginkgolide B","d11","L1700-03","in 10mM DMSO","PAFR","GPCR & G Protein","Ginkgolide B (BN52021) is a PAFR antagonist with IC50 of 3.6 μM.",{"v":424.4,"d":"424.40"},"15291-77-7",{"v":85,"d":"85.00"},200.28,"<1","N/A","http://selleckchem.com/products/Ginkgolide-B.html","C20H24O10","free base","BN52021","CC1C(=O)OC2C(O)C34C5CC(C(C)(C)C)C36C(O)C(=O)OC6OC4(C(=O)O5)C12O",-0.854,7,2,1]
["S1344","Glimepiride","e11","L1700-03","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Glimepiride(HOE-490) is a potent Kir6.2/SUR inhibitor with IC50 of 3.0 nM, 5.4 nM, and 7.3 nM for SUR1, SUR2A and SUR2B, used in the treatment of type 2 diabetes mellitus.",490.62,"93479-97-1",{"v":11,"d":"11.00"},22.42,"<1","N/A","http://selleckchem.com/products/Glimepiride.html","C24H34N4O5S","free base","HOE-490","CCC1=C(C)CN(C(=O)NCCC2=CC=C(C=C2)[S](=O)(=O)NC(=O)NC3CCC(C)CC3)C1=O",3.781,5,3,7]
["S1351","Ivermectin (MK-933)","f11","L1700-03","in 10mM DMSO","AChR,Autophagy,Chloride Channel,COVID-19,HIV,Mitophagy,P2 Receptor","Transmembrane Transporters","Ivermectin (MK-933, IVM) is a glutamate-gated chloride channel (GluCls) activator, used as a broad-spectrum antiparasitic drug. Ivermectin (MK-933, IVM) is a specific positive allosteric effector of P2X4 and α7 nicotinic acetylcholine receptors (nAChRs). Ivermectin has potent antiviral activity towards both HIV-1 and dengue virus. Ivermectin induces autophagy through the AKT/mTOR signaling pathway and mitophagy.",875.09,"70288-86-7",{"v":100,"d":"100.00"},114.27,"<1","N/A","http://selleckchem.com/products/Ivermectin.html","C48H74O14","Free Base","MK-933","CCC(C)C1OC2(CCC1C)CC3CC(C\\C=C(C)\\C(OC4CC(OC)C(OC5CC(OC)C(O)C(C)O5)C(C)O4)C(C)\\C=C\\C=C\\6COC7C(O)C(=CC(C(=O)O3)C67O)C)O2",4.743,11,2,8]
["S1352","TG100-115","g11","L1700-03","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","TG100-115 is a PI3Kγ/δ inhibitor with IC50 of 83 nM/235 nM, with little effect on PI3Kα/β. Phase 1/2.",346.34,"677297-51-7",{"v":9,"d":"9.00"},25.99,"<1","N/A","http://selleckchem.com/products/TG100-115.html","C18H14N6O2","free base","N/A","NC1=NC2=NC(=C(N=C2C(=N1)N)C3=CC(=CC=C3)O)C4=CC=CC(=C4)O",2.687,4,4,2]
["S1354","Lansoprazole","h11","L1700-03","in 10mM DMSO","ATPase,Proton Pump","Transmembrane Transporters","Lansoprazole (A-65006, AG-1749) is a proton-pump inhibitor (PPI) that binds covalently to parietal cell H(+),K(+)-ATPase. Lansoprazole prevents the stomach from producing gastric acid.",369.36,"103577-45-3",{"v":74,"d":"74.00"},200.35,"<1","N/A","http://selleckchem.com/products/Lansoprazole.html","C16H14F3N3O2S","free base","A-65006, AG-1749","CC1=C(OCC(F)(F)F)C=CN=C1C[S](=O)C2=NC3=CC=CC=C3[NH]2",3.442,4,1,6]
["S1356","Levetiracetam (UCB-L059)","a2","L1700-04","in 10mM DMSO","AChR,Calcium Channel","Transmembrane Transporters","Levetiracetam (UCB-L059, SIB-S1) is an anticonvulsant medication used to treat epilepsy. Levetiracetam (UCB-L059, SIB-S1) is an agonist of muscarinic acetylcholine receptors (mAChR). Levetiracetam modulates the presynaptic P/Q-type voltage-dependent calcium (Ca2+) channel.",170.21,"102767-28-2",{"v":34,"d":"34.00"},199.75,{"v":34,"d":"34.00"},199.75,"http://selleckchem.com/products/Levetiracetam.html","C8H14N2O2","free base","UCB-L059, SIB-S1","CCC(N1CCCC1=O)C(N)=O",-0.304,2,1,3]
["S1357","Lidocaine","b2","L1700-04","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Lidocaine (Alphacaine) is a selective inverse peripheral histamine H1-receptor agonist with an IC50 of >32 μM.",234.34,"137-58-6",{"v":47,"d":"47.00"},200.56,{"v":9,"d":"9.00"},38.41,"http://selleckchem.com/products/Lidocaine.html","C14H22N2O","Free Base","Alphacaine","CCN(CC)CC(=O)NC1=C(C)C=CC=C1C",2.626,1,1,5]
["S1358","Loratadine (SCH29851)","c2","L1700-04","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Loratadine (Alavert,Claritin,SCH29851) is a histamine H1 receptor antagonist, used to treat allergies. Also acts as a selective inhibitor of B(0)AT2 with IC50 of 4 μM.",382.88,"79794-75-5",{"v":17,"d":"17.00"},{"v":44.4,"d":"44.40"},"<1","N/A","http://selleckchem.com/products/Loratadine.html","C22H23ClN2O2","free base","Alavert,Claritin,SCH29851","CCOC(=O)N1CCC(CC1)=C2C3=C(CCC4=C2N=CC=C4)C=C(Cl)C=C3",{"v":5,"d":"5.000"},3,0,2]
["S1359","Losartan Potassium (DuP 753)","d2","L1700-04","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Losartan Potassium (DuP 753, MK 954) is an angiotensin II receptor antagonist, competes with the binding of angiotensin II to AT1 receptors with IC50 of 20 nM.",462.01,"124750-99-8",{"v":92,"d":"92.00"},199.13,{"v":92,"d":"92.00"},199.13,"http://selleckchem.com/products/losartan-potassium.html","C22H23ClKN6O","Potassium salt","MK 954,DuP 753","[KH].CCCCC1=NC(=C(CO)[N]1CC2=CC=C(C=C2)C3=C(C=CC=C3)C4=NN=N[NH]4)Cl",4.241,4,2,8]
["S1361","MGCD-265 analog","e2","L1700-04","in 10mM DMSO","c-Met,RON,Tie-2,VEGFR","Protein Tyrosine Kinase","MGCD-265 is a potent, multi-target and ATP-competitive inhibitor of c-Met and VEGFR1/2/3 with IC50 of 1 nM, 3 nM/3 nM/4 nM, respectively; also inhibits Ron and Tie2. Phase 1/2.",{"v":517.6,"d":"517.60"},"875337-44-3",{"v":104,"d":"104.00"},200.93,"<1","N/A","https://www.selleckchem.com/products/mgcd-265-analog.html","C26H20FN5O2S2","free base","N/A","C[N]1C=NC(=C1)C2=CC3=NC=CC(=C3S2)OC4=CC=C(NC(=S)NC(=O)CC5=CC=CC=C5)C=C4F",6.037,4,2,8]
["S1362","Rigosertib (ON-01910)","f2","L1700-04","in 10mM DMSO","Akt,Apoptosis related,PI3K,PLK","Cell Cycle","Rigosertib (ON-01910) is a non-ATP-competitive inhibitor of PLK1 with IC50 of 9 nM in a cell-free assay. It shows 30-fold greater selectivity against Plk2 and no activity to Plk3. Rigosertib inhibits PI3K/Akt pathway and activates oxidative stress signals. Rigosertib induces apoptosis in various cancer cells. Phase 3.",473.47,"1225497-78-8",{"v":95,"d":"95.00"},200.65,{"v":95,"d":"95.00"},200.65,"http://selleckchem.com/products/ON-01910.html","C21H24NNaO8S","Sodium Salt","N/A","[Na+].COC1=CC(=C(\\C=C\\[S](=O)(=O)CC2=CC=C(OC)C(=C2)NCC([O-])=O)C(=C1)OC)OC",0.632,6,1,11]
["S1363","Ki8751","g2","L1700-04","in 10mM DMSO","c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Ki8751 is a potent and selective inhibitor of VEGFR2 with IC50 of 0.9 nM, >40-fold selective for VEGFR2 than c-Kit, PDGFRα and FGFR-2, little activity to EGFR, HGFR and InsR.",469.41,"228559-41-9",{"v":47,"d":"47.00"},100.13,"<1","N/A","http://selleckchem.com/products/Ki8751.html","C24H18F3N3O4","free base","N/A","COC1=CC2=NC=CC(=C2C=C1OC)OC3=CC=C(NC(=O)NC4=CC=C(F)C=C4F)C(=C3)F",4.853,5,2,6]
["S1364","Patupilone (Epothilone B)","h2","L1700-04","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Patupilone (EPO906, Epothilone B) is a paclitaxel-like microtubule-stabilizing agent with EC0.01 of 1.8 μM. Phase 2.",507.68,"152044-54-7",{"v":102,"d":"102.00"},200.91,"<1","N/A","http://selleckchem.com/products/Epothilone-B.html","C27H41NO6S","free base","EPO906","CC1CCCC2(C)OC2CC(OC(=O)CC(O)C(C)(C)C(=O)C(C)C1O)\\C(C)=C\\C3=CSC(=N3)C",3.779,5,2,2]
["S1366","BMS-707035","a3","L1700-04","in 10mM DMSO","Integrase","Microbiology","BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.",410.42,"729607-74-3",{"v":38,"d":"38.00"},92.59,"<1","N/A","http://selleckchem.com/products/BMS-707035.html","C17H19FN4O5S","free base","N/A","CN1C(=O)C(=C(N=C1N2CCCC[S]2(=O)=O)C(=O)NCC3=CC=C(F)C=C3)O",0.385,5,2,4]
["S1367","Amonafide","b3","L1700-04","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Amonafide (NSC308847, AS1413) produces protein-associated DNA-strand breaks through a topoisomerase II-mediated reaction, but does not produce topoisomerase I-mediated DNA cleavage. Phase 3.",283.33,"69408-81-7",{"v":57,"d":"57.00"},201.18,"<1","N/A","http://selleckchem.com/products/Amonafide.html","C16H17N3O2","free base","NSC308847,AS1413","CN(C)CCN1C(=O)C2=C3C(=CC=C2)C=C(N)C=C3C1=O",1.162,2,1,3]
["S1368","Acitretin","c3","L1700-04","in 10mM DMSO","Retinoid Receptor","Metabolism","Acitretin (Etretin, RO 10-1670) is a second generation retinoid used for psoriasis.",326.43,"55079-83-9",{"v":20,"d":"20.00"},61.27,"<1","N/A","http://selleckchem.com/products/Acitretin.html","C21H26O3","free base","Etretin, RO 10-1670","COC1=CC(=C(\\C=C\\C(C)=C\\C=C\\C(C)=C\\C(O)=O)C(=C1C)C)C",5.665,2,0,6]
["S1369","Bafetinib (INNO-406)","d3","L1700-04","in 10mM DMSO","Bcr-Abl","Angiogenesis","Bafetinib (INNO-406, NS-187) is a potent and selective dual Bcr-Abl/Lyn inhibitor with IC50 of 5.8 nM/19 nM in cell-free assays, does not inhibit the phosphorylation of the T315I mutant and is less potent to PDGFR and c-Kit.",576.62,"859212-16-1",{"v":100,"d":"100.00"},173.42,"<1","N/A","http://selleckchem.com/products/Bafetinib.html","C30H31F3N8O","free base","NS-187","CN(C)C1CCN(C1)CC2=CC=C(C=C2C(F)(F)F)C(=O)NC3=CC=C(C)C(=C3)NC4=NC=CC(=N4)C5=CN=CN=C5",4.197,5,2,9]
["S1373","Daptomycin (LY146032)","e3","L1700-04","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture,Bacterial,DNA/RNA Synthesis","DNA Damage/DNA Repair","Daptomycin (Cubicin,LY146032) is a novel antibiotic with rapid in vitro bactericidal activity against gram-positive organisms.",1620.67,"103060-53-3",{"v":100,"d":"100.00"},{"v":61.7,"d":"61.70"},{"v":100,"d":"100.00"},{"v":61.7,"d":"61.70"},"http://selleckchem.com/products/Daptomycin.html","C72H101N17O26","free base","Cubicin,LY146032","CCCCCCCCCC(=O)NC(CC1=C[NH]C2=C1C=CC=C2)C(=O)NC(CC(N)=O)C(=O)NC(CC(O)=O)C(=O)NC3C(C)OC(=O)C(CC(=O)C4=CC=CC=C4N)NC(=O)C(NC(=O)C(CO)NC(=O)CNC(=O)C(CC(O)=O)NC(=O)C(C)NC(=O)C(CC(O)=O)NC(=O)C(CCCN)NC(=O)CNC3=O)C(C)CC(O)=O",-7.895,21,18,35]
["S1374","Doripenem Hydrate","f3","L1700-04","in 10mM DMSO","Antibiotics","Microbiology","Doripenem Hydrate (S-4661) is an ultra-broad-spectrum injectable antibiotic, used to treat complicated intra-abdominal infections and complicated urinary tract infections.",438.52,"364622-82-2",{"v":36,"d":"36.00"},82.09,{"v":26,"d":"26.00"},59.29,"http://selleckchem.com/products/Doripenem-Hydrate.html","C15H24N4O6S2.H2O","Hydrate","S-4661","O.CC(O)C1C2C(C)C(=C(N2C1=O)C(O)=O)SC3CNC(CN[S](N)(=O)=O)C3",-5.546,4,4,7]
["S1376","Gestodene","g3","L1700-04","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Gestodene (SH B 331,WL 70) is a progestogen hormonal contraceptive.",310.43,"60282-87-3",{"v":62,"d":"62.00"},199.72,"<1","N/A","http://selleckchem.com/products/Gestodene.html","C21H26O2","free base","SH B 331,WL 70","CCC12CCC3C(CCC4=CC(=O)CCC34)C1C=CC2(O)C#C",4.462,1,0,1]
["S1377","Drospirenone","h3","L1700-04","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Drospirenone (ZK 3059) is a synthetic progestin that is an analog to spironolactone.",366.49,"67392-87-4",{"v":73,"d":"73.00"},199.19,"<1","N/A","http://selleckchem.com/products/Drospirenone.html","C24H30O3","free base","ZK 3059","CC12CCC(=O)C=C1C3CC3C4C2CCC5(C)C4C6CC6C57CCC(=O)O7",3.383,3,0,0]
["S1378","Ruxolitinib (INCB018424)","a4","L1700-04","in 10mM DMSO","Apoptosis related,Autophagy,JAK,Mitophagy","JAK/STAT","Ruxolitinib (INCB018424) is the first potent, selective, JAK1/2 inhibitor to enter the clinic with IC50 of 3.3 nM/2.8 nM in cell-free assays, >130-fold selectivity for JAK1/2 versus JAK3. Ruxolitinib kills tumor cells through toxic mitophagy. Ruxolitinib induces autophagy and enhances apoptosis.",306.37,"941678-49-5",{"v":61,"d":"61.00"},199.11,"<1","N/A","http://selleckchem.com/products/INCB18424.html","C17H18N6","free base","INCB018424","N#CCC(C1CCCC1)[N]2C=C(C=N2)C3=NC=NC4=C3C=C[NH]4",{"v":2.88,"d":"2.880"},3,1,4]
["S1379","Isotretinoin","b4","L1700-04","in 10mM DMSO","Hydroxylase","Metabolism","Isotretinoin (13-cis retinoic acid) was developed to be used as a chemotherapy medication for the treatment of brain cancer, pancreatic cancer and more.",300.44,"4759-48-2",{"v":60,"d":"60.00"},199.71,"<1","N/A","http://selleckchem.com/products/Isotretinoin.html","C20H28O2","free base","13-cis retinoic acid","CC1=C(\\C=C\\C(C)=C\\C=C\\C(C)=C/C(O)=O)C(C)(C)CCC1",5.551,1,0,5]
["S1380","Lopinavir (ABT-378)","c4","L1700-04","in 10mM DMSO","COVID-19,HIV Protease","Proteases","Lopinavir (ABT-378) is a potent HIV protease inhibitor with Ki of 1.3 pM in a cell-free assay.",{"v":628.8,"d":"628.80"},"192725-17-0",{"v":126,"d":"126.00"},200.38,"<1","N/A","http://selleckchem.com/products/Lopinavir.html","C37H48N4O5","free base","ABT-378","CC(C)C(N1CCCNC1=O)C(=O)NC(CC(O)C(CC2=CC=CC=C2)NC(=O)COC3=C(C)C=CC=C3C)CC4=CC=CC=C4",4.926,4,4,15]
["S1381","Meropenem","d4","L1700-04","in 10mM DMSO","Antibiotics","Microbiology","Meropenem (SM 7338) is an ultra-broad spectrum injectable antibiotic.",383.46,"96036-03-2",{"v":76,"d":"76.00"},{"v":198.2,"d":"198.20"},{"v":8,"d":"8.00"},20.86,"http://selleckchem.com/products/Meropenem.html","C17H25N3O5S","free base","SM 7338","CC(O)C1C2C(C)C(=C(N2C1=O)C(O)=O)SC3CNC(C3)C(=O)N(C)C",-4.129,3,2,5]
["S1382","Mianserin HCl","e4","L1700-04","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Mianserin (Bolvidon, Norval, Tolvon,ORG GB-94 HCl,Mianserin hydrochloride) is an potent antagonist of H1 histamine receptor and 5-HT serotonin receptors, used for the treatment of depression.",300.83,"21535-47-7",{"v":60,"d":"60.00"},199.45,{"v":30,"d":"30.00"},99.72,"http://selleckchem.com/products/mianserin-hydrochloride.html","C18H20N2.HCl","Hydrochloride","Bolvidon, Norval, Tolvon,ORG GB-94 HCl,Mianserin hydrochloride","Cl.CN1CCN2C(C1)C3=C(CC4=C2C=CC=C4)C=CC=C3",4.088,0,0,0]
["S1385","Mosapride Citrate","f4","L1700-04","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Mosapride Citrate (TAK-370, AS-4370, Gasmotin) is a gastroprokinetic agent that acts as a selective 5HT4 agonist.",614.02,"112885-42-4",{"v":90,"d":"90.00"},146.58,"<1","N/A","http://selleckchem.com/products/Mosapride-citrate.html","C21H25ClFN3O3.C6H8O7","Citrate","TAK-370, AS-4370, Gasmotin","CCOC1=CC(=C(Cl)C=C1C(=O)NCC2CN(CCO2)CC3=CC=C(F)C=C3)N.OC(=O)CC(O)(CC(O)=O)C(O)=O",-1.422,6,2,12]
["S1386","Nafamostat mesilate (FUT-175)","g4","L1700-04","in 10mM DMSO","Apoptosis related,COVID-19,SARS-CoV,Serine Protease","Proteases","Nafamostat mesilate (Futhan, FUT-175) is a synthetic serine protease inhibitor, used as an anticoagulant during hemodialysis. Nafamostat mesylate blocks activation of SARS-CoV-2 and is investigated as a new treatment option for COVID-19. Nafamostat Mesilate attenuates inflammation and apoptosis.",539.58,"82956-11-4",{"v":20,"d":"20.00"},37.07,{"v":53,"d":"53.00"},98.22,"http://selleckchem.com/products/Nafamostat-mesylate.html","C19H17N5O2.2CH4O3S","Dimesylate","Futhan, FUT-175","C[S](O)(=O)=O.C[S](O)(=O)=O.NC(=N)NC1=CC=C(C=C1)C(=O)OC2=CC3=C(C=C2)C=C(C=C3)C(N)=N",1.364,2,3,6]
["S1387","Naftopidil DiHCl","h4","L1700-04","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Naftopidil DiHCl (Flivas, KT-611, Avishot,BM-15275) is a selective 5-HT1A and α1-adrenergic receptor antagonist with IC50 of 0.1 μM and 0.2 μM, respectively.",465.41,"57149-08-3",{"v":41,"d":"41.00"},88.09,"<1","N/A","http://selleckchem.com/products/Naftopidil-Dihydrochloride.html","C24H28N2O3.2HCl","Dihydrochloride","Flivas, KT-611, Avishot,BM-15275","Cl.Cl.COC1=CC=CC=C1N2CCN(CC2)CC(O)COC3=C4C=CC=CC4=CC=C3",4.726,2,1,7]
["S1389","Omeprazole","a5","L1700-04","in 10mM DMSO","ATPase,Autophagy,Proton Pump","Transmembrane Transporters","Omeprazole is a proton pump inhibitor that blocks H(+)-K(+)-ATPase, used to treat dyspepsia, peptic ulcer disease, gastroesophageal reflux disease, laryngopharyngeal reflux, and Zollinger–Ellison syndrome.",345.42,"73590-58-6",{"v":69,"d":"69.00"},199.76,"<1","N/A","http://selleckchem.com/products/Omeprazole.html","C17H19N3O3S","free base","N/A","COC1=CC=C2[NH]C(=NC2=C1)[S](=O)CC3=C(C)C(=C(C)C=N3)OC",2.904,5,1,5]
["S1390","Ondansetron HCl","b5","L1700-04","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Ondansetron HCl (Ondemet, Emeset, Emetron,GR 38032F,SN 307) is a serotonin 5-HT3 receptor antagonist, used to prevent nausea and vomiting caused by cancer chemotherapy, and radiation therapy.",329.82,"99614-01-4",{"v":66,"d":"66.00"},200.11,{"v":24,"d":"24.00"},72.77,"http://selleckchem.com/products/Ondansetron-hydrochloride.html","C18H19N3O.HCl","Hydrochloride","Ondemet, Emeset, Emetron,GR 38032F,SN 307","Cl.C[N]1C2=C(C(=O)C(CC2)C[N]3C=CN=C3C)C4=CC=CC=C14",3.016,2,0,2]
["S1391","Oxcarbazepine","c5","L1700-04","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Oxcarbazepine (GP47680) inhibits the binding of [3H]BTX to sodium channels with IC50 of 160 μM and also inhibits the influx of 22Na+ into rat brain synaptosomes with IC50 about 100 μM.",252.27,"28721-07-5",{"v":7,"d":"7.00"},27.75,"<1","N/A","http://selleckchem.com/products/Oxcarbazepine.html","C15H12N2O2","free base","GP47680","NC(=O)N1C2=C(CC(=O)C3=C1C=CC=C3)C=CC=C2",2.131,2,1,0]
["S1392","Pelitinib (EKB-569)","d5","L1700-04","in 10mM DMSO","EGFR,MEK,Src","Protein Tyrosine Kinase","Pelitinib (EKB-569) is a potent irreversible EGFR inhibitor with IC50 of 38.5 nM. Pelitinib (EKB-569) also slightly inhibits Src, MEK/ERK and ErbB2 with IC50s of 282 nM, 800 nM and 1255 nM, respectively. Phase2.",467.92,"257933-82-7",{"v":13,"d":"13.00"},27.78,"<1","N/A","http://selleckchem.com/products/Pelitinib.html","C24H23ClFN5O2","free base","N/A","CCOC1=C(NC(=O)\\C=C\\CN(C)C)C=C2C(=C1)N=CC(=C2NC3=CC(=C(F)C=C3)Cl)C#N",4.455,3,2,8]
["S1393","Pirarubicin (NSC-333054)","e5","L1700-04","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Topoisomerase","DNA Damage/DNA Repair","Pirarubicin (NSC-333054,THP) is an anthracycline antibiotic, and also a DNA/RNA synthesis inhibitor by intercalating into DNA and interacts with topoisomerase II, used as an antineoplastic agent.",627.64,"72496-41-4",{"v":7,"d":"7.00"},11.15,"<1","N/A","http://selleckchem.com/products/Pirarubicin.html","C32H37NO12","free base","NSC-333054,THP","COC1=CC=CC2=C1C(=O)C3=C(O)C4=C(CC(O)(CC4OC5CC(N)C(OC6CCCCO6)C(C)O5)C(=O)CO)C(=C3C2=O)O",1.091,8,4,7]
["S1394","Pizotifen Malate","f5","L1700-04","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Pizotifen Malate (Sandomigran, pizotyline,BC-105) is a benzocycloheptane based agent used for recurrent migraine headaches.",429.53,"5189-11-7",{"v":21,"d":"21.00"},48.89,"<1","N/A","http://selleckchem.com/products/Pizotifen-malate.html","C19H21NS.C4H6O5","Malate","Sandomigran, pizotyline,BC-105","CN1CCC(CC1)=C2C3=C(CCC4=C2C=CC=C4)SC=C3.OC(CC(O)=O)C(O)=O",0.292,2,1,3]
["S1396","Resveratrol (SRT501)","g5","L1700-04","in 10mM DMSO","AMPK,Apoptosis related,Autophagy,COX,ERK,IκB/IKK,JNK,Lipoxygenase,Mitophagy,Sirtuin,Src,STAT","Autophagy","Resveratrol (SRT501, trans-Resveratrol) has a wide spectrum of targets including cyclooxygenases(i.e. COX, IC50=1.1 μM), lipooxygenases（LOX, IC50=2.7 μM）, kinases, sirtuins and other proteins. It has anti-cancer, anti-inflammatory, blood-sugar-lowering and other beneficial cardiovascular effects. Resveratrol induces mitophagy/autophagy and autophagy-dependent apoptosis.",228.24,"501-36-0",{"v":45,"d":"45.00"},197.16,"<1","N/A","http://selleckchem.com/products/Resveratrol.html","C14H12O3","free base","trans-Resveratrol,SRT501","OC1=CC=C(C=C1)\\C=C\\C2=CC(=CC(=C2)O)O",{"v":3.09,"d":"3.090"},0,3,2]
["S1397","Rocuronium Bromide","h5","L1700-04","in 10mM DMSO","AChR","Neuronal Signaling","Rocuronium Bromide (ORG 9426) is a competitive AchR antagonist, used in modern anaesthesia.",609.68,"119302-91-9",{"v":122,"d":"122.00"},{"v":200.1,"d":"200.10"},{"v":122,"d":"122.00"},{"v":200.1,"d":"200.10"},"http://selleckchem.com/products/Rocuronium-bromide.html","C32H53N2O4.Br","Bromide","ORG 9426","[Br-].CC(=O)OC1C(CC2C3CCC4CC(O)C(CC4(C)C3CCC12C)N5CCOCC5)[N+]6(CCCC6)CC=C",0.282,3,1,6]
["S1398","Stavudine (d4T)","a6","L1700-04","in 10mM DMSO","Reverse Transcriptase","Microbiology","Stavudine (d4T, BMY-27857, Sanilvudine, NSC 163661) is a nucleoside analog reverse transcriptase inhibitor (NARTI) active against HIV.",224.21,"3056-17-5",{"v":45,"d":"45.00"},{"v":200.7,"d":"200.70"},"<1","N/A","http://selleckchem.com/products/Stavudine.html","C10H12N2O4","free base","BMY-27857, Sanilvudine, NSC 163661,d4T","CC1=CN(C2OC(CO)C=C2)C(=O)NC1=O",-0.515,3,2,2]
["S1400","Tenofovir (GS 1278) Disoproxil Fumarate","b6","L1700-04","in 10mM DMSO","HIV,Reverse Transcriptase","Microbiology","Tenofovir Disoproxil Fumarate (Tenofovir DF,GS-1278 Disoproxil Fumarate) belongs to a class of antiretroviral drugs, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination.",635.51,"202138-50-9",{"v":100,"d":"100.00"},157.35,"<1","N/A","http://selleckchem.com/products/Tenofovir-Disoproxil-Fumarate.html","C19H30N5O10P.C4H4O4","Fumarate","Tenofovir DF,GS-1278 Disoproxil Fumarate","CC(C)OC(=O)OCO[P](=O)(COC(C)C[N]1C=NC2=C1N=CN=C2N)OCOC(=O)OC(C)C.OC(=O)/C=C/C(O)=O",1.729,14,1,19]
["S1401","Tenofovir","c6","L1700-04","in 10mM DMSO","Antiviral,COVID-19,Reverse Transcriptase","Microbiology","Tenofovir (GS-1278) blocks reverse transcriptase and hepatitis B virus infections.",287.21,"147127-20-6",{"v":4,"d":"4.00"},13.93,{"v":2,"d":"2.00"},6.96,"http://selleckchem.com/products/Tenofovir.html","C9H14N5O4P","free base","GS-1278","CC(C[N]1C=NC2=C(N)N=CN=C12)OC[P](O)(O)=O",-0.772,4,1,5]
["S1403","Tigecycline (GAR-936)","d6","L1700-04","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Autophagy,Bacterial","Microbiology","Tigecycline (Tygacil, GAR-936, WAY-GAR-936, TBG-MINO) is bacteriostatic and is a protein synthesis inhibitor by binding to the 30S ribosomal subunit of bacteria and thereby blocking entry of Aminoacyl-tRNA into the A site of the ribosome during prokaryotic translation. Tigecycline induces autophagy by downregulating the PI3K-AKT-mTOR pathway.",585.65,"220620-09-7",{"v":100,"d":"100.00"},170.75,{"v":100,"d":"100.00"},170.75,"http://selleckchem.com/products/Tigecycline.html","C29H39N5O8","free base","Tygacil, GAR-936, WAY-GAR-936, TBG-MINO","CN(C)C1C2CC3CC4=C(C(=C(NC(=O)CNC(C)(C)C)C=C4N(C)C)O)C(=O)C3=C(O)C2(O)C(=O)C(=C1O)C(N)=O",-0.381,4,6,7]
["S1404","Trilostane","e6","L1700-04","in 10mM DMSO","Dehydrogenase","Metabolism","Trilostane (WIN 24540) is an inhibitor of 3β-hydroxysteroid dehydrogenase used in the treatment of Cushing’s syndrome.",329.43,"13647-35-3",{"v":65,"d":"65.00"},197.31,"<1","N/A","http://selleckchem.com/products/Trilostane.html","C20H27NO3","free base","WIN 24540","CC12CCC3C(CCC45OC4C(=C(CC35C)C#N)O)C1CCC2O",2.434,1,2,0]
["S1405","Vecuronium Bromide","f6","L1700-04","in 10mM DMSO","AChR","Neuronal Signaling","Vecuronium Bromide (ORG NC45) is a non-depolarizing neuromuscular blocking agent, used for skeletal muscle relaxation during surgery.",637.73,"50700-72-6",{"v":100,"d":"100.00"},156.81,{"v":4,"d":"4.00"},6.27,"http://selleckchem.com/products/Vecuronium-Bromide.html","C34H57N2O4.Br","Bromide","ORG NC45","[Br-].CC(=O)OC1CC2CCC3C(CCC4(C)C3CC(C4OC(C)=O)[N+]5(C)CCCCC5)C2(C)CC1N6CCCCC6",{"v":1.73,"d":"1.730"},4,0,6]
["S1407","Bimatoprost","g6","L1700-04","in 10mM DMSO","Prostaglandin Receptor","GPCR & G Protein","Bimatoprost(AGN 192024) is a prostaglandin analog used topically (as eye drops) to control the progression of glaucoma and in the management of ocular hypertension.",415.57,"155206-00-1",{"v":36,"d":"36.00"},86.63,"<1","N/A","http://selleckchem.com/products/Bimatoprost.html","C25H37NO4","free base","AGN 192024","CCNC(=O)CCC\\C=C/CC1C(O)CC(O)C1/C=C/C(O)CCC2=CC=CC=C2",{"v":3.03,"d":"3.030"},1,4,12]
["S1408","Linezolid (PNU-100766)","h6","L1700-04","in 10mM DMSO","Antibiotics","Microbiology","Linezolid (Zyvoxid, Zyvoxam,PNU-100766) is a synthetic antibiotic used for the treatment of serious infections.",337.35,"165800-03-3",{"v":67,"d":"67.00"},198.61,"<1","N/A","http://selleckchem.com/products/Linezolid(Zyvox).html","C16H20FN3O4","free base","Zyvoxid, Zyvoxam,PNU-100766","CC(=O)NCC1CN(C(=O)O1)C2=CC=C(N3CCOCC3)C(=C2)F",0.894,4,1,4]
["S1409","Alfuzosin HCl","a7","L1700-04","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Alfuzosin HCI(SL 77499 HCl)  is an alpha1 receptor antagonist used to treat benign prostatic hyperplasia (BPH).",425.91,"81403-68-1",{"v":85,"d":"85.00"},199.57,{"v":85,"d":"85.00"},199.57,"http://selleckchem.com/products/Alfuzosin-hydrochloride.html","C19H27N5O4.HCl","Hydrochloride","SL 77499 HCl","Cl.COC1=C(OC)C=C2C(=NC(=NC2=C1)N(C)CCCNC(=O)C3CCCO3)N",{"v":1.8,"d":"1.800"},6,2,8]
["S1415","Clopidogrel (SR-25990C) Bisulfate","b7","L1700-04","in 10mM DMSO","P2 Receptor","Neuronal Signaling","Clopidogrel Bisulfate (SR-25990C, Clopidogrel hydrogen sulfate, Iscover, Plavix) is an oral, thienopyridine class antiplatelet agent.",{"v":419.9,"d":"419.90"},"120202-66-6",{"v":83,"d":"83.00"},197.67,{"v":78,"d":"78.00"},185.76,"http://selleckchem.com/products/Clopidogrel-bisulfate.html","C16H16ClNO2S.H2SO4","Bisulfate","SR-25990C, Clopidogrel hydrogen sulfate, Iscover, Plavix","COC(=O)C(N1CCC2=C(C1)C=CS2)C3=C(Cl)C=CC=C3.O[S](O)(=O)=O",3.128,2,0,4]
["S1422","Droxinostat","c7","L1700-04","in 10mM DMSO","HDAC","Cytoskeletal Signaling","Droxinostat (NS 41080) is a selective inhibitor of HDAC, mostly for HDACs 6 and 8 with IC50 of 2.47 μM and 1.46 μM, greater than 8-fold selective against HDAC3 and no inhibition to HDAC1, 2, 4, 5, 7, 9, and 10.",243.69,"99873-43-5",{"v":49,"d":"49.00"},201.08,"<1","N/A","http://selleckchem.com/products/Droxinostat.html","C11H14ClNO3","free base","NS 41080","CC1=CC(=CC=C1OCCCC(=O)NO)Cl",{"v":2.4,"d":"2.400"},2,1,5]
["S1425","Ranolazine 2HCl","d7","L1700-04","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Ranolazine 2HCl (RS-43285,RS 43285-193,Ranexa, renolazine,Ranolazine dihydrochloride) is a calcium uptake inhibitor via the sodium/calcium channal, used to treat chronic angina.",500.46,"95635-56-6",{"v":100,"d":"100.00"},199.82,{"v":100,"d":"100.00"},199.82,"http://selleckchem.com/products/Ranolazine-dihydrochloride.html","C24H33N3O4.2HCl","Dihydrochloride","RS-43285,RS 43285-193,Ranexa, renolazine,Ranolazine dihydrochloride","Cl.Cl.COC1=CC=CC=C1OCC(O)CN2CCN(CC2)CC(=O)NC3=C(C)C=CC=C3C",3.755,3,2,9]
["S1426","Repaglinide","e7","L1700-04","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Repaglinide (AG-EE 623 ZW) is a potassium channel blocker, which lowers blood glucose by stimulating the release of insulin from the pancreas, used the treatment of type II diabetes.",452.59,"135062-02-1",{"v":91,"d":"91.00"},201.06,"<1","N/A","http://selleckchem.com/products/Repaglinide.html","C27H36N2O4","free base","AG-EE 623 ZW","CCOC1=C(C=CC(=C1)CC(=O)NC(CC(C)C)C2=CC=CC=C2N3CCCCC3)C(O)=O",5.307,3,1,10]
["S1430","Rolipram (ZK-62711)","f7","L1700-04","in 10mM DMSO","PDE","Metabolism","The PDE4 selective inhibitor, Rolipram (ZK-62711, SB 95952), inhibited immunopurified PDE4B and PDE4D activities similarly, with IC50 values of approx. 130 nM and 240 nM respectively; an anti-inflammatory agent.",275.34,"61413-54-5",{"v":55,"d":"55.00"},199.75,"<1","N/A","http://selleckchem.com/products/Rolipram.html","C16H21NO3","free base","ZK-62711, SB 95952","COC1=C(OC2CCCC2)C=C(C=C1)C3CNC(=O)C3",2.349,3,1,4]
["S1431","Sildenafil Citrate","g7","L1700-04","in 10mM DMSO","PDE","Metabolism","Sildenafil Citrate, a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5), is a well-tolerated and highly effective treatment for erectile dysfunction.",{"v":666.7,"d":"666.70"},"171599-83-0",{"v":20,"d":"20.00"},{"v":30,"d":"30.00"},"<1","N/A","http://selleckchem.com/products/Sildenafil-citrate.html","C22H30N6O4S.C6H8O7","Citrate","N/A","CCCC1=N[N](C)C2=C1N=C(NC2=O)C3=CC(=CC=C3OCC)[S](=O)(=O)N4CCN(C)CC4.OC(=O)CC(O)(CC(O)=O)C(O)=O",-2.107,9,1,12]
["S1432","Sumatriptan Succinate","h7","L1700-04","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Sumatriptan Succinate (GR 43175) is a triptan sulfa drug containing a sulfonamide group for the treatment of migraine headaches.",413.49,"103628-48-4",{"v":83,"d":"83.00"},200.73,{"v":83,"d":"83.00"},200.73,"http://selleckchem.com/products/Sumatriptan-succinate.html","C14H21N3O2S.C4H6O4","Succinate","GR 43175","CN[S](=O)(=O)CC1=CC=C2[NH]C=C(CCN(C)C)C2=C1.OC(=O)CCC(O)=O",-1.958,4,2,9]
["S1435","Tamsulosin hydrochloride","a8","L1700-04","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Tamsulosin (Flomax) hydrochloride is an antagonist of alpha1A adrenoceptors in the prostate.",444.97,"106463-17-6",{"v":89,"d":"89.00"},200.01,"<1","N/A","https://www.selleckchem.com/products/Tamsulosin-hydrochloride.html","C20H28N2O5S.HCl","HCl","Flomax hydrochloride","CCOC1=C(OCCNC(C)CC2=CC=C(OC)C(=C2)[S](N)(=O)=O)C=CC=C1",2.719,5,2,11]
["S1437","Tizanidine HCl","b8","L1700-04","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Tizanidine HCl (DS 103-282) is an α2-adrenergic receptor agonist and inhibits neurotransmitter release from CNS noradrenergic neurons.",290.17,"64461-82-1",{"v":10,"d":"10.00"},34.46,{"v":15,"d":"15.00"},51.69,"http://selleckchem.com/products/Tizanidine-hydrochloride.html","C9H8ClN5S.HCl","Hydrochloride","DS 103-282","Cl.ClC1=C(NC2=NCCN2)C3=NSN=C3C=C1",2.199,3,2,2]
["S1438","Topiramate","c8","L1700-04","in 10mM DMSO","Carbonic Anhydrase","Metabolism","Topiramate (MCN 4853, RWJ 17021) is a mutil-targeted inhibitor, including voltage-gated sodium channel and calcium channel, AMPA/kainate receptor and carbonic anhydrase, used to treat epilepsy.",339.36,"97240-79-4",{"v":68,"d":"68.00"},200.38,"<1","N/A","http://selleckchem.com/products/Topiramate.html","C12H21NO8S","free base","MCN 4853, RWJ 17021","CC1(C)OC2COC3(CO[S](N)(=O)=O)OC(C)(C)OC3C2O1",-1.932,6,1,3]
["S1439","Tranilast (SB 252218)","d8","L1700-04","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Tranilast (SB 252218, MK-341, Rizaben, MK 341, Tranpro) is an antiallergic drug by inhibiting lipid mediator and cytokine release from inflammatory cells, used for the treatment of allergic disorders such as asthma, allergic rhinitis and atopic dermatitis.",327.33,"53902-12-8",{"v":66,"d":"66.00"},201.63,"<1","N/A","http://selleckchem.com/products/Tranilast.html","C18H17NO5","free base","SB 252218, MK-341, Rizaben, MK 341, Tranpro","COC1=C(OC)C=C(\\C=C\\C(=O)NC2=CC=CC=C2C(O)=O)C=C1",2.679,4,1,6]
["S1441","Venlafaxine HCl","e8","L1700-04","in 10mM DMSO","Serotonin Transporter","Neuronal Signaling","Venlafaxine HCl(Wy 453 HCl) is an arylalkanolamine serotonin-norepinephrine reuptake inhibitor (SNRI), used to treat major depressive disorder (MDD), generalised anxiety disorder (GAD), panic disorder and social phobia.",313.86,"99300-78-4",{"v":55.5,"d":"55.50"},176.83,{"v":55.5,"d":"55.50"},176.83,"http://selleckchem.com/products/Venlafaxine-hydrochloride.html","C17H27NO2.HCl","Hydrochloride","Wy 453 HCl","Cl.COC1=CC=C(C=C1)C(CN(C)C)C2(O)CCCCC2",3.404,1,0,5]
["S1442","Voriconazole (UK-109496)","f8","L1700-04","in 10mM DMSO","Fungal,P450 (e.g. CYP17)","Metabolism","Voriconazole (Vfend,UK-109496) is a new triazole derivative similar to fluconazole and itraconazole that acts by inhibiting fungal cytochrome P-450-dependent, 14-alpha-sterol demethylase-mediated synthesis of ergosterol.",349.31,"137234-62-9",{"v":70,"d":"70.00"},{"v":200.4,"d":"200.40"},"<1","N/A","http://selleckchem.com/products/Voriconazole.html","C16H14F3N5O","free base","Vfend,UK-109496","CC(C1=NC=NC=C1F)C(O)(C[N]2C=NC=N2)C3=CC=C(F)C=C3F",2.071,4,0,5]
["S1443","Zileuton (A-64077)","g8","L1700-04","in 10mM DMSO","Apoptosis related,Ferroptosis,Lipoxygenase","Metabolism","Zileuton (A-64077, Abbott 64077, ZYFLO) is an orally active inhibitor of 5-lipoxygenase, and thus inhibits leukotrienes (LTB4, LTC4, LTD4, and LTE4) formation, used to decrease the symptoms of asthma. Zileuton induces apoptosis while inhibits ferroptosis.",236.29,"111406-87-2",{"v":47,"d":"47.00"},198.91,"<1","N/A","http://selleckchem.com/products/Zileuton.html","C11H12N2O2S","free base","A-64077, Abbott 64077, ZYFLO","CC(N(O)C(N)=O)C1=CC2=CC=CC=C2S1",2.184,1,1,2]
["S1444","Ziprasidone HCl","h8","L1700-04","in 10mM DMSO","5-HT Receptor,Dopamine Receptor","Neuronal Signaling","Ziprasidone HCl (CP-88059) is a novel and potent dopamine and serotonin (5-HT) receptor antagonist, used in the treatment of schizophrenia and bipolar disorder.",{"v":449.4,"d":"449.40"},"122883-93-6",{"v":90,"d":"90.00"},200.27,"<1","N/A","http://selleckchem.com/products/Ziprasidone-hydrochloride.html","C21H21ClN4OS.HCl","Hydrochloride","CP-88059","Cl.ClC1=CC2=C(CC(=O)N2)C=C1CCN3CCN(CC3)C4=NSC5=C4C=CC=C5",4.641,2,1,4]
["S1445","Zonisamide","a9","L1700-04","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Zonisamide (Zonegran,CI-912,AD 810) is a voltage-dependent sodium channel and T-type calcium channel blocker, used as an antiepileptic drug.",212.23,"68291-97-4",{"v":42,"d":"42.00"},{"v":197.9,"d":"197.90"},"<1","N/A","http://selleckchem.com/products/Zonisamide.html","C8H8N2O3S","free base","Zonegran,CI-912,AD 810","N[S](=O)(=O)CC1=NOC2=CC=CC=C12",0.411,4,1,2]
["S1451","Aurora A Inhibitor I (TC-S 7010)","b9","L1700-04","in 10mM DMSO","Apoptosis related,Aurora Kinase","Cell Cycle","Aurora A Inhibitor I (TC-S 7010) is a novel, potent, and selective inhibitor of Aurora A with IC50 of 3.4 nM in a cell-free assay. It is 1000-fold more selective for Aurora A than Aurora B. Aurora A Inhibitor I (TC-S 7010) triggers apoptosis through the ROS-mediated UPR signaling pathway.",588.07,"1158838-45-9",{"v":118,"d":"118.00"},200.66,"<1","N/A","http://selleckchem.com/products/Aurora-A-Inhibitor-I.html","C31H31ClFN7O2","free base","N/A","CCN1CCN(CC1)C(=O)CC2=CC=C(NC3=NC(=C(F)C=N3)NC4=CC=C(C=C4)C(=O)NC5=CC=CC=C5Cl)C=C2",5.621,4,3,9]
["S1452","Ispinesib (SB-715992)","c9","L1700-04","in 10mM DMSO","Apoptosis related,Kinesin","Cytoskeletal Signaling","Ispinesib (SB-715992, CK0238273) is a potent, specific and reversible inhibitor of kinesin spindle protein (KSP) with Ki app of 1.7 nM in a cell-free assay, no inhibition to CENP-E, RabK6, MCAK, MKLP1, KHC or Kif1A. Ispinesib induces mitotic arrest and apoptotic cell death.",517.06,"336113-53-2",{"v":103,"d":"103.00"},{"v":199.2,"d":"199.20"},"<1","N/A","http://selleckchem.com/products/Ispinesib-mesilate(SB-715992).html","C30H33ClN4O2","free base","CK0238273","CC(C)C(N(CCCN)C(=O)C1=CC=C(C)C=C1)C2=NC3=C(C=CC(=C3)Cl)C(=O)N2CC4=CC=CC=C4",5.259,3,1,9]
["S1453","Tipifarnib (R115777)","d9","L1700-04","in 10mM DMSO","FTase,Transferase","Metabolism","Tipifarnib (R115777, IND 58359) is a potent and specific farnesyltransferase (FTase) inhibitor with IC50 of 0.6 nM, its anti-proliferative effects are most prominent in H-ras or N-ras mutant cells. Phase 3.",{"v":489.4,"d":"489.40"},"192185-72-1",{"v":14,"d":"14.00"},28.61,"<1","N/A","http://selleckchem.com/products/Tipifarnib(R115777).html","C27H22Cl2N4O","free base","IND 58359","C[N]1C=NC=C1C(N)(C2=CC=C(Cl)C=C2)C3=CC4=C(C=C3)N(C)C(=O)C=C4C5=CC(=CC=C5)Cl",4.808,2,1,4]
["S1454","PHA-680632","e9","L1700-04","in 10mM DMSO","Aurora Kinase","Cell Cycle","PHA-680632 is a potent inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 27 nM, 135 nM and 120 nM, respectively. It has 10- to 200-fold higher IC50 for FGFR1, FLT3, LCK, PLK1, STLK2, and VEGFR2/3.",501.62,"398493-79-3",{"v":100,"d":"100.00"},199.35,"<1","N/A","http://selleckchem.com/products/PHA-680632.html","C28H35N7O2","free base","N/A","CCC1=CC=CC(=C1NC(=O)N2CC3=C(C2)C(=N[NH]3)NC(=O)C4=CC=C(C=C4)N5CCN(C)CC5)CC",4.339,3,3,6]
["S1455","Cilomilast","f9","L1700-04","in 10mM DMSO","PDE","Metabolism","Cilomilast (SB-207499) is a potent PDE4 inhibitor with IC50 of about 110 nM, has anti-inflammatory activity and low central nervous system activity. Phase 3.",343.42,"153259-65-5",{"v":69,"d":"69.00"},200.92,"<1","N/A","http://selleckchem.com/products/Cilomilast(SB-207499).html","C20H25NO4","free base","SB-207499","COC1=C(OC2CCCC2)C=C(C=C1)C3(CCC(CC3)C(O)=O)C#N",4.174,3,0,5]
["S1456","Zibotentan (ZD4054)","g9","L1700-04","in 10mM DMSO","Endothelin Receptor","GPCR & G Protein","Zibotentan (ZD4054) is a specific Endothelin (ET)A antagonist with IC50 of 21 nM, exhibiting no activity at ETB. Phase 3.",424.43,"186497-07-4",{"v":24,"d":"24.00"},56.55,"<1","N/A","http://selleckchem.com/products/Zibotentan(ZD4054).html","C19H16N6O4S","free base","N/A","COC1=NC(=CN=C1N[S](=O)(=O)C2=CC=CN=C2C3=CC=C(C=C3)C4=NN=CO4)C",1.456,9,1,6]
["S1457","Atazanavir (BMS-232632) Sulfate","h9","L1700-04","in 10mM DMSO","HIV Protease","Proteases","Atazanavir Sulfate (BMS-232632-05, Reyataz) is a HIV protease inhibitor with Ki of 2.66 nM in a cell-free assay.",802.93,"229975-97-7",{"v":104,"d":"104.00"},129.53,"<1","N/A","http://selleckchem.com/products/Atazanavir.html","C38H52N6O7.H2SO4","Sulfate","BMS-232632-05, Reyataz","COC(=O)NC(C(=O)NC(CC1=CC=CC=C1)C(O)CN(CC2=CC=C(C=C2)C3=NC=CC=C3)NC(=O)C(NC(=O)OC)C(C)(C)C)C(C)(C)C.O[S](O)(=O)=O",4.083,7,5,18]
["S1458","Neflamapimod (VX-745)","a10","L1700-04","in 10mM DMSO","p38 MAPK","MAPK","Neflamapimod (VX-745) is a potent and selective inhibitor of p38α with IC50 of 10 nM, 22-fold greater selectivity versus p38β and no inhibition to p38γ.",436.26,"209410-46-8",{"v":15,"d":"15.00"},34.38,"<1","N/A","http://selleckchem.com/products/VX-745.html","C19H9Cl2F2N3OS","free base","N/A","FC1=CC(=C(SC2=NN3C=NC(=O)C(=C3C=C2)C4=C(Cl)C=CC=C4Cl)C=C1)F",5.342,3,0,3]
["S1459","Thiazovivin","b10","L1700-04","in 10mM DMSO","ROCK","Cell Cycle","Thiazovivin is a novel ROCK inhibitor with IC50 of 0.5 μM in a cell-free assay, promotes hESC survival after single-cell dissociation.",311.36,"1226056-71-8",{"v":15,"d":"15.00"},48.18,"<1","N/A","http://selleckchem.com/products/Thiazovivin.html","C15H13N5OS","free base","N/A","O=C(NCC1=CC=CC=C1)C2=CSC(=N2)NC3=CC=NC=N3",2.357,4,2,5]
["S1460","SP600125","c10","L1700-04","in 10mM DMSO","Apoptosis related,Aurora Kinase,Autophagy,FLT3,JNK,Serine/threonin kinase,Trk receptor","MAPK","SP600125 (Nsc75890) is a broad-spectrum JNK inhibitor for JNK1, JNK2 and JNK3 with IC50 of 40 nM, 40 nM and 90 nM in cell-free assays, respectively; 10-fold greater selectivity against MKK4, 25-fold greater selectivity against MKK3, MKK6, PKB, and PKCα, and 100-fold selectivity against ERK2, p38, Chk1, EGFR etc. SP600125 is also a broad‐spectrum inhibitor of serine/threonine kinases including Aurora kinase A，FLT3 and TRKA with of IC50 of 60 nM, 90 nM and 70 nM. SP600125 inhibits autophagy and activates apoptosis.",220.23,"129-56-6",{"v":44,"d":"44.00"},199.79,"<1","N/A","http://selleckchem.com/products/SP600125.html","C14H8N2O","free base","Nsc75890","O=C1C2=C(C=CC=C2)C3=N[NH]C4=CC=CC1=C34",2.994,2,1,0]
["S1462","AZD6482","d10","L1700-04","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","AZD6482 (KIN-193) is a PI3Kβ inhibitor with IC50 of 10 nM, 8-, 87- and 109-fold more selective to PI3Kβ than PI3Kδ, PI3Kα and PI3Kγ in cell-free assays. Phase 1.",408.45,"1173900-33-8",{"v":82,"d":"82.00"},200.76,"<1","N/A","http://selleckchem.com/products/azd6482.html","C22H24N4O4","free base","KIN-193","CC(NC1=CC=CC=C1C(O)=O)C2=CC(=CN3C(=O)C=C(N=C23)N4CCOCC4)C",2.003,4,1,5]
["S1465","Moxifloxacin (BAY12-8039) HCl","e10","L1700-04","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Moxifloxacin (Avelox, Avalox,BAY12-8039 HCl) is a fourth-generation synthetic fluoroquinolone antibacterial agent.",437.89,"186826-86-8",{"v":87,"d":"87.00"},198.68,{"v":60,"d":"60.00"},137.02,"https://www.selleckchem.com/products/Moxifloxacin-hcl.html","C21H24FN3O4.HCl","Hydrochloride","Avelox, Avalox,BAY12-8039 HCl","Cl.COC1=C2N(C=C(C(O)=O)C(=O)C2=CC(=C1N3CC4CCCNC4C3)F)C5CC5",{"v":-0.32,"d":"-0.320"},3,1,4]
["S1467","Doxercalciferol","f10","L1700-04","in 10mM DMSO","Vitamin","Metabolism","Doxercalciferol (1α-hydroxyvitamin D2) is a synthetic vitamin D2 analog, suppressing parathyroid synthesis and secretion, used to treat secondary hyperparathyroidism and metabolic bone disease.",412.65,"54573-75-0",{"v":83,"d":"83.00"},201.14,"<1","N/A","http://selleckchem.com/products/Doxercalciferol(Hectorol).html","C28H44O2","free base","1α-hydroxyvitamin D2","CC(C)C(C)/C=C/C(C)C1CCC2C(/CCCC12C)=C/C=C/3CC(O)CC(O)C3=C",6.337,0,2,5]
["S1468","Alfacalcidol","g10","L1700-04","in 10mM DMSO","Vitamin","Metabolism","Alfacalcidol (1-hydroxycholecalciferol) is a non-selective VDR activator medication.",400.64,"41294-56-8",{"v":80,"d":"80.00"},199.68,"<1","N/A","http://selleckchem.com/products/Alfacalcidol.html","C27H44O2","free base","1-hydroxycholecalciferol","CC(C)CCCC(C)C1CCC2/C(CCCC12C)=C\\C=C3/CC(O)CC(O)C3=C",{"v":6.53,"d":"6.530"},0,2,6]
["S1470","Orantinib (SU6668)","h10","L1700-04","in 10mM DMSO","PDGFR","Protein Tyrosine Kinase","Orantinib (TSU-68, SU6668) has greatest potency against PDGFR autophosphorylation with Ki of 8 nM in a cell-free assay, but also strongly inhibits Flk-1 and FGFR1 trans-phosphorylation, little activity against IGF-1R, Met, Src, Lck, Zap70, Abl and CDK2; does not inhibit EGFR. Phase 3.",310.35,"252916-29-3",{"v":62,"d":"62.00"},199.77,"<1","N/A","http://selleckchem.com/products/TSU-68(SU6668).html","C18H18N2O3","free base","TSU-68","CC1=C(CCC(O)=O)C(=C([NH]1)/C=C/2C(=O)NC3=CC=CC=C23)C",2.868,2,2,4]
["S1472","Safinamide Mesylate","a11","L1700-04","in 10mM DMSO","MAO","Metabolism","Safinamide Mesylate (PNU-151774E, FCE28073) is mesylate salt of Safinamide, selectively and reversibly inhibits MAO-B with IC50 of 98 nM, exhibits 5918-fold selectivity against MAO-A. Phase 3.",398.45,"202825-46-5",{"v":80,"d":"80.00"},200.78,{"v":80,"d":"80.00"},200.78,"http://selleckchem.com/products/Safinamide-mesilate.html","C17H19FN2O2.CH4O3S","Mesylate","PNU-151774E,FCE28073","CC(NCC1=CC=C(OCC2=CC(=CC=C2)F)C=C1)C(N)=O.C[S](O)(=O)=O",2.064,2,2,7]
["S1474","GSK429286A","b11","L1700-04","in 10mM DMSO","ROCK","Cell Cycle","GSK429286A (RHO-15) is a selective inhibitor of ROCK1 and ROCK2 with IC50 of 14 nM and 63 nM, respectively.",432.37,"864082-47-3",{"v":87,"d":"87.00"},201.22,"<1","N/A","http://selleckchem.com/products/GSK429286A.html","C21H16F4N4O2","free base","RHO-15","CC1=C(C(CC(=O)N1)C2=CC=C(C=C2)C(F)(F)F)C(=O)NC3=C(F)C=C4[NH]N=CC4=C3",3.033,3,3,4]
["S1475","Pimasertib (AS-703026)","c11","L1700-04","in 10mM DMSO","MEK","MAPK","Pimasertib (AS-703026, MSC1936369B, SAR 245509) is a highly selective, potent, ATP non-competitive allosteric inhibitor of MEK1/2 with IC50 of 5 nM-2 μM in MM cell lines. Phase 2.",{"v":431.2,"d":"431.20"},"1236699-92-5",{"v":86,"d":"86.00"},199.44,"<1","N/A","http://selleckchem.com/products/AS703026.html","C15H15FIN3O3","free base","MSC1936369B, SAR 245509","OCC(O)CNC(=O)C1=CC=NC=C1NC2=C(F)C=C(I)C=C2",1.171,2,4,6]
["S1476","SB525334","d11","L1700-04","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","SB525334 is a potent and selective inhibitor of TGFβ receptor I (ALK5) with IC50 of 14.3 nM in a cell-free assay, 4-fold less potent to ALK4 than ALK5 and inactive to ALK2, 3, and 6.",343.42,"356559-20-1",{"v":68,"d":"68.00"},198.01,"<1","N/A","http://selleckchem.com/products/SB-525334.html","C21H21N5","free base","N/A","CC1=NC(=CC=C1)C2=C([NH]C(=N2)C(C)(C)C)C3=CC=C4N=CC=NC4=C3",4.305,4,1,3]
["S1480","Lomibuvir (VX-222)","e11","L1700-04","in 10mM DMSO","HCV Protease","Proteases","Lomibuvir (VX-222, VCH-222) is a novel, potent and selective inhibitor of HCV polymerase with IC50 of 0.94-1.2 μM, 15.3-fold less effective for mutant M423T, and 108-fold less effective for mutant I482L. Phase 2.",445.61,"1026785-59-0",{"v":89,"d":"89.00"},199.73,"<1","N/A","http://selleckchem.com/products/VX-222.html","C25H35NO4S","free base","VCH-222","CC1CCC(CC1)C(=O)N(C2CCC(O)CC2)C3=C(SC(=C3)C#CC(C)(C)C)C(O)=O",6.021,2,1,6]
["S1481","Zosuquidar (LY335979) 3HCl","f11","L1700-04","in 10mM DMSO","P-gp","Transmembrane Transporters","Zosuquidar 3HCl (LY335979, RS 33295-198, D06387) is a potent modulator of P-glycoprotein-mediated multi-drug resistance with Ki of 60 nM in a cell-free assay. Phase 3.",636.99,"167465-36-3",{"v":100,"d":"100.00"},156.99,{"v":23,"d":"23.00"},36.11,"http://selleckchem.com/products/LY335979.html","C32H31F2N3O2.3HCl","Trihydrochlorid","RS 33295-198 (D06387) 3HCl","Cl.Cl.Cl.OC(COC1=CC=CC2=C1C=CC=N2)CN3CCN(CC3)C4C5=C(C=CC=C5)C6C(C7=C4C=CC=C7)C6(F)F",5.845,2,1,6]
["S1482","Daclatasvir (BMS-790052)","g11","L1700-04","in 10mM DMSO","HCV Protease","Proteases","Daclatasvir (BMS-790052, EBP883) is a highly selective inhibitor of HCV NS5A with EC50 of 9-50 pM, for a broad range of HCV replicon genotypes and the JFH-1 genotype 2a infectious virus in cell culture. Phase 3.",738.88,"1009119-64-5",{"v":148,"d":"148.00"},{"v":200.3,"d":"200.30"},"<1","N/A","http://selleckchem.com/products/BMS-790052.html","C40H50N8O6","free base","EBP883","COC(=O)NC(C(C)C)C(=O)N1CCCC1C2=NC=C([NH]2)C3=CC=C(C=C3)C4=CC=C(C=C4)C5=CN=C([NH]5)C6CCCN6C(=O)C(NC(=O)OC)C(C)C",5.048,8,4,13]
["S1483","Iloperidone","h11","L1700-04","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Iloperidone (HP873) is a dopamine (D2)/serotonin (5-HT2) receptor antagonist, used for the treatment of schizophrenia.",426.48,"133454-47-4",{"v":27,"d":"27.00"},63.31,"<1","N/A","http://selleckchem.com/products/Iloperidone(Fanapt).html","C24H27FN2O4","free base","HP873","COC1=C(OCCCN2CCC(CC2)C3=NOC4=C3C=CC(=C4)F)C=CC(=C1)C(C)=O",4.016,5,0,8]
["S1484","MC1568","a2","L1700-05","in 10mM DMSO","HDAC","Cytoskeletal Signaling","MC1568 is a selective HDAC inhibitor for maize HD1-A with IC50 of 100 nM in a cell-free assay. It is 34-fold more selective for HD1-A than HD1-B.",314.31,"852475-26-4",{"v":13,"d":"13.00"},41.36,"<1","N/A","http://selleckchem.com/products/MC1568.html","C17H15FN2O3","free base","N/A","C[N]1C=C(/C=C/C(=O)C2=CC=CC(=C2)F)C=C1\\C=C\\C(=O)NO",2.981,2,1,5]
["S1485","HMN-214","b2","L1700-05","in 10mM DMSO","PLK","Cell Cycle","HMN-214 is a prodrug of HMN-176, which alters the cellular spatial orientation of Plk1.",424.47,"173529-46-9",{"v":12,"d":"12.00"},28.27,"<1","N/A","http://selleckchem.com/products/HMN-214.html","C22H20N2O5S","free base","N/A","COC1=CC=C(C=C1)[S](=O)(=O)N(C(C)=O)C2=C(C=CC=C2)\\C=C\\C3=CC=[N+]([O-])C=C3",2.282,4,0,6]
["S1486","AEE788 (NVP-AEE788)","c2","L1700-05","in 10mM DMSO","EGFR,HER2,VEGFR","Protein Tyrosine Kinase","AEE788 (NVP-AEE788) is a potent inhibitor of EGFR and HER2/ErbB2 with IC50 of 2 nM and 6 nM, less potent to VEGFR2/KDR, c-Abl, c-Src, and Flt-1, does not inhibit Ins-R, IGF-1R, PKCα and CDK1. Phase 1/2.",440.58,"497839-62-0",{"v":88,"d":"88.00"},199.74,"<1","N/A","http://selleckchem.com/products/AEE788.html","C27H32N6","free base","N/A","CCN1CCN(CC1)CC2=CC=C(C=C2)C3=CC4=C(NC(C)C5=CC=CC=C5)N=CN=C4[NH]3",5.042,2,2,7]
["S1487","PHA-793887","d2","L1700-05","in 10mM DMSO","Apoptosis related,CDK","Cell Cycle","PHA-793887 is a novel and potent inhibitor of CDK2, CDK5 and CDK7 with IC50 of 8 nM, 5 nM and 10 nM. It is greater than 6-fold more selective for CDK2, 5, and 7 than CDK1, 4, and 9. PHA-793887 induces cell-cycle arrest and apoptosis. Phase 1.",361.48,"718630-59-2",{"v":72,"d":"72.00"},199.18,"<1","N/A","http://selleckchem.com/products/PHA-793887.html","C19H31N5O2","free base","N/A","CC(C)CC(=O)NC1=N[NH]C2=C1CN(C(=O)C3CCN(C)CC3)C2(C)C",1.895,3,2,4]
["S1488","Naratriptan HCl","e2","L1700-05","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Naratriptan HCl is a triptan agent that is used for the treatment of migraine headaches.",371.93,"143388-64-1",{"v":74,"d":"74.00"},198.96,{"v":22,"d":"22.00"},59.15,"http://selleckchem.com/products/Naratriptan(Amerge).html","C17H25N3O2S.HCl","Hydrochloride","N/A","Cl.CN[S](=O)(=O)CCC1=CC=C2[NH]C=C(C3CCN(C)CC3)C2=C1",2.435,2,2,5]
["S1489","PIK-93","f2","L1700-05","in 10mM DMSO","PI4K","PI3K/Akt/mTOR","PIK-93 is the first potent, synthetic PI4K (PI4KIIIβ) inhibitor with IC50 of 19 nM; shown to inhibit PI3Kα with IC50 of 39 nM.",389.88,"593960-11-3",{"v":78,"d":"78.00"},200.06,"<1","N/A","http://selleckchem.com/products/PIK-93.html","C14H16ClN3O4S2","free base","N/A","CC(=O)NC1=NC(=C(S1)C2=CC(=C(Cl)C=C2)[S](=O)(=O)NCCO)C",1.076,4,3,6]
["S1490","Ponatinib (AP24534)","g2","L1700-05","in 10mM DMSO","Autophagy,Bcr-Abl,FGFR,PDGFR,Src,VEGFR","Angiogenesis","Ponatinib (AP24534) is a novel, potent multi-target inhibitor of Abl, PDGFRα, VEGFR2, FGFR1 and Src with IC50 of 0.37 nM, 1.1 nM, 1.5 nM, 2.2 nM and 5.4 nM in cell-free assays, respectively. Ponatinib (AP24534) inhibits autophagy.",532.56,"943319-70-8",{"v":30,"d":"30.00"},56.33,"<1","N/A","http://selleckchem.com/products/AP24534.html","C29H27F3N6O","free base","AP24534","CN1CCN(CC1)CC2=C(C=C(NC(=O)C3=CC(=C(C)C=C3)C#CC4=CN=C5C=CC=N[N]45)C=C2)C(F)(F)F",4.884,3,1,7]
["S1491","Fludarabine (NSC 118218)","h2","L1700-05","in 10mM DMSO","Apoptosis related,DNA/RNA Synthesis,Nucleoside Analog/Antimetabolite,STAT","JAK/STAT","Fludarabine (NSC 118218, FaraA, Fludarabinum) is a STAT1 activation inhibitor which causes a specific depletion of STAT1 protein (and mRNA) but not of other STATs. Also a DNA synthesis inhibitor in vascular smooth muscle cells. Fludarabine induces apoptosis.",285.23,"21679-14-1",{"v":57,"d":"57.00"},199.84,"<1","N/A","http://selleckchem.com/products/Fludarabine(Fludara).html","C10H12FN5O4","Free Base","FaraA, Fludarabinum, NSC 118218","NC1=NC(=NC2=C1N=C[N]2C3OC(CO)C(O)C3O)F",-1.312,4,4,2]
["S1497","Pralatrexate (NSC 754230)","a3","L1700-05","in 10mM DMSO","Apoptosis related,DHFR","Metabolism","Pralatrexate (NSC 754230) is an antifolate, and structurally a folate analog. Its IC50 is < 300 nM in some cell lines. Pralatrexate induces tumor cell apoptosis.",477.47,"146464-95-1",{"v":28,"d":"28.00"},58.64,"<1","N/A","http://selleckchem.com/products/Pralatrexate(Folotyn).html","C23H23N7O5","free base","NSC 754230","NC1=NC(=C2N=C(CC(CC#C)C3=CC=C(C=C3)C(=O)NC(CCC(O)=O)C(O)=O)C=NC2=N1)N",{"v":1.94,"d":"1.940"},7,3,10]
["S1499","Cefaclor","b3","L1700-05","in 10mM DMSO","Antibiotics","Microbiology","Cefaclor (Cefachlor, Cefaclorum) is a cephalosporin antibiotic.",385.82,"70356-03-5",{"v":11,"d":"11.00"},28.51,"<1","N/A","http://selleckchem.com/products/Cefaclor-(Ceclor).html","C15H14ClN3O4S.H2O","monohydrate","Cefachlor, Cefaclorum","O.NC(C(=O)NC1C2SCC(=C(N2C1=O)C(O)=O)Cl)C3=CC=CC=C3",{"v":-2.54,"d":"-2.540"},3,2,4]
["S1500","Betamethasone","c3","L1700-05","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Betamethasone (NSC-39470, SCH-4831) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive properties.",392.46,"378-44-9",{"v":79,"d":"79.00"},201.29,"<1","N/A","http://selleckchem.com/products/Betamethasone-(Celestone).html","C22H29FO5","Free Base","NSC-39470, SCH-4831","CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(O)C(=O)CO",1.708,2,2,2]
["S1501","Mycophenolate mofetil (RS-61443)","d3","L1700-05","in 10mM DMSO","Apoptosis related,Dehydrogenase","Metabolism","Mycophenolate Mofetil (RS 61443, Mycophenolic acid morpholinoethyl ester, CellCept, TM-MMF) is a non-competitive, selective and reversible inhibitor of inosine monophosphate dehydrogenase I/II with IC50 of 39 nM and 27 nM, respectively. Mycophenolate Mofetil induces caspase-dependent apoptosis and cell cycle inhibition in multiple myeloma cells.",433.49,"128794-94-5",{"v":86,"d":"86.00"},198.39,"<1","N/A","http://selleckchem.com/products/Mycophenolate-mofetil-(CellCept).html","C23H31NO7","free base","Mycophenolic acid morpholinoethyl ester, CellCept, RS 61443, TM-MMF","COC1=C(C)C2=C(C(=O)OC2)C(=C1C\\C=C(C)\\CCC(=O)OCCN3CCOCC3)O",3.209,6,1,10]
["S1504","Dyphylline","e3","L1700-05","in 10mM DMSO","PDE","Metabolism","Dyphylline (Diprophylline) is a xanthine derivative with bronchodilator and vasodilator effects.",254.24,"479-18-5",{"v":51,"d":"51.00"},{"v":200.6,"d":"200.60"},{"v":51,"d":"51.00"},{"v":200.6,"d":"200.60"},"http://selleckchem.com/products/Dyphylline(Dilor).html","C10H14N4O4","free base","Diprophylline","CN1C(=O)N(C)C2=C([N](CC(O)CO)C=N2)C1=O",-1.151,3,2,3]
["S1505","Aztreonam","f3","L1700-05","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Aztreonam (SQ 26776) is a synthetic monocyclic beta-lactam antibiotic, used to treat Gram-negative aerobic bacteria infection.",435.43,"78110-38-0",{"v":87,"d":"87.00"},{"v":199.8,"d":"199.80"},{"v":11,"d":"11.00"},25.26,"http://selleckchem.com/products/Aztreonam(Azactam).html","C13H17N5O8S2","free base","SQ 26776","CC1C(NC(=O)\\C(=N/OC(C)(C)C(O)=O)C2=CSC(=N2)N)C(=O)N1[S](O)(=O)=O",-1.035,6,2,7]
["S1508","Alprostadil","g3","L1700-05","in 10mM DMSO","PGES","Endocrinology & Hormones","Alprostadil (Prostaglandin-E1, PGE1, Edex, Muse, Liprostin) is used as a drug in the treatment of erectile dysfunction and has vasodilatory properties. It is a Prostaglandin Analog and Prostaglandin E1 Agonist.",354.48,"745-65-3",{"v":71,"d":"71.00"},200.29,"<1","N/A","http://selleckchem.com/products/Alprostadil(Caverject).html","C20H34O5","free base","Prostaglandin-E1, PGE1, Edex, Muse, Liprostin","CCCCCC(O)/C=C/C1C(O)CC(=O)C1CCCCCCC(O)=O",3.644,2,2,13]
["S1511","Lactulose","h3","L1700-05","in 10mM DMSO","Others","Others","Lactulose, a disaccharide composed of galactose and fructose, is a stimulator of health-promoting bacterium growth in the gastrointestinal tract, used to treat chronic constipation and hepatic encephalopathy.",{"v":342.3,"d":"342.30"},"4618-18-2",{"v":68,"d":"68.00"},198.66,{"v":68,"d":"68.00"},198.66,"http://selleckchem.com/products/Lactulose(Enulose).html","C12H22O11","free base","N/A","OCC(O)C(OC1OC(CO)C(O)C(O)C1O)C(O)C(=O)CO",-4.621,3,8,8]
["S1512","Tadalafil (IC351)","a4","L1700-05","in 10mM DMSO","PDE","Metabolism","Tadalafil (IC351) is a PDE-5 inhibitor with IC50 of 1.8 nM in a cell-free assay. Tadalafil is at least 9000 times more selective for PDE5 than most of the other families of PDEs, with the exception of PDE11. It can partial inhibits PDE11",{"v":389.4,"d":"389.40"},"171596-29-5",{"v":78,"d":"78.00"},200.31,"<1","N/A","http://selleckchem.com/products/Tadalafil(Cialis).html","C22H19N3O4","free base","IC351","CN1CC(=O)N2C(CC3=C([NH]C4=C3C=CC=C4)C2C5=CC=C6OCOC6=C5)C1=O",2.183,4,1,1]
["S1514","Cyclosporine","b4","L1700-05","in 10mM DMSO","Immunology & Inflammation related,phosphatase","Metabolism","Cyclosporine is a calcineurin phosphatase pathway inhibitor, used as an immunosuppressant drug to prevent rejection in organ transplantation.",1202.61,"79217-60-0",{"v":100,"d":"100.00"},83.15,"<1","N/A","http://selleckchem.com/products/Cyclosporine.html","C62H111N11O12","free base","Neoral","CCC1NC(=O)C(C(O)C(C)C\\C=C\\C)N(C)C(=O)C(C(C)C)N(C)C(=O)C(CC(C)C)N(C)C(=O)C(CC(C)C)N(C)C(=O)C(C)NC(=O)C(C)NC(=O)C(CC(C)C)N(C)C(=O)C(NC(=O)C(CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C",4.333,11,5,15]
["S1515","Pracinostat (SB939)","c4","L1700-05","in 10mM DMSO","Apoptosis related,HDAC","Cytoskeletal Signaling","Pracinostat (SB939) is a potent pan-HDAC inhibitor with IC50 of 40-140 nM with exception for HDAC6. It has no activity against the class III isoenzyme SIRT I. Pracinostat (SB939) induces apoptosis in tumor cells. Phase 2.",358.48,"929016-96-6",{"v":72,"d":"72.00"},200.85,"<1","N/A","http://selleckchem.com/products/SB939.html","C20H30N4O2","free base","N/A","CCCCC1=NC2=CC(=CC=C2[N]1CCN(CC)CC)\\C=C\\C(=O)NO",{"v":3.71,"d":"3.710"},2,1,10]
["S1517","Natamycin","d4","L1700-05","in 10mM DMSO","Fungal","Microbiology","Natamycin (Pimaricin), a natural and versatile anti-fungal agent during fermentation by the bacterium Streptomyces natalensis, commonly found in soil; with little to no flavour interference",665.73,"7681-93-8",{"v":7,"d":"7.00"},10.51,"<1","N/A","http://selleckchem.com/products/Natamycin(Pimaricin).html","C33H47NO13","free base","Pimaricin","CC1C/C=C/C=C/C=C/C=C/C(CC2OC(O)(CC(O)CC3OC3/C=C/C(=O)O1)CC(O)C2C(O)=O)OC4OC(C)C(O)C(N)C4O",-2.824,7,5,3]
["S1523","Voxtalisib (XL765) Analogue","e4","L1700-05","in 10mM DMSO","mTOR,PI3K","PI3K/Akt/mTOR","Voxtalisib (SAR245409, XL765) Analogue is a dual inhibitor of mTOR/PI3K, mostly for p110γ with IC50 of 9 nM; also inhibits DNA-PK and mTOR. Phase 1/2.",599.66,"1349796-36-6",{"v":12,"d":"12.00"},20.01,"<1","N/A","http://selleckchem.com/products/XL765(SAR245409).html","C31H29N5O6S","free base","SAR245409","COC1=CC(=CC(=C1)NC2=NC3=CC=CC=C3N=C2N[S](=O)(=O)C4=CC=C(NC(=O)C5=CC=C(C)C(=C5)OC)C=C4)OC",5.631,8,3,10]
["S1524","AT7519","f4","L1700-05","in 10mM DMSO","Apoptosis related,CDK,GSK-3","Cell Cycle","AT7519 is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9 with IC50 of 10-210 nM. It is less potent to CDK3 and little active to CDK7. AT7519 also decrease GSK3β phosphorylation. AT7519 induces apoptosis. Phase 2.",382.24,"844442-38-2",{"v":10,"d":"10.00"},26.16,"<1","N/A","http://selleckchem.com/products/AT7519.html","C16H17Cl2N5O2","Free Base","N/A","ClC1=CC=CC(=C1C(=O)NC2=C[NH]N=C2C(=O)NC3CCNCC3)Cl",1.599,3,4,4]
["S1525","Adavosertib (MK-1775)","g4","L1700-05","in 10mM DMSO","Wee1","Cell Cycle","Adavosertib (MK-1775, AZD1775) is a potent and selective Wee1 inhibitor with IC50 of 5.2 nM in a cell-free assay; hinders G2 DNA damage checkpoint. Phase 2.",{"v":500.6,"d":"500.60"},"955365-80-7",{"v":80,"d":"80.00"},159.81,"N/A","N/A","http://selleckchem.com/products/MK-1775.html","C27H32N8O2","free base","AZD1775","CN1CCN(CC1)C2=CC=C(NC3=NC4=C(C=N3)C(=O)N(CC=C)N4C5=NC(=CC=C5)C(C)(C)O)C=C2",4.158,4,1,7]
["S1526","Quizartinib (AC220)","h4","L1700-05","in 10mM DMSO","Apoptosis related,FLT3,Target Protein Ligand","Angiogenesis","Quizartinib (AC220) is a second-generation FLT3 inhibitor for Flt3(ITD/WT) with IC50 of 1.1 nM/4.2 nM in MV4-11 and RS4;11 cells, respectively, 10-fold more selective for Flt3 than KIT, PDGFRα, PDGFRβ, RET, and CSF-1R. Quizartinib (AC220) induces apoptosis of tumor cells. Phase 3.",560.67,"950769-58-1",{"v":33,"d":"33.00"},58.86,"<1","N/A","http://selleckchem.com/products/AC-220.html","C29H32N6O4S","free base","N/A","CC(C)(C)C1=CC(=NO1)NC(=O)NC2=CC=C(C=C2)C3=C[N]4C(=N3)SC5=CC(=CC=C45)OCCN6CCOCC6",5.064,6,2,8]
["S1528","LY2811376","a5","L1700-05","in 10mM DMSO","BACE,Beta Amyloid","Proteases","LY2811376 is the first orally available non-peptidic β-secretase(BACE1) inhibitor with IC50 of 239 nM-249 nM, that act to decrease Aβ secretion with EC50 of 300 nM, demonstrated to have 10-fold selectivity towards BACE1 over BACE2, and more than 50-fold inhibition over other aspartic proteases including cathepsin D, pepsin, or renin. Phase 1.",320.36,"1194044-20-6",{"v":16,"d":"16.00"},49.94,"<1","N/A","http://selleckchem.com/products/LY2811376.html","C15H14F2N4S","free base","N/A","CC1(CCSC(=N1)N)C2=CC(=C(F)C=C2F)C3=CN=CN=C3",2.478,3,1,2]
["S1529","Hesperadin","b5","L1700-05","in 10mM DMSO","Aurora Kinase","Cell Cycle","Hesperadin potently inhibits Aurora B with IC50 of 250 nM in a cell-free assay. It markedly reduces the activity of AMPK, Lck, MKK1, MAPKAP-K1, CHK1 and PHK while it does not inhibit MKK1 activity in vivo.",516.65,"422513-13-1",{"v":103,"d":"103.00"},199.36,"<1","N/A","http://selleckchem.com/products/Hesperadin.html","C29H32N4O3S","free base","N/A","CC[S](=O)(=O)NC1=CC=C2NC(=O)C(=C(NC3=CC=C(CN4CCCCC4)C=C3)/C5=CC=CC=C5)/C2=C1",4.071,3,3,8]
["S1530","BIX 02188","c5","L1700-05","in 10mM DMSO","MEK","MAPK","BIX02188 is a selective inhibitor of MEK5 with IC50 of 4.3 nM, also inhibits ERK5 catalytic activity with IC50 of 810 nM, and does not inhibit closely related kinases MEK1, MEK2, ERK2, and JNK2.",412.48,"1094614-84-2",{"v":43,"d":"43.00"},104.25,"<1","N/A","http://selleckchem.com/products/BIX-02188.html","C25H24N4O2","free base","N/A","CNC(=O)C1=CC=C\\2C(=C1)NC(=O)C2=C(\\NC3=CC(=CC=C3)CN(C)C)C4=CC=CC=C4",3.102,2,3,6]
["S1531","BIX 02189","d5","L1700-05","in 10mM DMSO","ERK,MEK","MAPK","BIX02189 is a selective inhibitor of MEK5 with IC50 of 1.5 nM, also inhibits ERK5 catalytic activity with IC50 of 59 nM in cell-free assays, and does not inhibit closely related kinases MEK1, MEK2, ERK2, and JNK2.",440.54,"1094614-85-3",{"v":60,"d":"60.00"},{"v":136.2,"d":"136.20"},"<1","N/A","http://selleckchem.com/products/BIX-02189.html","C27H28N4O2","free base","N/A","CN(C)CC1=CC=CC(=C1)N/C(C2=CC=CC=C2)=C/3C(=O)NC4=CC(=CC=C34)C(=O)N(C)C",3.308,2,2,6]
["S1532","AZD7762","e5","L1700-05","in 10mM DMSO","Chk","Cell Cycle","AZD7762 is a potent and selective inhibitor of Chk1 with IC50 of 5 nM in a cell-free assay. It is equally potent against Chk2 and less potent against CAM, Yes, Fyn, Lyn, Hck and Lck. Phase 1.",362.42,"860352-01-8",{"v":50,"d":"50.00"},137.96,"<1","N/A","http://selleckchem.com/products/AZD7762.html","C17H19FN4O2S","free base","N/A","NC(=O)NC1=C(SC(=C1)C2=CC(=CC=C2)F)C(=O)NC3CCCNC3",2.009,2,4,4]
["S1533","R406 (free base)","f5","L1700-05","in 10mM DMSO","Apoptosis related,FLT3,Syk","Angiogenesis","R406 (free base) is a potent Syk inhibitor with IC50 of 41 nM in a cell-free assay, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. R406 (free base) triggers apoptosis. Phase 1.",470.45,"841290-80-0",{"v":21,"d":"21.00"},44.64,"<1","N/A","http://selleckchem.com/products/R406(free-base).html","C22H23FN6O5","free base","N/A","COC1=C(OC)C(=CC(=C1)NC2=NC(=C(F)C=N2)NC3=NC4=C(OC(C)(C)C(=O)N4)C=C3)OC",3.881,8,3,7]
["S1534","Org 27569","g5","L1700-05","in 10mM DMSO","Cannabinoid Receptor","GPCR & G Protein","Org 27569 is an allosteric modulator of cannabinoid CB1 receptor, induces a CB1 receptor state that is characterized by enhanced agonist affinity and decreased inverse agonist affinity.",409.95,"868273-06-7",{"v":82,"d":"82.00"},200.02,"<1","N/A","http://selleckchem.com/products/Org-27569.html","C24H28ClN3O","free base","N/A","CCC1=C([NH]C2=CC=C(Cl)C=C12)C(=O)NCCC3=CC=C(C=C3)N4CCCCC4",6.213,1,2,6]
["S1536","CP-673451","h5","L1700-05","in 10mM DMSO","PDGFR","Protein Tyrosine Kinase","CP-673451 is a selective inhibitor of PDGFRα/β with IC50 of 10 nM/1 nM in cell-free assays, exhibits >450-fold selectivity over other angiogenic receptors, has antiangiogenic and antitumor activity.",{"v":417.5,"d":"417.50"},"343787-29-1",{"v":28,"d":"28.00"},67.07,"<1","N/A","http://selleckchem.com/products/CP-673451.html","C24H27N5O2","free base","N/A","COCCOC1=CC=C2[N](C=NC2=C1)C3=NC4=C(C=CC=C4C=C3)N5CCC(N)CC5",3.011,4,1,6]
["S1537","Vadimezan (ASA404)","a6","L1700-05","in 10mM DMSO","Antiviral,IFN,STING,TNF-alpha,VDA","Angiogenesis","Vadimezan (ASA404, NSC 640488, DMXAA) is a vascular disrupting agents (VDA) and competitive inhibitor of DT-diaphorase with Ki of 20 μM and IC50 of 62.5 μM in cell-free assays, respectively. DMXAA (Vadimezan) is also a STING agonist with potential antineoplastic activity. DMXAA (Vadimezan) potently induces IFN-β but relatively low TNF-α expression in vitro. DMXAA (Vadimezan) has antiviral activity. Phase 3.",282.29,"117570-53-3",{"v":7,"d":"7.00"},{"v":24.8,"d":"24.80"},"<1","N/A","http://selleckchem.com/products/DMXAA(ASA404).html","C17H14O4","free base","NSC 640488, DMXAA","CC1=C(C)C2=C(C=C1)C(=O)C3=C(O2)C(=CC=C3)CC(O)=O",3.601,3,0,2]
["S1538","Telaprevir (VX-950)","b6","L1700-05","in 10mM DMSO","COVID-19,HCV Protease","Proteases","Telaprevir (VX-950, LY-570310, MP-424) is an HCV NS3-4A serine protease inhibitor with IC50 of 0.35 μM.",679.85,"402957-28-2",{"v":136,"d":"136.00"},200.04,"<1","N/A","http://selleckchem.com/products/Telaprevir(VX-950).html","C36H53N7O6","free base","LY-570310, MP-424,VX-950","CCCC(NC(=O)C1C2CCCC2CN1C(=O)C(NC(=O)C(NC(=O)C3=NC=CN=C3)C4CCCCC4)C(C)(C)C)C(=O)C(=O)NC5CC5",2.685,8,4,14]
["S1540","Saxagliptin (BMS-477118)","c6","L1700-05","in 10mM DMSO","DPP","Proteases","Saxagliptin (BMS-477118, Onglyza) is a selective and reversible DPP4 inhibitor with IC50 of 26 nM.",315.41,"361442-04-8",{"v":63,"d":"63.00"},199.74,{"v":63,"d":"63.00"},199.74,"http://selleckchem.com/products/Saxagliptin(Onglyza).html","C18H25N3O2","Free Base","Onglyza,BMS-477118","NC(C(=O)N1C(CC2CC12)C#N)[C]34CC5[CH2]C(C[C](O)(C5)C3)C4",0.275,1,1,2]
["S1541","Selisistat (EX 527)","d6","L1700-05","in 10mM DMSO","Sirtuin","Epigenetics","Selisistat (EX 527, SEN0014196) is a potent and selective SIRT1 inhibitor with IC50 of 38 nM in a cell-free assay, exhibits >200-fold selectivity against SIRT2 and SIRT3. Phase 2.",248.71,"49843-98-3",{"v":49,"d":"49.00"},197.02,"<1","N/A","http://selleckchem.com/products/EX-527.html","C13H13ClN2O","free base","SEN0014196","NC(=O)C1CCCC2=C1[NH]C3=C2C=C(Cl)C=C3",3.149,1,2,1]
["S1544","AM1241","e6","L1700-05","in 10mM DMSO","Cannabinoid Receptor","GPCR & G Protein","AM-1241 is a selective cannabinoid CB2 receptor agonist with Ki of 3.4 nM, exhibits 82-fold selectivity over CB1 receptor.",503.33,"444912-48-5",{"v":101,"d":"101.00"},200.66,"<1","N/A","http://selleckchem.com/products/AM-1241.html","C22H22IN3O3","free base","N/A","CN1CCCCC1C[N]2C=C(C(=O)C3=CC(=CC=C3I)[N+]([O-])=O)C4=C2C=CC=C4",{"v":5.29,"d":"5.290"},1,0,5]
["S1545","SB408124","f6","L1700-05","in 10mM DMSO","OX Receptor","GPCR & G Protein","SB408124 is a non-peptide antagonist for OX1 receptor with Ki of 57 nM and 27 nM in both whole cell and membrane, respectively, exhibits 50-fold selectivity over OX2 receptor.",356.37,"288150-92-5",{"v":36,"d":"36.00"},101.02,"<1","N/A","http://selleckchem.com/products/sb-408124.html","C19H18F2N4O","free base","N/A","CN(C)C1=CC=C(NC(=O)NC2=CC(=NC3=C(F)C=C(F)C=C23)C)C=C1",3.565,2,2,3]
["S1547","Febuxostat","g6","L1700-05","in 10mM DMSO","ROS","Immunology & Inflammation","Febuxostat (TMX 67, TEI-6720) is a selective xanthine oxidase inhibitor with Ki of 0.6 nM.",316.37,"144060-53-7",{"v":63,"d":"63.00"},199.13,"<1","N/A","http://selleckchem.com/products/Febuxostat(Uloric).html","C16H16N2O3S","free base","TMX 67, TEI-6720","CC(C)COC1=C(C=C(C=C1)C2=NC(=C(S2)C(O)=O)C)C#N",3.468,3,0,5]
["S1548","Dapagliflozin (BMS-512148)","h6","L1700-05","in 10mM DMSO","SGLT","GPCR & G Protein","Dapagliflozin (BMS-512148) is a potent and selective hSGLT2 inhibitor with EC50 of 1.1 nM, exhibiting 1200-fold selectivity over hSGLT1. Phase 4.",408.87,"461432-26-8",{"v":82,"d":"82.00"},200.55,"<1","N/A","http://selleckchem.com/products/Dapagliflozin.html","C21H25ClO6","free base","BMS-512148","CCOC1=CC=C(CC2=CC(=CC=C2Cl)C3OC(CO)C(O)C(O)C3O)C=C1",2.409,2,4,6]
["S1549","Nebivolol hydrochloride (R-65824)","a7","L1700-05","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Nebivolol HCl (R-65824) selectively inhibits β1-adrenoceptor with IC50 of 0.8 nM.",{"v":441.9,"d":"441.90"},"152520-56-4",{"v":88,"d":"88.00"},199.14,"<1","N/A","http://selleckchem.com/products/Nebivolol(Bystolic).html","C22H25F2NO4.HCl","Hydrochloride","R-65824 hydrochloride","Cl.OC(CNCC(O)C1CCC2=C(O1)C=CC(=C2)F)C3CCC4=CC(=CC=C4O3)F",3.939,2,3,6]
["S1550","Pimobendan","b7","L1700-05","in 10mM DMSO","PDE","Metabolism","Pimobendan (UD-CG 115 BS) is a selective inhibitor of PDE3 with IC50 of 0.32 μM.",334.37,"74150-27-9",{"v":67,"d":"67.00"},200.38,"<1","N/A","http://selleckchem.com/products/Pimobendan(Vetmedin).html","C19H18N4O2","free base","UD-CG 115 BS","COC1=CC=C(C=C1)C2=NC3=CC(=CC=C3[NH]2)C4=NNC(=O)CC4C",2.936,4,2,3]
["S1553","Delafloxacin (ABT-492)","c7","L1700-05","in 10mM DMSO","Anti-infection","Immunology & Inflammation","Delafloxacin (ABT-492, RX-3341, WQ-3034) is a new fluoroquinolone against 155 aerobic and 171 anaerobic pathogens.",440.76,"189279-58-1, 339591-82-1 (sodium salt)",{"v":88,"d":"88.00"},199.66,"<1","N/A","http://www.selleck.cn/products/ABT-492.html","C18H12ClF3N4O4","free base","RX-3341J, WQ-3034","NC1=C(F)C=C(F)C(=N1)N2C=C(C(O)=O)C(=O)C3=CC(=C(N4CC(O)C4)C(=C23)Cl)F",2.682,3,2,3]
["S1555","AZD8055","d7","L1700-05","in 10mM DMSO","Apoptosis related,Autophagy,mTOR","PI3K/Akt/mTOR","AZD8055 is a novel ATP-competitive mTOR inhibitor with IC50 of 0.8 nM in MDA-MB-468 cells with excellent selectivity (∼1,000-fold) against PI3K isoforms and ATM/DNA-PK. AZD8055 induces caspase-dependent apoptosis and also induces autophagy. Phase 1.",465.54,"1009298-09-2",{"v":50,"d":"50.00"},{"v":107.4,"d":"107.40"},"<1","N/A","http://selleckchem.com/products/AZD8055.html","C25H31N5O4","free base","N/A","COC1=C(CO)C=C(C=C1)C2=NC3=C(C=C2)C(=NC(=N3)N4CCOCC4C)N5CCOCC5C",3.274,6,1,5]
["S1556","PHT-427","e7","L1700-05","in 10mM DMSO","Akt,PDPK1","PI3K/Akt/mTOR","PHT-427 (CS-0223) is a dual Akt and PDPK1 inhibitor (high affinity binding for the PH domains of Akt and PDPK1) with Ki of 2.7 μM and 5.2 μM, respectively.",409.61,"1191951-57-1",{"v":82,"d":"82.00"},200.19,"<1","N/A","http://selleckchem.com/products/PHT-427.html","C20H31N3O2S2","free base","CS-0223","CCCCCCCCCCCCC1=CC=C(C=C1)[S](=O)(=O)NC2=NN=CS2",6.296,4,1,14]
["S1557","KRN 633","f7","L1700-05","in 10mM DMSO","VEGFR","Protein Tyrosine Kinase","KRN 633 is an ATP-competitive inhibitor of VEGFR1/2/3 with IC50 of 170 nM/160 nM/125 nM, weakly inhibits PDGFR-α/β and c-Kit, does not block the phosphorylation of FGFR-1, EGFR or c-Met in cell.",416.86,"286370-15-8",{"v":9,"d":"9.00"},21.59,"<1","N/A","http://selleckchem.com/products/KRN-633.html","C20H21ClN4O4","free base","N/A","CCCNC(=O)NC1=CC=C(OC2=NC=NC3=CC(=C(OC)C=C23)OC)C=C1Cl",4.107,6,2,7]
["S1558","AT7867","g7","L1700-05","in 10mM DMSO","Akt,S6 Kinase","PI3K/Akt/mTOR","AT7867 is a potent ATP-competitive inhibitor of Akt1/2/3 and p70S6K/PKA with IC50 of 32 nM/17 nM/47 nM and 85 nM/20 nM in cell-free assays, respectively; little activity outside the AGC kinase family.",337.85,"857531-00-1",{"v":68,"d":"68.00"},201.27,"<1","N/A","http://selleckchem.com/products/AT7867.html","C20H20ClN3","free base","N/A","ClC1=CC=C(C=C1)C2(CCNCC2)C3=CC=C(C=C3)C4=C[NH]N=C4",{"v":3.85,"d":"3.850"},1,2,3]
["S1561","BMS-777607","h7","L1700-05","in 10mM DMSO","Axl,c-Met,RON,Tyro3","Protein Tyrosine Kinase","BMS-777607 (BMS 817378) is a Met-related inhibitor for c-Met, Axl, Ron and Tyro3 with IC50 of 3.9 nM, 1.1 nM, 1.8 nM and 4.3 nM in cell-free assays, 40-fold more selective for Met-related targets versus Lck, VEGFR-2, and TrkA/B, and more than 500-fold greater selectivity versus all other receptor and non receptor kinases.",512.89,"1025720-94-8",{"v":47,"d":"47.00"},91.64,"<1","N/A","http://selleckchem.com/products/BMS-777607.html","C25H19ClF2N4O4","free base","BMS 817378","CCOC1=C(C(=O)NC2=CC=C(OC3=CC=NC(=C3Cl)N)C(=C2)F)C(=O)N(C=C1)C4=CC=C(F)C=C4",3.517,5,2,7]
["S1565","Lumacaftor (VX-809)","a8","L1700-05","in 10mM DMSO","CFTR","Transmembrane Transporters","Lumacaftor (VX-809, VRT 826809) acts to correct CFTR mutations common in cystic fibrosis by increasing mutant CFTR (F508del-CFTR) maturation,EC50 of 0.1 μM in fisher rat thyroid cells. Phase 3.",452.41,"936727-05-8",{"v":90,"d":"90.00"},198.93,"<1","N/A","http://selleckchem.com/products/VX-809.html","C24H18F2N2O5","free base","VRT 826809","CC1=C(N=C(NC(=O)C2(CC2)C3=CC4=C(OC(F)(F)O4)C=C3)C=C1)C5=CC=CC(=C5)C(O)=O",6.411,5,1,5]
["S1567","Pomalidomide (CC-4047)","b8","L1700-05","in 10mM DMSO","Apoptosis related,E3 Ligase ,E3 ligase Ligand,TNF-alpha","Ubiquitin","Pomalidomide (CC-4047) inhibits LPS-induced TNF-α release with IC50 of 13 nM in PBMCs. Pomalidomide can be utilized in PROTAC as a ligand for targeting E3 ligase and inhibiting the E3 ligase protein cereblon (CRBN). Pomalidomide promotes apoptosis and cell cycle arrest.",273.24,"19171-19-8",{"v":54,"d":"54.00"},197.63,"<1","N/A","http://selleckchem.com/products/Pomalidomide(CC-4047).html","C13H11N3O4","free base","CC-4047","NC1=C2C(=O)N(C3CCC(=O)NC3=O)C(=O)C2=CC=C1",{"v":-0.65,"d":"-0.650"},4,2,1]
["S1568","PD318088","c8","L1700-05","in 10mM DMSO","MEK","MAPK","PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor, binds simultaneously with ATP in a region of the MEK1 active site that is adjacent to the ATP-binding site.",561.09,"391210-00-7",{"v":112,"d":"112.00"},199.61,"<1","N/A","http://selleckchem.com/products/PD318088.html","C16H13BrF3IN2O4","free base","N/A","OCC(O)CONC(=O)C1=C(NC2=CC=C(I)C=C2F)C(=C(F)C(=C1)Br)F",3.327,2,4,7]
["S1569","Tazarotene","d8","L1700-05","in 10mM DMSO","Retinoid Receptor","Metabolism","Tazarotene (AGN190168) is a retinoid prodrug of tazarotenic acid, which is a RAR agonist, used to treat psoriasis, acne, and sun damaged skin.",351.46,"118292-40-3",{"v":10,"d":"10.00"},28.45,"<1","N/A","http://selleckchem.com/products/Tazarotene(Avage).html","C21H21NO2S","free base","AGN190168","CCOC(=O)C1=CN=C(C=C1)C#CC2=CC3=C(SCCC3(C)C)C=C2",4.951,3,0,5]
["S1570","KU-60019","e8","L1700-05","in 10mM DMSO","ATM/ATR","DNA Damage/DNA Repair","KU-60019 is an improved analogue of KU-55933, with IC50 of 6.3 nM for ATM in cell-free assays, 270- and 1600-fold more selective for ATM than DNA-PK and ATR,and is a highly effective radiosensitizer.",547.67,"925701-49-1",{"v":18,"d":"18.00"},32.87,"<1","N/A","http://selleckchem.com/products/KU-60019.html","C30H33N3O5S","free base","N/A","CC1CN(CC(C)O1)CC(=O)NC2=CC3=C(SC4=C(C3)C=CC=C4C5=CC(=O)C=C(O5)N6CCOCC6)C=C2",3.818,5,1,5]
["S1572","BS-181 HCl","f8","L1700-05","in 10mM DMSO","CDK","Cell Cycle","BS-181 HCl is a highly selective CDK7 inhibitor with IC50 of 21 nM. It is more than 40-fold selective for CDK7 than CDK1, 2, 4, 5, 6, or 9.",416.99,"1397219-81-6",{"v":83,"d":"83.00"},199.05,{"v":3,"d":"3.00"},7.19,"http://selleckchem.com/products/BS-181.html","C22H32N6.HCl","Hydrochloride","N/A","Cl.CC(C)C1=C2N=C(NCCCCCCN)C=C(NCC3=CC=CC=C3)[N]2N=C1",4.684,2,3,11]
["S1573","Fasudil (HA-1077) HCl","g8","L1700-05","in 10mM DMSO","Autophagy,Calcium Channel,MLCK,PKA,PKC,PKG,Rho,ROCK","Cell Cycle","Fasudil (HA-1077, AT-877), a potent and selective inhibitor of Rho kinase, displays less potent inhibiton over PKA, PKG, PKC and MLCK with Ki of 1.6, 1.6, 3.3, and 36 μM in cell-free assays, respectively. Fasudil is also a calcium channel blocker.",327.83,"105628-07-7",{"v":5,"d":"5.00"},15.25,{"v":65,"d":"65.00"},198.27,"http://selleckchem.com/products/Fasudil-HCl(HA-1077).html","C14H17N3O2S.HCl","Hydrochloride","AT-877,HA-1077 HCl","Cl.O=[S](=O)(N1CCCNCC1)C2=C3C=CN=CC3=CC=C2",{"v":0.57,"d":"0.570"},3,1,2]
["S1574","Doramapimod (BIRB 796)","h8","L1700-05","in 10mM DMSO","JNK,p38 MAPK,Raf,Src","MAPK","Doramapimod (BIRB 796) is a  pan-p38 MAPK inhibitor with IC50 of  38 nM, 65 nM, 200 nM and 520 nM for p38α/β/γ/δ in cell-free assays, and binds p38α with Kd of 0.1 nM in THP-1 cells, 330-fold greater selectivity versus JNK2, weak inhibition for c-RAF, Fyn and Lck, insignificant inhibition of ERK-1, SYK, IKK2.",527.66,"285983-48-4",{"v":100,"d":"100.00"},189.52,"<1","N/A","http://selleckchem.com/products/BIRB-796-(Doramapimod).html","C31H37N5O3","free base","N/A","CC1=CC=C(C=C1)[N]2N=C(C=C2NC(=O)NC3=CC=C(OCCN4CCOCC4)C5=C3C=CC=C5)C(C)(C)C",5.907,4,2,8]
["S1576","Sulfasalazine (NSC 667219)","a9","L1700-05","in 10mM DMSO","Apoptosis related,Autophagy,COX,Ferroptosis,Immunology & Inflammation related,NF-κB,TGF-beta/Smad","Immunology & Inflammation","Sulfasalazine (NSC 667219, Azulfidine, Salazopyrin, Sulphasalazine) is a sulfa derivative of mesalazine, used as an anti-inflammatory agent to treat bowel disease and rheumatoid arthritis. Sulfasalazine is a potent and specific inhibitor of nuclear factor kappa B (NF-κB), TGF-β and COX-2. Sulfasalazine induces ferroptosis, apoptosis and autophagy.",398.39,"599-79-1",{"v":80,"d":"80.00"},200.81,"<1","N/A","http://selleckchem.com/products/Sulfasalazine(Azulfidine).html","C18H14N4O5S","free base","Azulfidine, Salazopyrin, Sulphasalazine, NSC 667219","OC(=O)C1=C(O)C=CC(=C1)N=NC2=CC=C(C=C2)[S](=O)(=O)NC3=CC=CC=N3",3.463,6,2,6]
["S1577","Tie2 kinase inhibitor","b9","L1700-05","in 10mM DMSO","Tie-2","Protein Tyrosine Kinase","Tie2 kinase inhibitor is an optimized compound of SB-203580, selective to Tie2 with IC50 of 0.25 μM, 200-fold more potent than p38.",439.53,"948557-43-5",{"v":35,"d":"35.00"},79.63,"<1","N/A","http://selleckchem.com/products/Tie2-kinase-inhibitor.html","C26H21N3O2S","free base","N/A","COC1=CC2=C(C=C1)C=C(C=C2)C3=C(N=C([NH]3)C4=CC=C(C=C4)[S](C)=O)C5=CC=NC=C5",{"v":4.57,"d":"4.570"},4,1,5]
["S1578","Candesartan (CV-11974)","c9","L1700-05","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Candesartan (CV-11974) is an angiotensin II receptor antagonist with IC50 of 0.26 nM.",440.45,"139481-59-7",{"v":88,"d":"88.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://selleckchem.com/products/Candesartan(Atacand).html","C24H20N6O3","free base","CV-11974","CCOC1=NC2=C([N]1CC3=CC=C(C=C3)C4=CC=CC=C4C5=N[NH]N=N5)C(=CC=C2)C(O)=O",4.626,6,1,7]
["S1582","H 89 2HCl","d9","L1700-05","in 10mM DMSO","Autophagy,PKA,PKG,S6 Kinase","PI3K/Akt/mTOR","H 89 2HCl is a potent PKA inhibitor with Ki of 48 nM in a cell-free assay, 10-fold selective for PKA than PKG,500-fold greater selectivity than PKC, MLCK, calmodulin kinase II and casein kinase I/II. H 89 2HCl induces autophagy.",519.28,"130964-39-5",{"v":104,"d":"104.00"},200.28,{"v":6,"d":"6.00"},11.55,"http://selleckchem.com/products/H-89-dihydrochloride.html","C20H20BrN3O2S.2HCl","Dihydrochloride","N/A","Cl.Cl.BrC1=CC=C(/C=C/CNCCN[S](=O)(=O)C2=CC=CC3=C2C=CN=C3)C=C1",3.665,3,2,8]
["S1590","TWS119","e9","L1700-05","in 10mM DMSO","Autophagy,GSK-3","PI3K/Akt/mTOR","TWS119 is a GSK-3β inhibitor with IC50 of 30 nM in a cell-free assay; capable of inducing neuronal differentiation and may be useful to stem cell biology. GSK-3β inhibition triggers autophagy.",318.33,"601514-19-6",{"v":64,"d":"64.00"},201.05,"<1","N/A","http://selleckchem.com/products/TWS119.html","C18H14N4O2","free base","N/A","NC1=CC(=CC=C1)C2=CC3=C([NH]2)N=CN=C3OC4=CC=CC(=C4)O",3.464,3,3,3]
["S1591","Bestatin (NK421)","f9","L1700-05","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Bestatin (Ubenimex,NK421) is a potent aminopeptidase-B and leukotriene (LT) A4 hydrolase inhibitor, used in the treatment of acute myelocytic leukemia.",308.37,"58970-76-6",{"v":4,"d":"4.00"},12.97,"<1","N/A","http://www.selleck.cn/products/Ubenimex(Bestatin).html","C16H24N2O4","Free Base","Ubenimex,NK421","CC(C)CC(NC(=O)C(O)C(N)CC1=CC=CC=C1)C(O)=O",{"v":-1.34,"d":"-1.340"},2,3,8]
["S1593","Apixaban (BMS 562247-01)","g9","L1700-05","in 10mM DMSO","Factor Xa","Metabolism","Apixaban (BMS 562247-01) is a highly selective, reversible inhibitor of Factor Xa with Ki of 0.08 nM and 0.17 nM in human and rabbit, respectively.",{"v":459.5,"d":"459.50"},"503612-47-3",{"v":18,"d":"18.00"},39.17,"<1","N/A","http://selleckchem.com/products/Apixaban(BMS-562247-01).html","C25H25N5O4","free base","BMS 562247-01","COC1=CC=C(C=C1)[N]2N=C(C(N)=O)C3=C2C(=O)N(CC3)C4=CC=C(C=C4)N5CCCCC5=O",2.865,5,1,5]
["S1594","Semagacestat (LY450139)","h9","L1700-05","in 10mM DMSO","Beta Amyloid,Notch,Secretase","Proteases","Semagacestat (LY450139) is a γ-secretase blocker for Aβ42, Aβ40 and Aβ38 with IC50 of 10.9 nM, 12.1 nM and 12.0 nM, also inhibits Notch signaling with IC50 of 14.1 nM in H4 human glioma cell. Phase 3.",361.44,"425386-60-3",{"v":72,"d":"72.00"},{"v":199.2,"d":"199.20"},"<1","N/A","http://selleckchem.com/products/Semagacestat(LY450139).html","C19H27N3O4","free base","N/A","CC(C)C(O)C(=O)NC(C)C(=O)NC1C(=O)N(C)CCC2=C1C=CC=C2",0.632,3,3,5]
["S1601","Reserpine","a10","L1700-05","in 10mM DMSO","VMAT","Transmembrane Transporters","Reserpine is an inhibitor of multidrug efflux pumps, used as an antipsychotic and antihypertensive drug. Reserpine is an inhibitor of the vesicular monoamine transporter 2 (VMAT2).",608.68,"50-55-5",{"v":13,"d":"13.00"},21.36,"<1","N/A","http://selleckchem.com/products/Reserpine.html","C33H40N2O9","free base","N/A","COC1C(CC2CN3CCC4=C([NH]C5=C4C=CC(=C5)OC)C3CC2C1C(=O)OC)OC(=O)C6=CC(=C(OC)C(=C6)OC)OC",4.242,9,1,10]
["S1603","Furosemide (NSC 269420)","b10","L1700-05","in 10mM DMSO","NKCC","Transmembrane Transporters","Furosemide (NSC 269420) is a potent NKCC2 (Na-K-2Cl symporter) inhibitor, used in the treatment of congestive heart failure and edema.",330.74,"54-31-9",{"v":66,"d":"66.00"},199.55,"<1","N/A","http://selleckchem.com/products/Furosemide(Lasix).html","C12H11ClN2O5S","free base","NSC 269420","N[S](=O)(=O)C1=C(Cl)C=C(NCC2=CC=CO2)C(=C1)C(O)=O",1.403,4,2,5]
["S1604","Olmesartan Medoxomil","c10","L1700-05","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Olmesartan Medoxomil (CS-866,RNH-6270) is a selective angiotensin II type 1 (AT(1)) receptor antagonist, used in the treatment of high blood pressure.",558.59,"144689-63-4",{"v":89,"d":"89.00"},159.33,"<1","N/A","http://selleckchem.com/products/olmesartan-medoxomil-Benicar.html","C29H30N6O6","free base","CS-866,RNH-6270","CCCC1=NC(=C([N]1CC2=CC=C(C=C2)C3=CC=CC=C3C4=N[NH]N=N4)C(=O)OCC5=C(C)OC(=O)O5)C(C)(C)O",4.814,9,1,11]
["S1605","Cefdinir","d10","L1700-05","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Cefdinir (FK 482, PD 134393, CI-983) is an oral cephalosporin antibiotic, used to treat bacterial infections in many different parts of the body.",395.41,"91832-40-5",{"v":79,"d":"79.00"},199.79,"<1","N/A","http://selleckchem.com/products/Cefdinir(Omnicef).html","C14H13N5O5S2","free base","FK 482, PD 134393, CI-983","NC1=NC(=CS1)C(=N/O)/C(=O)NC2C3SCC(=C(N3C2=O)C(O)=O)C=C",-0.172,5,2,5]
["S1606","Clotrimazole","e10","L1700-05","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Fungal","Microbiology","Clotrimazole (BAY b 5097, FB 5097) alters the permeability of the fungal cell wall by inhibiting the biosynthesis of ergosterol, used in the treatment of fungal infections.",344.84,"23593-75-1",{"v":11,"d":"11.00"},{"v":31.9,"d":"31.90"},"<1","N/A","http://selleckchem.com/products/Clotrimazole(Canesten).html","C22H17ClN2","free base","BAY b 5097, FB 5097","ClC1=C(C=CC=C1)C([N]2C=CN=C2)(C3=CC=CC=C3)C4=CC=CC=C4",5.222,1,0,4]
["S1607","Rizatriptan Benzoate","f10","L1700-05","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Rizatriptan Benzoate (MK-462) is an agonist at serotonin 5-HT1B and 5-HT1D receptors, used to treat acute migraine attacks.",391.47,"145202-66-0",{"v":20,"d":"20.00"},51.09,{"v":46,"d":"46.00"},117.51,"http://selleckchem.com/products/Rizatriptan-Benzoate(Maxalt).html","C22H25N5O2","Benzoate","MK-462 Benzoate","CN(C)CCC1=C[NH]C2=C1C=C(C[N]3C=NC=N3)C=C2.OC(=O)C4=CC=CC=C4",0.492,3,1,6]
["S1608","Pyridostigmine Bromide","g10","L1700-05","in 10mM DMSO","AChR","Neuronal Signaling","Pyridostigmine Bromide is a parasympathomimetic and a reversible cholinesterase inhibitor.",261.12,"101-26-8",{"v":52,"d":"52.00"},199.14,{"v":52,"d":"52.00"},199.14,"http://selleckchem.com/products/Pyridostigmine-Bromide(Mestinon).html","C9H13BrN2O2","Bromide","N/A","[Br-].CN(C)C(=O)OC1=C[N+](=CC=C1)C",-1.014,2,0,2]
["S1609","Methimazole","h10","L1700-05","in 10mM DMSO","Others","Others","Methimazole (Tapazole, Thiamazole) is an antithyroid medicine.",114.17,"60-56-0",{"v":23,"d":"23.00"},201.45,{"v":23,"d":"23.00"},201.45,"http://selleckchem.com/products/Methimazole(Tapazole).html","C4H6N2S","free base","Tapazole, Thiamazole","CN1C=CNC1=S",0.414,0,1,0]
["S1610","Metolazone","a11","L1700-05","in 10mM DMSO","Others","Others","Metolazone (SR 720-22) is a diuretic that primarily used to treat congestive heart failure and high blood pressure.",365.83,"17560-51-9",{"v":73,"d":"73.00"},199.55,"<1","N/A","http://selleckchem.com/products/Metolazone(Zaroxolyn).html","C16H16ClN3O3S","free base","SR 720-22","CC1NC2=CC(=C(C=C2C(=O)N1C3=CC=CC=C3C)[S](N)(=O)=O)Cl",2.463,3,2,2]
["S1611","Cefoperazone","b11","L1700-05","in 10mM DMSO","Antibiotics","Microbiology","Cefoperazone is a cephalosporin antibiotic for inhibition of rMrp2-mediated [3H]E217βG uptake with IC50 of 199 μM.",645.67,"62893-19-0",{"v":100,"d":"100.00"},154.88,"<1","N/A","http://selleckchem.com/products/cefoperazone-cefobid.html","C25H27N9O8S2","free base","N/A","CCN1CCN(C(=O)NC(C(=O)NC2C3SCC(=C(N3C2=O)C(O)=O)CSC4=NN=N[N]4C)C5=CC=C(O)C=C5)C(=O)C1=O",-0.792,9,3,9]
["S1613","Silodosin","c11","L1700-05","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Silodosin (KAD 3213, KMD 3213) is a highly selective α1A-adrenoceptor antagonist, used in treatment of benign prostatic hyperplasia.",495.53,"160970-54-7",{"v":99,"d":"99.00"},199.79,"<1","N/A","http://selleckchem.com/products/Silodosin(Rapaflo).html","C25H32F3N3O4","free base","KAD 3213, KMD 3213","CC(CC1=CC2=C(N(CCCO)CC2)C(=C1)C(N)=O)NCCOC3=CC=CC=C3OCC(F)(F)F",3.451,3,3,14]
["S1614","Riluzole (PK 26124)","d11","L1700-05","in 10mM DMSO","GluR,Sodium Channel","Transmembrane Transporters","Riluzole (PK 26124, RP-54274) is a glutamate release inhibitor with neuroprotective, anticonvulsant, anxiolytic and anesthetic qualities.",{"v":234.2,"d":"234.20"},"1744-22-5",{"v":46,"d":"46.00"},196.41,"<1","N/A","http://selleckchem.com/products/Riluzole(Rilutek).html","C8H5F3N2OS","free base","RP-54274, PK 26124","NC1=NC2=C(S1)C=C(OC(F)(F)F)C=C2",3.828,2,1,2]
["S1618","Sulfameter","e11","L1700-05","in 10mM DMSO","Bacterial","Immunology & Inflammation","Sulfameter  is a long-acting sulfonamide antibacterial.",{"v":280.3,"d":"280.30"},"651-06-9",{"v":56,"d":"56.00"},199.79,"<1","N/A","http://selleckchem.com/products/Sulfameter(Bayrena).html","C11H12N4O3S","free base","N/A","COC1=CN=C(N[S](=O)(=O)C2=CC=C(N)C=C2)N=C1",0.297,5,2,4]
["S1619","Prilocaine","f11","L1700-05","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Prilocaine (NSC 40027) is a local anesthetic of the amino amide type. It acts on sodium channels on the neuronal cell membrane, limiting the spread of seizure activity and reducing seizure propagation.",220.31,"721-50-6",{"v":44,"d":"44.00"},199.72,"<1","N/A","http://selleckchem.com/products/Prilocaine.html","C13H20N2O","free base","NSC 40027","CCCNC(C)C(=O)NC1=C(C)C=CC=C1",2.263,1,2,5]
["S1620","Darunavir Ethanolate","g11","L1700-05","in 10mM DMSO","COVID-19,HIV Protease","Proteases","Darunavir Ethanolate (TMC-114, UIC 94017) is a nonpeptidic HIV protease inhibitor, used to treat HIV infection.",593.73,"635728-49-3",{"v":100,"d":"100.00"},168.43,"<1","N/A","http://selleckchem.com/products/Darunavir-Ethanolate(Prezista).html","C27H37N3O7S.C2H5OH","Ethanolate","TMC-114, UIC 94017","CCO.CC(C)CN(CC(O)C(CC1=CC=CC=C1)NC(=O)OC2COC3OCCC23)[S](=O)(=O)C4=CC=C(N)C=C4",2.622,6,4,12]
["S1622","Prednisone (NSC-10023)","h11","L1700-05","in 10mM DMSO","Glucocorticoid Receptor,Immunology & Inflammation related","Endocrinology & Hormones","Prednisone (NSC-10023, Adasone) is a synthetic corticosteroid agent that is particularly effective as an immunosuppressant compound.",358.43,"53-03-2",{"v":71,"d":"71.00"},198.09,"<1","N/A","http://selleckchem.com/products/Prednisone.html","C21H26O5","free base","Adasone,NSC-10023","CC12CC(=O)C3C(CCC4=CC(=O)C=CC34C)C1CCC2(O)C(=O)CO",1.217,3,1,2]
["S1625","Ethinyl Estradiol","a2","L1700-06","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Ethinyl Estradiol is an orally bio-active estrogen used in almost all modern formulations of combined oral contraceptive pills.",{"v":296.4,"d":"296.40"},"57-63-6",{"v":59,"d":"59.00"},199.06,"<1","N/A","http://selleckchem.com/products/Ethinyl-Estradiol.html","C20H24O2","free base","N/A","CC12CCC3C(CCC4=CC(=CC=C34)O)C1CCC2(O)C#C",4.886,0,1,0]
["S1626","Naproxen Sodium","b2","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Naproxen Sodium (RS-3650) is a COX inhibitor for COX-1 and COX-2 with IC50 of 8.7 μM and 5.2 μM, respectively.",252.24,"26159-34-2",{"v":3,"d":"3.00"},11.89,{"v":50,"d":"50.00"},198.22,"http://selleckchem.com/products/Naproxen-Sodium(Aleve).html","C14H13NaO3","Sodium Salt","RS-3650","[Na+].COC1=CC=C2C=C(C=CC2=C1)C(C)C([O-])=O",1.375,1,0,3]
["S1627","Nitazoxanide (NSC 697855)","c2","L1700-06","in 10mM DMSO","Autophagy,Influenza Virus,mTOR,Serotonin Transporter","Microbiology","Nitazoxanide (NTZ, NSC 697855) is a synthetic nitrothiazolyl-salicylamide derivative and an antiprotozoal agent(IC50 for canine influenza virus ranges from 0.17 to 0.21 μM). Nitazoxanide modulates autophagy and inhibits mTORC1 signaling.",307.28,"55981-09-4",{"v":62,"d":"62.00"},201.77,"<1","N/A","http://selleckchem.com/products/Nitazoxanide(Alinia).html","C12H9N3O5S","free base","NTZ, NSC 697855","CC(=O)OC1=C(C=CC=C1)C(=O)NC2=NC=C(S2)[N+]([O-])=O",1.398,4,1,5]
["S1628","Triamcinolone Acetonide","d2","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Metabolism","Triamcinolone acetonide is a synthetic glucocorticoid, used in the symptomatic treatment of inflammation.",{"v":434.5,"d":"434.50"},"76-25-5",{"v":87,"d":"87.00"},200.23,"<1","N/A","http://selleckchem.com/products/Triamcinolone-Acetonide.html","C24H31FO6","free base","N/A","CC1(C)OC2CC3C4CCC5=CC(=O)C=CC5(C)C4(F)C(O)CC3(C)C2(O1)C(=O)CO",1.157,4,2,2]
["S1629","Orlistat (Ro 18-0647)","e2","L1700-06","in 10mM DMSO","Apoptosis related,Fatty Acid Synthase,Lipase","Metabolism","Orlistat (Ro 18-0647, Tetrahydrolipstatin) is a general lipase inhibitor with IC50 of 122 ng/ml for PL from human duodenal juice. Orlistat treatment reduces proliferation, induces apoptosis and arrests cell cycle.",495.73,"96829-58-2",{"v":99,"d":"99.00"},199.71,"<1","N/A","http://selleckchem.com/products/Orlistat(Alli).html","C29H53NO5","free base","Tetrahydrolipstatin,Ro 18-0647","CCCCCCCCCCCC(CC1OC(=O)C1CCCCCC)OC(=O)C(CC(C)C)NC=O",8.333,5,1,23]
["S1630","Allopurinol","f2","L1700-06","in 10mM DMSO","ROS","Immunology & Inflammation","Allopurinol is a purine analog inhibitor of the enzyme xanthine oxidase, used to treat gout or kidney stones, and to decrease levels of uric acid.",136.11,"315-30-0",{"v":27,"d":"27.00"},198.37,{"v":4,"d":"4.00"},29.39,"http://selleckchem.com/products/Allopurinol(Zyloprim).html","C5H4N4O","Free Base","N/A","O=C1N=CN=C2NNC=C12",-2.125,3,2,0]
["S1631","Allopurinol Sodium","g2","L1700-06","in 10mM DMSO","ROS","Immunology & Inflammation","Allopurinol Sodium  is a xanthine oxidase inhibitor with an IC50 of 7.82±0.12 μM.",{"v":159.1,"d":"159.10"},"17795-21-0",{"v":32,"d":"32.00"},201.13,{"v":32,"d":"32.00"},201.13,"http://selleckchem.com/products/Allopurinol-Sodium(Aloprim).html","C5H4N4NaO","Sodium Salt","N/A","[Na+].O=C1NC=NC2=C1C=N[NH]2",-0.681,3,2,0]
["S1633","Zafirlukast (ICI-204219)","h2","L1700-06","in 10mM DMSO","LTR","Immunology & Inflammation","Zafirlukast (ICI-204219) is an oral leukotriene receptor antagonist (LTRA), used to prevent asthma symptoms.",575.68,"107753-78-6",{"v":100,"d":"100.00"},173.71,"<1","N/A","http://selleckchem.com/products/Zafirlukast(Accolate).html","C31H33N3O6S","free base","ICI-204219","COC1=CC(=CC=C1CC2=C[N](C)C3=C2C=C(NC(=O)OC4CCCC4)C=C3)C(=O)N[S](=O)(=O)C5=CC=CC=C5C",6.299,6,2,9]
["S1635","Erythromycin","a3","L1700-06","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture","Microbiology","Erythromycin (E-Mycin) is a macrolide antibiotic that has an antimicrobial spectrum similar to or slightly wider than that of penicillin (IC50=1.5 μg/ml).",733.93,"114-07-8",{"v":147,"d":"147.00"},200.29,{"v":3,"d":"3.00"},4.09,"http://selleckchem.com/products/Erythromycin(E-Mycin).html","C37H67NO13","Free Base","E-Mycin","CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(O)CC(C)C(=O)C(C)C(O)C1(C)O",1.792,8,3,7]
["S1636","Amphotericin B","b3","L1700-06","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture","Microbiology","Amphotericin B (AMB, NSC 527017) is an amphipathic polyene antibiotic which permeabilizes ergosterol-containing membranes.",924.08,"1397-89-3",{"v":22,"d":"22.00"},23.81,"<1","N/A","http://selleckchem.com/products/Amphotericin-B(Abelcet).html","C47H73NO17","free base","NSC 527017","CC1OC(OC/2CC3OC(O)(CC(O)CC(O)C(O)CCC(O)CC(O)CC(=O)OC(C)C(C)C(O)C(C)\\C=C\\C=C\\C=C\\C=C\\C=C\\C=C\\C=C2)CC(O)C3C(O)=O)C(O)C(N)C1O",-2.617,6,10,3]
["S1638","Ibuprofen (NSC 256857)","c3","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Ibuprofen (NSC 256857, Dolgesic) is an anti-inflammatory inhibitor targeting COX-1 and COX-2 with IC50 of 13 μM and 370 μM, respectively.",206.28,"15687-27-1",{"v":41,"d":"41.00"},198.76,"<1","N/A","http://selleckchem.com/products/Ibuprofen(Advil).html","C13H18O2","free base","Dolgesic,NSC 256857","CC(C)CC1=CC=C(C=C1)C(C)C(O)=O",3.607,1,0,4]
["S1639","Amprenavir (VX-478)","d3","L1700-06","in 10mM DMSO","HIV Protease","Proteases","Amprenavir (VX-478, 141W94, KVX-478) is a potent PXR-selective agonist, and an HIV protease inhibitor, used to treat HIV.",505.63,"161814-49-9",{"v":16,"d":"16.00"},31.64,"<1","N/A","http://selleckchem.com/products/Amprenavir-(Agenerase).html","C25H35N3O6S","free base","141W94, VX-478, KVX-478","CC(C)CN(CC(O)C(CC1=CC=CC=C1)NC(=O)OC2CCOC2)[S](=O)(=O)C3=CC=C(N)C=C3",2.429,5,3,12]
["S1640","Albendazole (SKF-62979)","e3","L1700-06","in 10mM DMSO","ADC Cytotoxin,Microtubule Associated","Cytoskeletal Signaling","Albendazole (SKF-62979) is a member of the benzimidazole compounds used as a drug indicated for the treatment of a variety of worm infestations.",265.33,"54965-21-8",{"v":17,"d":"17.00"},64.07,"<1","N/A","http://selleckchem.com/products/Albendazole(Albenza).html","C12H15N3O2S","free base","SKF-62979","CCCSC1=CC=C2N=C(NC(=O)OC)[NH]C2=C1",3.065,3,2,5]
["S1641","Chlorothiazide","f3","L1700-06","in 10mM DMSO","Others","Others","Chlorothiazide is a diuretic and antihypertensive. (IC50=3.8 mM)",295.72,"58-94-6",{"v":59,"d":"59.00"},199.51,"<1","N/A","http://selleckchem.com/products/Chlorothiazide(Diuril).html","C7H6ClN3O4S2","free base","N/A","N[S](=O)(=O)C1=C(Cl)C=C2N=CN[S](=O)(=O)C2=C1",-0.177,5,2,1]
["S1643","Ursodiol","g3","L1700-06","in 10mM DMSO","FXR","GPCR & G Protein","Ursodiol (Ursodeoxycholic acid, UDCA) reduces cholesterol absorption and is used to dissolve (cholesterol) gallstones. (IC50=0.22 μM)",392.57,"128-13-2",{"v":79,"d":"79.00"},201.24,"<1","N/A","http://selleckchem.com/products/Ursodiol(Actigal).html","C24H40O4","free base","Ursodeoxycholic acid, UDCA","CC(CCC(O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CCC12C",4.014,1,2,4]
["S1644","Nitrofural","h3","L1700-06","in 10mM DMSO","Anti-infection","Microbiology","Nitrofural (Nitrofurazone) is a topical anti-infective agent with an IC50 of 22.83 ± 1.2 μM. (Rat LD50 = 590 mg/kg)",198.14,"59-87-0",{"v":40,"d":"40.00"},201.88,"<1","N/A","http://selleckchem.com/products/Nitrofurazone(ACTIN-N).html","C6H6N4O4","free base","Nitrofurazone","NC(=O)N/N=C/C1=CC=C(O1)[N+]([O-])=O",0.223,3,2,3]
["S1645","Ketoprofen","a4","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Ketoprofen (RP-19583) is a dual COX1/2 inhibitor, used as a nonsteroidal anti-inflammatory drug to treat arthritis-related inflammatory pains.",254.28,"22071-15-4",{"v":51,"d":"51.00"},200.57,"<1","N/A","http://selleckchem.com/products/Ketoprofen(Actron).html","C16H14O3","free base","RP-19583","CC(C(O)=O)C1=CC(=CC=C1)C(=O)C2=CC=CC=C2",3.361,2,0,4]
["S1646","Ketorolac","b4","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Ketorolac is a non-selective COX inhibitor of COX-1 and COX-2 with IC50 of 1.23 μM and 3.50 μM, respectively.",255.27,"74103-06-3",{"v":75,"d":"75.00"},293.81,"<1","N/A","http://selleckchem.com/products/Ketorolac-Tromethamine(Toradol).html","C15H13N1O3","free base","N/A","OC(=O)C1CC[N]2C1=CC=C2C(=O)C3=CC=CC=C3",2.832,2,0,3]
["S1647","Adenosine","c4","L1700-06","in 10mM DMSO","Adenosine Receptor,Nucleoside Analog/Antimetabolite","GPCR & G Protein","Adenosine is a nucleoside composed of a molecule of adenine attached to a ribose sugar molecule (ribofuranose) moiety via a β-N9-glycosidic bond.",267.24,"58-61-7",{"v":12,"d":"12.00"},{"v":44.9,"d":"44.90"},"<1","N/A","http://selleckchem.com/products/Adenosine(Adenocard).html","C10H13N5O4","free base","N/A","NC1=NC=NC2=C1N=C[N]2C3OC(CO)C(O)C3O",-1.881,4,4,2]
["S1649","Zolmitriptan","d4","L1700-06","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Zolmitriptan(BW-311C90) is a novel and highly selective 5-HT(1B/1D) receptor agonist, used in the treatment of acute migraines.",287.36,"139264-17-8",{"v":58,"d":"58.00"},201.84,"<1","N/A","http://selleckchem.com/products/Zolmitriptan(Zomig).html","C16H21N3O2","free base","BW-311C90","CN(C)CCC1=C[NH]C2=C1C=C(CC3COC(=O)N3)C=C2",2.457,2,2,5]
["S1651","Telbivudine","e4","L1700-06","in 10mM DMSO","Reverse Transcriptase","Microbiology","Telbivudine(NV 02B) is a potent, and selective HBV reverse transcriptase inhibitor, used to treat HBV infection.",242.23,"3424-98-4",{"v":48,"d":"48.00"},198.16,{"v":48,"d":"48.00"},198.16,"http://selleckchem.com/products/Telbivudine(Sebivo).html","C10H14N2O5","free base","NV 02B","CC1=CN(C2CC(O)C(CO)O2)C(=O)NC1=O",-1.238,3,3,2]
["S1652","Monobenzone","f4","L1700-06","in 10mM DMSO","Tyrosinase","Proteases","Monobenzone(Benoquin) is a compound used as a topical agent for medical depigmentation. It can specifically block tyrosinase.",200.23,"103-16-2",{"v":40,"d":"40.00"},199.77,"<1","N/A","http://selleckchem.com/products/Monobenzone(Benoquin).html","C13H12O2","free base","Benoquin","OC1=CC=C(OCC2=CC=CC=C2)C=C1",3.155,1,1,3]
["S1653","Tretinoin (NSC 122758)","g4","L1700-06","in 10mM DMSO","Retinoid Receptor","Metabolism","Tretinoin (Retinoic acid, All-trans Retinoic Acid, ATRA, Vitamin A acid, Vesanoid, Airol, Renova, Atralin, Retin-A, Avita, Stieva-A,NSC 122758), which is a ligand for both the retinoic acid receptor (RAR) and the retinoid X receptor (RXR), can induce granulocytic differentiation and apoptosis in acute promyelocytic leukemia (APL) cells.",{"v":300.4,"d":"300.40"},"302-79-4",{"v":60,"d":"60.00"},199.73,"<1","N/A","http://selleckchem.com/products/Tretinoin(Aberela).html","C20H28O2","free base","Retinoic acid, All-trans Retinoic Acid, ATRA, Vitamin A acid, Vesanoid, Airol, Renova, Atralin, Retin-A, Avita, Stieva-A,NSC 122758","CC1=C(\\C=C\\C(C)=C\\C=C\\C(C)=C\\C(O)=O)C(C)(C)CCC1",5.551,1,0,5]
["S1654","Phenylbutazone","h4","L1700-06","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Phenylbutazone (Butazolidine) is used as a non-steroidal anti-inflammatory agent for the treatment of chronic pain, including the symptoms of arthritis.",308.37,"50-33-9",{"v":62,"d":"62.00"},201.06,"<1","N/A","http://selleckchem.com/products/Phenylbutazone(Butazolidin).html","C19H20N2O2","free base","Butazolidine","CCCCC1C(=O)N(N(C1=O)C2=CC=CC=C2)C3=CC=CC=C3",3.954,2,0,5]
["S1655","Ezetimibe (SCH-58235)","a5","L1700-06","in 10mM DMSO","LDL","Metabolism","Ezetimibe (SCH-58235) is a potent, selective, cholesterol absorption inhibitor, used to lower cholesterol.",{"v":409.4,"d":"409.40"},"163222-33-1",{"v":81,"d":"81.00"},197.85,"<1","N/A","http://selleckchem.com/products/Ezetimibe(Zetia).html","C24H21F2NO3","free base","SCH-58235","OC(CCC1C(N(C1=O)C2=CC=C(F)C=C2)C3=CC=C(O)C=C3)C4=CC=C(F)C=C4",4.633,1,2,6]
["S1657","Enalaprilat Dihydrate","b5","L1700-06","in 10mM DMSO","RAAS","Endocrinology & Hormones","Enalaprilat (MK-422) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 1.94 nM.",{"v":348.4,"d":"348.40"},"84680-54-6",{"v":70,"d":"70.00"},200.92,"<1","N/A","http://selleckchem.com/products/Enalaprilat.html","C18H24N2O5.2H2O","Dihydrate","MK-422 Dihydrate","O.O.CC(NC(CCC1=CC=CC=C1)C(O)=O)C(=O)N2CCCC2C(O)=O",{"v":-1.53,"d":"-1.530"},3,1,8]
["S1658","Dofetilide","c5","L1700-06","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Dofetilide (UK-68798) is a selective potassium channel ((hERG)) blocker, used as a Class III antiarrhythmic drug.",441.56,"115256-11-6",{"v":88,"d":"88.00"},199.29,"<1","N/A","http://selleckchem.com/products/Dofetilide(Tikosyn).html","C19H27N3O5S2","free base","UK-68798","CN(CCOC1=CC=C(N[S](C)(=O)=O)C=C1)CCC2=CC=C(N[S](C)(=O)=O)C=C2",1.679,5,2,11]
["S1662","Isradipine","d5","L1700-06","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Isradipine (PN 200-110) is a potent and selective L-type voltage-gated calcium channel blocker, used to treat high blood pressure.",371.39,"75695-93-1",{"v":74,"d":"74.00"},199.25,"<1","N/A","http://selleckchem.com/products/Isradipine(Dynacirc).html","C19H21N3O5","free base","PN 200-110","COC(=O)C1=C(C)NC(=C(C1C2=CC=CC3=NON=C23)C(=O)OC(C)C)C",2.168,7,1,6]
["S1665","Estrone","e5","L1700-06","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Estrone is an estrogenic hormone.",270.37,"53-16-7",{"v":54,"d":"54.00"},199.73,"<1","N/A","http://selleckchem.com/products/Estrone.html","C18H22O2","free base","N/A","CC12CCC3C(CCC4=CC(=CC=C34)O)C1CCC2=O",3.938,1,1,0]
["S1666","Flucytosine","f5","L1700-06","in 10mM DMSO","Fungal","Microbiology","Flucytosine (5-Fluorocytosine, 5-FC, NSC 103805, Ro 2-9915) is an antifungal drug with IC50 of 0.93 μM in C. albicans.",129.09,"2022-85-7",{"v":8,"d":"8.00"},61.97,{"v":5,"d":"5.00"},38.73,"http://selleckchem.com/products/Flucytosine(Ancobon).html","C4H4FN3O","free base","5-Fluorocytosine, 5-FC, NSC 103805, Ro 2-9915","NC1=NC(=O)NC=C1F",-1.048,2,2,0]
["S1667","Trichlormethiazide","g5","L1700-06","in 10mM DMSO","Others","Others","Trichlormethiazide is a diuretic with properties similar to those of hydrochlorothiazide.",380.66,"133-67-5",{"v":54,"d":"54.00"},141.86,"<1","N/A","http://selleckchem.com/products/Trichlormethiazide(Achletin).html","C8H8Cl3N3O4S2","free base","N/A","N[S](=O)(=O)C1=C(Cl)C=C2NC(N[S](=O)(=O)C2=C1)C(Cl)Cl",1.046,4,3,2]
["S1669","Loteprednol etabonate","h5","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Loteprednol etabonate is a potent glucocorticoid receptor agonist, used in treatment of inflammation of the eye due to allergies.",466.95,"82034-46-6",{"v":93,"d":"93.00"},199.16,"<1","N/A","http://selleckchem.com/products/Loteprednol-etabonate.html","C24H31ClO7","free base","N/A","CCOC(=O)OC1(CCC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC12C)C(=O)OCCl",3.865,6,1,7]
["S1673","Aminophylline","a6","L1700-06","in 10mM DMSO","PDE","Metabolism","Aminophylline (Phyllocontin) is a competitive nonselective phosphodiesterase inhibitor with an IC50 of 0.12 mM and also a nonselective adenosine receptor antagonist.",420.43,"317-34-0",{"v":53,"d":"53.00"},126.06,{"v":84,"d":"84.00"},{"v":199.8,"d":"199.80"},"http://selleckchem.com/products/Aminophylline(Truphylline).html","C16H24N10O4","Ethylenediamine","Phyllocontin","CN1C(=O)N(C)C2=C([NH]C=N2)C1=O.CN3C(=O)N(C)C4=C([NH]C=N4)C3=O.NCCN",-2.089,6,4,1]
["S1675","Lubiprostone","b6","L1700-06","in 10mM DMSO","Chloride Channel","Transmembrane Transporters","Lubiprostone (RU 0211,SPI-0211) is an activator of ClC-2 chloride channels, used in the management of idiopathic chronic constipation.",390.46,"136790-76-6",{"v":78,"d":"78.00"},199.76,"<1","N/A","http://selleckchem.com/products/Lubiprostone(Amitiza).html","C20H32F2O5","Free Base","RU 0211,SPI-0211","CCCCC(F)(F)C(=O)CCC1C(O)CC(=O)C1CCCCCCC(O)=O",3.831,3,1,14]
["S1676","Amorolfine HCl","c6","L1700-06","in 10mM DMSO","Fungal","Microbiology","Amorolfine HCl(Ro 14-4767 HCl) is an antifungal reagent.",353.97,"78613-38-4",{"v":28,"d":"28.00"},{"v":79.1,"d":"79.10"},{"v":9,"d":"9.00"},25.43,"http://selleckchem.com/products/Amorolfine-Hydrochloride.html","C21H35NO.HCl","Hydrochloride","Ro 14-4767 HCl","Cl.CCC(C)(C)C1=CC=C(CC(C)CN2CC(C)OC(C)C2)C=C1",5.681,1,0,6]
["S1677","Chloramphenicol","d6","L1700-06","in 10mM DMSO","Antibiotics for Plant Cell Culture,Bacterial,Selection Antibiotics for Transfected Cell","Microbiology","Chloramphenicol (Chloromycetin) is a bacteriostatic by inhibiting protein synthesis.",323.13,"56-75-7",{"v":65,"d":"65.00"},201.16,"<1","N/A","http://selleckchem.com/products/Chloramphenicol(Chloromycetin).html","C11H12Cl2N2O5","free base","Chloromycetin","OCC(NC(=O)C(Cl)Cl)C(O)C1=CC=C(C=C1)[N+]([O-])=O",1.025,1,3,6]
["S1679","Flurbiprofen","e6","L1700-06","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Flurbiprofen is a member of the phenylalkanoic acid derivative family of non-steroidal anti-inflammatory drugs (NSAIDs).",244.26,"5104-49-4",{"v":49,"d":"49.00"},200.61,"<1","N/A","http://selleckchem.com/products/Flurbiprofen(Ansaid).html","C15H13FO2","free base","N/A","CC(C(O)=O)C1=CC(=C(C=C1)C2=CC=CC=C2)F",{"v":3.68,"d":"3.680"},1,0,3]
["S1680","Disulfiram (NSC 190940)","f6","L1700-06","in 10mM DMSO","Apoptosis related,COVID-19,Dehydrogenase,Pyroptosis","Metabolism","Disulfiram (NSC 190940, Tetraethylthiuram disulfide, TETD) is a specific inhibitor of aldehyde-dehydrogenase (ALDH) with IC50 of 0.15 μM and 1.45 μM for hALDH1 and hALDH2, respectively. Disulfiram is used for the treatment of chronic alcoholism by producing an acute sensitivity to alcohol. Disulfiram induces apoptosis. Disulfiram is also an inhibitor of pore formation by gasdermin D (GSDMD).",296.54,"97-77-8",{"v":59,"d":"59.00"},198.96,"<1","N/A","http://selleckchem.com/products/Disulfiram(Antabuse).html","C10H20N2S4","free base","NSC 190940, Tetraethylthiuram disulfide, TETD","CCN(CC)C(=S)SSC(=S)N(CC)CC",{"v":5.6,"d":"5.600"},0,0,9]
["S1681","Mesalamine (5-ASA)","g6","L1700-06","in 10mM DMSO","Immunology & Inflammation related,IκB/IKK","NF-κB","Mesalamine (5-Aminosalicylic acid, 5-ASA, Mesalazine, Apriso, Asacol, Pentasa, Canasa) is a specific inhibitor of TNFα-induced IKK activity, used to treat inflammatory bowel disease.",153.14,"89-57-6",{"v":31,"d":"31.00"},202.43,"<1","N/A","http://selleckchem.com/products/Mesalamine(Lialda).html","C7H7NO3","free base","5-Aminosalicylic acid, 5-ASA, Mesalazine, Apriso, Asacol, Pentasa, Canasa","NC1=CC=C(O)C(=C1)C(O)=O",0.471,1,2,1]
["S1683","Ipratropium Bromide","h6","L1700-06","in 10mM DMSO","AChR","Neuronal Signaling","Ipratropium Bromide is an antagonist of M3 type muscarinic acetylcholine receptors, used for the treatment of chronic obstructive pulmonary disease (COPD).",412.37,"22254-24-6",{"v":83,"d":"83.00"},201.28,{"v":83,"d":"83.00"},201.28,"http://selleckchem.com/products/Ipratropium-bromide.html","C20H30BrNO3","Bromide","N/A","[Br-].CC(C)[N+]1(C)C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3",-1.326,2,1,6]
["S1685","Sulfanilamide","a7","L1700-06","in 10mM DMSO","Bacterial","Microbiology","Sulfanilamide (Sulphanilamide) is a competitive inhibitor for bacterial enzyme dihydropteroate synthetase with IC50 of 320 μM.",{"v":172.2,"d":"172.20"},"63-74-1",{"v":34,"d":"34.00"},197.44,"<1","N/A","http://selleckchem.com/products/Sulfanilamide.html","C6H8N2O2S","free base","N/A","NC1=CC=C(C=C1)[S](N)(=O)=O",-0.212,2,2,1]
["S1688","Betamethasone Dipropionate","b7","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Betamethasone Dipropionate (SCH 11460) is a glucocorticoid steroid with anti-inflammatory and immunosuppressive abilities.",504.59,"5593-20-4",{"v":100,"d":"100.00"},198.18,"<1","N/A","http://selleckchem.com/products/Betamethasone-Dipropionate(Diprolene).html","C28H37FO7","Free Base","SCH 11460","CCC(=O)OCC(=O)C1(OC(=O)CC)C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC12C",{"v":3.8,"d":"3.800"},6,1,8]
["S1689","Meprednisone","c7","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Meprednisone (NSC 527579, SCH 4358) is a glucocorticoid and a methylated derivative of prednisone.",372.46,"1247-42-3",{"v":75,"d":"75.00"},201.37,"<1","N/A","http://selleckchem.com/products/Betapar(Meprednisone).html","C22H28O5","free base","NSC 527579, SCH 4358","CC1CC2C3CCC4=CC(=O)C=CC4(C)C3C(=O)CC2(C)C1(O)C(=O)CO",1.536,3,1,2]
["S1690","Betamethasone Valerate","d7","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Betamethasone Valerate is a moderately potent glucocorticoid steroid with anti-inflammatory and immunosuppressive properties.",476.58,"2152-44-5",{"v":95,"d":"95.00"},199.34,"<1","N/A","http://selleckchem.com/products/Betamethasone-valerate(Betnovate).html","C27H37FO6","free base","N/A","CCCCC(=O)OC1(C(C)CC2C3CCC4=CC(=O)C=CC4(C)C3(F)C(O)CC12C)C(=O)CO",3.666,4,2,7]
["S1691","Praziquantel","e7","L1700-06","in 10mM DMSO","COVID-19,Parasite","Microbiology","Praziquantel is an anthelmintic effective against flatworms.",312.41,"55268-74-1",{"v":63,"d":"63.00"},201.66,"<1","N/A","http://selleckchem.com/products/Praziquantel(Biltricide).html","C19H24N2O2","free base","N/A","O=C1CN(CC2N1CCC3=CC=CC=C23)C(=O)C4CCCCC4",2.477,2,0,1]
["S1692","Busulfan (NSC-750)","f7","L1700-06","in 10mM DMSO","Apoptosis related,DNA alkylator","DNA Damage/DNA Repair","Busulfan (NSC-750) is a cell cycle non-specific alkylating antineoplastic agent. Busulfan induces apoptosis.",{"v":246.3,"d":"246.30"},"55-98-1",{"v":49,"d":"49.00"},198.94,"<1","N/A","http://selleckchem.com/products/Busulfan(Busulfex).html","C6H14O6S2","free base","NSC-750","C[S](=O)(=O)OCCCCO[S](C)(=O)=O",-0.289,2,0,7]
["S1693","Carbamazepine","g7","L1700-06","in 10mM DMSO","Autophagy,Sodium Channel","Transmembrane Transporters","Carbamazepine (Carbatrol, NSC 169864) is a sodium channel blocker with IC50 of 131 μM in rat brain synaptosomes.",236.27,"298-46-4",{"v":47,"d":"47.00"},198.92,"<1","N/A","http://selleckchem.com/products/Carbamazepine(Carbatrol).html","C15H12N2O","free base","NSC 169864","NC(=O)N1C2=C(C=CC=C2)C=CC3=C1C=CC=C3",2.679,1,1,0]
["S1696","Hydrocortisone (NSC 10483)","h7","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Hydrocortisone (NSC 10483, Cortisol) is a steroid hormone or glucocorticoid produced by the adrenal gland.",362.46,"50-23-7",{"v":73,"d":"73.00"},{"v":201.4,"d":"201.40"},"<1","N/A","http://selleckchem.com/products/Hydrocortisone.html","C21H30O5","free base","Cortisol","CC12CCC(=O)C=C1CCC3C4CCC(O)(C(=O)CO)C4(C)CC(O)C23",1.283,2,2,2]
["S1701","Desonide","a8","L1700-06","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Desonide is a low potency topical corticosteroid.",416.51,"638-94-8",{"v":83,"d":"83.00"},199.27,"<1","N/A","http://selleckchem.com/products/Desonide.html","C24H32O6","free base","N/A","CC1(C)OC2CC3C4CCC5=CC(=O)C=CC5(C)C4C(O)CC3(C)C2(O1)C(=O)CO",1.028,4,2,2]
["S1702","Didanosine","b8","L1700-06","in 10mM DMSO","Reverse Transcriptase","Microbiology","Didanosine is a reverse transcriptase inhibitor with an IC50 of 0.49 μM.",236.23,"69655-05-6",{"v":47,"d":"47.00"},198.96,"<1","N/A","http://selleckchem.com/products/Didanosine(Videx).html","C10H12N4O3","free base","N/A","OCC1CCC(O1)[N]2C=NC3=C2N=CNC3=O",-0.844,4,2,2]
["S1703","Divalproex Sodium","c8","L1700-06","in 10mM DMSO","HDAC","Epigenetics","Divalproex Sodium, consisting of a compound of sodium valproate and valproic acid in a 1:1 molar relationship in an enteric coated form, is a HDAC inhibitor, used in the treatment for epilepsy.",310.41,"76584-70-8",{"v":62,"d":"62.00"},199.74,{"v":62,"d":"62.00"},199.74,"http://selleckchem.com/products/Divalproex-sodium.html","C8H16O2.C8H15O2.Na","Sodium Salt","N/A","[Na+].CCCC(CCC)C(O)=O.CCCC(CCC)C([O-])=O",4.025,1,0,10]
["S1704","Emtricitabine (BW 1592)","d8","L1700-06","in 10mM DMSO","HBV,HIV,Reverse Transcriptase","Microbiology","Emtricitabine (BW1592, FTC) is a new nucleoside agent that has activity against both human immunodeficiency virus (HIV) and hepatitis B virus. It is a reverse transcriptase inhibitor. Intracellular half-life is 39 h.",247.25,"143491-57-0",{"v":49,"d":"49.00"},198.18,{"v":49,"d":"49.00"},198.18,"http://selleckchem.com/products/Emtricitabine.html","C8H10FN3O3S","free base","FTC, BW1592","NC1=NC(=O)N(C=C1F)C2CSC(CO)O2",{"v":-0.68,"d":"-0.680"},3,2,2]
["S1705","Progesterone (NSC 9704)","e8","L1700-06","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Progesterone (NSC 9704, NSC 64377, Pregn-4-ene-3,20-dione) is an endogenous steroid hormone involved in the menstrual cycle, pregnancy, and embryogenesis of humans and other species. A potent agonist of the nuclear progesterone receptor (nPR) with Kd of 1 nM; An agonist of the membrane progesterone receptors(mPRs); An antagonist of the σ1 receptor.",314.46,"57-83-0",{"v":22,"d":"22.00"},69.96,"<1","N/A","http://selleckchem.com/products/Progesterone(Prometrium).html","C21H30O2","free base","NSC 64377, Pregn-4-ene-3,20-dione,NSC 9704","CC(=O)C1CCC2C3CCC4=CC(=O)CCC4(C)C3CCC12C",{"v":3.86,"d":"3.860"},2,0,1]
["S1706","Lamivudine (BCH-189)","f8","L1700-06","in 10mM DMSO","COVID-19,Reverse Transcriptase","Microbiology","Lamivudine (BCH-189, GR109714X) is a potent nucleoside analog reverse transcriptase inhibitor, used for treatment of chronic HBV and HIV/AIDS. It works by blocking the HIV reverse transcriptase and hepatitis B virus polymerase.",229.26,"134678-17-4",{"v":46,"d":"46.00"},200.65,{"v":46,"d":"46.00"},200.65,"http://selleckchem.com/products/Lamivudine(Epivir).html","C8H11N3O3S","free base","GR109714X, BCH-189","NC1=NC(=O)N(C=C1)C2CSC(CO)O2",{"v":-0.59,"d":"-0.590"},3,2,2]
["S1709","Estradiol","g8","L1700-06","in 10mM DMSO","Estrogen/progestogen Receptor,Interleukins","Endocrinology & Hormones","Estradiol (17β-estradiol, β-Estradiol, E2, 17β-Oestradiol) is a human sex hormone and steroid, and the primary female sex hormone. Estradiol upregulates IL-6 expression through the estrogen receptor β (ERβ) pathway.",272.38,"50-28-2",{"v":54,"d":"54.00"},198.25,"<1","N/A","http://selleckchem.com/products/Estradiol.html","C18H24O2","free base","17β-estradiol, β-Estradiol, E2, 17β-Oestradiol","CC12CCC3C(CCC4=C3C=CC(=C4)O)C1CCC2O",3.838,0,2,0]
["S1712","Deferasirox (ICL-670)","h8","L1700-06","in 10mM DMSO","Ferroptosis,P450 (e.g. CYP17)","Proteases","Deferasirox (ICL-670, CGP-72670) is an iron chelator, also a cytochrome P450 3A4 inducer, Cytochrome P450 2C8 inhibitor, and Cytochrome P450 1A2 inhibitor. Deferasirox-induced iron depletion promotes BclxL downregulation and cell death.",373.36,"201530-41-8",{"v":74,"d":"74.00"},{"v":198.2,"d":"198.20"},"<1","N/A","http://selleckchem.com/products/Deferasirox(Exjade).html","C21H15N3O4","free base","CGP-72670, ICL-670","OC(=O)C1=CC=C(C=C1)[N]2N=C(N=C2C3=CC=CC=C3O)C4=CC=CC=C4O",4.063,3,2,4]
["S1713","Piroxicam","a9","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Piroxicam (CP 16171) is a non-selective COX inhibitor, used in the treatment of rheumatoid and osteoarthritis.",331.35,"36322-90-4",{"v":66,"d":"66.00"},199.19,"<1","N/A","http://selleckchem.com/products/Piroxicam(Feldene).html","C15H13N3O4S","free base","CP 16171","CN1C(=C(O)C2=C(C=CC=C2)[S]1(=O)=O)C(=O)NC3=NC=CC=C3",0.501,4,2,2]
["S1714","Gemcitabine (LY-188011)","b9","L1700-06","in 10mM DMSO","Apoptosis related,Autophagy,DNA/RNA Synthesis,Nucleoside Analog/Antimetabolite","DNA Damage/DNA Repair","Gemcitabine (LY-188011, NSC 613327), a nucleic acid synthesis inhibitor, is a very potent and specific deoxycytidine analogue, used as chemotherapy. Gemcitabine induces a potent p53-dependent apoptosis.",{"v":263.2,"d":"263.20"},"95058-81-4",{"v":52,"d":"52.00"},197.57,{"v":52,"d":"52.00"},197.57,"http://selleckchem.com/products/Gemcitabine(Gemzar).html","C9H11F2N3O4","Free Base","LY-188011, NSC 613327","NC1=NC(=O)N(C=C1)C2OC(CO)C(O)C2(F)F",-1.394,3,3,2]
["S1715","Glipizide","c9","L1700-06","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Glipizide (CP-28720,K 4024) is used to treat high blood sugar levels caused by a type of diabetes mellitus called type 2 diabetes.",445.54,"29094-61-9",{"v":89,"d":"89.00"},199.76,"<1","N/A","http://selleckchem.com/products/Glipizide(Glucotrol).html","C21H27N5O4S","free base","CP-28720,K 4024","CC1=NC=C(N=C1)C(=O)NCCC2=CC=C(C=C2)[S](=O)(=O)NC(=O)NC3CCCCC3",1.902,6,3,7]
["S1716","Glyburide (Glibenclamide)","d9","L1700-06","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Glyburide (Glibenclamide) is a known blocker of vascular ATP-sensitive K+ channels (KATP), used in the treatment of type 2 diabetes.",{"v":494,"d":"494.00"},"10238-21-8",{"v":99,"d":"99.00"},{"v":200.4,"d":"200.40"},"<1","N/A","http://selleckchem.com/products/Glyburide(Diabeta).html","C23H28ClN3O5S","free base","Glibenclamide","COC1=C(C=C(Cl)C=C1)C(=O)NCCC2=CC=C(C=C2)[S](=O)(=O)NC(=O)NC3CCCCC3",{"v":4.14,"d":"4.140"},5,3,8]
["S1717","Fomepizole","e9","L1700-06","in 10mM DMSO","Dehydrogenase","Metabolism","Fomepizole (4-methylpyrazole, Antizol, Antizol-Vet) is a competitive inhibitor of alcohol dehydrogenase, the enzyme that catalyzes the initial steps in the metabolism of ethylene glycol and methanol to their toxic metabolites.",{"v":82.1,"d":"82.10"},"7554-65-6","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/Fomepizole(Antizol).html","C4H6N2","free base","4-methylpyrazole, Antizol, Antizol-Vet","CC1=C[NH]N=C1",{"v":0.76,"d":"0.760"},1,1,0]
["S1718","Adefovir Dipivoxil (GS 0840)","f9","L1700-06","in 10mM DMSO","Reverse Transcriptase","Microbiology","Adefovir Dipivoxil (GS 0840) is a reverse transcriptase inhibitor, used in the treatment of chronic hepatitis B virus (HBV).",501.47,"142340-99-6",{"v":100,"d":"100.00"},199.41,"<1","N/A","http://selleckchem.com/products/Adefovir-Dipivoxil(Preveon).html","C20H32N5O8P","free base","GS 0840","CC(C)(C)C(=O)OCO[P](=O)(COCC[N]1C=NC2=C1N=CN=C2N)OCOC(=O)C(C)(C)C",1.666,10,1,15]
["S1719","Zalcitabine","g9","L1700-06","in 10mM DMSO","Reverse Transcriptase","Microbiology","Zalcitabine (NSC 606170, Ro 24-2027/000) is a nucleoside analog HIV reverse transcriptase inhibitor (NARTI).",211.22,"7481-89-2",{"v":7,"d":"7.00"},33.14,{"v":42,"d":"42.00"},198.84,"http://selleckchem.com/products/Zalcitabine.html","C9H13N3O3","free base","NSC 606170, Ro 24-2027/000","NC1=NC(=O)N(C=C1)C2CCC(CO)O2",-0.991,3,2,2]
["S1721","Azathioprine","h9","L1700-06","in 10mM DMSO","Rho","Cell Cycle","Azathioprine(BW 57-322) is an immunosuppressive drug, inhibiting purine synthesis and GTP-binding protein Rac1 activation, used in the treatment of organ transplantation and autoimmune diseases.",277.26,"446-86-6",{"v":54,"d":"54.00"},194.76,"<1","N/A","http://selleckchem.com/products/Azathioprine(Azasan).html","C9H7N7O2S","free base","BW 57-322","C[N]1C=NC(=C1SC2=C3[NH]C=NC3=NC=N2)[N+]([O-])=O",1.071,4,1,3]
["S1723","Indomethacin (NSC-77541)","a10","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Indomethacin (NSC-77541, Indometacin) is a nonselective COX1 and COX2 inhibitor with IC50 of 0.1 μg/mL and 5 μg/mL, respectively, used to reduce fever, pain, stiffness, and swelling.",357.79,"53-86-1",{"v":72,"d":"72.00"},201.24,"<1","N/A","http://selleckchem.com/products/Indomethacin(Indocid).html","C19H16ClNO4","free base","Indometacin,NSC-77541","COC1=CC=C2[N](C(=C(CC(O)=O)C2=C1)C)C(=O)C3=CC=C(Cl)C=C3",4.235,3,0,4]
["S1725","Terbinafine","b10","L1700-06","in 10mM DMSO","Fungal","Microbiology","Terbinafine (SF 86-327,TDT 067) is used to treat infections caused by a fungus. It works by killing the fungus or preventing its growth.",291.43,"91161-71-6",{"v":58,"d":"58.00"},199.02,"<1","N/A","http://selleckchem.com/products/Terbinafine(Lamisil).html","C21H25N","Free Base","SF 86-327,TDT 067","CN(C\\C=C\\C#CC(C)(C)C)CC1=CC=CC2=CC=CC=C12",5.335,0,0,6]
["S1727","Levonorgestrel","c10","L1700-06","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Levonorgestrel (D-Norgestrel) is a female hormone that prevents ovulation.",312.45,"797-63-7",{"v":45,"d":"45.00"},144.02,"<1","N/A","http://selleckchem.com/products/Levonorgestrel(Levonelle).html","C21H28O2","free base","D-Norgestrel","CCC12CCC3C(CCC4=CC(=O)CCC34)C1CCC2(O)C#C",4.771,1,0,1]
["S1729","Gemfibrozil","d10","L1700-06","in 10mM DMSO","PPAR","Metabolism","Gemfibrozil (CI-719) is an activator of peroxisome proliferator-activated receptor-alpha (PPARα), used for the treatment of hypercholesterolemia and hypertriglyceridemia.",250.33,"25812-30-0",{"v":50,"d":"50.00"},199.74,"<1","N/A","http://selleckchem.com/products/Gemfibrozil(Lopid).html","C15H22O3","free base","CI-719","CC1=CC(=C(C)C=C1)OCCCC(C)(C)C(O)=O",4.172,2,0,6]
["S1730","Indapamide","e10","L1700-06","in 10mM DMSO","Others","Others","Indapamide is a non-thiazide sulphonamide diuretic compound, generally used in the treatment of hypertension, as well as decompensated cardiac failure.",365.83,"26807-65-8",{"v":73,"d":"73.00"},199.55,"<1","N/A","http://selleckchem.com/products/Indapamide(Lozol).html","C16H16ClN3O3S","free base","N/A","CC1CC2=C(C=CC=C2)N1NC(=O)C3=CC=C(Cl)C(=C3)[S](N)(=O)=O",2.664,3,2,3]
["S1732","Mitotane","f10","L1700-06","in 10mM DMSO","Others","Others","Mitotane (NCI-C04933), is an antineoplastic medication used in the treatment of adrenocortical carcinoma.",320.04,"53-19-0",{"v":64,"d":"64.00"},199.98,"<1","N/A","http://selleckchem.com/products/Mitotane(Lysodren).html","C14H10Cl4","free base","NCI-C04933","ClC(Cl)C(C1=CC=C(Cl)C=C1)C2=C(Cl)C=CC=C2",5.745,0,0,3]
["S1733","Methylprednisolone (NSC-19987)","g10","L1700-06","in 10mM DMSO","ACE,Apoptosis related,Autophagy,Glucocorticoid Receptor,Immunology & Inflammation related,Interleukins","Endocrinology & Hormones","Methylprednisolone (NSC-19987,U 7532) is a synthetic glucocorticoid receptor agonist, used to achieve prompt suppression of inflammation. Methylprednisolone activates ACE2 and reduces IL-6 levels, thus improves severe or critical COVID-19. Methylprednisolone markedly reduces autophagy and apoptosis.",374.47,"83-43-2",{"v":75,"d":"75.00"},200.28,"<1","N/A","http://selleckchem.com/products/Methylprednisolone.html","C22H30O5","free base","NSC-19987,U 7532","CC1CC2C3CCC(O)(C(=O)CO)C3(C)CC(O)C2C4(C)C=CC(=O)C=C14",1.512,2,2,2]
["S1734","Meloxicam","h10","L1700-06","in 10mM DMSO","COX","Neuronal Signaling","Meloxicam is a selective COX inhibitor, used to relieve pain and fever effects.",{"v":351.4,"d":"351.40"},"71125-38-7",{"v":30,"d":"30.00"},85.37,"<1","N/A","http://selleckchem.com/products/Meloxicam(Mobic).html","C14H13N3O4S2","free base","N/A","CN1C(=C(O)C2=C(C=CC=C2)[S]1(=O)=O)C(=O)NC3=NC=C(C)S3",0.255,4,2,2]
["S1735","Mesna","a11","L1700-06","in 10mM DMSO","Others","Others","Mesna, a sulfhydryl compound that is used to reduce the incidence of hemorrhagic cystitis associated with certain chemotherapeutic agents.",164.18,"19767-45-4",{"v":33,"d":"33.00"},{"v":201,"d":"201.00"},{"v":7,"d":"7.00"},42.64,"http://selleckchem.com/products/Mesna(Uromitexan).html","C2H5NaO3S2","Sodium Salt","N/A","[Na+].[O-][S](=O)(=O)CCS",-2.227,0,0,2]
["S1736","Methocarbamol","b11","L1700-06","in 10mM DMSO","Carbonic Anhydrase","Metabolism","Methocarbamol (AHR 85) is a carbonic anhydrase inhibitor, used as a central muscle relaxant to treat skeletal muscle spasms.",241.24,"532-03-6",{"v":48,"d":"48.00"},198.97,{"v":2,"d":"2.00"},8.29,"http://selleckchem.com/products/Methocarbamol(Robaxin).html","C11H15NO5","free base","AHR 85","COC1=C(OCC(O)COC(N)=O)C=CC=C1",0.916,4,2,7]
["S1737","Prednisolone (NSC-9900)","c11","L1700-06","in 10mM DMSO","Glucocorticoid Receptor,Immunology & Inflammation related","Endocrinology & Hormones","Prednisolone (NSC-9900) is a synthetic glucocorticoid with anti-inflammatory and immunomodulating properties.",360.44,"50-24-8",{"v":72,"d":"72.00"},199.76,"<1","N/A","http://selleckchem.com/products/Prednisolone(Hydroretrocortine).html","C21H28O5","Free Base","NSC-9900","CC12CC(O)C3C(CCC4=CC(=O)C=CC34C)C1CCC2(O)C(=O)CO",{"v":1.26,"d":"1.260"},2,2,2]
["S1738","Telmisartan","d11","L1700-06","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Telmisartan (BIBR 277) is an angiotensin II receptor antagonist (ARB) used in the management of hypertension.",514.62,"144701-48-4",{"v":13,"d":"13.00"},25.26,"<1","N/A","http://selleckchem.com/products/Telmisartan(Micardis).html","C33H30N4O2","free base","BIBR 277","CCCC1=NC2=C(C=C(C=C2C)C3=NC4=C(C=CC=C4)[N]3C)[N]1CC5=CC=C(C=C5)C6=CC=CC=C6C(O)=O",7.799,3,0,7]
["S1739","Thiabendazole","e11","L1700-06","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Thiabendazole inhibits the mitochondrial helminth-specific enzyme, fumarate reductase, with anthelminthic property, used as an anthelmintic and fungicide agent. It is a potent inhibitor of  cytochrome P450 1A2 (CYP1A2).",201.25,"148-79-8",{"v":40,"d":"40.00"},198.76,"<1","N/A","http://selleckchem.com/products/Thiabendazole.html","C10H7N3S","free base","N/A","[NH]1C2=C(C=CC=C2)N=C1C3=CSC=N3",2.154,2,1,1]
["S1740","Guaifenesin","f11","L1700-06","in 10mM DMSO","Others","Others","Guaifenesin is an expectorant used to relieve chest congestion.",198.22,"93-14-1",{"v":40,"d":"40.00"},{"v":201.8,"d":"201.80"},{"v":25,"d":"25.00"},126.12,"http://selleckchem.com/products/Guaifenesin(Guaiphenesin).html","C10H14O4","free base","N/A","COC1=C(OCC(O)CO)C=CC=C1",0.747,2,2,5]
["S1741","Rifabutin (LM427)","g11","L1700-06","in 10mM DMSO","Antibiotics,Antineoplastic and Immunosuppressive Antibiotics,Bacterial","Microbiology","Rifabutin (LM427, Ansamycin) is a semisynthetic ansamycin antibiotic, used in the treatment of Mycobacterium avium intracellulare (MAI) and tuberculosis.",{"v":847,"d":"847.00"},"72559-06-9",{"v":60,"d":"60.00"},70.84,"<1","N/A","http://selleckchem.com/products/Rifabutin(Mycobutin).html","C46H62N4O11","free base","LM427, Ansamycin","COC1\\C=C\\OC2(C)OC3=C(C2=O)C4=C(C(=C3C)O)C(=O)C(=C5NC6(CCN(CC6)CC(C)C)N=C45)NC(=O)/C(=C/C=C/C(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)C",3.931,9,5,5]
["S1742","Nevirapine (NSC 641530)","h11","L1700-06","in 10mM DMSO","Reverse Transcriptase","Microbiology","Nevirapine (NSC 641530,NVP) is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used to treat HIV-1 infection and AIDS.",{"v":266.3,"d":"266.30"},"129618-40-2",{"v":53,"d":"53.00"},199.02,"<1","N/A","http://selleckchem.com/products/Nevirapine(Viramune).html","C15H14N4O","free base","NSC 641530,NVP","CC1=CC=NC2=C1NC(=O)C3=C(N=CC=C3)N2C4CC4",2.293,3,1,1]
["S1743","Esomeprazole magnesium","a2","L1700-07","in 10mM DMSO","ATPase,Proton Pump","Transmembrane Transporters","Esomeprazole Magnesium(NEXIUM) is a proton pump inhibitor to reduce gastric acid secretion through inhibition of H(+)/K(+)-ATPase in gastric parietal cells.",713.12,"161973-10-0",{"v":143,"d":"143.00"},200.53,"<1","N/A","http://selleckchem.com/products/nexium-esomeprazole-magnesium.html","C34H36MgN6O6S2","Magnesium salt","NEXIUM","[Mg++].COC1=CC2=C([N-]C(=N2)[S](=O)CC3=C(C)C(=C(C)C=N3)OC)C=C1.COC4=CC5=C([N-]C(=N5)[S](=O)CC6=NC=C(C)C(=C6C)OC)C=C4",{"v":6.1,"d":"6.100"},10,0,10]
["S1744","Nicotinic Acid","b2","L1700-07","in 10mM DMSO","Vitamin","Metabolism","Nicotinic Acid is a water-soluble vitamin belonging to the vitamin B family.",123.11,"59-67-6",{"v":25,"d":"25.00"},203.07,{"v":2,"d":"2.00"},16.25,"http://selleckchem.com/products/Niacin(Nicotinic-acid).html","C6H5NO2","free base","N/A","OC(=O)C1=CC=CN=C1",0.309,2,0,1]
["S1747","Nimodipine","c2","L1700-07","in 10mM DMSO","Autophagy,Calcium Channel","Transmembrane Transporters","Nimodipine (BAY E 9736) is a dihydropyridine calcium channel blocker and an autophagy inhibitor, used in the treatment of high blood pressure.",418.44,"66085-59-4",{"v":84,"d":"84.00"},200.75,"<1","N/A","http://selleckchem.com/products/Nimodipine(Nimotop).html","C21H26N2O7","free base","BAY E 9736","COCCOC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OC(C)C)C",2.361,5,1,10]
["S1748","Nisoldipine","d2","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Nisoldipine (Sular, BAY K 5552) is a calcium channel blocker belonging to the dihydropyridines class, specific for L-type Cav1.2 with IC50 of 10 nM.",388.41,"63675-72-9",{"v":77,"d":"77.00"},198.24,"<1","N/A","http://selleckchem.com/products/Nisoldipine(Sular).html","C20H24N2O6","free base","BAY K 5552","COC(=O)C1=C(C)NC(=C(C1C2=CC=CC=C2[N+]([O-])=O)C(=O)OCC(C)C)C",2.958,4,1,8]
["S1750","Octocrylene","e2","L1700-07","in 10mM DMSO","Others","Others","Octocrylene is an organic compound used as an ingredient in sunscreens and cosmetics.",361.48,"6197-30-4","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/octocrylene.html","C24H27NO2","free base","N/A","CCCCC(CC)COC(=O)C(C#N)=C(C1=CC=CC=C1)C2=CC=CC=C2",6.487,2,0,10]
["S1754","Oxybutynin","f2","L1700-07","in 10mM DMSO","AChR","Neuronal Signaling","Oxybutynin is a competitive antagonist of the M1, M2, and M3 subtypes of the muscarinic acetylcholine receptor, used to relieve urinary and bladder difficulties.",357.49,"5633-20-5",{"v":71,"d":"71.00"},198.61,"<1","N/A","http://selleckchem.com/products/Oxybutynin(Ditropan).html","C22H31NO3","Free Base","N/A","CCN(CC)CC#CCOC(=O)C(O)(C1CCCCC1)C2=CC=CC=C2",4.646,2,0,10]
["S1756","Enoxacin","g2","L1700-07","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Enoxacin (AT-2266, CI919, Pd107779, NSC 629661) is an oral broad-spectrum fluoroquinolone antibacterial agent by inhibiting bacterial DNA gyrase and topoisomerase IV, used to treat a wide variety of infections.",320.32,"74011-58-8",{"v":32,"d":"32.00"},{"v":99.9,"d":"99.90"},"<1","N/A","http://selleckchem.com/products/Enoxacin(Penetrex).html","C15H17FN4O3","free base","AT-2266, CI919, Pd107779, NSC 629661","CCN1C=C(C(O)=O)C(=O)C2=CC(=C(N=C12)N3CCNCC3)F",-1.483,3,1,3]
["S1759","Pitavastatin (NK-104) calcium","h2","L1700-07","in 10mM DMSO","Apoptosis related,Autophagy,COVID-19,HMG-CoA Reductase,Mitophagy","Metabolism","Pitavastatin Calcium (NK-104, P-872441, itavastatin, nisvastatin), a novel member of the medication class of statins, is a calcium salt formulation of pitavastatin which is a highly effective HMG-CoA reductase inhibitor. Pitavastatin Calcium attenuates AGEs-induced mitophagy via inhibition of ROS generation. Pitavastatin Calcium induces autophagy and apoptosis.",880.98,"147526-32-7",{"v":51,"d":"51.00"},57.89,"<1","N/A","http://selleckchem.com/products/Pitavastatin-calcium(Livalo).html","C50H46CaF2N2O8","Calcium salt","NK-104, P-872441, itavastatin, nisvastatin","[Ca++].OC(CC(O)C=CC1=C(C2=CC=C(F)C=C2)C3=CC=CC=C3N=C1C4CC4)CC([O-])=O.OC(CC(O)C=CC5=C(C6=CC=C(F)C=C6)C7=CC=CC=C7N=C5C8CC8)CC([O-])=O",{"v":4.96,"d":"4.960"},2,4,16]
["S1760","Rifapentine","a3","L1700-07","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Rifapentine (MDL473) is an antibiotic, which inhibits DNA-dependent RNA polymerase activity, used to treat tuberculosis.",877.03,"61379-65-5",{"v":100,"d":"100.00"},114.02,"<1","N/A","http://selleckchem.com/products/Rifapentine(Priftin).html","C47H64N4O12","free base","MDL473","COC1\\C=C\\OC2(C)OC3=C(C2=O)C4=C(O)C(=C(NC(=O)\\C(=C\\C=C\\C(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)C)C(=C4C(=C3C)O)O)\\C=N\\N5CCN(CC5)C6CCCC6",4.664,8,6,6]
["S1761","Suprofen","b3","L1700-07","in 10mM DMSO","COX","Neuronal Signaling","Suprofen(TN-762) is a dual COX-1/COX-2 inhibitor, used as a non-steroidal anti-inflammatory analgesic and antipyretic.",260.31,"40828-46-4",{"v":52,"d":"52.00"},199.76,"<1","N/A","http://selleckchem.com/products/Suprofen(Profenal).html","C14H12O3S","free base","TN-762","CC(C(O)=O)C1=CC=C(C=C1)C(=O)C2=CC=CS2",3.314,2,0,4]
["S1762","Pyrazinamide","c3","L1700-07","in 10mM DMSO","Bacterial","Microbiology","Pyrazinamide (Pyrazinoic Acid Amide) is an agent used to treat tuberculosis.",123.11,"98-96-4",{"v":25,"d":"25.00"},203.07,{"v":12,"d":"12.00"},97.47,"http://selleckchem.com/products/Pyrazinamide(Pyrazinoic-acid-amide).html","C5H5N3O","free base","Pyrazinoic Acid Amide","NC(=O)C1=NC=CN=C1",-1.041,3,1,1]
["S1763","Quetiapine (ICI-204636) fumarate","d3","L1700-07","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Quetiapine Fumarate (ICI-204636) is an atypical antipsychotic used in the treatment of schizophrenia, bipolar I mania, bipolar II depression, bipolar I depression and shows affinity for various neurotransmitter receptors including serotonin, dopamine, histamine, and adrenergic receptors.",883.09,"111974-72-2",{"v":36,"d":"36.00"},40.77,"<1","N/A","http://selleckchem.com/products/Quetiapine-fumarate(Seroquel).html","C46H54N6O8S2","Fumarate","ICI-204636 fumarate","OCCOCCN1CCN(CC1)C2=NC3=CC=CC=C3SC4=C2C=CC=C4.OCCOCCN5CCN(CC5)C6=NC7=CC=CC=C7SC8=C6C=CC=C8.OC(=O)\\C=C\\C(O)=O",-0.718,6,2,14]
["S1764","Rifampin (NSC-113926)","e3","L1700-07","in 10mM DMSO","Antibiotics for Plant Cell Culture,Antineoplastic and Immunosuppressive Antibiotics,DNA/RNA Synthesis,Selection Antibiotics for Transfected Cell","DNA Damage/DNA Repair","Rifampin (NSC-113926, Rimactane, Rifampicin) is a DNA-dependent RNA polymerase inhibitor, used to treat a number of bacterial infections.",822.94,"13292-46-1",{"v":100,"d":"100.00"},121.52,"<1","N/A","http://selleckchem.com/products/Rifampin(Rifadin).html","C43H58N4O12","free base","Rimactane, Rifampicin,NSC-113926","COC1\\C=C\\OC2(C)OC3=C(C2=O)C4=C(O)C(=C(NC(=O)\\C(=C\\C=C\\C(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)C)C(=C4C(=C3C)O)O)\\C=N\\N5CCN(C)CC5",3.262,8,6,5]
["S1768","Cefditoren Pivoxil","f3","L1700-07","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Cefditoren Pivoxil (ME-1207) is a broad-spectrum antibiotic against Gram-negative and Gram-positive bacteria.",620.72,"117467-28-4",{"v":100,"d":"100.00"},{"v":161.1,"d":"161.10"},"<1","N/A","http://selleckchem.com/products/Cefditoren-pivoxil.html","C25H28N6O7S3","free base","ME-1207","CO\\N=C(/C(=O)NC1C2SCC(=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C)\\C=C/C3=C(C)N=CS3)C4=CSC(=N4)N",1.926,10,2,12]
["S1770","Sulfadiazine","g3","L1700-07","in 10mM DMSO","Antibiotics","Microbiology","Sulfadiazine is a sulfonamide antibiotic.",250.28,"68-35-9",{"v":50,"d":"50.00"},199.78,"<1","N/A","http://selleckchem.com/products/Sulfadiazine.html","C10H10N4O2S","free base","N/A","NC1=CC=C(C=C1)[S](=O)(=O)NC2=NC=CC=N2",0.313,4,2,3]
["S1771","Chlorprothixene","h3","L1700-07","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Chlorprothixene(Minithixen,Truxal) has strong binding affinities to dopamine and histamine receptors, such as D1, D2, D3, D5, H1, 5-HT2, 5-HT6 and 5-HT7, with Ki of 18 nM, 2.96 nM, 4.56 nM, 9 nM, 3.75 nM, 9.4 nM, 3 nM and 5.6 nM, respectively.",315.86,"113-59-7",{"v":6,"d":"6.00"},{"v":19,"d":"19.00"},"<1","N/A","http://selleckchem.com/products/Chlorprothixene.html","C18H18ClNS","free base","Minithixen,Truxal","CN(C)CC/C=C1/C2=CC=CC=C2SC3=C1C=C(Cl)C=C3",5.123,0,0,3]
["S1773","Oxytetracycline (Terramycin)","a4","L1700-07","in 10mM DMSO","Antibiotics,Bacterial,Selection Antibiotics for Transfected Cell","Others","Oxytetracycline(Terramycin) is a broad-spectrum tetracycline antibiotic, used to treat infections with bacteria.",460.43,"79-57-2",{"v":92,"d":"92.00"},199.81,"<1","N/A","http://selleckchem.com/products/Oxytetracycline(Terramycin).html","C22H24N2O9","free base","Terramycin","CN(C)C1C2C(O)C3C(=C(O)C4=C(C=CC=C4O)C3(C)O)C(=O)C2(O)C(=O)C(=C1O)C(N)=O",-1.904,3,5,2]
["S1774","Thioguanine (NSC 752)","b4","L1700-07","in 10mM DMSO","DNA Methyltransferase","Epigenetics","Thioguanine (NSC 752, 6-Thioguanine, 2-Amino-6-purinethiol), a purine antimetabolite, inhibits DNMT1 activity through ubiquitin-targeted degradation, used in the treatment of acute lymphoblastic leukemia, autoimmune disorders (e.g., Crohn's disease, rheumatoid arthritis) and organ transplant recipients.",167.19,"154-42-7",{"v":9,"d":"9.00"},53.83,"<1","N/A","http://selleckchem.com/products/Thioguanine.html","C5H5N5S","free base","NSC 752,6-Thioguanine, 2-Amino-6-purinethiol","NC1=NC(=S)C2=C(N1)N=C[NH]2",0.236,2,3,0]
["S1775","Thiotepa","c4","L1700-07","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics","Others","Thiotepa (Thioplex, Tiofosyl, Tiofosfamid, Triethylenethiophosphoramide) is an alkylating agent used to treat cancer.",189.22,"52-24-4",{"v":100,"d":"100.00"},528.49,{"v":100,"d":"100.00"},528.49,"http://selleckchem.com/products/thiotepa-thioplex.html","C6H12N3PS","free base","Tiofosyl, Tiofosfamid, Triethylenethiophosphoramide","S=[P](N1CC1)(N2CC2)N3CC3",-0.762,0,0,3]
["S1776","Toremifene Citrate (NK 622)","d4","L1700-07","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Toremifene Citrate (NK 622, NSC 613680) is an oral selective estrogen receptor modulator (SERM), used in the treatment of advanced breast cancer.",598.08,"89778-27-8",{"v":100,"d":"100.00"},{"v":167.2,"d":"167.20"},"<1","N/A","http://selleckchem.com/products/Toremifene-Citrate(Fareston).html","C32H36ClNO8","Citrate","NSC 613680,NK 622 Citrate","CN(C)CCOC1=CC=C(C=C1)\\C(=C(CCCl)/C2=CC=CC=C2)C3=CC=CC=C3.OC(=O)CC(O)(CC(O)=O)C(O)=O",1.945,4,0,14]
["S1777","Ethionamide","e4","L1700-07","in 10mM DMSO","Antibiotics","Microbiology","Ethionamide (Bayer 5312) is an antibiotic used in the treatment of tuberculosis.",166.24,"536-33-4",{"v":33,"d":"33.00"},198.51,"<1","N/A","http://selleckchem.com/products/Ethionamide.html","C8H10N2S","free base","Bayer 5312","CCC1=NC=CC(=C1)C(N)=S",1.498,1,1,2]
["S1778","Trifluridine (NSC 75520)","f4","L1700-07","in 10mM DMSO","DNA/RNA Synthesis,Thymidylate Synthase","DNA Damage/DNA Repair","Trifluridine (NSC 529182, NSC 75520, Viroptic, Trifluorothymidine, TFT) is an anti-herpesvirus antiviral agent by interacting viral DNA replication, used primarily on the eye.",{"v":296.2,"d":"296.20"},"70-00-8",{"v":59,"d":"59.00"},199.19,{"v":59,"d":"59.00"},199.19,"http://selleckchem.com/products/Trifluridine(Viroptic).html","C10H11F3N2O5","free base","NSC 529182, NSC 75520, Viroptic, Trifluorothymidine, TFT","OCC1OC(CC1O)N2C=C(C(=O)NC2=O)C(F)(F)F",-0.782,3,3,3]
["S1782","Azacitidine (5-Azacytidine)","g4","L1700-07","in 10mM DMSO","Autophagy,DNA Methyltransferase,Nucleoside Analog/Antimetabolite","DNA Damage/DNA Repair","Azacitidine (5-Azacytidine, 5-AzaC, Ladakamycin, AZA, 5-Aza, CC-486,NSC 102816) is a nucleoside analogue of cytidine that specifically inhibits DNA methylation by trapping DNA methyltransferases. Azacitidine induces mitochondrial apoptosis and autophagy.",{"v":244.2,"d":"244.20"},"320-67-2",{"v":48,"d":"48.00"},196.56,"<1","N/A","http://selleckchem.com/products/Azacitidine(Vidaza).html","C8H12N4O5","free base","5-AzaC,Ladakamycin, AZA,5-Aza, CC-486,NSC 102816,5-Azacytidine","NC1=NC(=O)N(C=N1)C2OC(CO)C(O)C2O",-2.505,4,4,2]
["S1784","Vidarabine","h4","L1700-07","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Vidarabine is an antiviral drug by interfering with the synthesis of viral DNA, used to treat herpes simplex and varicella zoster viruses.",267.24,"5536-17-4",{"v":53,"d":"53.00"},198.32,{"v":3,"d":"3.00"},11.23,"http://selleckchem.com/products/Vidarabine(Vira-A).html","C10H13N5O4","free base","N/A","NC1=C2N=C[N](C3OC(CO)C(O)C3O)C2=NC=N1",-1.881,4,4,2]
["S1786","Verteporfin (CL 318952)","a5","L1700-07","in 10mM DMSO","Apoptosis related,Autophagy,TEAD,VDA,YAP","Angiogenesis","Verteporfin (CL 318952, Visudyne) is a small molecule that inhibits TEAD–YAP association and YAP-induced liver overgrowth.  It is also a potent second-generation photosensitizing agent derived from porphyrin. Verteporfin is an autophagy inhibitor. Verteporfin inhibits cell proliferation and induces apoptosis.",718.79,"129497-78-5",{"v":100,"d":"100.00"},139.12,"<1","N/A","http://selleckchem.com/products/Verteporfin(Visudyne).html","C41H42N4O8","free base","CL 318952, Visudyne","COC(=O)CCC1=C(C)C2=CC3=NC(=CC4=C(C)C(=C([NH]4)C=C5N=C(C=C1[NH]2)C(=C5C)CCC(O)=O)C=C)C6=CC=C(C(C(=O)OC)C36C)C(=O)OC",7.789,9,2,12]
["S1787","Teniposide","b5","L1700-07","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Teniposide (NSC 122819, VM-26) is a chemotherapeutic medication mainly used in the treatment of childhood acute lymphocytic leukemia (ALL).",656.65,"29767-20-2",{"v":40,"d":"40.00"},60.92,"<1","N/A","http://selleckchem.com/products/Teniposide(Vumon).html","C32H32O13S","free base","NSC 122819, VM-26","COC1=CC(=CC(=C1O)OC)C2C3C(COC3=O)C(OC4OC5COC(OC5C(O)C4O)C6=CC=CS6)C7=CC8=C(OCO8)C=C27",2.516,10,3,6]
["S1789","Tetrabenazine (Xenazine)","c5","L1700-07","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Tetrabenazine(Xenazine,Ro 1-9569) acts primarily as a reversible high-affinity inhibitor of mono-amine uptake into granular vesicles of presynaptic neurons by binding selectively to VMAT-2; Also blocks dopamine D2 receptors, but this affinity is 1,000-fold lower than its affinity for VMAT-2.",317.42,"58-46-8",{"v":58,"d":"58.00"},182.72,"<1","N/A","http://selleckchem.com/products/Tetrabenazine(Nitoman).html","C19H27NO3","free base","Xenazine,Ro 1-9569","COC1=CC2=C(C=C1OC)C3CC(=O)C(CC(C)C)CN3CC2",3.365,3,0,4]
["S1790","Rifaximin","d5","L1700-07","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Rifaximin is a RNA synthesis inhibitor by binding the β subunit of the bacterial DNA-dependent RNA polymerase, used to treat traveler's diarrhea caused by certain bacteria.",785.88,"80621-81-4",{"v":47,"d":"47.00"},59.81,"<1","N/A","http://selleckchem.com/products/Rifaximin(Xifaxan).html","C43H51N3O11","free base","N/A","COC1\\C=C\\OC2(C)OC3=C(C2=O)C4=C(C(=C3C)O)C(=C(NC(=O)\\C(=C/C=C/C(C)C(O)C(C)C(O)C(C)C(OC(C)=O)C1C)C)C5=C4N=C6C=C(C)C=C[N]56)O",4.805,8,5,3]
["S1791","Bacitracin Zinc","e5","L1700-07","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Bacitracin(Zinc Bacitracin) is an antibiotic that interferes with the dephosphorylation of C55-isoprenyl pyrophosphate, a membrane carrier molecule that transports the building-blocks of the peptidoglycan bacterial cell wall outside of the inner membrane. It inhibits cleavage of Tyr from Met-enkephalin with IC50 of 10 μM.",1486.07,"1405-89-6",{"v":100,"d":"100.00"},67.29,"<1","N/A","http://www.selleck.cn/products/bacitracin-zinc.html","C66H101N17O16SZn","Free Base","Zinc Bacitracin","[Zn++].CCC(C)C(N)C1=NCC(S1)C(=O)NC(CC(C)C)C(=O)NC(CCC([O-])=O)C(=O)NC(C(C)CC)C(=O)NC2CCCCNC(=O)C(CC(N)=O)NC(=O)C(CC([O-])=O)NC(=O)C(CC3=C[NH]C=N3)NC(=O)C(CC4=CC=CC=C4)NC(=O)C(NC(=O)C(CCCN)NC2=O)C(C)CC",-3.993,14,15,31]
["S1792","Simvastatin (MK 733)","f5","L1700-07","in 10mM DMSO","Apoptosis related,Autophagy,Ferroptosis,HMG-CoA Reductase,Mitophagy","Metabolism","Simvastatin (MK-0733, MK 733) is a competitive inhibitor of HMG-CoA reductase with Ki of 0.1-0.2 nM in cell-free assays. Simvastatin induces ferroptosis, mitophagy, autophagy and apoptosis.",418.57,"79902-63-9",{"v":83,"d":"83.00"},198.29,"<1","N/A","http://selleckchem.com/products/Simvastatin(Zocor).html","C25H38O5","free base","MK-0733, MK 733","CCC(C)(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC3CC(O)CC(=O)O3)C12",4.634,4,1,7]
["S1793","Ramipril","g5","L1700-07","in 10mM DMSO","ACE,RAAS","Endocrinology & Hormones","Ramipril(HOE-498) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 5 nM.",416.51,"87333-19-5",{"v":83,"d":"83.00"},199.27,"<1","N/A","http://selleckchem.com/products/Ramipril(Altace).html","C23H32N2O5","free base","HOE-498","CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2C3CCCC3CC2C(O)=O",0.308,4,1,10]
["S1794","Fenofibrate (NSC-281319)","h5","L1700-07","in 10mM DMSO","Autophagy,P450 (e.g. CYP17),PPAR","Metabolism","Fenofibrate (NSC-281319) is a compound of the fibrate class and fibric acid derivative. Fenofibrate is a selective agonist of PPARα with EC50 of 30 μM. Fenofibrate binds to and inhibits cytochrome P450 epoxygenase (CYP)2C with IC50 of 0.2 μM, 0.7 μM and 9.7 μM for CYP2C19, CYP2B6 and CYP2C9, respectively. Fenofibrate induces autophagy.",360.83,"49562-28-9",{"v":72,"d":"72.00"},199.54,"<1","N/A","http://selleckchem.com/products/Fenofibrate(Tricor).html","C20H21ClO4","free base","NSC-281319","CC(C)OC(=O)C(C)(C)OC1=CC=C(C=C1)C(=O)C2=CC=C(Cl)C=C2",5.111,4,0,7]
["S1799","Ranolazine","a6","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Ranolazine (CVT 303, RS 43285-003) is a calcium uptake inhibitor via the sodium/calcium channel, used to treat chronic angina.",427.54,"95635-55-5",{"v":86,"d":"86.00"},201.15,"<1","N/A","http://selleckchem.com/products/Ranolazine(Ranexa).html","C24H33N3O4","Free Base","CVT 303, RS 43285-003","COC1=CC=CC=C1OCC(O)CN2CCN(CC2)CC(=O)NC3=C(C)C=CC=C3C",2.991,3,2,9]
["S1801","Ranitidine Hydrochloride","b6","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Ranitidine (AH19065) is a histamine H2-receptor antagonist, used to treat stomach or intestinal ulcers.",350.86,"66357-59-3",{"v":70,"d":"70.00"},199.51,{"v":70,"d":"70.00"},199.51,"http://selleckchem.com/products/Ranitidine-hydrochloride(Zantac).html","C13H22N4O3S.HCl","Hydrochloride","AH19065","Cl.CNC(/NCCSCC1=CC=C(CN(C)C)O1)=C\\[N+]([O-])=O",1.421,1,2,10]
["S1802","AICAR (Acadesine)","c6","L1700-07","in 10mM DMSO","AMPK,Mitophagy","PI3K/Akt/mTOR","AICAR (Acadesine, NSC105823, AICA Riboside), an AMPK activator, results in accumulation of ZMP, which mimics the stimulating effect of AMP on AMPK and AMPK kinase. AICAR (Acadesine) induces mitophagy. Phase 3.",258.23,"2627-69-2",{"v":51,"d":"51.00"},{"v":197.5,"d":"197.50"},"<1","N/A","http://selleckchem.com/products/Acadesine.html","C9H14N4O5","free base","NSC105823, AICA Riboside","NC(=O)C1=C(N)[N](C=N1)C2OC(CO)C(O)C2O",-2.913,3,5,3]
["S1805","Acetylcholine Chloride","d6","L1700-07","in 10mM DMSO","AChR","Neuronal Signaling","The chemical compound Acetylcholine Chloride(ACh chloride) is a neurotransmitter in both the peripheral nervous system (PNS) and central nervous system (CNS) in many organisms including humans.",181.66,"60-31-1",{"v":36,"d":"36.00"},198.17,{"v":36,"d":"36.00"},198.17,"http://www.selleck.cn/products/Acetylcholine-chloride.html","C7H16NO2.Cl","Chloride","ACh chloride","[Cl-].CC(=O)OCC[N+](C)(C)C",-3.869,2,0,4]
["S1806","Acipimox","e6","L1700-07","in 10mM DMSO","Others","Others","Acipimox (Olbemox,K-9321) is a niacin derivative used as a hypolipidemic agent.",154.12,"51037-30-0",{"v":31,"d":"31.00"},201.14,"<1","N/A","http://selleckchem.com/products/Acipimox.html","C6H6N2O3","free base","Olbemox,K-9321","CC1=CN=C(C=[N+]1[O-])C(O)=O",-0.975,2,0,1]
["S1807","Aciclovir (BW 248U)","f6","L1700-07","in 10mM DMSO","Antiviral,Apoptosis related,DNA/RNA Synthesis,Nucleoside Analog/Antimetabolite","Microbiology","Acyclovir (Acyclovir, Acycloguanosine, Zovirax, ACV, NSC 645011,BW 248U) is a synthetic nucleoside analogue active against herpesviruses. Acyclovir induces cell cycle perturbation and apoptosis in Jurkat leukemia cells.",{"v":225.2,"d":"225.20"},"59277-89-3",{"v":45,"d":"45.00"},199.82,"<1","N/A","http://selleckchem.com/products/Acyclovir(Aciclovir).html","C8H11N5O3","free base","Acyclovir, Acycloguanosine, Zovirax, ACV, NSC 645011,BW 248U","NC1=NC2=C(N=C[N]2COCCO)C(=O)N1",-1.423,4,3,4]
["S1808","Nifedipine (BAY-a-1040)","g6","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Nifedipine (BAY-a-1040) is a dihydropyridine calcium channel blocker, used to lower hypertension and to treat angina.",346.33,"21829-25-4",{"v":69,"d":"69.00"},199.23,"<1","N/A","http://selleckchem.com/products/Nifedipine(Adalat).html","C17H18N2O6","free base","BAY-a-1040","COC(=O)C1=C(C)NC(=C(C1C2=C(C=CC=C2)[N+]([O-])=O)C(=O)OC)C",1.766,4,1,6]
["S1811","Amiloride (MK-870) HCl","h6","L1700-07","in 10mM DMSO","Calcium Channel,Serine Protease,Sodium Channel","Transmembrane Transporters","Amiloride (MK-870 HCl) is a selective T-type calcium channel blocker, an epithelial sodium channel blocker and a selective inhibitor of urokinase plasminogen activator (uPA)(Ki=7 μM).",266.09,"2016-88-8",{"v":53,"d":"53.00"},199.18,{"v":6,"d":"6.00"},22.55,"http://selleckchem.com/products/Amiloride-hydrochloride(Midamor).html","C6H8ClN7O.HCl","Hydrochloride","MK-870 HCl","Cl.NC(=N)NC(=O)C1=NC(=C(N)N=C1N)Cl",-0.366,3,4,2]
["S1813","Amlodipine Besylate","a7","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Amlodipine Besylate is a long-acting calcium channel blocker, used to lower blood pressure and prevent chest pain.",567.05,"111470-99-6",{"v":113,"d":"113.00"},199.28,"<1","N/A","http://selleckchem.com/products/Amlodipine-besylate(Norvasc).html","C20H25ClN2O5.C6H6O3S","Besylate","N/A","CCOC(=O)C1=C(COCCN)NC(=C(C1C2=C(Cl)C=CC=C2)C(=O)OC)C.O[S](=O)(=O)C3=CC=CC=C3",2.739,5,2,11]
["S1816","Chlorpheniramine Maleate","b7","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Chlorpheniramine Maleate (Chlorpheniramine maleate, Chlorphenamine, NCI-C55265) is an histamine H1 receptor antagonist with IC50 of 12 nM.",390.86,"113-92-8",{"v":78,"d":"78.00"},199.56,{"v":78,"d":"78.00"},199.56,"http://selleckchem.com/products/Chlorpheniramine-maleate.html","C16H19ClN2.C4H4O4","Maleate","NCI-C55265","CN(C)CCC(C1=CC=C(Cl)C=C1)C2=NC=CC=C2.OC(=O)\\C=C/C(O)=O",{"v":0.7,"d":"0.700"},3,0,7]
["S1820","Clofibrate","c7","L1700-07","in 10mM DMSO","Others","Others","Clofibrate (Atromid-S), a fibric acid derivative used in the treatment of hyperlipoproteinemia type III and severe hypertriglyceridemia.",{"v":242.7,"d":"242.70"},"637-07-0",{"v":7,"d":"7.00"},28.84,"<1","N/A","http://www.selleck.cn/products/Clofibrate(Atromid-S).html","C12H15ClO3","Free Base","N/A","CCOC(=O)C(C)(C)OC1=CC=C(Cl)C=C1",3.329,3,0,5]
["S1823","Fenoprofen Calcium","d7","L1700-07","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Fenoprofen Calcium is a nonsteroidal, anti-inflammatory antiarthritic agent.",{"v":522.6,"d":"522.60"},"34597-40-5",{"v":105,"d":"105.00"},200.92,"<1","N/A","http://selleckchem.com/products/fenoprofen-calcium.html","C30H26CaO6","Calcium salt","N/A","[Ca++].CC(C([O-])=O)C1=CC(=CC=C1)OC2=CC=CC=C2.CC(C([O-])=O)C3=CC(=CC=C3)OC4=CC=CC=C4",4.086,2,0,8]
["S1825","Erdosteine","e7","L1700-07","in 10mM DMSO","NF-κB","NF-κB","Erdosteine (KW-9144,RV 144) is a mucolytic which is used in treatment of excessive viscous mucus. Erdosteine inhibits lipopolysaccharide (LPS)-induced NF-κB activation.",249.31,"84611-23-4",{"v":50,"d":"50.00"},200.55,"<1","N/A","http://selleckchem.com/products/erdosteine.html","C8H11NO4S2","free base","KW-9144,RV 144","OC(=O)CSCC(=O)NC1CCSC1=O",-0.382,3,1,5]
["S1827","Betaxolol HCl","f7","L1700-07","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Betaxolol (SL 75212) is a β1 adrenergic receptor blocker with IC50 of 6 μM.",343.89,"63659-19-8",{"v":69,"d":"69.00"},200.65,{"v":69,"d":"69.00"},200.65,"http://selleckchem.com/products/betaxolol-hydrochloride-betoptic.html","C18H29NO3.HCl","Hydrochloride","SL 75212 HCl","Cl.CC(C)NCC(O)COC1=CC=C(CCOCC2CC2)C=C1",2.959,2,2,11]
["S1828","Proparacaine HCl","g7","L1700-07","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Proparacaine HCl(Proxymetacaine Hydrochloride) is a voltage-gated sodium channels antagonist with ED50 of 3.4 mM.",330.85,"5875-06-9",{"v":12,"d":"12.00"},36.27,{"v":66,"d":"66.00"},199.49,"http://selleckchem.com/products/proparacaine-hcl.html","C16H26N2O3.HCl","Hydrochloride","Proxymetacaine Hydrochloride","Cl.CCCOC1=C(N)C=C(C=C1)C(=O)OCCN(CC)CC",3.013,3,1,10]
["S1829","Pranlukast","h7","L1700-07","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Pranlukast (ONO-1078,ono-rs-411) is an orally administered, and selective antagonist of the cysteinyl leukotrienes (LT) C(4), LTD(4) and LTE(4), used in the prophylactic treatment of chronic bronchial asthma.",{"v":481.5,"d":"481.50"},"103177-37-3",{"v":11,"d":"11.00"},22.85,"<1","N/A","http://selleckchem.com/products/pranlukast.html","C27H23N5O4","free base","ONO-1078,ono-rs-411","O=C(NC1=CC2=C(C=C1)C(=O)C=C(O2)C3=NN=N[NH]3)C4=CC=C(OCCCCC5=CC=CC=C5)C=C4",4.232,7,2,9]
["S1830","Oxfendazole","a8","L1700-07","in 10mM DMSO","Parasite","Microbiology","Oxfendazole (RS-8858,Fenbendazole sulfoxide) is a broad spectrum benzimidazole anthelmintic.",315.35,"53716-50-0",{"v":10,"d":"10.00"},31.71,"<1","N/A","http://selleckchem.com/products/oxfendazole.html","C15H13N3O3S","free base","RS-8858,Fenbendazole sulfoxide","COC(=O)NC1=NC2=C([NH]1)C=C(C=C2)[S](=O)C3=CC=CC=C3",2.657,4,2,4]
["S1831","Carvedilol","b8","L1700-07","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Carvedilol (BM-14190, SKF 105517) is a non-selective beta blocker/alpha-1 blocker, used to treat congestive heart failure (CHF) and high blood pressure.",406.47,"72956-09-3",{"v":81,"d":"81.00"},199.28,"<1","N/A","http://selleckchem.com/products/carvedilol.html","C24H26N2O4","free base","BM-14190, SKF 105517","COC1=CC=CC=C1OCCNCC(O)COC2=C3C(=CC=C2)[NH]C4=C3C=CC=C4",4.014,3,3,10]
["S1832","Atracurium Besylate","c8","L1700-07","in 10mM DMSO","AChR","Neuronal Signaling","Atracurium Besylate (BW 33A, 51W89) is a neuromuscular blocking agent with ED95 of 0.2 mg/kg.",1243.48,"64228-81-5",{"v":100,"d":"100.00"},80.42,{"v":33,"d":"33.00"},26.54,"http://selleckchem.com/products/atracurium-besylate.html","C53H72N2O12.2(C6H5O3S)","Dibesylate","BW 33A, 51W89","COC1=CC=C(CC2C3=CC(=C(OC)C=C3CC[N+]2(C)CCC(=O)OCCCCCOC(=O)CC[N+]4(C)CCC5=CC(=C(OC)C=C5C4CC6=CC=C(OC)C(=C6)OC)OC)OC)C=C1OC.[O-][S](=O)(=O)C7=CC=CC=C7.[O-][S](=O)(=O)C8=CC=CC=C8",3.646,12,0,28]
["S1833","Butoconazole nitrate","d8","L1700-07","in 10mM DMSO","Fungal,IFN,Interleukins,TNF-alpha","Microbiology","Butoconazole nitrate (RS-35887) is an anti-fungal agent that inhibits PHA-stimulated release of cytokines-- IL-2, TNFα, IFN and GM-CSF from human peripheral blood lymphocytes (IC50 of 7.2 μg/mL, 14.4 μg/mL, 7.36 μg/mL and 7.6 μg/mL, respectively).",474.79,"64872-77-1",{"v":95,"d":"95.00"},200.09,"<1","N/A","http://selleckchem.com/products/butoconazole-nitrate.html","C19H17Cl3N2S.HNO3","Nitrate","RS-35887","O[N+]([O-])=O.ClC1=CC=C(CCC(C[N]2C=CN=C2)SC3=C(Cl)C=CC=C3Cl)C=C1",5.238,1,0,7]
["S1835","Azithromycin (CP-62993)","e8","L1700-07","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture,Autophagy,Bacterial,COVID-19","Autophagy","Azithromycin (CP-62993, XZ-450) is an antibiotic by inhibiting protein synthesis, used for the treatment of bacterial infections.",748.98,"83905-01-5",{"v":100,"d":"100.00"},133.51,"<1","N/A","http://selleckchem.com/products/azithromycin-zithromax.html","C38H72N2O12","Free Base","XZ-450,CP-62993","CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(O)CC(C)CN(C)C(C)C(O)C1(C)O",2.078,7,3,7]
["S1836","Albendazole Oxide","f8","L1700-07","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Albendazole Oxide (Ricobendazole,Albendazole sulfoxide) is a tubulin polymerization or assembly inhibitor, used for the treatment of a variety of parasitic worm infestations.",281.33,"54029-12-8",{"v":11,"d":"11.00"},{"v":39.1,"d":"39.10"},"<1","N/A","http://selleckchem.com/products/albendazole-oxide-ricobendazole.html","C12H15N3O3S","free base","Ricobendazole,Albendazole sulfoxide","CCC[S](=O)C1=CC2=C(C=C1)N=C(NC(=O)OC)[NH]2",1.953,4,2,5]
["S1839","Chloroxine","g8","L1700-07","in 10mM DMSO","Bacterial","Microbiology","Chloroxine is a synthetic antibacterial compound that is effective in the treatment of dandruff and seborrheic dermatitis when incorporated in a shampoo.",214.05,"773-76-2",{"v":43,"d":"43.00"},200.89,"<1","N/A","http://selleckchem.com/products/Chloroxine.html","C9H5Cl2NO","free base","N/A","OC1=C(Cl)C=C(Cl)C2=C1N=CC=C2",3.103,1,1,0]
["S1840","Lomustine","h8","L1700-07","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Lomustine (NSC79037, Gleostine, CeeNU, CCNU) inhibits cancer cells by damaging the DNA and stops cells from dividing.",{"v":233.7,"d":"233.70"},"13010-47-4",{"v":46,"d":"46.00"},196.83,"<1","N/A","http://selleckchem.com/products/Lomustine(CeeNU).html","C9H16ClN3O2","free base","NSC79037, Gleostine, CeeNU, CCNU","ClCCN(N=O)C(=O)NC1CCCCC1",2.394,2,1,4]
["S1843","Chenodeoxycholic Acid","a9","L1700-07","in 10mM DMSO","FXR","Metabolism","Chenodeoxycholic Acid (Chenodiol, Chenodesoxycholic acid, Chenocholic acid,CDCA) is a naturally occurring human bile acid, and inhibits production of cholesterol in the liver and absorption in the intestines. Chenodeoxycholic Acid is a hydrophobic primary bile acid that activates nuclear receptors (FXR) involved in cholesterol metabolism.",392.57,"474-25-9",{"v":79,"d":"79.00"},201.24,"<1","N/A","http://selleckchem.com/products/Chenodeoxycholic-acid.html","C24H40O4","free base","Chenodiol, Chenodesoxycholic acid, Chenocholic acid,CDCA","CC(CCC(O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CCC12C",4.014,1,2,4]
["S1845","Cimetidine","b9","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Cimetidine (SKF-92334), a histamine congener, competitively inhibits histamine binding to histamine H2 receptors.",252.34,"51481-61-9",{"v":51,"d":"51.00"},202.11,"<1","N/A","http://selleckchem.com/products/Cimetidine(Tagamet).html","C10H16N6S","free base","SKF-92334","CNC(NCCSCC1=C(C)[NH]C=N1)=NC#N",0.007,2,3,7]
["S1847","Clemastine (HS-592) fumarate","c9","L1700-07","in 10mM DMSO","Autophagy,Histamine Receptor,mTOR","Neuronal Signaling","Clemastine Fumarate (HS-592, Meclastine) is a selective histamine H1 receptor antagonist with IC50 of 3 nM. Clemastine stimulates autophagy via mTOR pathway.",459.96,"14976-57-9",{"v":35,"d":"35.00"},76.09,"<1","N/A","http://selleckchem.com/products/Clemastine-Fumarate.html","C21H26ClNO.C4H4O4","Fumarate","HS-592 fumarate, Meclastine fumarate","CN1CCCC1CCOC(C)(C2=CC=CC=C2)C3=CC=C(Cl)C=C3.OC(=O)\\C=C\\C(O)=O",{"v":1.81,"d":"1.810"},3,0,8]
["S1848","Curcumin","d9","L1700-07","in 10mM DMSO","Apoptosis related,Autophagy,Epigenetic Reader Domain,Ferroptosis,HCV,HDAC,Histone Acetyltransferase,HIV,Influenza Virus,NF-κB,Nrf2","Epigenetics","Curcumin (Diferuloylmethane, Natural Yellow 3, Turmeric yellow) is the principal curcuminoid of the popular Indian spice turmeric, which is a member of the ginger family (Zingiberaceae). It is an inhibitor of p300 histone acetylatransferase（IC50~25 μM）and Histone deacetylase (HDAC); activates Nrf2 pathway and supresses the activation of NF-κB. Curcumin induces mitophagy, autophagy, apoptosis, and cell cycle arrest with antitumor activity. Curcumin reduces renal damage associated with rhabdomyolysis by decreasing ferroptosis-mediated cell death. Curcumin exhibits anti-infective properties against various human pathogens like the influenza virus, hepatitis C virus, HIV and so on.",368.38,"458-37-7",{"v":73,"d":"73.00"},198.16,"<1","N/A","http://selleckchem.com/products/Curcumin.html","C21H20O6","free base","Diferuloylmethane, Natural Yellow 3, Turmeric yellow","COC1=CC(=CC=C1O)/C=C/C(O)=C/C(=O)/C=C/C2=CC(=C(O)C=C2)OC",3.573,3,3,7]
["S1849","Daidzein","e9","L1700-07","in 10mM DMSO","PPAR","Metabolism","Daidzein is a natural isoflavone phytoestrogen found in Leguminosae, used as a component of foods and dietary supplements. Daidzein is a soy isoflavone, which acts as a PPAR activator.",254.24,"486-66-8",{"v":51,"d":"51.00"},{"v":200.6,"d":"200.60"},"<1","N/A","http://selleckchem.com/products/Daidzein.html","C15H10O4","free base","N/A","OC1=CC=C(C=C1)C2=COC3=CC(=CC=C3C2=O)O",2.382,2,2,1]
["S1854","Bifonazole","f9","L1700-07","in 10mM DMSO","Fungal","Microbiology","Bifonazole (Bay h 4502,(±)-bifonazole) is a substituted imidazole antifungal agent.",310.39,"60628-96-8",{"v":62,"d":"62.00"},199.75,"<1","N/A","http://selleckchem.com/products/bifonazole.html","C22H18N2","free base","Bay h 4502,(±)-bifonazole","C1=CC=C(C=C1)C([N]2C=CN=C2)C3=CC=C(C=C3)C4=CC=CC=C4",4.637,1,0,4]
["S1855","Pefloxacin Mesylate","g9","L1700-07","in 10mM DMSO","Bacterial","Microbiology","Pefloxacin Mesylate(Pefloxacinium mesylate) is a synthetic chemotherapeutic agent and an antibacterial agent with IC50 of 6.7 nM.",429.46,"70458-95-6",{"v":14,"d":"14.00"},{"v":32.6,"d":"32.60"},{"v":67,"d":"67.00"},156.01,"http://selleckchem.com/products/pefloxacin-mesylate.html","C17H20FN3O3.CH4O3S","Mesylate","Pefloxacinium mesylate","CCN1C=C(C(O)=O)C(=O)C2=CC(=C(C=C12)N3CCN(C)CC3)F.C[S](O)(=O)=O",-1.618,2,0,3]
["S1856","Metoprolol Tartrate","h9","L1700-07","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Metoprolol Tartrate (CGP 2175E) is a selective β1 receptor blocker medication, used to treat hypertension and heart failure.",684.81,"56392-17-7",{"v":100,"d":"100.00"},146.03,{"v":100,"d":"100.00"},146.03,"http://selleckchem.com/products/metoprolol-tartrate.html","2C15H25NO3.C4H6O6","Tartrate","CGP 2175E","COCCC1=CC=C(OCC(O)CNC(C)C)C=C1.COCCC2=CC=C(OCC(O)CNC(C)C)C=C2.OC(C(O)C(O)=O)C(O)=O",-3.559,6,6,21]
["S1858","Dienestrol","a10","L1700-07","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Dienestrol(Restrol) is a synthetic, non-steroidal estrogen. It is an estrogen receptor agonist.",266.33,"84-17-3",{"v":53,"d":"53.00"},{"v":199,"d":"199.00"},{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/Dienestrol(Restrol).html","C18H18O2","Free Base","Restrol","C/C=C(C1=CC=C(O)C=C1)/C(=C/C)C2=CC=C(O)C=C2",4.692,0,2,3]
["S1859","Diethylstilbestrol","b10","L1700-07","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Diethylstilbestrol (Stilbestrol) is a synthetic nonsteroidal estrogen, used to prevent miscarriage and other pregnancy complications.",268.35,"56-53-1",{"v":54,"d":"54.00"},201.23,"<1","N/A","http://selleckchem.com/products/Diethylstilbestrol(Stilbestrol).html","C18H20O2","free base","Stilbestrol","CCC(/C1=CC=C(O)C=C1)=C(CC)\\C2=CC=C(O)C=C2",5.137,0,2,4]
["S1865","Diltiazem HCl","c10","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Diltiazem (Tiazac, RG 83606) HCl is a benzothiazepine derivative with vasodilating action due to its antagonism of the actions of the calcium ion in membrane functions.",450.98,"33286-22-5",{"v":90,"d":"90.00"},199.57,{"v":90,"d":"90.00"},199.57,"http://selleckchem.com/products/Diltiazem-HCl(Tiazac).html","C22H26N2O4S.HCl","Hydrochloride","RG 83606 HCl","Cl.COC1=CC=C(C=C1)C2SC3=C(C=CC=C3)N(CCN(C)C)C(=O)C2OC(C)=O",3.475,4,0,7]
["S1866","Diphenhydramine HCl","d10","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Diphenhydramine HCl is a first-generation histamine H1 receptor antagonist, used in various allergic conditions such as rhinitis, urticaria and conjunctivitis.",291.82,"147-24-0",{"v":58,"d":"58.00"},198.75,{"v":58,"d":"58.00"},198.75,"http://selleckchem.com/products/Diphenhydramine-hydrochloride(Benadryl).html","C17H21NO.HCl","Hydrochloride","N/A","Cl.CN(C)CCOC(C1=CC=CC=C1)C2=CC=CC=C2",3.766,1,0,6]
["S1869","Dapoxetine HCl","e10","L1700-07","in 10mM DMSO","5-HT Receptor,Serotonin Transporter","Neuronal Signaling","Dapoxetine HCl (LY-210448) is a short-acting novel selective serotonin reuptake inhibitor, used for the treatment of premature ejaculation.",341.87,"129938-20-1",{"v":68,"d":"68.00"},198.91,{"v":68,"d":"68.00"},198.91,"http://selleckchem.com/products/Dapoxetine-hydrochloride(Priligy).html","C21H23NO.HCl","Hydrochloride","LY-210448","Cl.CN(C)C(CCOC1=C2C=CC=CC2=CC=C1)C3=CC=CC=C3",4.917,1,0,6]
["S1876","Valaciclovir HCl","f10","L1700-07","in 10mM DMSO","CMV","Microbiology","Valaciclovir HCl, an aciclovir prodrug, inhibits activity of virus DNA polymerase, used to treat infections caused by herpes simplex virus (HSV) and varicella zoster virus, and for prophylaxis against cytomegalovirus (CMV).",{"v":360.8,"d":"360.80"},"124832-27-5",{"v":14,"d":"14.00"},{"v":38.8,"d":"38.80"},{"v":72,"d":"72.00"},199.56,"http://selleckchem.com/products/valaciclovir-hcl.html","C13H20N6O4.HCl","Hydrochloride","N/A","Cl.CC(C)C(N)C(=O)OCCOC[N]1C=NC2=C1N=C(N)NC2=O",-0.296,6,3,8]
["S1878","Ganciclovir (BW 759)","g10","L1700-07","in 10mM DMSO","CMV","Microbiology","Ganciclovir (RS-21592, BW-759, 2'-Nor-2'-deoxyguanosine) is an antiviral drug for feline herpesvirus type-1 with IC50 of 5.2 μM in a cell-free assay.",255.23,"82410-32-0",{"v":27,"d":"27.00"},105.79,"<1","N/A","http://selleckchem.com/products/ganciclovir.html","C9H13N5O4","free base","RS-21592, BW-759, 2'-Nor-2'-deoxyguanosine","NC1=NC2=C(N=C[N]2COC(CO)CO)C(=O)N1",-1.934,4,4,5]
["S1880","Roxatidine Acetate HCl","h10","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Roxatidine Acetate HCl(HOE 760) is a specific and competitive histamin H2-receptor antagonist, with IC50 of 3.2 μM, inhibits gastric acid secretion and ulcer formation.",{"v":384.9,"d":"384.90"},"93793-83-0",{"v":77,"d":"77.00"},200.05,{"v":77,"d":"77.00"},200.05,"http://selleckchem.com/products/roxatidine-acetate-hcl.html","C19H28N2O4.HCl","Hydrochloride","HOE 760","Cl.CC(=O)OCC(=O)NCCCOC1=CC=CC(=C1)CN2CCCCC2",2.148,4,1,10]
["S1881","Protionamide","a11","L1700-07","in 10mM DMSO","Bacterial","Microbiology","Protionamide (Prothionamide, 1321-TH) is a drug used in the treatment of tuberculosis.",180.27,"14222-60-7",{"v":36,"d":"36.00"},{"v":199.7,"d":"199.70"},"<1","N/A","http://selleckchem.com/products/protionamide-prothionamide.html","C9H12N2S","free base","Prothionamide, 1321-TH","CCCC1=NC=CC(=C1)C(N)=S",1.954,1,1,3]
["S1883","Idoxuridine","b11","L1700-07","in 10mM DMSO","Antiviral","Microbiology","Idoxuridine (NSC 39661, SKF 14287,5-Iodo-2′-deoxyuridine,5-IUdR,IdUrd) is an antiviral agent for feline herpesvirus type-1 with IC50 of 4.3 μM.",{"v":354.1,"d":"354.10"},"54-42-2",{"v":35,"d":"35.00"},98.84,"<1","N/A","http://selleckchem.com/products/idoxuridine.html","C9H11IN2O5","free base","NSC 39661, SKF 14287,5-Iodo-2′-deoxyuridine,5-IUdR,IdUrd","OCC1OC(CC1O)N2C=C(I)C(=O)NC2=O",-1.402,3,3,2]
["S1884","Sparfloxacin","c11","L1700-07","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Sparfloxacin (AT-4140, CI-978, PD 131501,Zagam) is a fluoroquinolone antibiotic, shows broad and potent antibacterial activity.",{"v":392.4,"d":"392.40"},"110871-86-8",{"v":9,"d":"9.00"},22.94,"<1","N/A","http://selleckchem.com/products/sparfloxacin.html","C19H22F2N4O3","free base","AT-4140, CI-978, PD 131501,Zagam","CC1CN(CC(C)N1)C2=C(F)C3=C(C(=C2F)N)C(=O)C(=CN3C4CC4)C(O)=O",-1.056,2,2,3]
["S1885","Felodipine","d11","L1700-07","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Felodipine (CGH-869) is a selective L-type Ca2+ channel blocker with IC50 of 0.15 nM.",384.25,"72509-76-3",{"v":77,"d":"77.00"},200.39,"<1","N/A","http://selleckchem.com/products/Felodipine(Plendil).html","C18H19Cl2NO4","free base","CGH-869","CCOC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2Cl)Cl)C(=O)OC)C",3.549,4,1,6]
["S1888","Deflazacort","e11","L1700-07","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Deflazacort (MDL 458) is a glucocorticoid used as an anti-inflammatory and immunosuppressant.",441.52,"14484-47-0",{"v":88,"d":"88.00"},199.31,"<1","N/A","http://selleckchem.com/products/Deflazacor.html","C25H31NO6","free base","MDL 458","CC(=O)OCC(=O)C12N=C(C)OC1CC3C4CCC5=CC(=O)C=CC5(C)C4C(O)CC23C",{"v":1.67,"d":"1.670"},6,1,4]
["S1890","Nizatidine","f11","L1700-07","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Nizatidine is a histamine H2 receptor antagonist with IC50 of 0.9 nM, also inhibits AChE with IC50 of 6.7 μM.",331.46,"76963-41-2",{"v":66,"d":"66.00"},199.12,{"v":28,"d":"28.00"},84.47,"http://selleckchem.com/products/Nizatidine(Axid).html","C12H21N5O2S2","free base","N/A","CNC(/NCCSCC1=CSC(=N1)CN(C)C)=C/[N+]([O-])=O",0.643,1,2,10]
["S1891","Carbidopa","g11","L1700-07","in 10mM DMSO","Decarboxylase","Metabolism","Carbidopa is an aromatic-L-amino-acid decarboxylase inhibitor with an IC50 of 29 ± 2 μM.",226.23,"28860-95-9",{"v":4,"d":"4.00"},17.68,"<1","N/A","http://selleckchem.com/products/Carbidopa.html","C10H14N2O4","free base","N/A","CC(CC1=CC(=C(O)C=C1)O)(NN)C(O)=O",0.364,1,4,4]
["S1894","Valsartan (CGP-48933)","h11","L1700-07","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Valsartan (CGP-48933) is a selective angiotensin II receptor antagonist, used to treat high blood pressure and congestive heart failure.",435.52,"137862-53-4",{"v":87,"d":"87.00"},199.76,"<1","N/A","http://selleckchem.com/products/Valsartan(Diovan).html","C24H29N5O3","free base","CGP-48933","CCCCC(=O)N(CC1=CC=C(C=C1)C2=CC=CC=C2C3=N[NH]N=N3)C(C(C)C)C(O)=O",4.538,5,1,10]
["S1895","Dipyridamole (NSC 515776)","a2","L1700-08","in 10mM DMSO","PDE","Metabolism","Dipyridamole (NSC-515776, Persantine) is a phosphodiesterase inhibitor that blocks uptake and metabolism of adenosine by erythrocytes and vascular endothelial cells.",504.63,"58-32-2",{"v":101,"d":"101.00"},200.15,"<1","N/A","http://selleckchem.com/products/Dipyridamole(Permole,-Persantine).html","C24H40N8O4","free base","Persantine,NSC-515776","OCCN(CCO)C1=NC2=C(N=C(N=C2N3CCCCC3)N(CCO)CCO)C(=N1)N4CCCCC4",2.483,4,4,12]
["S1896","Hydroxyurea (NSC-32065)","b2","L1700-08","in 10mM DMSO","Apoptosis related,Autophagy,DNA/RNA Synthesis,HIV","DNA Damage/DNA Repair","Hydroxyurea (NSC-32065, NCI-C04831, Hydroxycarbamide) is an antineoplastic agent that inhibits DNA synthesis through the inhibition of ribonucleoside diphosphate reductase. Hydroxyurea activates apoptosis and autophagy. Hydroxyurea is used to treat HIV infection.",76.05,"127-07-1",{"v":15,"d":"15.00"},197.24,{"v":15,"d":"15.00"},197.24,"http://selleckchem.com/products/Hydroxyurea(Cytodrox).html","CH4N2O2","free base","NCI-C04831, Hydroxycarbamide,NSC-32065","NC(=O)NO",{"v":-1.03,"d":"-1.030"},1,2,0]
["S1897","Potassium Iodide","c2","L1700-08","in 10mM DMSO","Others","Others","Potassium Iodide is used to treat overactive thyroid and to protect the thyroid gland from the effects of radiation from inhaled or swallowed radioactive iodine.",{"v":166,"d":"166.00"},"7681-11-0",{"v":33,"d":"33.00"},{"v":198.8,"d":"198.80"},{"v":33,"d":"33.00"},{"v":198.8,"d":"198.80"},"http://selleckchem.com/products/Potassium-iodide.html","K+I-","Inorganic salt","N/A","[K+].[I-]",-3.113,0,0,0]
["S1898","Tropisetron HCl","d2","L1700-08","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Tropisetron HCl (ICS 205-930) is a potent and selective 5-HT3 receptor antagonist and α7-nicotinic receptor agonist, used to treat nausea and vomiting following chemotherapy.",320.81,"105826-92-4",{"v":35,"d":"35.00"},{"v":109.1,"d":"109.10"},{"v":46,"d":"46.00"},143.39,"http://selleckchem.com/products/Tropisetron-hydrochloride.html","C17H20N2O2.HCl","Hydrochloride","ICS 205-930","Cl.CN1C2CCC1CC(C2)OC(=O)C3C=NC4=CC=CC=C34",2.366,3,0,3]
["S1899","Nicotinamide (NSC 13128)","e2","L1700-08","in 10mM DMSO","Sirtuin","DNA Damage/DNA Repair","Nicotinamide (Niacinamide, Vitamin PP, Nicotinic acid amide, Vitamin B3, NSC 27452,NSC 13128), a water-soluble vitamin, is an active component of coenzymes NAD and NADP, and also act as an inhibitor of sirtuins.",122.12,"98-92-0",{"v":24,"d":"24.00"},196.53,{"v":24,"d":"24.00"},196.53,"http://selleckchem.com/products/Nicotinamide(Niacinamide).html","C6H6N2O","free base","Niacinamide, Vitamin PP, Nicotinic acid amide, Vitamin B3, NSC 27452,NSC 13128","NC(=O)C1=CC=CN=C1",-0.319,2,1,1]
["S1902","Vitamin B12","f2","L1700-08","in 10mM DMSO","Vitamin","Metabolism","Vitamin B12 (Cobalamin, Cyanocobalamin) is a water soluble vitamin with a key role in the normal functioning of the brain and nervous system, and for the formation of blood.",1355.37,"68-19-9",{"v":75,"d":"75.00"},55.34,{"v":6,"d":"6.00"},4.43,"http://selleckchem.com/products/Vitamin-B12.html","C63H88CoN14O14P","free base","Cobalamin, Cyanocobalamin","CC(CNC(=O)CCC1(C)C(CC(N)=O)C2N=C1/C(=C/3N=C(/C=C/4N=C(/C(=C/5[N-]C2(C)C(C)(CC(N)=O)C5CCC(N)=O)C)C(C)(CC(N)=O)C4CCC(N)=O)C(C)(C)C3CCC(N)=O)C)O[P]([O-])(=O)OC6C(O)C(OC6CO)[N]7C=NC8=C7C=C(C)C(=C8)C.[Co++]C#N",-1.129,14,9,26]
["S1903","Diclofenac Sodium","g2","L1700-08","in 10mM DMSO","COX","Neuronal Signaling","Diclofenac Sodium (GP 45840) is a non-selective COX inhibitor with IC50 of 0.5 μg/ml and 0.5 μg/ml for COX-1 and -2 in intact cells, respectively, used as a nonsteroidal anti-inflammatory drug (NSAID) to relieve pain and reduce swelling in flammation.",318.13,"15307-79-6",{"v":64,"d":"64.00"},201.18,{"v":14,"d":"14.00"},44.01,"http://selleckchem.com/products/Diclofenac-sodium.html","C14H10Cl2NNaO2","Sodium Salt","GP 45840","[Na+].[O-]C(=O)CC1=C(NC2=C(Cl)C=CC=C2Cl)C=CC=C1",2.899,0,1,4]
["S1904","Avobenzone","h2","L1700-08","in 10mM DMSO","Others","Others","Avobenzone (Butyl methoxydibenzoylmethane, BF2AVB) is an oil soluble ingredient used in sunscreen products to absorb the full spectrum of UVA rays and a dibenzoylmethane derivative.",310.39,"70356-09-1",{"v":62,"d":"62.00"},199.75,"<1","N/A","http://selleckchem.com/products/Avobenzone(Parsol-1789).html","C20H22O3","free base","Butyl methoxydibenzoylmethane, BF2AVB","COC1=CC=C(C=C1)C(=O)CC(=O)C2=CC=C(C=C2)C(C)(C)C",4.538,3,0,6]
["S1905","Amlodipine","a3","L1700-08","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Amlodipine (UK-48340) is a long-acting calcium channel blocker, used to lower blood pressure and prevent chest pain.",408.88,"88150-42-9",{"v":82,"d":"82.00"},200.55,"<1","N/A","http://selleckchem.com/products/Amlodipine(Norvasc).html","C20H25ClN2O5","free base","UK-48340","CCOC(=O)C1=C(COCCN)NC(=C(C1C2=C(Cl)C=CC=C2)C(=O)OC)C",1.576,5,2,10]
["S1907","Metronidazole","b3","L1700-08","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,DNA/RNA Synthesis","DNA Damage/DNA Repair","Metronidazole, a synthetic antibacterial and antiprotozoal agent of the nitroimidazole class, is used against protozoa.",171.15,"443-48-1",{"v":34,"d":"34.00"},198.66,"<1","N/A","http://selleckchem.com/products/Metronidazole(Flagyl).html","C6H9N3O3","free base","N/A","CC1=NC=C([N]1CCO)[N+]([O-])=O",-0.337,1,1,3]
["S1908","Flutamide","c3","L1700-08","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Flutamide (SCH-13521) is an antiandrogen drug, with its active metablolite binding at androgen receptor with Ki values of 55 nM, and primarily used to treat prostate cancer.",276.21,"13311-84-7",{"v":55,"d":"55.00"},199.12,"<1","N/A","http://selleckchem.com/products/Flutamide(Eulexin).html","C11H11F3N2O3","free base","SCH-13521","CC(C)C(=O)NC1=CC(=C(C=C1)[N+]([O-])=O)C(F)(F)F",2.916,1,1,4]
["S1909","Fluvastatin (XU-62-320) Sodium","d3","L1700-08","in 10mM DMSO","HMG-CoA Reductase","Metabolism","Fluvastatin Sodium (Vastin,XU-62-320) inhibits HMG-CoA reductase activity with IC50 of 8 nM in a cell-free assay.",433.45,"93957-55-2",{"v":87,"d":"87.00"},200.72,{"v":1,"d":"1.00"},2.31,"http://selleckchem.com/products/Fluvastatin-Sodium(Lescol).html","C24H25FNNaO4","Sodium","Vastin,XU-62-320","[Na+].CC(C)[N]1C2=C(C=CC=C2)C(=C1\\C=C\\C(O)CC(O)CC([O-])=O)C3=CC=C(F)C=C3",{"v":2.77,"d":"2.770"},0,2,8]
["S1910","Tioconazole","e3","L1700-08","in 10mM DMSO","Fungal","Microbiology","Tioconazole (UK-20349) is an antifungal medication with an average IC50 of 1.7 μM.",387.71,"65899-73-2",{"v":78,"d":"78.00"},201.18,"<1","N/A","http://selleckchem.com/products/tioconazole.html","C16H13Cl3N2OS","free base","UK-20349","ClC1=CC=C(C(C[N]2C=CN=C2)OCC3=C(Cl)SC=C3)C(=C1)Cl",4.437,2,0,6]
["S1913","Tropicamide","f3","L1700-08","in 10mM DMSO","AChR","Neuronal Signaling","Tropicamide(Ro 1-7683) is an anticholinergic and a muscarinic receptor subtype M4-preferring antagonist with IC50 of 8.0 nM.",284.35,"1508-75-4",{"v":57,"d":"57.00"},200.46,"<1","N/A","http://selleckchem.com/products/tropicamide.html","C17H20N2O2","free base","Ro 1-7683","CCN(CC1=CC=NC=C1)C(=O)C(CO)C2=CC=CC=C2",1.432,2,1,6]
["S1914","Pregnenolone","g3","L1700-08","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Pregnenolone(3β-Hydroxy-5-pregnen-20-one) is an endogenous steroid hormone, used in the treatment of fatigue, Alzheimer’s disease, trauma and injuries.",316.48,"145-13-1",{"v":22,"d":"22.00"},69.51,"<1","N/A","http://selleckchem.com/products/pregnenolone.html","C21H32O2","free base","3β-Hydroxy-5-pregnen-20-one","CC(=O)C1CCC2C3CC=C4CC(O)CCC4(C)C3CCC12C",3.624,1,1,1]
["S1915","Sulfamethoxazole","h3","L1700-08","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Sulfamethoxazole(Ro 4-2130) is a sulfonamide bacteriostatic antibiotic with an IC50 of 2.7 μM.",253.28,"723-46-6",{"v":51,"d":"51.00"},201.36,"<1","N/A","http://selleckchem.com/products/Sulfamethoxazole.html","C10H11N3O3S","free base","Ro 4-2130","CC1=CC(=NO1)N[S](=O)(=O)C2=CC=C(N)C=C2",0.709,4,2,3]
["S1916","Sulfisoxazole","a4","L1700-08","in 10mM DMSO","Bacterial","Microbiology","Sulfisoxazole (NU-445) is a sulfonamide antibacterial with an oxazole substituent.",{"v":267.3,"d":"267.30"},"127-69-5",{"v":53,"d":"53.00"},198.28,"<1","N/A","http://selleckchem.com/products/Sulfisoxazole.html","C11H13N3O3S","free base","NU-445","CC1=NOC(=C1C)N[S](=O)(=O)C2=CC=C(N)C=C2",0.918,4,2,3]
["S1917","Crystal Violet","b4","L1700-08","in 10mM DMSO","Dyes","Others","Crystal violet(Gentian Violet) is a triarylmethane dye.",407.98,"548-62-9",{"v":82,"d":"82.00"},200.99,{"v":14,"d":"14.00"},34.32,"http://selleckchem.com/products/Crystal-violet.html","C25H30ClN3","quaternary-N chloride salt","Gentian Violet","[Cl-].CN(C)C1=CC=C(C=C1)C(C2=CC=C(C=C2)N(C)C)=C3C=CC(C=C3)=[N+](C)C",{"v":2.25,"d":"2.250"},0,0,4]
["S1920","Haloperidol","c4","L1700-08","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Haloperidol (Haldol) is an antipsychotic and butyrophenone.",375.86,"52-86-8",{"v":75,"d":"75.00"},199.54,"<1","N/A","http://selleckchem.com/products/Haloperidol(Haldol).html","C21H23ClFNO2","free base","N/A","OC1(CCN(CCCC(=O)C2=CC=C(F)C=C2)CC1)C3=CC=C(Cl)C=C3",3.887,1,0,6]
["S1921","Phenindione","d4","L1700-08","in 10mM DMSO","Vitamin","Metabolism","Phenindione (Rectadione, phenylindandione) is an anticoagulant which functions as a Vitamin K antagonist.",222.24,"83-12-5",{"v":44,"d":"44.00"},197.98,"<1","N/A","http://selleckchem.com/products/Phenindione(Rectadione).html","C15H10O2","free base","Rectadione, phenylindandione","O=C1C(C2=CC=CC=C2)C(=O)C3=CC=CC=C13",2.819,2,0,1]
["S1928","Alibendol","e4","L1700-08","in 10mM DMSO","Others","Others","Alibendol (EB 1856) is an antispasmodic,choleretic, and cholekinetic.",251.28,"26750-81-2",{"v":50,"d":"50.00"},198.98,"<1","N/A","http://selleckchem.com/products/alibendol.html","C13H17NO4","free base","EB 1856","COC1=CC(=CC(=C1O)C(=O)NCCO)CC=C",1.248,2,3,6]
["S1933","Triamcinolone","f4","L1700-08","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Triamcinolone is a glucocorticoid given, as the free alcohol or in esterified form, orally, intramuscularly, by local injection, by inhalation, or applied topically in the management of various disorders in which corticosteroids are indicated.",394.43,"124-94-7",{"v":78,"d":"78.00"},197.75,"<1","N/A","http://selleckchem.com/products/Triamcinolone(Aristocort).html","C21H27FO6","free base","N/A","CC12CC(O)C3(F)C(CCC4=CC(=O)C=CC34C)C1CC(O)C2(O)C(=O)CO",0.422,2,3,2]
["S1934","Nystatin (Fungicidin)","g4","L1700-08","in 10mM DMSO","Antibiotics for Mammalian Cell Culture,Fungal","Microbiology","Nystatin(Fungicidin), which belongs to the polyene group of antimycotics, is frequently used as a topical agent in the treatment of oro-pharyngeal candidosis.",1056.24,"62997-67-5",{"v":19,"d":"19.00"},17.99,"<1","N/A","http://selleckchem.com/products/Nystatin(Mycostatin).html","C53H85NO20","free base","Fungicidin","CC1OC(=O)CC(O)CC(O)CC(O)CCC(O)C(O)CC2(O)CC(O)C(C(CC(OC3OC(C)C(O)C(N)C3O)/C=C/C=C/C=C/C=C/CC/C=C/C=C/C(C)C(O)C1C)O2)C(O)=O",-2.265,8,11,5]
["S1937","Isoniazid","h4","L1700-08","in 10mM DMSO","Fatty Acid Synthase","Metabolism","Isoniazid is a prodrug that blocks the action of fatty acid synthase by interacting with KatG , used for the prevention and treatment of tuberculosis.",137.14,"54-85-3",{"v":27,"d":"27.00"},196.88,{"v":27,"d":"27.00"},196.88,"http://selleckchem.com/products/Isoniazid(Tubizid).html","C6H7N3O","free base","N/A","NNC(=O)C1=CC=NC=C1",-0.811,2,2,1]
["S1940","Levofloxacin","a5","L1700-08","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Levofloxacin (Fluoroquinolone) is a broad-spectrum antibiotic topoisomerase II and topoisomerase IV inhibitor, used to treat respiratory, urinary tract, gastrointestinal, and abdominal infections.",361.37,"100986-85-4",{"v":24,"d":"24.00"},66.41,{"v":11,"d":"11.00"},30.44,"http://selleckchem.com/products/levofloxacin-levaquin.html","C18H20FN3O4","Free Base","Fluoroquinolone","CC1COC2=C(N3CCN(C)CC3)C(=CC4=C2N1C=C(C(O)=O)C4=O)F",-1.374,3,0,2]
["S1941","Enalapril Maleate","b5","L1700-08","in 10mM DMSO","ACE,RAAS","Endocrinology & Hormones","Enalapril (MK-421) Maleate is an angiotensin-converting enzyme (ACE) inhibitor, used in the treatment of hypertension, diabetic nephropathy, and chronic heart failure.",492.52,"76095-16-4",{"v":99,"d":"99.00"},201.01,"<1","N/A","http://selleckchem.com/products/Enalapril-maleate(Vasotec).html","C20H28N2O5.C4H4O4","Maleate","MK-421 Maleate","CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2CCCC2C(O)=O.OC(=O)\\C=C/C(O)=O",-0.502,6,1,12]
["S1949","Menadione (NSC 4170)","c5","L1700-08","in 10mM DMSO","CDK,DNA/RNA Synthesis,phosphatase","Metabolism","Menadione (NSC 4170, Vitamin K3), a fat-soluble compound, is an inhibitor of Cdc25 phosphatase and mitochondrial DNA polymerase γ (pol γ), used as a nutritional supplement.",172.18,"58-27-5",{"v":34,"d":"34.00"},197.47,"<1","N/A","http://selleckchem.com/products/Menadione.html","C11H8O2","free base","Vitamin K3,NSC 4170","CC1=CC(=O)C2=CC=CC=C2C1=O",2.204,2,0,0]
["S1950","Metformin HCl","d5","L1700-08","in 10mM DMSO","Autophagy,Carbohydrate Metabolism,JNK,Mitophagy,p38 MAPK","Metabolism","Metformin HCl (1,1-Dimethylbiguanide HCl) decreases hyperglycemia in hepatocytes primarily by suppressing glucose production by the liver (hepatic gluconeogenesis). Metformin promotes mitophagy in mononuclear cells. Metformin induces apoptosis of lung cancer cells through activating JNK/p38 MAPK pathway and GADD153.",165.62,"1115-70-4",{"v":33,"d":"33.00"},199.25,{"v":33,"d":"33.00"},199.25,"http://selleckchem.com/products/Metformin-hydrochloride(Glucophage).html","C4H11N5.HCl","Hydrochloride","1,1-Dimethylbiguanide HCl","Cl.CN(C)C(=N)NC(N)=N",{"v":-0.36,"d":"-0.360"},0,2,3]
["S1952","Methoxsalen","e5","L1700-08","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Methoxsalen (Xanthotoxin, NCI-C55903) is a naturally occurring photoactive substance found in the seeds of the Ammi majus (Umbelliferae) plant, used in the diagnosis and treatment of psoriasis; A CYP2A5/6 inhibitor.",216.19,"298-81-7",{"v":43,"d":"43.00"},{"v":198.9,"d":"198.90"},"<1","N/A","http://selleckchem.com/products/Methoxsalen(Oxsoralen).html","C12H8O4","free base","Xanthotoxin, NCI-C55903","COC1=C2OC=CC2=CC3=C1OC(=O)C=C3",2.187,4,0,1]
["S1956","Miconazole Nitrate","f5","L1700-08","in 10mM DMSO","Fungal","Microbiology","Miconazole (NSC 169434) Nitrate is an imidazole antifungal agent by inhibiting ergosterol biosynthesis and inducing ROS, used to treat vaginal yeast infections.",479.14,"22832-87-7",{"v":96,"d":"96.00"},200.36,"<1","N/A","http://selleckchem.com/products/Miconazole-nitrate.html","C18H14Cl4N2O.HNO3","Nitrate","NSC 169434 Nitrate","O[N+]([O-])=O.ClC1=CC=C(COC(C[N]2C=CN=C2)C3=CC=C(Cl)C=C3Cl)C(=C1)Cl",4.387,2,0,6]
["S1957","Sulfamethizole","g5","L1700-08","in 10mM DMSO","Bacterial","Microbiology","Sulfamethizole is a sulfathiazole antibacterial agent.",270.33,"144-82-1",{"v":54,"d":"54.00"},199.76,"<1","N/A","http://selleckchem.com/products/Sulfamethizole(Proklar).html","C9H10N4O2S2","free base","N/A","CC1=NN=C(N[S](=O)(=O)C2=CC=C(N)C=C2)S1",0.305,4,2,3]
["S1958","Sulbactam","h5","L1700-08","in 10mM DMSO","Anti-infection","Microbiology","Sulbactam(CP45899) is a beta-lactamase inhibitor with an average IC50 of 0.8 μM.",233.24,"68373-14-8",{"v":47,"d":"47.00"},201.51,{"v":47,"d":"47.00"},201.51,"http://selleckchem.com/products/sulbactam.html","C8H11NO5S","free base","CP45899","CC1(C)C(N2C(CC2=O)[S]1(=O)=O)C(O)=O",-0.671,4,0,1]
["S1959","Tolfenamic Acid","a6","L1700-08","in 10mM DMSO","COX","Neuronal Signaling","Tolfenamic Acid(Clotam) is a COX-2 inhibitor with IC50 of 0.2 μM.",{"v":261.7,"d":"261.70"},"13710-19-5",{"v":52,"d":"52.00"},{"v":198.7,"d":"198.70"},"<1","N/A","http://selleckchem.com/products/tolfenamic-acid.html","C14H12ClNO2","free base","Clotam","CC1=C(Cl)C=CC=C1NC2=C(C=CC=C2)C(O)=O",{"v":4.16,"d":"4.160"},1,1,3]
["S1960","Pranoprofen","b6","L1700-08","in 10mM DMSO","COX,PGES","Neuronal Signaling","Pranoprofen (Pyranoprofen,Pranopulin) is a non-steroidal COX inhibitor, used as an anti-inflammatory drug in ophthalmology.",255.27,"52549-17-4",{"v":51,"d":"51.00"},199.79,"<1","N/A","http://selleckchem.com/products/pranoprofen.html","C15H13NO3","free base","Pyranoprofen,Pranopulin","CC(C(O)=O)C1=CC2=C(OC3=NC=CC=C3C2)C=C1",{"v":3.05,"d":"3.050"},3,0,2]
["S1962","Sulphadimethoxine","c6","L1700-08","in 10mM DMSO","Anti-infection","Microbiology","Sulphadimethoxine is a non-reducing glucuronide.",310.33,"122-11-2",{"v":62,"d":"62.00"},199.79,"<1","N/A","http://selleckchem.com/products/sulphadimethoxine.html","C12H14N4O4S","free base","N/A","COC1=CC(=NC(=N1)OC)N[S](=O)(=O)C2=CC=C(N)C=C2",1.358,6,2,5]
["S1964","Rimantadine","d6","L1700-08","in 10mM DMSO","Influenza Virus","Microbiology","Rimantadine (Flumadine) is an anti-influenza virus drug for T. brucei with IC50 of 7 μM.",{"v":179.3,"d":"179.30"},"13392-28-4",{"v":33,"d":"33.00"},184.05,{"v":33,"d":"33.00"},184.05,"http://selleckchem.com/products/rimantadine-flumadine.html","C12H21N","free base","N/A","CC(N)[C]12C[CH]3[CH2]C([CH2][CH](C3)C1)C2",2.204,0,1,1]
["S1965","Primidone","e6","L1700-08","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Primidone (NCI-C56360) is an anticonvulsant of the pyrimidinedione class.",218.25,"125-33-7",{"v":44,"d":"44.00"},{"v":201.6,"d":"201.60"},"<1","N/A","http://selleckchem.com/products/Primidone(Mysoline).html","C12H14N2O2","free base","NCI-C56360","CCC1(C(=O)NCNC1=O)C2=CC=CC=C2",0.931,2,2,2]
["S1969","Nefiracetam","f6","L1700-08","in 10mM DMSO","GABA Receptor","Neuronal Signaling","Nefiracetam (DZL 221) is a GABAergic, cholinergic, and monoaminergic neuronal system enhancer for Ro 5-4864-induced convulsions. Phase 2.",{"v":246.3,"d":"246.30"},"77191-36-7",{"v":49,"d":"49.00"},198.94,{"v":5,"d":"5.00"},{"v":20.3,"d":"20.30"},"http://selleckchem.com/products/Nefiracetam(Translon).html","C14H18N2O2","free base","DZL 221","CC1=CC=CC(=C1NC(=O)CN2CCCC2=O)C",1.443,2,1,3]
["S1971","Nicorandil","g6","L1700-08","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Nicorandil (SG-75) is a potassium channel activator, and stimulates guanylate cyclase to increase formation of cyclic GMP (cGMP).",211.17,"65141-46-0",{"v":42,"d":"42.00"},198.89,{"v":17,"d":"17.00"},{"v":80.5,"d":"80.50"},"http://selleckchem.com/products/Nicorandil(Ikorel).html","C8H9N3O4","free base","SG-75","[O-][N+](=O)OCCNC(=O)C1=CC=CN=C1",1.758,3,1,5]
["S1972","Tamoxifen (ICI 46474) Citrate","h6","L1700-08","in 10mM DMSO","Apoptosis related,Autophagy,Estrogen/progestogen Receptor,HSP (HSP90)","Endocrinology & Hormones","Tamoxifen Citrate (Istubal,ICI 46474 Citrate) is a selective estrogen receptor modulator (SERM). Tamoxifen Citrate is also a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen induces apoptosis and autophagy.",563.64,"54965-24-1",{"v":100,"d":"100.00"},177.42,"<1","N/A","http://selleckchem.com/products/Tamoxifen-Citrate(Nolvadex).html","C26H29NO.C6H8O7","Citrate","Istubal,ICI 46474 Citrate","CC/C(C1=CC=CC=C1)=C(C2=CC=CC=C2)/C3=CC=C(OCCN(C)C)C=C3.OC(=O)CC(O)(CC(O)=O)C(O)=O",1.966,4,0,13]
["S1973","Cyclocytidine HCl","a7","L1700-08","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Cyclocytidine (NSC 145668) is the prodrug of cytarabine, which is a pyrimidine nucleoside analog that inhibits the DNA synthesis and used mainly in the treatment of leukemia.",261.66,"10212-25-6",{"v":10,"d":"10.00"},38.22,{"v":44,"d":"44.00"},168.16,"http://selleckchem.com/products/cyclocytidine-hcl.html","C9H12ClN3O4","Hydrochloride","NSC 145668 HCl","Cl.OCC1OC2C(OC3=NC(=N)C=CN23)C1O",-1.395,3,2,1]
["S1974","Meglumine","b7","L1700-08","in 10mM DMSO","Others","Others","Meglumine(Meglumin,Methylglucamine) is an amino sugar derived from sorbitol for THP-1 cells with IC50 of 22 μg/mL.",195.21,"6284-40-8",{"v":39,"d":"39.00"},199.78,{"v":39,"d":"39.00"},199.78,"http://selleckchem.com/products/meglumine.html","C7H17NO5","free base","Meglumin,Methylglucamine","CNCC(O)C(O)C(O)C(O)CO",-2.798,0,6,6]
["S1975","Aripiprazole","c7","L1700-08","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Aripiprazole (OPC-14597) is a novel atypical antipsychotic drug that is reported to be a high-affinity 5-HT receptor partial agonist.",448.39,"129722-12-9",{"v":90,"d":"90.00"},200.72,"<1","N/A","http://selleckchem.com/products/aripiprazole-abilify.html","C23H27Cl2N3O2","free base","OPC-14597","ClC1=CC=CC(=C1Cl)N2CCN(CCCCOC3=CC=C4CCC(=O)NC4=C3)CC2",4.998,2,1,7]
["S1978","Methscopolamine","d7","L1700-08","in 10mM DMSO","AChR","Neuronal Signaling","Methscopolamine is a muscarinic acetylcholine receptor blocker.",398.29,"155-41-9",{"v":79,"d":"79.00"},198.35,{"v":67,"d":"67.00"},168.22,"http://selleckchem.com/products/Methscopolamine-bromide(Pamine).html","C18H24BrNO4","quaternary-N bromide salt","N/A","[Br-].C[N+]1(C)C2CC(CC1C3OC23)OC(=O)C(CO)C4=CC=CC=C4",-2.949,3,1,5]
["S1979","Amiodarone (NSC 85442) HCl","e7","L1700-08","in 10mM DMSO","Autophagy,Potassium Channel","Transmembrane Transporters","Amiodarone (NSC 85442,Amiodar,Amiodarone hydrochloride,Nexterone) HCl is a sodium/potassium-ATPase inhibitor and an autophagy activator, used to treat various types of cardiac dysrhythmias.",681.77,"19774-82-4",{"v":23,"d":"23.00"},33.74,"<1","N/A","http://selleckchem.com/products/amiodarone-hcl.html","C25H29I2NO3.HCl","Hydrochloride","Amiodar,Amiodarone hydrochloride,Nexterone","Cl.CCCCC1=C(C(=O)C2=CC(=C(OCCN(CC)CC)C(=C2)I)I)C3=C(O1)C=CC=C3",{"v":7.62,"d":"7.620"},3,0,11]
["S1983","Adenine HCl","f7","L1700-08","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Adenine HCl(6-Aminopurine hydrochloride) is a hydrochloride salt form of adenine which is a purine derivative and a nucleobase with a variety of roles in biochemistry.",171.59,"2922-28-3",{"v":8,"d":"8.00"},46.62,{"v":4,"d":"4.00"},23.31,"http://selleckchem.com/products/adenine-hydrochloride.html","C5H5N5.HCl","Hydrochloride","6-Aminopurine hydrochloride","Cl.NC1=NC=NC2=C1N=C[NH]2",{"v":-0.06,"d":"-0.060"},3,2,0]
["S1987","Mometasone furoate","g7","L1700-08","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Mometasone Furoate (SCH-32088,mometasone 17-furoate) is a glucocorticoid receptor agonist, used topically to reduce inflammation of the skin or in the airways.",521.43,"83919-23-7",{"v":6,"d":"6.00"},11.51,"<1","N/A","http://selleckchem.com/products/mometasone-furoate.html","C27H30Cl2O6","Furoate","SCH-32088,mometasone 17-furoate","CC1CC2C3CCC4=CC(=O)C=CC4(C)C3(Cl)C(O)CC2(C)C1(OC(=O)C5=CC=CO5)C(=O)CCl",4.616,5,1,5]
["S1988","Propylthiouracil","h7","L1700-08","in 10mM DMSO","Peroxidases","Metabolism","Propylthiouracil (NSC 6498, NSC 70461) is a thyroperoxidase and 5'-deiodinase inhibitor, used to treat hyperthyroidism.",170.23,"51-52-5",{"v":34,"d":"34.00"},199.73,"<1","N/A","http://selleckchem.com/products/Propylthiouracil.html","C7H10N2OS","free base","NSC 6498, NSC 70461","CCCC1=CC(=O)NC(=S)N1",1.575,1,2,2]
["S1990","Capsaicin(Vanilloid)","a8","L1700-08","in 10mM DMSO","TRP Channel","Transmembrane Transporters","Capsaicin (Qutenza, Vanilloid) is an active component of chili peppers, which are plants belonging to the genus Capsicum.Capsaici is a TRPV1 agonist with an EC50 of 0.29 μM in HEK293 cells.",305.41,"404-86-4",{"v":61,"d":"61.00"},199.73,"<1","N/A","http://selleckchem.com/products/capsaicin.html","C18H27NO3","free base","Qutenza, Vanilloid","COC1=C(O)C=CC(=C1)CNC(=O)CCCC\\C=C\\C(C)C",{"v":3.91,"d":"3.910"},2,2,9]
["S1992","Fluticasone propionate","b8","L1700-08","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Fluticasone Propionate (CCI-187881) is a synthetic glucocorticoid, used to treat non-allergic and allergic rhinitis.",500.57,"80474-14-2",{"v":100,"d":"100.00"},199.77,"<1","N/A","http://selleckchem.com/products/fluticasone-propionate-Flonase-Veramyst.html","C25H31F3O5S","free base","CCI-187881","CCC(=O)OC1(C(C)CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC12C)C(=O)SCF",4.086,4,1,6]
["S1994","Lacidipine","c8","L1700-08","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Lacidipine (GX-1048, GR-43659X, SN-305) is a L-type calcium channel blocker, used for treating high blood pressure.",455.54,"103890-78-4",{"v":91,"d":"91.00"},199.76,"<1","N/A","http://selleckchem.com/products/lacidipine-lacipil-motens.html","C26H33NO6","free base","GX-1048, GR-43659X, SN-305","CCOC(=O)C1=C(C)NC(=C(C1C2=C(C=CC=C2)\\C=C\\C(=O)OC(C)(C)C)C(=O)OCC)C",3.824,6,1,11]
["S2001","Elvitegravir (JTK-303)","d8","L1700-08","in 10mM DMSO","Integrase","Microbiology","Elvitegravir (GS-9137,JTK-303,D06677) is an HIV integrase inhibitor for HIV-1 IIIB, HIV-2 EHO and HIV-2 ROD with IC50 of 0.7 nM, 2.8 nM and 1.4 nM in cell-free assays, respectively.",447.88,"697761-98-1",{"v":89,"d":"89.00"},198.71,"<1","N/A","http://selleckchem.com/products/Elvitegravir.html","C23H23ClFNO5","free base","GS-9137,JTK-303,D06677","COC1=CC2=C(C=C1CC3=C(F)C(=CC=C3)Cl)C(=O)C(=CN2C(CO)C(C)C)C(O)=O",4.665,3,1,7]
["S2003","Maraviroc (UK-427857)","e8","L1700-08","in 10mM DMSO","CCR,HIV","Microbiology","Maraviroc (Celsentri,UK-427857) is a CCR5 antagonist for MIP-1α, MIP-1β and RANTES with IC50 of 3.3 nM, 7.2 nM and 5.2 nM in cell-free assays, respectively. Maraviroc is used in the treatment of HIV infection.",513.67,"376348-65-1",{"v":100,"d":"100.00"},194.68,"<1","N/A","http://selleckchem.com/products/Maraviroc.html","C29H41F2N5O","free base","Celsentri,UK-427857","CC(C)C1=NN=C(C)[N]1C2CC3CCC(C2)N3CCC(NC(=O)C4CCC(F)(F)CC4)C5=CC=CC=C5",3.921,3,1,8]
["S2005","Raltegravir (MK-0518)","f8","L1700-08","in 10mM DMSO","Integrase","Microbiology","Raltegravir (MK-0518) is a potent integrase (IN) inhibitor for WT and S217Q PFV IN with IC50 of 90 nM and 40 nM in cell-free assays, respectively. It shows greater than 1000-fold selectivity for HIV-1 IN over several related Mg2+-dependent enzyme such as HCV polymerase, HIV reverse transcriptase, HIV RNaseH and human α-, β-, γ-polymerases.",444.42,"518048-05-0",{"v":88,"d":"88.00"},198.01,"<1","N/A","http://selleckchem.com/products/Raltegravir-(MK-0518).html","C20H21FN6O5","free base","MK-0518","CN1C(=O)C(=C(N=C1C(C)(C)NC(=O)C2=NN=C(C)O2)C(=O)NCC3=CC=C(F)C=C3)O",-0.291,7,3,6]
["S2006","Pyrimethamine","g8","L1700-08","in 10mM DMSO","DHFR","Metabolism","Pyrimethamine(RP 4753) is a dihydrofolate reductase (DHFR) inhibitor, used as an antimalarial drug.",248.71,"58-14-0",{"v":10,"d":"10.00"},40.21,"<1","N/A","http://selleckchem.com/products/Pyrimethamine.html","C12H13ClN4","free base","RP 4753","CCC1=NC(=NC(=C1C2=CC=C(Cl)C=C2)N)N",{"v":2.75,"d":"2.750"},2,2,2]
["S2007","Sulindac","h8","L1700-08","in 10mM DMSO","COX","Neuronal Signaling","Sulindac(MK-231) is a non-steroidal COX inhibitor, which potently inhibits prostaglandin synthesis, used in the treatment of acute or chronic inflammatory conditions.",356.41,"38194-50-2",{"v":71,"d":"71.00"},199.21,"<1","N/A","http://selleckchem.com/products/Sulindac(Clinoril).html","C20H17FO3S","free base","MK-231","CC1=C(CC(O)=O)C2=C(C=CC(=C2)F)\\C1=C/C3=CC=C(C=C3)[S](C)=O",3.639,2,0,4]
["S2011","Pramipexole 2HCl Monohydrate","a9","L1700-08","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Pramipexole 2HCl Monohydrate is a novel non-ergoline dopamine (DA) agonist, used to treat Parkinson's disease.",302.26,"191217-81-9",{"v":41,"d":"41.00"},135.64,{"v":60,"d":"60.00"},{"v":198.5,"d":"198.50"},"http://selleckchem.com/products/Pramipexole-dihydrochloride-monohydrate.html","C10H17N3S.2HCl.H2O","Dihydrochloride monohydrate","N/A","O.Cl.Cl.CCCNC1CCC2=C(C1)SC(=N2)N",{"v":1.94,"d":"1.940"},1,2,3]
["S2012","PCI-34051","b9","L1700-08","in 10mM DMSO","Apoptosis related,HDAC","Epigenetics","PCI-34051 is a potent and specific HDAC8 inhibitor with IC50 of 10 nM in a cell-free assay. It has greater than 200-fold selectivity over HDAC1 and 6, more than 1000-fold selectivity over HDAC2, 3, and 10. PCI-34051 induces caspase-dependent apoptosis.",296.32,"950762-95-5",{"v":59,"d":"59.00"},199.11,"<1","N/A","http://selleckchem.com/products/pci-34051.html","C17H16N2O3","free base","N/A","COC1=CC=C(C[N]2C=CC3=C2C=C(C=C3)C(=O)NO)C=C1",2.911,2,1,4]
["S2013","PF-573228","c9","L1700-08","in 10mM DMSO","Apoptosis related,FAK","Angiogenesis","PF-573228 is an ATP-competitive inhibitor of FAK with IC50 of 4 nM in a cell-free assay, ~50- to 250-fold selective for FAK than Pyk2, CDK1/7 and GSK-3β. PF-573228 induces apoptosis.",491.49,"869288-64-2",{"v":26,"d":"26.00"},{"v":52.9,"d":"52.90"},"<1","N/A","http://selleckchem.com/products/pf-573228.html","C22H20F3N5O3S","free base","N/A","C[S](=O)(=O)C1=CC(=CC=C1)CNC2=NC(=NC=C2C(F)(F)F)NC3=CC4=C(NC(=O)CC4)C=C3",3.967,5,3,7]
["S2014","BMS-265246","d9","L1700-08","in 10mM DMSO","CDK","Cell Cycle","BMS-265246 is a potent and selective CDK1/2 inhibitor with IC50 of 6 nM/9 nM in a cell-free assay. It is 25-fold more selective for CDK1/2 than CDK4.",345.34,"582315-72-8",{"v":20,"d":"20.00"},57.91,"<1","N/A","http://selleckchem.com/products/bms-265246.html","C18H17F2N3O2","free base","N/A","CCCCOC1=C2C=N[NH]C2=NC=C1C(=O)C3=C(F)C=C(C)C=C3F",4.135,4,1,6]
["S2015","Suplatast Tosylate","e9","L1700-08","in 10mM DMSO","Interleukins","Immunology & Inflammation","Suplatast Tosylate (IPD-1151T, Suplatast Tosilate) is a novel capsular anti-asthmatic agent that suppresses both IgE production, IL-4 and IL-5 synthesis with IC50 above 100 μM.",499.64,"94055-76-2",{"v":100,"d":"100.00"},200.14,{"v":100,"d":"100.00"},200.14,"http://selleckchem.com/products/suplatast-tosilate.html","C23H33NO7S2","Tosylate","IPD-1151T, Suplatast Tosilate","CCOCC(O)COC1=CC=C(NC(=O)CC[S+](C)C)C=C1.CC2=CC=C(C=C2)[S]([O-])(=O)=O",0.877,3,2,11]
["S2016","Mirtazapine","f9","L1700-08","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Mirtazapine (Org3770,6-Azamianserin) is an adrenergic and seroton receptor antagonist, used to treat depression.",265.35,"85650-52-8",{"v":53,"d":"53.00"},199.74,"<1","N/A","http://selleckchem.com/products/mirtazapine-remeron-avanza.html","C17H19N3","free base","Org3770,6-Azamianserin","CN1CCN2C(C1)C3=C(CC4=C2N=CC=C4)C=CC=C3",3.094,1,0,0]
["S2017","Benidipine HCl","g9","L1700-08","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Benidipine HCl (KW-3049,(±)- Benidipine) is a hydrochloride salt form of benidipine which is a dihydropyridine calcium channel blocker.",542.02,"91599-74-5",{"v":8,"d":"8.00"},14.76,"<1","N/A","http://selleckchem.com/products/benidipine-hydrochloride.html","C28H31N3O6.HCl","Hydrochloride","KW-3049,(±)- Benidipine","Cl.COC(=O)C1=C(C)NC(=C(C1C2=CC(=CC=C2)[N+]([O-])=O)C(=O)OC3CCCN(C3)CC4=CC=CC=C4)C",{"v":4.36,"d":"4.360"},4,1,9]
["S2018","ENMD-2076 L-(+)-Tartaric acid","h9","L1700-08","in 10mM DMSO","Aurora Kinase,FLT3,VEGFR","Angiogenesis","ENMD-2076 L-(+)-Tartaric acid is the tartaric acid of ENMD-2076, selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.86 nM, 25-fold more selective for Aurora A than Aurora B and less potent to VEGFR2/KDR and VEGFR3, FGFR1 and FGFR2 and PDGFRα. Phase 2.",525.56,"1291074-87-7",{"v":100,"d":"100.00"},190.27,"<1","N/A","http://selleckchem.com/products/enmd-2076-l-tartaric-acid.html","C25H31N7O6","free base","N/A","CN1CCN(CC1)C2=NC(=NC(=C2)NC3=N[NH]C(=C3)C)\\C=C\\C4=CC=CC=C4.OC(C(O)C(O)=O)C(O)=O",-0.683,5,4,8]
["S2020","Formoterol Hemifumarate","a10","L1700-08","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Formoterol Hemifumarate (Eformoterol, CGP 25827A, NSC 299587, YM 08316,Formoterol fumarate) is a potent, selective and long-acting β2-adrenoceptor agonist used in the management of asthma and chronic obstructive pulmonary disease(COPD).",{"v":402.4,"d":"402.40"},"43229-80-7",{"v":80,"d":"80.00"},198.81,"<1","N/A","http://selleckchem.com/products/formoterol-hemifumarate.html","C19H24N2O4.1/2C4H4O4","Hemifumarate","Eformoterol, CGP 25827A, NSC 299587, YM 08316,Formoterol fumarate","COC1=CC=C(CC(C)NCC(O)C2=CC=C(O)C(=C2)NC=O)C=C1.COC3=CC=C(CC(C)NCC(O)C4=CC=C(O)C(=C4)NC=O)C=C3.OC(=O)\\C=C\\C(O)=O",-1.526,6,8,18]
["S2021","Chlormezanone","b10","L1700-08","in 10mM DMSO","Others","Others","Chlormezanone，a non-benzodiazepine that is used in the management of anxiety. It has been suggested for use in the treatment of muscle spasm.",273.74,"80-77-3",{"v":55,"d":"55.00"},200.92,"<1","N/A","http://selleckchem.com/products/Chlormezanone(Trancopal).html","C11H12ClNO3S","free base","N/A","CN1C(C2=CC=C(Cl)C=C2)[S](=O)(=O)CCC1=O",1.559,3,0,1]
["S2024","Ketotifen Fumarate","c10","L1700-08","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Ketotifen Fumarate(HC 20511 fumarate) is a fumaric acid salt of ketotifen which is a H1-antihistamine and mast cell stabilizer.",{"v":425.5,"d":"425.50"},"34580-14-8",{"v":8,"d":"8.00"},{"v":18.8,"d":"18.80"},"<1","N/A","http://selleckchem.com/products/ketotifen-fumarate-zaditor.html","C19H19NOS.C4H4O4","Fumarate","HC 20511 fumarate","CN1CCC(CC1)=C2C3=C(CC(=O)C4=C2C=CS4)C=CC=C3.OC(=O)\\C=C\\C(O)=O",0.772,3,0,2]
["S2025","Urapidil HCl","d10","L1700-08","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Urapidil HCl is a hydrochloride salt form of urapidil which is α1-adrenoceptor antagonist and 5-HT1A receptor agonist with pIC50 of 6.13 and 6.4 respectively.",423.94,"64887-14-5",{"v":24,"d":"24.00"},56.61,{"v":85,"d":"85.00"},{"v":200.5,"d":"200.50"},"http://selleckchem.com/products/urapidil-hydrochloride.html","C20H29N5O3.HCl","Hydrochloride","N/A","Cl.COC1=CC=CC=C1N2CCN(CCCNC3=CC(=O)N(C)C(=O)N3C)CC2",1.808,3,1,7]
["S2026","Ginkgolide A","e10","L1700-08","in 10mM DMSO","GABA Receptor","Neuronal Signaling","Ginkgolide A (BN52020) is an extract from in Ginkgo biloba and a g-aminobutyric acid (GABA) antagonist with a Ki of 14.5 μM.",{"v":408.4,"d":"408.40"},"15291-75-5",{"v":81,"d":"81.00"},198.33,"<1","N/A","http://selleckchem.com/products/ginkgolide-a.html","C20H24O9","free base","BN52020","CC1C(=O)OC2CC34C5CC(C(C)(C)C)C36C(O)C(=O)OC6OC4(C(=O)O5)C12O",-0.022,7,1,1]
["S2028","Diclazuril","f10","L1700-08","in 10mM DMSO","Parasite","Microbiology","Diclazuril(R-64433) is an anti-coccidial drug.",407.64,"101831-37-2",{"v":16,"d":"16.00"},39.25,"<1","N/A","http://selleckchem.com/products/diclazuril.html","C17H9Cl3N4O2","free base","R-64433","ClC1=CC=C(C=C1)C(C#N)C2=C(Cl)C=C(C=C2Cl)N3N=CC(=O)NC3=O",4.191,3,1,3]
["S2029","Uridine","g10","L1700-08","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Uridine (NSC 20256,β-Uridine, Uridin) is a nucleoside, contains a uracil attached to a ribose ring via a β-N1-glycosidic bond.",{"v":244.2,"d":"244.20"},"58-96-8",{"v":49,"d":"49.00"},200.66,{"v":49,"d":"49.00"},200.66,"http://selleckchem.com/products/uridine.html","C9H12N2O6","free base","NSC 20256,β-Uridine, Uridin","OCC1OC(C(O)C1O)N2C=CC(=O)NC2=O",-2.451,3,4,2]
["S2030","Flunarizine 2HCl","h10","L1700-08","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Flunarizine 2HCl (KW-3149, R14950) is a dihydrochloride salt form which is a calcium channel blocker with a Ki of 68 nM.",477.42,"30484-77-6",{"v":5,"d":"5.00"},10.47,"<1","N/A","http://selleckchem.com/products/flunarizine-dihydrochloride.html","C26H26F2N2.2HCl","2HCl","KW-3149, R14950","Cl.Cl.FC1=CC=C(C=C1)C(N2CCN(CC2)C\\C=C\\C3=CC=CC=C3)C4=CC=C(F)C=C4",6.699,0,0,6]
["S2031","Fenticonazole Nitrate","a11","L1700-08","in 10mM DMSO","Fungal","Microbiology","Fenticonazole Nitrate(Lomexin,REC 15-1476,Falvin) is an azole antifungal agent.",518.41,"73151-29-8",{"v":104,"d":"104.00"},200.61,"<1","N/A","http://selleckchem.com/products/fenticonazole-nitrate.html","C24H20Cl2N2OS.HNO3","Nitrate","Lomexin,REC 15-1476,Falvin","O[N+]([O-])=O.ClC1=CC=C(C(C[N]2C=CN=C2)OCC3=CC=C(SC4=CC=CC=C4)C=C3)C(=C1)Cl",5.176,2,0,8]
["S2032","Rebamipide","b11","L1700-08","in 10mM DMSO","CCK receptor","GPCR & G Protein","Rebamipide (OPC-12759,Proamipide) is a cholecystokinin type 1 (CCK1) receptor inhibitor for inhibiting [125I]BH-CCK-8S with IC50 of 37.7 μM.",370.79,"90098-04-7",{"v":74,"d":"74.00"},199.57,"<1","N/A","http://selleckchem.com/products/rebamipide.html","C19H15ClN2O4","free base","OPC-12759,Proamipide","OC(=O)C(CC1=CC(=O)NC2=C1C=CC=C2)NC(=O)C3=CC=C(Cl)C=C3",2.606,3,2,5]
["S2036","Aspartame","c11","L1700-08","in 10mM DMSO","Others","Others","Aspartame (SC-18862,Nutrasweet) is an artificial, non-saccharide sweetener used as a sugar substitute in some foods and beverages.",{"v":294.3,"d":"294.30"},"22839-47-0",{"v":33,"d":"33.00"},112.13,{"v":4,"d":"4.00"},13.59,"http://selleckchem.com/products/aspartame.html","C14H18N2O5","free base","SC-18862,Nutrasweet","COC(=O)C(CC1=CC=CC=C1)NC(=O)C(N)CC(O)=O",-2.455,4,2,8]
["S2037","Candesartan Cilexetil","d11","L1700-08","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Candesartan Cilexetil (TCV-116) is an angiotensin II receptor antagonist with IC50 of 0.26 nM, used in the treatment of hypertension.",610.66,"145040-37-5",{"v":122,"d":"122.00"},199.78,"<1","N/A","http://selleckchem.com/products/Candesartan-cilexetil-Atacand.html","C33H34N6O6","free base","TCV-116","CCOC1=NC2=C([N]1CC3=CC=C(C=C3)C4=C(C=CC=C4)C5=NN=N[NH]5)C(=CC=C2)C(=O)OC(C)OC(=O)OC6CCCCC6",6.913,10,1,13]
["S2038","Phentolamine Mesylate","e11","L1700-08","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Phentolamine Mesylate(Phentolamine methanesulfonate) is a reversible and nonselective alpha-adrenergic receptor antagonist, used for the prevention or control of hypertensive episodes.",377.46,"65-28-1",{"v":76,"d":"76.00"},201.35,{"v":76,"d":"76.00"},201.35,"http://selleckchem.com/products/phentolamine-mesilate.html","C17H19N3O.CH4O3S","Mesylate","Phentolamine methanesulfonate","CC1=CC=C(C=C1)N(CC2=NCCN2)C3=CC(=CC=C3)O.C[S](O)(=O)=O",2.555,1,2,4]
["S2040","Nimesulide","f11","L1700-08","in 10mM DMSO","COX","Neuronal Signaling","Nimesulide is a relatively COX-2 selective inhibitor with IC50 of 26 μM.",308.31,"51803-78-2",{"v":62,"d":"62.00"},{"v":201.1,"d":"201.10"},"<1","N/A","http://selleckchem.com/products/Nimesulide.html","C13H12N2O5S","free base","N/A","C[S](=O)(=O)NC1=C(OC2=CC=CC=C2)C=C(C=C1)[N+]([O-])=O",2.195,3,1,5]
["S2041","Dyclonine HCl","g11","L1700-08","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Dyclonine HCl(Dyclocaine HCl) is a hydrochloride salt form of dyclonine which is an oral anaesthetic, reversibly binds to activated sodium channels on the neuronal membrane, thereby decreasing the neuronal membrane's permeability to sodium ions, leading to an increased threshold for excitation.",325.87,"536-43-6",{"v":15,"d":"15.00"},46.03,{"v":6,"d":"6.00"},18.41,"http://selleckchem.com/products/dyclonine-hydrochloride.html","C18H27NO2.HCl","Hydrochloride","Dyclocaine HCl","Cl.CCCCOC1=CC=C(C=C1)C(=O)CCN2CCCCC2",4.435,2,0,8]
["S2042","Cyproterone Acetate","h11","L1700-08","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Cyproterone acetate is an androgen receptor (AR) antagonist with IC50 of 7.1 nM, as well as a weak progesterone receptor agonist with weak pro-gestational and glucocorticoid activity.",416.94,"427-51-0",{"v":83,"d":"83.00"},199.07,"<1","N/A","http://selleckchem.com/products/cyproterone-acetate.html","C24H29ClO4","free base","N/A","CC(=O)OC1(CCC2C3C=C(Cl)C4=CC(=O)C5CC5C4(C)C3CCC12C)C(C)=O",3.314,4,0,3]
["S2043","Memantine HCl","a2","L1700-09","in 10mM DMSO","NMDAR","Neuronal Signaling","Memantine HCl is an antagonist of NMDAR. It is also a CYP2B6 and CYP2D6 inhibitor for recombinant CYP2B6 and CYP2D6 with IC50 of 1.12 μM and 242.4 μM, Ki of 0.51 μM and 84.4 μM, respectively.",215.76,"41100-52-1",{"v":43,"d":"43.00"},{"v":199.3,"d":"199.30"},{"v":30,"d":"30.00"},139.04,"http://selleckchem.com/products/memantine-hydrochloride-namenda.html","C12H21N.HCl","Hydrochloride","N/A","Cl.CC12C[CH]3CC(C)([CH2]1)C[C](N)(C3)C2",2.289,0,1,0]
["S2044","Cyproheptadine HCl","b2","L1700-09","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Cyproheptadine HCl(Periactin) is a hydrochloride salt form of cyproheptadine which is a histamine receptor antagonist.",323.86,"969-33-5",{"v":65,"d":"65.00"},{"v":200.7,"d":"200.70"},"<1","N/A","http://selleckchem.com/products/cyproheptadine-hydrochloride-periactin.html","C21H21N.HCl","Hydrochloride","Periactin","Cl.CN1CCC(CC1)=C2C3=C(C=CC=C3)C=CC4=C2C=CC=C4",4.744,0,0,0]
["S2045","Doxifluridine","c2","L1700-09","in 10mM DMSO","Phosphorylase","Metabolism","Doxifluridine (5'-DFUR, AMC 0101) is an oral prodrug that is converted to the cytotoxic agent 5-fluorouracil (5-FU).",246.19,"3094-09-5",{"v":49,"d":"49.00"},199.03,{"v":49,"d":"49.00"},199.03,"http://selleckchem.com/products/doxifluridine.html","C9H11FN2O5","free base","5'-DFUR, AMC 0101","CC1OC(C(O)C1O)N2C=C(F)C(=O)NC2=O",-1.653,3,3,1]
["S2046","Pioglitazone HCl","d2","L1700-09","in 10mM DMSO","Ferroptosis,P450 (e.g. CYP17),PPAR","Metabolism","Pioglitazone HCl (AD-4833, U-72107E) is an inhibitor of cytochrome P450 (CYP)2C8 and CYP3A4 enzymes. Pioglitazone HCl inhibits CYP2C8, CYP3A4 and CYP2C9 with Ki of 1.7 μM, 11.8 μM and 32.1 μM, respectively. Pioglitazone HCl is also a selective peroxisome proliferator-activated receptor-gamma (PPARγ) agonist with EC50 of 0.93 μM and 0.99 μM for human PPARγ and mouse PPARγ, respectively. Pioglitazone HCl inhibits mitochondrial iron uptake, lipid peroxidation, and subsequent ferroptosis.",{"v":392.9,"d":"392.90"},"112529-15-4",{"v":79,"d":"79.00"},201.07,"<1","N/A","http://selleckchem.com/products/pioglitazone-hydrochloride-actos.html","C19H20N2O3S.HCl","Hydrochloride","AD-4833, U-72107E","Cl.CCC1=CC=C(CCOC2=CC=C(CC3SC(=O)NC3=O)C=C2)N=C1",4.289,4,1,7]
["S2051","Captopril","e2","L1700-09","in 10mM DMSO","ACE,RAAS","Endocrinology & Hormones","Captopril (SQ 14225,Capoten) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 6 nM.",217.29,"62571-86-2",{"v":43,"d":"43.00"},197.89,{"v":2,"d":"2.00"},{"v":9.2,"d":"9.20"},"http://selleckchem.com/products/captopril-capoten.html","C9H15NO3S","free base","SQ 14225,Capoten","CC(CS)C(=O)N1CCCC1C(O)=O",0.667,2,0,3]
["S2052","Oxytetracycline Dihydrate","f2","L1700-09","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Oxytetracycline Dihydrate is a prescription antibiotic, interfering with the ability of bacteria to produce essential proteins.",496.46,"6153-64-6",{"v":5,"d":"5.00"},10.07,"<1","N/A","http://selleckchem.com/products/oxytetracycline-dihydrate.html","C22H24N2O9.2H2O","Dihydrate","N/A","O.O.CN(C)C1C2C(O)C3C(=C(O)C2(O)C(=O)C(=C1O)C(N)=O)C(=O)C4=C(O)C=CC=C4C3(C)O",-2.309,3,5,2]
["S2053","Cytidine","g2","L1700-09","in 10mM DMSO","Nucleoside Analog/Antimetabolite","DNA Damage/DNA Repair","Cytidine is a nucleoside molecule that is formed when cytosine is attached to a ribose ring, cytidine is a component of RNA.",243.22,"65-46-3",{"v":49,"d":"49.00"},201.46,{"v":49,"d":"49.00"},201.46,"http://selleckchem.com/products/cytidine.html","C9H13N3O5","free base","N/A","NC1=NC(=O)N(C=C1)C2OC(CO)C(O)C2O",-2.396,3,4,2]
["S2054","Orphenadrine Citrate","h2","L1700-09","in 10mM DMSO","AChR","Neuronal Signaling","Orphenadrine Citrate is a skeletal muscle relaxant, it acts in the central nervous system to produce its muscle relaxant effects.",{"v":461.5,"d":"461.50"},"4682-36-4",{"v":92,"d":"92.00"},199.35,"<1","N/A","http://selleckchem.com/products/orphenadrine-citrate-norflex.html","C18H23NO.C6H8O7","Citrate","N/A","CN(C)CCOC(C1=CC=CC=C1)C2=CC=CC=C2C.OC(=O)CC(O)(CC(O)=O)C(O)=O",-0.483,4,0,11]
["S2055","Gimeracil","a3","L1700-09","in 10mM DMSO","Dehydrogenase","Metabolism","Gimeracil is an inhibitor of dihydropyrimidine dehydrogenase, which inhibits the early step in homologous recombination for double strand breaks repair.",145.54,"103766-25-2",{"v":29,"d":"29.00"},199.26,"<1","N/A","http://selleckchem.com/products/gimeracil.html","C5H4ClNO2","free base","N/A","OC1=CC(=O)NC=C1Cl",-0.493,1,2,0]
["S2057","Cyclophosphamide (NSC-26271) Monohydrate","b3","L1700-09","in 10mM DMSO","DNA alkylator","DNA Damage/DNA Repair","Cyclophosphamide (NSC-26271, Cytoxan) Monohydrate is a nitrogen mustard alkylating agent, it attaches the alkyl group to the guanine base of DNA, shown to crosslink DNA, causing strand breakage and inducing mutations.",{"v":279.1,"d":"279.10"},"6055-19-2",{"v":55,"d":"55.00"},197.06,{"v":7,"d":"7.00"},25.08,"http://selleckchem.com/products/cyclophosphamide-monohydrate.html","C7H15Cl2N2O2P.H2O","Monohydrate","Cytoxan Monohydrate","O.ClCCN(CCCl)[P]1(=O)NCCCO1",-0.063,2,1,5]
["S2058","Tolnaftate","c3","L1700-09","in 10mM DMSO","Fungal","Microbiology","Tolnaftate is a synthetic thiocarbamate used as an anti-fungal agent.",307.41,"2398-96-1",{"v":62,"d":"62.00"},201.69,"<1","N/A","http://selleckchem.com/products/tolnaftate.html","C19H17NOS","free base","N/A","CN(C(=S)OC1=CC=C2C=CC=CC2=C1)C3=CC(=CC=C3)C",6.289,1,0,4]
["S2059","Terazosin HCl Dihydrate","d3","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Terazosin HCl is a selective α1-adrenoceptor antagonist, used for treatment of symptoms of an enlarged prostate (BPH).",459.92,"70024-40-7",{"v":26,"d":"26.00"},56.53,"<1","N/A","http://selleckchem.com/products/terazosin-hydrochloride-hytrin.html","C19H25N5O4.HCl.2H2O","HCl & Dihydrate","N/A","O.O.Cl.COC1=CC2=C(C=C1OC)C(=NC(=N2)N3CCN(CC3)C(=O)C4CCCO4)N",1.348,6,1,4]
["S2060","Bromhexine HCl","e3","L1700-09","in 10mM DMSO","Others","Others","Bromhexine HCl is a medication prescribed for coughs which works by dissolving hard phlegm.",412.59,"611-75-6",{"v":6,"d":"6.00"},14.54,"<1","N/A","http://selleckchem.com/products/bromhexine-hydrochloride.html","C14H20Br2N2.HCl","HCl","N/A","Cl.CN(CC1=CC(=CC(=C1N)Br)Br)C2CCCCC2",4.894,0,1,3]
["S2061","Lovastatin (MK-803)","f3","L1700-09","in 10mM DMSO","Autophagy,HMG-CoA Reductase","Metabolism","Lovastatin (MK-803, Mevinolin,Mevacor) is an inhibitor of HMG-CoA reductase with IC50 of 3.4 nM in a cell-free assay, used for lowering cholesterol (hypolipidemic agent). Lovastatin triggers autophagy.",404.54,"75330-75-5",{"v":8,"d":"8.00"},19.78,"<1","N/A","http://selleckchem.com/products/lovastatin-mevacor.html","C24H36O5","free base","Mevinolin,Mevacor","CCC(C)C(=O)OC1CC(C)C=C2C=CC(C)C(CCC3CC(O)CC(=O)O3)C12",4.218,4,1,7]
["S2062","Tiopronin","g3","L1700-09","in 10mM DMSO","ROS","Immunology & Inflammation","Tiopronin is an antioxidant agent, used for the treatment of cystinuria by controlling the rate of cystine precipitation and excretion.",163.19,"1953-02-2",{"v":32,"d":"32.00"},196.09,{"v":32,"d":"32.00"},196.09,"http://selleckchem.com/products/tiopronin-thiola.html","C5H9NO3S","free base","N/A","CC(S)C(=O)NCC(O)=O",-0.362,2,1,3]
["S2064","Balofloxacin","h3","L1700-09","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Balofloxacin (Q-35,Q-roxin) is a quinolone antibiotic, inhibiting the synthesis of bacterial DNA by interference with the enqyme DNA gyrase.",389.42,"127294-70-6",{"v":5,"d":"5.00"},12.84,"<1","N/A","http://selleckchem.com/products/balofloxacin.html","C20H24FN3O4","free base","Q-35,Q-roxin","CNC1CCCN(C1)C2=C(OC)C3=C(C=C2F)C(=O)C(=CN3C4CC4)C(O)=O",-0.615,3,1,5]
["S2065","Lafutidine","a4","L1700-09","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Lafutidine (FRG-8813), a newly developed histamine H(2)-receptor antagonist, inhibits gastric acid secretion.",431.55,"118288-08-7",{"v":86,"d":"86.00"},199.28,"<1","N/A","http://selleckchem.com/products/lafutidine.html","C22H29N3O4S","free base","FRG-8813","O=C(C[S](=O)CC1=CC=CO1)NC\\C=C/COC2=CC(=CC=N2)CN3CCCCC3",1.987,5,1,11]
["S2066","Moxonidine","b4","L1700-09","in 10mM DMSO","Imidazoline Receptor","GPCR & G Protein","Moxonidine (BDF5895) is a selective agonist at the imidazoline receptor subtype 1, used as antihypertensive agent.",241.68,"75438-57-2",{"v":24,"d":"24.00"},{"v":99.3,"d":"99.30"},"<1","N/A","http://selleckchem.com/products/moxonidine.html","C9H12ClN5O","free base","BDF5895","COC1=NC(=NC(=C1NC2=NCCN2)Cl)C",0.598,4,2,3]
["S2067","Ozagrel HCl","c4","L1700-09","in 10mM DMSO","P450 (e.g. CYP17),Prostaglandin Receptor","Metabolism","Ozagrel HCl (OKY-046) is a selective <n>thromboxane A(2) (TXA(2)) synthetase inhibitor with IC50 of 11 nM for rabbit platelet, used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.",264.71,"78712-43-3",{"v":52,"d":"52.00"},196.44,{"v":52,"d":"52.00"},196.44,"http://selleckchem.com/products/ozagrel-hydrochloride.html","C13H12N2O2.HCl","HCl","OKY-046 HCl","Cl.OC(=O)/C=C/C1=CC=C(C[N]2C=CN=C2)C=C1",1.986,2,0,4]
["S2069","Argatroban (MCI-9038)","d4","L1700-09","in 10mM DMSO","Thrombin","Proteases","Argatroban (MCI-9038) is a potent and selective synthetic thrombin inhibitor with Ki ranging from 5 nM to 39 nM, used as an anticoagulant.",508.63,"74863-84-6",{"v":9,"d":"9.00"},17.69,"<1","N/A","http://selleckchem.com/products/argatroban.html","C23H36N6O5S","free base","MCI-9038","CC1CCN(C(C1)C(O)=O)C(=O)C(CCCNC(N)=N)N[S](=O)(=O)C2=CC=CC3=C2NCC(C)C3",1.266,4,4,10]
["S2071","Prulifloxacin (NM441)","e4","L1700-09","in 10mM DMSO","COVID-19","Microbiology","Prulifloxacin (NM441, AF 3013), the prodrug of ulifloxacin, is a broad-spectrum oral fluoroquinolone antibacterial agent.",461.46,"123447-62-1",{"v":11,"d":"11.00"},23.84,"<1","N/A","http://www.selleckchem.com/products/prulifloxacin-pruvel.html","C21H20FN3O6S","Free Base","AF 3013","CC1SC2=C(C(O)=O)C(=O)C3=CC(=C(C=C3N12)N4CCN(CC4)CC5=C(C)OC(=O)O5)F",0.031,5,0,4]
["S2072","Seratrodast(AA-2414)","f4","L1700-09","in 10mM DMSO","Prostaglandin Receptor","Metabolism","Seratrodast (AA-2414, ABT-001) is a potent and selective thromboxane A2 receptor (TP) antagonist which is used primarily in the treatment of asthma and used as anti-inflammatory agent.",354.44,"112665-43-7",{"v":71,"d":"71.00"},200.32,"<1","N/A","http://www.selleck.cn/products/seratrodast.html","C22H26O4","Free Base","ABT-001","CC1=C(C)C(=O)C(=C(C)C1=O)C(CCCCCC(O)=O)C2=CC=CC=C2",5.216,3,0,8]
["S2074","Mecarbinate","g4","L1700-09","in 10mM DMSO","HCV Protease","Proteases","Mecarbinate (Dimecarbin) is a chemical intermediate of arbidol hydrochloride.",233.26,"15574-49-9",{"v":47,"d":"47.00"},201.49,"<1","N/A","http://selleckchem.com/products/mecarbinate.html","C13H15NO3","free base","Dimecarbin","CCOC(=O)C1=C(C)[N](C)C2=CC=C(O)C=C12",2.437,2,1,3]
["S2075","Rosiglitazone (BRL-49653) HCl","h4","L1700-09","in 10mM DMSO","PPAR","Metabolism","Rosiglitazone HCl (BRL-49653) is a blood glucose-lowering drugs, stimulating insulin secretion by binding to the PPAR receptors in fat cells.",393.89,"302543-62-0",{"v":79,"d":"79.00"},200.56,"<1","N/A","http://selleckchem.com/products/rosiglitazone-hydrochloride.html","C18H19N3O3S.HCl","HCl","BRL-49653 HCl","Cl.CN(CCOC1=CC=C(CC2SC(=O)NC2=O)C=C1)C3=CC=CC=N3",{"v":3.65,"d":"3.650"},4,1,7]
["S2077","Atorvastatin Calcium","a5","L1700-09","in 10mM DMSO","Apoptosis related,Autophagy,HMG-CoA Reductase","Metabolism","Atorvastatin Calcium is an inhibitor of HMG-CoA reductase used as a cholesterol-lowering medication that blocks the production of cholesterol. Atorvastatin Calcium induces apoptosis and autophagy.",1155.34,"134523-03-8",{"v":100,"d":"100.00"},86.55,"<1","N/A","http://selleckchem.com/products/atorvastatin-calcium-lipitor.html","2(C33H34FN2O5).Ca","Calcium","N/A","[Ca++].CC(C)C1=C(C(=O)NC2=CC=CC=C2)C(=C([N]1CCC(O)CC(O)CC([O-])=O)C3=CC=C(F)C=C3)C4=CC=CC=C4.CC(C)C5=C(C(=O)NC6=CC=CC=C6)C(=C([N]5CCC(O)CC(O)CC([O-])=O)C7=CC=C(F)C=C7)C8=CC=CC=C8",8.163,2,6,24]
["S2078","Famotidine","b5","L1700-09","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Famotidine (MK208) is a histamine H2–receptor antagonist with IC50 of 0.6 mM, commonly used to treat heartburn, GERD, ulcers, and other digestive conditions.",337.45,"76824-35-6",{"v":67,"d":"67.00"},198.55,"<1","N/A","http://selleckchem.com/products/famotidine-pepcid.html","C8H15N7O2S3","free base","MK208","NC(=N)NC1=NC(=CS1)CSCCC(=N)N[S](N)(=O)=O",-1.328,3,4,9]
["S2079","Moexipril HCl","c5","L1700-09","in 10mM DMSO","ACE,COVID-19,RAAS","Endocrinology & Hormones","Moexipril HCl (RS-10085) is a potent orally active nonsulfhydryl angiotensin converting enzyme (ACE) inhibitor, used for the treatment of hypertension and congestive heart failure.",535.03,"82586-52-5",{"v":20,"d":"20.00"},37.38,"<1","N/A","http://selleckchem.com/products/moexipril-hydrochloride.html","C27H34N2O7.HCl","Hydrochloride","RS-10085","Cl.CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2CC3=CC(=C(OC)C=C3CC2C(O)=O)OC",1.005,6,1,12]
["S2080","Clevidipine Butyrate","d5","L1700-09","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Clevidipine Butyrate(Cleviprex) is a dihydropyridine calcium channel blocker,  uses as an agent for the reduction of blood pressure.",456.32,"167221-71-8",{"v":91,"d":"91.00"},199.42,"<1","N/A","http://selleckchem.com/products/cleviprex-clevidipine.html","C21H23Cl2NO6","free base","Cleviprex","CCCC(=O)OCOC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2Cl)Cl)C(=O)OC)C",4.145,6,1,10]
["S2082","Adiphenine HCl","e5","L1700-09","in 10mM DMSO","AChR","Neuronal Signaling","Adiphenine HCl(NSC 129224) is a nicotinic receptor inhibitor, used as an antispasmodic drug.",347.88,"50-42-0",{"v":30,"d":"30.00"},86.24,{"v":70,"d":"70.00"},201.22,"http://selleckchem.com/products/adiphenine-hcl.html","C20H25NO2.HCl","HCl","NSC 129224","Cl.CCN(CC)CCOC(=O)C(C1=CC=CC=C1)C2=CC=CC=C2",4.433,2,0,9]
["S2083","Procaterol HCl","f5","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Procaterol HCl (OPC-2009) is a short-acting β2-adrenergic receptor agonist with Kp of 8 nM, used for the treatment of asthma",326.82,"62929-91-3",{"v":65,"d":"65.00"},198.89,{"v":65,"d":"65.00"},198.89,"http://www.selleckchem.com/products/procaterol-hcl.html","C16H22N2O3.HCl","hydrochloride","OPC-2009","Cl.CCC(NC(C)C)C(O)C1=CC=C(O)C2=C1C=CC(=O)N2",2.781,1,4,5]
["S2084","Duloxetine HCl","g5","L1700-09","in 10mM DMSO","5-HT Receptor,Serotonin Transporter","Neuronal Signaling","Duloxetine HCl (LY-248686) is a serotonin-norepinephrine reuptake inhibitor with Ki of 4.6 nM, used for treatment of major depressive disorder and generalized anxiety disorder (GAD).",333.88,"136434-34-9",{"v":67,"d":"67.00"},200.67,"<1","N/A","http://selleckchem.com/products/duloxetine-hcl-cymbalta.html","C18H19NOS.HCl","HCl","LY-248686 HCl","Cl.CNCCC(OC1=C2C=CC=CC2=CC=C1)C3=CC=CS3",4.228,1,1,6]
["S2085","Trimebutine","h5","L1700-09","in 10mM DMSO","Opioid Receptor","Neuronal Signaling","Trimebutine (Mebutin) is an agonist of peripheral mu, kappa and delta opiate receptors, used as spasmolytic agent for treatment of both acute and chronic abdominal pain.",387.47,"39133-31-8",{"v":50,"d":"50.00"},129.04,"<1","N/A","http://selleckchem.com/products/trimebutine.html","C22H29NO5","free base","Mebutin","CCC(COC(=O)C1=CC(=C(OC)C(=C1)OC)OC)(N(C)C)C2=CC=CC=C2",4.115,5,0,10]
["S2086","Ivabradine HCl","a6","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Ivabradine HCl (S 16257-2,S-18982 D6 hydrochloride), a new If inhibitor with IC 50 of 2.9 μM which acts specifically on the pacemaker activity of the sinoatrial node, is a pure heart rate lowering agent.",505.05,"148849-67-6",{"v":101,"d":"101.00"},199.98,{"v":82,"d":"82.00"},162.36,"http://selleckchem.com/products/ivabradine-hcl-procoralan.html","C27H36N2O5.HCl","HCl","S 16257-2,S-18982 D6 hydrochloride","Cl.COC1=CC2=C(CC(=O)N(CCCN(C)CC3CC4=CC(=C(OC)C=C34)OC)CC2)C=C1OC",3.753,5,0,10]
["S2087","Rivastigmine Tartrate","b6","L1700-09","in 10mM DMSO","AChR","Neuronal Signaling","Rivastigmine Tartrate (ENA 713) is a cholinesterase inhibitor with IC50 of 5.5 μM, and used as a parasympathomimetic or cholinergic agent for the treatment of mild to moderate Alzheimer disease.",400.42,"129101-54-8",{"v":42,"d":"42.00"},104.89,{"v":80,"d":"80.00"},199.79,"http://selleckchem.com/products/rivastigmine-tartrate-exelon.html","C14H22N2O2.C4H6O6","Tartrate","ENA 713","CCN(C)C(=O)OC1=CC=CC(=C1)C(C)N(C)C.OC(C(O)C(O)=O)C(O)=O",-2.099,4,2,8]
["S2090","Dexmedetomidine HCl","c6","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Dexmedetomidine HCl((+)-Medetomidine Hydrochloride) is a highly selective and potent alpha-2 adrenoceptor agonist, which reduces anesthetic requirements for patients by providing significant sedation.",236.74,"145108-58-3",{"v":48,"d":"48.00"},202.75,"<1","N/A","http://selleckchem.com/products/dexmedetomidine-hcl-precedex.html","C13H16N2.HCl","HCl","(+)-Medetomidine Hydrochloride","Cl.CC(C1=CN=C[NH]1)C2=CC=CC(=C2C)C",3.378,1,1,2]
["S2091","Betaxolol","d6","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Betaxolol (SL 75212,Dextrobetaxolol) is a selective beta1 adrenergic receptor blocker used in the treatment of hypertension and glaucoma.",307.43,"63659-18-7",{"v":62,"d":"62.00"},201.67,{"v":62,"d":"62.00"},201.67,"http://selleckchem.com/products/betaxolol-betoptic.html","C18H29NO3","free base","SL 75212,Dextrobetaxolol","CC(C)NCC(O)COC1=CC=C(CCOCC2CC2)C=C1",2.577,2,2,11]
["S2092","Detomidine HCl","e6","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Detomidine HCl(MPV 253AII) produce dose-dependent sedative and analgesic effects, mediatated by activation of α2 catecholamine receptors.",222.71,"90038-01-0",{"v":45,"d":"45.00"},202.06,{"v":45,"d":"45.00"},202.06,"http://selleckchem.com/products/detomidine-hcl.html","C12H14N2.HCl","HCl","MPV 253AII","Cl.CC1=C(C)C(=CC=C1)CC2=C[NH]C=N2",3.053,1,1,2]
["S2096","Almotriptan Malate","f6","L1700-09","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Almotriptan Malate (LAS 31416) is a selective 5-hydroxytryptamine1B/1D (5-HT1B/1D) receptor agonist, used for the treatment of Migraine attacks in adults.",469.55,"181183-52-8",{"v":94,"d":"94.00"},200.19,"<1","N/A","http://selleckchem.com/products/almotriptan-malate-axert.html","C17H25N3O2S.C4H6O5","Malate","LAS 31416","CN(C)CCC1=C[NH]C2=CC=C(C[S](=O)(=O)N3CCCC3)C=C12.OC(CC(O)=O)C(O)=O",-1.943,4,2,9]
["S2097","Ambrisentan","g6","L1700-09","in 10mM DMSO","Endothelin Receptor","GPCR & G Protein","Ambrisentan (LU-208075, BSF-208075) is a highly selective antagonist of the endothelin-1 type A receptor, used in the treatment of pulmonary arterial hypertension (PAH).",378.42,"177036-94-1",{"v":76,"d":"76.00"},200.84,"<1","N/A","http://selleckchem.com/products/ambrisentan.html","C22H22N2O4","free base","LU-208075, BSF-208075","COC(C(OC1=NC(=CC(=N1)C)C)C(O)=O)(C2=CC=CC=C2)C3=CC=CC=C3",3.659,5,0,7]
["S2098","Bexarotene (LGD1069)","h6","L1700-09","in 10mM DMSO","Retinoid Receptor","Metabolism","Bexarotene (Targretin, LGD1069) is a retinoid specifically selective for retinoid X receptors, used as an oral antineoplastic agent in the treatment of cutaneous T-cell lymphoma.",{"v":348,"d":"348.00"},"153559-49-0",{"v":8,"d":"8.00"},22.99,"<1","N/A","http://selleckchem.com/products/bexarotene.html","C24H28O2","free base","Targretin","CC1=CC2=C(C=C1C(=C)C3=CC=C(C=C3)C(O)=O)C(C)(C)CCC2(C)C",6.405,1,0,3]
["S2099","Temocapril HCl","a7","L1700-09","in 10mM DMSO","ACE,RAAS","Endocrinology & Hormones","Temocapril HCl (CS-622) is the hydrochloride of Temocapril, which is a long-acting angiotensin-converting enzyme (ACE) inhibitor, used for the treatment of hypertension.",513.07,"110221-44-8",{"v":103,"d":"103.00"},200.75,"<1","N/A","http://selleckchem.com/products/temocapril-hcl.html","C23H28N2O5S2.HCl","Hydrochloride","CS-622 HCl","Cl.CCOC(=O)C(CCC1=CC=CC=C1)NC2CSC(CN(CC(O)=O)C2=O)C3=CC=CS3",0.787,4,1,11]
["S2101","Gabexate Mesylate","b7","L1700-09","in 10mM DMSO","Serine Protease","Proteases","Gabexate Mesylate(FOY) is a serine protease inhibitor with IC50 of 0.19 μM which is used therapeutically in the treatment of pancreatitis and disseminated intravascular coagulation.",417.48,"56974-61-9",{"v":83,"d":"83.00"},198.81,{"v":12,"d":"12.00"},28.74,"http://selleckchem.com/products/gabexate-mesylate.html","C16H23N3O4.CH4O3S","Mesylate","FOY","CCOC(=O)C1=CC=C(OC(=O)CCCCCNC(N)=N)C=C1.C[S](O)(=O)=O",1.774,4,2,12]
["S2102","Rasagiline Mesylate","c7","L1700-09","in 10mM DMSO","MAO","Metabolism","Rasagiline Mesylate (TVP-1012,(R)-AGN1135 mesylate,TVP1012 mesylate) is a new MAO-B inhibitor for the treatment of idiopathic Parkinson's disease.",267.34,"161735-79-1",{"v":53,"d":"53.00"},198.25,{"v":53,"d":"53.00"},198.25,"http://selleckchem.com/products/rasagiline-mesylate.html","C12H13N.CH4O3S","Mesylate","TVP-1012,(R)-AGN1135 mesylate,TVP1012 mesylate","C[S](O)(=O)=O.C#CCNC1CCC2=CC=CC=C12",2.705,0,1,2]
["S2103","Naltrexone HCl","d7","L1700-09","in 10mM DMSO","Opioid Receptor","Neuronal Signaling","Naltrexone HCl(PTI-901) is an opioid receptor antagonist used primarily in the management of alcohol dependence and opioid dependence.",377.86,"16676-29-2",{"v":14,"d":"14.00"},37.05,{"v":14,"d":"14.00"},37.05,"http://selleckchem.com/products/naltrexone-hcl.html","C20H23NO4.HCl","Hydrochloride","PTI-901","Cl.OC1=CC=C2CC3N(CCC45C(OC1=C24)C(=O)CCC35O)CC6CC6",2.039,2,1,2]
["S2104","Levosulpiride","e7","L1700-09","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Levosulpiride(RV-12309,S-(-)-Sulpiride) is a selective antagonist for D2 dopamine receptors used as an antipsychotic and prokinetic agent.",341.43,"23672-07-3",{"v":69,"d":"69.00"},202.09,"<1","N/A","http://selleckchem.com/products/levosulpiride-levogastrol.html","C15H23N3O4S","free base","RV-12309,S-(-)-Sulpiride","CCN1CCCC1CNC(=O)C2=C(OC)C=CC(=C2)[S](N)(=O)=O",0.704,4,2,6]
["S2105","Pantoprazole","f7","L1700-09","in 10mM DMSO","ATPase,Proton Pump","Transmembrane Transporters","Pantoprazole (SKF96022, BY-1023) is a proton pump inhibitor drug that inhibits gastric acid secretion. It works on gastric parietal cells to irreversibly inhibit (H+/K+)-ATPase function and suppress the production of gastric acid.",383.37,"102625-70-7",{"v":76,"d":"76.00"},198.24,"<1","N/A","http://selleckchem.com/products/pantoprazole-protonix.html","C16H15F2N3O4S","free base","SKFSKF96022, BY-1023","COC1=C(OC)C(=NC=C1)C[S](=O)C2=NC3=CC=C(OC(F)F)C=C3[NH]2",2.737,6,1,7]
["S2108","Flunixin Meglumin","g7","L1700-09","in 10mM DMSO","COX","Neuronal Signaling","Flunixin Meglumin(Banamine) is a potent inhibitor of the enzyme cyclooxygenase (COX) used as analgesic agent with anti-inflammatory and antipyretic activity.",491.46,"42461-84-7",{"v":98,"d":"98.00"},199.41,{"v":98,"d":"98.00"},199.41,"http://selleckchem.com/products/flunixin-meglumin.html","C14H11F3N2O2.C7H17NO5","Meglumin","Banamine","CNCC(O)C(O)C(O)C(O)CO.CC1=C(C=CC=C1NC2=NC=CC=C2C(O)=O)C(F)(F)F",-1.676,2,7,10]
["S2109","Imidapril HCl","h7","L1700-09","in 10mM DMSO","ACE,RAAS","Endocrinology & Hormones","Imidapril HCl(TA-6366) is an angiotensin-converting enzyme (ACE) inhibitor with IC50 of 2.6 nM, used for the treatment of hypertension.",441.91,"89396-94-1",{"v":88,"d":"88.00"},199.14,{"v":54,"d":"54.00"},{"v":122.2,"d":"122.20"},"http://selleckchem.com/products/imidapril-tanatril.html","C20H27N3O6.HCl","Hydrochloride","TA-6366","Cl.CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2C(CN(C)C2=O)C(O)=O",-1.197,5,1,10]
["S2111","Lapatinib (GW-572016)","a8","L1700-09","in 10mM DMSO","Autophagy,EGFR,Ferroptosis,HER2","Protein Tyrosine Kinase","Lapatinib (GW-572016, GSK572016, GW2016), used in the form of Lapatinib Ditosylate, is a potent EGFR and ErbB2 inhibitor with IC50 of 10.8 and 9.2 nM in cell-free assays, respectively. Lapatinib induces ferroptosis and autophagic cell death.",581.06,"231277-92-2",{"v":100,"d":"100.00"},{"v":172.1,"d":"172.10"},"<1","N/A","http://selleckchem.com/products/lapatinib.html","C29H26ClFN4O4S","free base","GSK572016, GW2016","C[S](=O)(=O)CCNCC1=CC=C(O1)C2=CC=C3N=CN=C(NC4=CC=C(OCC5=CC=CC(=C5)F)C(=C4)Cl)C3=C2",6.041,6,2,11]
["S2113","Cisatracurium Besylate","b8","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Cisatracurium Besylate(51W89) is a nondepolarizing neuromuscular blocking agent, antagonizing the action of acetylcholine by inhibiting neuromuscular transmission.",1243.48,"96946-42-8",{"v":249,"d":"249.00"},200.24,{"v":47,"d":"47.00"},{"v":37.8,"d":"37.80"},"http://selleckchem.com/products/cisatracurium-besylate-nimbex.html","C53H72N2O12.2C6H5O3S","Besylate","51W89","COC1=CC=C(CC2C3=CC(=C(OC)C=C3CC[N+]2(C)CCC(=O)OCCCCCOC(=O)CC[N+]4(C)CCC5=CC(=C(OC)C=C5C4CC6=CC=C(OC)C(=C6)OC)OC)OC)C=C1OC.[O-][S](=O)(=O)C7=CC=CC=C7.[O-][S](=O)(=O)C8=CC=CC=C8",3.646,12,0,28]
["S2114","Dronedarone HCl","c8","L1700-09","in 10mM DMSO","Calcium Channel,Potassium Channel,Sodium Channel","Transmembrane Transporters","Dronedarone HCl (SR33589) is a multichannel blocker targeting potassium channel, sodium channel and calcium channel, used as an antiarrhythmic drug for treatment of atrial fibrillation (AF).",593.22,"141625-93-6",{"v":80,"d":"80.00"},134.86,"<1","N/A","http://selleckchem.com/products/dronedarone-hcl-multaq.html","C31H44N2O5S.HCl","HCl","SR33589","Cl.CCCCN(CCCC)CCCOC1=CC=C(C=C1)C(=O)C2=C(CCCC)OC3=CC=C(N[S](C)(=O)=O)C=C23",7.397,5,1,18]
["S2116","Conivaptan HCl","d8","L1700-09","in 10mM DMSO","Vasopressin Receptor","GPCR & G Protein","Conivaptan HCl(YM 087) is an orally active, non-peptide, vasopressin V1A and V2 receptor antagonist, used in the treatment of euvolemic and hypervolemic hyponatremia.",535.04,"168626-94-6",{"v":107,"d":"107.00"},199.99,"<1","N/A","http://selleckchem.com/products/conivaptan-hcl-vaprisol.html","C32H26N4O2.HCl","HCl","YM 087","Cl.CC1=NC2=C([NH]1)C3=C(C=CC=C3)N(CC2)C(=O)C4=CC=C(NC(=O)C5=C(C=CC=C5)C6=CC=CC=C6)C=C4",{"v":5.68,"d":"5.680"},3,2,4]
["S2118","Ibutilide Fumarate","e8","L1700-09","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Ibutilide Fumarate (U-70226E,Corvert Fumarate) is a Class III antiarrhythmic agent that is indicated for acute cardioconversion of atrial fibrillation and atrial flutter of a recent onset to sinus rhythm by induction of slow inward sodium current, which prolongs action potential and refractory period of myocardial cells.",885.23,"122647-32-9",{"v":89,"d":"89.00"},100.54,{"v":89,"d":"89.00"},100.54,"http://selleckchem.com/products/ibutilide-fumarate.html","(C20H36N2O3S)2.C4H4O4","Fumarate","U-70226E,Corvert Fumarate","CCCCCCCN(CC)CCCC(O)C1=CC=C(N[S](C)(=O)=O)C=C1.CCCCCCCN(CC)CCCC(O)C2=CC=C(N[S](C)(=O)=O)C=C2.OC(=O)\\C=C\\C(O)=O",1.954,6,4,30]
["S2119","Probucol","f8","L1700-09","in 10mM DMSO","LDL","Metabolism","Probucol (DH-581) is an anti-hyperlipidemic drug by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism.",516.84,"23288-49-5",{"v":103,"d":"103.00"},199.29,"<1","N/A","http://selleckchem.com/products/probucol.html","C31H48O2S2","free base","DH-581","CC(C)(C)C1=CC(=CC(=C1O)C(C)(C)C)SC(C)(C)SC2=CC(=C(O)C(=C2)C(C)(C)C)C(C)(C)C",9.779,0,2,8]
["S2120","Arbidol HCl","g8","L1700-09","in 10mM DMSO","Influenza Virus","Microbiology","Arbidol HCl (Umifenovir) is a broad-spectrum antiviral compound that blocks viral fusion, used in treatment of influenza and other respiratory viral infections.",513.88,"131707-23-8",{"v":103,"d":"103.00"},200.44,"<1","N/A","http://selleckchem.com/products/Arbidol-hcl.html","C22H25BrN2O3S.HCl","Hydrochloride","Umifenovir hydrochloride, Arbidol hydrochloride","Cl.CCOC(=O)C1=C(CSC2=CC=CC=C2)[N](C)C3=CC(=C(O)C(=C13)CN(C)C)Br",5.698,2,1,8]
["S2123","Dextrose","h8","L1700-09","in 10mM DMSO","Others","Others","Dextrose (D-glucose), a simple sugar (monosaccharide), is an important carbohydrate in biology.",180.16,"50-99-7",{"v":36,"d":"36.00"},199.82,{"v":36,"d":"36.00"},199.82,"http://selleckchem.com/products/Dextrose(D-glucose).html","C6H12O6","free base","D-glucose","OCC(O)C(O)C(O)C(O)C=O",-2.791,1,5,5]
["S2124","Xylose","a9","L1700-09","in 10mM DMSO","Others","Others","Xylose(Wood sugar) is a sugar first isolated from wood.",150.13,"25990-60-7, 58-86-6",{"v":30,"d":"30.00"},199.83,{"v":30,"d":"30.00"},199.83,"http://selleckchem.com/products/Xylose.html","C5H10O5","free base","Wood sugar","OCC(O)C(O)C(O)C=O",{"v":-2.28,"d":"-2.280"},1,4,4]
["S2125","Mestranol","b9","L1700-09","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Mestranol is the 3-methyl ether of ethinyl estradiol, which is a potent estrogen receptor agonist and used as oral contraceptives.",310.43,"72-33-3",{"v":15,"d":"15.00"},48.32,"<1","N/A","http://selleckchem.com/products/Mestranol.html","C21H26O2","free base","N/A","COC1=CC2=C(C=C1)C3CCC4(C)C(CCC4(O)C#C)C3CC2",5.112,1,0,1]
["S2126","Naftopidil","c9","L1700-09","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Naftopidil (KT-611) is a selective α1-adrenergic receptor antagonist with Ki of 3.7 nM, 20 nM, and 1.2 nM for α1a, α1b, and α1d, respectively, used for the treatment of benign prostatic hyperplasia.",392.49,"57149-07-2",{"v":79,"d":"79.00"},201.28,"<1","N/A","http://selleckchem.com/products/Naftopidil(Flivas).html","C24H28N2O3","Free Base","KT-611","COC1=CC=CC=C1N2CCN(CC2)CC(O)COC3=C4C=CC=CC4=CC=C3",3.962,2,1,7]
["S2127","S-(+)-Rolipram","d9","L1700-09","in 10mM DMSO","PDE","Metabolism","S-(+)-Rolipram inhibits human monocyte cyclic AMP-specific PDE4 with IC50 of 0.75 μM, has anti-inflammatory and anti-depressant activity in the central nervous system, less potent than its R enantiomer.",275.34,"85416-73-5",{"v":55,"d":"55.00"},199.75,"<1","N/A","http://selleckchem.com/products/sRolipram.html","C16H21NO3","free base","N/A","COC1=C(OC2CCCC2)C=C(C=C1)C3CNC(=O)C3",2.349,3,1,4]
["S2128","Bazedoxifene (WAY-140424) HCl","e9","L1700-09","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Bazedoxifene HCl (WAY-140424, TSE-424) is a novel, non-steroidal, indole-based estrogen receptor modulator (SERM) binding to both ERα and ERβ with IC50 of  23 nM and 89 nM, respectively.",507.06,"198480-56-7",{"v":101,"d":"101.00"},199.19,"<1","N/A","http://selleckchem.com/products/bazedoxifene-hcl.html","C30H34N2O3.HCl","Hydrochloride","TSE-424","Cl.CC1=C([N](CC2=CC=C(OCCN3CCCCCC3)C=C2)C4=CC=C(O)C=C14)C5=CC=C(O)C=C5",7.602,1,2,7]
["S2130","Atropine sulfate monohydrate","f9","L1700-09","in 10mM DMSO","AChR,ADC Cytotoxin","Neuronal Signaling","Atropine sulfate monohydrate is a competitive antagonist for the muscarinic acetylcholine receptor, used to decrease the production of saliva and secretions of the airway prior to surgery.",694.83,"5908-99-6",{"v":139,"d":"139.00"},200.05,{"v":139,"d":"139.00"},200.05,"http://selleckchem.com/products/Atropine-sulfate-monohydrate.html","2(C17H23NO3).H2O.H2SO4","Sulfate monohydrate","N/A","O.CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3.CN4C5CCC4CC(C5)OC(=O)C(CO)C6=CC=CC=C6.O[S](O)(=O)=O",2.628,4,2,10]
["S2131","Roflumilast (B9302-107)","g9","L1700-09","in 10mM DMSO","PDE","Metabolism","Roflumilast (APTA 2217, B9302-107, BY 217, BYK 20869) is a selective inhibitor of PDE4 with IC50 of 0.2-4.3 nM in a cell-free assay.",403.21,"162401-32-3",{"v":81,"d":"81.00"},200.89,"<1","N/A","http://selleckchem.com/products/Roflumilast(Daxas).html","C17H14Cl2F2N2O3","free base","APTA 2217, B9302-107, BY 217, BYK 20869","FC(F)OC1=CC=C(C=C1OCC2CC2)C(=O)NC3=C(Cl)C=NC=C3Cl",4.402,4,1,7]
["S2134","AZD8330","h9","L1700-09","in 10mM DMSO","MEK","MAPK","AZD8330 (ARRY704) is a novel, selective, non-ATP competitive MEK 1/2 inhibitor with IC50 of 7 nM. Phase 1.",461.23,"869357-68-6",{"v":92,"d":"92.00"},199.47,"<1","N/A","http://selleckchem.com/products/AZD8330(ARRY-424704).html","C16H17FIN3O4","free base","ARRY704","CN1C(=O)C(=CC(=C1NC2=C(F)C=C(I)C=C2)C(=O)NOCCO)C",1.653,3,3,6]
["S2149","GSK1292263","a10","L1700-09","in 10mM DMSO","GPR","Endocrinology & Hormones","GSK1292263 is a novel GPR119 agonist, showing potential for the treatment of type 2 diabetes. Phase 2.",456.56,"1032823-75-8",{"v":34,"d":"34.00"},74.47,"<1","N/A","http://selleckchem.com/products/GSK1292263.html","C23H28N4O4S","free base","N/A","CC(C)C1=NOC(=N1)N2CCC(CC2)COC3=CN=C(C=C3)C4=CC=C(C=C4)[S](C)(=O)=O",3.893,7,0,7]
["S2151","Sonidegib (NVP-LDE225)","b10","L1700-09","in 10mM DMSO","Hedgehog/Smoothened","Stem Cells & Wnt","Sonidegib (Erismodegib, NVP-LDE225) is a Smoothened (Smo) antagonist, inhibiting Hedgehog (Hh) signaling with IC50 of 1.3 nM (mouse) and 2.5 nM (human) in cell-free assays, respectively. Phase 3.",{"v":485.5,"d":"485.50"},"956697-53-3",{"v":97,"d":"97.00"},199.79,"<1","N/A","http://selleckchem.com/products/LDE225(NVP-LDE225).html","C26H26F3N3O3","free base","Erismodegib","CC1CN(CC(C)O1)C2=CC=C(NC(=O)C3=C(C)C(=CC=C3)C4=CC=C(OC(F)(F)F)C=C4)C=N2",6.732,4,1,6]
["S2153","CGS 21680 HCl","c10","L1700-09","in 10mM DMSO","Adenosine Receptor","GPCR & G Protein","CGS 21680 HCl is an adenosine A2 receptor agonist with IC50 of 22 nM, exhibits 140-fold over A1 receptor.",535.98,"124431-80-7",{"v":100,"d":"100.00"},186.57,"<1","N/A","http://selleckchem.com/products/CGS-21680-hydrochloride.html","C23H29N7O6.HCl","Hydrochloride","N/A","Cl.CCNC(=O)C1OC(C(O)C1O)[N]2C=NC3=C2N=C(NCCC4=CC=C(CCC(O)=O)C=C4)N=C3N",0.911,6,5,10]
["S2154","Dabigatran (BIBR-1048) etexilate","d10","L1700-09","in 10mM DMSO","Thrombin","Proteases","Dabigatran Etexilate (BIBR-1048) is the prodrug of dabigatran, a potent, nonpeptidic small molecule that specifically and reversibly inhibits both free and clot-bound thrombin by binding to the active site of the thrombin molecule.",627.73,"211915-06-9",{"v":126,"d":"126.00"},200.72,"<1","N/A","http://selleckchem.com/products/BIBR-1048(Dabigatran-etexilate).html","C34H41N7O5","free base","BIBR-1048","CCCCCCOC(=O)N=C(N)C1=CC=C(NCC2=NC3=C(C=CC(=C3)C(=O)N(CCC(=O)OCC)C4=CC=CC=N4)[N]2C)C=C1",5.751,8,2,17]
["S2155","LY2608204","e10","L1700-09","in 10mM DMSO","Carbohydrate Metabolism","Metabolism","LY2608204 activates glucokinase (GK) with EC50 of 42 nM. Phase 2.",559.81,"1234703-40-2",{"v":112,"d":"112.00"},200.07,"<1","N/A","http://selleckchem.com/products/ly2608204.html","C28H37N3O3S3","free base","N/A","O=C(NC1=NC=C(SCCN2CCCC2)S1)C3(CC3C4CCCCC4)C5=CC=C(C=C5)[S](=O)(=O)C6CC6",5.393,4,1,10]
["S2156","LY2886721","f10","L1700-09","in 10mM DMSO","BACE","Neuronal Signaling","LY2886721 is a BACE inhibitor used for the treatment of Alzheimer's Disease. Phase 1/2.",390.41,"1262036-50-9",{"v":9,"d":"9.00"},23.05,"<1","N/A","http://selleckchem.com/products/LY-2886721.html","C18H16F2N4O2S","free base","N/A","NC1=NC2(COCC2CS1)C3=CC(=CC=C3F)NC(=O)C4=NC=C(F)C=C4",2.134,4,2,3]
["S2158","KW-2449","g10","L1700-09","in 10mM DMSO","Aurora Kinase,Bcr-Abl,FLT3","Angiogenesis","KW-2449 is a multiple-targeted inhibitor, mostly for Flt3 with IC50 of 6.6 nM, modestly potent to FGFR1, Bcr-Abl and Aurora A; little effect on PDGFRβ, IGF-1R, EGFR. Phase 1.",{"v":332.4,"d":"332.40"},"1000669-72-6",{"v":67,"d":"67.00"},201.56,"<1","N/A","http://selleckchem.com/products/KW-2449.html","C20H20N4O","free base","N/A","O=C(N1CCNCC1)C2=CC=C(C=C2)/C=C/C3=N[NH]C4=C3C=CC=C4",2.723,2,2,3]
["S2159","Tebipenem Pivoxil","h10","L1700-09","in 10mM DMSO","Antibiotics","Microbiology","Tebipenem pivoxil (L-084, ME1211,TBPM-PI,LJC 11036) is an oral carbapenem antibiotic, use to treat otolaryngologic and respiratory infections.",497.63,"161715-24-8",{"v":99,"d":"99.00"},198.94,"<1","N/A","http://selleckchem.com/products/Tebipenem-pivoxil(L-084).html","C22H31N3O6S2","free base","L-084, ME1211,TBPM-PI,LJC 11036","CC(O)C1C2C(C)C(=C(N2C1=O)C(=O)OCOC(=O)C(C)(C)C)SC3CN(C3)C4=NCCS4",1.782,6,1,10]
["S2160","Almorexant HCl","a11","L1700-09","in 10mM DMSO","OX Receptor","GPCR & G Protein","Almorexant HCl (ACT-078573) is an orally active, dual orexin receptor antagonist with IC50 of 6.6 nM and 3.4 nM for OX1 and OX2 receptor, respectively. Phase 3.",549.02,"913358-93-7",{"v":72,"d":"72.00"},131.14,"<1","N/A","http://selleckchem.com/products/almorexant-hcl.html","C29H32ClF3N2O3","Hydrochloride","ACT-078573 HCl","Cl.CNC(=O)C(N1CCC2=C(C=C(OC)C(=C2)OC)C1CCC3=CC=C(C=C3)C(F)(F)F)C4=CC=CC=C4",6.438,3,1,9]
["S2161","RAF265 (CHIR-265)","b11","L1700-09","in 10mM DMSO","Apoptosis related,Raf,VEGFR","MAPK","RAF265 (CHIR-265) is a potent selective inhibitor of C-Raf/B-Raf/B-Raf V600E with IC50 of 3-60 nM, and exhibits potent inhibition on VEGFR2 phosphorylation with EC50 of 30 nM in cell-free assays. RAF265 (CHIR-265) induces cell cycle arrest and apoptosis. Phase 2.",518.41,"927880-90-8",{"v":100,"d":"100.00"},{"v":192.9,"d":"192.90"},"<1","N/A","http://selleckchem.com/products/RAF265(CHIR-265).html","C24H16F6N6O","free base","N/A","C[N]1C(=NC2=C1C=CC(=C2)OC3=CC=NC(=C3)C4=NC=C([NH]4)C(F)(F)F)NC5=CC=C(C=C5)C(F)(F)F",6.469,4,2,7]
["S2162","AZD1480","c11","L1700-09","in 10mM DMSO","JAK","JAK/STAT","AZD1480 is a novel ATP-competitive JAK2 inhibitor with IC50 of 0.26 nM in a cell-free assay, selectivity against JAK3 and Tyk2, and to a smaller extent against JAK1. Phase 1.",348.77,"935666-88-9",{"v":70,"d":"70.00"},200.71,"<1","N/A","http://www.selleck.cn/products/AZD1480.html","C14H14ClFN8","free base","N/A","CC(NC1=NC=C(Cl)C(=N1)NC2=N[NH]C(=C2)C)C3=NC=C(F)C=N3",2.645,5,3,5]
["S2163","PF-4708671","d11","L1700-09","in 10mM DMSO","Autophagy,S6 Kinase","PI3K/Akt/mTOR","PF-4708671 is a cell-permeable inhibitor of p70 ribosomal S6 kinase (S6K1 isoform) with Ki/IC50 of 20 nM/160 nM in cell-free assays, 400-fold greater selectivity for S6K1 than S6K2, and 4- and >20-fold selectivity for S6K1 than MSK1 and RSK1/2, respectively. PF-4708671 induces autophagy. First S6K1-specific inhibitor to be reported.",390.41,"1255517-76-0",{"v":30,"d":"30.00"},76.84,"<1","N/A","http://selleckchem.com/products/pf-4708671.html","C19H21F3N6","free base","N/A","CCC1=CN=CN=C1N2CCN(CC2)CC3=NC4=C([NH]3)C=CC(=C4)C(F)(F)F",3.886,3,1,5]
["S2167","Bazedoxifene (TSE-424) acetate","e11","L1700-09","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Bazedoxifene Acetate (WAY-140424,TSE-424 acetate) is a third generation selective estrogen receptor modulator (SERM).",530.65,"198481-33-3",{"v":100,"d":"100.00"},188.45,"<1","N/A","http://selleckchem.com/products/Bazedoxifene-acetate.html","C30H34N2O3.C2H4O2","Acetate","WAY-140424,TSE-424 acetate","CC(O)=O.CC1=C([N](CC2=CC=C(OCCN3CCCCCC3)C=C2)C4=CC=C(O)C=C14)C5=CC=C(O)C=C5",3.981,2,2,7]
["S2168","PD128907 HCl","f11","L1700-09","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","PD 128907 HCl is a potent and selective dopamine D3 receptor agonist, with EC50 of 0.64 nM, exhibits 53-fold selectivity over dopamine D2 receptor.",285.77,"112960-16-4",{"v":12,"d":"12.00"},41.99,{"v":50,"d":"50.00"},174.97,"http://selleckchem.com/products/PD-128907.html","C14H19NO3.HCl","Hydrochloride","N/A","Cl.CCCN1CCOC2C1COC3=CC=C(O)C=C23",2.463,2,1,2]
["S2169","Rosuvastatin (ZD4522) calcium","g11","L1700-09","in 10mM DMSO","COVID-19,HMG-CoA Reductase","Metabolism","Rosuvastatin Calcium (ZD4522 calcium) is a competitive inhibitor of HMG-CoA reductase with IC50 of 11 nM in a cell-free assay.",500.57,"147098-20-2",{"v":100,"d":"100.00"},199.77,"<1","N/A","http://selleckchem.com/products/Rosuvastatin-calcium(Crestor).html","C22H28FN3O6S.1/2Ca","Calcium salt","ZD4522 calcium","[Ca++].CC(C)C1=C(\\C=C\\C(O)CC(O)CC([O-])=O)C(=NC(=N1)N(C)[S](C)(=O)=O)C2=CC=C(F)C=C2.CC(C)C3=C(\\C=C\\C(O)CC(O)CC([O-])=O)C(=NC(=N3)N(C)[S](C)(=O)=O)C4=CC=C(F)C=C4",1.906,8,4,20]
["S2170","Givinostat (ITF2357)","h11","L1700-09","in 10mM DMSO","HDAC","Cytoskeletal Signaling","Givinostat (ITF2357) is a potent HDAC inhibitor for maize HD2, HD1B and HD1A with IC50 of 10 nM, 7.5 nM and 16 nM in cell-free assays. Phase 2.",475.97,"732302-99-7",{"v":95,"d":"95.00"},199.59,"<1","N/A","http://selleckchem.com/products/ITF2357(Givinostat).html","C24H27N3O4.HCl.H2O","Chloride","N/A","O.Cl.CCN(CC)CC1=CC2=C(C=C1)C=C(COC(=O)NC3=CC=C(C=C3)C(=O)NO)C=C2",4.046,3,2,9]
["S2173","Telotristat Etiprate (LX 1606 Hippurate)","a2","L1700-10","in 10mM DMSO","Hydroxylase","Metabolism","Telotristat Etiprate (LX 1606 Hippurate) is an orally bioavailable, tryptophan hydroxylase (TPH) inhibitor with potential antiserotonergic activity. Phase 3.",754.15,"1137608-69-5",{"v":100,"d":"100.00"},{"v":132.6,"d":"132.60"},"<1","N/A","http://selleckchem.com/products/telotristat-etiprate-lx-1606-hippurate.html","C27H26ClF3N6O3.C9H9NO3","Hippuric acid","N/A","CCOC(=O)C(N)CC1=CC=C(C=C1)C2=CC(=NC(=N2)N)OC(C3=CC=C(Cl)C=C3[N]4C=CC(=N4)C)C(F)(F)F.OC(=O)CNC(=O)C5=CC=CC=C5",3.747,8,3,14]
["S2177","Dichlorphenamide","b2","L1700-10","in 10mM DMSO","Carbonic Anhydrase","Metabolism","Dichlorphenamide (Diclofenamide) is a sulfonamide and a carbonic anhydrase inhibitor of the meta-Disulfamoylbenzene class.",305.16,"120-97-8",{"v":61,"d":"61.00"},199.89,"N/A","N/A","http://www.selleckchem.com/products/Dichlorphenamide(Diclofenamide).html","C6H6Cl2N2O4S2","Free Base","Diclofenamide","N[S](=O)(=O)C1=CC(=C(Cl)C(=C1)[S](N)(=O)=O)Cl","N/A","N/A","N/A","N/A"]
["S2178","AG-14361","c2","L1700-10","in 10mM DMSO","PARP","DNA Damage/DNA Repair","AG14361 is a potent inhibitor of PARP1 with Ki of <5 nM in a cell-free assay. It is at least 1000-fold more potent than the benzamides.",320.39,"328543-09-5",{"v":12,"d":"12.00"},37.45,"<1","N/A","http://selleckchem.com/products/AG14361.html","C19H20N4O","free base","N/A","CN(C)CC1=CC=C(C=C1)C2=NC3=CC=CC4=C3[N]2CCNC4=O",2.576,2,1,3]
["S2179","Gandotinib (LY2784544)","d2","L1700-10","in 10mM DMSO","JAK","JAK/STAT","Gandotinib (LY2784544) is a potent JAK2 inhibitor with IC50 of 3 nM, effective in JAK2V617F, 8- and 20-fold selective versus JAK1 and JAK3. Phase 2.",469.94,"1229236-86-5",{"v":94,"d":"94.00"},200.03,"<1","N/A","http://selleckchem.com/products/LY2784544.html","C23H25ClFN7O","free base","N/A","CC1=N[NH]C(=C1)NC2=N[N]3C(=C(C)N=C3C(=C2)CN4CCOCC4)CC5=CC=C(Cl)C=C5F",3.938,4,2,6]
["S2180","Ixazomib (MLN2238)","e2","L1700-10","in 10mM DMSO","Autophagy,Proteasome","Proteases","Ixazomib (MLN2238) inhibits the chymotrypsin-like proteolytic (β5) site of the 20S proteasome with IC50 and Ki of 3.4 nM and 0.93 nM in cell-free assays, respectively, also inhibits the caspase-like (β1) and trypsin-like (β2) proteolytic sites, with IC50 of 31 and 3500 nM. Ixazomib (MLN2238) induces autophagy. Phase 3.",361.03,"1072833-77-2",{"v":72,"d":"72.00"},199.43,"<1","N/A","http://selleckchem.com/products/MLN-2238.html","C14H19BCl2N2O4","Free Base","N/A","CC(C)CC(NC(=O)CNC(=O)C1=C(Cl)C=CC(=C1)Cl)B(O)O",3.344,2,2,7]
["S2181","Ixazomib Citrate (MLN9708) Analogue","f2","L1700-10","in 10mM DMSO","Autophagy,Proteasome","Proteases","Ixazomib Citrate (MLN9708) Analogue is the analogue of Ixazomib Citrate (MLN9708) from WO2016165677A1. Ixazomib Citrate (MLN9708) immediately hydrolyzed to Ixazomib (MLN2238), the biologically active form, on exposure to aqueous solutions or plasma. Ixazomib (MLN2238) inhibits the chymotrypsin-like proteolytic (β5) site of the 20S proteasome with IC50/Ki of 3.4 nM/0.93 nM in cell-free assays, less potent to β1 and little activity to β2. Ixazomib (MLN2238) induces autophagy. Phase 3.",517.12,"1201902-80-8",{"v":100,"d":"100.00"},193.38,"<1","N/A","http://selleckchem.com/products/MLN9708.html","C20H23BCl2N2O9","free base","N/A","CC(C)CC(NC(=O)CNC(=O)C1=C(Cl)C=CC(=C1)Cl)B2OC(=O)CC(CC(O)=O)(O2)C(O)=O",3.497,7,2,10]
["S2182","SB743921 HCl","g2","L1700-10","in 10mM DMSO","Kinesin","Cytoskeletal Signaling","SB743921 is a kinesin spindle protein (KSP) inhibitor with Ki of 0.1 nM, almost no affinity to MKLP1, Kin2, Kif1A, Kif15, KHC, Kif4 and CENP-E. Phase 1/2.",553.52,"940929-33-9",{"v":111,"d":"111.00"},200.53,{"v":22,"d":"22.00"},39.75,"http://selleckchem.com/products/SB-743921.html","C31H33N2O3.HCl","Hydrochloride","N/A","Cl.CC(C)C(N(CCCN)C(=O)C1=CC=C(C)C=C1)C2=C(CC3=CC=CC=C3)C(=O)C4=C(O2)C=C(Cl)C=C4",6.536,3,1,9]
["S2183","Infigratinib (BGJ398)","h2","L1700-10","in 10mM DMSO","FGFR","Angiogenesis","Infigratinib (BGJ398) is a potent and selective FGFR inhibitor for FGFR1/2/3 with IC50 of 0.9 nM/1.4 nM/1 nM in cell-free assays, >40-fold selective for FGFR versus FGFR4 and VEGFR2, and little activity to Abl, Fyn, Kit, Lck, Lyn and Yes. Phase 2.",560.48,"872511-34-7",{"v":27,"d":"27.00"},48.17,"<1","N/A","http://www.selleck.cn/products/bgj398-nvp-bgj398.html","C26H31Cl2N7O3","Free Base","NVP-BGJ398","CCN1CCN(CC1)C2=CC=C(NC3=NC=NC(=C3)N(C)C(=O)NC4=C(Cl)C(=CC(=C4Cl)OC)OC)C=C2",5.342,5,2,8]
["S2185","Allitinib tosylate","a3","L1700-10","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","Allitinib tosylate (AST-1306 TsOH, AST-6) is a novel irreversible inhibitor of EGFR and ErbB2 with IC50 of 0.5 nM and 3 nM, also effective in mutation EGFR T790M/L858R, more potent to ErbB2-overexpressing cells, 3000-fold selective for ErbB family than other kinases.",621.08,"1050500-29-2",{"v":124,"d":"124.00"},199.65,"<1","N/A","https://www.selleckchem.com/products/allitinib-tosylate.html","C24H18ClFN4O2,C7H8O3S","Mesylate","AST-1306 TsOH, AST-6","CC1=CC=C(C=C1)[S](O)(=O)=O.FC2=CC(=CC=C2)COC3=CC=C(NC4=C5C=C(NC(=O)C=C)C=CC5=NC=N4)C=C3Cl",7.381,4,2,8]
["S2186","SB505124","b3","L1700-10","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","SB505124 is a selective inhibitor of TGFβR for ALK4, ALK5 with IC50 of 129 nM and 47 nM in cell-free assays, respectively, also inhibits ALK7, but does not inhibit ALK1, 2, 3, or 6.",{"v":335.4,"d":"335.40"},"694433-59-5",{"v":67,"d":"67.00"},199.76,"<1","N/A","http://selleckchem.com/products/sb-505124.html","C20H21N3O2","free base","N/A","CC1=CC=CC(=N1)C2=C(N=C([NH]2)C(C)(C)C)C3=CC4=C(OCO4)C=C3",4.609,4,1,3]
["S2187","Avasimibe (CI-1011)","c3","L1700-10","in 10mM DMSO","Acyltransferase,P450 (e.g. CYP17)","Metabolism","Avasimibe (CI-1011, PD-148515) inhibits ACAT with IC50 of 3.3 μM, also inhibits human P450 isoenzymes CYP2C9, CYP1A2 and CYP2C19 with IC50 of 2.9 μM, 13.9 μM and 26.5 μM, respectively.",501.72,"166518-60-1",{"v":100,"d":"100.00"},199.31,"<1","N/A","http://selleckchem.com/products/Avasimibe(CI-1011).html","C29H43NO4S","free base","PD-148515","CC(C)C1=CC(=C(CC(=O)N[S](=O)(=O)OC2=C(C=CC=C2C(C)C)C(C)C)C(=C1)C(C)C)C(C)C",8.227,2,1,10]
["S2188","Phenprocoumon","d3","L1700-10","in 10mM DMSO","5-alpha Reductase","Angiogenesis","Phenprocoumon (Marcoumar, Marcumar and Falithrom,Ro 1-4849) is a vitamin K reductase with an IC50 of 1 μM",280.32,"435-97-2,53621-47-9 (sodium salt)",{"v":56,"d":"56.00"},199.77,"<1","N/A","http://www.selleck.cn/products/Phenprocoumon(Marcumar).html","C18H16O3","free base","Marcoumar, Marcumar and Falithrom,Ro 1-4849","CCC(C1=CC=CC=C1)C2=C(O)C3=CC=CC=C3OC2=O",4.004,2,1,3]
["S2192","Sapitinib (AZD8931)","e3","L1700-10","in 10mM DMSO","EGFR,HER2","Protein Tyrosine Kinase","Sapitinib (AZD8931) is a reversible, ATP competitive inhibitor of EGFR, ErbB2 and ErbB3 with IC50 of 4 nM, 3 nM and 4 nM in cell-free assays, more potent than Gefitinib or Lapatinib against NSCLC cell, 100-fold more selective for the ErbB family than MNK1 and Flt. Phase 2.",473.93,"848942-61-0",{"v":40,"d":"40.00"},{"v":84.4,"d":"84.40"},"<1","N/A","http://selleckchem.com/products/AZD8931.html","C23H25ClFN5O3","free base","N/A","CNC(=O)CN1CCC(CC1)OC2=C(OC)C=C3N=CN=C(NC4=C(F)C(=CC=C4)Cl)C3=C2",3.485,5,2,7]
["S2193","GSK461364","f3","L1700-10","in 10mM DMSO","PLK","Cell Cycle","GSK461364 (GSK461364A) inhibits purified Plk1 with Ki of 2.2 nM in a cell-free assay. It is more than 1000-fold selective against Plk2/3.",{"v":543.6,"d":"543.60"},"929095-18-1",{"v":10,"d":"10.00"},{"v":18.4,"d":"18.40"},"<1","N/A","http://selleckchem.com/products/GSK461364.html","C27H28F3N5O2S","free base","GSK461364A","CC(OC1=C(SC(=C1)[N]2C=NC3=C2C=C(CN4CCN(C)CC4)C=C3)C(N)=O)C5=CC=CC=C5C(F)(F)F",5.125,3,1,8]
["S2194","R406","g3","L1700-10","in 10mM DMSO","Apoptosis related,FLT3,Syk","Angiogenesis","R406 is a potent Syk inhibitor with IC50 of 41 nM in cell-free assays, strongly inhibits Syk but not Lyn, 5-fold less potent to Flt3. R406 induces apoptosis. Phase 1.",628.63,"841290-81-1",{"v":100,"d":"100.00"},159.08,"<1","N/A","http://selleckchem.com/products/R406.html","C22H23FN6O5.C6H6O3S","Besylate","N/A","COC1=C(OC)C(=CC(=C1)NC2=NC(=C(F)C=N2)NC3=NC4=C(OC(C)(C)C(=O)N4)C=C3)OC.O[S](=O)(=O)C5=CC=CC=C5",5.044,8,3,8]
["S2195","Lexibulin (CYT997)","h3","L1700-10","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Lexibulin (CYT997, SRI-32007) is a potent microtubule polymerization inhibitor with IC50 of 10-100 nM in cancer cell lines. Phase 2.",434.53,"917111-44-5",{"v":86,"d":"86.00"},197.91,"<1","N/A","http://selleckchem.com/products/CYT997.html","C24H30N6O2","free base","SRI-32007","CCCC(NC1=C(C)C=NC(=N1)C2=CC(=C(NC(=O)NCC)C=C2)OC)C3=CC=CN=C3",3.744,5,3,9]
["S2197","A-966492","a4","L1700-10","in 10mM DMSO","PARP","DNA Damage/DNA Repair","A-966492 is a novel and potent inhibitor of PARP1 and PARP2 with Ki of 1 nM and 1.5 nM, respectively.",324.35,"934162-61-5",{"v":64,"d":"64.00"},197.32,"<1","N/A","http://selleckchem.com/products/A-966492.html","C18H17FN4O","free base","N/A","NC(=O)C1=C2[NH]C(=NC2=CC=C1)C3=CC=C(C=C3F)C4CCCN4",2.505,2,3,3]
["S2198","SGI-1776 free base","b4","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,FLT3,Haspin Kinase,Pim","JAK/STAT","SGI-1776 free base is a novel ATP competitive inhibitor of Pim1 with IC50 of 7 nM in a cell-free assay, 50- and 10-fold selective versus Pim2 and Pim3, also potent to Flt3 and haspin. SGI-1776 induces apoptosis and autophagy.",405.42,"1025065-69-3",{"v":81,"d":"81.00"},199.79,"<1","N/A","http://selleckchem.com/products/SGI-1776.html","C20H22F3N5O","free base","N/A","CN1CCC(CC1)CNC2=N[N]3C(=NC=C3C4=CC=CC(=C4)OC(F)(F)F)C=C2",5.206,3,1,6]
["S2199","Aliskiren Hemifumarate","c4","L1700-10","in 10mM DMSO","RAAS","Endocrinology & Hormones","Aliskiren hemifumarate(CGP 60536 hemifumarate, CGP60536B hemifumarate, SPP 100 hemifumarate) is a direct renin inhibitor with IC50 of 1.5 nM.",609.83,"173334-58-2",{"v":100,"d":"100.00"},163.98,{"v":100,"d":"100.00"},163.98,"http://selleckchem.com/products/Aliskiren-hemifumarate.html","C30H53N3O6.1/2C4H4O4","fumarate salt","CGP 60536 hemifumarate, CGP60536B hemifumarate, SPP 100 hemifumarate","COCCCOC1=C(OC)C=CC(=C1)CC(CC(N)C(O)CC(C(C)C)C(=O)NCC(C)(C)C(N)=O)C(C)C.COCCCOC2=C(OC)C=CC(=C2)CC(CC(N)C(O)CC(C(C)C)C(=O)NCC(C)(C)C(N)=O)C(C)C.OC(=O)\\C=C\\C(O)=O",1.735,12,8,40]
["S2201","BMS-794833","d4","L1700-10","in 10mM DMSO","c-Met,RON,VEGFR","Protein Tyrosine Kinase","BMS-794833 is a potent ATP competitive inhibitor of Met (c-Met)/VEGFR2 with IC50 of 1.7 nM/15 nM, also inhibits Ron, Axl and Flt3 with IC50 of <3 nM; a prodrug of BMS-817378. Phase 1.",468.84,"1174046-72-0",{"v":94,"d":"94.00"},200.49,"<1","N/A","http://selleckchem.com/products/BMS-794833.html","C23H15ClF2N4O3","free base","N/A","NC1=NC=CC(=C1Cl)OC2=CC=C(NC(=O)C3=CNC=C(C3=O)C4=CC=C(F)C=C4)C=C2F",{"v":2.85,"d":"2.850"},4,3,5]
["S2202","NVP-BHG712","e4","L1700-10","in 10mM DMSO","Bcr-Abl,Ephrin receptor,Raf,Src","Protein Tyrosine Kinase","NVP-BHG712 is a specific EphB4 inhibitor with ED50 of 25 nM that discriminates between VEGFR and EphB4 inhibition; also shows activity against c-Raf, c-Src and c-Abl with IC50 of 0.395 μM, 1.266 μM and 1.667 μM, respectively.",503.48,"940310-85-0",{"v":101,"d":"101.00"},{"v":200.6,"d":"200.60"},"<1","N/A","http://selleckchem.com/products/NVP-BHG712.html","C26H20F3N7O","free base","N/A","C[N]1N=CC2=C1N=C(N=C2NC3=CC(=CC=C3C)C(=O)NC4=CC=CC(=C4)C(F)(F)F)C5=CC=CN=C5",4.871,5,2,6]
["S2205","OSI-420","f4","L1700-10","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","OSI-420 (DesMethyl Erlotinib, CP-473420) is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).",415.87,"183320-51-6",{"v":83,"d":"83.00"},199.58,"<1","N/A","http://selleckchem.com/products/OSI-420-Desmethyl-Erlotinib,CP-473420.html","C21H21N3O4.HCl","Hydrochloride","DesMethyl Erlotinib (CP-473420) HCl","Cl.COCCOC1=CC2=C(C=C1OCCO)C(=NC=N2)NC3=CC=CC(=C3)C#C",4.283,5,2,9]
["S2207","PIK-293","g4","L1700-10","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","PIK-293 is a PI3K inhibitor, mostly for PI3Kδ with IC50 of 0.24 μM, 500-, 100- and 50-fold less potent to PI3Kα/β/γ, respectively.",397.43,"900185-01-5",{"v":80,"d":"80.00"},201.29,"<1","N/A","http://selleckchem.com/products/PIK-293.html","C22H19N7O","free base","N/A","CC1=C(C=CC=C1)N2C(=NC3=C(C(=CC=C3)C)C2=O)C[N]4N=CC5=C4N=CN=C5N",3.162,5,1,3]
["S2214","AZ 960","h4","L1700-10","in 10mM DMSO","Apoptosis related,JAK","JAK/STAT","AZ 960 is a novel ATP competitive JAK2 inhibitor with IC50 and Ki of <3 nM and 0.45 nM, 3-fold selectivity of AZ960 for JAK2 over JAK3. AZ 960 induces apoptosis and growth arrest.",354.36,"905586-69-8",{"v":71,"d":"71.00"},200.36,"<1","N/A","http://selleckchem.com/products/AZ-960.html","C18H16F2N6","free base","N/A","CC(NC1=NC(=C(F)C=C1C#N)NC2=N[NH]C(=C2)C)C3=CC=C(F)C=C3",4.495,2,3,5]
["S2215","DAPT (GSI-IX)","a5","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,Beta Amyloid,Secretase","Proteases","DAPT (GSI-IX, LY-374973) is a novel γ-secretase inhibitor, which inhibits Aβ production with IC50 of 20 nM in HEK 293 cells. DAPT enhances the apoptosis of human tongue carcinoma cells and regulates autophagy.",432.46,"208255-80-5",{"v":86,"d":"86.00"},198.86,"<1","N/A","http://selleckchem.com/products/DAPT-GSI-IX.html","C23H26F2N2O4","free base","LY-374973","CC(NC(=O)CC1=CC(=CC(=C1)F)F)C(=O)NC(C(=O)OC(C)(C)C)C2=CC=CC=C2",3.385,4,2,9]
["S2216","Mubritinib (TAK 165)","b5","L1700-10","in 10mM DMSO","HER2","Protein Tyrosine Kinase","Mubritinib (TAK-165) is a potent inhibitor of HER2/ErbB2 with IC50 of 6 nM in BT-474 cell; no activity to EGFR, FGFR, PDGFR, JAK1, Src and Blk in BT-474 cell line.",468.47,"366017-09-6",{"v":13,"d":"13.00"},27.75,"<1","N/A","http://selleckchem.com/products/Mubritinib-TAK-165.html","C25H23F3N4O2","free base","N/A","FC(F)(F)C1=CC=C(\\C=C\\C2=NC(=CO2)COC3=CC=C(CCCC[N]4C=CN=N4)C=C3)C=C1",5.844,5,0,11]
["S2217","Irinotecan (CPT-11) HCl Trihydrate","c5","L1700-10","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Irinotecan (CPT-11) prevents DNA from unwinding by inhibition of topoisomerase 1.",677.18,"136572-09-3",{"v":100,"d":"100.00"},147.67,{"v":1,"d":"1.00"},1.48,"http://selleckchem.com/products/Irinotecan-Hcl-Trihydrate-Campto.html","C33H38N4O6.HCl.3H2O","HCl & trihydrat","CPT-11 HCl Trihydrate","O.O.O.Cl.CCC1=C2CN3C(=O)C4=C(C=C3C2=NC5=CC=C(OC(=O)N6CCC(CC6)N7CCCCC7)C=C15)C(O)(CC)C(=O)OC4",3.446,6,0,5]
["S2218","Torkinib (PP242)","d5","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,Mitophagy,mTOR","PI3K/Akt/mTOR","Torkinib (PP242) is a selective mTOR inhibitor with IC50 of 8 nM in cell-free assays; targets both mTOR complexes with >10- and 100-fold selectivity for mTOR than PI3Kδ or PI3Kα/β/γ, respectively. Torkinib (PP242) induces mitophagy and apoptosis.",308.34,"1092351-67-1",{"v":61,"d":"61.00"},197.83,"<1","N/A","http://selleckchem.com/products/PP242.html","C16H16N6O","free base","N/A","CC(C)[N]1N=C(C2=CC3=C([NH]2)C=CC(=C3)O)C4=C(N)N=CN=C14",2.908,3,3,2]
["S2219","Momelotinib (CYT387)","e5","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,JAK","JAK/STAT","Momelotinib (CYT387, LM-1149 , CYT11387) is an ATP-competitive inhibitor of JAK1/JAK2 with IC50 of 11 nM/18 nM, ~10-fold selectivity versus JAK3. Momelotinib (CYT387) induces apoptosis and autophagy. Phase 3.",414.46,"1056634-68-4",{"v":74,"d":"74.00"},178.55,"<1","N/A","http://selleckchem.com/products/Cyt387.html","C23H22N6O2","free base","LM-1149 , CYT11387","O=C(NCC#N)C1=CC=C(C=C1)C2=NC(=NC=C2)NC3=CC=C(C=C3)N4CCOCC4",2.857,4,2,6]
["S2220","SB590885","f5","L1700-10","in 10mM DMSO","Raf","MAPK","SB590885 is a potent B-Raf inhibitor with Ki of 0.16 nM in a cell-free assay, 11-fold greater selectivity for B-Raf over c-Raf, no inhibition to other human kinases.",453.54,"405554-55-4",{"v":5,"d":"5.00"},11.02,"<1","N/A","http://selleckchem.com/products/SB590885.html","C27H27N5O2","free base","N/A","CN(C)CCOC1=CC=C(C=C1)C2=NC(=C([NH]2)C3=CC=C\\4C(=C3)CCC4=N\\O)C5=CC=NC=C5",4.503,4,1,7]
["S2222","PF-3716556","g5","L1700-10","in 10mM DMSO","ATPase,Proton Pump","Transmembrane Transporters","PF 3716556 is a potent and selective P-CAB (potassium-competitive acid blocker), with pIC50 of 6.026 and 7.095 for the inhibition of porcine H+,K+-ATPase activity in ion-leaky and ion-tight assay, respectively, inhibits gastric acid secretion, displays no activity at Na+,K+-ATPase, used for the treatment of gastroesophageal reflux disease.",394.47,"928774-43-0",{"v":79,"d":"79.00"},200.27,"<1","N/A","http://selleckchem.com/products/PF-3716556.html","C22H26N4O3","Free Base","N/A","CN(CCO)C(=O)C1=C[N]2C=C(C)N=C2C(=C1)NC3CCOC4=CC=CC(=C34)C",1.499,3,2,5]
["S2224","UK 383367","h5","L1700-10","in 10mM DMSO","Procollagen C Proteinase","Metabolism","UK-383367 is a procollagen C-proteinase inhibitor with IC50 of 44 nM, has excellent selectivity over MMPs.",324.38,"348622-88-8",{"v":65,"d":"65.00"},200.38,"<1","N/A","http://selleckchem.com/products/UK-383367.html","C15H24N4O4","free base","N/A","NC(=O)C1=NOC(=N1)C(CCCC2CCCCC2)CC(=O)NO",1.731,5,2,8]
["S2225","TAME","a6","L1700-10","in 10mM DMSO","APC,E3 Ligase","Cell Cycle","Tosyl-L-Arginine Methyl Ester (TAME) is an APC inhibitor.",342.41,"901-47-3",{"v":69,"d":"69.00"},201.51,{"v":69,"d":"69.00"},201.51,"http://selleckchem.com/products/TAME.html","C14H22N4O4S","free base","N/A","COC(=O)C(CCCNC(N)=N)N[S](=O)(=O)C1=CC=C(C)C=C1",0.749,4,3,10]
["S2226","Idelalisib","b6","L1700-10","in 10mM DMSO","Autophagy,PI3K","PI3K/Akt/mTOR","Idelalisib (CAL-101, GS-1101) is a selective p110δ inhibitor with IC50 of 2.5 nM in cell-free assays; shown to have 40- to 300-fold greater selectivity for p110δ than p110α/β/γ, and 400- to 4000-fold more selectivity to p110δ than C2β, hVPS34, DNA-PK and mTOR. Idelalisib also stimulates autophagy.",415.42,"870281-82-6",{"v":83,"d":"83.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://selleckchem.com/products/CAL-101.html","C22H18FN7O","free base","CAL-101, GS-1101","CCC(NC1=C2N=C[NH]C2=NC=N1)C3=NC4=CC=CC(=C4C(=O)N3C5=CC=CC=C5)F",3.624,5,2,5]
["S2227","PIK-294","c6","L1700-10","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","PIK-294 is a highly selective p110δ inhibitor with IC50 of 10 nM, 1000-, 49- and 16-fold less potent to PI3Kα/β/γ, respectively.",489.53,"900185-02-6",{"v":98,"d":"98.00"},200.19,"<1","N/A","http://selleckchem.com/products/PIK-294.html","C28H23N7O2","free base","N/A","CC1=C(C=CC=C1)N2C(=O)C3=C(C=CC=C3C)N=C2C[N]4N=C(C5=CC(=CC=C5)O)C6=C(N)N=CN=C46",4.867,5,2,4]
["S2228","Belnacasan (VX-765)","d6","L1700-10","in 10mM DMSO","Caspase","Apoptosis","Belnacasan (VX-765) is a potent and selective inhibitor of caspase-1 with Ki of 0.8 nM in a cell-free assay. Phase 2.",{"v":509,"d":"509.00"},"273404-37-8",{"v":100,"d":"100.00"},196.46,"<1","N/A","http://selleckchem.com/products/VX-765.html","C24H33ClN4O6","free base","N/A","CCOC1OC(=O)CC1NC(=O)C2CCCN2C(=O)C(NC(=O)C3=CC(=C(N)C=C3)Cl)C(C)(C)C",1.698,6,3,8]
["S2229","Eltrombopag (SB497115) Olamine","e6","L1700-10","in 10mM DMSO","TpoR","Immunology & Inflammation","Eltrombopag Olamine (SB-497115-GR, Revolade, Promacta,Promacta Olamine) is a member of the biarylhydrazone class, which is a nonpeptide agonist of the thrombopoietin receptor (TpoR).",564.63,"496775-62-3",{"v":89,"d":"89.00"},157.63,"<1","N/A","http://selleckchem.com/products/Eltrombopag-SB-497115-GR.html","C29H36N6O6","diolamine","SB-497115-GR, Revolade, Promacta,Promacta Olamine","CC1=CC=C(C=C1C)N2N=C(C)C(=N/NC3=CC=CC(=C3O)C4=CC(=CC=C4)C(O)=O)/C2=O.NCCO.NCCO",-0.151,4,6,7]
["S2230","Galunisertib (LY2157299)","f6","L1700-10","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","Galunisertib (LY2157299) is a potent TGFβ receptor I (TβRI) inhibitor with IC50 of 56 nM in a cell-free assay. Phase 2/3.",369.42,"700874-72-2",{"v":74,"d":"74.00"},200.31,"<1","N/A","http://selleckchem.com/products/ly2157299.html","C22H19N5O","free base","N/A","CC1=CC=CC(=N1)C2=N[N]3CCCC3=C2C4=CC=NC5=C4C=C(C=C5)C(N)=O",3.095,4,1,3]
["S2231","Telatinib","g6","L1700-10","in 10mM DMSO","c-Kit,PDGFR,VEGFR","Protein Tyrosine Kinase","Telatinib (BAY 57-9352) is a potent inhibitor of VEGFR2/3, c-Kit and PDGFRα with IC50 of 6 nM/4 nM, 1 nM and 15 nM, respectively. Phase 2.",409.83,"332012-40-5",{"v":82,"d":"82.00"},200.08,"<1","N/A","http://selleckchem.com/products/Telatinib-BAY-57-9352.html","C20H16ClN5O3","free base","BAY 57-9352","CNC(=O)C1=NC=CC(=C1)COC2=NN=C(NC3=CC=C(Cl)C=C3)C4=C2OC=C4",3.861,6,2,6]
["S2233","Esomeprazole sodium","h6","L1700-10","in 10mM DMSO","ATPase","Transmembrane Transporters","Esomeprazole Sodium((S)-Omeprazole sodium, (-)-Omeprazole sodium) is a sodium salt of esomeprazole that is a potent proton pump inhibitor with an IC50 of 0.076 mg/kg.",{"v":367.4,"d":"367.40"},"161796-78-7",{"v":73,"d":"73.00"},198.69,{"v":73,"d":"73.00"},198.69,"http://selleckchem.com/products/esomeprazole-sodium.html","C17H18N3O3S.Na","Sodium salt","(S)-Omeprazole sodium, (-)-Omeprazole sodium","COC1=CC=C2[N]([Na])C(=NC2=C1)[S](=O)CC3=NC=C(C)C(=C3C)OC",3.008,5,0,5]
["S2235","Volasertib (BI 6727)","a7","L1700-10","in 10mM DMSO","Apoptosis related,PLK","Cell Cycle","Volasertib (BI 6727) is a highly potent Plk1 inhibitor with IC50 of 0.87 nM in a cell-free assay. It shows 6- and 65-fold greater selectivity against Plk2 and Plk3. Volasertib induces cell cycle arrest and apoptosis in various cancer cells. Phase 3.",618.81,"755038-65-4",{"v":20,"d":"20.00"},32.32,"<1","N/A","http://selleckchem.com/products/BI6727-Volasertib.html","C34H50N8O3","free base","N/A","CCC1N(C(C)C)C2=C(C=NC(=N2)NC3=CC=C(C=C3OC)C(=O)NC4CCC(CC4)N5CCN(CC5)CC6CC6)N(C)C1=O",4.838,5,2,10]
["S2238","Palomid 529 (P529)","b7","L1700-10","in 10mM DMSO","mTOR","PI3K/Akt/mTOR","Palomid 529 (P529, SG 00529) inhibits both the mTORC1 and mTORC2 complexes, reduces phosphorylation of pAktS473, pGSK3βS9, and pS6. Phase 1.",406.43,"914913-88-5",{"v":81,"d":"81.00"},{"v":199.3,"d":"199.30"},"<1","N/A","http://selleckchem.com/products/Palomid-529-P529.html","C24H22O6","free base","SG 00529","COC1=CC=C(COC2=C(OC)C=C3C(=C2)OC(=O)C4=C3C=CC(=C4)C(C)O)C=C1",4.257,5,1,6]
["S2243","Degrasyn (WP1130)","c7","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,Bcr-Abl,DUB","Angiogenesis","Degrasyn (WP1130) is a selective deubiquitinase (DUB: USP5, UCH-L1, USP9x, USP14, and UCH37) inhibitor and also suppresses Bcr/Abl, also a JAK2 transducer (without affecting 20S proteasome) and activator of transcription (STAT). Degrasyn (WP1130) induces apoptosis and blocks autophagy.",384.27,"856243-80-6",{"v":77,"d":"77.00"},200.38,"<1","N/A","http://selleckchem.com/products/WP1130.html","C19H18BrN3O","free base","N/A","CCCC(NC(=O)/C(=C/C1=NC(=CC=C1)Br)C#N)C2=CC=CC=C2",4.546,2,1,6]
["S2244","AR-42","d7","L1700-10","in 10mM DMSO","HDAC","Epigenetics","AR-42 (HDAC-42) is an HDAC inhibitor with IC50 of 30 nM. Phase 1.",312.36,"935881-37-1",{"v":63,"d":"63.00"},201.69,"<1","N/A","http://selleckchem.com/products/AR-42-HDAC-42.html","C18H20N2O3","free base","HDAC-42","CC(C)C(C(=O)NC1=CC=C(C=C1)C(=O)NO)C2=CC=CC=C2",2.834,2,2,5]
["S2246","Abiraterone Acetate (CB7630)","e7","L1700-10","in 10mM DMSO","Androgen Receptor,P450 (e.g. CYP17)","Metabolism","Abiraterone Acetate (CB7630, CB-7630) is an acetate salt form of Abiraterone which is a steroidal cytochrome CYP17 inhibitor with IC50 of 72 nM in a cell-free assay. Abiraterone acetate is an oral androgen biosynthesis inhibitor.",391.55,"154229-18-2",{"v":20,"d":"20.00"},51.08,"<1","N/A","http://www.selleck.cn/products/Abiraterone-Acetate-CB7630.html","C26H33NO2","Acetate","CB7630, CB-7630","CC(=O)OC1CCC2(C)C3CCC4(C)C(CC=C4C5=CC=CN=C5)C3CC=C2C1",4.602,3,0,3]
["S2247","Buparlisib (BKM120)","f7","L1700-10","in 10mM DMSO","Apoptosis related,PI3K","PI3K/Akt/mTOR","Buparlisib (BKM120, NVP-BKM120) is a selective PI3K inhibitor of p110α/β/δ/γ with IC50 of 52 nM/166 nM/116 nM/262 nM in cell-free assays, respectively. Reduced potency against VPS34, mTOR, DNAPK, with little activity to PI4Kβ. Buparlisib induces apoptosis. Phase 2.",410.39,"944396-07-0",{"v":82,"d":"82.00"},199.81,"<1","N/A","http://selleckchem.com/products/BKM-120.html","C18H21F3N6O2","free base","NVP-BKM120","NC1=CC(=C(C=N1)C2=NC(=NC(=C2)N3CCOCC3)N4CCOCC4)C(F)(F)F",2.342,5,1,4]
["S2248","Silmitasertib (CX-4945)","g7","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,Casein Kinase","Metabolism","Silmitasertib (CX-4945) is a potent and selective inhibitor of CK2 (casein kinase 2) with IC50 of 1 nM in a cell-free assay, less potent to Flt3, Pim1 and CDK1 (inactive in cell-based assay). Silmitasertib induces autophagy and promotes apoptosis. Phase 1/2.",349.77,"1009820-21-6",{"v":16,"d":"16.00"},45.74,"<1","N/A","http://selleckchem.com/products/cx-4945-silmitasertib.html","C19H12ClN3O2","free base","N/A","OC(=O)C1=CC2=C(C=C1)C3=CN=CC=C3C(=N2)NC4=CC(=CC=C4)Cl",4.157,3,1,3]
["S2250","(-)-Epigallocatechin Gallate","h7","L1700-10","in 10mM DMSO","DNA Methyltransferase,EGFR,Fatty Acid Synthase,HER2,Telomerase","DNA Damage/DNA Repair","(-)-Epigallocatechin Gallate(EGCG) is the main catechin extraction of green tea that inhibits telomerase and DNA methyltransferase. EGCG blocks the activation of EGF receptors and HER-2 receptors. ECGG inhibits fatty acid synthase and glutamate dehydrogenase activity.",458.37,"989-51-5",{"v":72,"d":"72.00"},157.08,{"v":23,"d":"23.00"},50.18,"http://selleckchem.com/products/(-)-Epigallocatechin-gallate.html","C22H18O11","free base","EGCG","OC1=CC2=C(CC(OC(=O)C3=CC(=C(O)C(=C3)O)O)C(O2)C4=CC(=C(O)C(=C4)O)O)C(=C1)O",3.097,3,8,4]
["S2252","(+)-Usniacin","a8","L1700-10","in 10mM DMSO","Others","Others","(+)-Usniacin (D-Usnic Acid) is a naturally occurring dibenzofuran derivative found in several lichen species.",344.32,"7562-61-0",{"v":4,"d":"4.00"},11.62,"<1","N/A","http://selleckchem.com/products/Usniacin-D-Usnic-acid.html","C18H16O7","free base","D-Usnic Acid","CC(=O)C1=C(O)C(=C(O)C2=C1OC3=CC(=O)C(=C(O)C23C)C(C)=O)C",1.087,4,3,2]
["S2253","3-Indolebutyric acid (IBA)","b8","L1700-10","in 10mM DMSO","Others","Others","3-Indolebutyric acid(IBA) is a plant hormone in the auxin family and is an ingredient in many commercial plant rooting horticultural products.",203.24,"133-32-4",{"v":41,"d":"41.00"},201.73,"<1","N/A","http://selleckchem.com/products/3-Indolebutyric-acid(IBA).html","C12H13NO2","free base","N/A","OC(=O)CCCC1=C[NH]C2=C1C=CC=C2",{"v":2.7,"d":"2.700"},1,1,4]
["S2254","4-Demethylepipodophyllotoxin(NSC-122819,VM-26)","c8","L1700-10","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","4-Demethylepipodophyllotoxin (NSC-122819, VM-26, DMEP) is an antimitotic agent which binds to monomeric tubulin, preventing micro-tubule polymerization. It is a potent inhibitor of microtubule assembly.",400.38,"6559-91-7",{"v":80,"d":"80.00"},199.81,"N/A","N/A","http://selleckchem.com/products/4-Demethylepipodophyllotoxin.html","C21H20O8","free base","DMEP","COC1=C(O)C(=CC(=C1)C2C3C(COC3=O)C(O)C4=CC5=C(OCO5)C=C24)OC",1.886,6,2,3]
["S2256","4-Methylumbelliferone (4-MU)","d8","L1700-10","in 10mM DMSO","Others","Others","4-Methylumbelliferone is a hyaluronic acid (HA) synthesis inhibitor with an IC50 of 0.4 mM.",176.17,"90-33-5",{"v":35,"d":"35.00"},198.67,"<1","N/A","http://selleckchem.com/products/4-Methylumbelliferone(4-MU).html","C10H8O3","free base","N/A","CC1=CC(=O)OC2=C1C=CC(=C2)O",2.104,2,1,0]
["S2258","Esculin","e8","L1700-10","in 10mM DMSO","Others","Others","Esculin (Aesculin) is a glucoside found in horse chestnuts.",340.28,"531-75-9",{"v":68,"d":"68.00"},199.84,{"v":2,"d":"2.00"},5.88,"http://selleckchem.com/products/Aesculin(Esculin).html","C15H16O9","free base","Aesculin","OCC1OC(OC2=C(O)C=C3OC(=O)C=CC3=C2)C(O)C(O)C1O",-0.514,4,5,3]
["S2259","Aloe-emodin","f8","L1700-10","in 10mM DMSO","IFN","Immunology & Inflammation","Aloe-emodin (NSC 38628, Rhabarberone) is an interferon-inducing agent with IC50 of about 1 μg/mL for JEV and of about 0.33 μg/mL for EV71.",270.24,"481-72-1",{"v":3,"d":"3.00"},{"v":11.1,"d":"11.10"},"<1","N/A","http://selleckchem.com/products/Aloe-emodin.html","C15H10O5","free base","NSC 38628, Rhabarberone","OCC1=CC2=C(C(=C1)O)C(=O)C3=C(C=CC=C3O)C2=O",1.719,2,3,1]
["S2260","Amygdalin","g8","L1700-10","in 10mM DMSO","Others","Others","Amygdalin is a glycoside initially isolated from the seeds of the tree Prunus dulcis, also known as bitter almonds.",457.43,"29883-15-6",{"v":91,"d":"91.00"},198.94,"<1","N/A","http://selleckchem.com/products/Amygdalin.html","C20H27NO11","free base","N/A","OCC1OC(OCC2OC(OC(C#N)C3=CC=CC=C3)C(O)C(O)C2O)C(O)C(O)C1O",-2.403,4,7,7]
["S2261","Andrographolide","h8","L1700-10","in 10mM DMSO","NF-κB","NF-κB","Andrographolide is a labdane diterpenoid that is the main bioactive component of the medicinal plant Andrographis paniculata.",350.45,"5508-58-7",{"v":70,"d":"70.00"},199.74,"<1","N/A","http://selleckchem.com/products/Andrographolide.html","C20H30O5","free base","N/A","CC1(CO)C(O)CCC2(C)C(C\\C=C\\3C(O)COC3=O)C(=C)CCC12",2.056,2,3,3]
["S2262","Apigenin (LY 080400)","a9","L1700-10","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Apigenin (NSC 83244, LY 080400) is a potent P450 inhibitor for CYP2C9 with Ki of 2 μM.",270.24,"520-36-5",{"v":54,"d":"54.00"},199.82,"<1","N/A","http://selleckchem.com/products/Apigenin.html","C15H10O5","free base","NSC 83244","OC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(O)C=C3O",{"v":2.41,"d":"2.410"},2,3,1]
["S2263","Arbutin","b9","L1700-10","in 10mM DMSO","Tyrosinase","Proteases","Arbutin (Uva, p-Arbutin, β-Arbutin) is a tyrosinase inhibitor with IC50 of 0.9 mM and 0.7 mM for Monophenolase and Diphenolase, respectively.",272.25,"497-76-7",{"v":55,"d":"55.00"},202.02,{"v":55,"d":"55.00"},202.02,"http://selleckchem.com/products/Arbutin(Uva,-p-Arbutin).html","C12H16O7","free base","Uva,p-Arbutin, β-Arbutin","OCC1OC(OC2=CC=C(O)C=C2)C(O)C(O)C1O",-0.584,2,5,3]
["S2264","Artemether","c9","L1700-10","in 10mM DMSO","ADC Cytotoxin,Anti-infection","Microbiology","Artemether (SM-224, CGP 56696) is an antimalarial for the treatment of resistant strains of falciparum malaria.",298.37,"71963-77-4",{"v":60,"d":"60.00"},201.09,"<1","N/A","http://selleckchem.com/products/Artemether(SM-224).html","C16H26O5","free base","SM-224, CGP 56696","COC1OC2OC3(C)CCC4C(C)CCC(C1C)C24OO3",2.029,5,0,1]
["S2265","Artesunate (WR-256283)","d9","L1700-10","in 10mM DMSO","ADC Cytotoxin,STAT","JAK/STAT","Artesunate (WR-256283) is a part of the artemisinin group of agents with an IC50 of < 5 μM for small cell lung carcinoma cell line H69. It is a potential inhibitor of STAT-3 and exhibits selective cytotoxicity of cancer cells over normal cells in vitro; A potent inhibitor of EXP1.",384.42,"88495-63-0",{"v":77,"d":"77.00"},{"v":200.3,"d":"200.30"},"<1","N/A","http://selleckchem.com/products/Artesunate.html","C19H28O8","free base","WR-256283","CC1CCC2C(C)C(OC3OC4(C)CCC1C23OO4)OC(=O)CCC(O)=O",1.845,7,0,5]
["S2266","Asiatic Acid","e9","L1700-10","in 10mM DMSO","p38 MAPK","MAPK","Asiatic acid (Dammarolic acid, Asiantic acid) is the aglycone of asiaticoside isolated from the plant Centella asiatica, commonly used in wound healing.",{"v":488.7,"d":"488.70"},"464-92-6",{"v":97,"d":"97.00"},198.49,"<1","N/A","http://selleckchem.com/products/Asiatic-acid.html","C30H48O5","free base","Dammarolic acid, Asiantic acid","CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5CCC34C)C2C1C)C(O)=O",4.435,1,3,2]
["S2267","Azomycin","f9","L1700-10","in 10mM DMSO","Others","Others","Azomycin (2-Nitroimidazole) is an antimicrobial antibiotic produced by a strain of Nocardia mesenterica.",113.07,"527-73-1",{"v":22,"d":"22.00"},194.57,"<1","N/A","http://selleckchem.com/products/Azomycin(2-Nitroimidazole).html","C3H3N3O2","free base","2-Nitroimidazole","[O-][N+](=O)C1=NC=C[NH]1",0.153,1,1,1]
["S2268","Baicalein","g9","L1700-10","in 10mM DMSO","P450 (e.g. CYP17),PREP","Metabolism","Baicalein is a CYP2C9 and prolyl endopeptidase inhibitor.",270.24,"491-67-8",{"v":54,"d":"54.00"},199.82,"<1","N/A","http://selleckchem.com/products/Baicalein.html","C15H10O5","free base","N/A","OC1=C(O)C(=C2C(=O)C=C(OC2=C1)C3=CC=CC=C3)O",{"v":2.41,"d":"2.410"},2,3,1]
["S2269","Baicalin (NSC-661431)","h9","L1700-10","in 10mM DMSO","GABA Receptor,PREP","Neuronal Signaling","Baicalin (NSC-661431) is a known prolyl endopeptidase inhibitor and affects the GABA receptors.",446.36,"21967-41-9",{"v":89,"d":"89.00"},199.39,"<1","N/A","http://selleckchem.com/products/Baicalin.html","C21H18O11","free base","N/A","OC1C(O)C(OC(C1O)C(O)=O)OC2=C(O)C(=C3C(=O)C=C(OC3=C2)C4=CC=CC=C4)O",0.608,5,5,4]
["S2270","Bergenin","a10","L1700-10","in 10mM DMSO","Others","Others","Bergenin (Cuscutin) is trihydroxybenzoic acid glycoside and the C-glycoside of 4-O-methyl gallic acid.",328.27,"477-90-7",{"v":66,"d":"66.00"},201.05,"<1","N/A","http://selleckchem.com/products/Bergenin-(Cuscutin).html","C14H16O9","free base","Cuscutin","COC1=C(O)C2=C(C=C1O)C(=O)OC3C(O)C(O)C(CO)OC23",-0.849,4,5,2]
["S2271","Berberine chloride (NSC 646666)","b10","L1700-10","in 10mM DMSO","Anti-infection,Apoptosis related,Autophagy,Bcl-2,Caspase,IAP,JNK,p38 MAPK,P450 (e.g. CYP17),PARP,ROS,Topoisomerase","Microbiology","Berberine chloride (NSC 646666, Natural Yellow 18) is a quaternary ammonium salt from the group of isoquinoline alkaloids. Berberine activates caspase 3 and caspase 8, cleavage of poly ADP-ribose polymerase (PARP) and the release of cytochrome c. Berberine chloride decreases the expression of c-IAP1, Bcl-2 and Bcl-XL. Berberine chloride induces apoptosis with sustained phosphorylation of JNK and p38 MAPK, as well as generation of the ROS. Berberine chloride is a dual topoisomerase I and II inhibitor. Berberine chloride is also a potential autophagy modulator.",371.81,"633-65-8",{"v":40,"d":"40.00"},107.58,"<1","N/A","http://selleckchem.com/products/Berberine-Hydrochloride.html","C20H18NO4.Cl","chloride","Natural Yellow 18 chloride","[Cl-].COC1=CC=C2C=C3C4=C(CC[N+]3=CC2=C1OC)C=C5OCOC5=C4",1.289,4,0,2]
["S2276","Bilobalide","c10","L1700-10","in 10mM DMSO","Others","Others","Bilobalide is a biologically active terpenic trilactone present in Ginkgo biloba.",{"v":326.3,"d":"326.30"},"33570-04-6",{"v":65,"d":"65.00"},{"v":199.2,"d":"199.20"},"<1","N/A","http://selleckchem.com/products/Bilobalide.html","C15H18O8","free base","N/A","CC(C)(C)C1(O)CC2OC(=O)CC23C(=O)OC4OC(=O)C(O)C134",-0.641,6,1,1]
["S2277","Caffeic Acid","d10","L1700-10","in 10mM DMSO","Lipoxygenase,TRP Channel","Transmembrane Transporters","Caffeic acid is a hydroxycinnamic acid, a naturally occurring organic compound. Caffeic acid is an inhibitor of both TRPV1 ion channel and 5-Lipoxygenase (5-LO).",180.16,"331-39-5",{"v":36,"d":"36.00"},199.82,"<1","N/A","http://selleckchem.com/products/Caffeic-acid.html","C9H8O4","free base","N/A","OC(=O)/C=C/C1=CC=C(O)C(=C1)O",1.443,1,2,2]
["S2280","Chlorogenic Acid","e10","L1700-10","in 10mM DMSO","Others","Others","Chlorogenic acid (NSC 407296, Heriguard) is a hydroxycinnamic acid and a member of a family of naturally occurring organic compounds.",354.31,"327-97-9",{"v":71,"d":"71.00"},200.39,{"v":18,"d":"18.00"},{"v":50.8,"d":"50.80"},"http://selleckchem.com/products/Chlorogenic-acid.html","C16H18O9","free base","NSC 407296, Heriguard","OC1CC(O)(CC(OC(=O)\\C=C\\C2=CC(=C(O)C=C2)O)C1O)C(O)=O",{"v":-0.34,"d":"-0.340"},3,4,5]
["S2281","Chrysin","f10","L1700-10","in 10mM DMSO","Others","Others","Chrysin (NSC 407436) is a naturally occurring flavone chemically extracted from the blue passion flower (Passiflora caerulea).",254.24,"480-40-0",{"v":51,"d":"51.00"},{"v":200.6,"d":"200.60"},"<1","N/A","http://selleckchem.com/products/Chrysin.html","C15H10O4","free base","NSC 407436","OC1=CC2=C(C(=C1)O)C(=O)C=C(O2)C3=CC=CC=C3",2.652,2,2,1]
["S2282","Cinchonidine","g10","L1700-10","in 10mM DMSO","Anti-infection,Serotonin Transporter","Microbiology","Cinchonidine is an alkaloid used in asymmetric synthesis in organic chemistry.",294.39,"485-71-2",{"v":59,"d":"59.00"},200.41,"<1","N/A","http://selleckchem.com/products/Cinchonidine.html","C19H22N2O","free base","N/A","OC(C1CC2CCN1CC2C=C)C3=CC=NC4=CC=CC=C34",{"v":2.75,"d":"2.750"},1,1,3]
["S2283","Cinchonine(LA40221)","h10","L1700-10","in 10mM DMSO","5-alpha Reductase","Angiogenesis","Cinchonine (LA40221) is an alkaloid and a stereoisomer and pseudo-enantiomer of cinchonidine.",{"v":294.4,"d":"294.40"},"118-10-5",{"v":9,"d":"9.00"},30.57,"N/A","N/A","http://selleckchem.com/products/cinchonine.html","C19H22N2O","free base","N/A","OC(C1CC2CCN1CC2C=C)C3=CC=NC4=CC=CC=C34",{"v":2.75,"d":"2.750"},1,1,3]
["S2284","Colchicine (NSC 757)","a11","L1700-10","in 10mM DMSO","Microtubule Associated","Cell Cycle","Colchicine (NSC 757, Colchineos, Colchisol, Colcin) is a microtubule polymerization inhibitor with an IC50 of 3 nM.",399.44,"64-86-8",{"v":80,"d":"80.00"},200.28,{"v":80,"d":"80.00"},200.28,"http://selleckchem.com/products/colchicine.html","C22H25NO6","free base","Colchineos, Colchisol, Colcin,NSC 757","COC1=CC=C2C(=CC1=O)C(CCC3=C2C(=C(OC)C(=C3)OC)OC)NC(C)=O",2.044,6,1,5]
["S2285","Cryptotanshinone","b11","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,STAT","JAK/STAT","Cryptotanshinone is a STAT3 inhibitor with IC50 of 4.6 μM in a cell-free assay, strongly inhibits phosphorylation of STAT3 Tyr705, with a small effect on STAT3 Ser727, but none against STAT1 nor STAT5. Cryptotanshinone induces ROS-dependent autophagy and mitochondria-mediated apoptosis.",296.36,"35825-57-1",{"v":5,"d":"5.00"},16.87,"<1","N/A","http://selleckchem.com/products/Cryptotanshinone.html","C19H20O3","free base","Tanshinone C","CC1COC2=C1C(=O)C(=O)C3=C4CCCC(C)(C)C4=CC=C23",3.761,3,0,0]
["S2286","Cyclosporin A (NSC 290193)","c11","L1700-10","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Complement System,Immunology & Inflammation related,phosphatase","Immunology & Inflammation","Cyclosporin A (Cyclosporine A, Cyclosporine, Ciclosporin, CsA,NSC 290193) is an immunosuppressive agent, binds to the cyclophilin and then inhibits calcineurin with IC50 of 7 nM in a cell-free assay, widely used in organ transplantation to prevent rejection.",1202.61,"59865-13-3",{"v":100,"d":"100.00"},83.15,"<1","N/A","http://selleckchem.com/products/Cyclosporin-A(Cyclosporine-A).html","C62H111N11O12","free base","Cyclosporine A, Cyclosporine, Ciclosporin, CsA,NSC 290193","CCC1NC(=O)C(C(O)C(C)C\\C=C\\C)N(C)C(=O)C(C(C)C)N(C)C(=O)C(CC(C)C)N(C)C(=O)C(CC(C)C)N(C)C(=O)C(C)NC(=O)C(C)NC(=O)C(CC(C)C)N(C)C(=O)C(NC(=O)C(CC(C)C)N(C)C(=O)CN(C)C1=O)C(C)C",4.333,11,5,15]
["S2287","Cytisine","d11","L1700-10","in 10mM DMSO","AChR","Neuronal Signaling","Cytisine (Baphitoxine, Sophorine) is a nicotinic acetylcholine receptor agonist.",190.24,"485-35-8",{"v":38,"d":"38.00"},199.75,{"v":38,"d":"38.00"},199.75,"http://selleckchem.com/products/Cytisine(Baphitoxine,-Sophorine).html","C11H14N2O","free base","Baphitoxine,Sophorine","O=C1C=CC=C2C3CNCC(C3)CN12",-0.338,1,1,0]
["S2289","Daidzin","e11","L1700-10","in 10mM DMSO","Dehydrogenase","Metabolism","Daidzin (Daidzoside, Daidzein 7-O-glucoside, Daidzein 7-glucoside), a natural organic compound in the class of phytochemicals known as isoflavones, is a potent and selective inhibitor of human mitochondrial aldehyde dehydrogenase and inhibits ALDH-I selectively (Ki=20 nM); at least 500 times less effective against ALDH-Ⅱ, the cytosolic isozyme (Ki=10 μM).",416.38,"552-66-9",{"v":83,"d":"83.00"},199.34,"<1","N/A","http://selleckchem.com/products/Daidzin.html","C21H20O9","Free Base","Daidzoside, Daidzein 7-O-glucoside, Daidzein 7-glucoside","OCC1OC(OC2=CC3=C(C=C2)C(=O)C(=CO3)C4=CC=C(O)C=C4)C(O)C(O)C1O",0.452,4,5,4]
["S2290","Dihydroartemisinin (DHA)","f11","L1700-10","in 10mM DMSO","Apoptosis related,Autophagy,NF-κB","NF-κB","Dihydroartemisinin (DHA, Dihydroqinghaosu, β-Dihydroartemisinin, Artenimol) is a semi-synthetic derivative of artemisinin and isolated from the traditional Chinese herb Artemisia annua. Dihydroartemisinin induces autophagy and apoptosis by suppressing NF-κB activation.",284.35,"71939-50-9",{"v":56,"d":"56.00"},196.94,"<1","N/A","http://selleckchem.com/products/Dihydroartemisinin(DHA).html","C15H24O5","free base","Dihydroqinghaosu, β-Dihydroartemisinin, Artenimol","CC1CCC2C(C)C(O)OC3OC4(C)CCC1C23OO4",1.621,4,0,0]
["S2293","DL-Carnitine HCl","g11","L1700-10","in 10mM DMSO","Others","Others","DL-Carnitine HCl is a quaternary ammonium compound biosynthesized from the amino acids lysine and methionine.",197.66,"461-05-2",{"v":40,"d":"40.00"},202.37,{"v":40,"d":"40.00"},202.37,"http://selleckchem.com/products/DL-Carnitine-hydrochloride.html","C7H15NO3.HCl","Hydrochloride","N/A","[Cl-].C[N+](C)(C)CC(O)CC(O)=O",{"v":-4.49,"d":"-4.490"},1,1,4]
["S2295","Emodin","h11","L1700-10","in 10mM DMSO","Dehydrogenase","Metabolism","Emodin is a purgative resin, 6-methyl-1,3,8-trihydroxyanthraquinone, from rhubarb, the buckthorn and Japanese Knotweed (Fallopia japonica).",270.24,"518-82-1",{"v":54,"d":"54.00"},199.82,"<1","N/A","http://selleckchem.com/products/Emodin.html","C15H10O5","free base","N/A","CC1=CC2=C(C(=C1)O)C(=O)C3=C(C=C(O)C=C3O)C2=O",2.568,2,3,0]
["S2296","Enoxolone","a2","L1700-11","in 10mM DMSO","Dehydrogenase","Metabolism","Enoxolone (Glycyrrhetin) is a pentacyclic triterpenoid derivative of the beta-amyrin type obtained from the hydrolysis of glycyrrhizic acid, which was obtained from the herb liquorice.",470.68,"471-53-4",{"v":94,"d":"94.00"},199.71,"<1","N/A","http://selleckchem.com/products/Enoxolone(Glycyrrhetin).html","C30H46O4","free base","Glycyrrhetin","CC1(C)C(O)CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(O)=O",5.656,2,1,1]
["S2298","Fisetin","b2","L1700-11","in 10mM DMSO","Sirtuin","Epigenetics","Fisetin (Fustel) is a potent sirtuin activating compound (STAC) and an agent that modulates sirtuins.",286.24,"528-48-3",{"v":57,"d":"57.00"},199.13,"<1","N/A","http://selleckchem.com/products/Fisetin(Fustel).html","C15H10O6","free base","N/A","OC1=CC2=C(C=C1)C(=O)C(=C(O2)C3=CC(=C(O)C=C3)O)O",1.872,2,4,1]
["S2299","Formononetin","c2","L1700-11","in 10mM DMSO","Others","Endocrinology & Hormones","Formononetin (Formononetol, Biochanin B) is a phytoestrogen from the root of Astragalus membranaceus and an O-methylated isoflavone.",268.26,"485-72-3",{"v":54,"d":"54.00"},{"v":201.3,"d":"201.30"},"<1","N/A","http://selleckchem.com/products/Formononetin(Formononetol).html","C16H12O4","free base","Formononetol, Biochanin B","COC1=CC=C(C=C1)C2=COC3=C(C=CC(=C3)O)C2=O",2.608,3,1,2]
["S2300","Ferulic Acid","d2","L1700-11","in 10mM DMSO","FGFR","Angiogenesis","Ferulic Acid (Fumalic) is a hydroxycinnamic acid and a type of organic compound found in the Ferula assafoetida L. or Ligusticum chuanxiong. Ferulic acid is a novel fibroblast growth factor receptor (FGFR) inhibitor with IC50s of 3.78 μM and 12.5 μM for FGFR1 and FGFR2, respectively.",194.19,"1135-24-6",{"v":39,"d":"39.00"},200.83,"<1","N/A","http://selleckchem.com/products/Fumalic-acid(Ferulic-acid).html","C10H10O4","free base","Fumalic Acid","COC1=CC(=CC=C1O)\\C=C\\C(O)=O",1.669,2,1,3]
["S2301","Genistin (Genistoside)","e2","L1700-11","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Genistin (Genistoside, Genistine, Genistein 7-glucoside, Genistein glucoside) is an isoflavone found in a number of dietary plants like soy and kudzu. Genistin attenuates cellular growth and promotes apoptotic cell death breast cancer cells through modulation of Estrogen Receptor α (ERα) signaling pathway.",432.37,"529-59-9",{"v":86,"d":"86.00"},{"v":198.9,"d":"198.90"},"<1","N/A","http://selleckchem.com/products/Genistin(Genistoside).html","C21H20O10","free base","Genistoside, Genistine, Genistein 7-glucoside, Genistein glucoside","OCC1OC(OC2=CC3=C(C(=C2)O)C(=O)C(=CO3)C4=CC=C(O)C=C4)C(O)C(O)C1O",{"v":0.21,"d":"0.210"},4,6,4]
["S2302","Glycyrrhizin (NSC 167409)","f2","L1700-11","in 10mM DMSO","Dehydrogenase,High-mobility Group,MAO","Metabolism","Glycyrrhizin (NSC 167409, Glycyrrhizic Acid) is a direct HMGB1(high mobility group box 1) inhibitor that inhibits HMGB1-dependent inflammatory molecule expression and oxidative stress; modulates P38 and P-JNK but not p-ERK signalling; Also inhibits 11 beta-hydroxysteroid dehydrogenase and monoamine oxidase (MAO).",822.93,"1405-86-3",{"v":100,"d":"100.00"},121.52,"<1","N/A","http://selleckchem.com/products/Glycyrrhizic-acid.html","C42H62O16","free base","N/A","CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(O)=O)OC6OC(C(O)C(O)C6OC7OC(C(O)C(O)C7O)C(O)=O)C(O)=O",2.417,8,5,7]
["S2303","Gossypol Acetate","g2","L1700-11","in 10mM DMSO","Dehydrogenase","Metabolism","Gossypol Acetate (Gossypol Acetic acid, Pogosin, AT101) is a polyphenolic aldehyde that permeates cells and acts as an inhibitor for several dehydrogenase enzymes such as lactate dehydrogenase, NAD-linked enzymes.",578.61,"12542-36-8",{"v":100,"d":"100.00"},172.83,"<1","N/A","https://www.selleckchem.com/products/gossypol-acetate.html","C32H34O10","Acetate","Gossypol Acetic acid, Pogosin, AT101","CC(C)C1=C2C=C(C)C(=C(O)C2=C(C=O)C(=C1O)O)C3=C(O)C4=C(C=C3C)C(=C(O)C(=C4C=O)O)C(C)C.CC(O)=O",6.388,3,6,5]
["S2304","Gramine","h2","L1700-11","in 10mM DMSO","ADC Cytotoxin,AdipoR,Adrenergic Receptor","Metabolism","Gramine (Donaxine) is a natural indole alkaloid isolated from giant reed, acts as an active adiponectin receptor (AdipoR) agonist, with IC50 of 3.2 µM and 4.2 µM for AdipoR2 and AdipoR1, respectively. Gramine is also a human and mouse β2-Adrenergic receptor (β2-AR) agonist.",174.24,"87-52-5",{"v":35,"d":"35.00"},200.87,"<1","N/A","http://selleckchem.com/products/Gramine.html","C11H14N2","free base","N/A","CN(C)CC1=C[NH]C2=C1C=CC=C2",2.197,0,1,2]
["S2305","Grape Seed Extract","a3","L1700-11","in 10mM DMSO","Others","Others","Grape Seed Extract are industrial derivatives from whole grape seeds that have a great concentration of vitamin E, flavonoids, linoleic acid, and OPCs.","N/A","84929-27-1",{"v":94,"d":"94.00"},{"v":10,"d":"10.00"},"<1","N/A","http://selleckchem.com/products/Grape-Seed-Extract.html","N/A","Polyphenols","N/A","N/A",{"v":0,"d":"0.000"},0,0,0]
["S2306","Gynostemma Extract","b3","L1700-11","in 10mM DMSO","Others","Others","Gynostemma Extract (Gynostemma Pentaphyllum, Gypenoside) is a saponins extract derived from the Gynostemma pentaphyllum.",917.13,"80321-63-7",{"v":189,"d":"189.00"},206.08,"<1","N/A","http://selleckchem.com/products/Gynostemma-Extract.html","C48H82O18","free base","Gynostemma Pentaphyllum, Gypenoside","CC(C)=CCCC(C)(OC1OC(COC2OCC(O)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7O)C(C)(C)C6CCC45C",1.059,6,11,12]
["S2308","Hesperetin","c3","L1700-11","in 10mM DMSO","Histamine Receptor,TGF-beta/Smad","TGF-beta/Smad","Hesperetin is a bioflavonoid and, to be more specific, a flavanone.",302.27,"520-33-2",{"v":60,"d":"60.00"},{"v":198.5,"d":"198.50"},"<1","N/A","http://selleckchem.com/products/Hesperetin.html","C16H14O6","free base","N/A","COC1=CC=C(C=C1O)C2CC(=O)C3=C(O)C=C(O)C=C3O2",2.357,3,3,2]
["S2309","Hesperidin","d3","L1700-11","in 10mM DMSO","Others","Others","Hesperidin (Cirantin) is a flavanone glycoside found abundantly in citrus fruits.",610.56,"520-26-3",{"v":100,"d":"100.00"},163.78,"<1","N/A","http://selleckchem.com/products/Hesperidin.html","C28H34O15","free base","Cirantin","COC1=CC=C(C=C1O)C2CC(=O)C3=C(O)C=C(OC4OC(COC5OC(C)C(O)C(O)C5O)C(O)C(O)C4O)C=C3O2",-0.431,7,8,7]
["S2310","Honokiol (NSC 293100)","e3","L1700-11","in 10mM DMSO","Akt,Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,Autophagy,HCV,MEK","PI3K/Akt/mTOR","Honokiol (NSC 293100) is the active principle of magnolia extract that inhibits Akt-phosphorylation and promotes ERK1/2 phosphorylation. Honokiol causes G0/G1 phase arrest, induces apoptosis, and autophagy via the ROS/ERK1/2 signaling pathway. Honokiol inhibits hepatitis C virus (HCV) infection. Phase 3.",266.33,"35354-74-6",{"v":53,"d":"53.00"},{"v":199,"d":"199.00"},"<1","N/A","http://selleckchem.com/products/Honokiol.html","C18H18O2","free base","N/A","OC1=C(CC=C)C=C(C=C1)C2=CC(=CC=C2O)CC=C",{"v":4.88,"d":"4.880"},0,2,5]
["S2311","Hyodeoxycholic acid (HDCA)","f3","L1700-11","in 10mM DMSO","GPCR19","GPCR & G Protein","Hyodeoxycholic (HDCA, NSC 60672) acid is a secondary bile acid, one of the metabolic byproducts of intestinal bacteria.",392.57,"83-49-8",{"v":78,"d":"78.00"},198.69,"<1","N/A","http://selleckchem.com/products/Hyodeoxycholic-acid(HDCA).html","C24H40O4","free base","NSC 60672","CC(CCC(O)=O)C1CCC2C3CC(O)C4CC(O)CCC4(C)C3CCC12C",4.014,1,2,4]
["S2312","Icariin","g3","L1700-11","in 10mM DMSO","PDE","Metabolism","Icariin is a cGMP-specific PDE5 inhibitor with IC50 of 0.432 μM, 167-fold more selective for PDE5 than PDE4.",676.66,"489-32-7",{"v":50,"d":"50.00"},73.89,"<1","N/A","http://selleckchem.com/products/Icariin.html","C33H40O15","free base","N/A","COC1=CC=C(C=C1)C2=C(OC3OC(C)C(O)C(O)C3O)C(=O)C4=C(O2)C(=C(OC5OC(CO)C(O)C(O)C5O)C=C4O)CC=C(C)C",0.983,7,8,9]
["S2313","Indole-3-carbinol","h3","L1700-11","in 10mM DMSO","NF-κB","NF-κB","Indole-3-carbinol is produced by the breakdown of the glucosinolate glucobrassicin, which can be found at relatively high levels in cruciferous vegetables. Indole-3-carbinol suppresses NF-κB and IκBα kinase activation.",147.18,"700-06-1",{"v":29,"d":"29.00"},197.04,{"v":7,"d":"7.00"},47.56,"http://selleckchem.com/products/Indole-3-carbinol.html","C9H9NO","free base","N/A","OCC1=C[NH]C2=C1C=CC=C2",1.518,0,2,1]
["S2314","Kaempferol (NSC 407289)","a4","L1700-11","in 10mM DMSO","Estrogen/progestogen Receptor,Fatty Acid Synthase","Endocrinology & Hormones","Kaempferol (NSC 407289, Robigenin), a natural flavonol, functions as an ERRα and ERRγ inverse agonist. It inhibits topoisomerase I catalyzed DNA religation and may also inhibit the activity of fatty acid synthase.",286.23,"520-18-3",{"v":57,"d":"57.00"},199.14,"<1","N/A","http://selleckchem.com/products/Kaempferol.html","C15H10O6","free base","Robigenin","OC1=CC=C(C=C1)C2=C(O)C(=O)C3=C(O)C=C(O)C=C3O2",1.872,2,4,1]
["S2316","Kinetin","b4","L1700-11","in 10mM DMSO","Others","Others","Kinetin (6-Furfuryladenine) is a type of cytokinin, a class of plant hormone that promotes cell division.",215.21,"525-79-1",{"v":8,"d":"8.00"},37.17,"<1","N/A","http://selleckchem.com/products/Kinetin(6-Furfuryladenine).html","C10H9N5O","free base","6-Furfuryladenine","C(NC1=NC=NC2=C1[NH]C=N2)C3=CC=CO3",0.875,4,2,3]
["S2317","L-(+)-Rhamnose Monohydrate","c4","L1700-11","in 10mM DMSO","Others","Others","L(+)-Rhamnose (Rham) is a naturally-occurring deoxy sugar that is found primarily in plants and some bacteria.",182.17,"10030-85-0",{"v":36,"d":"36.00"},197.62,{"v":36,"d":"36.00"},197.62,"http://selleckchem.com/products/l-positive-rotation-rhamnose-monohydrate.html","C6H12O5.H2O","Monohydrate","N/A","O.CC1OC(O)C(O)C(O)C1O",-1.833,1,3,0]
["S2318","Lappaconitine","d4","L1700-11","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Lappaconitine (LC) is a natural diterpenoid alkaloid (DTA), acting as a human heart sodium channel blocker and possessing a wide range of biological activities, including anti-arrhythmic, anti-inflammatory, antioxidative, anticancer, epileptiform etc.",{"v":584.7,"d":"584.70"},"32854-75-4",{"v":16,"d":"16.00"},27.36,"N/A","N/A","http://selleckchem.com/products/lappaconitine.html","C32H44N2O8","free base","N/A","CCN1CC2(CCC(OC)C34C2CC(C13)C5(O)CC(OC)C6CC4C5(O)C6OC)OC(=O)C7=CC=CC=C7NC(C)=O",0.029,6,1,8]
["S2319","Limonin","e4","L1700-11","in 10mM DMSO","HIV Protease","Microbiology","Limonin is a triterpenoid enriched in citrus fruits, which has antivirus and antitumor ability.",470.51,"1180-71-8",{"v":44,"d":"44.00"},93.52,"<1","N/A","http://selleckchem.com/products/Limonin.html","C26H30O8","free base","N/A","CC1(C)OC2CC(=O)OCC23C4CCC5(C)C(OC(=O)C6OC56C4(C)C(=O)CC13)C7=COC=C7",1.447,8,0,1]
["S2320","Luteolin","f4","L1700-11","in 10mM DMSO","ADC Cytotoxin,PDE","Metabolism","Luteolin (Luteoline, Luteolol, Digitoflavone) is a flavonoid found in Terminalia chebula, which is a non-selective phisphodiesterase PDE inhibitor for PDE1-5 with Ki of 15.0 μM, 6.4 μM, 13.9 μM, 11.1 μM and 9.5 μM, respectively.",286.24,"491-70-3",{"v":57,"d":"57.00"},199.13,"<1","N/A","https://www.selleckchem.com/products/luteolin.html","C15H10O6","free base","Luteoline, Luteolol, Digitoflavone","OC1=CC(=C2C(=O)C=C(OC2=C1)C3=CC=C(O)C(=C3)O)O",2.168,2,4,1]
["S2321","Magnolol","g4","L1700-11","in 10mM DMSO","Fungal,NF-κB","NF-κB","Magnolol (NSC 293099) is a bioactive lignin found in the bark of the Houpu magnolia (Magnolia officinalis) which shows antifungal properties. It can block TNF-α-induced NF-KB activation.",266.33,"528-43-8",{"v":53,"d":"53.00"},{"v":199,"d":"199.00"},"<1","N/A","http://selleckchem.com/products/Magnolol(2,2-Bichavicol).html","C18H18O2","free base","NSC 293099","OC1=C(C=C(CC=C)C=C1)C2=CC(=CC=C2O)CC=C",{"v":4.88,"d":"4.880"},0,2,5]
["S2322","(+)-Matrine","h4","L1700-11","in 10mM DMSO","Opioid Receptor","Neuronal Signaling","Matrine((+)-Matrine) is an alkaloid found in plants from the Sophora family, which has a variety of pharmacological effects, including anti-cancer effects, and action as a kappa opioid receptor agonist.",248.36,"519-02-8",{"v":49,"d":"49.00"},197.29,{"v":11,"d":"11.00"},44.29,"http://selleckchem.com/products/matrine.html","C15H24N2O","free base","N/A","O=C1CCCC2C3CCCN4CCCC(CN12)C34",1.417,1,0,0]
["S2323","Methyl-Hesperidin","a5","L1700-11","in 10mM DMSO","Akt,PKC","PI3K/Akt/mTOR","Methyl Hesperidin is a flavanone glycoside (flavonoid) (C28H34O15) found abundantly in citrus fruits. Its aglycone form is called hesperetin.",624.59,"11013-97-1",{"v":100,"d":"100.00"},155.62,{"v":100,"d":"100.00"},155.62,"http://selleckchem.com/products/Methyl-Hesperidin.html","C29H36O15","free base","N/A","COC1=CC=C(C=C1O)C2CC(=O)C3=C(OC)C=C(OC4OC(COC5OC(C)C(O)C(O)C5O)C(O)C(O)C4O)C=C3O2",{"v":-0.79,"d":"-0.790"},7,8,7]
["S2325","Morin Hydrate","b5","L1700-11","in 10mM DMSO","Others","Others","Morin hydrate (Aurantica) is a flavonoid isolated from Maclura pomifera (Osage orange), Maclura tinctoria (old fustic) and from leaves of Psidium guajava (common guava).",320.25,"6202-27-3",{"v":64,"d":"64.00"},199.84,"<1","N/A","https://www.selleckchem.com/products/Morin-hydrate.html","C15H10O7.H2O","Hydrate","Aurantica","O.OC1=CC=C(C(=C1)O)C2=C(O)C(=O)C3=C(O)C=C(O)C=C3O2",1.423,2,5,1]
["S2326","Myricetin","c5","L1700-11","in 10mM DMSO","MEK","MAPK","Myricetin, a natural flavonoid with antioxidant and anti tumor properties, is a novel inhibitor of MEK1 activity and transformation of JB6 P+ mouse epidermal cells. It also inhibits PI3Kγ with Kd of 0.17 μM.",318.24,"529-44-2",{"v":63,"d":"63.00"},197.96,"<1","N/A","http://selleckchem.com/products/Myricetin(Cannabiscetin).html","C15H10O8","free base","Cannabiscetin","OC1=CC(=C2C(=O)C(=C(OC2=C1)C3=CC(=C(O)C(=C3)O)O)O)O",1.388,2,6,1]
["S2327","Myricitrin","d5","L1700-11","in 10mM DMSO","PKC","TGF-beta/Smad","Myricitrin (Myricitrine), a flavonoid compound isolated from the root bark of Myrica cerifera, which exerts antinociceptive effects.",464.38,"17912-87-7",{"v":93,"d":"93.00"},200.27,"<1","N/A","http://selleckchem.com/products/Myricitrin(Myricitrine).html","C21H20O12","free base","Myricitrine","CC1OC(OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(O)C(=C4)O)O)C(O)C(O)C1O",0.347,4,8,3]
["S2328","Nalidixic acid","e5","L1700-11","in 10mM DMSO","Selection Antibiotics for Transfected Cell,Topoisomerase","DNA Damage/DNA Repair","Nalidixic acid (NSC-82174) is a synthetic 1,8-naphthyridine antimicrobial agent with a limited bacteriocidal spectrum. It is an inhibitor of the A subunit of bacterial DNA gyrase.",232.24,"389-08-2",{"v":6,"d":"6.00"},25.84,"<1","N/A","http://selleckchem.com/products/Nalidixic-acid(NegGram).html","C12H12N2O3","free base","NSC-82174","CCN1C=C(C(O)=O)C(=O)C2=C1N=C(C)C=C2",1.176,3,0,2]
["S2329","Naringin","f5","L1700-11","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Naringin (Naringoside) is a flavanone glycoside, which exerts a variety of pharmacological effects such as antioxidant activity, blood lipid lowering, anticancer activity, and inhibition of cytochrome P450 enzymes.",580.53,"10236-47-2",{"v":100,"d":"100.00"},172.26,"<1","N/A","http://selleckchem.com/products/Naringin(Naringoside).html","C27H32O14","free base","Naringoside","CC1OC(OC2C(O)C(O)C(CO)OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(O)C=C5)O)C(O)C(O)C1O",-0.415,6,8,6]
["S2331","Neohesperidin Dihydrochalcone (Nhdc)","g5","L1700-11","in 10mM DMSO","Others","Others","Neohesperidin dihydrochalcone(Nhdc, NCI-c60764), sometimes abbreviated to neohesperidin DC or simply NHDC, is an artificial sweetener derived from citrus.",612.58,"20702-77-6",{"v":100,"d":"100.00"},163.24,"<1","N/A","http://selleckchem.com/products/Neohesperidin-dihydrochalcone(Nhdc).html","C28H36O15","free base","NCI-c60764","COC1=C(O)C=C(CCC(=O)C2=C(O)C=C(OC3OC(CO)C(O)C(O)C3OC4OC(C)C(O)C(O)C4O)C=C2O)C=C1",-0.048,6,9,10]
["S2332","Neohesperidin","h5","L1700-11","in 10mM DMSO","ROS","Immunology & Inflammation","Neohesperidin (NSC 31048), a flavanone glycoside found in citrus fruits, is an antioxidant agent., Neohesperidin (NSC 31048) 是一种抗氧化剂，在1,1-diphenyl-2-picryldydrazyl（DPPH）自由基清除测定中，IC50为22.31 μg/ml。",610.56,"13241-33-3",{"v":122,"d":"122.00"},199.82,"<1","N/A","http://selleckchem.com/products/Neohesperidin.html","C28H34O15","free base","NSC 31048","COC1=CC(=CC(=C1)C2CC(=O)C3=C(O)C=C(OC4OC(CO)C(O)C(O)C4OC5OC(C)C(O)C(O)C5O)C=C3O2)O",-0.431,7,8,7]
["S2333","Nobiletin (NSC 76751)","a6","L1700-11","in 10mM DMSO","MMP","Proteases","Nobiletin (NSC 76751, Hexamethoxyflavone), a citrus flavonoid isolated from citrus peels like in tangerine, which has anti-inflammatory and anti-tumor activities.",402.39,"478-01-3",{"v":81,"d":"81.00"},{"v":201.3,"d":"201.30"},"<1","N/A","http://selleckchem.com/products/Nobiletin(Hexamethoxyflavone).html","C21H22O8","free base","Hexamethoxyflavone","COC1=C(OC)C=C(C=C1)C2=CC(=O)C3=C(OC)C(=C(OC)C(=C3O2)OC)OC",3.038,8,0,7]
["S2334","Oleanolic Acid","b6","L1700-11","in 10mM DMSO","Antiviral","Microbiology","Oleanolic Acid (Caryophyllin) is a non-toxic, hepatoprotective triterpenoid found in Phytolacca Americana, which exerts antitumor and antiviral properties.",{"v":456.7,"d":"456.70"},"508-02-1",{"v":21,"d":"21.00"},45.98,"<1","N/A","http://selleckchem.com/products/Oleanolic-Acid(Caryophyllin).html","C30H48O3","free base","Caryophyllin","CC1(C)CC(C2CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC34C)C2C1)C(O)=O",6.282,1,1,1]
["S2335","Oridonin (NSC-250682)","c6","L1700-11","in 10mM DMSO","Akt,Bacterial","PI3K/Akt/mTOR","Oridonin (Isodonol, Rubescenin, NSC-250682), a diterpenoid purified from Rabdosia rubescens, is a traditional agent with antitumor, anti-bacterial and anti-inflammatory effects. Oridonin inhibits AKT1 and AKT2 kinase activity with IC50 of 8.4 μM and 8.9 μM, respectively.",364.43,"28957-04-2",{"v":72,"d":"72.00"},197.57,"<1","N/A","http://selleckchem.com/products/Oridonin(Isodonol).html","C20H28O6","free base","Isodonol, Rubescenin","CC1(C)CCC(O)C23COC(O)(C(O)C12)C45C(O)C(CCC34)C(=C)C5=O",{"v":0.2,"d":"0.200"},2,3,0]
["S2336","Orotic acid (6-Carboxyuracil)","d6","L1700-11","in 10mM DMSO","Others","Others","Orotic acid(6-Carboxyuracil) is a heterocyclic compound and an acid.",{"v":156.1,"d":"156.10"},"65-86-1",{"v":2,"d":"2.00"},12.81,"<1","N/A","http://selleckchem.com/products/Orotic-acid(6-Carboxyuracil).html","C5H4N2O4","free base","N/A","OC(=O)C1=CC(=O)NC(=O)N1",-1.152,3,2,1]
["S2337","Osthole","e6","L1700-11","in 10mM DMSO","Others","Others","Osthol is an O-methylated coumarin, which is found in the plants such as Cnidium monnieri, Angelica archangelica and Angelica pubescens.",244.29,"484-12-8",{"v":49,"d":"49.00"},200.58,"<1","N/A","http://selleckchem.com/products/Osthole(Osthol).html","C15H16O3","free base","Osthol","COC1=CC=C2C=CC(=O)OC2=C1CC=C(C)C",{"v":3.74,"d":"3.740"},3,0,3]
["S2338","Oxymatrine","f6","L1700-11","in 10mM DMSO","Immunology & Inflammation related","TGF-beta/Smad","Oxymatrine (Matrine N-oxide) is a quinolizidine alkaloid extracted from the root of Sophora flavescens with anti-inflammatory, antifibrosis, and antitumor effects, inhibits the iNOS expression and TGF-β/Smad pathway. It is used for the treatment of viral hepatitis, cancer, viral myocarditis, gastrointestinal hemorrhage and skin diseases.",264.36,"16837-52-8",{"v":53,"d":"53.00"},200.48,{"v":53,"d":"53.00"},200.48,"http://selleckchem.com/products/Oxymatrine(Matrine-N-oxide).html","C15H24N2O2","free base","Matrine N-oxide","[O-][N+]12CCCC3CN4C(CCCC4=O)C(CCC1)C23",{"v":0.61,"d":"0.610"},1,0,0]
["S2339","Paeonol","g6","L1700-11","in 10mM DMSO","MAO","Metabolism","Paeonol (Peonol), a phenolic compound extracted from Chinese herbs Paeonia suffruticosa (moutan cortex) and Cynanchum paniculatum, inhibits MAO with an IC50 of about 50 μM.",166.17,"552-41-0",{"v":33,"d":"33.00"},198.59,"<1","N/A","http://selleckchem.com/products/Paeonol(Peonol).html","C9H10O3","free base","Peonol","COC1=CC(=C(C=C1)C(C)=O)O",1.311,2,1,2]
["S2341","(-)-Parthenolide","h6","L1700-11","in 10mM DMSO","HDAC,MDM2/MDMX,NF-κB,p53","NF-κB","(-)-Parthenolide, an inhibitor of the Nuclear Factor-κB Pathway, specifically depletes HDAC1 protein without affecting other class I/II HDACs; Also promotes the ubiquitination of MDM2 and activates p53 cellular functions.",248.32,"20554-84-1",{"v":49,"d":"49.00"},197.33,"<1","N/A","http://selleckchem.com/products/Parthenolide((-)-Parthenolide).html","C15H20O3","free base","N/A","CC/1=C\\CCC2(C)OC2C3OC(=O)C(=C)C3CC1",2.923,3,0,0]
["S2342","Phloretin (RJC 02792)","a7","L1700-11","in 10mM DMSO","SGLT","GPCR & G Protein","Phloretin (RJC 02792, NSC 407292, Dihydronaringenin) is a dihydrochalcone found in apple tree leaves, which shows beneficial effects on diabetes.",274.27,"60-82-2",{"v":54,"d":"54.00"},196.89,"<1","N/A","http://selleckchem.com/products/Phloretin(Dihydronaringenin).html","C15H14O5","free base","NSC 407292, Dihydronaringenin","OC1=CC=C(CCC(=O)C2=C(O)C=C(O)C=C2O)C=C1",2.757,1,4,4]
["S2343","Phlorizin","b7","L1700-11","in 10mM DMSO","ATPase,SGLT","GPCR & G Protein","Phlorizin (Phloridzin) is a dihydrochalcone found in the bark of pear (Pyrus communis), apple, cherry and other fruit trees. Phlorizin is a non-selective SGLT inhibitor with Ki of 300 nM and 39 nM for hSGLT1 and hSGLT2, respectively. Phlorizin is also a Na+/K+-ATPase inhibitor.",436.41,"60-81-1",{"v":87,"d":"87.00"},199.35,"<1","N/A","http://selleckchem.com/products/Phlorizin(Phloridzin).html","C21H24O10","free base","Phloridzin","OCC1OC(OC2=C(C(=O)CCC3=CC=C(O)C=C3)C(=CC(=C2)O)O)C(O)C(O)C1O",0.827,3,7,7]
["S2344","Piperine","c7","L1700-11","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Piperine (1-Piperoylpiperidine) is the alkaloid responsible for the pungency of black pepper and long pepper, which has also been used in some forms of traditional medicine and as an insecticide.",285.34,"94-62-2",{"v":57,"d":"57.00"},199.76,"<1","N/A","http://selleckchem.com/products/Piperine(1-Piperoylpiperidine).html","C17H19NO3","free base","1-Piperoylpiperidine","O=C(\\C=C\\C=C\\C1=CC2=C(OCO2)C=C1)N3CCCCC3",2.864,3,0,3]
["S2346","Puerarin","d7","L1700-11","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Puerarin (Kakonein), an isoflavones found in the root of Radix puerariae, is a 5-HT2C receptor and benzodiazepine site antagonist.",416.38,"3681-99-0",{"v":86,"d":"86.00"},206.54,"<1","N/A","http://selleckchem.com/products/Puerarin(Kakonein).html","C21H20O9","free base","Kakonein","OCC1OC(OC2=C(O)C=CC3=C2OC=C(C3=O)C4=CC=C(O)C=C4)C(O)C(O)C1O",{"v":0.21,"d":"0.210"},4,6,4]
["S2347","Quercetin Dihydrate","e7","L1700-11","in 10mM DMSO","PI3K,Sirtuin","PI3K/Akt/mTOR","Quercetin (Sophoretin), a polyphenolic flavonoid found in a wide variety of plant-based foods, such as apples, onions, berries, and red wine, is utilized in many different cultures for their nervous system and anticancer effects. Quercetin (dihydrate), a natural flavonoid, is a stimulator of recombinant SIRT1 and a PI3K inhibitor with IC50s of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively.",338.27,"6151-25-3",{"v":67,"d":"67.00"},198.07,"<1","N/A","http://selleckchem.com/products/Quercetin-dihydrate(Sophoretin).html","C15H10O7.2H2O","Dihydrate","Sophoretin","O.O.OC1=CC(=C2C(=O)C(=C(OC2=C1)C3=CC=C(O)C(=C3)O)O)O",1.216,2,5,1]
["S2348","Rotenone (Barbasco)","f7","L1700-11","in 10mM DMSO","Apoptosis related,Mitochondrial Metabolism,Mitophagy,NADPH-oxidase,ROS","Immunology & Inflammation","Rotenone (Barbasco, Dactinol, Paraderil, Rotenon, Rotocide) is a botanical insecticide that is an inhibitor of mitochondrial electron transport. Rotenone inhibits NADH/DB oxidoreductase and NADH oxidase with IC50 of 28.8 nM and 5.1 nM, respectively. Rotenone induces apoptosis through enhancing mitochondrial reactive oxygen species production.",394.42,"83-79-4",{"v":78,"d":"78.00"},197.76,"N/A","N/A","http://selleckchem.com/products/rotenone-barbasco.html","C23H22O6","free base","Barbasco, Dactinol, Paraderil, Rotenon, Rotocide","COC1=CC2=C(C=C1OC)C3C(CO2)OC4=C(C=CC5=C4CC(O5)C(C)=C)C3=O",{"v":3.93,"d":"3.930"},6,0,3]
["S2349","Rutaecarpine","g7","L1700-11","in 10mM DMSO","COX","Neuronal Signaling","Rutaecarpine (Rutecarpine) is an indolopyridoquinazolinone alkaloid isolated from Evodia rutaecarpa and related herbs; a new class of COX-2 inhibitor.",287.32,"84-26-4",{"v":24,"d":"24.00"},83.53,"<1","N/A","http://selleckchem.com/products/Rutaecarpine(Rutecarpine).html","C18H13N3O","free base","Rutecarpine","O=C1N2CCC3=C([NH]C4=C3C=CC=C4)C2=NC5=C1C=CC=C5",3.359,2,1,0]
["S2350","Rutin","h7","L1700-11","in 10mM DMSO","ADC Cytotoxin,Immunology & Inflammation related","Immunology & Inflammation","Rutin (Rutoside), a flavonol glycoside found in many plants including buckwheat; tobacco; forsythia; hydrangea; viola, etc., which possesses healthy effects for human.",610.52,"153-18-4",{"v":100,"d":"100.00"},163.79,"<1","N/A","http://selleckchem.com/products/Rutin(Rutoside).html","C27H30O16","free base","Rutoside","CC1OC(OCC2OC(OC3=C(OC4=C(C(=CC(=C4)O)O)C3=O)C5=CC(=C(O)C=C5)O)C(O)C(O)C2O)C(O)C(O)C1O",-1.158,6,10,6]
["S2351","Salicin","a8","L1700-11","in 10mM DMSO","COX","Neuronal Signaling","Salicin (Salicoside, Salicine) is a phenol β-glycosid produced from willow bark that shows anti-inflammatory effects. It is a natural, non-selective COX-1 and COX-2 inhibitor.",286.28,"138-52-3",{"v":57,"d":"57.00"},199.11,{"v":24,"d":"24.00"},83.83,"http://selleckchem.com/products/Salicin(Salicoside,-Salicine).html","C13H18O7","free base","Salicoside,Salicine","OCC1OC(OC2=CC=CC=C2CO)C(O)C(O)C1O",-0.947,2,5,4]
["S2354","Sclareol","b8","L1700-11","in 10mM DMSO","Others","Others","Sclareol, a labdane-type diterpene isolated from clary sage (Salvia sclarea), exerts growth inhibition and cytotoxic activity against a variety of human cancer cell lines.",{"v":308.5,"d":"308.50"},"515-03-7",{"v":61,"d":"61.00"},197.73,"<1","N/A","http://selleckchem.com/products/Sclareol.html","C20H36O2","free base","N/A","CC1(C)CCCC2(C)C1CCC(C)(O)C2CCC(C)(O)C=C",{"v":4.27,"d":"4.270"},0,0,4]
["S2355","Sclareolide","c8","L1700-11","in 10mM DMSO","Others","Others","Sclareolide (Norambreinolide) is a sesquiterpene lactone natural product derived from various plant sources including Salvia sclarea, Salvia yosgadensis, and cigar tobacco.",250.38,"564-20-5",{"v":50,"d":"50.00"},{"v":199.7,"d":"199.70"},"<1","N/A","http://selleckchem.com/products/Sclareolide(Norambreinolide).html","C16H26O2","free base","Norambreinolide","CC1(C)CCCC2(C)C1CCC3(C)OC(=O)CC23",3.495,2,0,0]
["S2356","Shikimic Acid","d8","L1700-11","in 10mM DMSO","Others","Others","Shikimic acid (Shikimate), more commonly known as its anionic form shikimate, is an important biochemical intermediate in plants and microorganisms.",174.15,"138-59-0",{"v":35,"d":"35.00"},200.98,{"v":35,"d":"35.00"},200.98,"http://selleckchem.com/products/Shikimic-acid(Shikimate).html","C7H10O5","free base","Shikimate","OC1CC(=CC(O)C1O)C(O)=O",-1.154,1,3,1]
["S2357","Silibinin (NSC 651520)","e8","L1700-11","in 10mM DMSO","Others","Others","Silibinin (NSC 651520, Silybin, Silibinin A, Silymarin I, Flavobin), the main flavonoid extracted from the milk thistle Silybum marianum, displays hepatoprotective properties in acute and chronic liver injury.",482.44,"22888-70-6",{"v":96,"d":"96.00"},198.99,"<1","N/A","http://selleckchem.com/products/Silibinin(Silybin).html","C25H22O10","free base","Silybin, Silibinin A, Silymarin I, Flavobin","COC1=CC(=CC=C1O)C2OC3=CC(=CC=C3OC2CO)C4OC5=CC(=CC(=C5C(=O)C4O)O)O",2.592,5,5,4]
["S2358","Silymarin","f8","L1700-11","in 10mM DMSO","Antioxidant","Angiogenesis","Silymarin (Silybin B), a polyphenolic flavonoid extracted from the seeds of Silybum marianum or milk thistle, is used in the prevention and treatment of liver diseases and primary liver cancer.",482.44,"65666-07-1",{"v":96,"d":"96.00"},198.99,"<1","N/A","http://selleckchem.com/products/Silymarin(Silybin-B).html","C25H22O10","free base","Silybin B","COC1=CC(=CC=C1O)C2OC3=CC=C(C=C3OC2CO)C4OC5=C(C(=CC(=C5)O)O)C(=O)C4O",2.592,5,5,4]
["S2359","Sinomenine","g8","L1700-11","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Sinomenine (Cucoline, Kukoline), a pure alkaloid extracted from the chinese medical plant Sinomenium acutum, is used for the treatment of rheumatism and arthritis.",329.39,"115-53-7",{"v":65,"d":"65.00"},197.33,{"v":65,"d":"65.00"},197.33,"http://selleckchem.com/products/Sinomenine(Cucoline).html","C19H23NO4","free base","Cucoline, Kukoline","COC1=CC2C3CC4=C(C(=C(OC)C=C4)O)C2(CCN3C)CC1=O",1.674,3,1,2]
["S2362","Synephrine","h8","L1700-11","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Synephrine (Oxedrine), a natural protoalkaloid in the extract of bitter orange and other citrus species, is commonly used for weight loss.",167.21,"94-07-5",{"v":33,"d":"33.00"},197.36,"<1","N/A","http://selleckchem.com/products/Synephrine(Oxedrine).html","C9H13NO2","free base","Oxedrine","CNCC(O)C1=CC=C(O)C=C1",0.615,0,3,3]
["S2363","Tangeretin","a9","L1700-11","in 10mM DMSO","Antioxidant","Apoptosis","Tangeretin (Tangeritin), a natural polymethoxylated flavone concentrated in the peel of citrus fruits, is known to have antiproliferative, antiinvasive, antimetastatic and antioxidant activities.",372.37,"481-53-8",{"v":8,"d":"8.00"},21.48,"<1","N/A","http://selleckchem.com/products/Tangeretin(Tangeritin).html","C20H20O7","free base","Tangeritin","COC1=CC=C(C=C1)C2=CC(=O)C3=C(OC)C(=C(OC)C(=C3O2)OC)OC",3.054,7,0,6]
["S2364","Tanshinone I","b9","L1700-11","in 10mM DMSO","Phospholipase (e.g. PLA)","Metabolism","Tanshinone I, an active principle isolated from Salvia miltiorrhiza (Danshen), is structurally similar to tanshinone IIA and may possess similar cytotoxic effects on tumor cells.",276.29,"568-73-0",{"v":23,"d":"23.00"},83.25,"<1","N/A","http://selleckchem.com/products/Tanshinone-I.html","C18H12O3","free base","N/A","CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C(C)C=CC=C34",4.084,3,0,0]
["S2365","Tanshinone IIA","c9","L1700-11","in 10mM DMSO","Lipase","Metabolism","Tanshinone IIA (Tanshinone B) is the most abundant diterpene quinone in Danshen, Salviae miltiorrhizae Radix, a widely prescribed traditional herbal medicine that is used to treat cardiovascular and inflammatory diseases; A natural monoacylglycerol lipase inhibitor.",294.34,"568-72-9",{"v":5,"d":"5.00"},16.99,"<1","N/A","http://selleckchem.com/products/Tanshinone-IIA(Tanshinone-B).html","C19H18O3","free base","Tanshinone B","CC1=COC2=C1C(=O)C(=O)C3=C2C=CC4=C3CCCC4(C)C",{"v":4.66,"d":"4.660"},3,0,0]
["S2366","Taxifolin (Dihydroquercetin)","d9","L1700-11","in 10mM DMSO","VEGFR","Angiogenesis","Taxifolin, type I inhibitor for VEGFR-2 kinase, is a flavonoid in many plants such as Taxus chinensis, Siberian larch, Cedrus deodara and so on.",304.25,"480-18-2",{"v":60,"d":"60.00"},197.21,"<1","N/A","http://selleckchem.com/products/Taxifolin(Dihydroquercetin).html","C15H12O7","free base","N/A","OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(O)C=C3)O",1.479,2,5,1]
["S2369","Troxerutin","e9","L1700-11","in 10mM DMSO","NLR,ROS","Immunology & Inflammation","Troxerutin, a natural bioflavonoid isolated from Sophora japonica, has been reported to have many benefits and medicinal properties. Troxerutin, also known as vitamin P4, is a tri-hydroxyethylated derivative of natural bioflavonoid rutins which can inhibit the production of reactive oxygen species (ROS) and depress ER stress-mediated NOD activation.",742.68,"7085-55-4",{"v":100,"d":"100.00"},134.65,{"v":100,"d":"100.00"},134.65,"http://selleckchem.com/products/Troxerutin.html","C33H42O19","free base","N/A","CC1OC(OCC2OC(OC3=C(OC4=CC(=CC(=C4C3=O)O)OCCO)C5=CC(=C(OCCO)C=C5)OCCO)C(O)C(O)C2O)C(O)C(O)C1O",{"v":-2.1,"d":"-2.100"},9,10,15]
["S2370","Ursolic Acid","f9","L1700-11","in 10mM DMSO","Others","Others","Ursolic acid (NSC 167406, NSC-4060, Prunol, Urson, Malol) is a pentacyclic triterpene acid, used in cosmetics.",{"v":456.7,"d":"456.70"},"77-52-1",{"v":91,"d":"91.00"},199.26,"<1","N/A","http://selleckchem.com/products/Ursolic-acid(Malol).html","C30H48O3","free base","NSC 167406, NSC-4060, Prunol, Urson, Malol","CC1CC(C2CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC34C)C2C1C)C(O)=O",6.327,1,1,1]
["S2371","Vanillylacetone","g9","L1700-11","in 10mM DMSO","NF-κB","NF-κB","Vanillylacetone (NSC 15335) is similar in chemical structure to other flavor chemicals such as vanillin and eugenol and is used as a flavor additive in spice oils and in perfumery to introduce spicy aromas. Vanillylacetone (Zingerone) alleviates oxidative stress and inflammation, down-regulates NF-κB mediated signaling pathways. Zingerone acts as an anti-mitotic agent, and inhibits the growth of neuroblastoma cells.",194.23,"122-48-5",{"v":38,"d":"38.00"},195.64,{"v":10,"d":"10.00"},51.49,"http://selleckchem.com/products/Vanillylacetone.html","C11H14O3","free base","NSC 15335","COC1=CC(=CC=C1O)CCC(C)=O",1.792,2,1,4]
["S2372","Xanthone","h9","L1700-11","in 10mM DMSO","ADC Cytotoxin","Others","Xanthone (Genicide) is an organic compound, which can be prepared by the heating of phenyl salicylate.",{"v":196.2,"d":"196.20"},"90-47-1",{"v":39,"d":"39.00"},198.78,"<1","N/A","http://selleckchem.com/products/Xanthone(Genicide).html","C13H8O2","free base","Genicide","O=C1C2=CC=CC=C2OC3=C1C=CC=C3",2.964,2,0,0]
["S2373","Yohimbine HCl","a10","L1700-11","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Yohimbine (Antagonil) has been used as a mydriatic and in the treatment of impotence. It is also alleged to be an aphrodisiac.",{"v":390.9,"d":"390.90"},"65-19-0",{"v":12,"d":"12.00"},{"v":30.7,"d":"30.70"},"<1","N/A","http://selleckchem.com/products/Yohimbine-hydrochloride(Antagonil).html","C21H26N2O3.HCl","Hydrochloride","Antagonil","Cl.COC(=O)C1C(O)CCC2CN3CCC4=C([NH]C5=C4C=CC=C5)C3CC12",3.204,2,2,2]
["S2374","5-hydroxytryptophan (5-HTP)","b10","L1700-11","in 10mM DMSO","Others","Others","5-Hydroxytryptophan (5-HTP, NSC-92523), also known as oxitriptan (INN), is a naturally occurring amino acid and chemical precursor for the treatment of depression.",220.22,"56-69-9",{"v":44,"d":"44.00"},{"v":199.8,"d":"199.80"},{"v":4,"d":"4.00"},18.16,"http://selleckchem.com/products/5-hydroxytryptophan(5-HTP).html","C11H12N2O3","free base","NSC-92523","NC(CC1=C[NH]C2=CC=C(O)C=C12)C(O)=O",-1.554,1,3,3]
["S2375","Aloin","c10","L1700-11","in 10mM DMSO","Tyrosinase","Proteases","Aloin (Barbaloin, Barbalin), a natural anthracycline from Aloe vera, is a tyrosinase inhibitor.",418.39,"1415-73-2",{"v":83,"d":"83.00"},198.38,{"v":83,"d":"83.00"},198.38,"http://selleckchem.com/products/Aloin(Barbaloin).html","C21H22O9","free base","Barbaloin, Barbalin","OCC1OC(C(O)C(O)C1O)C2C3=C(C(=CC=C3)O)C(=O)C4=C2C=C(CO)C=C4O",-0.404,2,7,3]
["S2376","Ammonium Glycyrrhizinate","d10","L1700-11","in 10mM DMSO","Dehydrogenase,High-mobility Group","Metabolism","Ammonium Glycyrrhizinate (AMGZ, Glycyram, Glycyrrhizin ammonium salt, Glycyrrhizic acid ammonium salt) is a unique product from Licorice root with a very high sweetness. Ammonium glycyrrhizinate is a direct inhibitor of HMGB1 with anti-inflammatory, anti-tumor, anti-diabetic activities. Ammonium Glycyrrhizinate inhibits growth and cytopathology of several unrelated DNA and RNA viruses. Ammonium Glycyrrhizinate also inhibits both hepatic delta 4-5-reductase and 11 beta-hydroxysteroid dehydrogenase.",839.96,"1407-03-0",{"v":168,"d":"168.00"},200.01,{"v":5,"d":"5.00"},5.95,"http://selleckchem.com/products/Ammonium-Glycyrrhizinate(AMGZ).html","C42H62O16.NH3","Glycyrrhizic acid salt","AMGZ, Glycyram, Glycyrrhizin ammonium salt, Glycyrrhizic acid ammonium salt","N.CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(O)=O)OC6OC(C(O)C(O)C6OC7OC(C(O)C(O)C7O)C(O)=O)C(O)=O",-0.915,8,5,7]
["S2377","Biochanin A","e10","L1700-11","in 10mM DMSO","FAAH","Metabolism","Biochanin A (4-Methylgenistein), an O-methylated isoflavone from Trifolium pratense, inhibits protein tyrosine kinase (PTK) of epidermal growth factor receptor with IC50 values of 91.5 μM.",284.26,"491-80-5",{"v":57,"d":"57.00"},200.52,"<1","N/A","http://selleckchem.com/products/Biochanin-A(4-Methylgenistein).html","C16H12O5","free base","4-Methylgenistein","COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O",2.366,3,2,2]
["S2378","Butylscopolamine Bromide","f10","L1700-11","in 10mM DMSO","AChR","Neuronal Signaling","Butylscopolamine Bromide (Scopolamine Butylbromide,(-)-Scopolamine butylbromide, Hyoscine butylbromide), is a peripherally acting antimuscarinic, anticholinergic agent used as an abdominal-specific antispasmodic.",440.37,"149-64-4",{"v":88,"d":"88.00"},199.83,{"v":88,"d":"88.00"},199.83,"http://selleckchem.com/products/butylscopolamine-bromide.html","C21H30NO4.Br","Bromide","Scopolamine Butylbromide,(-)-Scopolamine butylbromide, Hyoscine butylbromide","[Br-].CCCC[N+]1(C)C2CC(CC1C3OC23)OC(=O)C(CO)C4=CC=CC=C4",{"v":-1.62,"d":"-1.620"},3,1,8]
["S2379","Dioscin","g10","L1700-11","in 10mM DMSO","Others","Others","Dioscin (Collettiside III, Saponin) is a saponin extracted and isolated from Polygonatum Zanlanscianense Pamp, showing antitumor activities.",869.04,"19057-60-4",{"v":100,"d":"100.00"},115.07,"<1","N/A","http://selleckchem.com/products/Dioscin(Collettiside-III).html","C45H72O16","free base","Collettiside III, Saponin","CC1CCC2(OC1)OC3CC4C5CC=C6CC(CCC6(C)C5CCC4(C)C3C2C)OC7OC(CO)C(OC8OC(C)C(O)C(O)C8O)C(O)C7OC9OC(C)C(O)C(O)C9O",1.169,8,8,7]
["S2380","Diosmetin","h10","L1700-11","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Diosmetin (Luteolin 4-methyl ether) is a bioflavonoid found in spearmint, oregano, and many other plants.",300.26,"520-34-3",{"v":60,"d":"60.00"},199.83,"<1","N/A","http://selleckchem.com/products/Diosmetin(Luteolin-4-methyl-ether).html","C16H12O6","free base","Luteolin 4-methyl ether","COC1=CC=C(C=C1O)C2=CC(=O)C3=C(O)C=C(O)C=C3O2",2.394,3,3,2]
["S2381","D-Mannitol","a11","L1700-11","in 10mM DMSO","Others","Others","D-Mannitol is an osmotic diuretic agent and a weak renal vasodilator.",182.17,"69-65-8",{"v":36,"d":"36.00"},197.62,{"v":36,"d":"36.00"},197.62,"http://selleckchem.com/products/D-Mannitol(Osmitrol).html","C6H14O6","free base","Osmitrol","OCC(O)C(O)C(O)C(O)CO",-2.941,0,6,5]
["S2382","Evodiamine","b11","L1700-11","in 10mM DMSO","NF-κB","NF-κB","Evodiamine (Isoevodiamine), an alkaloid extract from the fruit of Evodiae Fructus exhibits antitumor activities against the human tumor cells. It is shown to inhibit NF-kB activation through suppression of IkB kinase activity.",303.36,"518-17-2",{"v":12,"d":"12.00"},39.56,"<1","N/A","http://www.selleck.cn/products/Evodiamine(Isoevodiamine).html","C19H17N3O","Free Base","Isoevodiamine","CN1C2N(CCC3=C2[NH]C4=CC=CC=C34)C(=O)C5=C1C=CC=C5",3.673,1,1,0]
["S2383","Gastrodin","c11","L1700-11","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Gastrodin (Gastrodine), an anti-inflammatory polyphenol extracted from Chinese natural herbal Gastrodia elata Blume., benefits neurodegenerative diseases.",286.28,"62499-27-8",{"v":50,"d":"50.00"},174.65,"<1","N/A","http://selleckchem.com/products/Gastrodin(Gastrodine).html","C13H18O7","free base","Gastrodine","OCC1OC(OC2=CC=C(CO)C=C2)C(O)C(O)C1O",-0.947,2,5,4]
["S2384","Hematoxylin","d11","L1700-11","in 10mM DMSO","Dyes","Others","Hematoxylin (Hydroxybrazilin) is a compound that forms strongly colored complexes with certain metal ions, notably Fe(III) and Al(III) salts and a kind of stain in histology.",302.28,"517-28-2",{"v":61,"d":"61.00"},{"v":201.8,"d":"201.80"},{"v":61,"d":"61.00"},{"v":201.8,"d":"201.80"},"http://selleckchem.com/products/Hematoxylin(Hydroxybrazilin).html","C16H14O6","free base","Hydroxybrazilin","OC1=CC2=C(C=C1O)C3C4=C(OCC3(O)C2)C(=C(O)C=C4)O",1.691,1,4,0]
["S2385","Hordenine","e11","L1700-11","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Hordenine (N,N-dimethyl-4-hydroxyphenylethylamine) is a phenylethylamine alkaloid with antibacterial and antibiotic properties.",165.23,"539-15-1",{"v":33,"d":"33.00"},199.72,"<1","N/A","http://selleckchem.com/products/Hordenine.html","C10H15NO","free base","N/A","CN(C)CCC1=CC=C(O)C=C1",1.982,0,1,3]
["S2386","Indirubin (NSC 105327)","f11","L1700-11","in 10mM DMSO","GSK-3","PI3K/Akt/mTOR","Indirubin (NSC 105327) is a potent cyclin-dependent kinases and GSK-3β inhibitor with IC50 of about 5 μM and 0.6 μM.",262.26,"479-41-4",{"v":53,"d":"53.00"},202.09,"<1","N/A","http://selleckchem.com/products/Indirubin.html","C16H10N2O2","free base","NSC 105327","O=C1NC2=CC=CC=C2\\C1=C3/NC4=C(C=CC=C4)C3=O",1.876,2,2,0]
["S2387","Lappaconite HBr","g11","L1700-11","in 10mM DMSO","ADC Cytotoxin,Immunology & Inflammation related","Immunology & Inflammation","Lappaconite Hydrobromide is a kind of alkaloid extracted from Aconitum sinomontanum Nakai and has anti-inflammatory effects.",665.61,"97792-45-5",{"v":28,"d":"28.00"},42.07,"<1","N/A","http://selleckchem.com/products/Lappaconite-Hydrobromide.html","C32H44N2O8.HBr","Hydrobromide","N/A","Br.CCN1CC2(CCC(OC)C34C2CC(C13)C5(O)CC(OC)C6CC4C5(O)C6OC)OC(=O)C7=C(NC(C)=O)C=CC=C7",{"v":0.52,"d":"0.520"},6,1,8]
["S2388","L-carnitine","h11","L1700-11","in 10mM DMSO","Others","Others","L-carnitine (Levocarnitine,Carnitor, vitamin BT, Karnitin,L(-)-Carnitine) is constituent of striated muscle and liver. It is used therapeutically to stimulate gastric and pancreatic secretions and in the treatment of hyperlipoproteinemias.",{"v":161.2,"d":"161.20"},"541-15-1",{"v":12,"d":"12.00"},74.44,{"v":32,"d":"32.00"},198.51,"http://selleckchem.com/products/L-carnitine(Levocarnitine).html","C7H15NO3","quaternary-N  salt","Levocarnitine,Carnitor, vitamin BT, Karnitin,L(-)-Carnitine","C[N+](C)(C)CC(O)CC([O-])=O",{"v":-3.29,"d":"-3.290"},0,1,4]
["S2389","Naringin Dihydrochalcone","a2","L1700-12","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Naringin Dihydrochalcone(Naringin DC) is a new-style sweetening agent and an artificial sweetener derived from naringin and also an inhibitor of CYP enzymes.",582.55,"18916-17-1",{"v":100,"d":"100.00"},171.66,"<1","N/A","http://selleckchem.com/products/Naringin-Dihydrochalcone(Naringin-DC).html","C27H34O14","free base","N/A","CC1OC(OC2C(O)C(O)C(CO)OC2OC3=CC(=C(C(=O)CCC4=CC=C(O)C=C4)C(=C3)O)O)C(O)C(O)C1O",-0.032,5,9,9]
["S2390","Polydatin","b2","L1700-12","in 10mM DMSO","Phospholipase (e.g. PLA)","Metabolism","Polydatin (Piceid) is a crystal component extracted from the root stem of perennial herbage Polygonum Cuspidatum Sieb.et Zucc.",390.38,"65914-17-2",{"v":78,"d":"78.00"},199.81,"<1","N/A","http://selleckchem.com/products/Polydatin(Piceid).html","C20H22O8","free base","Piceid","OCC1OC(OC2=CC(=CC(=C2)\\C=C\\C3=CC=C(O)C=C3)O)C(O)C(O)C1O",{"v":1.16,"d":"1.160"},2,6,5]
["S2391","Quercetin (NSC 9221)","c2","L1700-12","in 10mM DMSO","Apoptosis related,Autophagy,Mitophagy,PI3K,PKC,Sirtuin,Src","Epigenetics","Quercetin (NSC 9221, Sophoretin, C.I. 75720), a natural flavonoid present in vegetables, fruit and wine, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4-5.4 μM. Quercetin induces mitophagy, apoptosis and protective autophagy. Phase 4.",302.24,"117-39-5",{"v":61,"d":"61.00"},201.83,"<1","N/A","http://selleckchem.com/products/Quercetin(Sophoretin).html","C15H10O7","Free Base","Sophoretin, C.I. 75720","OC1=CC(=C2C(=O)C(=C(OC2=C1)C3=CC=C(O)C(=C3)O)O)O",{"v":1.63,"d":"1.630"},2,5,1]
["S2392","Sesamin","d2","L1700-12","in 10mM DMSO","Others","Others","Sesamin (Fagarol, Fsesamin), a lignan isolated from the bark of Fagara plants and from sesame oil, exhibits various health benefits.",354.35,"607-80-7",{"v":70,"d":"70.00"},197.54,"<1","N/A","http://selleckchem.com/products/Sesamin(Fagarol).html","C20H18O6","free base","Fagarol, Fsesamin","C1OC2=C(O1)C=C(C=C2)C3OCC4C3COC4C5=CC6=C(OCO6)C=C5",2.237,6,0,2]
["S2393","Sorbitol","e2","L1700-12","in 10mM DMSO","Others","Others","Sorbitol (Glucitol) is a sugar alcohol and a sugar substitute.",182.17,"50-70-4",{"v":36,"d":"36.00"},197.62,{"v":36,"d":"36.00"},197.62,"http://selleckchem.com/products/Sorbitol(Glucitol).html","C6H14O6","free base","Glucitol","OCC(O)C(O)C(O)C(O)CO",-2.941,0,6,5]
["S2394","Naringenin","f2","L1700-12","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Naringenin (NSC 34875, S-Dihydrogenistein, NSC 11855, Salipurol) is a natural predominant flavanone derived from plant food, which is considered to have a bioactive effect on human health as antioxidant, free radical scavenger, anti-inflammatory, carbohydrate metabolism promoter, and immune system modulator.",272.25,"480-41-1",{"v":54,"d":"54.00"},198.35,"<1","N/A","http://selleckchem.com/products/naringenin.html","C15H12O5","free base","NSC 34875, S-Dihydrogenistein, NSC 11855, Salipurol","OC1=CC=C(C=C1)C2CC(=O)C3=C(O)C=C(O)C=C3O2",2.373,2,3,1]
["S2396","Salidroside","g2","L1700-12","in 10mM DMSO","Mitophagy,mTOR,PREP","PI3K/Akt/mTOR","Salidroside (Rhodioloside), a phenylpropanoid glycoside isolated from Rhodiola rosea, has been reported to have a broad spectrum of pharmacological properties. Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.",{"v":300.3,"d":"300.30"},"10338-51-9",{"v":60,"d":"60.00"},{"v":199.8,"d":"199.80"},{"v":60,"d":"60.00"},{"v":199.8,"d":"199.80"},"http://selleckchem.com/products/Salidroside-Rhodioloside.html","C14H20O7","free base","Rhodioloside","OCC1OC(OCCC2=CC=C(O)C=C2)C(O)C(O)C1O",-0.443,2,5,5]
["S2397","Palmatine chloride","h2","L1700-12","in 10mM DMSO","Calcium Channel","Neuronal Signaling","Palmatine hydrochloride (Palmatine chloride (6CI,7CI); Fibrauretin) is a hydrochloride salt of palmatine which is a protoberberine alkaloid.",387.86,"10605-02-4",{"v":77,"d":"77.00"},198.53,{"v":5,"d":"5.00"},12.89,"http://selleckchem.com/products/Palmatine-chloride.html","C21H22NO4.Cl","Chloride","N/A","[Cl-].COC1=CC=C2C=C3C4=C(CC[N+]3=CC2=C1OC)C=C(OC)C(=C4)OC",1.488,4,0,4]
["S2399","Dihydromyricetin","a3","L1700-12","in 10mM DMSO","GABA Receptor,ROS","Neuronal Signaling","Dihydromyricetin (Ampelopsin, Ampeloptin) is a natural antioxidant flavonoid from Ampelopsis grossedentata.",320.25,"27200-12-0",{"v":64,"d":"64.00"},199.84,"<1","N/A","http://selleckchem.com/products/Dihydromyricetin-Ampeloptin.html","C15H12O8","free base","Ampeloptin","OC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(O)C(=C3)O)O",1.237,2,6,1]
["S2400","Rheic Acid","b3","L1700-12","in 10mM DMSO","FTO,Immunology & Inflammation related","Immunology & Inflammation","Rhein (Monorhein, NSC 38629, Rheinic) is an anthraquinone compound enriched in the fresh rhizome of Rheum coreanum Nakai, showing anti-inflammation and antitumor activities. Rhein is an FTO (mRNA N6-methyladenine demethylase) inhibitor and also inhibits AlkB repair enzymes.",284.22,"478-43-3",{"v":3,"d":"3.00"},10.56,"<1","N/A","http://www.selleck.cn/products/Rhein-Monorhein.html","C15H8O6","Free Base","Rhein, Monorhein, NSC 38629, Rheinic Acid","OC(=O)C1=CC(=C2C(=O)C3=C(C=CC=C3O)C(=O)C2=C1)O",1.954,3,2,1]
["S2401","Sodium Danshensu","c3","L1700-12","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Sodium Danshensu is a mono sodium of danshensu, which is a natural phenolic acid of caffeic acid derivatives isolated from Salvia miltiorrhiza.",220.15,"67920-52-9",{"v":7,"d":"7.00"},{"v":31.8,"d":"31.80"},{"v":2,"d":"2.00"},9.08,"http://selleckchem.com/products/Sodium-Danshensu.html","C9H9O5.Na","Sodium Salt","N/A","[Na+].OC(CC1=CC(=C(O)C=C1)O)C([O-])=O",-0.795,0,3,3]
["S2403","Tetrandrine (NSC-77037)","d3","L1700-12","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Tetrandrine (NSC-77037, Fanchinine, d-Tetrandrine), a bis-benzylisoquinoline alkaloid derived from Stephania tetrandra, is a calcium channel blocker.",622.75,"518-34-3",{"v":7,"d":"7.00"},11.24,"<1","N/A","http://www.selleck.cn/products/Tetrandrine-Fanchinine.html","C38H42N2O6","Free Base","Fanchinine, d-Tetrandrine","COC1=CC=C2CC3N(C)CCC4=CC(=C(OC)C(=C34)OC5=C(OC)C=C6CCN(C)C(CC7=CC=C(OC1=C2)C=C7)C6=C5)OC",7.218,6,0,4]
["S2404","Isoliquiritigenin","e3","L1700-12","in 10mM DMSO","Aldose Reductase","Metabolism","Isoliquiritigenin, an anti-tumor flavonoid from the root of Glycyrrhiza glabra, inhibits aldose reductase with an IC50 of 320 nM.",256.25,"961-29-5",{"v":12,"d":"12.00"},46.83,"<1","N/A","http://selleckchem.com/products/Isoliquiritigenin.html","C15H12O4","free base","N/A","OC1=CC=C(C=C1)\\C=C\\C(=O)C2=C(O)C=C(O)C=C2",2.975,1,3,3]
["S2405","Sophocarpine","f3","L1700-12","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Sophocarpine, a major ingredient of Sophora alopecuroides, has a wide range of pharmacological effects.",246.35,"6483-15-4",{"v":49,"d":"49.00"},{"v":198.9,"d":"198.90"},{"v":6,"d":"6.00"},24.36,"http://selleckchem.com/products/Sophocarpine.html","C15H22N2O","free base","N/A","O=C1C=CCC2C3CCCN4CCCC(CN12)C34",1.394,1,0,0]
["S2406","Chrysophanic Acid","g3","L1700-12","in 10mM DMSO","EGFR,mTOR","Protein Tyrosine Kinase","Chrysophanic Acid (Chrysophanol) a natural anthraquinone isolated from Dianella longifolia, is a EGFR/mTOR pathway inhibitor.",254.24,"481-74-3",{"v":5,"d":"5.00"},19.67,"<1","N/A","http://selleckchem.com/products/Chrysophanic-acid-Chrysophanol.html","C15H10O4","free base","Chrysophanol","CC1=CC2=C(C(=C1)O)C(=O)C3=C(O)C=CC=C3C2=O",{"v":2.81,"d":"2.810"},2,2,0]
["S2407","Curcumol","h3","L1700-12","in 10mM DMSO","JAK","JAK/STAT","Curcumol is a pure monomer isolated from Rhizoma Curcumaeis with antitumor activities.",236.35,"4871-97-0",{"v":47,"d":"47.00"},198.86,"<1","N/A","http://selleckchem.com/products/Curcumol.html","C15H24O2","free base","N/A","CC(C)C1CC23OC1(O)CC(=C)C2CCC3C",2.786,1,0,1]
["S2408","Cephalomannine","a4","L1700-12","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics","Others","Cephalomannine (Baccatin III) is an active anti-cancer agent obtained from Taxus yunnanensis and has an antineoplastic effect on tumors found in mice.",{"v":831.9,"d":"831.90"},"71610-00-9",{"v":100,"d":"100.00"},120.21,"<1","N/A","http://selleckchem.com/products/cephalomannine.html","C45H53NO14","free base","Baccatin III","C/C=C(C)/C(=O)NC(C(O)C(=O)OC1CC2(O)C(OC(=O)C3=CC=CC=C3)C4C(C)(C(O)CC5OCC45OC(C)=O)C(=O)C(OC(C)=O)C(=C1C)C2(C)C)C6=CC=CC=C6",2.937,11,3,14]
["S2409","10-Deacetylbaccatin-III","b4","L1700-12","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics","Others","10-Deacetylbaccatin-III(10-DB III) is an antineoplastic agent and an anti-cancer intermediate.",544.59,"32981-86-5",{"v":109,"d":"109.00"},200.15,"<1","N/A","http://selleckchem.com/products/10-dab-10-deacetylbaccatin.html","C29H36O10","free base","10-DB III","CC(=O)OC12COC1CC(O)C3(C)C2C(OC(=O)C4=CC=CC=C4)C5(O)CC(O)C(=C(C(O)C3=O)C5(C)C)C",0.364,6,3,5]
["S2410","Paeoniflorin (NSC 178886)","c4","L1700-12","in 10mM DMSO","COX,HIF","Immunology & Inflammation","Paeoniflorin (NSC 178886,Peoniflorin) is a herbal constituent extracted from the root of Paeonia albiflora Pall. Paeoniflorin reduces COX-2 expression. Paeoniflorin alleviates liver fibrosis by inhibiting HIF-1α through mTOR-dependent pathway.",480.46,"23180-57-6",{"v":96,"d":"96.00"},199.81,{"v":96,"d":"96.00"},199.81,"http://selleckchem.com/products/paeoniflorin.html","C23H28O11","free base","NSC 178886,Peoniflorin","CC12CC3(O)OC(O1)C4(COC(=O)C5=CC=CC=C5)C3CC24OC6OC(CO)C(O)C(O)C6O",-1.283,6,4,7]
["S2411","Geniposide","d4","L1700-12","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Geniposide is an iridoid glycoside isolated from the fruit of Gardenia jasminoides Ellis.",388.37,"24512-63-8",{"v":78,"d":"78.00"},200.84,{"v":78,"d":"78.00"},200.84,"http://selleckchem.com/products/geniposide.html","C17H24O10","free base","N/A","COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C3C1CC=C3CO",-2.066,5,5,6]
["S2412","Genipin","e4","L1700-12","in 10mM DMSO","Apoptosis related","Apoptosis","Genipin((+)-Genipin) is an active aglycone derived from an iridoid glycoside called geniposide, which is found in the fruit of Gardenia jasminoides Ellis.",226.23,"6902-77-8",{"v":45,"d":"45.00"},198.91,"<1","N/A","http://selleckchem.com/products/genipin.html","C11H14O5","free base","(+)-Genipin","COC(=O)C1=COC(O)C2C1CC=C2CO",-0.319,3,1,3]
["S2413","Geniposidic acid","f4","L1700-12","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Geniposidic acid is an iridoid glucoside, used to treat inflammation, jaundice and hepatic disorders.",374.34,"27741-01-1",{"v":16,"d":"16.00"},42.74,"<1","N/A","http://selleckchem.com/products/geniposidic-acid.html","C16H22O10","free base","N/A","OCC1OC(OC2OC=C(C3CC=C(CO)C23)C(O)=O)C(O)C(O)C1O",-2.291,4,5,5]
["S2415","Astragaloside A","g4","L1700-12","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Astragaloside A (Astragaloside IV) is the primary pure saponin isolated from Astragalus membranaceus, which has been widely used for the treatment of cardiovascular diseases.",784.97,"83207-58-3",{"v":100,"d":"100.00"},127.39,"<1","N/A","http://selleckchem.com/products/astragaloside-a.html","C41H68O14","free base","N/A","CC(C)(O)C1CCC(C)(O1)C2C(O)CC3(C)C4CC(OC5OC(CO)C(O)C(O)C5O)C6C(C)(C)C(CCC67CC47CCC23C)OC8OCC(O)C(O)C8O",-0.348,5,8,7]
["S2422","Ipriflavone (Osteofix)","h4","L1700-12","in 10mM DMSO","Others","Others","Ipriflavone (7-Isopropoxyisoflavon) is used to inhibit bone resorption.",280.32,"35212-22-7",{"v":56,"d":"56.00"},199.77,"<1","N/A","http://selleckchem.com/products/ipriflavone.html","C18H16O3","free base","N/A","CC(C)OC1=CC=C2C(=C1)OC=C(C2=O)C3=CC=CC=C3",3.576,3,0,3]
["S2423","(S)-10-Hydroxycamptothecin","a5","L1700-12","in 10mM DMSO","Topoisomerase","DNA Damage/DNA Repair","(S)-10-Hydroxycamptothecin (10-HCPT) is a DNA topoisomerase I inhibitor with potent anti-tumor activity.",364.35,"19685-09-7",{"v":8,"d":"8.00"},21.96,"<1","N/A","http://selleckchem.com/products/10-hydroxycamptothecin.html","C20H16N2O5","free base","10-HCPT","CCC1(O)C(=O)OCC2=C1C=C3N(CC4=CC5=CC(=CC=C5N=C34)O)C2=O",1.504,4,1,1]
["S2425","Apocynin (NSC 2146)","b5","L1700-12","in 10mM DMSO","NADPH-oxidase","Immunology & Inflammation","Apocynin (NSC 2146, Acetovanillone, NSC 209524) is a selective NADPH-oxidase inhibitor with IC50 of 10 μM.",166.17,"498-02-2",{"v":33,"d":"33.00"},198.59,"<1","N/A","http://selleckchem.com/products/apocynin-acetovanillone.html","C9H10O3","free base","Acetovanillone, NSC 209524","COC1=C(O)C=CC(=C1)C(C)=O",1.311,2,1,2]
["S2437","Rotundine","c5","L1700-12","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Rotundine (L-tetrahydropalmatine, L-THP) is a selective dopamine D1 receptor antagonist with IC50 of 166 nM.",355.43,"483-14-7",{"v":8,"d":"8.00"},22.51,"<1","N/A","http://selleckchem.com/products/rotundine.html","C21H25NO4","free base","L-tetrahydropalmatine, L-THP","COC1=CC2=C(C=C1OC)C3CC4=CC=C(OC)C(=C4CN3CC2)OC",3.599,4,0,4]
["S2438","Synephrine HCl","d5","L1700-12","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","SynephrineHCl (Oxedrine, p-Synephrine) is a sympathomimetic α-adrenergic receptor (AR) agonist.",203.67,"5985-28-4",{"v":14,"d":"14.00"},68.74,{"v":41,"d":"41.00"},201.31,"http://selleckchem.com/products/synephrine-hcl.html","C9H13NO2.HCl","Hydrochloride","N/A","Cl.CNCC(O)C1=CC=C(O)C=C1",0.997,0,3,3]
["S2439","Guanosine","e5","L1700-12","in 10mM DMSO","Nucleoside Analog/Antimetabolite","DNA Damage/DNA Repair","Guanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond.",283.24,"118-00-3",{"v":56,"d":"56.00"},197.71,"<1","N/A","http://selleckchem.com/products/guanosine.html","C10H13N5O5","free base","N/A","NC1=NC2=C(N=C[N]2C3OC(CO)C(O)C3O)C(=O)N1",{"v":-2.38,"d":"-2.380"},4,5,2]
["S2442","Inosine","f5","L1700-12","in 10mM DMSO","Others","Others","Inosine (NSC 20262, INO 495) is a nucleoside that is formed when hypoxanthine is attached to a ribose ring via a β-N9-glycosidic bond.",268.23,"58-63-9",{"v":53,"d":"53.00"},197.59,{"v":47,"d":"47.00"},175.22,"http://selleckchem.com/products/inosine.html","C10H12N4O5","free base","NSC 20262, INO 495","OCC1OC(C(O)C1O)[N]2C=NC3=C2N=CNC3=O",-2.249,4,4,2]
["S2443","Tolbutamide (HLS 831)","g5","L1700-12","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Tolbutamide (HLS 831) is an inhibitor of potassium channel, used for type II diabetes.",270.35,"64-77-7",{"v":54,"d":"54.00"},199.74,"<1","N/A","http://selleckchem.com/products/tolbutamide.html","C12H18N2O3S","free base","HLS 831","CCCCNC(=O)N[S](=O)(=O)C1=CC=C(C)C=C1",2.336,3,2,5]
["S2446","Levosimendan","h5","L1700-12","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Levosimendan(OR1259,OR1855,Simsndan) is a calcium sensitizer acting through calcium-dependent binding to cardiac troponin C (cTnC), provides treatment for heart failure.",280.28,"141505-33-1",{"v":56,"d":"56.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://selleckchem.com/products/levosimendan.html","C14H12N6O","free base","OR1259,OR1855,Simsndan","CC1CC(=O)NN=C1C2=CC=C(NN=C(C#N)C#N)C=C2",1.486,3,2,3]
["S2448","Gambogic Acid","a6","L1700-12","in 10mM DMSO","Bcl-2,Caspase","Apoptosis","Gambogic Acid (Guttatic Acid, Guttic Acid, Beta-Guttiferrin) activates caspases with EC50 of 0.78-1.64 μM and competitively inhibits Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1 with IC50 of 1.47, 1.21, 2.02, 0.66, 1.06 and 0.79 μM, respectively.",628.75,"2752-65-0",{"v":100,"d":"100.00"},159.05,"<1","N/A","http://selleckchem.com/products/gambogic-acid.html","C38H44O8","free base","Guttatic Acid, Guttic Acid, Beta-Guttiferrin","CC(C)=CCCC1(C)OC2=C(CC=C(C)C)C3=C(C(=C2C=C1)O)C(=O)C4=CC5CC6C(C)(C)OC(C\\C=C(C)/C(O)=O)(C5=O)C46O3",6.957,6,1,8]
["S2449","Colforsin","b6","L1700-12","in 10mM DMSO","Autophagy,cAMP,FXR","GPCR & G Protein","Colforsin (Forskolin, HL 362, Coleonol) is a ubiquitous activator of eukaryotic adenylyl cyclase (AC) in a wide variety of cell types, commonly used to raise levels of cAMP in the study and research of cell physiology. Forskolin also activates PXR and FXR activity. Forskolin stimulates autophagy.",{"v":410.5,"d":"410.50"},"66575-29-9",{"v":82,"d":"82.00"},199.76,"<1","N/A","http://selleckchem.com/products/forskolin.html","C22H34O7","free base","Forskolin, HL 362, Coleonol","CC(=O)OC1C(O)C2C(C)(C)CCC(O)C2(C)C3(O)C(=O)CC(C)(OC13C)C=C",0.837,4,2,3]
["S2450","Equol","c6","L1700-12","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Equol ,a metabolite of soybeans, is an important isoflavone in humans，specifically binds to 5α-DHT, has a modest affinity for recombinant estrogen receptor ERβ. Phase 2.",242.27,"531-95-3",{"v":48,"d":"48.00"},198.13,"<1","N/A","http://selleckchem.com/products/equol.html","C15H14O3","free base","N/A","OC1=CC=C(C=C1)C2COC3=CC(=CC=C3C2)O",3.211,1,2,1]
["S2451","Amantadine HCl","d6","L1700-12","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Amantadine HCl (1-adamantanamine) is used to treat or prevent infections of the respiratory tract caused by a certain virus.",{"v":187.7,"d":"187.70"},"665-66-7",{"v":38,"d":"38.00"},202.45,{"v":38,"d":"38.00"},202.45,"http://selleckchem.com/products/Amantadine-hydrochloride(Symmetrel).html","C10H17N.HCl","Hydrochloride","1-adamantanamine HCl","Cl.N[C]12CC3[CH2][CH](C[CH]([CH2]3)C1)C2",1.877,0,1,0]
["S2452","Amfebutamone (Bupropion) HCl","e6","L1700-12","in 10mM DMSO","AChR,Dopamine Receptor","Neuronal Signaling","Amfebutamone (Bupropion) HCl(Wellbutrin) is a selective norepinephrine-dopamine reuptake inhibitor with IC50 of 6.5 and 3.4 μM for the reuptake of dopamine and norepinephrine, respectively.",{"v":276.2,"d":"276.20"},"31677-93-7",{"v":8,"d":"8.00"},28.96,"<1","N/A","http://selleckchem.com/products/Amfebutamone-hydrochloride(Bupropion).html","C13H18ClNO.HCl","Hydrochloride","Wellbutrin","Cl.CC(NC(C)(C)C)C(=O)C1=CC=CC(=C1)Cl",3.501,1,1,4]
["S2454","Bupivacaine HCl","f6","L1700-12","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Bupivacaine HCl binds to the intracellular portion of voltage-gated sodium channels and blocks sodium influx into nerve cells, used for treating cardiac arrhythmias.",324.89,"18010-40-7",{"v":65,"d":"65.00"},200.07,{"v":23,"d":"23.00"},70.79,"http://selleckchem.com/products/Bupivacaine-hydrochloride(Marcain).html","C18H28N2O.HCl","Hydrochloride","N/A","Cl.CCCCN1CCCCC1C(=O)NC2=C(C)C=CC=C2C",4.692,1,1,5]
["S2455","Bethanechol chloride","g6","L1700-12","in 10mM DMSO","AChR","Neuronal Signaling","Bethanechol chloride(Myocholine,Urecholine) is a selective muscarinic receptor agonist without any effect on nicotinic receptors.",196.68,"590-63-6",{"v":39,"d":"39.00"},198.29,{"v":39,"d":"39.00"},198.29,"http://selleckchem.com/products/Carbamyl-beta-methylcholine-chloride(Bethanechol-chloride).html","C7H17N2O2.Cl","quaternary-N Chloride salt","Myocholine,Urecholine","[Cl-].CC(C[N+](C)(C)C)OC(N)=O",-3.702,2,1,4]
["S2456","Chlorpromazine HCl","h6","L1700-12","in 10mM DMSO","Dopamine Receptor,Potassium Channel","Neuronal Signaling","Chlorpromazine HCl (Sonazine) is a dopamine and potassium channel inhibitor with IC50 of 6.1 and 16 μM for inward-rectifying K+ currents and time-independent outward currents.",355.33,"69-09-0",{"v":71,"d":"71.00"},199.81,{"v":71,"d":"71.00"},199.81,"http://selleckchem.com/products/Chlorpromazine-hydrochloride(Sonazine).html","C17H19ClN2S.HCl","Hydrochloride","Sonazine","Cl.CN(C)CCCN1C2=C(SC3=C1C=C(Cl)C=C3)C=CC=C2",5.121,0,0,4]
["S2457","Clindamycin HCl","a7","L1700-12","in 10mM DMSO","Bacterial","Microbiology","Clindamycin HCl inhibits protein synthesis by acting on the 50S ribosomal, used for the treatment of bacterial infections.",461.44,"21462-39-5",{"v":92,"d":"92.00"},199.38,{"v":92,"d":"92.00"},199.38,"http://selleckchem.com/products/Clindamycin-hydrochloride(Dalacin).html","C18H33ClN2O5S.HCl","Hydrochloride","N/A","Cl.CCCC1CC(N(C)C1)C(=O)NC(C(C)Cl)C2OC(SC)C(O)C(O)C2O",1.659,2,4,7]
["S2458","Clonidine HCl","b7","L1700-12","in 10mM DMSO","Adrenergic Receptor,Autophagy","Neuronal Signaling","Clonidine HCl(Kapvay) is a direct-acting α2 adrenergic agonist with an ED50 of 0.02±0.01 mg/kg.",{"v":266.5,"d":"266.50"},"4205-91-8",{"v":53,"d":"53.00"},198.87,{"v":53,"d":"53.00"},198.87,"http://selleckchem.com/products/Clonidine-hydrochloride(Catapres).html","C9H9Cl2N3.HCl","Hydrochloride","Kapvay","Cl.ClC1=C(NC2=NCCN2)C(=CC=C1)Cl",2.736,1,2,2]
["S2459","Clozapine","c7","L1700-12","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Clozapine (HF 1854, LX 100-129) is an atypical antipsychotic drug by acting as a 5-HT antagonist, used in the treatment of schizophrenia.",326.82,"5786-21-0",{"v":65,"d":"65.00"},198.89,"<1","N/A","http://selleckchem.com/products/Clozapine(Clozaril).html","C18H19ClN4","free base","HF 1854, LX 100-129","CN1CCN(CC1)C2=NC3=C(NC4=C2C=CC=C4)C=CC(=C3)Cl",3.422,1,1,1]
["S2460","Pramipexole","d7","L1700-12","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Pramipexole (SND 919,Mirapexin,Sifrol,Mirapex) is a partial/full D2S, D2L, D3, D4 receptor agonist with a Ki of 3.9, 2.2, 0.5 and 5.1 nM for D2S, D2L, D3, D4 receptor, respectively.",211.33,"104632-26-0",{"v":42,"d":"42.00"},198.74,"<1","N/A","http://selleckchem.com/products/Pramipexole-Mirapex.html","C10H17N3S","Free Base","SND 919,Mirapexin,Sifrol,Mirapex","CCCNC1CCC2=C(C1)SC(=N2)N",1.383,1,2,3]
["S2461","Domperidone","e7","L1700-12","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Domperidone is an oral dopamine D2 receptor antagonist, used to treat nausea and vomiting.",425.91,"57808-66-9",{"v":48,"d":"48.00"},{"v":112.7,"d":"112.70"},"<1","N/A","http://selleckchem.com/products/Domperidone(Motilium).html","C22H24ClN5O2","free base","N/A","ClC1=CC2=C(C=C1)N(C3CCN(CCCN4C(=O)NC5=C4C=CC=C5)CC3)C(=O)N2",2.453,2,2,5]
["S2466","Estriol","f7","L1700-12","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Estriol (NSC-12169) is an antagonist of the G-protein coupled estrogen receptor in estrogen receptor-negative breast cancer cells.",288.39,"50-27-1",{"v":57,"d":"57.00"},197.65,"<1","N/A","http://selleckchem.com/products/Estriol(Oestriol).html","C18H24O3","free base","NSC-12169","CC12CCC3C(CCC4=CC(=CC=C34)O)C1CC(O)C2O",2.871,0,3,0]
["S2467","Famciclovir","g7","L1700-12","in 10mM DMSO","Antiviral","Microbiology","Famciclovir (BRL-42810) is a guanine analogue antiviral drug used for the treatment of various herpesvirus infections.",321.34,"104227-87-4",{"v":64,"d":"64.00"},199.17,{"v":64,"d":"64.00"},199.17,"http://selleckchem.com/products/Famciclovir(Famvir).html","C14H19N5O4","free base","BRL-42810","CC(=O)OCC(CC[N]1C=NC2=CN=C(N)N=C12)COC(C)=O",-0.294,7,1,9]
["S2468","Fenbendazole","h7","L1700-12","in 10mM DMSO","Parasite","Microbiology","Fenbendazole(Fenbendazol,Phenbendasol) is a broad spectrum benzimidazole anthelmintic used against gastrointestinal parasites with an IC50 of about 0.01 μg/mL.",299.35,"43210-67-9",{"v":4,"d":"4.00"},13.36,"<1","N/A","http://selleckchem.com/products/Fenbendazole(Panacur).html","C15H13N3O2S","free base","Fenbendazol,Phenbendasol","COC(=O)NC1=NC2=C([NH]1)C=C(SC3=CC=CC=C3)C=C2",3.769,3,2,4]
["S2470","Fluocinolone Acetonide","a8","L1700-12","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Fluocinolone Acetonide (Flucort-N) is a corticosteroid that binds to the cytosolic glucocorticoid receptor.",{"v":452.5,"d":"452.50"},"67-73-2",{"v":90,"d":"90.00"},{"v":198.9,"d":"198.90"},"<1","N/A","http://selleckchem.com/products/Fluocinolone-acetonide(Flucort-N).html","C24H30F2O6","free base","Flucort-N","CC1(C)OC2CC3C4CC(F)C5=CC(=O)C=CC5(C)C4(F)C(O)CC3(C)C2(O1)C(=O)CO",0.995,4,2,2]
["S2471","Gallamine Triethiodide","b8","L1700-12","in 10mM DMSO","AChR","Neuronal Signaling","Gallamine Triethiodide  is a cholinergic receptor blocker with an IC50 of 68.0 ± 8.4 μM.",891.53,"65-29-2",{"v":100,"d":"100.00"},112.17,{"v":100,"d":"100.00"},112.17,"http://selleckchem.com/products/Gallamine-triethiodide(Flaxedil).html","C30H60I3N3O3","tri-quaternary-N iodide salt","N/A","[I-].[I-].[I-].CC[N+](CC)(CC)CCOC1=C(OCC[N+](CC)(CC)CC)C(=CC=C1)OCC[N+](CC)(CC)CC",-8.065,3,0,21]
["S2473","Hexestrol","c8","L1700-12","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Hexestrol (Bibenzyl) binds to ERα and ERβ with EC50 of 0.07 nM and 0.175 nM, respectively.",270.37,"84-16-2",{"v":42,"d":"42.00"},155.34,"<1","N/A","http://selleckchem.com/products/Hexestrol(Bibenzyl).html","C18H22O2","free base","Bibenzyl","CCC(C(CC)C1=CC=C(O)C=C1)C2=CC=C(O)C=C2",5.192,0,2,5]
["S2475","Imatinib (STI571)","d8","L1700-12","in 10mM DMSO","Autophagy,Bcr-Abl,c-Kit,PDGFR","Protein Tyrosine Kinase","Imatinib (STI571,Gleevec, Glivec, CGP057148B) is a multi-target inhibitor of tyrosine kinase with inhibition for v-Abl, c-Kit and PDGFR, IC50 values are 0.6 μM, 0.1 μM and 0.1 μM in cell-free or cell-based assays, respectively. Imatinib (STI571) induces autophagy.",{"v":493.6,"d":"493.60"},"152459-95-5",{"v":33,"d":"33.00"},66.86,"<1","N/A","http://selleckchem.com/products/Imatinib(STI571).html","C29H31N7O","free base","STI571,Gleevec, Glivec, CGP057148B","CN1CCN(CC1)CC2=CC=C(C=C2)C(=O)NC3=CC=C(C)C(=C3)NC4=NC=CC(=N4)C5=CC=CN=C5",{"v":4.22,"d":"4.220"},4,2,7]
["S2479","Lincomycin HCl","e8","L1700-12","in 10mM DMSO","Antibiotics for Mammalian Cell Culture,Anti-infection","Microbiology","Lincomycin  hydrochloride (Lincocin, NSC 70731,U10149A) is the monohydrated salt of lincomycin, a substance produced by the growth of a member of the lincolnensis group of Streptomyces lincolnensis.",{"v":443,"d":"443.00"},"859-18-7",{"v":89,"d":"89.00"},{"v":200.9,"d":"200.90"},{"v":89,"d":"89.00"},{"v":200.9,"d":"200.90"},"http://selleckchem.com/products/Lincomycin-hydrochloride(Lincocin).html","C18H34N2O6S.HCl","Hydrochloride","Lincocin, NSC 70731,U10149A","Cl.CCCC1CC(N(C)C1)C(=O)NC(C(C)O)C2OC(SC)C(O)C(O)C2O",0.454,2,5,7]
["S2480","Loperamide HCl","f8","L1700-12","in 10mM DMSO","Autophagy,Opioid Receptor","Neuronal Signaling","Loperamide HCl (ADL 2-1294,R-18553 hydrochloride) is a selective μ-opioid receptor agonist opioid with Ki of 3.3 nM, 15-fold and 350-fold selective over the δ subtype and the κ subtype of the opioid receptor, used against diarrhea resulting from gastroenteritis or inflammatory bowel disease.",{"v":513.5,"d":"513.50"},"34552-83-5",{"v":22,"d":"22.00"},42.84,"<1","N/A","http://selleckchem.com/products/Loperamide-hydrochloride.html","C29H33ClN2O2.HCl","Hydrochloride","ADL 2-1294,R-18553 hydrochloride","Cl.CN(C)C(=O)C(CCN1CCC(O)(CC1)C2=CC=C(Cl)C=C2)(C3=CC=CC=C3)C4=CC=CC=C4",5.017,1,0,7]
["S2481","Manidipine","g8","L1700-12","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Manidipine(CV-4093,(±)-Manidipine) is a calcium channel blocker (dihydropyridine type) that is used clinically as an antihypertensive.",{"v":610.7,"d":"610.70"},"89226-50-6",{"v":122,"d":"122.00"},199.77,"<1","N/A","http://selleckchem.com/products/Manidipine(Manyper).html","C35H38N4O6","free base","CV-4093,(±)-Manidipine","COC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OCCN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=CC=C5)C",5.058,4,1,12]
["S2482","Manidipine 2HCl","h8","L1700-12","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Manidipine 2HCl (CV-4093) is a HCl salt form of Manidipine, which is a calcium channel blocker with IC50 of 2.6 nM, used clinically as an antihypertensive. Phase 4.",683.62,"89226-75-5",{"v":21,"d":"21.00"},30.72,"<1","N/A","http://selleckchem.com/products/Manidipine-dihydrochloride(CV-4093).html","C35H38N4O6.2HCl","Dihydrochloride","CV-4093","Cl.Cl.COC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OCCN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=CC=C5)C",5.822,4,1,12]
["S2484","Milrinone","a9","L1700-12","in 10mM DMSO","PDE","Metabolism","Milrinone (Win 47203,Primacor) is a phosphodiesterase 3 (PDE3) inhibitor, used to increase the heart's contractility.",211.22,"78415-72-2",{"v":42,"d":"42.00"},198.84,"<1","N/A","http://selleckchem.com/products/Milrinone(Primacor).html","C12H9N3O","free base","Win 47203,Primacor","CC1=C(C=C(C#N)C(=O)N1)C2=CC=NC=C2",0.356,2,1,1]
["S2485","Mitoxantrone (NSC-301739) 2HCl","b9","L1700-12","in 10mM DMSO","Apoptosis related,COVID-19,PKC,Topoisomerase","DNA Damage/DNA Repair","Mitoxantrone 2HCl (NSC-301739) is a dihydrochloride salt of Mitoxantrone. Mitoxantrone is an inhibitor of type II topoisomerase and protein kinase C (PKC) with IC50 of 8.5 μM for PKC. Mitoxantrone inhibits cell proliferative growth of MCF-7/wt cells with IC50 of 0.42 μM. Mitoxantrone also induces apoptosis.",{"v":517.4,"d":"517.40"},"70476-82-3",{"v":89,"d":"89.00"},172.01,{"v":89,"d":"89.00"},172.01,"http://selleckchem.com/products/Mitoxantrone-Hydrochloride.html","C22H29ClN4O6.2HCl","Dihydrochloride","NSC-301739 2HCl","Cl.Cl.OCCNCCNC1=CC=C(NCCNCCO)C2=C1C(=O)C3=C(O)C=CC(=C3C2=O)O",0.832,2,8,12]
["S2486","Moroxydine HCl","c9","L1700-12","in 10mM DMSO","Antiviral","Microbiology","Moroxydine HCl(ABOB hydrochloride) is a synthetic antiviral compound chemically belonging to the series of the heterocyclic biguanidines.",207.66,"3160-91-6",{"v":42,"d":"42.00"},202.25,{"v":42,"d":"42.00"},202.25,"http://selleckchem.com/products/Moroxydine-hydrochloride.html","C6H13N5O.HCl","Hydrochloride","ABOB hydrochloride","Cl.NC(=N)NC(=N)N1CCOCC1",-0.672,1,2,3]
["S2487","Mycophenolic acid","d9","L1700-12","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Dehydrogenase,Selection Antibiotics for Transfected Cell","Metabolism","Mycophenolic acid (Mycophenolate, RS-61443) is a potent IMPDH inhibitor and the active metabolite of an immunosuppressive drug, used to prevent rejection in organ transplantation.",320.34,"24280-93-1",{"v":64,"d":"64.00"},199.79,"<1","N/A","http://selleckchem.com/products/Mycophenolic-acid(Mycophenolate).html","C17H20O6","free base","Mycophenolate, RS-61443","COC1=C(C)C2=C(C(=C1C\\C=C(/C)CCC(O)=O)O)C(=O)OC2",3.157,4,1,6]
["S2489","Nateglinide","e9","L1700-12","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Nateglinide (Starlix,A-4166,SDZ DJN 608) is an insulin secretagog agent that lowers blood glucose levels by stimulating insulin secretion from the pancreas.",317.42,"105816-04-4",{"v":63,"d":"63.00"},198.48,"<1","N/A","http://selleckchem.com/products/Nateglinide(Starlix).html","C19H27NO3","free base","Starlix,A-4166,SDZ DJN 608","CC(C)C1CCC(CC1)C(=O)NC(CC2=CC=CC=C2)C(O)=O",3.981,2,1,6]
["S2491","Nitrendipine","f9","L1700-12","in 10mM DMSO","Autophagy,Calcium Channel","Transmembrane Transporters","Nitrendipine (Bayotensin) is a dihydropyridine calcium channel blocker with an IC50 of 95 nM.",360.37,"39562-70-4",{"v":72,"d":"72.00"},199.79,"<1","N/A","http://selleckchem.com/products/Nitrendipine.html","C18H20N2O6","free base","Bayotensin","CCOC(=O)C1=C(C)NC(=C(C1C2=CC(=CC=C2)[N+]([O-])=O)C(=O)OC)C",2.115,4,1,7]
["S2492","Novobiocin Sodium (NSC 2382)","g9","L1700-12","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,Topoisomerase","DNA Damage/DNA Repair","Novobiocin Sodium (NSC 2382, Albamycin, Cathomycin) is an aminocoumarin antibiotic that targets bacterial DNA gyrase (TopoIV), used to treat susceptible gram positive bacteria.",634.61,"1476-53-5",{"v":100,"d":"100.00"},157.58,{"v":100,"d":"100.00"},157.58,"http://selleckchem.com/products/Novobiocin-sodium(Albamycin).html","C31H35N2O11.Na","Sodium Salt","Albamycin,Cathomycin,NSC 2382","[Na+].COC1C(OC(N)=O)C(O)C(OC2=CC=C3C(=C(NC(=O)C4=CC=C([O-])C(=C4)CC=C(C)C)C(=O)OC3=C2C)O)OC1(C)C",2.747,8,4,9]
["S2493","Olanzapine","h9","L1700-12","in 10mM DMSO","5-HT Receptor,Dopamine Receptor","Neuronal Signaling","Olanzapine (LY170053,Zyprexa, Zalasta, Zolafren, Olzapin, Oferta, Zypadhera) is a high affinity for 5-HT2 serotonin and D2 dopamine receptor antagonist.",312.44,"132539-06-1",{"v":62,"d":"62.00"},198.44,"<1","N/A","http://selleckchem.com/products/Olanzapine(Zyprexa).html","C17H20N4S","free base","LY170053,Zyprexa, Zalasta, Zolafren, Olzapin, Oferta, Zypadhera","CN1CCN(CC1)C2=NC3=C(NC4=C2C=C(C)S4)C=CC=C3",{"v":2.69,"d":"2.690"},1,1,1]
["S2494","Olopatadine HCl","a10","L1700-12","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Olopatadine HCl(ALO4943A,KW4679) is a histamine blocker and mast cell stabilizer with an IC50 of 559 μM for the release of histamine.",373.87,"140462-76-6",{"v":75,"d":"75.00"},{"v":200.6,"d":"200.60"},{"v":13,"d":"13.00"},34.77,"http://selleckchem.com/products/Olopatadine-hydrochloride(Opatanol).html","C21H23NO3.HCl","Hydrochloride","ALO4943A,KW4679","Cl.CN(C)CC\\C=C/1C2=C(COC3=C1C=C(CC(O)=O)C=C3)C=CC=C2",{"v":0.92,"d":"0.920"},2,0,5]
["S2496","Ozagrel","b10","L1700-12","in 10mM DMSO","P450 (e.g. CYP17),Prostaglandin Receptor","GPCR & G Protein","Ozagrel (OKY-046) is a selective thromboxane A(2) (TXA(2)) synthetase inhibitor with IC50 of 11 nM for rabbit platelet, used for the improvement of postoperative cerebrovascular contraction and accompanying cerebral ischaemia.",228.25,"82571-53-7",{"v":46,"d":"46.00"},201.53,"<1","N/A","http://selleckchem.com/products/Ozagrel.html","C13H12N2O2","free base","OKY-046","OC(=O)/C=C/C1=CC=C(C[N]2C=CN=C2)C=C1",1.604,2,0,4]
["S2497","Pancuronium dibromide","c10","L1700-12","in 10mM DMSO","AChR","Neuronal Signaling","Pancuronium dibromide(Pavulon) is a competitive nicotinic acetylcholine receptor antagonist, used as a muscle relaxant.",732.67,"15500-66-0",{"v":100,"d":"100.00"},136.49,{"v":100,"d":"100.00"},136.49,"http://selleckchem.com/products/Pancuronium-bromide(Pavulon).html","C35H60N2O4.2Br","di-quaternary-N bromide salt","Pavulon","[Br-].[Br-].CC(=O)OC1CC2CCC3C(CCC4(C)C3CC(C4OC(C)=O)[N+]5(C)CCCCC5)C2(C)CC1[N+]6(C)CCCCC6",-2.043,4,0,6]
["S2499","Phenoxybenzamine HCl","d10","L1700-12","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Phenoxybenzamine HCl (NSC 37448, NCI-c01661) is a non-specific, irreversible alpha antagonist with an IC50 of 550 nM.",{"v":340.3,"d":"340.30"},"63-92-3",{"v":68,"d":"68.00"},199.82,{"v":17,"d":"17.00"},49.96,"http://selleckchem.com/products/Phenoxybenzamine-hydrochloride.html","C18H22ClNO.HCl","HCl","NSC 37448, NCI-c01661","Cl.CC(COC1=CC=CC=C1)N(CCCl)CC2=CC=CC=C2",{"v":4.96,"d":"4.960"},1,0,8]
["S2500","Propafenone HCl","e10","L1700-12","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Propafenone HCl is a classic anti-arrhythmic medication, which treats illnesses associated with rapid heartbeats such as atrial and ventricular arrhythmias.",{"v":377.9,"d":"377.90"},"34183-22-7",{"v":69,"d":"69.00"},182.59,"<1","N/A","http://selleckchem.com/products/Propafenone(Rytmonorm).html","C21H27NO3.HCl","Hydrochloride","N/A","CCCNCC(O)COC1=CC=CC=C1C(=O)CCC2=CC=CC=C2",3.673,2,2,11]
["S2501","Pyrantel Pamoate","f10","L1700-12","in 10mM DMSO","Parasite","Microbiology","Pyrantel pamoate (Pyrantel Embonate), a broad-spectrum anthelmintic drug, is used to treat a number of parasitic worm infections.",594.69,"22204-24-6",{"v":100,"d":"100.00"},168.15,"<1","N/A","http://selleckchem.com/products/Pyrantel-pamoate(Pyrantel-embonate).html","C23H16O6.C11H14N2S","salt","Pyrantel Embonate","CN1CCCN=C1\\C=C\\C2=CC=CS2.OC(=O)C3=CC4=CC=CC=C4C(=C3O)CC5=C6C=CC=CC6=CC(=C5O)C(O)=O",6.203,3,2,6]
["S2502","Quinine HCl Dihydrate","g10","L1700-12","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Quinine HCl Dihydrate is a white crystalline K+ channel blocker, used to treat malaria.",396.91,"6119-47-7",{"v":79,"d":"79.00"},199.04,{"v":43,"d":"43.00"},108.34,"http://selleckchem.com/products/Quinine-hydrochloride-dihydrate.html","C20H24N2O2.HCl.2H2O","Hydrochloride dihydrate","N/A","O.O.Cl.COC1=CC2=C(C=C1)N=CC=C2C(O)C3CC4CCN3CC4C=C",2.701,2,1,4]
["S2503","Racecadotril","h10","L1700-12","in 10mM DMSO","Opioid Receptor","Neuronal Signaling","Racecadotril (Acetorphan) is a peripherally acting enkephalinase inhibitor with an IC50 of 4.5 μM.",385.48,"81110-73-8",{"v":22,"d":"22.00"},57.07,"<1","N/A","http://selleckchem.com/products/Racecadotril(Acetorphan).html","C21H23NO4S","free base","Acetorphan","CC(=O)SCC(CC1=CC=CC=C1)C(=O)NCC(=O)OCC2=CC=CC=C2",3.128,4,1,11]
["S2504","Ribavirin (ICN-1229)","a11","L1700-12","in 10mM DMSO","Antiviral","Microbiology","Ribavirin (NSC-163039, ICN-1229, RTCA, Tribavirin), a synthetic guanosine analogue, possesses a broad spectrum of activity against DNA and RNA viruses.",244.21,"36791-04-5",{"v":49,"d":"49.00"},200.65,{"v":49,"d":"49.00"},200.65,"http://selleckchem.com/products/Ribavirin(Copegus).html","C8H12N4O5","free base","NSC-163039, RTCA, Tribavirin","NC(=O)C1=N[N](C=N1)C2OC(CO)C(O)C2O",-2.745,4,4,3]
["S2505","Rosiglitazone (BRL-49653) maleate","b11","L1700-12","in 10mM DMSO","Autophagy,Ferroptosis,PPAR,TRP Channel","Metabolism","Rosiglitazone maleate (BRL-49653C), a member of the thiazolidinedione class of antihyperglycaemic agents, is a high-affinity selective agonist of the peroxisome proliferator-activated receptor-γ (PPAR-γ) with IC50 of 42 nM. Rosiglitazone maleate also modulates TRP channels and induces autophagy. Rosiglitazone prevents ferroptosis.",{"v":473.5,"d":"473.50"},"155141-29-0",{"v":94,"d":"94.00"},198.52,"<1","N/A","http://selleckchem.com/products/Rosiglitazone-maleate.html","C18H19N3O3S.C4H4O4","Maleate","BRL-49653C","CN(CCOC1=CC=C(CC2SC(=O)NC2=O)C=C1)C3=NC=CC=C3.OC(=O)\\C=C/C(O)=O",3.307,6,1,9]
["S2506","Roxithromycin","c11","L1700-12","in 10mM DMSO","Antibiotics,Antineoplastic and Immunosuppressive Antibiotics","Microbiology","Roxithromycin (Roxl-150, Roxo, Surlid, Rulide, Biaxsig, Roxar, Roximycin, Roxomycin, Tirabicin, Coroxin,RU-28965) is a semi-synthetic macrolide antibiotic. It is used to treat respiratory tract, urinary and soft tissue infections.",837.07,"80214-83-1",{"v":167,"d":"167.00"},199.51,"<1","N/A","http://selleckchem.com/products/Roxithromycin(Roxl-150).html","C41H76N2O15","free base","Roxl-150, Roxo, Surlid, Rulide, Biaxsig, Roxar, Roximycin, Roxomycin, Tirabicin, Coroxin,RU-28965","CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(O)CC(C)C(=N/OCOCCOC)/C(C)C(O)C1(C)O",1.619,11,3,13]
["S2508","Scopolamine (LSM-4015) HBr","d11","L1700-12","in 10mM DMSO","AChR","Neuronal Signaling","Scopolamine HBr (LSM-4015,NSC 61806,(-)-Scopolamine hydrobromide, Hyoscine hydrobromide, Scopine hydrobromide) is a competitive muscarinic acetylcholine receptor antagonist with an IC50 of 55.3 nM.",384.26,"114-49-8",{"v":76,"d":"76.00"},197.78,{"v":76,"d":"76.00"},197.78,"http://selleckchem.com/products/Scopolamine-hydrobromide.html","C17H21NO4.HBr","Hydrobromide","LSM-4015,NSC 61806,(-)-Scopolamine hydrobromide, Hyoscine hydrobromide, Scopine hydrobromide","Br.CN1C2CC(CC1C3OC23)OC(=O)C(CO)C4=CC=CC=C4",1.314,3,1,5]
["S2509","Sotalol HCl","e11","L1700-12","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Sotalol(MJ-1999)  is a non-selective beta blocker and a potassium channel blocker with an IC50 of 43 μM.",308.82,"959-24-0",{"v":61,"d":"61.00"},197.53,{"v":61,"d":"61.00"},197.53,"http://selleckchem.com/products/Sotalol-hydrochloride(Betapace).html","C12H20N2O3S.HCl","Hydrochloride","MJ-1999","Cl.CC(C)NCC(O)C1=CC=C(N[S](C)(=O)=O)C=C1",0.876,2,3,6]
["S2510","Spectinomycin 2HCl","f11","L1700-12","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture,Selection Antibiotics for Transfected Cell","Microbiology","Spectinomycin 2HCl (Actinospectacin) is a new parenteral antibiotic prepared from Streptomyces spectabilis.",405.27,"21736-83-4",{"v":81,"d":"81.00"},199.87,{"v":81,"d":"81.00"},199.87,"http://selleckchem.com/products/Spectinomycin-hydrochloride.html","C14H24N2O7.2HCl","dihydrochloride","Actinospectacin","Cl.Cl.CNC1C(O)C(NC)C2OC3(O)C(OC(C)CC3=O)OC2C1O",-1.566,4,4,2]
["S2511","Sulfadoxine","g11","L1700-12","in 10mM DMSO","Anti-infection","Microbiology","Sulfadoxine (Sulphadoxine) is an ultra-long-lasting sulfonamide with an IC50 of 249 μg/ml for P. vivax.",310.33,"2447-57-6",{"v":62,"d":"62.00"},199.78,"<1","N/A","http://selleckchem.com/products/Sulfadoxine(Sulphadoxine).html","C12H14N4O4S","free base","Sulphadoxine","COC1=C(OC)C(=NC=N1)N[S](=O)(=O)C2=CC=C(N)C=C2",0.837,6,2,5]
["S2512","Tenoxicam","h11","L1700-12","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Tenoxicam(Ro-12-0068) is a good HO. radicals scavenger with an IC50 of 56.7 μM.",337.38,"59804-37-4",{"v":68,"d":"68.00"},201.55,"<1","N/A","http://selleckchem.com/products/Tenoxicam(Mobiflex).html","C13H11N3O4S2","free base","Ro-12-0068","CN1C(=C(O)C2=C(C=CS2)[S]1(=O)=O)C(=O)NC3=CC=CC=N3",0.454,4,2,2]
["S2515","Vardenafil HCl Trihydrate","a2","L1700-13","in 10mM DMSO","PDE","Metabolism","Vardenafil HCl Trihydrate (BAY38-9456) is a new type PDE inhibitor with IC50 of 0.7 and 180 nM for PDE5 and PDE1, respectively.",579.11,"330808-88-3",{"v":100,"d":"100.00"},172.68,{"v":10,"d":"10.00"},17.27,"http://selleckchem.com/products/Vardenafil(Vivanza).html","C23H32N6O4S.HCl.3H2O","Hydrochloride trihydrate","BAY38-9456","O.O.O.Cl.CCCC1=NC(=C2[N]1N=C(NC2=O)C3=CC(=CC=C3OCC)[S](=O)(=O)N4CCN(CC)CC4)C",2.109,6,1,8]
["S2516","Xylazine HCl","b2","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Xylazine(BAY 1470 hydrochloride) is an α2-Adrenergic receptor agonist, used as a sedative and muscle relaxant.",256.79,"23076-35-9",{"v":50,"d":"50.00"},194.71,{"v":12,"d":"12.00"},46.73,"http://selleckchem.com/products/Xylazine(Rompun).html","C12H16N2S.HCl","Hydrochloride","BAY 1470 hydrochloride","Cl.CC1=C(NC2=NCCCS2)C(=CC=C1)C",3.647,1,1,2]
["S2517","Maprotiline HCl","c2","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Maprotiline HCl is a selective noradrenalin re-uptake inhibitor, used in the treatment of depression.",313.86,"10347-81-6",{"v":63,"d":"63.00"},200.73,"<1","N/A","http://selleckchem.com/products/Maprotiline-hydrochloride.html","C20H23N.HCl","Hydrochloride","N/A","Cl.CNCCCC12CCC(C3=CC=CC=C13)C4=C2C=CC=C4",4.498,0,1,4]
["S2519","Naphazoline HCl","d2","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Naphazoline HCl is an ocular vasoconstrictor and imidazoline derivative sympathomimetic amine.",246.74,"550-99-2",{"v":17,"d":"17.00"},{"v":68.9,"d":"68.90"},{"v":49,"d":"49.00"},198.59,"http://selleckchem.com/products/Naphazoline-hydrochloride-Naphcon.html","C14H14N2.HCl","Hydrochloride","N/A","Cl.C1CN=C(CC2=C3C=CC=CC3=CC=C2)N1",2.442,1,1,2]
["S2521","Epinephrine bitartrate","e2","L1700-13","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Epinephrine bitartrate (Adrenalinium) is an alpha- and beta-adrenergic receptor stimulator.",333.29,"51-42-3",{"v":67,"d":"67.00"},201.03,{"v":67,"d":"67.00"},201.03,"http://selleckchem.com/products/Epinephrine-bitartrate-Adrenalinium.html","C9H13NO3.C4H6O6","tartrate","Adrenalinium","CNCC(O)C1=CC(=C(O)C=C1)O.OC(C(O)C(O)=O)C(O)=O",-3.996,2,6,6]
["S2524","Phenytoin Sodium","f2","L1700-13","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Phenytoin Sodium (Aleviatin, Diphenylhydantoin sodium, Eptoin, Phenytoin soluble, Prompt; Phenytek,Dilantin sodium, Diphantoine) is an inactive voltage-gated sodium channel stabilizer.",274.25,"630-93-3",{"v":32,"d":"32.00"},116.68,{"v":3,"d":"3.00"},10.94,"http://selleckchem.com/products/Phenytoin-sodium-Dilantin.html","C15H11N2NaO2","Sodium Salt","Aleviatin, Diphenylhydantoin sodium, Eptoin, Phenytoin soluble, Prompt,Phenytek,Dilantin sodium, Diphantoine","[Na+].[O-]C1=NC(=O)C(N1)(C2=CC=CC=C2)C3=CC=CC=C3",2.084,2,1,2]
["S2525","Phenytoin","g2","L1700-13","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Phenytoin (Di-Hydan, Dihycon, Dilabid, Diphedan, Diphenat, Diphenylan, Diphenylhydantoin, Hydantol, Lehydan, NSC 8722) is an inactive voltage-gated sodium channel stabilizer.",252.27,"57-41-0",{"v":50,"d":"50.00"},{"v":198.2,"d":"198.20"},"<1","N/A","http://selleckchem.com/products/Phenytoin-Lepitoin.html","C15H12N2O2","Free Base","Di-Hydan, Dihycon, Dilabid, Diphedan, Diphenat, Diphenylan, Diphenylhydantoin, Hydantol, Lehydan, NSC 8722","O=C1NC(=O)C(N1)(C2=CC=CC=C2)C3=CC=CC=C3",2.105,2,2,2]
["S2526","Alizarin","h2","L1700-13","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Alizarin (Anthraquinonic) strongly inhibits P450 isoform CYP1A1, CYP1A2 and CYP1B1 with IC50 of 6.2 μM, 10.0 μM and 2.7 μM, respectively; weakly inhibits CYP2A6 and CYP2E1, and does not inhibit CYP2C19, CYP3A4 and CYP3A5.",240.21,"72-48-0",{"v":48,"d":"48.00"},199.83,"<1","N/A","http://selleckchem.com/products/Alizarin.html","C14H8O4","free base","Anthraquinonic","OC1=C(O)C2=C(C=C1)C(=O)C3=CC=CC=C3C2=O",2.324,2,2,0]
["S2528","Ciclopirox","a3","L1700-13","in 10mM DMSO","ATPase,Fungal","Transmembrane Transporters","Ciclopirox(HOE 296b, Penlac) is a broad-spectrum antifungal agent working as an iron chelator.",207.27,"29342-05-0",{"v":42,"d":"42.00"},202.63,"<1","N/A","http://selleckchem.com/products/Ciclopirox-Penlac.html","C12H17NO2","Free Base","HOE 296b, Penlac","CC1=CC(=O)N(O)C(=C1)C2CCCCC2",2.489,1,0,1]
["S2529","Dopamine HCl","b3","L1700-13","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Dopamine HCl(ASL279, NSC 173182) is a catecholamine neurotransmitter present in a wide variety of animals,And a dopamine D1-5 receptors agonist.",189.64,"62-31-7",{"v":38,"d":"38.00"},200.38,{"v":38,"d":"38.00"},200.38,"http://selleckchem.com/products/Dopamine-hydrochloride-Inotropin.html","C8H11NO2.HCl","Hydrochloride","ASL279, NSC 173182","Cl.NCCC1=CC(=C(O)C=C1)O",1.155,0,3,2]
["S2531","Asaraldehyde","c3","L1700-13","in 10mM DMSO","COX","Neuronal Signaling","Asaraldehyde (Asaronaldehyde) is a natural COX-2 inhibitor, exhibiting 17-fold selectivity over COX-1.",{"v":196.2,"d":"196.20"},"4460-86-0",{"v":39,"d":"39.00"},198.78,"<1","N/A","http://selleckchem.com/products/Asaraldehyde-Asaronaldehyde.html","C10H12O4","free base","Asaronaldehyde","COC1=C(OC)C=C(C=O)C(=C1)OC",{"v":1.54,"d":"1.540"},4,0,4]
["S2532","L-Ascorbyl 6-palmitate","d3","L1700-13","in 10mM DMSO","N/A","Others","Ascorbyl palmitate is an ester formed from ascorbic acid and palmitic acid creating a fat-soluble form of vitamin C.",414.53,"137-66-6",{"v":83,"d":"83.00"},200.23,"<1","N/A","http://selleckchem.com/products/L-Ascorbyl-6-palmitate.html","C22H38O7","free base","N/A","CCCCCCCCCCCCCCCC(=O)OCC(O)C1OC(=O)C(=C1O)O",5.268,4,3,18]
["S2533","Ritodrine HCl","e3","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Ritodrine HCl (NSC 291565,DU 21220, Ritodrine) is a hydrochloride salt of ritodrine which is a β-2 adrenergic receptor agonist.",323.81,"23239-51-2",{"v":65,"d":"65.00"},200.73,{"v":65,"d":"65.00"},200.73,"http://selleckchem.com/products/Ritodrine-hydrochloride-Yutopar.html","C17H21NO3.HCl","Hydrochloride","NSC 291565,DU 21220, Ritodrine","Cl.CC(NCCC1=CC=C(O)C=C1)C(O)C2=CC=C(O)C=C2",3.037,0,4,6]
["S2534","Isoconazole nitrate","f3","L1700-13","in 10mM DMSO","Fungal","Microbiology","Isoconazole nitrate (Travogen,Adestan G 100, R 15454) is an azole antifungal reagent.",479.14,"24168-96-5",{"v":41,"d":"41.00"},85.57,"<1","N/A","http://selleckchem.com/products/Isoconazole-nitrate-Travogen.html","C18H14Cl4N2O.HNO3","Nitrate","Travogen,Adestan G 100, R 15454","O[N+]([O-])=O.ClC1=CC=C(C(C[N]2C=CN=C2)OCC3=C(Cl)C=CC=C3Cl)C(=C1)Cl",4.387,2,0,6]
["S2535","Econazole nitrate","g3","L1700-13","in 10mM DMSO","Calcium Channel,Fungal","Transmembrane Transporters","Econazole Nitrate (NSC 243115,Spectazole) is a Ca2+ channel blocker, used as an antifungal medicine that fights infections caused by fungus.",{"v":444.7,"d":"444.70"},"24169-02-6",{"v":89,"d":"89.00"},200.13,"<1","N/A","http://selleckchem.com/products/Econazole-nitrate-Spectazole.html","C18H15Cl3N2O.HNO3","Nitrate","NSC 243115,Spectazole","O[N+]([O-])=O.ClC1=CC=C(COC(C[N]2C=CN=C2)C3=CC=C(Cl)C=C3Cl)C=C1",3.722,2,0,6]
["S2536","Miconazole","h3","L1700-13","in 10mM DMSO","Fungal","Microbiology","Miconazole (Monistat,R18134) is an imidazole antifungal agent.",416.13,"22916-47-8",{"v":83,"d":"83.00"},199.46,"<1","N/A","http://selleckchem.com/products/Miconazole-Monistat.html","C18H14Cl4N2O","Free Base","Monistat,R18134","ClC1=CC=C(COC(C[N]2C=CN=C2)C3=C(Cl)C=C(Cl)C=C3)C(=C1)Cl",5.645,2,0,6]
["S2537","Secnidazole","a4","L1700-13","in 10mM DMSO","Anti-infection","Microbiology","Secnidazole (Flagentyl, PM 185184, RP 14539) is a nitroimidazole anti-infective.",185.18,"3366-95-8",{"v":37,"d":"37.00"},199.81,{"v":37,"d":"37.00"},199.81,"http://selleckchem.com/products/Secnidazole-Flagentyl.html","C7H11N3O3","free base","PM 185184, RP 14539","CC(O)C[N]1C(=NC=C1[N+]([O-])=O)C",{"v":0.04,"d":"0.040"},1,1,3]
["S2541","Clomipramine HCl","b4","L1700-13","in 10mM DMSO","Serotonin Transporter","Neuronal Signaling","Clomipramine HCl(Anafranil) is a hydrochloride salt of clomipramine which is a serotonin transporter (SERT), norepinephrine transporter (NET) dopamine transporter (DAT) blocker with Ki of 0.14, 54 and 3 nM, respectively.",351.31,"17321-77-6",{"v":70,"d":"70.00"},199.25,{"v":70,"d":"70.00"},199.25,"http://selleckchem.com/products/Clomipramine-hydrochloride-Anafranil.html","C19H23ClN2.HCl","Hydrochloride","Anafranil","Cl.CN(C)CCCN1C2=C(CCC3=C1C=C(Cl)C=C3)C=CC=C2",5.434,0,0,4]
["S2543","Ceftiofur HCl","c4","L1700-13","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Ceftiofur HCl (U-67279A,Excenel hydrochloride) is a cephalosporin antibiotic, used to treat both Gram-positive and Gram-negative bacteria infection.",560.02,"103980-44-5",{"v":100,"d":"100.00"},178.57,"<1","N/A","http://selleckchem.com/products/Ceftiofur-hydrochloride.html","C19H17N5O7S3.HCl","Hydrochloride","U-67279A,Excenel hydrochloride","Cl.CO/N=C(/C(=O)NC1C2SCC(=C(N2C1=O)C(O)=O)CSC(=O)C3=CC=CO3)C4=CSC(=N4)N",{"v":1.09,"d":"1.090"},8,2,9]
["S2545","Scopine","d4","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Scopine(6,7-Epoxytropine) is the metabolite of anisodine, which is a α1-adrenergic receptor agonist and used in the treatment of acute circulatory shock.",155.19,"498-45-3",{"v":31,"d":"31.00"},199.76,"<1","N/A","http://selleckchem.com/products/scopine.html","C8H13NO2","free base","6,7-Epoxytropine","CN1C2CC(O)CC1C3OC23",-0.627,1,1,0]
["S2547","Tiotropium Bromide hydrate","e4","L1700-13","in 10mM DMSO","AChR","Neuronal Signaling","Tiotropium Bromide hydrate (BA 679BR) is a monohydrate of tiotropium bromide (Spiriva; Tiova; BA 679BR; tiopropium) that is an anticholinergic and bronchodilator and a muscarinic receptor antagonist.",490.43,"139404-48-1",{"v":8,"d":"8.00"},16.31,"<1","N/A","http://selleckchem.com/products/Tiotropium-Bromide-hydrate.html","C19H22NO4S2.Br.xH2O","quaternary-N bromide salt&hydr","BA 679BR","O.[Br-].C[N+]1(C)C2CC(CC1C3OC23)OC(=O)C(O)(C4=CC=CS4)C5=CC=CS5",-1.727,3,0,5]
["S2549","Trospium chloride","f4","L1700-13","in 10mM DMSO","AChR","Neuronal Signaling","Trospium chloride  is a competitive muscarinic cholinergic receptor antagonist.",427.96,"10405-02-4",{"v":41,"d":"41.00"},{"v":95.8,"d":"95.80"},{"v":86,"d":"86.00"},200.95,"http://selleckchem.com/products/Trospium-chloride-Sanctura.html","C25H30NO3.Cl","quaternary-N chloride salt","N/A","[Cl-].OC(C(=O)OC1CC2CCC(C1)[N+]23CCCC3)(C4=CC=CC=C4)C5=CC=CC=C5",-0.324,2,0,5]
["S2551","Sulbactam sodium","g4","L1700-13","in 10mM DMSO","β-lactamase","Microbiology","Sulbactam sodium (Unasyn, CP-45899-2) is an irreversible β-lactamase inhibitor.",255.22,"69388-84-7",{"v":3,"d":"3.00"},11.75,{"v":51,"d":"51.00"},199.83,"http://selleckchem.com/products/sulbactam-sodium-unasyn.html","C8H10NO5S.Na","Sodium  salt","Unasyn, CP-45899-2","[Na+].CC1(C)C(N2C(CC2=O)[S]1(=O)=O)C([O-])=O",-2.145,3,0,1]
["S2552","Azelastine HCl","h4","L1700-13","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Azelastine HCl is a potent, second-generation, selective, histamine receptor antagonist, used in the treatment of rhinitis.",418.36,"79307-93-0",{"v":28,"d":"28.00"},66.93,{"v":35,"d":"35.00"},83.66,"http://selleckchem.com/products/azelastine.html","C22H24ClN3O.HCl","Hydrochloride","N/A","Cl.CN1CCCC(CC1)N2N=C(CC3=CC=C(Cl)C=C3)C4=CC=CC=C4C2=O",4.476,2,0,3]
["S2553","5-Aminolevulinic acid HCl","a5","L1700-13","in 10mM DMSO","Others","Others","5-Aminolevulinic Acid HCl(5-ALA hydrochloride) is an intermediate in the porphyrin synthesis pathway, used as a photosensitizing agent and a antineoplastic agent.",167.59,"5451-09-2",{"v":34,"d":"34.00"},202.88,{"v":34,"d":"34.00"},202.88,"http://selleckchem.com/products/5-Aminolevulinic-acid-hydrochloride.html","C5H9NO3.HCl","Hydrochloride","5-ALA hydrochloride","Cl.NCC(=O)CCC(O)=O",-3.318,2,1,4]
["S2554","Daphnetin","b5","L1700-13","in 10mM DMSO","EGFR,PKA,PKC","Angiogenesis","Daphnetin, a natural coumarin derivative, is a protein kinase inhibitor, inhibits EGFR, PKA and PKC with IC50 of 7.67 μM, 9.33 μM and 25.01 μM, respectively, also known to exhibit anti-inflammatory and anti-oxidant activities.",178.14,"486-35-1",{"v":35,"d":"35.00"},196.47,"<1","N/A","http://selleckchem.com/products/Daphnetin.html","C9H6O4","free base","N/A","OC1=CC=C2C=CC(=O)OC2=C1O",1.415,2,2,0]
["S2555","Clarithromycin","c5","L1700-13","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Clarithromycin (A-56268) is a macrolide antibiotic and a CYP3A4 inhibitor, used to treat a number of bacterial infections.",747.95,"81103-11-9",{"v":25,"d":"25.00"},33.42,"<1","N/A","http://selleckchem.com/products/clarithromycin.html","C38H69NO13","free base","A-56268","CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(CC(C)C(=O)C(C)C(O)C1(C)O)OC",{"v":2.2,"d":"2.200"},9,3,8]
["S2556","Rosiglitazone (BRL 49653)","d5","L1700-13","in 10mM DMSO","Autophagy,Ferroptosis,PPAR,TRP Channel","Metabolism","Rosiglitazone (BRL 49653) is a potent antihyperglycemic agent and a potent thiazolidinedione insulin sensitizer with IC50 of 12, 4 and 9 nM for rat, 3T3-L1 and human adipocytes, respectively. Rosiglitazone is a pure ligand of PPAR-gamma, and has no PPAR-alpha-binding action. Rosiglitazone modulates TRP channels and induces autophagy. Rosiglitazone prevents ferroptosis.",357.43,"122320-73-4",{"v":71,"d":"71.00"},198.64,"<1","N/A","http://selleckchem.com/products/Rosiglitazone-Avandia.html","C18H19N3O3S","Free Base","BRL 49653","CN(CCOC1=CC=C(CC2SC(=O)NC2=O)C=C1)C3=CC=CC=N3",3.268,4,1,7]
["S2557","Terbinafine HCl","e5","L1700-13","in 10mM DMSO","Fungal","Microbiology","Terbinafine HCl (KWD 201,KWD 2019,TDT 067 hydrochloride) inhibits ergosterol synthesis by inhibiting squalene epoxidase, used as an antifungal drug.",327.89,"78628-80-5",{"v":66,"d":"66.00"},201.29,"<1","N/A","http://selleckchem.com/products/Terbinafine-hydrochloride-Lamisil.html","C21H25N.HCl","Hydrochloride","KWD 201,KWD 2019,TDT 067 hydrochloride","Cl.CN(C\\C=C\\C#CC(C)(C)C)CC1=CC=CC2=C1C=CC=C2",5.717,0,0,6]
["S2559","Cortisone acetate","f5","L1700-13","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Cortisone acetate (Cortone, NSC 49420) is an acetate salt form of cortisone that is a steroid hormone and a glucocorticoid.",402.48,"50-04-4",{"v":7,"d":"7.00"},17.39,"<1","N/A","http://selleckchem.com/products/Cortisone-acetate-Cortone.html","C23H30O6","free base","Cortone,NSC 49420","CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3C(=O)CC12C",1.619,5,0,4]
["S2561","Clomifene citrate","g5","L1700-13","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Clomifene citrate (NSC 35770, Clomiphene citrate) is a selective estrogen receptor modulator, used in the treatment of ovulation induction.",598.08,"50-41-9",{"v":120,"d":"120.00"},200.64,"<1","N/A","http://selleckchem.com/products/Clomifene-citrate-Serophene.html","C26H28ClNO.C6H8O7","Citrate","NSC 35770, Clomiphene citrate","CCN(CC)CCOC1=CC=C(C=C1)C(=C(Cl)/C2=CC=CC=C2)/C3=CC=CC=C3.OC(=O)CC(O)(CC(O)=O)C(O)=O",2.129,4,0,14]
["S2564","Cloxacillin Sodium","h5","L1700-13","in 10mM DMSO","Anti-infection","Microbiology","Cloxacillin Sodium(Cloxacap,BRL 1621 sodium salt) is a sodium salt of cloxacillin that is a penicillinase-resistant, acid resistant, semi-synthetic penicillin.",475.88,"7081-44-9",{"v":55,"d":"55.00"},115.58,{"v":55,"d":"55.00"},115.58,"http://selleckchem.com/products/Cloxacillin-sodium-Cloxacap.html","C19H19ClN3NaO6S","Sodium Salt & hydrate","Cloxacap,BRL 1621 sodium salt","O.[Na+].CC1=C(C(=O)NC2C3SC(C)(C)C(N3C2=O)C([O-])=O)C(=NO1)C4=CC=CC=C4Cl",0.619,4,1,4]
["S2565","Amoxicillin Sodium","a6","L1700-13","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Amoxicillin Sodium (Clavulanate,Amoxycillin sodium) is a moderate- spectrum, bacteriolytic, β-lactam antibiotic.",387.39,"34642-77-8",{"v":78,"d":"78.00"},201.35,{"v":78,"d":"78.00"},201.35,"http://selleckchem.com/products/amoxicillin-amox.html","C16H18N3O5S.Na","Sodium Salt","Clavulanate,Amoxycillin sodium","[Na+].CC1(C)SC2C(NC(=O)C(N)C3=CC=C(O)C=C3)C(=O)N2C1C([O-])=O",-1.534,2,3,4]
["S2566","Isoprenaline (NCI-C55630) HCl","b6","L1700-13","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Isoprenaline HCl (NCI-c55630,Isoproterenol hydrochloride) is a non-selective beta-adrenergic receptor agonist, used for the treatment of bradycardia and heart block.",247.72,"51-30-9",{"v":50,"d":"50.00"},201.84,{"v":50,"d":"50.00"},201.84,"http://selleckchem.com/products/Isoprenaline-hydrochloride.html","C11H17NO3.HCl","Hydrochloride","NCI-c55630,Isoproterenol hydrochloride","Cl.CC(C)NCC(O)C1=CC=C(O)C(=C1)O",1.481,0,4,4]
["S2567","Medroxyprogesterone acetate (NSC-26386)","c6","L1700-13","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Medroxyprogesterone acetate (MPA, NSC-26386, Medroxyprogesterone 17-acetate, Farlutin) is a synthetic progestin and act as a potent progesterone receptor agonist, used to treat abnormal menstruation or irregular vaginal bleeding.",386.52,"71-58-9",{"v":12,"d":"12.00"},31.05,"<1","N/A","http://selleckchem.com/products/Medroxyprogesterone-acetate.html","C24H34O4","Free Base","MPA, NSC-26386, Medroxyprogesterone 17-acetate, Farlutin","CC1CC2C(CCC3(C)C2CCC3(OC(C)=O)C(C)=O)C4(C)CCC(=O)C=C14",3.755,4,0,3]
["S2569","Phenylephrine (NCI-C55641) HCl","d6","L1700-13","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Phenylephrine HCl (NCI-c55641,Phenylephrine hydrochloride,(R)-(-)-Phenylephrine hydrochloride, L-Phenylephrine hydrochloride) is a selective α1-adrenergic receptor agonist, used primarily as a decongestant.",203.67,"61-76-7",{"v":41,"d":"41.00"},201.31,{"v":41,"d":"41.00"},201.31,"http://selleckchem.com/products/Phenylephrine-hydrochloride.html","C9H13NO2.HCl","Hydrochloride","NCI-c55641,Phenylephrine hydrochloride,(R)-(-)-Phenylephrine hydrochloride, L-Phenylephrine hydrochloride","Cl.CNCC(O)C1=CC(=CC=C1)O",0.997,0,3,3]
["S2570","Prednisolone Acetate","e6","L1700-13","in 10mM DMSO","Glucocorticoid Receptor","Endocrinology & Hormones","Prednisolone Acetate (Omnipred,Prednisolone-21-acetate) is a synthetic corticosteroid drug that is particularly effective as an immunosuppressant agent.",402.48,"52-21-1",{"v":81,"d":"81.00"},201.25,"<1","N/A","http://selleckchem.com/products/Prednisolone-acetate-Omnipred.html","C23H30O6","free base","Omnipred,Prednisolone-21-acetate","CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC12C",1.639,4,1,4]
["S2573","Tetracaine HCl","f6","L1700-13","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Tetracaine HCl (Amethocaine hydrochloride) is a hydrochloride salt form of tetracaine which is a potent local anaesthetic and a channel function allosteric inhibitor.",300.82,"136-47-0",{"v":60,"d":"60.00"},199.45,{"v":60,"d":"60.00"},199.45,"http://selleckchem.com/products/tetracaine-hydrochloride-pontocaine.html","C15H24N2O2.HCl","Hydrochloride","Amethocaine hydrochloride","Cl.CCCCNC1=CC=C(C=C1)C(=O)OCCN(C)C",3.343,2,1,9]
["S2574","Tetracycline HCl","g6","L1700-13","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture,Selection Antibiotics for Transfected Cell","Microbiology","Tetracycline HCl (NCI-c55561) is a hydrochloride salt of tetracycline that is a broad-spectrum polyketide antibiotic.",{"v":480.9,"d":"480.90"},"64-75-5",{"v":96,"d":"96.00"},199.63,{"v":96,"d":"96.00"},199.63,"http://selleckchem.com/products/tetracycline-hydrochloride.html","C22H24N2O8.HCl","Hydrochloride","NCI-c55561","Cl.CN(C)C1C2CC3C(=C(O)C2(O)C(=O)C(=C1O)C(N)=O)C(=O)C4=C(O)C=CC=C4C3(C)O",-0.513,3,4,2]
["S2585","Brompheniramine hydrogen maleate","f7","L1700-13","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Brompheniramine hydrogen maleate(Brompheniramine maleate) is a histamine H1 receptors antagonist.",435.31,"980-71-2",{"v":87,"d":"87.00"},199.86,{"v":46,"d":"46.00"},105.67,"http://selleckchem.com/products/brompheniramine.html","C16H19BrN2.C4H4","Maleate","Brompheniramine maleate","CN(C)CCC(C1=CC=C(Br)C=C1)C2=CC=CC=N2.OC(=O)\\C=C/C(O)=O",0.784,3,0,7]
["S2599","L-Thyroxine","e8","L1700-13","in 10mM DMSO","THR","Metabolism","L-Thyroxine (NSC 36397,Levothyroxine) is a synthetic form of thyroxine and a hormone replacement drug.",776.87,"51-48-9",{"v":100,"d":"100.00"},128.72,"<1","N/A","http://selleckchem.com/products/l-thyroxine.html","C15H11I4NO4","free base","NSC 36397,Levothyroxine","NC(CC1=CC(=C(OC2=CC(=C(O)C(=C2)I)I)C(=C1)I)I)C(O)=O",2.026,2,2,5]
["S2613","Clorsulon","a10","L1700-13","in 10mM DMSO","Anti-infection","Microbiology","Clorsulon (MK-401,L631529) is used in the treatment of Fasciola hepatica infections in calves and sheep.",380.66,"60200-06-8",{"v":76,"d":"76.00"},199.65,"<1","N/A","http://selleckchem.com/products/clorsulon.html","C8H8Cl3N3O4S2","free base","MK-401,L631529","NC1=CC(=C(C=C1[S](N)(=O)=O)[S](N)(=O)=O)C(Cl)=C(Cl)Cl",0.155,4,3,3]
["S2619","MG132","e10","L1700-13","in 10mM DMSO","Proteasome","Proteases","MG132 ((S,R,S)-(-)-MG132, Z-Leu-D-Leu-Leu-al) is a potent proteasome (ChTL, TL, and PGPH) inhibitor.  MG132 also inhibits calpain (IC50=1.2 μM).",475.62,"1211877-36-9",{"v":90,"d":"90.00"},189.23,"<1","N/A","http://selleckchem.com/products/MG132.html","C26H41N3O5","free base","(S,R,S)-(-)-MG-132, Z-Leu-D-Leu-Leu-al","CC(C)CC(NC(=O)C(CC(C)C)NC(=O)C(CC(C)C)NC(=O)OCC1=CC=CC=C1)C=O",4.371,5,3,15]
["S2637","Fasiglifam(TAK-875) Hemihydrate","e2","L1700-14","in 10mM DMSO","GPR","Endocrinology & Hormones","Fasiglifam(TAK-875) Hemihydrate is a selective GPR40 agonist with EC50 of 14 nM in human GPR40 expressing CHO cell line, 400-fold more potent than oleic acid.",533.63,"1374598-80-7",{"v":100,"d":"100.00"},{"v":187.4,"d":"187.40"},"<1","N/A","http://selleckchem.com/products/tak-875.html","C29H32O7S.1/2H2O","Hemihydrate","N/A","O.CC1=CC(=CC(=C1C2=CC=CC(=C2)COC3=CC=C4C(COC4=C3)CC(O)=O)C)OCCC[S](C)(=O)=O.CC5=CC(=CC(=C5C6=CC=CC(=C6)COC7=CC=C8C(COC8=C7)CC(O)=O)C)OCCC[S](C)(=O)=O",9.968,12,0,22]
["S2658","Omipalisib (GSK2126458)","h2","L1700-14","in 10mM DMSO","Autophagy,mTOR,PI3K","PI3K/Akt/mTOR","Omipalisib (GSK2126458, GSK458) is a highly selective and potent inhibitor of p110α/β/δ/γ, mTORC1/2 with Ki of 0.019 nM/0.13 nM/0.024 nM/0.06 nM and 0.18 nM/0.3 nM in cell-free assays, respectively. Omipalisib induces autophagy. Phase 1.",{"v":505.5,"d":"505.50"},"1086062-66-9",{"v":100,"d":"100.00"},197.82,"<1","N/A","http://selleckchem.com/products/gsk2126458.html","C25H17F2N5O3S","free base","GSK458","COC1=NC=C(C=C1N[S](=O)(=O)C2=CC=C(F)C=C2F)C3=CC=C4N=CC=C(C5=CC=NN=C5)C4=C3",3.705,7,1,6]
["S2666","PF-3845","g3","L1700-14","in 10mM DMSO","FAAH","Metabolism","PF-3845 is a potent, selective and irreversible FAAH inhibitor with Ki of 230 nM, showing negligible activity against FAAH2.",456.46,"1196109-52-0",{"v":91,"d":"91.00"},199.36,"<1","N/A","http://selleckchem.com/products/pf-3845.html","C24H23F3N4O2","free base","N/A","FC(F)(F)C1=CN=C(OC2=CC(=CC=C2)CC3CCN(CC3)C(=O)NC4=CN=CC=C4)C=C1",{"v":4.55,"d":"4.550"},4,1,6]
["S2689","WAY-600","h5","L1700-14","in 10mM DMSO","mTOR","PI3K/Akt/mTOR","WAY-600 is a potent, ATP-competitive and selective inhibitor of mTOR with IC50 of 9 nM; blocks mTORC1/P-S6K(T389) and mTORC2/P-AKT(S473) but not P-AKT(T308); selective for mTOR than PI3Kα (>100-fold) and PI3Kγ (>500-fold).",494.59,"1062159-35-6",{"v":22,"d":"22.00"},44.48,"<1","N/A","http://selleckchem.com/products/way-600.html","C28H30N8O","free base","N/A","C1CN(CCO1)C2=NC(=NC3=C2C=N[N]3C4CCN(CC4)CC5=CC=CN=C5)C6=CC7=C([NH]C=C7)C=C6",2.946,5,1,5]
["S2692","TG101209","c6","L1700-14","in 10mM DMSO","c-RET,FLT3,JAK","JAK/STAT","TG101209 is a selective JAK2 inhibitor with IC50 of 6 nM, less potent to Flt3 and RET (c-RET) with IC50 of 25 nM and 17 nM in cell-free assays, ~30-fold selective for JAK2 than JAK3, sensitive to JAK2V617F and MPLW515L/K mutations.",509.67,"936091-14-4",{"v":102,"d":"102.00"},200.13,"<1","N/A","http://selleckchem.com/products/tg101209.html","C26H35N7O2S","free base","N/A","CN1CCN(CC1)C2=CC=C(NC3=NC=C(C)C(=N3)NC4=CC(=CC=C4)[S](=O)(=O)NC(C)(C)C)C=C2",4.659,4,3,8]
["S2714","LY411575","g7","L1700-14","in 10mM DMSO","Apoptosis related,Notch,Secretase","Proteases","LY411575 is a potent γ-secretase inhibitor with IC50 of 0.078 nM/0.082 nM (membrane/cell-based), also inhibits Notch cleavage with IC50 of 0.39 nM in APP or NΔE expressing HEK293 cells. LY411575 induces apoptosis.",479.48,"209984-57-6",{"v":95,"d":"95.00"},198.13,"<1","N/A","http://selleckchem.com/products/ly-411575.html","C26H23F2N3O4","free base","N/A","CC(NC(=O)C(O)C1=CC(=CC(=C1)F)F)C(=O)NC2C(=O)N(C)C3=C(C=CC=C3)C4=C2C=CC=C4",2.625,3,3,5]
["S2738","PAC-1","e9","L1700-14","in 10mM DMSO","Caspase","Apoptosis","PAC-1 is a potent procaspase-3 activator with EC50 of 0.22 μM and the first small molecule known to directly activate procaspase-3 to caspase-3.",392.49,"315183-21-2",{"v":78,"d":"78.00"},198.73,"<1","N/A","http://selleckchem.com/products/pac-1.html","C23H28N4O2","free base","N/A","OC1=C(CC=C)C=CC=C1/C=N/NC(=O)CN2CCN(CC2)CC3=CC=CC=C3",3.331,2,2,8]
["S2746","AZ 628","c10","L1700-14","in 10mM DMSO","Apoptosis related,Raf","MAPK","AZ628 is a new pan-Raf inhibitor for BRAF, BRAFV600E, and c-Raf-1 with IC50 of 105 nM, 34 nM and 29 nM in cell-free assays, also inhibits VEGFR2, DDR2, Lyn, Flt1, FMS, etc. AZ628 induces apoptosis.",451.52,"878739-06-1",{"v":90,"d":"90.00"},199.33,"<1","N/A","http://selleckchem.com/products/az628.html","C27H25N5O2","free base","N/A","CN1C=NC2=C(C=C(NC3=CC(=CC=C3C)NC(=O)C4=CC(=CC=C4)C(C)(C)C#N)C=C2)C1=O",{"v":4.57,"d":"4.570"},3,2,5]
["S2760","Canagliflozin (JNJ 28431754)","g11","L1700-14","in 10mM DMSO","SGLT","GPCR & G Protein","Canagliflozin (TA 7284, JNJ 28431754) is a highly potent and selective SGLT2 inhibitor for hSGLT2 with IC50 of 2.2 nM in a cell-free assay, exhibits 413-fold selectivity over hSGLT1.",444.52,"842133-18-0",{"v":88,"d":"88.00"},197.97,"<1","N/A","http://selleckchem.com/products/canagliflozin.html","C24H25FO5S","free base","TA 7284","CC1=C(CC2=CC=C(S2)C3=CC=C(F)C=C3)C=C(C=C1)C4OC(CO)C(O)C(O)C4O",3.446,1,4,5]
["S2765","MK-2048","b2","L1700-15","in 10mM DMSO","Integrase","Microbiology","MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.",461.87,"869901-69-9",{"v":9,"d":"9.00"},19.49,"<1","N/A","http://selleckchem.com/products/mk-2048.html","C21H21ClFN5O4","free base","N/A","CCN1CC(C)[N]2C(=C(O)C3=C2C(=NN(CC4=CC=C(F)C(=C4)Cl)C3=O)C(=O)NC)C1=O",2.446,4,2,4]
["S2776","Devimistat (CPI-613)","b3","L1700-15","in 10mM DMSO","Apoptosis related,Dehydrogenase","Metabolism","Devimistat (CPI-613), a lipoate analog, inhibits mitochondrial enzymes pyruvate dehydrogenase (PDH) and α-ketoglutarate dehydrogenase in NCI-H460 cell line, disrupts tumor cell mitochondrial metabolism. CPI-613 induces apoptosis in pancreatic cancer cells. Phase 2.",388.59,"95809-78-2",{"v":77,"d":"77.00"},198.15,"<1","N/A","http://selleckchem.com/products/cpi-613.html","C22H28O2S2","free base","N/A","OC(=O)CCCCC(CCSCC1=CC=CC=C1)SCC2=CC=CC=C2",{"v":5.63,"d":"5.630"},1,0,13]
["S2790","Istradefylline","f4","L1700-15","in 10mM DMSO","Adenosine Receptor","GPCR & G Protein","Istradefylline (KW-6002) is a selective adenosine A2A receptor (A2AR) antagonist with Ki of 2.2 nM. Phase 3.",384.43,"155270-99-8",{"v":6,"d":"6.00"},15.61,"<1","N/A","http://selleckchem.com/products/istradefylline-kw-6002.html","C20H24N4O4","free base","KW-6002","CCN1C(=O)N(CC)C2=C([N](C)C(=N2)\\C=C\\C3=CC=C(OC)C(=C3)OC)C1=O",2.957,5,0,6]
["S2799","Daporinad","e5","L1700-15","in 10mM DMSO","Autophagy,NAMPT,Transferase","Metabolism","Daporinad (FK866, APO866) effectively inhibits nicotinamide phosphoribosyltransferase (NMPRTase; Nampt) with IC50 of 0.09 nM in a cell-free assay. Daporinad (FK866, APO866) triggers autophagy. Phase 1/2.",391.51,"658084-64-1",{"v":78,"d":"78.00"},199.23,"<1","N/A","http://www.selleck.cn/products/apo866-fk866.html","C24H29N3O2","Free Base","FK866, APO866","O=C(NCCCCC1CCN(CC1)C(=O)C2=CC=CC=C2)/C=C/C3=CC=CN=C3",3.269,3,1,8]
["S2816","Tyrphostin AG 879","a7","L1700-15","in 10mM DMSO","HER2","Protein Tyrosine Kinase","Tyrphostin AG 879 potently inhibits HER2/ErbB2 with IC50 of 1 μM, 100- and 500-fold higher selective to ErbB2 than PDGFR and EGFR.",316.46,"148741-30-4",{"v":36,"d":"36.00"},113.76,"<1","N/A","http://selleckchem.com/products/tyrphostin-ag-879-ag-879.html","C18H24N2OS","free base","AG 879","CC(C)(C)C1=C(O)C(=CC(=C1)/C=C(C#N)/C(N)=S)C(C)(C)C",4.565,0,2,4]
["S2840","Apalutamide (ARN-509)","e8","L1700-15","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Apalutamide (ARN-509) is a selective and competitive androgen receptor inhibitor with IC50 of 16 nM in a cell-free assay, useful for prostate cancer treatment. Phase 3.",477.43,"956104-40-8",{"v":18,"d":"18.00"},{"v":37.7,"d":"37.70"},"<1","N/A","http://selleckchem.com/products/arn-509.html","C21H15F4N5O2S","free base","N/A","CNC(=O)C1=CC=C(C=C1F)N2C(=S)N(C(=O)C23CCC3)C4=CN=C(C#N)C(=C4)C(F)(F)F",4.452,3,1,4]
["S2853","Carfilzomib (PR-171)","e9","L1700-15","in 10mM DMSO","Apoptosis related,Autophagy,COVID-19,Proteasome","Proteases","Carfilzomib (PR-171) is an irreversible proteasome inhibitor with IC50 of <5 nM in ANBL-6 cells, displayed preferential in vitro inhibitory potency against the ChT-L activity in the β5 subunit, but little or no effect on the PGPH and T-L activities. Carfilzomib activates prosurvival autophagy and induces cell apoptosis.",719.91,"868540-17-4",{"v":50,"d":"50.00"},69.45,"<1","N/A","http://selleckchem.com/products/carfilzomib-pr-171.html","C40H57N5O7","free base","N/A","CC(C)CC(NC(=O)C(CCC1=CC=CC=C1)NC(=O)CN2CCOCC2)C(=O)NC(CC3=CC=CC=C3)C(=O)NC(CC(C)C)C(=O)C4(C)CO4",3.799,7,4,20]
["S2865","VUF 10166","a11","L1700-15","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","VUF10166 is a novel, potent and competitive antagonist for 5-HT3A receptor with Ki of 0.04 nM, its affinity at 5-HT3AB receptor is significantly lower.",262.74,"155584-74-0",{"v":21,"d":"21.00"},79.93,"<1","N/A","http://selleckchem.com/products/vuf-10166.html","C13H15ClN4","free base","N/A","CN1CCN(CC1)C2=NC3=CC=CC=C3N=C2Cl",2.826,2,0,1]
["S2872","GW5074","f11","L1700-15","in 10mM DMSO","Apoptosis related,Raf","MAPK","GW5074 is a potent and selective c-Raf inhibitor with IC50 of 9 nM, no effect on the activities of JNK1/2/3, MEK1, MKK6/7, CDK1/2, c-Src, p38 MAP, VEGFR2 or c-Fms is noted. GW5074 inhibits LK-induced apoptosis.",520.94,"220904-83-6",{"v":104,"d":"104.00"},199.64,"<1","N/A","http://selleckchem.com/products/gw5074.html","C15H8Br2INO2","free base","N/A","OC1=C(Br)C=C(C=C1Br)C=C2C(=O)NC3=CC=C(I)C=C23",4.564,1,2,1]
["S2884","Acesulfame Potassium","d2","L1700-16","in 10mM DMSO","Others","Others","Acesulfame potassium is a non-nutritive sweetener.",202.25,"55589-62-3",{"v":40,"d":"40.00"},197.78,{"v":40,"d":"40.00"},197.78,"http://selleckchem.com/products/acesulfame-potassium.html","C4H5NO4S.K","Potassium Salt","N/A","[KH].CC1=CC(=O)N[S](=O)(=O)O1",-0.858,2,1,0]
["S2901","CCG 50014","h3","L1700-16","in 10mM DMSO","RGS","GPCR & G Protein","CCG 50014 is a potent and selective inhibitor of RGS4 with IC50 of 30 nM.",316.35,"883050-24-6",{"v":63,"d":"63.00"},199.15,"<1","N/A","http://selleckchem.com/products/ccg-50014.html","C16H13FN2O2S","free base","N/A","CC1=CC=C(C=C1)N2SC(=O)N(CC3=CC=C(F)C=C3)C2=O",4.414,2,0,3]
["S2910","Tempol","g4","L1700-16","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Tempol (4-Hydroxy-TEMPO) is a superoxide scavenger that displays neuroprotective, anti-inflammatory and analgesic effects. Phase 2.",172.24,"2226-96-2",{"v":34,"d":"34.00"},{"v":197.4,"d":"197.40"},{"v":34,"d":"34.00"},{"v":197.4,"d":"197.40"},"http://selleckchem.com/products/tempol-4-hydroxy-tempo.html","C9H18NO2","free base","4-Hydroxy-TEMPO","CC1(C)CC(O)CC(C)(C)N1[O]",0.413,0,1,0]
["S2919","IOX2","g5","L1700-16","in 10mM DMSO","HIF","Angiogenesis","IOX2 (JICL38) is a potent inhibitor of HIF-1α prolyl hydroxylase-2 (PHD2) with IC50 of 21 nM in a cell-free assay, >100-fold selectivity over JMJD2A, JMJD2C, JMJD2E, JMJD3, or the 2OG oxygenase FIH.",352.34,"931398-72-0",{"v":7,"d":"7.00"},19.87,"<1","N/A","http://selleckchem.com/products/iox2.html","C19H16N2O5","free base","JICL38","OC(=O)CNC(=O)C1=C(O)C2=C(C=CC=C2)N(CC3=CC=CC=C3)C1=O",1.153,3,2,5]
["S3012","Pazopanib","h7","L1700-16","in 10mM DMSO","Autophagy,Cathepsin B,c-Kit,CSF-1R,Cysteine Protease,FGFR,PDGFR,VEGFR","Protein Tyrosine Kinase","Pazopanib (GW786034) is a novel multi-target inhibitor of VEGFR1, VEGFR2, VEGFR3, PDGFR, FGFR, c-Kit and c-Fms/CSF1R with IC50 of 10 nM, 30 nM, 47 nM, 84 nM, 74 nM, 140 nM and 146 nM in cell-free assays, respectively. Pazopanib induces cathepsin B activation and autophagy.",437.52,"444731-52-6",{"v":87,"d":"87.00"},198.85,"<1","N/A","http://selleckchem.com/products/pazopanib.html","C21H23N7O2S","Free Base","GW786034","C[N]1N=C2C=C(C=CC2=C1C)N(C)C3=NC(=NC=C3)NC4=CC=C(C)C(=C4)[S](N)(=O)=O",3.741,5,2,5]
["S3023","Bufexamac","g8","L1700-16","in 10mM DMSO","COX,IFN","Neuronal Signaling","Bufexamac(Bufexamic acid) is a COX inhibitor for IFN-α release with EC50 of 8.9 μM.",223.27,"2438-72-4",{"v":45,"d":"45.00"},201.55,"<1","N/A","http://selleckchem.com/products/bufexamac.html","C12H17NO3","free base","Bufexamic acid","CCCCOC1=CC=C(CC(=O)NO)C=C1",2.191,2,1,6]
["S3038","Fosaprepitant dimeglumine salt","c10","L1700-16","in 10mM DMSO","Neurokinin Receptor","Neuronal Signaling","Fosaprepitant dimeglumine salt (MK-0517) is a water-soluble phosphoryl prodrug for Aprepitant which is a NK1 antagonist.",1004.83,"265121-04-8",{"v":201,"d":"201.00"},200.03,{"v":135,"d":"135.00"},134.35,"http://selleckchem.com/products/fosaprepitant.html","C23H22F7N4O6P.2C7H17NO5","dimeglumine salt","MK-0517","CNCC(O)C(O)C(O)C(O)CO.CNCC(O)C(O)C(O)C(O)CO.CC(OC1OCCN(CC2=NN(C(=O)N2)[P](O)(O)=O)C1C3=CC=C(F)C=C3)C4=CC(=CC(=C4)C(F)(F)F)C(F)(F)F",-1.235,4,13,21]
["S3046","Azilsartan","f10","L1700-16","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Azilsartan (TAK-536) is an angiotensin II type 1 (AT1) receptor antagonist with IC50 of 2.6 nM.",456.45,"147403-03-0",{"v":91,"d":"91.00"},199.36,"<1","N/A","http://selleckchem.com/products/azilsartan-tak-536.html","C25H20N4O5","free base","TAK-536","CCOC1=NC2=CC=CC(=C2[N]1CC3=CC=C(C=C3)C4=CC=CC=C4C5=NC(=O)ON5)C(O)=O",4.662,6,1,7]
["S3061","Epinephrine HCl","f11","L1700-16","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Epinephrine HCl (Adrenaline) is a hormone and a neurotransmitter.",219.67,"55-31-2",{"v":44,"d":"44.00"},{"v":200.3,"d":"200.30"},{"v":44,"d":"44.00"},{"v":200.3,"d":"200.30"},"http://selleckchem.com/products/epinephrine-hcl-adrenaline.html","C9H13NO3.HCl","HCl","Adrenaline","Cl.CNCC(O)C1=CC=C(O)C(=C1)O",0.754,0,4,3]
["S3081","Ulipristal Acetate (CDB 2914)","b3","L1700-17","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Ulipristal acetate (CDB-2914, HRP 2000, RU 44675) is a selective SPRM for emergency contraception after an unprotected intercourse or contraceptive failure.",475.62,"126784-99-4",{"v":83,"d":"83.00"},191.43,"<1","N/A","http://selleckchem.com/products/ulipristal.html","C30H37NO4","free base","HRP 2000, RU 44675","CN(C)C1=CC=C(C=C1)C2CC3(C)C(CCC3(OC(C)=O)C(C)=O)C4CCC5=CC(=O)CCC5=C24",4.309,2,0,3]
["S3117","Oxybutynin hydrochloride","c4","L1700-17","in 10mM DMSO","AChR","Neuronal Signaling","Oxybutynin(MJ4309-1) is an anticholinergic medication used to relieve urinary and bladder difficulties.",393.95,"1508-65-2",{"v":79,"d":"79.00"},200.53,{"v":4,"d":"4.00"},10.15,"https://www.selleckchem.com/products/oxybutynin-hydrochloride.html","C22H31NO3.HCl","hydrochloride","MJ4309-1","Cl.CCN(CC)CC#CCOC(=O)C(O)(C1CCCCC1)C2=CC=CC=C2",5.028,2,0,10]
["S3144","Darifenacin HBr","f5","L1700-17","in 10mM DMSO","AChR","Neuronal Signaling","Darifenacin HBr (UK-88525) is a selective M3 muscarinic receptor antagonist with pKi of 8.9.",507.46,"133099-07-7",{"v":100,"d":"100.00"},197.06,"<1","N/A","http://selleckchem.com/products/darifenacin-hydrobromide.html","C28H30N2O2.HBr","HBr","UK-88525","Br.NC(=O)C(C1CCN(CCC2=CC=C3OCCC3=C2)C1)(C4=CC=CC=C4)C5=CC=CC=C5",5.048,2,1,7]
["S3167","Altrenogest","b7","L1700-17","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Altrenogest (A35957, RU2267,R2267) is a progestogen structurally related to veterinary steroid trenbolone.",310.43,"850-52-2",{"v":62,"d":"62.00"},199.72,"<1","N/A","http://selleckchem.com/products/altrenogest.html","C21H26O2","free base","A35957, RU2267,R2267","CC12C=CC3=C4CCC(=O)C=C4CCC3C1CCC2(O)CC=C",3.561,1,0,2]
["S3179","Carbenicillin disodium","a8","L1700-17","in 10mM DMSO","Antibiotics,Antibiotics for Plant Cell Culture,Bacterial,Selection Antibiotics for Transfected Cell","Microbiology","Carbenicillin (BRL-2064,α-carboxybenzylpenicillin) is a semi-synthetic penicillin antibiotic which interferes with cell wall synthesis of gram-negative bacteria while displaying low toxicity.",422.36,"4800-94-6",{"v":5,"d":"5.00"},11.84,{"v":84,"d":"84.00"},198.88,"http://selleckchem.com/products/carbenicillin-disodium.html","C17H16N2Na2O6S","Disodium","BRL-2064,α-carboxybenzylpenicillin","[Na+].[Na+].CC1(C)SC2C(NC(=O)C(C([O-])=O)C3=CC=CC=C3)C(=O)N2C1C([O-])=O",-2.218,2,1,5]
["S3201","Trifluoperazine 2HCl","f9","L1700-17","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Trifluoperazine (NSC-17474, RP-7623, SKF-5019) 2HCl is a dopamine D2 receptor inhibitor with IC50 of 1.1 nM. Trifluoperazine also inhibits calmodulin (CaM).",480.42,"440-17-5",{"v":88,"d":"88.00"},183.17,{"v":96,"d":"96.00"},199.83,"http://selleckchem.com/products/trifluoperazine-dihydrochloride.html","C21H24F3N3S.2HCl","2HCl","SKF5019","Cl.Cl.CN1CCN(CCCN2C3=C(SC4=CC=C(C=C24)C(F)(F)F)C=CC=C3)CC1",5.739,0,0,5]
["S3606","Fangchinoline","f10","L1700-17","in 10mM DMSO","Reverse Transcriptase","Microbiology","Fangchinoline, a bisbenzylisoquinoline alkaloid, is a novel HIV-1 inhibitor with pain-relieving, blood pressure-depressing, and antibiotic activities.",608.72,"33889-68-8",{"v":100,"d":"100.00"},164.28,"<1","N/A","http://selleckchem.com/products/r-s-fangchinoline.html","C37H40N2O6","free base","N/A","COC1=C2OC3=CC=C(CC4N(C)CCC5=C4C=C(OC6=C(O)C(=CC7=C6C(CC(=C2)C=C1)N(C)CC7)OC)C(=C5)OC)C=C3",6.992,5,1,3]
["S3610","Cordycepin","a11","L1700-17","in 10mM DMSO","MMP","Proteases","Cordycepin (3'-Deoxyadenosine) is an adenosine analogue, which is readily phosphorylated to its mono-, di-, and triphosphate intracellularly. It has a very potent anti-cancer, anti-oxidant and anti-inflammatory activities.",251.24,"73-03-0",{"v":50,"d":"50.00"},199.01,{"v":25,"d":"25.00"},99.51,"http://selleckchem.com/products/cordycepin.html","C10H13N5O3","free base","3'-Deoxyadenosine","NC1=NC=NC2=C1N=C[N]2C3OC(CO)CC3O",-1.308,4,3,2]
["S3622","Diammonium Glycyrrhizinate","b2","L1700-18","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Diammonium glycyrrhizinate (DG), a traditional Chinese medicine (TCM), is extracted and purified from liquorices (Radix glycyrrhizae). It is known for its anti-inflammatory effects, resistance to biologic oxidation and membranous protection. DG is able to reduce inflammatory injury via suppression of NF‑κB, TNF‑α and intercellular adhesion molecule 1.",856.99,"79165-06-3",{"v":100,"d":"100.00"},116.69,{"v":100,"d":"100.00"},116.69,"http://selleckchem.com/products/diammonium-glycyrrhizinate.html","C42H62O16.2H3N","ammonium salt","N/A","N.N.CC1(C)C(CCC2(C)C1CCC3(C)C2C(=O)C=C4C5CC(C)(CCC5(C)CCC34C)C(O)=O)OC6OC(C(O)C(O)C6OC7OC(C(O)C(O)C7O)C(O)=O)C(O)=O",-4.247,8,5,7]
["S3635","Medroxyprogesterone","e3","L1700-18","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Medroxyprogesterone (MP) is a synthetic pregnane steroid and a derivative of progesterone. It is a potent progesterone receptor agonist.",344.49,"520-85-4",{"v":68,"d":"68.00"},197.39,"<1","N/A","http://selleckchem.com/products/medroxyprogesterone.html","C22H32O3","free base","MP","CC1CC2C(CCC3(C)C2CCC3(O)C(C)=O)C4(C)CCC(=O)C=C14",3.376,2,0,1]
["S3652","3-Nitropropionic acid","a5","L1700-18","in 10mM DMSO","Dehydrogenase","Metabolism","3-Nitropropionic acid (β-Nitropropionic Acid, 3-NP) is an irreversible inhibitor of mitochondrial respiratory Complex II succinate dehydrogenase, resulting in energy depletion through disruption of the electron transport chain.",119.08,"504-88-1",{"v":23,"d":"23.00"},193.15,{"v":23,"d":"23.00"},193.15,"http://selleckchem.com/products/3-nitropropionic-acid.html","C3H5NO4","free base","β-Nitropropionic Acid, 3-NP","OC(=O)CC[N+]([O-])=O",{"v":0.02,"d":"0.020"},1,0,3]
["S3659","Fludrocortisone acetate","h5","L1700-18","in 10mM DMSO","Others","Others","Fludrocortisone (9α-fluorocortisol) is a synthetic pregnane steroid and a halogenated derivative of cortisol. It is used to treat adrenogenital syndrome, postural hypotension, and adrenal insufficiency.",422.49,"514-36-3",{"v":84,"d":"84.00"},198.82,"<1","N/A","http://selleckchem.com/products/fludrocortisone-acetate.html","C23H31FO6","free base","9α-fluorocortisol acetate","CC(=O)OCC(=O)C1(O)CCC2C3CCC4=CC(=O)CCC4(C)C3(F)C(O)CC12C",1.791,4,1,4]
["S3672","Cefonicid sodium","a7","L1700-18","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Cefonicid sodium (Monocid) is a cephalosporin antibiotic. It interferes with cell wall biosynthesis in bacteria, leading to lysis of the infectious organism.",586.53,"61270-78-8",{"v":100,"d":"100.00"},170.49,{"v":100,"d":"100.00"},170.49,"http://selleckchem.com/products/cefonicid-sodium.html","C18H16N6O8S3.2Na","disodium salt","Monocid sodium","[Na+].[Na+].OC(C(=O)NC1C2SCC(=C(N2C1=O)C([O-])=O)CSC3=NN=N[N]3C[S]([O-])(=O)=O)C4=CC=CC=C4",-4.327,5,2,9]
["S3689","Ethidium bromide","a9","L1700-18","in 10mM DMSO","Others","Others","Ethidium Bromide (Homidium bromide, EtBr, EB) is an intercalating agent which resembles a DNA base pair and commonly used as a fluorescent tag (nucleic acid stain) in molecular biology laboratories for techniques such as agarose gel electrophoresis.",394.31,"1239-45-8",{"v":78,"d":"78.00"},197.81,{"v":7,"d":"7.00"},17.75,"http://selleckchem.com/products/ethidium-bromide.html","C21H20N3.Br","bromide","Homidium bromide, EtBr, EB","[Br-].CC[N+]1=C2C=C(N)C=CC2=C3C=CC(=CC3=C1C4=CC=CC=C4)N",{"v":1.79,"d":"1.790"},0,2,2]
["S3696","PTP Inhibitor I","h9","L1700-18","in 10mM DMSO","phosphatase","Metabolism","PTP Inhibitor I is a cell-permeable, protein tyrosine phosphatase (PTP) inhibitor with Ki values of 43 and 42 μM for SHP-1(ΔSH2) and PTP1B, respectively.",215.04,"2491-38-5",{"v":43,"d":"43.00"},199.96,"<1","N/A","http://selleckchem.com/products/ptp-inhibitor-i.html","C8H7BrO2","free base","α-Bromo-4-hydroxyacetophenone, 2-Bromo-4'-hydroxyacetophenone, 4-Hydroxyphenacyl bromide, SHP-1 Inhibitor II","OC1=CC=C(C=C1)C(=O)CBr",2.005,1,1,2]
["S3699","2,3-Butanedione-2-monoxime","c10","L1700-18","in 10mM DMSO","MLCK","Cytoskeletal Signaling","2,3-Butanedione monoxime (BDM, Diacetyl monoxime, Diacetylmonoxime) is the well-characterized, low-affinity, non-competitive inhibitor of skeletal muscle myosin-II and inhibits skeletal and cardiac muscle contraction.",{"v":101.1,"d":"101.10"},"57-71-6",{"v":20,"d":"20.00"},197.82,{"v":20,"d":"20.00"},197.82,"http://selleckchem.com/products/2-3-butanedione-2-monoxime.html","C4H7NO2","free base","Diacetyl monoxime, Diacetylmonoxime","CC(=O)\\C(C)=N\\O",-0.161,2,0,1]
["S3720","Elafibranor","d2","L1700-19","in 10mM DMSO","PPAR","Metabolism","Elafibranor (GFT505) is an agonist of the peroxisome proliferator-activated receptor-α(PPAR-alpha) and peroxisome proliferator-activated receptor-δ(PPAR-δ). It improves insulin sensitivity, glucose homeostasis, and lipid metabolism and reduces inflammation.",384.49,"923978-27-2",{"v":76,"d":"76.00"},197.66,"<1","N/A","http://selleckchem.com/products/elafibranor.html","C22H24O4S","free base","GFT505","CSC1=CC=C(C=C1)C(=O)\\C=C\\C2=CC(=C(OC(C)(C)C(O)=O)C(=C2)C)C",5.477,3,0,7]
["S3724","Velpatasvir","g2","L1700-19","in 10mM DMSO","COVID-19,HCV Protease","Proteases","Velpatasvir (GS-5816,VEL) is a second-generation NS5A inhibitor that inhibits hepatitis C viral replication through acting on the crucial \"membranous web\" that facilitates RNA replication.",{"v":883,"d":"883.00"},"1377049-84-7",{"v":100,"d":"100.00"},113.25,{"v":100,"d":"100.00"},113.25,"http://selleckchem.com/products/velpatasvir.html","C49H54N8O8","free base","GS-5816,VEL","COCC1CC(N(C1)C(=O)C(NC(=O)OC)C2=CC=CC=C2)C3=NC=C([NH]3)C4=CC=C5C(=C4)COC6=C5C=C7C=CC8=C(N=C([NH]8)C9CCC(C)N9C(=O)C(NC(=O)OC)C(C)C)C7=C6",5.789,10,4,13]
["S3739","Calcipotriene","c4","L1700-19","in 10mM DMSO","Vitamin","Metabolism","Calcipotriene (Calcipotriol, MC903) is a synthetic derivative of calcitriol, a form of vitamin D. It can induce differentiation and suppresses proliferation of keratinocytes, reversing abnormal keratinocyte changes in psoriasis, and lead to normalization of epidermal growth.  Calcipotriol is a synthetic VitD3 analogue with a high affinity for the vitamin D receptor.",{"v":412.6,"d":"412.60"},"112965-21-6",{"v":82,"d":"82.00"},198.74,"<1","N/A","http://selleckchem.com/products/calcipotriene.html","C27H40O3","free base","Calcipotriol, MC903","CC(\\C=C\\C(O)C1CC1)C2CCC3/C(CCCC23C)=C/C=C\\4CC(O)CC(O)C4=C",4.679,0,3,5]
["S3757","2'-Deoxyinosine","e5","L1700-19","in 10mM DMSO","Others","Others","2’-Deoxyinosine (Guanine deoxyriboside, Deoxyinosine) is the nucleoside form of hypoxanthine. It is a product of DNA damage that is formed from 2’-deoxyadenosine by adenosine deaminase or reactive nitrogen species. 2’-deoxyinosine enhances apoptosis induced by 5-fluorouracil in HT-29 and SW620 cancer cells.",252.23,"890-38-0",{"v":24,"d":"24.00"},95.15,"N/A","N/A","http://selleckchem.com/products/2-deoxyinosine.html","C10H12N4O4","free base","Guanine deoxyriboside, Deoxyinosine","OCC1OC(CC1O)[N]2C=NC3=C2N=CNC3=O",-1.482,4,3,2]
["S3772","5-Hydroxymethylfurfural","g6","L1700-19","in 10mM DMSO","Others","Others","5-Hydroxymethylfurfural (5-HMF) is an important bio-sourced intermediate, formed from carbohydrates such as glucose or fructose and used for production of fuels and chemical intermediates.",126.11,"67-47-0",{"v":25,"d":"25.00"},198.24,"N/A","N/A","http://selleckchem.com/products/5-hydroxymethylfurfural.html","C6H6O3","free base","N/A","OCC1=CC=C(O1)C=O",0.458,2,1,2]
["S3784","Obacunone (AI3-37934)","c8","L1700-19","in 10mM DMSO","Aromatase,Nrf2","Endocrinology & Hormones","Obacunone (AI3-37934, CCRIS 8657), a natural compound present in citrus fruits, has been demonstrated for various biological activities including anti-cancer and anti-inflammatory properties. It significantly inhibits aromatase activity in an in vitro enzyme assay with an IC50 value of 28.04 μM; also a novel activator of Nrf2.",454.51,"751-03-1",{"v":90,"d":"90.00"},198.02,"N/A","N/A","http://selleckchem.com/products/obacunone.html","C26H30O7","free base","CCRIS 8657","CC1(C)OC(=O)C=CC2(C)C3CCC4(C)C(OC(=O)C5OC45C3(C)C(=O)CC12)C6=COC=C6",2.715,7,0,1]
["S3791","Succinic acid","b9","L1700-19","in 10mM DMSO","Others","Metabolism","Succinic acid (1,4-Butandioic Acid, 1,2-Ethanedicarboxylic acid, Amber acid, Asuccin, Butanedioic acid) is a crystalline organic acid which occurs in living tissue as an intermediate in glucose metabolism.",118.09,"110-15-6",{"v":23,"d":"23.00"},194.77,"N/A","N/A","http://selleckchem.com/products/succinic-acid.html","C4H6O4","free base","1,4-Butandioic Acid, 1,2-Ethanedicarboxylic acid, Amber acid, Asuccin, Butanedioic acid","OC(=O)CCC(O)=O",{"v":-0.36,"d":"-0.360"},2,0,3]
["S3796","Rebaudioside A","f9","L1700-19","in 10mM DMSO","Carbohydrate Metabolism","Metabolism","Rebaudioside A (Stevia Extract, Reb A, Glycoside A3, Stevioside A3), an natural sweetening ingredient extracted from the stevia leaf, is used in powder or liquid form to heighten sweetening intensity and improve taste. Rebaudioside A is a steviol glycoside, α-glucosidase inhibitor with IC50 of 35.01 μg/ml.can inhibit ATP-sensitive K+-channels.",967.01,"58543-16-1",{"v":40,"d":"40.00"},41.36,"N/A","N/A","http://selleckchem.com/products/rebaudioside-a.html","C44H70O23","free base","Reb A, Glycoside A3, Stevioside A3","CC12CCCC(C)(C1CCC34CC(=C)C(CCC23)(C4)OC5OC(CO)C(O)C(OC6OC(CO)C(O)C(O)C6O)C5OC7OC(CO)C(O)C(O)C7O)C(=O)OC8OC(CO)C(O)C(O)C8O",-3.476,9,14,13]
["S3814","Tubeimoside I","f11","L1700-19","in 10mM DMSO","Apoptosis related","Apoptosis","Tubeimoside I (Lobatoside H, TBMS1), a triterpenoid saponin, isolated from the tubers of Bolbostemma paniculatum, shows potent antitumor and antitumor-promoting effects.",1319.43,"102040-03-9",{"v":100,"d":"100.00"},268.55,"N/A","N/A","http://selleckchem.com/products/tubeimoside-i.html","C63H98O29","free base","Lobatoside H","CC1OC(OC2C(O)C(O)COC2OC(=O)C34CCC(C)(C)CC3C5=CCC6C7(C)CC(O)C8OC9OC(CO)C(O)C(O)C9OC%10OCC(O)C(O)C%10OC(=O)CC(C)(O)CC(=O)OCC8(C)C7CCC6(C)C5(C)CC4)C(O)C(OC%11OCC(O)C(O)C%11O)C1O",-1.606,15,13,8]
["S3817","Harmine hydrochloride","a2","L1700-20","in 10mM DMSO","5-HT Receptor,ADC Cytotoxin,DYRK,MAO","Cell Cycle","Harmine (Telepathine), a fluorescent harmala alkaloid belonging to the beta-carboline family of compounds, is a highly cell-permeant and competitive inhibitor of ATP binding to the kinase pocket of DYRK1A, with about 60-fold higher IC50 value for DYRK2. Harmine also inhibits monoamine oxidases (MAOs), PPARγ and cdc-like kinases (CLKs). Harmine inhibits 5-HT2A serotonin receptor with Ki of 397 nM.",248.71,"343-27-1",{"v":21,"d":"21.00"},84.44,"N/A","N/A","http://selleckchem.com/products/harmine-hydrochloride.html","C13H12N2O.HCl","hydrochloride","Telepathine hydrochloride","Cl.COC1=CC2=C(C=C1)C3=CC=NC(=C3[NH]2)C",{"v":2.82,"d":"2.820"},2,1,1]
["S3832","Euphorbiasteroid","e3","L1700-20","in 10mM DMSO","AMPK","PI3K/Akt/mTOR","Euphorbiasteroid (Euphorbia factor L1), a component of Euphorbia lathyris L., inhibits adipogenesis of 3T3-L1 cells through activation of the AMPK pathway and induces HL-60 cells to apoptosis via promoting Bcl-2/Bax apoptotic signaling pathway in a dose-dependent manner. Euphorbiasteroid is a tricyclic diperpene of Euphorbia lathyris L., inhibits tyrosinase, and increases the phosphorylation of AMPK, with anti-cancer, anti-virus, anti-obesity and multidrug resistance-modulating effect.",552.66,"28649-59-4",{"v":21,"d":"21.00"},{"v":38,"d":"38.00"},"N/A","N/A","http://selleckchem.com/products/euphorbiasteroid.html","C32H40O8","free base","Euphorbia factor L1","CC1CC2(OC(C)=O)C(C1OC(=O)CC3=CC=CC=C3)C(OC(C)=O)C4(CCC5C(\\C=C(C)\\C2=O)C5(C)C)CO4",4.183,8,0,8]
["S3840","Baohuoside I","e4","L1700-20","in 10mM DMSO","ROS","Immunology & Inflammation","Baohuoside I (Icariside II) is a flavonoid isolated from Epimedium koreanum Nakai with anti-inflammatory and anti-cancer activities. It may exert cytotoxic effect via the ROS/MAPK pathway.",514.52,"113558-15-9",{"v":100,"d":"100.00"},194.36,"N/A","N/A","http://selleckchem.com/products/baohuoside-i.html","C27H30O10","Flavonoid glycoside","Icariside II","COC1=CC=C(C=C1)C2=C(OC3OC(C)C(O)C(O)C3O)C(=O)C4=C(O)C=C(O)C(=C4O2)CC=C(C)C",2.913,5,5,6]
["S3854","Tetrahydropalmatine hydrochloride","a6","L1700-20","in 10mM DMSO","ADC Cytotoxin,Dopamine Receptor","Neuronal Signaling","Tetrahydropalmatine (THP, Gindarine, 1-Tetrahydropalmitine) is an isoquinoline alkaloid found in several different plant species, mainly in the Corydalis genus (Yan Hu Suo), but also in other plants such as Stephania rotunda. It is a potent  muscle relaxant. Tetrahydropalmatine hydrochloride acts through inhibition of amygdaloid release of dopamine to inhibit an epileptic attack in rats.",391.89,"6024-85-7",{"v":12,"d":"12.00"},30.62,"N/A","N/A","http://selleckchem.com/products/tetrahydropalmatine-hydrochloride.html","C21H25NO4.HCl","hydrochloride","Gindarine hydrochloride, 1-Tetrahydropalmitine HCl","Cl.COC1=C(OC)C2=C(CC3N(CCC4=C3C=C(OC)C(=C4)OC)C2)C=C1",3.981,4,0,4]
["S3867","(E)-Cardamonin","e7","L1700-20","in 10mM DMSO","NF-κB,TRP Channel","NF-κB","(E)-Cardamonin (Alpinetin chalcone, cardamomin) is a naturally occurring chalcone with strong anti-inflammatory activity. It is a novel TRPA1 antagonist with IC50 of 454 nM and also a NF-kB inhibitor.",270.28,"19309-14-9",{"v":54,"d":"54.00"},199.79,"N/A","N/A","http://selleckchem.com/products/e-cardamoni.html","C16H14O4","free base","Alpinetin chalcone, cardamomin","COC1=CC(=CC(=C1C(=O)\\C=C\\C2=CC=CC=C2)O)O",3.201,2,2,4]
["S3872","Guaiacol","b8","L1700-20","in 10mM DMSO","COX,NF-κB","NF-κB","Guaiacol (O-methoxyphenol, 2-hydroxyanisole, O-methylcatechol) is a phenolic natural product first isolated from Guaiac resin and the oxidation of lignin. It is a precursor to various flavorants, such as eugenoland vanillin. Guaiacol, a phenolic compound isolated from Guaiac resin, inhibits LPS-stimulated COX-2 expression and NF-κB activation. Anti-inflammatory activity.",124.14,"90-05-1",{"v":24,"d":"24.00"},193.33,"N/A","N/A","http://selleckchem.com/products/guaiacol.html","C7H8O2","free base","o-methoxyphenol, 2-hydroxyanisole, O-methylcatechol","COC1=C(O)C=CC=C1",1.571,1,1,1]
["S3878","Bavachinin","h8","L1700-20","in 10mM DMSO","PPAR","Metabolism","Bavachinin (7-O-Methylbavachin) is a novel natural pan-PPAR agonist from the fruit of the traditional Chinese glucose-lowering herb malaytea scurfpea. It shows stronger activities with PPAR-γ than with PPAR-α and PPAR-β/δ (EC50 = 0.74 μmol/l, 4.00 μmol/l and 8.07 μmol/l in 293T cells, respectively).",{"v":338.4,"d":"338.40"},"19879-30-2",{"v":67,"d":"67.00"},197.99,"N/A","N/A","http://selleckchem.com/products/bavachinin.html","C21H22O4","free base","7-O-Methylbavachin","COC1=CC2=C(C=C1CC=C(C)C)C(=O)CC(O2)C3=CC=C(O)C=C3",4.698,3,1,4]
["S3896","(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine","h10","L1700-20","in 10mM DMSO","Others","Others","(1R,2R)-trans-N-Boc-1,2-cyclohexanediamine is an intermediate in organic synthesis.",{"v":214.3,"d":"214.30"},"146504-07-6",{"v":42,"d":"42.00"},195.99,"N/A","N/A","http://selleckchem.com/products/1r-2r-trans-n-boc-1-2-cyclohexanediamine.html","C11H22N2O2","free base","N/A","CC(C)(C)OC(=O)NC1CCCCC1N",{"v":1.55,"d":"1.550"},2,2,3]
["S3899","Hederagenin","c11","L1700-20","in 10mM DMSO","COX,NF-κB,NOS","Immunology & Inflammation","Hederagenin (Caulosapogenin, Hederagenol, Hederagenic acid, Astrantiagenin E) is a highly water insoluble triterpenoid compound that can be found in various plants including Hedera helix and Chenopodium quinoa. It exhibits a variety of biological activities, including potent antitumor properties both in vitro and in vivo. Hederagenin inhibits LPS-stimulated expression of iNOS, COX-2, and NF-κB.",{"v":472.7,"d":"472.70"},"465-99-6",{"v":94,"d":"94.00"},198.86,"N/A","N/A","http://selleckchem.com/products/hederagenin.html","C30H48O4","free base","Caulosapogenin, Hederagenol, Hederagenic acid, Astrantiagenin E","CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(CO)C5CCC34C)C2C1)C(O)=O",5.356,1,2,2]
["S3907","Bulleyaconi cine A","c2","L1700-21","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Bulleyaconi cine A (Bulleyaconitine A, BLA) is an active ingredient of Aconitum bulleyanum plants and classified as an \"aconitine-like\" alkaloid. It is a potent use-dependent blocker for both Nav1.7 and Nav1.8 Na+ currents.",627.76,"107668-79-1",{"v":7,"d":"7.00"},11.15,"N/A","N/A","http://selleckchem.com/products/bulleyaconi-cine-a.html","C35H49NO9","free base","Bulleyaconitine A","CCN1CC2(CCC(OC)C34C5CC6(O)C(CC(OC(C)=O)(C(C(OC)C23)C14)C5C6C(=O)C7=CC=C(OC)C=C7)OC)COC",0.816,8,0,11]
["S3920","7β-Hydroxylathyrol","g3","L1700-21","in 10mM DMSO","Others","Others","7β-Hydroxylathyrol (7beta-Hydroxylathyrol, 7-Hydroxylathyrol) is natural occuring product extracted from the seeds of Euphorbia lathyris L.",350.45,"34208-98-5",{"v":66,"d":"66.00"},188.33,"N/A","N/A","http://selleckchem.com/products/7-beta-hydroxylathyrol.html","C20H30O5","free base","7beta-Hydroxylathyrol, 7-Hydroxylathyrol","CC1CC2(O)C(C1O)C(O)C(=C)C(O)CC3C(/C=C(C)/C2=O)C3(C)C",1.319,1,3,0]
["S3932","Astilbin","c5","L1700-21","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Astilbin (Isoastilbin, Neoastilbin, Neoisoastilbin, Taxifolin 3-O-rhamnoside), a flavonoid compound isolated from the rhizome of Smilax glabra Roxb, displays anticancer, antioxidative, anti-inflammatory, and immunosuppressive activities.",450.39,"29838-67-3",{"v":100,"d":"100.00"},222.03,"N/A","N/A","http://selleckchem.com/products/astilbin.html","C21H22O11","free base","Isoastilbin, Neoastilbin, Neoisoastilbin, Taxifolin 3-O-rhamnoside, Taxifolin 3-rhamnoside","CC1OC(OC2C(OC3=C(C(=CC(=C3)O)O)C2=O)C4=CC(=C(O)C=C4)O)C(O)C(O)C1O",0.621,4,7,3]
["S3945","L-Cycloserine","g6","L1700-21","in 10mM DMSO","Transferase","Metabolism","L-Cycloserine (Levcycloserine, Levcicloserina, Levcycloserinum, (-)-Cycloserine, (S)-Cycloserine) is a potent inhibitor of the sphingolipid pathway via inhibiting 3-ketodihydrosphingosine synthetase. It also inhibits HIV-1 cytopathic effects, replication, and infectivity.",102.09,"339-72-0",{"v":8,"d":"8.00"},78.36,{"v":20,"d":"20.00"},195.91,"http://selleckchem.com/products/l-cycloserine.html","C3H6N2O2","free base","Levcycloserine, Levcicloserina, Levcycloserinum, (-)-Cycloserine, (S)-Cycloserine","NC1CONC1=O",-1.788,2,2,0]
["S3950","Maltitol","b7","L1700-21","in 10mM DMSO","Others","Others","Maltitol (Maltisorb, 4-O-α-glucopyranosyl-D-sorbitol) is a sugar alcohol (polyol) used as a sugar substitute. It is especially useful in the production of sweets, including sugarless hard candies, chewing gum, chocolates.",344.31,"585-88-6",{"v":20,"d":"20.00"},58.09,"N/A","N/A","http://selleckchem.com/products/maltitol.html","C12H24O11","free base","Maltisorb, 4-O-α-glucopyranosyl-D-sorbitol","OCC(O)C(O)C(OC1OC(CO)C(O)C(O)C1O)C(O)CO",-4.688,2,9,8]
["S3962","Dihydroactinidiolide","b8","L1700-21","in 10mM DMSO","Others","Others","Dihydroactinidiolide is known to be a bioactive molecule in animals. It is a component of pheromones in insects, such as red fire ants and in mammals such as the Cat and the Red Fox.",180.24,"17092-92-1",{"v":36,"d":"36.00"},199.73,"N/A","N/A","http://selleckchem.com/products/dihydroactinidiolide.html","C11H16O2","free base","N/A","CC1(C)CCCC2(C)OC(=O)C=C12",2.483,2,0,0]
["S3982","Batyl alcohol","b10","L1700-21","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Batyl alcohol (Batilol, Stearyl monoglyceride, 1-O-Octadecylglycerol, Batilolum), isolated from shark liver oil, is also present in yellow bone marrow of animals and has been described as an inflammatory agent.",344.57,"544-62-7",{"v":68,"d":"68.00"},197.35,"N/A","N/A","http://selleckchem.com/products/batyl-alcohol.html","C21H44O3","free base","Batilol, Stearyl monoglyceride, 1-O-Octadecylglycerol, Batilolum","CCCCCCCCCCCCCCCCCCOCC(O)CO",6.715,1,2,20]
["S3987","L-Tryptophan","g10","L1700-21","in 10mM DMSO","Others","Others","L-tryprophan is an essential amino acid that acts like a natural mood regulator that is necessary for normal growth in infants and for nitrogen balance in adults.",204.23,"73-22-3",{"v":11,"d":"11.00"},53.86,"N/A","N/A","http://selleckchem.com/products/l-tryptophan.html","C11H12N2O2","free base","N/A","NC(CC1=C[NH]C2=C1C=CC=C2)C(O)=O",-1.312,1,2,3]
["S3999","α-santonin","b2","L1700-22","in 10mM DMSO","Parasite","Microbiology","α-santonin, a naturally occurring sesquiterpene lactone, is a potent antiparasitic agent.",{"v":246.3,"d":"246.30"},"481-06-1",{"v":49,"d":"49.00"},198.94,"N/A","N/A","http://selleckchem.com/products/alpha-santonin.html","C15H18O3","free base","N/A","CC1C2CCC3(C)C=CC(=O)C(=C3C2OC1=O)C",2.601,3,0,0]
["S4009","Mirabegron","a3","L1700-22","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Mirabegron (YM 178) is a selective β3-adrenoceptor agonist with EC50 of 22.4 nM.",396.51,"223673-61-8",{"v":79,"d":"79.00"},199.24,"<1","N/A","http://selleckchem.com/products/mirabegron-ym178.html","C21H24N4O2S","free base","YM 178","NC1=NC(=CS1)CC(=O)NC2=CC=C(CCNCC(O)C3=CC=CC=C3)C=C2",{"v":2.26,"d":"2.260"},2,4,9]
["S4023","Procaine HCl","e4","L1700-22","in 10mM DMSO","AChR,NMDAR,Sodium Channel","Transmembrane Transporters","Procaine (Novocaine) is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 μM, 0.296 mM and 45.5 μM, which is also an inhibitor of 5-HT3 with KD of 1.7 μM.",272.77,"51-05-8",{"v":55,"d":"55.00"},201.64,{"v":55,"d":"55.00"},201.64,"http://selleckchem.com/products/procaine-novocaine-hcl.html","C13H20N2O2.HCl","HCl","Novocaine HCl","Cl.CCN(CC)CCOC(=O)C1=CC=C(N)C=C1",2.157,2,1,7]
["S4040","Norethindrone","f5","L1700-22","in 10mM DMSO","Others,0","Others","Norethindrone (Norethisterone) is a synthetic progestin, which mimic the actions of the endogenous ovarian hormone progesterone.",298.42,"68-22-4",{"v":60,"d":"60.00"},201.06,"<1","N/A","http://selleckchem.com/products/norethindrone-norethisterone.html","C20H26O2","free base","Norethisterone","CC12CCC3C(CCC4=CC(=O)CCC34)C1CCC2(O)C#C",4.315,1,0,0]
["S4051","Nabumetone","a7","L1700-22","in 10mM DMSO","COX","Neuronal Signaling","Nabumetone (BRL-14777) is a non-steroidal anti-inflammatory drug and its active metabolite inhibits the COX.",228.29,"42924-53-8",{"v":46,"d":"46.00"},{"v":201.5,"d":"201.50"},"<1","N/A","http://selleckchem.com/products/nabumetone.html","C15H16O2","free base","BRL-14777","COC1=CC=C2C=C(CCC(C)=O)C=CC2=C1",2.943,2,0,4]
["S4056","Retapamulin","d7","L1700-22","in 10mM DMSO","Antibiotics","Microbiology","Retapamulin (SB-275833) is a topical antibiotic, which binds to both E. coli and S. aureus ribosomes with similar potencies with Kd of 3 nM.",517.76,"224452-66-8",{"v":104,"d":"104.00"},200.87,"<1","N/A","http://selleckchem.com/products/retapamulin.html","C30H47NO4S","free base","SB-275833","CC1CCC23CCC(=O)C2C1(C)C(CC(C)(C=C)C(O)C3C)OC(=O)CSC4CC5CCC(C4)N5C",4.154,3,1,6]
["S4076","Propranolol HCl","c9","L1700-22","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Propranolol HCl (AY-64043, ICI-45520, NCS-91523) is a competitive non-selective beta-adrenergic receptors inhibitor.",{"v":295.8,"d":"295.80"},"318-98-9",{"v":59,"d":"59.00"},199.46,{"v":6,"d":"6.00"},20.28,"http://selleckchem.com/products/propranolol-hcl.html","C16H21NO2.HCl","Hydrochloride","AY-64043, ICI-45520, NCS-91523","Cl.CC(C)NCC(O)COC1=CC=CC2=CC=CC=C12",2.922,1,2,6]
["S4081","Sulfacetamide Sodium","h9","L1700-22","in 10mM DMSO","Anti-infection,Autophagy","Immunology & Inflammation","Sulfacetamide Sodium is an anti-biotic.",236.22,"127-56-0",{"v":19,"d":"19.00"},80.43,{"v":51,"d":"51.00"},{"v":215.9,"d":"215.90"},"http://selleckchem.com/products/sulfacetamide-sodium.html","C8H10N2O3S.Na","Sodium Salt","N/A","[Na+].CC(=O)[N-][S](=O)(=O)C1=CC=C(N)C=C1",-0.118,3,1,2]
["S4096","Droperidol","d11","L1700-22","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Droperidol (NSC 169874,Dehydrobenzperidol) is a potent antagonist of dopamine subtype 2 receptors in the limbic system.",379.43,"548-73-2",{"v":76,"d":"76.00"},{"v":200.3,"d":"200.30"},"<1","N/A","http://selleckchem.com/products/droperidol.html","C22H22FN3O2","free base","NSC 169874,Dehydrobenzperidol","FC1=CC=C(C=C1)C(=O)CCCN2CCC(=CC2)N3C(=O)NC4=C3C=CC=C4",3.049,2,1,6]
["S4105","Closantel Sodium","c2","L1700-23","in 10mM DMSO","Bacterial","Microbiology","Closantel is a gram positive antibacterial activity inhibitor, inhibiting the KinA/Spo0F system with IC50 of 3.8 μM.",685.06,"61438-64-0",{"v":100,"d":"100.00"},145.97,"<1","N/A","http://selleckchem.com/products/closantel-sodium.html","C22H13Cl2I2N2O2.Na","Sodium Salt","N/A","[Na+].CC1=C(NC(=O)C2=CC(=CC(=C2[O-])I)I)C=C(Cl)C(=C1)C(C#N)C3=CC=C(Cl)C=C3",6.049,1,1,4]
["S4118","Histamine 2HCl","d3","L1700-23","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Histamine(Ceplene) is an organic nitrogen compound, acts on target cells in mammalian brain via stimulation of Histamine 1/2.",184.07,"56-92-8",{"v":3,"d":"3.00"},{"v":16.3,"d":"16.30"},{"v":37,"d":"37.00"},201.01,"http://selleckchem.com/products/histamine-2hcl.html","C5H9N3.2HCl","Dihydrochloride","Ceplene","Cl.Cl.NCCC1=C[NH]C=N1",{"v":0.05,"d":"0.050"},1,2,2]
["S4136","Carprofen","g4","L1700-23","in 10mM DMSO","COX","Neuronal Signaling","Carprofen inhibits canine COX2 with IC50 of 30 nM.",273.71,"53716-49-7",{"v":55,"d":"55.00"},200.94,"<1","N/A","http://selleckchem.com/products/carprofen.html","C15H12ClNO2","free base","N/A","CC(C(O)=O)C1=CC2=C(C=C1)C3=C([NH]2)C=CC(=C3)Cl",4.114,1,1,2]
["S4160","Penicillin G Sodium","c6","L1700-23","in 10mM DMSO","Antibiotics,Antibiotics for Mammalian Cell Culture,Antibiotics for Plant Cell Culture","Microbiology","Penicillin G Sodium (Benzylpenicillin) is a β-lactam antibiotic produced by Penicillin spp.",356.37,"69-57-8",{"v":71,"d":"71.00"},199.23,{"v":71,"d":"71.00"},199.23,"http://selleckchem.com/products/benzylpenicillin-sodium.html","C16H18N2O4S.Na","Sodium Salt","Benzylpenicillin Sodium","[Na+].CC1(C)SC2C(NC(=O)CC3=CC=CC=C3)C(=O)N2C1C([O-])=O",{"v":-0.35,"d":"-0.350"},2,1,4]
["S4163","Doxycycline Hyclate (WC2031)","f6","L1700-23","in 10mM DMSO","Antineoplastic and Immunosuppressive Antibiotics,MMP","Proteases","Doxycycline Hyclate (WC2031, Doxycycline hydrochloride hemiethanolate hemihydrate) is a member of the tetracycline antibiotics group, and is commonly used to treat a variety of infections. It is also an inhibitor of matrix metallo-proteinases (MMP).",512.94,"24390-14-5",{"v":100,"d":"100.00"},194.95,{"v":100,"d":"100.00"},194.95,"http://selleckchem.com/products/doxycycline-hyclate.html","C22H24N2O8.1/2C2H6O.HCl.1/2H2O","hyclate","Doxycycline hydrochloride hemiethanolate hemihydrate","O.Cl.Cl.CCO.CC1C2C(O)C3C(N(C)C)C(=C(C(N)=O)C(=O)C3(O)C(=C2C(=O)C4=C(O)C=CC=C14)O)O.CC5C6C(O)C7C(N(C)C)C(=C(C(N)=O)C(=O)C7(O)C(=C6C(=O)C8=C(O)C=CC=C58)O)O",-0.955,6,11,4]
["S4178","Climbazole","c8","L1700-23","in 10mM DMSO","Fungal","Microbiology","Climbazole(BAY-e 6975) is a broad-spectrum imidazole antifungal agent that can provide anti-dandruff benefits.",292.76,"38083-17-9",{"v":59,"d":"59.00"},201.53,"<1","N/A","http://selleckchem.com/products/climbazole.html","C15H17ClN2O2","free base","BAY-e 6975","CC(C)(C)C(=O)C(OC1=CC=C(Cl)C=C1)[N]2C=CN=C2",3.766,3,0,5]
["S4187","Salicylanilide","b9","L1700-23","in 10mM DMSO","Fungal,Integrase,Reverse Transcriptase","Microbiology","Salicylanilides (WR10019,2-Hydroxybenzanilide) are a group of compounds with a wide range of biological activities including antiviral potency, antibacterial (including antimycobacterial) and antifungal activities.",213.23,"87-17-2",{"v":43,"d":"43.00"},201.66,"<1","N/A","http://selleckchem.com/products/salicylanilide.html","C13H11NO2","free base","WR10019,2-Hydroxybenzanilide","OC1=CC=CC=C1C(=O)NC2=CC=CC=C2",2.372,1,2,2]
["S4201","Florfenicol","f10","L1700-23","in 10mM DMSO","Bacterial","Microbiology","Florfenicol (SCH-25298,(-)-Florfenicol) is a fluorinated synthetic analog of thiamphenicol with broad-spectrum, primarily bacteriostatic activity.",358.21,"73231-34-2",{"v":72,"d":"72.00"},{"v":201,"d":"201.00"},"<1","N/A","http://selleckchem.com/products/florfenicol.html","C12H14Cl2FNO4S","free base","SCH-25298,(-)-Florfenicol","C[S](=O)(=O)C1=CC=C(C=C1)C(O)C(CF)NC(=O)C(Cl)Cl",1.597,3,2,6]
["S4213","Dirithromycin","h11","L1700-23","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Dirithromycin (LY-237216, ASE 136,Dynabac) is a macrolide glycopeptide antibiotic by binding to the 50S subunit of the 70S bacterial ribosome to inhibit the translocation of peptides.",835.07,"62013-04-1",{"v":11,"d":"11.00"},13.17,"<1","N/A","http://selleckchem.com/products/dirithromycin.html","C42H78N2O14","free base","LY-237216, ASE 136,Dynabac","CCC1OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(O)CC(C)C4NC(COCCOC)OC(C4C)C1(C)O",1.869,10,3,12]
["S4227","Fidaxomicin","b3","L1700-24","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","Fidaxomicin (OPT-80, PAR-101,Dificid) is a narrow spectrum macrocyclic antibiotic that inhibits RNA polymerase sigma subunit.",1058.04,"873857-62-6",{"v":100,"d":"100.00"},94.51,"<1","N/A","http://selleckchem.com/products/fidaxomicin.html","C52H74Cl2O18","free base","OPT-80, PAR-101,Dificid","CCC1\\C=C(C)/C(O)C\\C=C\\C=C(COC2OC(C)C(OC(=O)C3=C(CC)C(=C(O)C(=C3O)Cl)Cl)C(O)C2OC)\\C(=O)OC(C\\C=C(C)\\C=C(C)\\C1OC4OC(C)(C)C(OC(=O)C(C)C)C(O)C4O)C(C)O",7.774,11,7,15]
["S4235","Phenazopyridine HCl","a4","L1700-24","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","Phenazopyridine HCl is a local analgesic that has been used in urinary tract disorders. It is an inhibitor of sodium channel protein type 1 subunit alpha.",{"v":249.7,"d":"249.70"},"136-40-3",{"v":50,"d":"50.00"},200.24,"<1","N/A","http://selleckchem.com/products/phenazopyridine-hcl.html","C11H11N5.HCl","Hydrochloride","N/A","Cl.NC1=NC(=C(C=C1)N=NC2=CC=CC=C2)N",3.015,3,2,2]
["S4250","Sulfamethoxypyridazine","e5","L1700-24","in 10mM DMSO","Anti-infection","Microbiology","Sulfamethoxypyridazine (CL 13494) is a long-acting sulfonamide for treatment of Dermatitis herpetiformis.",{"v":280.3,"d":"280.30"},"80-35-3",{"v":56,"d":"56.00"},199.79,"<1","N/A","http://selleckchem.com/products/sulfamethoxypyridazine.html","C11H12N4O3S","free base","CL 13494","COC1=NN=C(N[S](=O)(=O)C2=CC=C(N)C=C2)C=C1",1.014,5,2,4]
["S4256","Buspirone HCl","a6","L1700-24","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Buspirone(Buspirone hydrochloride) is a serotonergic (5HT(1A) receptor agonist) anxiolytic drug with some D(2) dopaminergic effect, used for anxiety disorders.",421.96,"33386-08-2",{"v":84,"d":"84.00"},199.07,{"v":84,"d":"84.00"},199.07,"http://selleckchem.com/products/buspirone-hcl.html","C21H31N5O2.HCl","Hydrochloride","Buspirone hydrochloride","Cl.O=C1CC2(CCCC2)CC(=O)N1CCCCN3CCN(CC3)C4=NC=CC=N4",2.403,4,0,6]
["S4278","Carteolol HCl","a8","L1700-24","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Carteolol HCl(Carteolol hydrochloride,OPC-1085 hydrochloride) is a β-adrenoceptor antagonist, used for the treatment of glaucoma.",328.83,"51781-21-6",{"v":65,"d":"65.00"},197.67,{"v":65,"d":"65.00"},197.67,"http://selleckchem.com/products/carteolol-hci.html","C16H25ClN2O3","Hydrochloride","Carteolol hydrochloride,OPC-1085 hydrochloride","Cl.CC(C)(C)NCC(O)COC1=C2CCC(=O)NC2=CC=C1",1.664,2,3,6]
["S4281","Tasimelteon","d8","L1700-24","in 10mM DMSO","MT Receptor","Neuronal Signaling","Tasimelteon (BMS 214778, VEC 162) is a selective dual melatonin receptor (MT1/MT2) agonist with 2.1-4.4 times greater affinity for the MT2 receptor believed to mediate circadian rhythm phase-shifting (Ki = 0.0692 nM and Ki = 0.17 nM in NIH-3T3 and CHOeK1 cells, respectively), than for the MT1 receptor (Ki = 0.304 nM and Ki = 0.35 nM, respectively).",245.32,"609799-22-6",{"v":49,"d":"49.00"},199.74,{"v":-1,"d":"-1.00"},-4.08,"https://www.selleckchem.com/products/tasimelteon.html","C15H19NO2","free base","BMS 214778, VEC 162","CCC(=O)NCC1CC1C2=C3CCOC3=CC=C2",2.203,2,1,4]
["S4301","(R)-(+)-Atenolol HCl","d10","L1700-24","in 10mM DMSO","Adrenergic Receptor","Others","(R)-(+)-Atenolol binds to but does not activate beta-adrenergic receptors thereby blocking the actions of endogenous or exogenous beta-adrenergic agonists.",266.34,"56715-13-0",{"v":53,"d":"53.00"},198.99,{"v":18,"d":"18.00"},67.58,"http://selleckchem.com/products/atenolol.html","C9H16ClNO2","Hydrochloride","N/A","Cl.CC(=O)OC1CN2CCC1CC2",0.939,2,0,2]
["S4307","Auranofin","h10","L1700-24","in 10mM DMSO","Bacterial,Thioredoxin Reductase","Microbiology","Auranofin (Ridaura, SKF-39162) is an inhibitor of thioredoxin reductase (TrxR) with IC50 of 88 nM for purified H. pylori TrxR in cell-free assay. Auranofin has anti-cancer activity and can completely inhibit bacterial growth at 1.2 μM. Auranofin is an FDA-approved gold-containing compound used for the treatment of rheumatoid arthritis.",678.48,"34031-32-8",{"v":100,"d":"100.00"},147.39,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/auranofin.html","C20H34AuO9PS","Free Base","Ridaura, SKF39162","CCP(|[Au]SC1OC(COC(C)=O)C(OC(C)=O)C(OC(C)=O)C1OC(C)=O)(CC)CC",1.407,9,0,14]
["S4330","Isoetharine Mesylate","d2","L1700-25","in 10mM DMSO","Others","Others","Isoetharine is a selective beta2-adrenergic receptor agonist, which gives quick relief for bronchospasm and asthma.",335.42,"7279-75-6",{"v":67,"d":"67.00"},199.75,{"v":67,"d":"67.00"},199.75,"http://www.selleckchem.com/products/isoetharine-mesylate.html","C14H25NO6S","mesylate","N/A","CCC(NC(C)C)C(O)C1=CC=C(O)C(=C1)O.C[S](O)(=O)=O",1.586,0,4,5]
["S4338","Methoxamine HCl","c3","L1700-25","in 10mM DMSO","Others","Others","Methoxamine is an α1-adrenergic receptor agonist, it induces vasoconstriction of skin and splanchnic blood vessels.",247.72,"61-16-5",{"v":50,"d":"50.00"},201.84,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/methoxamine-hcl.html","C11H17NO3.HCl","Hydrochloride","Vasoxine HCl","Cl.COC1=CC(=C(OC)C=C1)C(O)C(C)N",1.151,2,2,4]
["S4357","Tacrine HCl","e4","L1700-25","in 10mM DMSO","AChR","Neuronal Signaling","Tacrine is a centrally acting anticholinesterase and indirect cholinergic agonist. Tacrine hydrochloride hydrate is an inhibitor of both acetyl (AChE) and butyryl-cholinestrase (BChE) with IC50s of 31 nM and 25.6 nM, respectively.",234.72,"1684-40-8",{"v":46,"d":"46.00"},195.98,{"v":46,"d":"46.00"},195.98,"http://www.selleckchem.com/products/tacrine-hcl.html","C13H14N2.HCl","hydrochlorid","N/A","Cl.NC1=C2C=CC=CC2=NC3=C1CCCC3",3.172,1,1,0]
["S4367","Suxibuzone","c5","L1700-25","in 10mM DMSO","Others","Others","Suxibuzone is a prodrug of the non steroidal anti inflammatory drug phenylbutazone, and is commonly used in horses.",438.47,"27470-51-5",{"v":88,"d":"88.00"},{"v":200.7,"d":"200.70"},{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/suxibuzone.html","C24H26N2O6","Free Base","N/A","CCCCC1(COC(=O)CCC(O)=O)C(=O)N(N(C1=O)C2=CC=CC=C2)C3=CC=CC=C3",3.504,5,0,11]
["S4396","Digoxigenin","c7","L1700-25","in 10mM DMSO","Others","Others","N/A",390.51,"1672-46-4",{"v":78,"d":"78.00"},199.74,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/digoxigenin.html","C23H34O5","Free Base","Lanadigigenin","CC12CCC(O)CC1CCC3C2CC(O)C4(C)C(CCC34O)C5=CC(=O)OC5",2.276,2,2,1]
["S4402","Oxeladin Citrate","f7","L1700-25","in 10mM DMSO","Others","Others","Oxeladin citrate (OL), a cough suppressant, is a highly potent and effective drug applied in the treatment of all types of cough of various etiologies.",{"v":527.6,"d":"527.60"},"52432-72-1",{"v":100,"d":"100.00"},189.54,{"v":100,"d":"100.00"},189.54,"http://www.selleckchem.com/products/oxeladin-citrate.html","C20H33NO3.C6H8O7","citrate","OL","CCN(CC)CCOCCOC(=O)C(CC)(CC)C1=CC=CC=C1.OC(=O)CC(O)(CC(O)=O)C(O)=O",-0.137,6,0,18]
["S4505","Vinblastine (NSC-49842) sulfate","d9","L1700-25","in 10mM DMSO","AChR,Antineoplastic and Immunosuppressive Antibiotics,Apoptosis related,Autophagy,Microtubule Associated","Cytoskeletal Signaling","Vinblastine sulfate (NSC49842, Vincaleukoblastine sulfate salt, 29060-LE, Exal, Velban, Velbe) inhibits microtubule formation and suppresses nAChR activity with IC50 of 8.9 μM in a cell-free assay, used to treat certain kinds of cancer. Vinblastine sulfate induces autophagy and apoptosis.",909.05,"143-67-9",{"v":100,"d":"100.00"},{"v":110,"d":"110.00"},"<1","N/A","http://selleckchem.com/products/vinblastine-sulfate.html","C46H58N4O9.H2SO4","sulfate","Vincaleukoblastine sulfate salt, 29060-LE, Exal, Velban, Velbe","CCC1(O)CC2CN(CCC3=C([NH]C4=CC=CC=C34)C(C2)(C(=O)OC)C5=C(OC)C=C6N(C)C7C(O)(C(OC(C)=O)C8(CC)C=CCN9CCC7(C89)C6=C5)C(=O)OC)C1.O[S](O)(=O)=O",{"v":4.28,"d":"4.280"},7,1,10]
["S4511","6-Benzylaminopurine","b10","L1700-25","in 10mM DMSO","ROS","Immunology & Inflammation","6-Benzylaminopurine is a first-generation synthetic cytokinin which could regulate the activities of the antioxidant defense system of plants.Its treatment elicits plant growth and development.",225.25,"1214-39-7",{"v":45,"d":"45.00"},199.78,"<1","N/A","http://selleckchem.com/products/6-benzylaminopurine.html","C12H11N5","free base","N/A","C(NC1=NC=NC2=C1[NH]C=N2)C3=CC=CC=C3",1.693,3,2,3]
["S4526","Fenbufen","f11","L1700-25","in 10mM DMSO","COX","Neuronal Signaling","Fenbufen (Lederfen, CL-82204) is an orally active phenylalkanoic derivative with anti-inflammatory, analgesic and antipyretic activity. It is a non-steroidal anti-inflammatory drug.",254.28,"36330-85-5",{"v":50,"d":"50.00"},196.63,"<1","N/A","http://selleckchem.com/products/fenbufen.html","C16H14O3","free base","Lederfen, CL-82204","OC(=O)CCC(=O)C1=CC=C(C=C1)C2=CC=CC=C2",2.933,2,0,5]
["S4535","Methylene Blue","e2","L1700-26","in 10mM DMSO","Dyes,Guanylate Cyclase,Microtubule Associated","GPCR & G Protein","Methylene Blue (Basic Blue 9, Tetramethylthionine chloride, methylthioninium chloride, CI-52015) is used as a dye in chromoendoscopy. It Inhibits tau filament formation with IC50 of 1.9μM. Also it inhibits soluble guanylyl cyclase.",319.85,"61-73-4",{"v":63,"d":"63.00"},196.97,{"v":63,"d":"63.00"},196.97,"http://selleckchem.com/products/methylene-blue.html","C16H18ClN3S","free base","Basic Blue 9, Tetramethylthionine chloride, methylthioninium chloride, CI-52015","[Cl-].CN(C)C1=CC2=C(C=C1)N=C3C=CC(C=C3S2)=[N+](C)C",0.369,1,0,1]
["S4546","Xylitol","e3","L1700-26","in 10mM DMSO","Autophagy","Autophagy","Xylitol (Adonitol, Ribitol, Xylite, D-Xylitol, Adonite) is a sugar alcohol derived from XYLOSE by reduction of the carbonyl group. It is as sweet as sucrose and used as a noncariogenic sweetener.",152.15,"87-99-0",{"v":30,"d":"30.00"},197.17,{"v":30,"d":"30.00"},197.17,"http://selleckchem.com/products/xylitol.html","C5H12O5","free base","Adonitol, Ribitol, Xylite, D-Xylitol, Adonite","OCC(O)C(O)C(O)CO",{"v":-2.43,"d":"-2.430"},0,5,4]
["S4562","Dehydrocholic acid","a5","L1700-26","in 10mM DMSO","Others","Others","Dehydrocholic acid (Decholin, Dehystolin, Felacrinos, Sanocholen) is a semisynthetic bile acid made from cholic acid. It is used as a cholagogue, hydrocholeretic, diuretic, and as a diagnostic aid.",402.52,"81-23-2",{"v":80,"d":"80.00"},198.75,"<1","N/A","http://selleckchem.com/products/dehydrocholic-acid.html","C24H34O5","free base","Decholin, Dehystolin, Felacrinos, Sanocholen","CC(CCC(O)=O)C1CCC2C3C(CC(=O)C12C)C4(C)CCC(=O)CC4CC3=O",2.784,4,0,4]
["S4581","Triacetin","e6","L1700-26","in 10mM DMSO","Fungal","Microbiology","Triacetin (Glycerol triacetate, Glyceryl triacetate, Glycerin triacetate, 1,2,3-Triacetoxypropane) is a triglyceride that is used as an antifungal agent.",{"v":218.2,"d":"218.20"},"102-76-1","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/triacetin.html","C9H14O6","free base","Glycerol triacetate, Glyceryl triacetate, Glycerin triacetate, 1,2,3-Triacetoxypropane","CC(=O)OCC(COC(C)=O)OC(C)=O",-0.271,6,0,8]
["S4588","Docusate Sodium","b7","L1700-26","in 10mM DMSO","Opioid Receptor","Neuronal Signaling","Docusate Sodium (Aerosol OT, Bis(2-ethylhexyl) sulfosuccinate sodium salt, Constonate) is a laxative used to treat constipation, for constipation due to the use of opiates it maybe used with a stimulant laxative, can be taken by mouth or rectally.",444.56,"577-11-7",{"v":88,"d":"88.00"},197.95,{"v":18,"d":"18.00"},40.49,"http://selleckchem.com/products/docusate-sodium.html","C20H37O7S.Na","sodium salt","Aerosol OT, Bis(2-ethylhexyl) sulfosuccinate sodium salt, Constonate","[Na+].CCCCC(CC)COC(=O)CC(C(=O)OCC(CC)CCCC)[S]([O-])(=O)=O",3.172,4,0,18]
["S4607","2,2′-Dihydroxy-4-methoxybenzophenone","a9","L1700-26","in 10mM DMSO","Others","Others","2,2′-Dihydroxy-4-methoxybenzophenone (Dioxybenzone, Dioxybenzon, Advastab 47, Cyasorb UV 24, Benzophenone-8) is an organic compound used in sunscreen to block UVB and short-wave UVA (ultraviolet) rays.",244.24,"131-53-3",{"v":48,"d":"48.00"},196.53,"<1","N/A","http://selleckchem.com/products/2-2-dihydroxy-4-methoxybenzophenone.html","C14H12O4","free base","Dioxybenzone, Dioxybenzon, Advastab 47, Cyasorb UV 24, Benzophenone-8","COC1=CC(=C(C=C1)C(=O)C2=C(O)C=CC=C2)O",2.733,2,2,3]
["S4612","Dapson","d9","L1700-26","in 10mM DMSO","Antibiotics","Microbiology","Dapson (Dapsone, 4,4′-Diaminodiphenyl sulfone, 4,4′-Sulfonyldianiline, 4-Aminophenyl sulfone, Bis(4-aminophenyl) sulfone, DDS), also known as diaminodiphenyl sulfone (DDS), is an antibiotic commonly used in combination with rifampicin and clofazimine for the treatment of leprosy.",{"v":248.3,"d":"248.30"},"80-08-0",{"v":49,"d":"49.00"},197.34,"<1","N/A","http://selleckchem.com/products/dapson.html","C12H12N2O2S","free base","Dapsone, 4,4′-Diaminodiphenyl sulfone, 4,4′-Sulfonyldianiline, 4-Aminophenyl sulfone, Bis(4-aminophenyl) sulfone, DDS","NC1=CC=C(C=C1)[S](=O)(=O)C2=CC=C(N)C=C2",1.439,2,2,2]
["S4630","Diazoxide","h10","L1700-26","in 10mM DMSO","ADC Cytotoxin,Potassium Channel","Transmembrane Transporters","Diazoxide (Sch-6783, SRG-95213, Proglycem) is a well-known small molecule that activates KATP channels in the smooth muscle of blood vessels and pancreatic beta-cells by increasing membrane permeability to potassium ions.",230.67,"364-98-7",{"v":46,"d":"46.00"},199.42,"<1","N/A","http://selleckchem.com/products/diazoxide.html","C8H7ClN2O2S","free base","Sch-6783, SRG-95213, Proglycem","CC1=NC2=CC=C(Cl)C=C2[S](=O)(=O)N1",1.196,3,1,0]
["S4641","Tedizolid Phosphate","a2","L1700-27","in 10mM DMSO","Antibiotics","Microbiology","Tedizolid (TR-701FA) is an oxazolidinone-class antibiotic. Tedizolid phosphate is a phosphate ester prodrug of the active compound tedizolid.",450.32,"856867-55-5",{"v":22,"d":"22.00"},48.85,"<1","N/A","http://selleckchem.com/products/tedizolid-phosphate.html","C17H16FN6O6P","free base","TR-701FA","C[N]1N=NC(=N1)C2=NC=C(C=C2)C3=CC=C(C=C3F)N4CC(CO[P](O)(O)=O)OC4=O",1.712,7,0,6]
["S4658","Hydroquinidine","d3","L1700-27","in 10mM DMSO","Others","Others","Hydroquinidine (Dihydroquinidine, Hydroconchinine, Hydroconquinine, Dihydroquinine) is an antiarrhythmic agent.",326.43,"1435-55-8",{"v":65,"d":"65.00"},199.12,"<1","N/A","http://selleckchem.com/products/hydroquinidine.html","C20H26N2O2","free base","Dihydroquinidine, Hydroconchinine, Hydroconquinine, Dihydroquinine","CCC1CN2CCC1CC2C(O)C3=C4C=C(OC)C=CC4=NC=C3",3.124,2,1,4]
["S4666","Sivelestat sodium tetrahydrate","c4","L1700-27","in 10mM DMSO","Serine Protease","Proteases","Sivelestat sodium tetrahydrate (ONO5046-Na, EI546, LY544349) is a competitive inhibitor of human neutrophil elastase, also inhibits leukocyte elastase obtained from rabbit, rat, hamster and mouse.",528.51,"201677-61-4",{"v":100,"d":"100.00"},189.21,"<1","N/A","http://selleckchem.com/products/sivelestat-sodium.html","C20H21N2O7S.4H2O.Na","sodium salt","Sivelestat sodium, ONO5046-Na, Sodium sivelestat, EI546 sodium, LY544349 sodium","O.O.O.O.[Na+].CC(C)(C)C(=O)OC1=CC=C(C=C1)[S](=O)(=O)NC2=CC=CC=C2C(=O)NCC([O-])=O",0.018,5,2,9]
["S4685","Efavirenz","f5","L1700-27","in 10mM DMSO","Reverse Transcriptase","Microbiology","Efavirenz (Sustiva, Stocrin, DMP-266) is a synthetic non-nucleoside reverse transcriptase (RT) inhibitor with antiviral activity.",315.67,"154598-52-4",{"v":63,"d":"63.00"},199.58,"<1","N/A","http://selleckchem.com/products/efavirenz.html","C14H9ClF3NO2","free base","Sustiva, Stocrin, DMP-266, DMP 266","FC(F)(F)C1(OC(=O)NC2=C1C=C(Cl)C=C2)C#CC3CC3",4.381,2,1,3]
["S4691","Oxybenzone","c6","L1700-27","in 10mM DMSO","Others","Others","Oxybenzone is a benzophenone derivative used as a sunscreen agent.",228.24,"131-57-7",{"v":45,"d":"45.00"},197.16,"<1","N/A","http://selleckchem.com/products/oxybenzone.html","C14H12O3","free base","Eusolex 4360, Escalol 567, KAHSCREEN BZ-3, Benzophenone 3","COC1=CC(=C(C=C1)C(=O)C2=CC=CC=C2)O",2.975,2,1,3]
["S4714","(-)-Menthol","c8","L1700-27","in 10mM DMSO","TRP Channel","Transmembrane Transporters","(-)-Menthol is a levo isomer of menthol and used as a cooling agent that strongly activates TRPM8.",156.27,"2216-51-5",{"v":31,"d":"31.00"},198.37,{"v":16,"d":"16.00"},102.39,"http://selleckchem.com/products/-menthol.html","C10H20O","free base","L-Menthol, Levomenthol, Menthomenthol, Menthacamphor","CC(C)C1CCC(C)CC1O",2.779,0,1,1]
["S4717","Isatin","f8","L1700-27","in 10mM DMSO","MAO","Metabolism","Isatin (2,3-Indolinedione) is an endogenous MAO inhibitor with an IC50 of 15 μM and more active against MAO-B than MAO-A.",147.13,"91-56-5",{"v":29,"d":"29.00"},{"v":197.1,"d":"197.10"},"<1","N/A","http://selleckchem.com/products/isatin.html","C8H5NO2","free base","2,3-Indolinedione","O=C1NC2=C(C=CC=C2)C1=O",{"v":0.67,"d":"0.670"},2,1,0]
["S4728","3,3'-Diindolylmethane","g9","L1700-27","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","3,3'-Diindolylmethane(DIM) is a major digestive product of indole-3-carbinol, a potential anticancer component of cruciferous vegetables. 3,3'-Diindolylmethane is a strong, pure androgen receptor (AR) antagonist.",246.31,"1968-05-4",{"v":49,"d":"49.00"},198.94,"<1","N/A","http://selleckchem.com/products/3-3-diindolylmethane.html","C17H14N2","free base","DIM","C(C1=C[NH]C2=C1C=CC=C2)C3=C[NH]C4=C3C=CC=C4",4.391,0,2,2]
["S4743","Wogonin","b11","L1700-27","in 10mM DMSO","CDK,Transferase","Cell Cycle","Wogonin (Vogonin), a natural and biologically-active flavonoid found in plants, is an inhibitor of CDK9 and does not inhibit CDK2, CDK4 and CDK6 at doses that inhibit CDK9 activity; Also inhibits N-acetyltransferase.",284.26,"632-85-9",{"v":56,"d":"56.00"},{"v":197,"d":"197.00"},"<1","N/A","http://selleckchem.com/products/wogonin.html","C16H12O5","free base","Vogonin","COC1=C(O)C=C(O)C2=C1OC(=CC2=O)C3=CC=CC=C3",2.636,3,2,2]
["S4759","p-Coumaric Acid","f2","L1700-28","in 10mM DMSO","Anti-infection","Microbiology","p-Coumaric acid (4-Hydroxycinnamic acid, P-Hydroxycinnamic acid, 4-Coumaric acid, Trans-p-Coumaric acid, para-Coumaric Acid) is a hydroxy derivative of cinnamic acid found in a variety of edible plants and is reported to have antioxidant, anti-inflammatory, and antimicrobial activity.",164.16,"501-98-4",{"v":32,"d":"32.00"},194.93,"<1","N/A","http://selleckchem.com/products/p-coumaric-acid.html","C9H8O3","free base","4-Hydroxycinnamic acid, P-Hydroxycinnamic acid, 4-Coumaric acid, Trans-p-Coumaric acid, para-Coumaric Acid","OC(=O)\\C=C\\C1=CC=C(O)C=C1",1.685,1,1,2]
["S4766","Gibberellic acid","e3","L1700-28","in 10mM DMSO","Others","Others","Gibberellic acid (Gibberellin, Gibberellin A3, GA3, GA), a plant hormone stimulating plant growth and development, is a tetracyclic di-terpenoid compound.",346.37,"77-06-5",{"v":69,"d":"69.00"},199.21,"N/A","N/A","http://selleckchem.com/products/gibberellic-acid.html","C19H22O6","free base","Gibberellin, Gibberellin A3, GA3","CC12C(O)C=CC3(OC1=O)C4CCC5(O)CC4(CC5=C)C(C23)C(O)=O",0.442,3,1,1]
["S4778","o-Veratraldehyde","f4","L1700-28","in 10mM DMSO","Others","Others","o-Veratraldehyde (2,3-Dimethoxybenzaldehyde) is used as the materials for the organic synthesis intermediates.",166.17,"86-51-1",{"v":33,"d":"33.00"},198.59,"N/A","N/A","http://selleckchem.com/products/o-veratraldehyde.html","C9H10O3","free base","2,3-Dimethoxybenzaldehyde","COC1=CC=CC(=C1OC)C=O",1.556,3,0,3]
["S4785","Nicotinamide N-oxide","e5","L1700-28","in 10mM DMSO","CXCR","Immunology & Inflammation","Nicotinamide N-oxide (Nicotinamide 1-oxide, 1-oxynicotinamide) is recognized as an in vivo metabolite of nicotinamide which is a precurser of nicotinamide-adenine dinucleotide (NAD+) in animals. Nicotinamide N-oxide is novel, potent, and selective antagonists of the  CXCR2 receptor.",138.12,"1986-81-8",{"v":8,"d":"8.00"},57.92,"N/A","N/A","http://selleckchem.com/products/nicotinamide-n-oxide.html","C6H6N2O2","free base","Nicotinamide 1-oxide, 1-oxynicotinamide, 1-Oxy-nicotinamide","NC(=O)C1=CC=C[N+](=C1)[O-]",{"v":0,"d":"0.000"},0,0,0]
["S4809","3-Indolepropionic acid","e7","L1700-28","in 10mM DMSO","Others","Others","3-Indolepropionic acid (IPA, indole-3-propionic acid), a gut microbial metabolite, is a potent neuroprotective antioxidant and plant auxin.",189.21,"830-96-6",{"v":37,"d":"37.00"},195.55,"N/A","N/A","http://selleckchem.com/products/3-indolepropionic-acid.html","C11H11NO2","free base","indole-3-propionic acid, Indolepropionic acid","OC(=O)CCC1=C[NH]C2=C1C=CC=C2",{"v":0,"d":"0.000"},0,0,0]
["S4819","Saccharin","c8","L1700-28","in 10mM DMSO","Others","Others","Saccharin (Benzoic sulfimide, O-Sulfobenzimide, O-Benzoic sulfimide, Saccharimide) is an artificial sweetener with effectively no food energy.",183.18,"81-07-2",{"v":36,"d":"36.00"},196.53,"N/A","N/A","http://selleckchem.com/products/saccharin.html","C7H5NO3S","free base","Benzoic sulfimide, O-Sulfobenzimide, O-Benzoic sulfimide, Saccharimide","O=C1N[S](=O)(=O)C2=C1C=CC=C2",0.359,3,1,0]
["S4833","Cefoxitin sodium","h8","L1700-28","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Cefoxitin Sodium is the sodium salt form of cefoxitin, a beta-lactam, second-generation cephalosporin antibiotic with bactericidal activity.",449.43,"33564-30-6",{"v":89,"d":"89.00"},198.03,{"v":89,"d":"89.00"},198.03,"http://selleckchem.com/products/cefoxitin-sodium.html","C16H16N3O7S2.Na","sodium salt","N/A","[Na+].COC1(NC(=O)CC2=CC=CS2)C3SCC(=C(N3C1=O)C([O-])=O)COC(N)=O",-1.151,5,2,8]
["S4847","Faropenem Sodium","d10","L1700-28","in 10mM DMSO","Antibiotics","Microbiology","Faropenem sodium is an orally active beta-lactam antibiotic that has been used in trials studying the treatment of Tuberculosis, Pulmonary Tuberculosis, and Community Acquired Pneumonia.",{"v":307.3,"d":"307.30"},"122547-49-3",{"v":12,"d":"12.00"},39.05,{"v":61,"d":"61.00"},{"v":198.5,"d":"198.50"},"http://selleckchem.com/products/faropenem-sodium.html","C12H14NO5S.Na","sodium","N/A","[Na+].CC(O)C1C2SC(=C(N2C1=O)C([O-])=O)C3CCCO3",-1.793,2,1,3]
["S4861","Oxindole","h11","L1700-28","in 10mM DMSO","Bacterial,HIV","Microbiology","Oxindole (2-indolone, 2-Oxindole, Indolin-2-one) is an aromatic heterocyclic organic compound which causes sedation, muscle weakness, hypotension, and coma when dosed in excess. Oxindole has anti-cancer, anti-HIV, anti-diabetic, antibacterial and other pharmacological activities.",133.15,"59-48-3",{"v":26,"d":"26.00"},195.27,"N/A","N/A","http://selleckchem.com/products/oxindole.html","C8H7NO","free base","2-indolone, 2-Oxindole, Indolin-2-one","O=C1CC2=C(N1)C=CC=C2",0.819,1,1,0]
["S4872","Titanium tetrafluoride","b3","L1700-29","in 10mM DMSO","Others","Others","Titanium tetrafluoride is an inorganic compound that is an effective but instable caries preventive agent.",123.86,"7783-63-3","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/titanium-tetrafluoride.html","TiF4","salt","N/A","F[Ti](F)(F)F",0.795,0,0,0]
["S4883","Lynestrenol","d4","L1700-29","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Lynestrenol (Ethinylestrenol) is a synthetic progestational hormone, an agonist of the progesterone receptor and has weak androgenic and estrogenic activity.",284.44,"52-76-6",{"v":56,"d":"56.00"},196.88,"N/A","N/A","http://selleckchem.com/products/lynestrenol.html","C20H28O","free base","Ethinylestrenol","CC12CCC3C(CCC4=CCCCC34)C1CCC2(O)C#C",5.316,0,0,0]
["S4886","Menbutone","g4","L1700-29","in 10mM DMSO","Others","Others","Menbutone (Genabilin, Naftobil, Genabilic acid), or genabilic acid, is a derivative of oxybutyric acid which acts as a choleretic stimulating secretion, a trypsinogen and a pepsinogen.",258.27,"3562-99-0",{"v":51,"d":"51.00"},197.47,"N/A","N/A","http://selleckchem.com/products/menbutone.html","C15H14O4","Organophosphates","Genabilin, Naftobil, Genabilic acid","COC1=C2C=CC=CC2=C(C=C1)C(=O)CCC(O)=O",2.307,3,0,5]
["S4908","SN-38","g6","L1700-29","in 10mM DMSO","ADC Cytotoxin,Autophagy,Topoisomerase","DNA Damage/DNA Repair","SN-38 (NK012) is an active metabolite of CPT-11, inhibits DNA topoisomerase I, DNA synthesis and causes frequent DNA single-strand breaks. SN-38 induces autophagy.",{"v":392.4,"d":"392.40"},"86639-52-3",{"v":21,"d":"21.00"},53.52,"<1","N/A","http://selleckchem.com/products/sn-38.html","C22H20N2O5","free base","NK012","CCC1=C2CN3C(=O)C4=C(C=C3C2=NC5=C1C=C(O)C=C5)C(O)(CC)C(=O)OC4",2.446,4,1,2]
["S4927","Cyclen","c7","L1700-29","in 10mM DMSO","Others","Others","Cyclen (1,4,7,10-tetraazacyclododecane) is a macrocycle capable of selectively binding cations that used as a ligand in chemistry for instance with chemicals used in MRI contrast agents.",172.27,"294-90-6",{"v":34,"d":"34.00"},197.36,{"v":34,"d":"34.00"},197.36,"http://selleckchem.com/products/cyclen.html","C8H20N4","free base","1,4,7,10-tetraazacyclododecane","C1CNCCNCCNCCN1",-1.589,0,4,0]
["S4939","cis-Aconitic acid","b8","L1700-29","in 10mM DMSO","Others","Others","Cis-Aconitic acid (cis-aconitate, Achilleic acid, Citridinic acid, Equisetic acid, Pyrocitric acid) is an intermediate in the tricarboxylic acid cycle produced by the dehydration of citric acid.",174.11,"585-84-2",{"v":34,"d":"34.00"},195.28,"N/A","N/A","http://selleckchem.com/products/cis-aconitic-acid.html","C6H6O6","free base","cis-aconitate, Achilleic acid, Citridinic acid, Equisetic acid, Pyrocitric acid","OC(=O)CC(=C/C(O)=O)/C(O)=O",-0.337,3,0,4]
["S4958","Glycocholic acid","f9","L1700-29","in 10mM DMSO","Others","Others","Glycocholic acid (Cholylglycine, Glycocholate) is a natural secondary bile acid involved in the emulsification of fats.",465.62,"475-31-0",{"v":93,"d":"93.00"},199.73,"N/A","N/A","http://selleckchem.com/products/glycocholic-acid.html","C26H43NO6","free base","Cholylglycine, Glycocholate","CC(CCC(=O)NCC(O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C",1.972,2,4,6]
["S4971","Buparvaquone","h10","L1700-29","in 10mM DMSO","Anti-infection","Microbiology","Buparvaquone (Butalex) is a second-generation hydroxynaphthoquinone related to parvaquone, with novel features that make it a promising compound for the therapy and prophylaxis of all forms of theileriosis.",326.43,"88426-33-9",{"v":65,"d":"65.00"},199.12,"<1","N/A","http://selleckchem.com/products/buparvaquone.html","C21H26O3","free base","Butalex","CC(C)(C)C1CCC(CC1)CC2=C(O)C(=O)C3=C(C=CC=C3)C2=O",4.993,2,1,3]
["S4984","2,2'-Cyclouridine","b2","L1700-30","in 10mM DMSO","Others","Others","2,2'-Cyclouridine is a research tool for antiviral and anticancer studies.",226.19,"3736-77-4",{"v":45,"d":"45.00"},198.95,{"v":-1,"d":"-1.00"},-4.42,"http://selleckchem.com/products/2-2-cyclouridine.html","C9H10N2O5","free base","N/A","OCC1OC2C(OC3=NC(=O)C=CN23)C1O",-1.185,4,2,1]
["S4999","Avermectin B1","f3","L1700-30","in 10mM DMSO","Parasite","Microbiology","Avermectin B1 (Abamectin) is a widely used insecticide and anthelmintic.",873.08,"71751-41-2",{"v":100,"d":"100.00"},114.54,"N/A","N/A","http://selleckchem.com/products/avermectin.html","C48H72O14","Macrocyclic lactones","abamectin","CCC(C)C1OC2(CC3CC(C\\C=C(C)\\C(OC4CC(OC)C(OC5CC(OC)C(O)C(C)O5)C(C)O4)C(C)\\C=C\\C=C\\6COC7C(O)C(=CC(C(=O)O3)C67O)C)O2)C=CC1C",4.692,11,2,8]
["S5007","Delamanid","e4","L1700-30","in 10mM DMSO","Bacterial","Microbiology","Delamanid (OPC-67683) is a new anti-tuberculosis drug with an excellent intracellular bactericidal activity and a high accumulation rate.",534.48,"681492-22-8",{"v":100,"d":"100.00"},{"v":187.1,"d":"187.10"},"<1","N/A","http://selleckchem.com/products/delamanid.html","C25H25F3N4O6","free base","OPC-67683","CC1(COC2=CC=C(C=C2)N3CCC(CC3)OC4=CC=C(OC(F)(F)F)C=C4)C[N]5C=C(N=C5O1)[N+]([O-])=O",6.452,5,0,9]
["S5020","Tilorone dihydrochloride","g5","L1700-30","in 10mM DMSO","Antiviral,IFN","Immunology & Inflammation","Tilorone dihydrochloride is a broad-spectrum, orally active antiviral agent that activates interferon production. It has antitumor, anti-inflammatory properties.",483.47,"27591-69-1",{"v":43,"d":"43.00"},88.94,{"v":96,"d":"96.00"},198.56,"http://selleckchem.com/products/tilorone-dihydrochloride.html","C25H34N2O3.2HCl","dihydrochloride","N/A","Cl.Cl.CCN(CC)CCOC1=CC2=C(C=C1)C3=C(C=C(OCCN(CC)CC)C=C3)C2=O",5.326,3,0,12]
["S5032","Mephenesin","e6","L1700-30","in 10mM DMSO","NMDAR","Neuronal Signaling","Mephenesin (Decontractyl, Cresoxydiol, Memphenesin, Mephedan) is centrally acting muscle relaxant, a topical analgesic and may be an NMDA receptor antagonist.",182.22,"59-47-2",{"v":36,"d":"36.00"},197.56,{"v":30,"d":"30.00"},164.64,"http://selleckchem.com/products/mephenesin.html","C10H14O3","free base","Decontractyl, Cresoxydiol, Memphenesin, Mephedan","CC1=C(OCC(O)CO)C=CC=C1",1.249,1,2,4]
["S5042","Bevantolol hydrochloride","d7","L1700-30","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Bevantolol hydrochloride (NC-1400) is a cardioselective, beta adrenoceptor antagonist, devoid of intrinsic β sympathomimetic activity and with weak membrane-stabilizing and local anesthetic properties.",381.89,"42864-78-8",{"v":76,"d":"76.00"},199.01,{"v":52,"d":"52.00"},136.16,"http://selleckchem.com/products/bevantolol-hydrochloride.html","C20H27NO4.HCl","hydrochloride","NC-1400 hydrochloride","Cl.COC1=C(OC)C=C(CCNCC(O)COC2=CC=CC(=C2)C)C=C1",3.645,3,2,10]
["S5058","Revaprazan Hydrochloride","h8","L1700-30","in 10mM DMSO","ATPase,Proton Pump","Transmembrane Transporters","Revaprazan Hydrochloride (YH1885) is a new reversible proton pump inhibitor with long-lasting acid-suppressive effects. Revaprazan Hydrochloride reversibly inhibits H(+)/K(+)-ATPase via binding to the K+-binding site of the pump.",{"v":398.9,"d":"398.90"},"178307-42-1",{"v":16,"d":"16.00"},40.11,"N/A","N/A","http://selleckchem.com/products/revaprazan-hydrochloride.html","C22H23FN4.HCl","HCl","YH1885","Cl.CC1N(CCC2=C1C=CC=C2)C3=NC(=NC(=C3C)C)NC4=CC=C(F)C=C4",6.215,2,1,3]
["S5069","Dabrafenib Mesylate","h9","L1700-30","in 10mM DMSO","Raf","MAPK","Dabrafenib Mesylate (GSK2118436) is the mesylate salt form of dabrafenib, an orally bioavailable inhibitor of B-raf (BRAF) protein with IC50s of 0.8 nM, 3.2 nM and 5 nM for B-Raf (V600E), B-Raf (WT) and C-Raf, respectively.",615.67,"1195768-06-9",{"v":100,"d":"100.00"},162.42,"<1","N/A","http://selleckchem.com/products/dabrafenib-mesylate.html","C23H20F3N5O2S2.CH4O3S","mesylate","GSK2118436 Mesylate","CC(C)(C)C1=NC(=C(S1)C2=CC=NC(=N2)N)C3=C(F)C(=CC=C3)N[S](=O)(=O)C4=C(F)C=CC=C4F.C[S](O)(=O)=O",4.963,5,2,6]
["S5083","Lentinan","d11","L1700-30","in 10mM DMSO","Fungal,Immunology & Inflammation related","Immunology & Inflammation","Lentinan (A823605, Bromoduline), isolated and purified from a hot water extract of Lentinula edodes fruit bodies, is a fungal polysaccharide immunomodulator with anti-tumor effects.","N/A","37339-90-5",{"v":100,"d":"100.00"},{"v":10,"d":"10.00"},"N/A","N/A","http://selleckchem.com/products/lentinan.html","C42H70O35R2","Polysaccharides","A823605, Bromoduline","O(C1C(O)C(CO)OC(OCC2OC(OC3C(O)C(CO)OC(OC4C(O)C(COC5OC(CO)C(O)C(O)C5O)OC(OC6C(O)C(OC(CO)C6O)[*])C4O)C3O)C(O)C(OC7OC(CO)C(O)C(O)C7O)C2O)C1O)[*]",-10.494,14,21,20]
["S5100","Pralidoxime Iodide","h2","L1700-31","in 10mM DMSO","AChR","Neuronal Signaling","Pralidoxime Iodide (2-PAM) is an antidote approved for reactivation of inhibited acetylcholinesterase (AChE) in organophosphate poisoning.",264.06,"94-63-3",{"v":52,"d":"52.00"},196.92,"N/A","N/A","http://selleckchem.com/products/pralidoxime-lodide.html","C7H9N2O.I","iodide salt","2-PAM","[I-].C[N+]1=C(C=CC=C1)\\C=N\\O",{"v":-1.56,"d":"-1.560"},1,0,1]
["S5113","Propyl gallate","c4","L1700-31","in 10mM DMSO","PPAR","Metabolism","Propyl gallate (Gallic acid propyl esterZ, n-Propyl gallate) is an antioxidant used in foods especially animal fats and vegetable oils, also in a wide variety of cosmetics and beauty care products.",{"v":212.2,"d":"212.20"},"121-79-9",{"v":42,"d":"42.00"},197.93,"N/A","N/A","http://selleckchem.com/products/propyl-gallate.html","C10H12O5","free base","Gallic acid propyl esterZ, n-Propyl gallate","CCCOC(=O)C1=CC(=C(O)C(=C1)O)O",{"v":0,"d":"0.000"},0,0,0]
["S5130","Taurocholic acid sodium salt hydrate","d5","L1700-31","in 10mM DMSO","Others","Others","Taurocholic acid (Sodium taurocholate hydrate), a bile salt formed in the liver, is the product of conjugation of cholic acid with taurine that is involved in the emulsification of lipids. Its sodium salt is the chief ingredient of the bile of carnivorous animals.","537.68 (anhydrous basis)","345909-26-4",{"v":100,"d":"100.00"},185.98,"N/A","N/A","http://selleckchem.com/products/taurocholic-acid-sodium-salt-hydrate.html","C26H45NO7S.xH2O.Na","sodium salt, hydrate","Sodium taurocholate hydrate","[Na+].CC(CCC(=O)NCC[S]([O-])(=O)=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C",{"v":0,"d":"0.000"},0,0,0]
["S5134","D(-)-Arabinose","g5","L1700-31","in 10mM DMSO","Others","Others","D-Arabinose is a reducing sugar useful as a substrate in analysis of arabinose isomerases and synthesis of D-erythroascorbic acid in yeast.",150.13,"28697-53-2",{"v":30,"d":"30.00"},199.83,"N/A","N/A","http://selleckchem.com/products/d-arabinose.html","C5H10O5","free base","D-arabinose","OC1COC(O)C(O)C1O",{"v":0,"d":"0.000"},0,0,0]
["S5144","Neferine","f6","L1700-31","in 10mM DMSO","Akt,Apoptosis related,Autophagy,HIV,NF-κB,Nrf2","NF-κB","Neferine ((R)-1,2-Dimethoxyaporphine), a natural component of Nelumbo nucifera, has antitumor efficiency. Neferine induces apoptosis in renal cancer cells. Neferine prevents autophagy through activation of Akt/mTOR pathway and Nrf2 in muscle cells. Neferine strongly inhibits NF-κB activation. Neferine possesses a number of therapeutic effects such as anti-diabetic, anti-aging, anti-microbial, anti-thrombotic, anti-arrhythmic, anti-inflammatory and even anti-HIV.",624.77,"2292-16-2",{"v":100,"d":"100.00"},160.06,"N/A","N/A","http://selleckchem.com/products/neferine.html","C38H44N2O6","free base","(R)-1,2-Dimethoxyaporphine","COC1=CC=C(CC2N(C)CCC3=C2C=C(OC4=CC(=CC=C4O)CC5N(C)CCC6=C5C=C(OC)C(=C6)OC)C(=C3)OC)C=C1",{"v":0,"d":"0.000"},0,0,0]
["S5162","Isovanillic acid","d8","L1700-31","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Isovanillic acid (Acide isovanillique, 3-Hydroxyanisic acid, 3-Hydroxy-p-anisic acid), a metabolite of isovanillin, is a selective inhibitor of neutrophil migration into inflamed tissue.",168.15,"645-08-9",{"v":33,"d":"33.00"},196.25,"N/A","N/A","http://selleckchem.com/products/isovanillic-acid.html","C8H8O4","free base","Acide isovanillique, 3-Hydroxyanisic acid, 3-Hydroxy-p-anisic acid","COC1=C(O)C=C(C=C1)C(O)=O",{"v":0,"d":"0.000"},0,0,0]
["S5175","(-)-Ambroxide","g9","L1700-31","in 10mM DMSO","Others","Others","Ambroxide, a naturally occurring terpenoid, is one of the key constituents responsible for the odor of ambergris and an autoxidation product of ambrein.",236.39,"6790-58-5",{"v":31,"d":"31.00"},131.14,"N/A","N/A","http://selleckchem.com/products/ambroxide.html","C16H28O","free base","N/A","CC1(C)CCCC2(C)C1CCC3(C)OCCC23",{"v":0,"d":"0.000"},0,0,0]
["S5201","Acetylisovaleryltylosin Tartrate","f10","L1700-31","in 10mM DMSO","Bacterial","Microbiology","Acetylisovaleryltylosin tartrate (AK105039) is an antimicrobial of the macrolide group with antibacterial activity against Gram-positive bacteria.",1192.34,"63428-13-7",{"v":100,"d":"100.00"},83.87,"N/A","N/A","http://selleckchem.com/products/acetylisovaleryltylosin-tartrate.html","C53H87NO19.C4H6O6","tartrate","AK105039","CCC1OC(=O)CC(OC(C)=O)C(C)C(OC2OC(C)C(OC3CC(C)(O)C(OC(=O)CC(C)C)C(C)O3)C(C2O)N(C)C)C(CC=O)CC(C)C(=O)/C=C/C(=C/C1COC4OC(C)C(O)C(OC)C4OC)C.OC(C(O)C(O)=O)C(O)=O",-0.856,18,4,22]
["S5214","Imidocarb dipropionate","a2","L1700-32","in 10mM DMSO","Anti-infection","Microbiology","Imidocarb is an antiprotozoal agent, used as dipropionate in the treatment of babesiosis and ehrlichiosis.",496.56,"55750-06-6",{"v":39,"d":"39.00"},78.54,"N/A","N/A","http://selleckchem.com/products/Imidocarb-dipropionate.html","C19H20N6O.2C3H6O2","dipropionate","N/A","CCC(O)=O.CCC(O)=O.O=C(NC1=CC=CC(=C1)C2=NCCN2)NC3=CC=CC(=C3)C4=NCCN4",2.022,5,4,6]
["S5230","Elubiol","b3","L1700-32","in 10mM DMSO","Others","Others","Elubiol (dichlorophenyl imidazoldioxolan) is used as a cosmetic ingredient for the conditioning of oily skin, effective in oil control.",561.46,"67914-69-6",{"v":15,"d":"15.00"},26.72,"N/A","N/A","http://selleckchem.com/products/elubiol.html","C27H30Cl2N4O5","free base","dichlorophenyl imidazoldioxolan","CCOC(=O)N1CCN(CC1)C2=CC=C(OCC3COC(C[N]4C=CN=C4)(O3)C5=CC=C(Cl)C=C5Cl)C=C2",4.602,6,0,9]
["S5246","Entecavir","f4","L1700-32","in 10mM DMSO","Reverse Transcriptase","Microbiology","Entecavir(BMS200475,SQ34676), a new deoxyguanine nucleoside analogue, is a selective inhibitor of the replication of the hepatitis B virus (HBV).",277.28,"142217-69-4",{"v":55,"d":"55.00"},198.36,"<1","N/A","https://www.selleckchem.com/products/s5246-entecavir.html","C12H15N5O3","free base","BMS200475,SQ34676","NC1=NC(=O)C2=C(N1)[N](C=N2)C3CC(O)C(CO)C3=C",-1.404,3,4,2]
["S5253","Cisapride (R 51619)","a5","L1700-32","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Cisapride (R 51619, Kaudalit, Kinestase, Prepulsid, Presid, Pridesia, Propulsid) is a nonselective 5-HT4 receptor agonist with gastroprokinetic effects.",465.95,"81098-60-4",{"v":93,"d":"93.00"},199.59,"<1","N/A","http://selleckchem.com/products/cisapride.html","C23H29ClFN3O4","Benzamide","Kaudalit, Kinestase, Prepulsid, Presid, Pridesia, Propulsid","COC1CN(CCCOC2=CC=C(F)C=C2)CCC1NC(=O)C3=C(OC)C=C(N)C(=C3)Cl",2.785,4,2,9]
["S5277","INCB032304","h6","L1700-32","in 10mM DMSO","Others","Others","INCB032304 is a pharmaceutical intermediate.",315.45,"941685-27-4",{"v":63,"d":"63.00"},199.72,{"v":-1,"d":"-1.00"},-3.17,"https://www.selleckchem.com/products/incb032304.html","C15H21N5OSi","Pyrrolo[2,3-d]pyrimidine","4-(1h-pyrazol-4-yl)-7-((2-(trimethylsilyl)ethoxy) methyl)-7h-pyrrolo[2, 3-d]pyrimidine","C[Si](C)(C)CCOC[N]1C=CC2=C(N=CN=C12)C3=C[NH]N=C3",2.738,4,1,6]
["S5283","TMB-PS","e7","L1700-32","in 10mM DMSO","Dyes","Others","TMB-PS (TMBZ-PS, TetraMethyl BisPhenol S, Bis-(2,6dimethyl-4-hydroxyphenyl)-sulfone) is a chromogenic reagent for the detection of hydrogen peroxide e.g. in the enzymatic analysis of body fluids.",362.49,"102062-36-2",{"v":72,"d":"72.00"},198.63,"N/A","N/A","http://selleckchem.com/products/tmb-ps.html","C19H26N2O3S","free base","TMBZ-PS, TetraMethyl BisPhenol S, Bis-(2,6dimethyl-4-hydroxyphenyl)-sulfone","CC1=C(N)C(=CC(=C1)C2=CC(=C(NCCC[S](O)(=O)=O)C(=C2)C)C)C",3.822,0,2,6]
["S5292","Diazolidinyl urea","d8","L1700-32","in 10mM DMSO","Anti-infection","Microbiology","Diazolidinyl urea (Germall II) is an antimicrobial preservative used in cosmetics.",278.22,"78491-02-8",{"v":55,"d":"55.00"},197.69,"N/A","N/A","http://selleckchem.com/products/diazolidinyl-urea.html","C8H14N4O7","free base","Germall II","OCNC(=O)N(CO)C1N(CO)C(=O)N(CO)C1=O",-3.165,3,5,5]
["S5306","Forchlorfenuron (CPPU)","h9","L1700-32","in 10mM DMSO","Others","Cytoskeletal Signaling","Forchlorfenuron (CPPU) is a synthetic cytokinin that inhibits septins and exhibits anti-parasitic, anticancer, and anti-angiogenic activities.",247.68,"68157-60-8",{"v":49,"d":"49.00"},197.84,"N/A","N/A","http://selleckchem.com/products/forchlorfenuron.html","C12H10ClN3O","free base","KT-30","ClC1=NC=CC(=C1)NC(=O)NC2=CC=CC=C2",2.245,2,2,2]
["S5315","PRT4165","a11","L1700-32","in 10mM DMSO","BMI-1,E3 Ligase","Ubiquitin","PRT4165 is a Bmi1/Ring1A inhibitor with an IC50 of 3.9 µM in the cell-free assay and also inhibits PRC1-mediated H2A ubiquitylation in vivo and in vitro.",235.24,"31083-55-3",{"v":11,"d":"11.00"},46.76,"<1","N/A","http://selleckchem.com/products/prt4165.html","C15H9NO2","free base","N/A","O=C1C2=C(C=CC=C2)C(=O)C1=CC3=CC=CN=C3",2.085,3,0,1]
["S5328","Gamithromycin","d2","L1700-33","in 10mM DMSO","Antibiotics","Microbiology","Gamithromycin (ML-1709460) is a new macrolide antibiotic that is only registered for use in cattle to treat respiratory disorders such as bovine respiratory disease.",777.04,"145435-72-9",{"v":100,"d":"100.00"},128.69,"<1","N/A","http://www.selleckchem.com/products/gamithromycin.html","C40H76N2O12","Free Base","ML-1709460","CCCN1CC(C)C(O)C(C)(O)C(CC)OC(=O)C(C)C(OC2CC(C)(OC)C(O)C(C)O2)C(C)C(OC3OC(C)CC(C3O)N(C)C)C(C)(O)CC1C",2.562,7,3,9]
["S5346","2-Phenylethylamine hydrochloride","h3","L1700-33","in 10mM DMSO","Others","Others","2-Phenylethylamine hydrochloride (β-Phenylethylamine, benzeneethanamine, β-aminoethylbenzene) is the hydrochloride salt form of 2-Phenylethylamine, which is an aromatic amine acting as a monoaminergic neuromodulator or a neurotransmitter in the human central nervous system.",157.64,"156-28-5",{"v":31,"d":"31.00"},196.65,"N/A","N/A","http://selleckchem.com/products/2-phenylethylamine-hydrochloride.html","C8H11N.HCl","hydrochloride","β-Phenylethylamine hydrochloride, benzeneethanamine hydrochloride, β-aminoethylbenzene hydrochloride","Cl.NCCC1=CC=CC=C1",1.639,0,1,2]
["S5352","Cefminox Sodium","f4","L1700-33","in 10mM DMSO","Bacterial","Microbiology","Cefminox Sodium (Meicelin, MT-141) is the sodium salt form of cefminox, a semi-synthetic, second-generation, beta-lactamase-stable cephalosporin with antibacterial activity.",541.56,"75498-96-3",{"v":100,"d":"100.00"},184.65,{"v":100,"d":"100.00"},184.65,"http://selleckchem.com/products/cefminox-sodium.html","C16H20N7O7S3.Na","sodium salt","Meicelin, MT-141","[Na+].COC1(NC(=O)CSCC(N)C(O)=O)C2SCC(=C(N2C1=O)C([O-])=O)CSC3=NN=N[N]3C",-5.601,7,2,11]
["S5359","Butoconazole","c5","L1700-33","in 10mM DMSO","Fungal","Microbiology","Butoconazole is an imidazole antifungal used in gynecology.",411.78,"64872-76-0",{"v":82,"d":"82.00"},199.14,"N/A","N/A","http://selleckchem.com/products/butoconazole.html","C19H17Cl3N2S","free base","N/A","ClC1=CC=C(CCC(C[N]2C=CN=C2)SC3=C(Cl)C=CC=C3Cl)C=C1",6.496,1,0,7]
["S5372","Methyl Aminolevulinate Hydrochloride","g6","L1700-33","in 10mM DMSO","Others","Others","Methyl Aminolevulinate (Aminolevulinic acid methyl ester Hydrochloride, Methyl 5-aminolevulinate Hydrochloride) is a prodrug that is metabolised to protoporphyrin IX used in photodynamic therapy.",181.62,"79416-27-6",{"v":36,"d":"36.00"},198.22,{"v":-1,"d":"-1.00"},-5.51,"https://www.selleckchem.com/products/methyl-aminolevulinate-hydrochloride.html","C6H12ClNO3","free base","Aminolevulinic acid methyl ester Hydrochloride, Methyl 5-aminolevulinate Hydrochloride","Cl.COC(=O)CCC(=O)CN",-0.613,3,1,5]
["S5380","7-Hydroxyflavone","f7","L1700-33","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","7-Hydroxyflavone is a potent inhibitor of CYP1A1 with a Ki value of 0.015 μM and exhibits 6-fold greater selectivity for CYP1A1 over CYP1A2. It also has excellent antioxidant properties and great potential to be applied as medicines.",238.24,"6665-86-7",{"v":47,"d":"47.00"},197.28,"N/A","N/A","http://selleckchem.com/products/7-hydroxyflavone.html","C15H10O3","free base","N/A","OC1=CC=C2C(=O)C=C(OC2=C1)C3=CC=CC=C3",2.894,2,1,1]
["S5397","Chlorhexidine","e9","L1700-33","in 10mM DMSO","Anti-infection","Microbiology","Chlorhexidine is a disinfectant and topical anti-infective agent that is active against Gram-positive and Gram-negative organisms, facultative anaerobes, aerobes, and yeasts.",505.45,"55-56-1",{"v":100,"d":"100.00"},197.84,{"v":-1,"d":"-1.00"},-1.98,"https://www.selleckchem.com/products/chlorhexidine.html","C22H30Cl2N10","free base","N/A","ClC1=CC=C(NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC2=CC=C(Cl)C=C2)C=C1",4.373,0,6,17]
["S5407","Squalane","g10","L1700-33","in 10mM DMSO","Others","Others","Squalane (Perhydrosqualene, Dodecahydrosqualene) is a naturally occuring lipid in both plants and animals. It is usually used as an emollient and moisturizer in cosmetics manufacturing.",422.81,"111-01-3","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/squalane.html","C30H62","free base","Perhydrosqualene, Dodecahydrosqualene","CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C",12.831,0,0,21]
["S5418","Parecoxib Sodium","f11","L1700-33","in 10mM DMSO","COX","Immunology & Inflammation","Parecoxib Sodium (SC-69124) is a water-soluble, injectable sodium salt form of parecoxib, which is a potent and selective inhibitor of cyclo-oxygenase-2 (COX2).",{"v":392.4,"d":"392.40"},"198470-85-8",{"v":78,"d":"78.00"},198.77,{"v":-1,"d":"-1.00"},-2.55,"https://www.selleckchem.com/products/parecoxib-sodium.html","C19H17N2NaO4S","free base","SC-69124 Sodium","CCC(=O)N([Na])[S](=O)(=O)C1=CC=C(C=C1)C2=C(C)ON=C2C3=CC=CC=C3",{"v":3.36,"d":"3.360"},5,0,5]
["S5434","AS057278","b3","L1700-34","in 10mM DMSO","Others","Neuronal Signaling","AS057278 (3-Methylpyrazole-5-carboxylic acid, MPC) is an inhibitor of D-amino acid oxidase (DAAO).",126.11,"402-61-9",{"v":25,"d":"25.00"},198.24,"N/A","N/A","http://selleckchem.com/products/as057278.html","C5H6N2O2","free base","3-Methylpyrazole-5-carboxylic acid","CC1=CC(=N[NH]1)C(O)=O",0.477,2,1,1]
["S5438","Biphenyl-4-sulfonyl chloride","f3","L1700-34","in 10mM DMSO","HDAC","Epigenetics","Biphenyl-4-sulfonyl chloride (p-Phenylbenzenesulfonyl, 4-Phenylbenzenesulfonyl, p-Biphenylsulfonyl) is a HDAC inhibitor with synthetic applications in palladium-catalyzed desulfitative C-arylation.",252.72,"1623-93-4",{"v":50,"d":"50.00"},197.85,"N/A","N/A","http://selleckchem.com/products/biphenyl-4-sulfonyl-chloride.html","C12H9ClO2S","free base","p-Phenylbenzenesulfonyl chloride, 4-Phenylbenzenesulfonyl chloride, p-Biphenylsulfonyl chloride","Cl[S](=O)(=O)C1=CC=C(C=C1)C2=CC=CC=C2",3.257,2,0,2]
["S5446","2-Chloro-1-(4-fluorobenzyl)benzimidazole","e4","L1700-34","in 10mM DMSO","Aldose Reductase","Metabolism","2-Chloro-1-(4-fluorobenzyl)benzimidazole is an aldose reductase (ALR2) inhibitor which is used for preparation of disubstituted benzimidazole derivative.",260.69,"84946-20-3",{"v":52,"d":"52.00"},199.47,"N/A","N/A","http://selleckchem.com/products/2-chloro-1-4-fluorobenzyl-benzimidazole.html","C14H10ClFN2","free base","N/A","FC1=CC=C(C[N]2C(=NC3=CC=CC=C23)Cl)C=C1",4.216,1,0,2]
["S5459","Aucubin","a6","L1700-34","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Aucubin (Rhinanthin), an iridoid glycoside existing in medicinal plants, has been reported to show an anti-inflammatory activity by suppression of TNF-α production in murine macrophages.",346.33,"479-98-1",{"v":69,"d":"69.00"},199.23,{"v":15,"d":"15.00"},43.31,"http://selleckchem.com/products/aucubin.html","C15H22O9","free base","Rhinanthin","OCC1OC(OC2OC=CC3C(O)C=C(CO)C23)C(O)C(O)C1O",-2.916,3,6,4]
["S5465","Morroniside","g6","L1700-34","in 10mM DMSO","MMP,Pyroptosis","Proteases","Morroniside, an iridoid glycoside, is the main active ingredient from Cornus officinalis Sieb. et Zucc. and Sambucus williamsii Hance. It has therapeutic effects on diabetic angiopathies, renal damage, lipid metabolism and inflammation and bone resorption. Morroniside has neuroprotective effect by inhibiting neuron apoptosis and MMP2/9 expression.",406.38,"25406-64-8",{"v":81,"d":"81.00"},199.32,{"v":81,"d":"81.00"},199.32,"http://selleckchem.com/products/morroniside.html","C17H26O11","free base","N/A","COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C3C(C)OC(O)CC13",{"v":-2.28,"d":"-2.280"},6,4,5]
["S5481","Molindone hydrochloride","e8","L1700-34","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Molindone hydrochloride is the hydrochloride salt form of molindone, a conventional antipsychotic used in the therapy of schizophrenia. It is a dopamine D2/D5 receptor antagonist.",312.83,"15622-65-8",{"v":9,"d":"9.00"},28.77,"N/A","N/A","http://selleckchem.com/products/molindone-hydrochloride.html","C16H24N2O2.HCl","hydrochloride","N/A","Cl.CCC1=C(C)[NH]C2=C1C(=O)C(CC2)CN3CCOCC3",2.522,2,1,3]
["S5494","Salbutamol","a10","L1700-34","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Salbutamol (Albuterol) is a short-acting, selective beta2-adrenergic receptor agonist used to treat or prevent bronchospasm in patients with asthma, bronchitis, emphysema, and other lung diseases.",239.31,"18559-94-9",{"v":47,"d":"47.00"},{"v":196.4,"d":"196.40"},"N/A","N/A","https://www.selleckchem.com/products/salbutamol.html","C13H21NO3","free base","Albuterol","CC(C)(C)NCC(O)C1=CC=C(O)C(=C1)CO",0.941,0,4,5]
["S5504","Ropivacaine","h10","L1700-34","in 10mM DMSO","Others","Others","Ropivacaine is a member of the amino amide class of local anesthetics.",{"v":274.4,"d":"274.40"},"84057-95-4",{"v":23,"d":"23.00"},83.82,"<1","N/A","https://www.selleckchem.com/products/ropivacaine.html","C17H26N2O","Amide local anesthetics","N/A","CCCN1CCCCC1C(=O)NC2=C(C)C=CC=C2C",3.853,1,1,4]
["S5521","Eosin Y Disodium","b2","L1700-35","in 10mM DMSO","Others","Others","Eosin Y is a form of eosin. It is most commonly used as an acidic red stain for highlighting cytoplasm material in samples.",691.85,"17372-87-1",{"v":100,"d":"100.00"},144.54,"N/A","N/A","http://selleckchem.com/products/eosin-y-disodium.html","C20H6Br4O5.2Na","disodium salt","N/A","[Na+].[Na+].[O-]C1=C(Br)C2=C(C=C1Br)C3(OC(=O)C4=C3C=CC=C4)C5=C(O2)C(=C([O-])C(=C5)Br)Br",5.324,3,0,0]
["S5537","Tizanidine","d3","L1700-35","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Tizanidine is an imidazoline derivative and a centrally acting α2 adrenergic agonist used as a muscle relaxant for therapy of acute muscle spasms and chronic spasticity.",253.71,"51322-75-9",{"v":50,"d":"50.00"},197.07,{"v":15,"d":"15.00"},59.12,"http://selleckchem.com/products/tizanidine.html","C9H8ClN5S","α2-adrenergic agonists","N/A","ClC1=C(NC2=NCCN2)C3=NSN=C3C=C1",1.817,3,2,2]
["S5540","Landiolol hydrochloride","g3","L1700-35","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Landiolol hydrochloride (ONO-1101) is the hydrochloride salt form of Landiolol, which is an ultra-short-acting β1 selective adrenoceptor antagonist.",546.05,"144481-98-1",{"v":100,"d":"100.00"},183.13,{"v":100,"d":"100.00"},183.13,"https://www.selleckchem.com/products/landiolol-hydrochloride.html","C25H39N3O8.HCl","hydrochloride","ONO-1101 hydrochloride","Cl.CC1(C)OCC(COC(=O)CCC2=CC=C(OCC(O)CNCCNC(=O)N3CCOCC3)C=C2)O1",{"v":0.4,"d":"0.400"},7,3,14]
["S5554","Lanatoside C","c5","L1700-35","in 10mM DMSO","Akt,Antiviral,Apoptosis related,Autophagy,JAK,mTOR,PI3K,STAT,Wnt/beta-catenin","Immunology & Inflammation","Lanatoside C is a cardiac glycoside with antiviral and anti-tumor activity. Lanatoside C induces G2/M cell cycle arrest and induces autophagy and apoptosis via attenuating MAPK, Wnt, JAK-STAT, and PI3K/AKT/mTOR signaling pathways.",985.12,"17575-22-3","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/lanatoside-c.html","C49H76O20","free base","N/A","CC1OC(CC(O)C1OC2CC(O)C(OC3CC(OC(C)=O)C(OC4OC(CO)C(O)C(O)C4O)C(C)O3)C(C)O2)OC5CCC6(C)C(CCC7C6CC(O)C8(C)C(CCC78O)C9=CC(=O)OC9)C5",0.631,12,7,12]
["S5568","Tocofersolan","a7","L1700-35","in 10mM DMSO","Vitamin","Metabolism","Tocofersolan (Tocophersolan) is a synthetic water-soluble version of vitamin E that is used in treatment of vitamin E deficiency.",574.83,"9002-96-4",{"v":100,"d":"100.00"},173.96,{"v":-1,"d":"-1.00"},-1.74,"https://www.selleckchem.com/products/tocofersolan.html","(C2H4O)nC33H54O5","free base","Tocophersolan","CC(C)CCCC(C)CCCC(C)CCCC1(C)CCC2=C(C)C(=C(C)C(=C2O1)C)OC(=O)CCC(=O)OCCO",10.716,5,1,20]
["S5579","Chelidonic acid","g7","L1700-35","in 10mM DMSO","Caspase,Decarboxylase,Immunology & Inflammation related,Interleukins,NF-κB","Immunology & Inflammation","Chelidonic acid (Jerva acid, Jervaic acid, γ-Pyrone-2,6-dicarboxylic acid) is a secondary metabolite found in several plants with therapeutic potential in allergic disorders in experimental animals. Chelidonic acid inhibits IL-6 production by blocking NF-κB and caspase-1 in HMC-1 cells. Chelidonic acid is also an inhibitor of glutamate decarboxylase with Ki of 1.2 μM.",{"v":184.1,"d":"184.10"},"99-32-1",{"v":4,"d":"4.00"},21.73,"N/A","N/A","http://selleckchem.com/products/chelidonic-acid.html","C7H4O6","free base","Jerva acid, Jervaic acid, γ-Pyrone-2,6-dicarboxylic acid","OC(=O)C1=CC(=O)C=C(O1)C(O)=O",-0.479,4,0,2]
["S5599","Sodium cholate","c9","L1700-35","in 10mM DMSO","Others","Others","Sodium cholate (NaCh) is the sodium salt of the naturally occurring cholic acid, a bile salt produced by the liver, with strong solubilization capacity of water-insoluble substances.",430.55,"361-09-1",{"v":86,"d":"86.00"},199.74,"N/A","N/A","http://selleckchem.com/products/sodium-cholate.html","C24H39O5.Na","sodium salt","N/A","[Na+].CC(CCC([O-])=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CC(O)C12C",1.438,0,3,4]
["S5614","(+)-Longifolene","f10","L1700-35","in 10mM DMSO","Others","Others","(+)-Longifolene is a naturally occurring, oily liquid hydrocarbon found primarily in the high-boiling fraction of certain pine resins",204.35,"475-20-7","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://selleckchem.com/products/longifolene.html","C15H24","free base","N/A","CC1(C)CCCC2(C)C3CCC(C13)C2=C",4.177,0,0,0]
["S5626","Benzalkonium chloride","g11","L1700-35","in 10mM DMSO","Others","Others","Benzalkonium chloride, a detergent and preservative found in health care and household products, is an established irritant.","N/A","63449-41-2, 8001-54-5",{"v":51,"d":"51.00"},{"v":10,"d":"10.00"},"N/A","N/A","https://www.selleckchem.com/products/benzalkonium-chloride.html","C15H26ClNR","free base","N/A","[Cl-].CCCCCC[N+](C)(C)CC1=CC=CC=C1",{"v":0.85,"d":"0.850"},0,0,7]
["S5642","Homovanillic acid","f2","L1700-36","in 10mM DMSO","Others","Others","Homovanillic acid (Vanillacetic acid) is a major catecholamine metabolite that is used as a reagent to detect oxidative enzymes, and is associated with dopamine levels in the brain.",182.17,"306-08-1",{"v":36,"d":"36.00"},197.62,"N/A","N/A","https://www.selleckchem.com/products/homovanillic-acid.html","C9H10O4","Dopamine","Vanillacetic acid","COC1=C(O)C=CC(=C1)CC(O)=O",1.236,2,1,3]
["S5649","Hydroxyzine pamoate","a3","L1700-36","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Hydroxyzine Pamoate is the pamoate salt form of hydroxyzine, a synthetic piperazine histamine H1-receptor antagonist with anti-allergic, antispasmodic, sedative, anti-emetic and anti-anxiety properties.",763.27,"10246-75-0",{"v":100,"d":"100.00"},131.01,{"v":-1,"d":"-1.00"},-1.31,"https://www.selleckchem.com/products/hydroxyzine-pamoate.html","C44H43ClN2O8","free base","N/A","OCCOCCN1CCN(CC1)C(C2=CC=CC=C2)C3=CC=C(Cl)C=C3.OC(=O)C4=C(O)C(=C5C=CC=CC5=C4)CC6=C7C=CC=CC7=CC(=C6O)C(O)=O",1.794,3,3,12]
["S5665","Drofenine Hydrochloride","g4","L1700-36","in 10mM DMSO","BChE","Neuronal Signaling","Drofenine hydrochloride is a potent competitive inhibitor of BChE. It is an anticholinergic that acts both at the level of the nerves and the muscle fibers.",353.93,"548-66-3",{"v":71,"d":"71.00"},{"v":200.6,"d":"200.60"},{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/drofenine-hydrochloride.html","C20H32ClNO2","hydrochloride","N/A","Cl.CCN(CC)CCOC(=O)C(C1CCCCC1)C2=CC=CC=C2",5.106,2,0,9]
["S5672","Hydroxyhexamide","e5","L1700-36","in 10mM DMSO","Others","Others","Hydroxyhexamide is a pharmacologically active metabolite of acetohexamide, which is a sulfonylurea hypoglycemic agent.",326.41,"3168-01-2",{"v":65,"d":"65.00"},199.14,"<1","N/A","https://www.selleckchem.com/products/hydroxyhexamide.html","C15H22N2O4S","free base","N/A","CC(O)C1=CC=C(C=C1)[S](=O)(=O)NC(=O)NC2CCCCC2",2.152,3,3,4]
["S5688","Tropolone (NSC 89303)","a7","L1700-36","in 10mM DMSO","Others","Metabolism","Tropolone (NSC 89303, 2-Hydroxytropone, Purpurocatechol), a metal chelator, possesses weak antioxidative and radical-scavenging properties and shows a strong affinity for ferric ion. It is able to inhibit ferric iron reduction by catecholates, lowering the redox potential of the iron couple.",122.12,"533-75-5",{"v":24,"d":"24.00"},196.53,"N/A","N/A","https://www.selleckchem.com/products/tropolone.html","C7H6O2","free base","2-Hydroxytropone, Purpurocatechol","OC1=CC=CC=CC1=O",0.741,1,1,0]
["S5698","Ketorolac tromethamine salt","h7","L1700-36","in 10mM DMSO","COX","Immunology & Inflammation","Ketorolac tromethamine is a synthetic pyrrolizine carboxylic acid derivative with anti-inflammatory, analgesic and antipyretic properties. It is a non-selective COX inhibitor with IC50s of 20 nM for both COX-1 and COX-2.",{"v":376.4,"d":"376.40"},"74103-07-4",{"v":75,"d":"75.00"},199.26,{"v":75,"d":"75.00"},199.26,"http://www.selleckchem.com/products/ketorolac-tromethamine-salt.html","C19H24N2O6","tromethamine salt","N/A","NC(CO)(CO)CO.OC(=O)C1CC[N]2C1=CC=C2C(=O)C3=CC=CC=C3",-2.028,2,4,6]
["S5716","Abemaciclib (LY2835219)","e9","L1700-36","in 10mM DMSO","CDK","Cell Cycle","Abemaciclib (LY2835219) is a cell cycle inhibitor selective for CDK4/6 with IC50 of 2 nM and 10 nM in cell-free assays, respectively.",506.59,"1231929-97-7",{"v":6,"d":"6.00"},11.84,"<1","N/A","http://selleckchem.com/products/abemaciclib.html","C27H32F2N8","free base","LY2835219","CCN1CCN(CC1)CC2=CN=C(NC3=NC=C(F)C(=N3)C4=CC(=C5N=C(C)[N](C(C)C)C5=C4)F)C=C2",4.957,4,1,7]
["S5729","Fosfosal","a11","L1700-36","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Fosfosal (2-phosphonoxy benzoic acid) is a non-acetylated salicylic acid derivative, with analgesic and anti-inflammatory activity, but without effects on PG biosynthesis in vitro.",{"v":218.1,"d":"218.10"},"6064-83-1",{"v":43,"d":"43.00"},197.16,{"v":-1,"d":"-1.00"},-4.59,"https://www.selleckchem.com/products/fosfosal.html","C7H7O6P","free base","2-phosphonoxy benzoic acid","OC(=O)C1=C(O[P](O)(O)=O)C=CC=C1",0.963,2,0,3]
["S5736","Benzathine penicilline","h11","L1700-36","in 10mM DMSO","Antibiotics,Bacterial","Microbiology","Benzathine penicilline (Benzathine penicillin G) is an antibiotic useful for the treatment of a number of bacterial infections.",909.12,"1538-09-6",{"v":100,"d":"100.00"},{"v":110,"d":"110.00"},{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/benzathine-penicilline.html","C48H56N6O8S2","Free Base","Benzathine penicillin G","CC1(C)SC2C(NC(=O)CC3=CC=CC=C3)C(=O)N2C1C(O)=O.CC4(C)SC5C(NC(=O)CC6=CC=CC=C6)C(=O)N5C4C(O)=O.C(CNCC7=CC=CC=C7)NCC8=CC=CC=C8",-0.608,6,4,15]
["S5750","DL-Norepinephrine hydrochloride","c3","L1700-37","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Norepinephrine (noradrenaline) is the neurotransmitter at most sympathetic neuroeffector junctions and has pharmacologic effects on both α1 and β1 adrenoceptors.",205.64,"55-27-6",{"v":41,"d":"41.00"},199.38,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/dl-norepinephrine-hydrochloride.html","C8H12ClNO3","hydrochloride","noradrenaline hydrochloride","Cl.NCC(O)C1=CC(=C(O)C=C1)O",0.323,0,4,2]
["S5756","Methyl Stearate","h3","L1700-37","in 10mM DMSO","Others","Others","Methyl Stearate (Methyl Octadecanoate, Stearic Acid methyl ester), found in cloves, is an antifoaming agent and fermentation nutrient.",{"v":298.5,"d":"298.50"},"112-61-8",{"v":8,"d":"8.00"},{"v":26.8,"d":"26.80"},{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/methyl-stearate.html","C19H38O2","Free Base","Methyl Octadecanoate, Stearic Acid methyl ester","CCCCCCCCCCCCCCCCCC(=O)OC",{"v":7.53,"d":"7.530"},2,0,17]
["S5763","D-Mannose","g4","L1700-37","in 10mM DMSO","Others","Others","D-mannose is a naturally occurring simple sugar that may help your body cleanse the urinary tract and maintain a healthy bladder lining.",180.16,"3458-28-4",{"v":36,"d":"36.00"},199.82,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/d-mannose.html","C6H12O6","Free Base","N/A","OCC1OC(O)C(O)C(O)C1O",-2.514,1,4,1]
["S5778","Esmolol","c6","L1700-37","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Esmolol is a cardioselective beta1 receptor blocker with rapid onset, a very short duration of action, and no significant intrinsic sympathomimetic or membrane stabilising activity at therapeutic dosages.",295.37,"81147-92-4",{"v":59,"d":"59.00"},199.75,{"v":59,"d":"59.00"},199.75,"http://www.selleckchem.com/products/esmolol.html","C16H25NO4","Free Base","N/A","COC(=O)CCC1=CC=C(OCC(O)CNC(C)C)C=C1",1.978,3,2,10]
["S5783","Montelukast","h6","L1700-37","in 10mM DMSO","LTR","Immunology & Inflammation","Montelukast(MK0476) is a leukotriene receptor antagonist used for the maintenance treatment of asthma and to relieve symptoms of seasonal allergies.",586.18,"158966-92-8",{"v":100,"d":"100.00"},{"v":170.6,"d":"170.60"},{"v":1,"d":"1.00"},1.71,"http://www.selleckchem.com/products/montelukast.html","C35H36ClNO3S","Free Base","MK0476","CC(C)(O)C1=CC=CC=C1CCC(SCC2(CC2)CC(O)=O)C3=CC=CC(=C3)\\C=C\\C4=CC=C5C=CC(=CC5=N4)Cl",8.284,2,0,12]
["S5807","HMN-176","g8","L1700-37","in 10mM DMSO","PLK","Cell Cycle","HMN-176 is an active metabolite of HMN-214, which has a potent antitumor activity in mouse xenograft models. HMN-176 effectively inhibits PLK-1 by interference with its normal subcellular spatial distribution at centrosomes and along the cytoskeletal structure.",382.43,"173529-10-7",{"v":76,"d":"76.00"},198.73,"<1","N/A","http://www.selleckchem.com/products/hmn-176.html","C20H18N2O4S","Free Base","N/A","COC1=CC=C(C=C1)[S](=O)(=O)NC2=C(C=CC=C2)\\C=C\\C3=CC=[N+]([O-])C=C3",2.292,3,1,6]
["S5822","Butyl benzyl phthalate","c10","L1700-37","in 10mM DMSO","Others","Others","Butyl benzyl phthalate (BBP, 1,2-benzenedicarboxylic acid, butyl phenylmethyl ester) is a member of the group of chemicals known as phthalates. It is a toxicant and may be used as a plasticiser.",312.36,"85-68-7","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleckchem.com/products/butyl-benzyl-phthalate.html","C19H20O4","Free Base","BBP; 1,2-benzenedicarboxylic acid; butyl phenylmethyl ester","CCCCOC(=O)C1=C(C=CC=C1)C(=O)OCC2=CC=CC=C2",4.452,4,0,9]
["S5824","Cinnamyl alcohol","e10","L1700-37","in 10mM DMSO","PPAR","Metabolism","Cinnamyl alcohol is a naturally occurring compound that is found within cinnamon. Cinnamyl alcohol can be significantly attenuated the enhanced expression of obesity-related proteins PPARγ in MDI medium-cultivated 3T3-L1 cells.",134.18,"104-54-1",{"v":27,"d":"27.00"},201.22,{"v":7,"d":"7.00"},52.17,"http://www.selleckchem.com/products/cinnamyl-alcohol.html","C9H10O","Free Base","N/A","OC/C=C/C1=CC=CC=C1",1.693,0,1,2]
["S5835","3-(4-Hydroxyphenyl)-1-propanol","f11","L1700-37","in 10mM DMSO","Others","Others","3-(4-Hydroxyphenyl)-1-propanol is a reagent in the synthesis of (−)-Centrolobine, which is an anti-Leishmania agent.",152.19,"10210-17-0",{"v":30,"d":"30.00"},197.12,{"v":30,"d":"30.00"},197.12,"http://www.selleckchem.com/products/3-4-hydroxyphenyl-1-propanol.html","C9H12O2","Free Base","N/A","OCCCC1=CC=C(O)C=C1",{"v":1.76,"d":"1.760"},0,2,3]
["S5848","Frovatriptan Succinate","b3","L1700-38","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Frovatriptan Succinate(SB 209509 Succinate,VML 251 Succinate) is the succinate salt form of frovatriptan, a synthetic triptan with serotonin (5-HT) receptor agonist activity especially for the 5-HT1B/1D receptors.",361.39,"158930-09-7",{"v":72,"d":"72.00"},199.23,{"v":72,"d":"72.00"},199.23,"http://www.selleck.cn/products/frovatriptan-succinate.html","C18H23N3O5","Succinate","SB 209509 Succinate,VML 251 Succinate","CNC1CCC2=C(C1)C3=C([NH]2)C=CC(=C3)C(N)=O.OC(=O)CCC(O)=O",{"v":-1.65,"d":"-1.650"},3,3,5]
["S5861","Lercanidipine","a4","L1700-38","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Lercanidipine is a vasoselective dihydropyridine calcium antagonist used for the treatment of essential hypertension.",611.73,"100427-26-7",{"v":55,"d":"55.00"},89.91,{"v":1,"d":"1.00"},1.63,"http://www.selleckchem.com/products/lercanidipine.html","C36H41N3O6","Free Base","N/A","COC(=O)C1=C(C)NC(=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OC(C)(C)CN(C)CCC(C3=CC=CC=C3)C4=CC=CC=C4)C",6.132,4,1,14]
["S5904","WHI-P97","h5","L1700-38","in 10mM DMSO","JAK","JAK/STAT","WHI-P97 is a potent inhibitor of JAK-3 with an estimated Ki value of 0.09 μM in modeling studies and a measured IC50 value of 2.5 μM in EGFR kinase inhibition assays.",{"v":455.1,"d":"455.10"},"211555-05-4",{"v":8,"d":"8.00"},17.58,"<1","N/A","http://www.selleckchem.com/products/whi-p97.html","C16H13Br2N3O3","Free Base","N/A","COC1=CC2=NC=NC(=C2C=C1OC)NC3=CC(=C(O)C(=C3)Br)Br",4.699,4,2,4]
["S5911","Bictegravir","e6","L1700-38","in 10mM DMSO","COVID-19,Integrase","Microbiology","Bictegravir (GS-9883) is a novel, potent, once-daily, unboosted inhibitor of HIV-1 integrase.",449.38,"1611493-60-7",{"v":90,"d":"90.00"},200.28,"<1","N/A","http://www.selleckchem.com/products/bictegravir.html","C21H18F3N3O5","Free Base","GS-9883","OC1=C2N(CC3OC4CCC(C4)N3C2=O)C=C(C(=O)NCC5=C(F)C=C(F)C=C5F)C1=O",0.646,4,2,3]
["S5925","Olodaterol hydrochloride","a8","L1700-38","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Olodaterol hydrochloride (BI-1744) is the hydrochloride salt form of Olodaterol, which is a long-acting beta2-adrenergic agonist.",{"v":422.9,"d":"422.90"},"869477-96-3",{"v":85,"d":"85.00"},200.99,{"v":85,"d":"85.00"},200.99,"http://www.selleckchem.com/products/olodaterol-hydrochloride.html","C21H27ClN2O5","hydrochloride","BI-1744 HCl","Cl.COC1=CC=C(CC(C)(C)NCC(O)C2=C3OCC(=O)NC3=CC(=C2)O)C=C1",2.257,3,4,7]
["S5939","Bendamustine (SDX105)","e9","L1700-38","in 10mM DMSO","Others","Others","Bendamustine (SDX105) is a nitrogen mustard drug used in the treatment of chronic lymphocytic leukemia (CLL), multiple myeloma, and non-Hodgkin's lymphoma.",358.26,"16506-27-7",{"v":72,"d":"72.00"},200.97,"<1","N/A","http://www.selleck.cn/products/bendamustine.html","C16H21Cl2N3O2","Free Base","SDX105","C[N]1C(=NC2=C1C=CC(=C2)N(CCCl)CCCl)CCCC(O)=O",3.606,2,0,9]
["S6003","Ataluren (PTC124)","g10","L1700-38","in 10mM DMSO","CFTR","Transmembrane Transporters","Ataluren (PTC124) selectively induces ribosomal read-through of premature but not normal termination codons, with EC50 of 0.1 μM in HEK293 cells, may provide treatment for genetic disorders caused by nonsense mutations (e.g. CF caused by CFTR nonsense mutation). Phase 3.",284.24,"775304-57-9",{"v":57,"d":"57.00"},200.53,"<1","N/A","http://selleckchem.com/products/PTC124.html","C15H9FN2O3","free base","N/A","OC(=O)C1=CC=CC(=C1)C2=NOC(=N2)C3=CC=CC=C3F",{"v":2.98,"d":"2.980"},4,0,3]
["S6005","VX-702","h10","L1700-38","in 10mM DMSO","p38 MAPK","MAPK","VX-702 is a highly selective inhibitor of p38α MAPK, 14-fold higher potency against the p38α versus p38β.",{"v":404.3,"d":"404.30"},"745833-23-2",{"v":81,"d":"81.00"},200.35,"<1","N/A","http://selleckchem.com/products/VX-702.html","C19H12F4N4O2","free base","N/A","NC(=O)N(C1=NC(=C(C=C1)C(N)=O)C2=C(F)C=C(F)C=C2)C3=C(F)C=CC=C3F",3.682,3,2,4]
["S6028","α-D-Glucose anhydrous","h2","L1700-39","in 10mM DMSO","Others","Others","Alpha-D-Glucose is a primary source of energy for living organisms. It is naturally occurring and is found in fruits and other parts of plants in its free state. It is an intermediate in glycolysis/gluconeogenesis pathway.",180.16,"492-62-6",{"v":36,"d":"36.00"},199.82,"N/A","N/A","http://www.selleck.cn/products/a-d-glucose-anhydrous.html","C6H12O6","free base","N/A","OCC1OC(O)C(O)C(O)C1O",-2.514,1,4,1]
["S6030","3-(3-Methoxyphenyl)propionic acid","b3","L1700-39","in 10mM DMSO","Others","Others","3-(3-Methoxyphenyl)propionic acid is a naturally occurring human metabolite, It is an organic acid and excreted in human urine.",{"v":180.2,"d":"180.20"},"10516-71-9",{"v":36,"d":"36.00"},199.78,"N/A","N/A","http://www.selleck.cn/products/3-3-methoxyphenyl-propionic-acid.html","C10H12O3","free base","N/A","COC1=CC=CC(=C1)CCC(O)=O",1.934,2,0,4]
["S6048","3-Oxopentanedioic acid","h4","L1700-39","in 10mM DMSO","Others","Others","3-Oxopentanedioic acid (1,3-Acetonedicarboxylic acid; 3-Oxoglutaric acid) is an intermediate for organic compound synthesis.",{"v":146.1,"d":"146.10"},"542-05-2",{"v":29,"d":"29.00"},198.49,"N/A","N/A","http://www.selleck.cn/products/3-oxopentanedioic-acid.html","C5H6O5","free base","1,3-Acetonedicarboxylic acid; 3-Oxoglutaric acid","OC(=O)CC(=O)CC(O)=O",-0.483,3,0,4]
["S6057","2-Ethylbutyric Acid","g5","L1700-39","in 10mM DMSO","Others","Others","2-Ethylbutyric Acid (2-ethyl hexanoic acid) is a chemical used to make paint dryers and plasticizers.",116.16,"88-09-5","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleck.cn/products/ethylbutyric-acid.html","C6H12O2","free base","2-ethyl hexanoic acid","CCC(CC)C(O)=O",1.837,1,0,3]
["S6074","3-(3-Hydroxyphenyl)propionic Acid","c7","L1700-39","in 10mM DMSO","Others","Others","3-(3-Hydroxyphenyl)propionic acid (m-Hydroxyphenylpropionic acid, 3-Hydroxyhydrocinnamic acid) is one of the major metabolites of ingested caffeic acid and of the phenolic degradation products of proanthocyanidins by the microflora in the colon.",166.17,"621-54-5",{"v":33,"d":"33.00"},198.59,"N/A","N/A","http://www.selleck.cn/products/3-3-hydroxyphenyl-propionic-acid.html","C9H10O3","free base","m-Hydroxyphenylpropionic acid, 3-Hydroxyhydrocinnamic acid","OC(=O)CCC1=CC(=CC=C1)O",1.708,1,1,3]
["S6095","Quinoline-4-carboxylic acid","e8","L1700-39","in 10mM DMSO","Others","Others","Quinoline-4-carboxylic acid (4-Carboxyquinoline) is a very important structure in a synthetic medicinal chemistry.",173.17,"486-74-8",{"v":34,"d":"34.00"},196.34,"N/A","N/A","http://www.selleck.cn/products/quinoline-4-carboxylic-acid.html","C10H7NO2","free base","4-Carboxyquinoline","OC(=O)C1=C2C=CC=CC2=NC=C1",1.646,2,0,1]
["S6111","L-Hydroorotic acid","g9","L1700-39","in 10mM DMSO","Others","Others","L-Dihydroorotic acid (L-dihydroorotate) is an intermediate in the metabolism of Pyrimidine. It is a substrate for Dihydroorotate dehydrogenase (mitochondrial).",158.11,"5988-19-2",{"v":31,"d":"31.00"},196.07,"N/A","N/A","http://www.selleck.cn/products/l-hydroorotic-acid.html","C5H6N2O4","free base","L-dihydroorotate","OC(=O)C1CC(=O)NC(=O)N1",-1.296,3,2,1]
["S6114","D-Arabitol","b10","L1700-39","in 10mM DMSO","Others","Others","D-Arabitol is a water soluble sugar alcohol.",152.15,"488-82-4",{"v":30,"d":"30.00"},197.17,"N/A","N/A","http://www.selleck.cn/products/d-arabitol.html","C5H12O5","free base","N/A","OCC(O)C(O)C(O)CO",{"v":-2.43,"d":"-2.430"},0,5,4]
["S6143","Ureidopropionic acid","b2","L1700-40","in 10mM DMSO","Others","Others","Ureidopropionic acid is an intermediate in the metabolism of uracil.",132.12,"462-88-4",{"v":26,"d":"26.00"},196.79,"N/A","N/A","http://www.selleck.cn/products/ureidopropionic-acid.html","C4H8N2O3","free base","N/A","NC(=O)NCCC(O)=O",-1.107,2,2,3]
["S6158","Acid orange 7","d3","L1700-40","in 10mM DMSO","Others","Others","Acid orange 7 (2-naphthol orange, Orange II, CI 15510, D&C Orange 4, COLIPA C015) is an azo dye used for dyeing wool.",350.32,"633-96-5",{"v":19.4,"d":"19.40"},55.38,"N/A","N/A","http://www.selleck.cn/products/acid-orange-7.html","C16H11N2NaO4S","free base","2-naphthol orange, Orange II, CI 15510,  D&C Orange 4, COLIPA C015","[Na+].OC1=CC=C2C=CC=CC2=C1N=NC3=CC=C(C=C3)[S]([O-])(=O)=O",1.953,2,1,3]
["S6165","Erythrosine B","b4","L1700-40","in 10mM DMSO","Dyes","Others","Erythrosine B is cherry or melon-pink synthetic, primarily used for food coloring.",879.86,"16423-68-0",175.97,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/erythrosine-b.html","C20H6I4Na2O5","free base","N/A","[Na+].[Na+].[O-]C1=C(I)C2=C(C=C1I)C3(OC(=O)C4=C3C=CC=C4)C5=C(O2)C(=C([O-])C(=C5)I)I",4.643,3,0,0]
["S6173","Amylmetacresol","a5","L1700-40","in 10mM DMSO","Anti-infection","Microbiology","Amylmetacresol is an antiseptic used to treat infections of the mouth and throat.",178.27,"1300-94-3","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleck.cn/products/amylmetacresol.html","C12H18O","free base","N/A","CCCCCC1=C(O)C=C(C)C=C1",4.385,0,1,4]
["S6204","Allyl Methyl Sulfide","a7","L1700-40","in 10mM DMSO","Others","Others","Allyl Methyl Sulfide (3-Methylthio-1-propene), a bioactive organosulfur compound found in garlic, is reported to modulate disease states such as cancer and infection.",88.17,"10152-76-8","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleck.cn/products/allyl-methyl-sulfide.html","C4H8S","free base","3-Methylthio-1-propene","CSCC=C",1.411,0,0,2]
["S6218","Sodium lauryl sulfate","b8","L1700-40","in 10mM DMSO","Others","Others","Sodium lauryl sulfate is an anionic detergent and surfactant found in many personal care products.",288.38,"151-21-3",57.68,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/sodium-lauryl-sulfate.html","C12H25NaO4S","free base","N/A","[Na+].CCCCCCCCCCCCO[S]([O-])(=O)=O",2.165,1,0,12]
["S6229","Lauryl gallate","a9","L1700-40","in 10mM DMSO","Others","Others","Lauryl gallate (Dodecyl gallate) is the ester of dodecanol and gallic acid that exhibits both potent chain-breaking and preventive antioxidant activity.",338.44,"1166-52-5",67.69,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/lauryl-gallate.html","C19H30O5","free base","Dodecyl gallate","CCCCCCCCCCCCOC(=O)C1=CC(=C(O)C(=C1)O)O",5.937,2,3,13]
["S6233","Tartaric acid","d9","L1700-40","in 10mM DMSO","Others","Others","Tartaric acid (2,3-Dihydroxysuccinic acid, Threaric acid, Racemic acid, Uvic acid, Paratartaric acid, Winestone) is a white crystalline organic acid that occurs naturally in many plants, most notably in grapes. It has several applications for industrial and pharmaceutical use.",150.09,"87-69-4",30.02,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/tartaric-acid.html","C4H6O6","free base","2,3-Dihydroxysuccinic acid; Threaric acid; Racemic acid; Uvic acid; Paratartaric acid; Winestone","OC(C(O)C(O)=O)C(O)=O",-1.664,2,2,3]
["S6251","Terephthalic acid","f10","L1700-40","in 10mM DMSO","Others","Others","Terephthalic acid (para-Phthalic acid, 1,4-Benzenedioic acid), a raw material for polyethylene terephthalate (PET) production, is one of the most important chemicals in petrochemical industry.",166.13,"100-21-0",33.23,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/terephthalic-acid.html","C8H6O4","free base","para-Phthalic acid; 1,4-Benzenedioic acid","OC(=O)C1=CC=C(C=C1)C(O)=O",1.089,2,0,2]
["S6262","Ammonium formate","h11","L1700-40","in 10mM DMSO","Others","Others","Ammonium Formate is the ammonium salt of formic acid. It is widely used in various organic reactions.",63.06,"540-69-2",12.61,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/ammonium-formate.html","CH5NO2","free base","N/A","NOC=O",-0.942,1,1,1]
["S6279","Cyclohexanecarboxylic Acid","d3","L1700-41","in 10mM DMSO","Others","Others","Cyclohexanecarboxylic Acid, a component of the growth stimulant naphthenic acid, is the starting reagent for the synthesis of polyketide-type antibiotics, Phoslactomycins.",128.17,"98-89-5","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleck.cn/products/cyclohexanecarboxylic-acid.html","C7H12O2","free base","N/A","OC(=O)C1CCCCC1",1.921,1,0,1]
["S6286","Tricarballylic acid","c4","L1700-41","in 10mM DMSO","Others","Metabolism","Tricarballylic acid (β-Carboxyglutaric acid, Propane-1,2,3-tricarboxylic acid) is an inhibitor of aconitase and therefore interferes with the Krebs cycle.",176.12,"99-14-9",35.22,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/tricarballylic-acid.html","C6H8O6","free base","Carballylic acid; 1,2,3-Propanetricarboxylic acid; β-Carboxyglutaric acid; Propane-1,2,3-tricarboxylic acid","OC(=O)CC(CC(O)=O)C(O)=O",-0.719,3,0,5]
["S6307","2-Methyllactic acid","h5","L1700-41","in 10mM DMSO","Others","Others","2-Methyllactic acid (2-Hydroxyisobutyric acid, Acetonic acid) is a metabolite of methyl tertiary-butyl ether.",{"v":104.1,"d":"104.10"},"594-61-6",20.82,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/2-methyllactic-acid.html","C4H8O3","free base","2-Hydroxyisobutyric acid, Acetonic acid","CC(C)(O)C(O)=O",-0.081,1,0,1]
["S6317","2-Picolinic acid methyl ester","g6","L1700-41","in 10mM DMSO","Others","Others","2-Picolinic acid methyl ester (Methyl picolinate, 2-Pyridinecarboxylic acid methyl ester, Methyl pyridine-2-carboxylate) is used as pharmaceutical intermediate.",137.14,"2459-07-6",27.43,{"v":200,"d":"200.00"},"N/A","N/A","http://www.selleck.cn/products/2-picolinic-acid-methyl-ester.html","C7H7NO2","free base","Methyl picolinate, 2-Pyridinecarboxylic acid methyl ester, Methyl pyridine-2-carboxylate, 2-Carbomethoxypyridine","COC(=O)C1=NC=CC=C1",0.963,3,0,2]
["S6339","Black PN","c8","L1700-41","in 10mM DMSO","Others","Others","Black PN (Brilliant Black BN) is a black dye that provides a blackish violet shade in applications.",867.68,"2519-30-4",85.71,98.79,"N/A","N/A","http://www.selleck.cn/products/black-pn.html","C28H17N5Na4O14S4","free base","Brilliant Black BN","[Na+].[Na+].[Na+].[Na+].CC(=O)NC1=C2C(=C(N=NC3=CC=C(N=NC4=CC=C(C=C4)[S]([O-])(=O)=O)C5=CC=C(C=C35)[S]([O-])(=O)=O)C(=CC2=C(C=C1)[S]([O-])(=O)=O)[S]([O-])(=O)=O)O",-4.385,5,2,9]
["S6357","1,5-Diaminopentane dihydrochloride","f9","L1700-41","in 10mM DMSO","Others","Others","1,5-Diaminopentane (Cadaverine) is a foul-smelling diamine formed by bacterial decarboxylation of lysine that occurs during protein hydrolysis during putrefaction of animal tissue.",{"v":175.1,"d":"175.10"},"1476-39-7",5.04,{"v":28.8,"d":"28.80"},"N/A","N/A","http://www.selleck.cn/products/1-5-diaminopentane-dihydrochloride.html","C5H16Cl2N2","dihydrochloride","Cadaverine dihydrochloride","Cl.Cl.NCCCCCN",0.386,0,2,4]
["S6410","Clemizole","g10","L1700-41","in 10mM DMSO","Dopamine Receptor,TRP Channel","Neuronal Signaling","Clemizole, a first-generation histamine receptor (H1) antagonist, is a potent inhibitor of behavioural and electrographic seizure activity. It has a potential therapeutic effect on hepatitis C infection and also potently inhibits TRPC5 ion channels.",325.84,"442-52-4",{"v":65,"d":"65.00"},199.48,{"v":-1,"d":"-1.00"},"N/A","http://www.selleck.cn/products/clemizole.html","C19H20ClN3","Free Base","N/A","ClC1=CC=C(C[N]2C(=NC3=C2C=CC=C3)CN4CCCC4)C=C1",4.527,1,0,4]
["S6413","fexaramine","b11","L1700-41","in 10mM DMSO","FXR","Metabolism","Fexaramine is a potent, selective farnesoid X receptor (FXR) agonist with an EC50 of 25 nM and it displays no activity at hRXRα, hPPARα, hPPARγ, hPPARδ, mPXR, hPXR, hLXRα, hTRβ, hRARβ, mCAR, mERRγ and hVDR receptors.",496.64,"574013-66-4",{"v":99,"d":"99.00"},199.34,{"v":-1,"d":"-1.00"},"N/A","http://www.selleck.cn/products/fexaramine.html","C32H36N2O3","Free Base","N/A","COC(=O)/C=C/C1=CC=CC(=C1)N(CC2=CC=C(C=C2)C3=CC=C(C=C3)N(C)C)C(=O)C4CCCCC4",{"v":6.87,"d":"6.870"},3,0,9]
["S6425","JNJ 63533054","f2","L1700-42","in 10mM DMSO","GPR","GPCR & G Protein","JNJ 63533054 is a potent and selective GPR139 agonist. It specifically activated human GPR139 in the calcium mobilization (EC50 = 16 ± 6 nM) and GTPγS binding (EC50 = 17 ± 4 nM) assays.",316.78,"1802326-66-4",{"v":63,"d":"63.00"},198.88,{"v":-1,"d":"-1.00"},"N/A","http://www.selleck.cn/products/jnj-63533054.html","C17H17ClN2O2","Free Base","N/A","CC(NC(=O)CNC(=O)C1=CC=CC(=C1)Cl)C2=CC=CC=C2",2.723,2,2,5]
["S6431","Damascenone","c3","L1700-42","in 10mM DMSO","Others","Others","Damascenone is a potent flavor compound, possessing an extremely low odor threshold of 0.002 ppb in water.",190.28,"23696-85-7","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleck.cn/products/damascenone.html","C13H18O","Free Base","N/A","C/C=C/C(=O)C1=C(C)C=CCC1(C)C",3.542,1,0,2]
["S6452","Delavirdine mesylate","b5","L1700-42","in 10mM DMSO","Reverse Transcriptase","Microbiology","Delavirdine Mesylate(U 90152 mesylate) is a mesylate salt form of delavirdine, which is a synthetic, non-nucleoside reverse transcriptase inhibitor.",552.67,"147221-93-0",{"v":100,"d":"100.00"},180.94,"<1","N/A","http://www.selleck.cn/products/delavirdine.html","C23H32N6O6S2","mesylate","U 90152 mesylate","CC(C)NC1=CC=CN=C1N2CCN(CC2)C(=O)C3=CC4=C([NH]3)C=CC(=C4)N[S](C)(=O)=O.C[S](O)(=O)=O",1.879,4,3,6]
["S6461","Permethrin","a6","L1700-42","in 10mM DMSO","Anti-infection","Microbiology","Permethrin(NRDC-143) is a synthetic Type I pyrethroidal neurotoxic pesticide that has been responsible for accidental animal deaths.",391.29,"52645-53-1",{"v":78,"d":"78.00"},199.34,"<1","N/A","http://www.selleck.cn/products/permethrin.html","C21H20Cl2O3","Free Base","NRDC-143","CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC2=CC(=CC=C2)OC3=CC=CC=C3",5.438,3,0,7]
["S6470","Fluralaner","h6","L1700-42","in 10mM DMSO","Chloride Channel,GABA Receptor","Neuronal Signaling","Fluralaner (A1443, AH252723) is a systemic insecticide and acaricide that is administered orally.Fluralaner inhibits γ-aminobutyric acid (GABA)-gated chloride channels (GABAA receptors) and L-glutamate-gated chloride channels (GluCls)",556.29,"864731-61-3",{"v":100,"d":"100.00"},179.76,"<1","N/A","http://www.selleck.cn/products/fluralaner.html","C22H17Cl2F6N3O3","Free Base","A1443, AH252723","CC1=CC(=CC=C1C(=O)NCC(=O)NCC(F)(F)F)C2=NOC(C2)(C3=CC(=CC(=C3)Cl)Cl)C(F)(F)F",5.176,4,2,8]
["S6487","fluticasone furoate","a8","L1700-42","in 10mM DMSO","Adrenergic Receptor","Neuronal Signaling","Fluticasone furoate (GW685698) is an inhaled corticosteroid/long-acting beta-agonist combination with a prolonged bronchodilator duration of action. It is used for the treatment of non-allergic and allergic rhinitis administered by a nasal spray.",538.58,"397864-44-7",{"v":100,"d":"100.00"},185.67,"<1","N/A","http://www.selleck.cn/products/fluticasone-furoate.html","C27H29F3O6S","free base","GW685698","CC1CC2C3CC(F)C4=CC(=O)C=CC4(C)C3(F)C(O)CC2(C)C1(OC(=O)C5=CC=CO5)C(=O)SCF",4.479,5,1,6]
["S6509","AG 494","a10","L1700-42","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","AG-494, a member of the tyrphostin family of tyrosine kinase inhibitors, is a potent inhibitor of EGF receptor autophosphorylation (IC50=1.2 μM) and EGF-dependent cell growth (IC50=6 μM).",280.28,"133550-35-3",{"v":56,"d":"56.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://www.selleck.cn/products/ag-494.html","C16H12N2O3","free base","N/A","OC1=C(O)C=C(C=C1)\\C=C(C#N)\\C(=O)NC2=CC=CC=C2",2.437,1,3,3]
["S6512","Defensamide (MHP)","d10","L1700-42","in 10mM DMSO","SPHK","Immunology & Inflammation","Defensamide (MHP) is an activator of sphingosine kinase (SPHK1). It can modulate the innate epidermal immune response by potentiating SPHK1 activity and inducing cAMP production.",293.36,"1104874-94-3",{"v":100,"d":"100.00"},340.88,{"v":100,"d":"100.00"},340.88,"http://www.selleck.cn/products/defensamide.html","C16H23NO4","free base","N/A","CCCCCC(=O)NC(CC1=CC=C(O)C=C1)C(=O)OC",2.914,3,2,9]
["S6527","Kobe2602","g11","L1700-42","in 10mM DMSO","Ras","Cell Cycle","Kobe2602 is a selective Ras inhibitor that blocks H-Ras GTP binding to c-Raf-1 (Ki = 149 µM).",419.31,"454453-49-7",{"v":84,"d":"84.00"},200.33,"<1","N/A","http://www.selleck.cn/products/kobe2602.html","C14H9F4N5O4S","free base","N/A","[O-][N+](=O)C1=CC(=CC(=C1NNC(=S)NC2=CC=C(F)C=C2)[N+]([O-])=O)C(F)(F)F",4.976,0,3,8]
["S6544","SR-3029","h2","L1700-43","in 10mM DMSO","Casein Kinase","Metabolism","SR-3029 is a potent and selective casein kinase 1δ/1ε (CK1δ/ε) inhibitor with IC50 values of 44 and 260 nM for CK1δ and CK1ε, respectively.",480.45,"1454585-06-8",{"v":47,"d":"47.00"},97.82,"<1","N/A","http://www.selleck.cn/products/sr-3029.html","C23H19F3N8O","free base","N/A","FC1=CC(=CC=C1)[N]2C=NC3=C2N=C(N=C3NCC4=NC5=C(F)C(=CC=C5[NH]4)F)N6CCOCC6",4.175,5,2,5]
["S6571","BQR695","d4","L1700-43","in 10mM DMSO","PI4K","PI3K/Akt/mTOR","BQR695 (NVP-BQR695) is a quinoxaline that displays sub-micromolar potency against human PI4KIIIβ (IC50~90 nM).",352.39,"1513879-21-4",{"v":70,"d":"70.00"},198.64,"<1","N/A","http://www.selleck.cn/products/bqr695.html","C19H20N4O3","free base","NVP-BQR695","CNC(=O)CNC1=CN=C2C=CC(=CC2=N1)C3=CC=C(OC)C(=C3)OC",2.187,5,2,6]
["S6585","Triethylenetetramine Dihydrochloride","c5","L1700-43","in 10mM DMSO","Others","Others","Triethylenetetramine Dihydrochloride (TETA 2HCl, Trientine Dihydrochloride), a Cu(II)-selective chelator, is commonly used for the treatment of Wilson's disease.",219.16,"38260-01-4",{"v":15,"d":"15.00"},68.44,{"v":44,"d":"44.00"},200.77,"http://www.selleck.cn/products/triethylenetetramine-dihydrochloride.html","C6H20Cl2N4","Dihydrochloride","TETA 2HCl, Trientine Dihydrochloride","Cl.Cl.NCCNCCNCCN",-1.508,0,4,7]
["S7006","BAY-61-3606","b7","L1700-43","in 10mM DMSO","Apoptosis related,Syk","Angiogenesis","BAY-61-3606 is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM). BAY-61-3606 induces cell cycle arrest and apoptosis.",463.32,"648903-57-5",{"v":14,"d":"14.00"},30.22,"<1","N/A","http://selleckchem.com/products/bay-61-3606.html","C20H18N6O3.2HCl","dihydrochloride","N/A","Cl.Cl.COC1=CC=C(C=C1OC)C2=CC3=NC=C[N]3C(=N2)NC4=NC=CC=C4C(N)=O",3.082,6,2,6]
["S7007","Binimetinib (MEK162)","c7","L1700-43","in 10mM DMSO","Apoptosis related,Autophagy,MEK","MAPK","Binimetinib (MEK162, ARRY-162, ARRY-438162) is a potent inhibitor of MEK1/2 with IC50 of 12 nM in a cell-free assay. Binimetinib induces G1 cell cycle arrest and apoptosis in human NSCLC cell lines and induces autophagy. Phase 3.",441.23,"606143-89-9",{"v":88,"d":"88.00"},199.44,"<1","N/A","http://selleckchem.com/products/mek162.html","C17H15BrF2N4O3","free base","ARRY-162,ARRY-438162","C[N]1C=NC2=C1C=C(C(=O)NOCCO)C(=C2F)NC3=C(F)C=C(Br)C=C3",2.775,3,3,6]
["S7038","Epoxomicin (BU-4061T)","c9","L1700-43","in 10mM DMSO","Apoptosis related,Proteasome","Proteases","Epoxomicin (BU-4061T, Aids010837) is a selective proteasome inhibitor with anti-inflammatory activity, inhibits primarily the CH-L activity of the 20S proteasome, while T-L and PGPH catalytic activities are also inhibited at 100- and 1000-fold reduced rate. Epoxomicin promotes apoptosis.",554.72,"134381-21-8",{"v":100,"d":"100.00"},180.27,"<1","N/A","http://selleckchem.com/products/epoxomicin-bu-4061t.html","C28H50N4O7","free base","Aids010837","CCC(C)C(NC(=O)C(C(C)CC)N(C)C(C)=O)C(=O)NC(=O)C(NC(CC(C)C)C(=O)C1(C)CO1)C(C)O",1.793,6,4,16]
["S7040","AZD3514","e9","L1700-43","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","AZD3514 is a potent and oral androgen receptor downregulator with Ki of 2.2 μM and has ability of reducing AR protein expression.Phase 1.",519.56,"1240299-33-5",{"v":100,"d":"100.00"},192.47,"<1","N/A","http://selleckchem.com/products/azd3514.html","C25H32F3N7O2","free base","N/A","CC(=O)N1CCN(CCOC2=CC=C(C=C2)C3CCN(CC3)C4=N[N]5C(=NN=C5C(F)(F)F)CC4)CC1",2.235,5,0,7]
["S7080","RN486","g11","L1700-43","in 10mM DMSO","BTK","Angiogenesis","RN486 is a potent and selective BTK inhibitor with IC50 of 4 nM.",606.69,"1242156-23-5",{"v":62,"d":"62.00"},102.19,"<1","N/A","http://selleckchem.com/products/rn486.html","C35H35FN6O3","free base","N/A","CN1CCN(CC1)C2=CN=C(NC3=CC(=CN(C)C3=O)C4=CC=CC(=C4CO)N5C=CC6=CC(=CC(=C6C5=O)F)C7CC7)C=C2",3.061,3,2,7]
["S7087","GSK2334470","b2","L1700-44","in 10mM DMSO","PDPK1","PI3K/Akt/mTOR","GSK2334470 is a novel PDK1 inhibitor with IC50 of ~10 nM in a cell-free assay, with no activity at other close related AGC-kinases.",462.59,"1227911-45-6",{"v":90,"d":"90.00"},194.56,"<1","N/A","http://selleckchem.com/products/gsk2334470.html","C25H34N8O","free base","N/A","CNC1=NC(=CC(=N1)N2CC(CCC2C)C(=O)NC3CCCCC3)C4=CC5=C(C=C4)C(=N[NH]5)N",4.516,4,4,5]
["S7103","Taselisib (GDC 0032)","f3","L1700-44","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","Taselisib (GDC 0032, RG7604) is a potent, next-generation β isoform-sparing PI3K inhibitor targeting PI3Kα/δ/γ with Ki of 0.29 nM/0.12 nM/0.97nM, >10 fold selective over PI3Kβ.",460.53,"1282512-48-4",{"v":70,"d":"70.00"},{"v":152,"d":"152.00"},"<1","N/A","http://selleckchem.com/products/gdc-0032.html","C24H28N8O2","free base","RG7604","CC(C)[N]1N=C(C)N=C1C2=C[N]3CCOC4=CC(=CC=C4C3=N2)C5=C[N](N=C5)C(C)(C)C(N)=O",{"v":2.47,"d":"2.470"},6,1,5]
["S7114","NU6027","d4","L1700-44","in 10mM DMSO","CDK","Cell Cycle","NU6027 is a potent ATR/CDK inhibitor, inhibits CDK1/2, ATR and DNA-PK with Ki of 2.5 μM/1.3 μM, 0.4 μM and 2.2 μM, enter cells more readily than the 6-aminopurine-based inhibitors.",251.28,"220036-08-8",{"v":50,"d":"50.00"},198.98,"<1","N/A","http://selleckchem.com/products/nu6027.html","C11H17N5O2","free base","N/A","NC1=NC(=C(N=O)C(=N1)OCC2CCCCC2)N",2.576,4,2,4]
["S7135","LDN-57444","b6","L1700-44","in 10mM DMSO","DUB","Proteases","LDN-57444 is a reversible, competitive proteasome inhibitor for Uch-L1 with IC50 of 0.88 μM, 28-fold selectivity over isoform Uch-L3.",397.64,"668467-91-2",{"v":11,"d":"11.00"},27.66,"<1","N/A","http://selleckchem.com/products/ldn-57444.html","C17H11Cl3N2O3","free base","N/A","CC(=O)O\\N=C/1C(=O)N(CC2=CC(=CC=C2Cl)Cl)C3=CC=C(Cl)C=C13",4.343,4,0,4]
["S7138","BMS-833923","e6","L1700-44","in 10mM DMSO","Hedgehog/Smoothened","GPCR & G Protein","BMS-833923 (XL139) is an orally bioavailable Smoothened antagonist. Phase 2.",473.57,"1059734-66-5",{"v":95,"d":"95.00"},{"v":200.6,"d":"200.60"},"<1","N/A","http://selleckchem.com/products/bms-833923.html","C30H27N5O","free base","XL139","CNCC1=CC(=C(C)C=C1)NC(=O)C2=CC=C(NC3=NC4=CC=CC=C4C(=N3)C5=CC=CC=C5)C=C2",6.214,3,3,7]
["S7158","Abemaciclib mesylate (LY2835219)","e8","L1700-44","in 10mM DMSO","CDK","Cell Cycle","Abemaciclib (LY2835219) is a potent and selective inhibitor of CDK4 and CDK6 with IC50 of 2 nM and 10 nM in cell-free assays, respectively. Phase 3.",{"v":602.7,"d":"602.70"},"1231930-82-7",{"v":83,"d":"83.00"},137.71,{"v":100,"d":"100.00"},165.92,"http://selleckchem.com/products/ly2835219.html","C27H32F2N8.CH4O3S","mesylate","N/A","CCN1CCN(CC1)CC2=CC=C(NC3=NC(=C(F)C=N3)C4=CC(=C5N=C(C)[N](C(C)C)C5=C4)F)N=C2.C[S](O)(=O)=O",4.543,4,1,7]
["S7173","Spebrutinib (CC-292)","g9","L1700-44","in 10mM DMSO","BTK","Angiogenesis","Spebrutinib (CC-292, AVL-292) is a covalent, orally active, and highly selective BTK inhibitor with IC50 of <0.5 nM, displaying at least 1400-fold selectivity over the other kinases assayed. Phase 1.",423.44,"1202757-89-8",{"v":85,"d":"85.00"},200.74,"<1","N/A","http://selleckchem.com/products/avl-292.html","C22H22FN5O3","free base","AVL-292","COCCOC1=CC=C(NC2=NC=C(F)C(=N2)NC3=CC(=CC=C3)NC(=O)C=C)C=C1",4.087,5,3,10]
["S7193","1-Azakenpaullone","a11","L1700-44","in 10mM DMSO","GSK-3","PI3K/Akt/mTOR","1-Azakenpaullone (1-Akp) is a potent and selective GSK-3β inhibitor with IC50 of 18 nM, >100-fold selectivity over CDK1/cyclin B and CDK5/p25.",328.16,"676596-65-9",{"v":66,"d":"66.00"},201.12,"<1","N/A","http://selleckchem.com/products/1-azakenpaullone.html","C15H10BrN3O","free base","1-Akp","BrC1=CC2=C([NH]C3=C2CC(=O)NC4=C3N=CC=C4)C=C1",2.949,2,2,0]
["S7198","BIO","d11","L1700-44","in 10mM DMSO","Apoptosis related,CDK,GSK-3,JAK","PI3K/Akt/mTOR","BIO (GSK-3 Inhibitor IX, 6-bromoindirubin-3-oxime, 6-Bromoindirubin-3'-oxime, MLS 2052) is a specific inhibitor of GSK-3 with IC50 of 5 nM for GSK-3α/β in a cell-free assay, shows >16-fold selectivity over CDK5, also a pan-JAK inhibitor with IC50 of 30 nM for Tyk2. BIO induces apoptosis in human melanoma cells.",356.17,"667463-62-9",{"v":71,"d":"71.00"},199.34,"<1","N/A","http://selleckchem.com/products/bio.html","C16H10BrN3O2","free base","GSK-3 Inhibitor IX, 6-bromoindirubin-3-oxime, 6-Bromoindirubin-3'-oxime, MLS 2052","O\\N=C/1\\C(NC2=CC=CC=C12)=C3\\C(=O)NC4=C3C=CC(=C4)Br",2.692,2,2,0]
["S7230","UNC0642","d3","L1700-45","in 10mM DMSO","G9a/GLP,Histone Methyltransferase","Epigenetics","UNC0642 is a potent, selective inhibitor of histone methyltransferases G9a/GLP with IC50s less than 2.5 nM for G9a and GLP and shows more than 300-fold selective for G9a and GLP over a broad range of kinases, GPCRs, transporters, and ion channels.",{"v":546.7,"d":"546.70"},"1481677-78-4",{"v":100,"d":"100.00"},182.92,"<1","N/A","http://selleckchem.com/products/unc0642.html","C29H44F2N6O2","free base","N/A","COC1=CC2=C(C=C1OCCCN3CCCC3)N=C(N=C2NC4CCN(CC4)C(C)C)N5CCC(F)(F)CC5",4.706,4,1,10]
["S7237","OG-L002","h3","L1700-45","in 10mM DMSO","Histone Demethylase,LSD1","Epigenetics","OG-L002 is a potent and specific LSD1 inhibitor with IC50 of 20 nM in a cell-free assay, exhibiting 36- and 69-fold selectivity over MAO-B and MAO-A, respectively.",225.29,"1357302-64-7",{"v":45,"d":"45.00"},199.74,"<1","N/A","http://selleckchem.com/products/og-l002.html","C15H15NO","free base","N/A","NC1CC1C2=CC=C(C=C2)C3=CC=CC(=C3)O",{"v":2.47,"d":"2.470"},0,2,2]
["S7258","SKLB1002","d5","L1700-45","in 10mM DMSO","VEGFR","Protein Tyrosine Kinase","SKLB1002 is a potent and ATP-competitive VEGFR2 inhibitor with IC50 of 32 nM.",320.39,"1225451-84-2",{"v":7,"d":"7.00"},21.85,"<1","N/A","http://selleckchem.com/products/sklb1002.html","C13H12N4O2S2","free base","N/A","COC1=C(OC)C=C2C(=NC=NC2=C1)SC3=NN=C(C)S3",2.747,6,0,4]
["S7269","PD173955","c6","L1700-45","in 10mM DMSO","Bcr-Abl","Angiogenesis","PD173955 is a potent Bcr-Abl inhibitor with IC50 of 1-2 nM, also inhibiting Src activity with IC50 of 22 nM.",443.35,"260415-63-2",{"v":15,"d":"15.00"},33.83,"<1","N/A","http://selleckchem.com/products/pd173955.html","C21H16Cl2N4OS","free base","N/A","CSC1=CC(=CC=C1)NC2=NC3C(C=N2)C=C(C(=O)N3C)C4=C(Cl)C=CC=C4Cl",4.854,3,1,4]
["S7278","HPOB","a7","L1700-45","in 10mM DMSO","HDAC","Cytoskeletal Signaling","HPOB is a potent, selective HDAC6 inhibitor with IC50 of 56 nM, >30-fold selectivity over other HDACs.",314.34,"1429651-50-2",{"v":62,"d":"62.00"},197.24,"<1","N/A","http://selleckchem.com/products/hpob.html","C17H18N2O4","free base","N/A","OCCN(C(=O)CC1=CC=C(C=C1)C(=O)NO)C2=CC=CC=C2",{"v":1.33,"d":"1.330"},2,2,6]
["S7293","ZCL278","c8","L1700-45","in 10mM DMSO","Rho","Cell Cycle","ZCL278 is a selective Cdc42 GTPase inhibitor with Kd of 11.4 μM.",584.89,"587841-73-4",{"v":100,"d":"100.00"},170.97,"<1","N/A","http://selleckchem.com/products/zcl278.html","C21H19BrClN5O4S2","free base","N/A","CC1=CC(=NC(=N1)N[S](=O)(=O)C2=CC=C(NC(=S)NC(=O)COC3=C(Cl)C=C(Br)C=C3)C=C2)C",4.809,6,3,9]
["S7312","Z-DEVD-FMK","c10","L1700-45","in 10mM DMSO","Caspase","Apoptosis","Z-DEVD-FMK (Caspase-3 Inhibitor) is a specific, irreversible Caspase-3 inhibitor, and also shows potent inhibition on caspase-6, caspase-7, caspase-8, and caspase-10.",668.66,"210344-95-9",{"v":100,"d":"100.00"},149.55,"<1","N/A","http://selleckchem.com/products/z-devd-fmk.html","C30H41FN4O12","free base","Caspase-3 Inhibitor","COC(=O)CCC(CC(=O)C(CC(=O)OC)NC(=O)OCC1=CC=CC=C1)C(=O)NC(C(C)C)C(=O)NC(CC(=O)OC)C(=O)CF",1.347,12,3,24]
["S7317","WZ4003","f10","L1700-45","in 10mM DMSO","AMPK","PI3K/Akt/mTOR","WZ4003 is a highly specific NUAK kinase inhibitor with IC50 of 20 nM and 100 nM for NUAK1 and NUAK2 in cell-base assays, respectively, without significant inhibition on 139 other kinases.",496.99,"1214265-58-3",{"v":7,"d":"7.00"},14.08,"<1","N/A","http://selleckchem.com/products/wz4003.html","C25H29ClN6O3","free base","N/A","CCC(=O)NC1=CC=CC(=C1)OC2=NC(=NC=C2Cl)NC3=C(OC)C=C(C=C3)N4CCN(C)CC4",4.776,5,2,8]
["S7333","K-Ras(G12C) inhibitor 6","c2","L1700-46","in 10mM DMSO","Ras","Cell Cycle","K-Ras(G12C) inhibitor 6 is an allosteric, and selective inhibitor of oncogenic K-Ras(G12C).",405.34,"2060530-16-5",{"v":81,"d":"81.00"},199.83,"<1","N/A","http://selleckchem.com/products/k-ras-g12c-inhibitor-6.html","C17H22Cl2N2O3S","free base","N/A","SCCCC(=O)NC1CCN(CC1)C(=O)COC2=CC=C(Cl)C=C2Cl",2.441,3,1,7]
["S7340","CH5138303","b3","L1700-46","in 10mM DMSO","HSP (HSP90)","Cytoskeletal Signaling","CH5138303 is an orally available Hsp90 inhibitor with Kd of 0.48 nM.",{"v":415.9,"d":"415.90"},"959763-06-5",{"v":83,"d":"83.00"},199.57,"<1","N/A","http://selleckchem.com/products/ch5138303.html","C19H18ClN5O2S","free base","N/A","NC(=O)CCCSC1=NC(=NC(=N1)C2=C(Cl)C=C3COCC4=CC=CC2=C34)N",2.956,5,2,6]
["S7364","Atglistatin","f4","L1700-46","in 10mM DMSO","Lipase","Metabolism","Atglistatin is a highly potent, and selective inhibitor of adipose triglyceride lipase (ATGL) with IC50 of 0.7 μM, high selectivity over other key metabolic lipases.",283.37,"1469924-27-3",{"v":56,"d":"56.00"},197.62,"<1","N/A","http://selleckchem.com/products/atglistatin.html","C17H21N3O","free base","N/A","CN(C)C(=O)NC1=CC=CC(=C1)C2=CC=C(C=C2)N(C)C",2.832,1,1,3]
["S7372","PTC-209","e5","L1700-46","in 10mM DMSO","BMI-1","Cell Cycle","PTC-209 is a potent and selective BMI-1 inhibitor with IC50 of 0.5 μM in HEK293T cell line, and results in irreversible reduction of cancer-initiating cells (CICs).",495.19,"315704-66-6",{"v":99,"d":"99.00"},199.92,"<1","N/A","http://selleckchem.com/products/ptc-209.html","C17H13Br2N5OS","Free Base","N/A","COC1=CC(=C(NC2=NC(=CS2)C3=C(C)N=C4N=CC=C[N]34)C(=C1)Br)Br",4.871,4,1,4]
["S7397","Sorafenib (BAY 43-9006)","b7","L1700-46","in 10mM DMSO","Apoptosis related,Autophagy,Ferroptosis,FLT3,PDGFR,Raf,VEGFR","MAPK","Sorafenib (BAY 43-9006, NSC-724772) is a multikinase inhibitor of Raf-1 and B-Raf with IC50 of 6 nM and 22 nM in cell-free assays, respectively. Sorafenib inhibits VEGFR-2, VEGFR-3, PDGFR-β, Flt-3 and c-KIT with IC50 of 90 nM, 20 nM, 57 nM, 59 nM and 68 nM, respectively. Sorafenib induces autophagy and apoptosis and activates ferroptosis with anti-tumor activity.",464.82,"284461-73-0",{"v":63,"d":"63.00"},135.54,"<1","N/A","http://selleckchem.com/products/sorafenib.html","C21H16ClF3N4O3","Free Base","NSC-724772,BAY 43-9006","CNC(=O)C1=CC(=CC=N1)OC2=CC=C(NC(=O)NC3=CC=C(Cl)C(=C3)C(F)(F)F)C=C2",4.175,4,3,6]
["S7411","Ascomycin (FK520)","e7","L1700-46","in 10mM DMSO","Anti-infection","Microbiology","Ascomycin (FK520, FR 900520, Immunomycin), an FK-506 analog, is a neutral macrolide immunosuppressant, which prevents rejection after an organ transplant. Phase 3.",792.01,"104987-12-4",{"v":100,"d":"100.00"},126.26,"<1","N/A","http://selleckchem.com/products/ascomycin-fk520.html","C43H69NO12","free base","FR 900520, Immunomycin","CCC1/C=C(C)/CC(C)CC(OC)C2OC(O)(C(C)CC2OC)C(=O)C(=O)N3CCCCC3C(=O)OC(C(C)C(O)CC1=O)\\C(C)=C\\C4CCC(O)C(C4)OC",4.766,9,2,6]
["S7441","WS3","e9","L1700-46","in 10mM DMSO","IκB/IKK","NF-κB","WS3 is a β cell proliferation inducer via modulation of Erb3 binding protein-1 (EBP1) and the IκB kinase pathway.",569.58,"1421227-52-2",{"v":100,"d":"100.00"},175.57,"<1","N/A","http://selleckchem.com/products/ws3.html","C28H30F3N7O3","free base","N/A","CN1CCN(CC1)CC2=C(C=C(NC(=O)NC3=CC=C(OC4=CC(=NC=N4)NC(=O)C5CC5)C=C3)C=C2)C(F)(F)F",4.234,5,3,9]
["S7442","WS6","f9","L1700-46","in 10mM DMSO","IκB/IKK","NF-κB","WS6 is a β cell proliferation inducer via modulation of Erb3 binding protein-1 (EBP1) and the IκB kinase pathway.",568.59,"1421227-53-3",{"v":100,"d":"100.00"},175.87,"<1","N/A","http://selleckchem.com/products/ws6.html","C29H31F3N6O3","free base","N/A","CN1CCN(CC1)CC2=C(C=C(NC(=O)CC3=CC=C(OC4=CC(=NC=N4)NC(=O)C5CC5)C=C3)C=C2)C(F)(F)F",{"v":4.36,"d":"4.360"},5,2,10]
["S7457","XEN445","h10","L1700-46","in 10mM DMSO","Lipase","Metabolism","XEN445 is a potent and selective endothelial lipase inhibitor with IC50 of 0.237 μM.",366.33,"1515856-92-4",{"v":80,"d":"80.00"},218.38,"<1","N/A","http://selleckchem.com/products/xen445.html","C18H17F3N2O3","free base","N/A","OC(=O)C1=CC(=CC=C1N2CCC(C2)OCC3=NC=CC=C3)C(F)(F)F",3.725,3,0,6]
["S7482","EHT 1864 2HCl","d2","L1700-47","in 10mM DMSO","Rho","Cell Cycle","EHT 1864 2HCl is a potent Rac family GTPase inhibitor with Kd of 40 nM, 50 nM, 60 nM and 250 nM for Rac1, Rac1b, Rac2 and Rac3, respectively.",581.47,"754240-09-0",{"v":100,"d":"100.00"},171.98,{"v":100,"d":"100.00"},171.98,"http://selleckchem.com/products/eht-1864.html","C25H29Cl2F3N2O4S","dihydrochloride","N/A","Cl.Cl.FC(F)(F)C1=CC2=C(C=C1)C(=CC=N2)SCCCCCOC3=COC(=CC3=O)CN4CCOCC4",4.663,5,0,11]
["S7493","INH1","c3","L1700-47","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","INH1 (IBT 13131) is a cell-permeable Hec1 inhibitor, which specifically disrupts the Hec1/Nek2 interaction.",{"v":308.4,"d":"308.40"},"313553-47-8",{"v":61,"d":"61.00"},{"v":197.8,"d":"197.80"},"<1","N/A","http://selleckchem.com/products/inh1.html","C18H16N2OS","free base","IBT 13131","CC1=CC(=C(C=C1)C2=CSC(=N2)NC(=O)C3=CC=CC=C3)C",4.531,2,1,3]
["S7515","VGX-1027","h4","L1700-47","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","VGX-1027 (GIT 27) is an orally active immunomodulator. Phase 1.",205.21,"6501-72-0",{"v":41,"d":"41.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://selleckchem.com/products/vgx-1027.html","C11H11NO3","free base","GIT 27","OC(=O)CC1CC(=NO1)C2=CC=CC=C2",1.368,3,0,3]
["S7530","Vactosertib (TEW-7197)","d6","L1700-47","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","Vactosertib  (TEW-7197, EW-7197) is a highly potent, selective, and orally bioavailable TGF-β receptor ALK4/ALK5 inhibitor with IC50 of 13 nM and 11 nM, respectively. Phase 1.",399.42,"1352608-82-2",{"v":79,"d":"79.00"},197.79,"<1","N/A","http://selleckchem.com/products/ew-7197.html","C22H18FN7","free base","EW-7197","CC1=NC(=CC=C1)C2=C(N=C(CNC3=CC=CC=C3F)[NH]2)C4=C[N]5N=CN=C5C=C4",3.621,4,2,5]
["S7536","Lorlatinib (PF-6463922)","g6","L1700-47","in 10mM DMSO","ALK,Apoptosis related,ROS1","Protein Tyrosine Kinase","Lorlatinib (PF-6463922) is a potent, dual ALK/ROS1 inhibitor with Ki of <0.02 nM, <0.07 nM, and 0.7 nM for ROS1, ALK (WT), and ALK (L1196M), respectively. PF-06463922 induces apoptosis. Phase 1.",406.41,"1454846-35-5",{"v":81,"d":"81.00"},199.31,"<1","N/A","http://selleckchem.com/products/pf-06463922.html","C21H19FN6O2","free base","N/A","CC1OC2=C(N)N=CC(=C2)C3=C(C#N)[N](C)N=C3CN(C)C(=O)C4=C1C=C(F)C=C4",2.343,4,1,0]
["S7555","Domatinostat (4SC-202)","b8","L1700-47","in 10mM DMSO","HDAC","Epigenetics","Domatinostat (4SC-202) is a selective class I HDAC inhibitor with IC50 of 1.20 μM, 1.12 μM, and 0.57 μM for HDAC1, HDAC2, and HDAC3, respectively. Also displays inhibitory activity against Lysine specific demethylase 1 (LSD1). Phase 1.",447.51,"910462-43-0",{"v":89,"d":"89.00"},198.88,"<1","N/A","http://selleckchem.com/products/4sc-202.html","C23H21N5O3S","free base","N/A","C[N]1C=C(C=N1)C2=CC=C(C=C2)[S](=O)(=O)[N]3C=CC(=C3)\\C=C\\C(=O)NC4=CC=CC=C4N",2.955,4,2,6]
["S7572","A-366","c9","L1700-47","in 10mM DMSO","G9a/GLP,Histone Methyltransferase","Epigenetics","A-366 is a potent and selective G9a/GLP histone lysine methyltransferase inhibitor with IC50 of 3.3nM and 38nM, exhibiting >1000-fold selectivity for G9a/GLP over 21 other methyltransferases.",329.44,"1527503-11-2",{"v":65,"d":"65.00"},{"v":197.3,"d":"197.30"},"<1","N/A","http://selleckchem.com/products/a-366.html","C19H27N3O2","free base","N/A","COC1=C(OCCCN2CCCC2)C=C3N=C(N)C4(CCC4)C3=C1",2.467,3,1,6]
["S7581","GSK J1","b10","L1700-47","in 10mM DMSO","Histone Demethylase,JMJD","Epigenetics","GSK-J1 is a highly potent inhibitor of H3K27 histone demethylase JMJD3 (KDM6B) and UTX (KDM6A) with IC50 of 60 nM  in cell-free assays for JMJD3 (KDM6B) , respectively, >10-fold selectivity over other tested demethylases, with IC50 of 0.95μM and 1.76μM towards JARID1B/C.",389.45,"1373422-53-7",{"v":77,"d":"77.00"},197.71,"<1","N/A","http://selleckchem.com/products/gsk-j1.html","C22H23N5O2","free base","N/A","OC(=O)CCNC1=CC(=NC(=N1)C2=CC=CC=N2)N3CCC4=C(CC3)C=CC=C4",3.707,4,1,6]
["S7597","BV-6","f11","L1700-47","in 10mM DMSO","IAP","Apoptosis","BV-6 is a SMAC mimetic, dual cIAP and XIAP inhibitor.",1205.57,"1001600-56-1(free base)",{"v":100,"d":"100.00"},82.95,{"v":25,"d":"25.00"},20.74,"http://selleckchem.com/products/bv-6.html","C70H96N10O8.xCF3COOH","free base","N/A","CNC(C)C(=O)NC(C1CCCCC1)C(=O)N2CCCC2C(=O)NC(C(C3=CC=CC=C3)C4=CC=CC=C4)C(=O)NCCCCCCNC(=O)C(NC(=O)C5CCCN5C(=O)C(NC(=O)C(C)NC)C6CCCCC6)C(C7=CC=CC=C7)C8=CC=CC=C8",8.158,8,8,29]
["S7631","TH287","e3","L1700-48","in 10mM DMSO","MTH1,NUDIX","DNA Damage/DNA Repair","TH287 is a potent and selective MTH1 (NUDT1) inhibitor with IC50 of 0.8 nM.",269.13,"1609960-30-6",{"v":53,"d":"53.00"},196.93,"<1","N/A","http://selleckchem.com/products/th287.html","C11H10Cl2N4","free base","N/A","CNC1=CC(=NC(=N1)N)C2=C(Cl)C(=CC=C2)Cl",3.449,2,2,2]
["S7636","SU9516","b4","L1700-48","in 10mM DMSO","CDK","Cell Cycle","SU 9516 is a 3-substituted indolinone CDK inhibitor with IC50 of 22 nM, 40 nM, and 200 nM for CDK2, CDK1, and CDK4, respectively.",241.25,"377090-84-1",{"v":48,"d":"48.00"},198.96,"<1","N/A","http://selleckchem.com/products/su9516.html","C13H11N3O2","free base","N/A","COC1=CC=C2NC(=O)C(=C\\C3=CN=C[NH]3)/C2=C1",0.893,3,2,2]
["S7651","SB225002","f5","L1700-48","in 10mM DMSO","CXCR","GPCR & G Protein","SB225002 is a potent, and selective CXCR2 antagonist with IC50 of 22 nM for inhibiting interleukin IL-8 binding to CXCR2, > 150-fold selectivity over the other 7-TMRs tested.",352.14,"182498-32-4",{"v":70,"d":"70.00"},198.78,"<1","N/A","http://selleckchem.com/products/sb225002.html","C13H10BrN3O4","free base","N/A","OC1=CC(=CC=C1NC(=O)NC2=C(Br)C=CC=C2)[N+]([O-])=O",2.923,1,3,3]
["S7653","PND-1186 (VS-4718)","h5","L1700-48","in 10mM DMSO","Apoptosis related,FAK","Angiogenesis","PND-1186 (VS-4718, SR-2156) is a reversible and selective FAK inhibitor with IC50 of 1.5 nM. PND-1186 selectively promotes tumor cell apoptosis. Phase 1.",{"v":501.5,"d":"501.50"},"1061353-68-1",{"v":24,"d":"24.00"},47.86,"<1","N/A","http://selleckchem.com/products/pnd-1186-vs-4718.html","C25H26F3N5O3","free base","SR-2156","CNC(=O)C1=CC=CC=C1NC2=CC(=NC=C2C(F)(F)F)NC3=CC=C(C=C3OC)N4CCOCC4",4.302,4,3,8]
["S7681","OF-1","b8","L1700-48","in 10mM DMSO","Epigenetic Reader Domain","Epigenetics","OF-1 is a potent inhibitor of BRPF1B and BRPF2 bromodomain with Kd of 100 nM and 500 nM, respectively.",440.31,"919973-83-4",{"v":76,"d":"76.00"},172.61,"<1","N/A","http://selleckchem.com/products/of-1.html","C17H18BrN3O4S","free base","N/A","COC1=CC2=C(C=C1N[S](=O)(=O)C3=C(C)C=C(Br)C=C3)N(C)C(=O)N2C",{"v":2.81,"d":"2.810"},4,1,4]
["S7685","SecinH3","e8","L1700-48","in 10mM DMSO","cytohesin","Apoptosis","SecinH3 is a selective cytohesin inhibitor with IC50 of 2.4 μM, 5.4 μM, 5.4 μM, 5.6 μM, 5.6 μM, and 65 μM for hCyh2, hCyh1, mCyh3, hCyh3, drosophila steppke, and yGea2-S7, respectively.",{"v":460.5,"d":"460.50"},"853625-60-2",{"v":92,"d":"92.00"},199.78,"<1","N/A","http://selleckchem.com/products/secinh3.html","C24H20N4O4S","free base","N/A","COC1=N[N](C2=CC=C(NC(=O)CSC3=CC=CC=C3)C=C2)C(=N1)C4=CC=C5OCOC5=C4",4.748,6,1,7]
["S7697","LY2409881","d9","L1700-48","in 10mM DMSO","IκB/IKK","NF-κB","LY2409881 is a potent and selective IKK2 inhibitor with IC50 of 30 nM, >10-fold selectivity over IKK1 and other common kinases.",594.43,"946518-60-1",{"v":20,"d":"20.00"},33.65,"<1","N/A","http://selleckchem.com/products/ly2409881.html","C24H32Cl4N6OS","trihydrochloride","N/A","Cl.Cl.Cl.CN1CCN(CCCNC2=NC=C(Cl)C(=N2)C3=CC4=C(S3)C=CC=C4C(=O)NC5CC5)CC1",5.147,3,2,8]
["S7721","Monomethyl auristatin E (MMAE)","g10","L1700-48","in 10mM DMSO","ADC Cytotoxin,Microtubule Associated","Cytoskeletal Signaling","Monomethyl auristatin E (MMAE, SGD-1010) is a synthetic antineoplastic agent, which is linked to a monoclonal antibody (MAB). It is also a microtubule-disrupting agent .",717.98,"474645-27-7",{"v":100,"d":"100.00"},139.28,"<1","N/A","http://selleckchem.com/products/monomethyl-auristatin-e-mmae.html","C39H67N5O7","free base","SGD-1010","CCC(C)C(C(CC(=O)N1CCCC1C(OC)C(C)C(=O)NC(C)C(O)C2=CC=CC=C2)OC)N(C)C(=O)C(NC(=O)C(NC)C(C)C)C(C)C",{"v":3.46,"d":"3.460"},6,4,20]
["S7743","CCT196969","e2","L1700-49","in 10mM DMSO","Raf,Src","MAPK","CCT196969 is a novel orally available, pan-RAF inhibitor with anti-SRC activity. It also inhibits SRC, LCK, and the p38 MAPKs.",513.52,"1163719-56-9",{"v":100,"d":"100.00"},194.73,"<1","N/A","http://selleckchem.com/products/cct196969.html","C27H24FN7O3","free base","N/A","CC(C)(C)C1=N[N](C(=C1)NC(=O)NC2=CC=C(OC3=C4N=CC(=O)NC4=NC=C3)C=C2F)C5=CC=CC=C5",4.782,6,3,6]
["S7753","BPTES","d3","L1700-49","in 10mM DMSO","Glutaminase","Proteases","BPTES is a potent and selective Glutaminase GLS1 (KGA) inhibitor with IC50 of 0.16 μM. It has no effect on glutamate dehydrogenase activity and causes only a very slight inhibition of γ-glutamyl transpeptidase activity.",524.68,"314045-39-1",{"v":100,"d":"100.00"},190.59,"<1","N/A","http://selleckchem.com/products/bptes.html","C24H24N6O2S3","free base","N/A","O=C(CC1=CC=CC=C1)NC2=NN=C(CCSCCC3=NN=C(NC(=O)CC4=CC=CC=C4)S3)S2",3.432,6,2,12]
["S7775","Emricasan (IDN-6556)","h4","L1700-49","in 10mM DMSO","Antiviral,Caspase","Apoptosis","Emricasan (IDN-6556, PF 03491390, PF-03491390) is a potent irreversible pan-caspase inhibitor. Emricasan is an inhibitor of Zika virus infection.",{"v":569.5,"d":"569.50"},"254750-02-2",{"v":100,"d":"100.00"},175.59,"<1","N/A","http://selleckchem.com/products/emricasan-idn-6556-pf-03491390.html","C26H27F4N3O7","free base","PF 03491390, PF-03491390","CC(NC(=O)C(=O)NC1=C(C=CC=C1)C(C)(C)C)C(=O)NC(CC(O)=O)C(=O)COC2=C(F)C(=CC(=C2F)F)F",3.017,6,3,12]
["S7783","Combretastatin A4","f5","L1700-49","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","Combretastatin A4 is a microtubule-targeting agent that binds β-tubulin with Kd of 0.4 μM.Phase 3.",316.35,"117048-59-6",{"v":63,"d":"63.00"},199.15,"<1","N/A","http://selleckchem.com/products/combretastatin-a4.html","C18H20O5","free base","N/A","COC1=C(O)C=C(\\C=C/C2=CC(=C(OC)C(=C2)OC)OC)C=C1",3.508,4,1,6]
["S7811","MHY1485","d7","L1700-49","in 10mM DMSO","Autophagy,mTOR","PI3K/Akt/mTOR","MHY1485 is a potent, and cell-permeable mTOR activator, and also potently inhibits autophagy.",387.39,"326914-06-1",{"v":4,"d":"4.00"},10.33,"<1","N/A","http://selleckchem.com/products/mhy1485.html","C17H21N7O4","free base","N/A","[O-][N+](=O)C1=CC=C(NC2=NC(=NC(=N2)N3CCOCC3)N4CCOCC4)C=C1",2.653,5,1,5]
["S7814","AI-10-49","g7","L1700-49","in 10mM DMSO","Others","Apoptosis","AI-10-49 is a selective inhibitor of the binding of CBFβ-SMMHC to RUNX1 with IC50 of 260 nM.",660.52,"1256094-72-0",{"v":100,"d":"100.00"},{"v":151.4,"d":"151.40"},"<1","N/A","http://selleckchem.com/products/ai-10-49.html","C30H22F6N6O5","Free Base","N/A","FC(F)(F)OC1=CC=C2[NH]C(=NC2=C1)C3=NC=C(OCCOCCOC4=CN=C(C=C4)C5=NC6=C([NH]5)C=CC(=C6)OC(F)(F)F)C=C3",8.991,9,2,14]
["S7835","I-BRD9","c9","L1700-49","in 10mM DMSO","Epigenetic Reader Domain","Epigenetics","I-BRD9 (GSK602) is a potent and selective BRD9 inhibitor with pIC50 of 7.3, while it displayed a pIC50 of 5.3 against BRD4.",497.55,"1714146-59-4",{"v":99,"d":"99.00"},198.97,"<1","N/A","http://selleckchem.com/products/i-brd9-gsk602.html","C22H22F3N3O3S2","free base","GSK602","CCN1C=C(C2=CC(=CC=C2)C(F)(F)F)C3=C(C=C(S3)C(=N)NC4CC[S](=O)(=O)CC4)C1=O",2.779,3,1,6]
["S7852","Eliglustat","c10","L1700-49","in 10mM DMSO","Glucosylceramide Synthase","Metabolism","Eliglustat (GENZ-112638) inhibits glucosylceramide synthase(GCS) (IC50=20 nM in intact MDCK cells), thus reducing the load of glucosylceramide influx into the lysosome.",404.54,"491833-29-5",{"v":80,"d":"80.00"},197.76,"<1","N/A","http://selleckchem.com/products/eliglustat.html","C23H36N2O4","Tartrate","GENZ-112638","CCCCCCCC(=O)NC(CN1CCCC1)C(O)C2=CC=C3OCCOC3=C2",3.808,3,2,11]
["S7877","ONO-4059 analogue","g11","L1700-49","in 10mM DMSO","BTK","Angiogenesis","ONO-4059 analogue (ONO-WG-307) is an analogue of ONO-4059, which is a highly potent and selective oral BTK inhibitor with IC50 of 23.9 nM. Phase 1.",{"v":456.5,"d":"456.50"},"1351635-67-0",{"v":20,"d":"20.00"},43.81,"<1","N/A","http://selleckchem.com/products/ono-4059.html","C25H24N6O3","free base","ONO-WG-307","NC1=C2N(C(=O)N(C3CCCN(C3)C(=O)C=C)C2=NC=N1)C4=CC=C(OC5=CC=CC=C5)C=C4",{"v":3.38,"d":"3.380"},5,1,5]
["S7891","CC-115","f2","L1700-50","in 10mM DMSO","DNA-PK,mTOR","DNA Damage/DNA Repair","CC-115 is a dual inhibitor of DNA-dependent protein kinase (DNA-PK) and mammalian target of rapamycin (mTOR) with IC50 values of 0.013 μM and 0.021 μM, respectively. It has potential antineoplastic activity.",336.35,"1228013-15-7",{"v":67,"d":"67.00"},{"v":199.2,"d":"199.20"},"<1","N/A","http://selleckchem.com/products/cc-115.html","C16H16N8O","free base","N/A","CCN1C(=O)CNC2=NC=C(N=C12)C3=C(C)N=C(C=C3)C4=N[NH]C=N4",0.664,6,2,3]
["S7909","Dp44mT","d3","L1700-50","in 10mM DMSO","Others","Others","Dp44mT is a potent iron chelator, which shows selective antitumor activity.",285.37,"152095-12-0",{"v":57,"d":"57.00"},199.74,"<1","N/A","http://selleckchem.com/products/dp44mt.html","C14H15N5S","free base","N/A","CN(C)C(=S)N\\N=C(/C1=NC=CC=C1)C2=CC=CC=N2",2.968,3,1,5]
["S7928","DASA-58","b5","L1700-50","in 10mM DMSO","PKM","Metabolism","DASA-58 is a specific and potent Pyruvate kinase M2 (PKM2) activator.",453.53,"1203494-49-8",{"v":91,"d":"91.00"},200.65,"<1","N/A","http://selleckchem.com/products/dasa-58.html","C19H23N3O6S2","free base","N/A","NC1=CC(=CC=C1)[S](=O)(=O)N2CCCN(CC2)[S](=O)(=O)C3=CC4=C(OCCO4)C=C3",0.632,6,1,4]
["S7943","O4I1","f6","L1700-50","in 10mM DMSO","OCT","Transmembrane Transporters","O4I1 is a potent Oct3/4 inducer.",{"v":253.3,"d":"253.30"},"175135-47-4",{"v":51,"d":"51.00"},201.34,"<1","N/A","http://selleckchem.com/products/o4i1.html","C16H15NO2","free base","N/A","COC1=CC=C(COC2=CC=C(CC#N)C=C2)C=C1",3.294,2,0,5]
["S7947","PX-12","a7","L1700-50","in 10mM DMSO","COVID-19,Thioredoxin","Metabolism","PX-12 (DB05448, 1-methyl propyl 2-imidazolyl disulfide) is a potent thioredoxin-1 (Trx-1) inhibitor by irreversibly thioalkylation of Cys73 of Trx-1. Phase 2.",188.31,"141400-58-0",{"v":38,"d":"38.00"},201.79,"<1","N/A","http://selleckchem.com/products/px-12.html","C7H12N2S2","free base","DB05448, 1-methyl propyl 2-imidazolyl disulfide","CCC(C)SSC1=NC=C[NH]1",2.641,1,1,4]
["S7958","Lificiguat (YC-1)","a8","L1700-50","in 10mM DMSO","Guanylate Cyclase,HIF","Angiogenesis","Lificiguat (YC-1) is an nitric oxide (NO)-independent activator of soluble guanylyl cyclase(sGC) and an inhibitor of Hypoxia-inducible factor-1alpha (HIF-1alpha).",304.34,"170632-47-0",{"v":60,"d":"60.00"},197.15,"<1","N/A","http://selleckchem.com/products/lificiguat-yc-1.html","C19H16N2O2","free base","N/A","OCC1=CC=C(O1)C2=N[N](CC3=CC=CC=C3)C4=C2C=CC=C4",4.078,2,1,4]
["S7977","Napabucasin (BBI608)","e9","L1700-50","in 10mM DMSO","STAT","JAK/STAT","Napabucasin (BBI608) is an orally available Stat3 and cancer cell stemness inhibitor.",240.21,"83280-65-3",{"v":10,"d":"10.00"},41.63,"<1","N/A","http://selleckchem.com/products/napabucasin.html","C14H8O4","free base","BBI608","CC(=O)C1=CC2=C(O1)C(=O)C3=CC=CC=C3C2=O",2.234,4,0,1]
["S8003","PQ 401","a11","L1700-50","in 10mM DMSO","IGF-1R","Protein Tyrosine Kinase","PQ401 inhibits autophosphorylation of IGF-1R domain with IC50 of <1 μM.",341.79,"196868-63-0",{"v":32,"d":"32.00"},93.62,"<1","N/A","http://selleckchem.com/products/pq-401.html","C18H16ClN3O2","free base","N/A","COC1=C(NC(=O)NC2=C3C=CC=CC3=NC(=C2)C)C=C(Cl)C=C1",3.639,3,2,3]
["S8014","GW9508","h11","L1700-50","in 10mM DMSO","GPR","Endocrinology & Hormones","GW9508 is a potent and selective agonist for FFA1 (GPR40) with pEC50 of 7.32, 100-fold selective against GPR120, stimulates insulin secretion in a glucose-sensitive manner.",347.41,"885101-89-3",{"v":69,"d":"69.00"},198.61,"<1","N/A","http://selleckchem.com/products/gw9508.html","C22H21NO3","free base","N/A","OC(=O)CCC1=CC=C(NCC2=CC=CC(=C2)OC3=CC=CC=C3)C=C1",4.903,2,1,8]
["S8032","PRT062607 (P505-15) HCl","e3","L1700-51","in 10mM DMSO","FAK,FLT3,Mixed Lineage Kinase,PAK,Pyk2,Src,Syk","Angiogenesis","PRT062607 (P505-15, BIIB057, PRT-2607) HCl is a novel, highly selective Syk inhibitor with IC50 of 1 nM in cell-free assays, >80-fold selective for Syk than Fgr, PAK5, Lyn, FAK, Pyk2, FLT3, MLK1 and Zap70.",429.91,"1370261-97-4",{"v":86,"d":"86.00"},200.04,{"v":86,"d":"86.00"},200.04,"http://selleckchem.com/products/prt062607-p505-15-hcl.html","C19H23N9O.HCl","Hydrochloride","BIIB057, PRT-2607","Cl.NC1CCCCC1NC2=NC=C(C(N)=O)C(=N2)NC3=CC(=CC=C3)[N]4N=CC=N4",2.033,5,4,6]
["S8040","GDC-0349","d4","L1700-51","in 10mM DMSO","mTOR","PI3K/Akt/mTOR","GDC-0349 (RG-7603) is a potent and selective ATP-competitive inhibitor of mTOR with Ki of 3.8 nM, 790-fold inhibitory effect against PI3Kα and other 266 kinases. Phase 1.",452.55,"1207360-89-1",{"v":91,"d":"91.00"},201.08,"<1","N/A","http://selleckchem.com/products/gdc-0349.html","C24H32N6O3","free base","RG-7603","CCNC(=O)NC1=CC=C(C=C1)C2=NC(=C3CCN(CC3=N2)C4COC4)N5CCOCC5C",1.982,5,2,5]
["S8057","Pacritinib (SB1518)","h5","L1700-51","in 10mM DMSO","FLT3,JAK","JAK/STAT","Pacritinib (SB1518) is a potent and selective inhibitor of Janus Kinase 2 (JAK2) and Fms-Like Tyrosine Kinase-3 (FLT3) with IC50s of 23 and 22 nM in cell-free assays, respectively. Phase 3.",472.58,"937272-79-2",{"v":11,"d":"11.00"},23.28,"<1","N/A","http://selleckchem.com/products/pacritinib-sb1518.html","C28H32N4O3","free base","N/A","C1CCN(C1)CCOC2=CC=C3NC4=NC=CC(=N4)C5=CC(=CC=C5)COC\\C=C\\COCC2=C3",4.547,5,1,4]
["S8058","Riviciclib hydrochloride (P276-00)","a6","L1700-51","in 10mM DMSO","Apoptosis related,CDK","Cell Cycle","Riviciclib hydrochloride (P276-00) is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Riviciclib hydrochloride (P276-00) induces apoptosis. Phase 2/3.",{"v":438.3,"d":"438.30"},"920113-03-7",{"v":88,"d":"88.00"},200.78,{"v":88,"d":"88.00"},200.78,"http://selleckchem.com/products/p276-00.html","C21H20ClNO5.HCl","hydrochloride","N/A","Cl.CN1CCC(C1CO)C2=C(O)C=C(O)C3=C2OC(=CC3=O)C4=C(Cl)C=CC=C4",{"v":3.49,"d":"3.490"},2,3,3]
["S8078","Bardoxolone Methyl","c7","L1700-51","in 10mM DMSO","Apoptosis related,Autophagy,Ferroptosis,IκB/IKK,NF-κB,Nrf2","NF-κB","Bardoxolone Methyl (RTA 402, TP-155, NSC 713200, CDDO Methyl Ester, CDDO-Me) is an IKK inhibitor, showing potent proapoptotic and anti-inflammatory activities; Also a potent Nrf2 activator and nuclear factor-κB (NF-κB) inhibitor. Bardoxolone Methyl abrogates ferroptosis. Bardoxolone methyl induces apoptosis and autophagy in cancer cells.",505.69,"218600-53-4",{"v":21,"d":"21.00"},41.53,"<1","N/A","http://selleckchem.com/products/bardoxolone-methyl.html","C32H43NO4","free base","RTA 402, TP-155, NSC 713200, CDDO Methyl Ester, CDDO-Me","COC(=O)C12CCC(C)(C)CC1C3C(=O)C=C4C(C)(CCC5C(C)(C)C(=O)C(=CC45C)C#N)C3(C)CC2",5.798,4,0,2]
["S8111","GSK591","g8","L1700-51","in 10mM DMSO","Histone Methyltransferase,PRMT","Epigenetics","GSK591 (EPZ015866, GSK3203591) is a potent selective inhibitor of the arginine methyltransferase PRMT5 with IC50 of 4 nM.",380.48,"1616391-87-7",{"v":76,"d":"76.00"},199.75,"<1","N/A","http://selleckchem.com/products/gsk591-epz015866-gsk3203591.html","C22H28N4O2","free base","EPZ015866, GSK3203591","OC(CNC(=O)C1=CC(=NC=C1)NC2CCC2)CN3CCC4=C(C3)C=CC=C4",2.467,2,3,7]
["S8136","Sivelestat (ONO-5046)","d10","L1700-51","in 10mM DMSO","Serine Protease","Proteases","Sivelestat (ONO5046, LY544349, EI546) is a potent and selective inhibitor of neutrophil elastase with IC50 of 44nM. It almost shows no activity at a range of other proteases.",434.46,"127373-66-4",{"v":86,"d":"86.00"},197.95,"<1","N/A","http://selleckchem.com/products/sivelestat-ono-5046.html","C20H22N2O7S","Free Base","ONO5046, LY544349, EI546","CC(C)(C)C(=O)OC1=CC=C(C=C1)[S](=O)(=O)NC2=CC=CC=C2C(=O)NCC(O)=O",2.321,6,2,9]
["S8149","NSC348884","c11","L1700-51","in 10mM DMSO","Apoptosis related,p53","Apoptosis","NSC348884, as a nucleophosmin inhibitor, inhibit cell proliferation and induce apoptosis in various cancer cell lines with IC50 values ranging from 1.4-4 µM.",636.79,"81624-55-7",{"v":100,"d":"100.00"},157.04,"<1","N/A","http://selleckchem.com/products/nsc348884.html","C38H40N10","free base","N/A","CC1=CC2=C(C=C1)N=C(CN(CCN(CC3=NC4=C([NH]3)C=C(C)C=C4)CC5=NC6=C([NH]5)C=C(C)C=C6)CC7=NC8=C([NH]7)C=C(C)C=C8)[NH]2",7.572,4,4,11]
["S8173","Verubecestat (MK-8931) Trifluoroacetate","g2","L1700-52","in 10mM DMSO","BACE","Neuronal Signaling","Verubecestat (MK-8931) Trifluoroacetate is a potent and selective beta-secretase inhibitor and BACE1 protein inhibitor or Beta-site APP-cleaving enzyme 1 inhibitor.",523.43,"2095432-65-6",{"v":81,"d":"81.00"},154.75,"<1","N/A","http://selleckchem.com/products/verubecestat-mk-8931.html","C19H18F5N5O5S","Trifluoroacetat","MK-8931","CN1C(=N)NC(C)(C[S]1(=O)=O)C2=CC(=CC=C2F)NC(=O)C3=CC=C(F)C=N3.OC(=O)C(F)(F)F",2.198,5,2,4]
["S8182","NSC87877","f3","L1700-52","in 10mM DMSO","phosphatase","Metabolism","NSC-87877 is a cell-permeable inhibitor of both SHP-1 and SHP-2 with IC50 values of 355 and 318 nM respectively. It also inhibits EGF-induced Erk1/2 activation in HEK293 cells and significantly reduces MDA-MB-468 cell viability/proliferation.",503.42,"56932-43-5",{"v":100,"d":"100.00"},198.64,{"v":100,"d":"100.00"},198.64,"http://selleckchem.com/products/nsc87877.html","C19H13N3O7S2.2Na","sodium salt","N/A","OC1=C2N=CC=CC2=C(C=C1N=NC3=CC4=CC=C(C=C4C=C3)[S](=O)(=O)O[Na])[S](=O)(=O)O[Na]",3.899,5,1,6]
["S8193","Lanabecestat (AZD3293)","e4","L1700-52","in 10mM DMSO","BACE","Neuronal Signaling","Lanabecestat (AZD3293, LY3314814) is an oral beta-secretase 1 cleaving enzyme (BACE) inhibitor with an inhibitory constant Ki  of 0.4 nM.",412.53,"1383982-64-6",{"v":82,"d":"82.00"},198.77,"<1","N/A","http://selleckchem.com/products/azd3293-ly3314814.html","C26H28N4O","free base","LY3314814","COC1CCC2(CC1)CC3=C(C=C(C=C3)C4=CN=CC(=C4)C#CC)C25N=C(C)C(=N5)N",3.882,4,1,3]
["S8208","Hydroxyfasudil (HA-1100) HCl","f5","L1700-52","in 10mM DMSO","ROCK","Cell Cycle","Hydroxyfasudil (HA-1100), an active metabolite of fasudil hydrochloride, is a specific Rho-kinase(ROCK) inhibitor with IC50 values of 0.73 μM and 0.72 μM for ROCK1 and ROCK2, respectively.",343.83,"155558-32-0 (HCl salt)",{"v":68,"d":"68.00"},197.77,{"v":60,"d":"60.00"},{"v":174.5,"d":"174.50"},"http://selleckchem.com/products/hydroxyfasudil-ha-1100.html","C14H17N3O3S.HCl.xH2O","hydrochloride","N/A","Cl.O=C1NC=CC2=C1C=CC=C2[S](=O)(=O)N3CCCNCC3",0.443,3,2,2]
["S8234","RS-1","e6","L1700-52","in 10mM DMSO","CRISPR/Cas9,RAD51","DNA Damage/DNA Repair","RS-1 is a RAD51-stimulatory compound, which increases the DNA binding activity of RAD51. It is an HDR(homology-directed repair) enhancer that enhances Cas9- and TALEN-mediated knock-in efficiency in rabbit embryos both in vitro and in vivo.",524.23,"312756-74-4",{"v":100,"d":"100.00"},190.76,"<1","N/A","http://selleckchem.com/products/rs-1.html","C20H16Br2N2O3S","free base","N/A","BrC1=CC=C(NC(=O)C2=CC=C(Br)C(=C2)[S](=O)(=O)NCC3=CC=CC=C3)C=C1",4.606,3,2,6]
["S8250","79-6 (CID5721353)","a8","L1700-52","in 10mM DMSO","Bcl-6","Apoptosis","79-6 (CID5721353) (BCL6 inhibitor) is a BCL6 inhibitor with Kd value of 138 μM.",457.28,"301356-95-6",{"v":91,"d":"91.00"},{"v":199,"d":"199.00"},"<1","N/A","http://selleckchem.com/products/79-6-cid5721353-bcl6-inhibitor.html","C15H9BrN2O6S2","free base","BCL6 inhibitor","OC(=O)CC(N1C(=S)S/C(C1=O)=C/2C(=O)NC3=CC=C(Br)C=C23)C(O)=O",2.057,4,1,4]
["S8276","FCCP","d9","L1700-52","in 10mM DMSO","ATPase,OXPHOS","Apoptosis","FCCP (Trifluoromethoxy carbonylcyanide phenylhydrazone, Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone) is a potent uncoupler of oxidative phosphorylation in mitochondria that disrupts ATP synthesis by transporting protons across cell membranes.",254.17,"370-86-5",{"v":50,"d":"50.00"},196.72,"<1","N/A","http://selleckchem.com/products/fccp.html","C10H5F3N4O","free base","Trifluoromethoxy carbonylcyanide phenylhydrazone, Carbonyl cyanide 4-(trifluoromethoxy)phenylhydrazone","FC(F)(F)OC1=CC=C(NN=C(C#N)C#N)C=C1",3.924,2,1,4]
["S8288","VLX1570","e10","L1700-52","in 10mM DMSO","DUB","Ubiquitin","VLX1570 is a competitive inhibitor of proteasome DUB activity, with an IC50 of ~10 μM in vitro.",469.39,"1431280-51-1",{"v":93,"d":"93.00"},198.13,"<1","N/A","http://selleckchem.com/products/vlx1570.html","C23H17F2N3O6","free base","N/A","[O-][N+](=O)C1=C(F)C=CC(=C1)\\C=C2/CCN(C\\C(=C/C3=CC=C(F)C(=C3)[N+]([O-])=O)C2=O)C(=O)C=C",4.385,2,0,5]
["S8305","TRC051384","a2","L1700-53","in 10mM DMSO","HSP (HSP90)","Metabolism","TRC051384 is an inducer of heat shock protein 70 (HSP70) and potent anti-inflammatory agent.",465.54,"867164-40-7",{"v":93,"d":"93.00"},199.77,"<1","N/A","http://selleckchem.com/products/trc051384.html","C25H31N5O4","free base","N/A","O=C(NCCN1CCOCC1)NC2=CC=C(C=C2)C(=O)\\C=C\\C3=CC=CC(=N3)N4CCOCC4",2.311,5,2,8]
["S8320","SKL2001","a3","L1700-53","in 10mM DMSO","Wnt/beta-catenin","Stem Cells & Wnt","SKL2001 is a novel agonist of the Wnt/β-catenin pathway. It disrupts the Axin/β-catenin interaction.",286.29,"909089-13-0",{"v":57,"d":"57.00"},{"v":199.1,"d":"199.10"},"<1","N/A","http://selleckchem.com/products/skl2001.html","C14H14N4O3","free base","N/A","O=C(NCCC[N]1C=CN=C1)C2=NOC(=C2)C3=CC=CO3",0.929,5,1,6]
["S8337","1400W 2HCl","e4","L1700-53","in 10mM DMSO","NOS","Immunology & Inflammation","1400W (N-(3-(Aminomethyl)benzyl)acetamidine) is a slow, tight binding, and highly selective inhibitor of inducible nitric-oxide synthase(iNOS).",250.17,"214358-33-5",{"v":35,"d":"35.00"},{"v":139.9,"d":"139.90"},{"v":35,"d":"35.00"},{"v":139.9,"d":"139.90"},"http://selleckchem.com/products/1400w.html","C10H15N3.2HCl","dihydrochloride","N-(3-(Aminomethyl)benzyl)acetamidine","Cl.Cl.CC(=N)NCC1=CC=CC(=C1)CN",0.881,0,2,4]
["S8355","APS-2-79 HCl","d5","L1700-53","in 10mM DMSO","MEK","MAPK","APS-2-79 is a MAPK antagonist that modulating KSR-dependent MAPK signalling by antagonizing RAF heterodimerization as well as the conformational changes required for phosphorylation and activation of KSR-bound MEK. IC50=120 ± 23 nM.",423.89,"2002381-31-7",{"v":97,"d":"97.00"},228.83,"<1","N/A","http://selleckchem.com/products/aps-2-79.html","C23H21N3O3.HCl","hydrochloride","N/A","Cl.COC1=C(OC)C=C2C(=NC=NC2=C1)NC3=CC=C(OC4=CC=CC=C4)C=C3C",5.873,5,1,6]
["S8362","Tucatinib","g5","L1700-53","in 10mM DMSO","EGFR,HER2","Protein Tyrosine Kinase","Tucatinib (Irbinitinib, ONT-380, ARRY-380) is an oral, potent, selective, reversible and ATP-competitive small-molecule inhibitor of ErbB-2 (also called HER2) with IC50s of 8 nM and 7 nM for ErbB-2 and p95 HER2, respectively in cell-based assays, showing ~500-fold selective for HER2 vs EGFR. It has potential antineoplastic activity.",480.52,"937263-43-9",{"v":96,"d":"96.00"},199.78,"<1","N/A","http://selleckchem.com/products/arry-380-ont-380.html","C26H24N8O2","free base","Irbinitinib, ONT-380, ARRY-380","CC1=CC(=CC=C1OC2=CC3=NC=N[N]3C=C2)NC4=NC=NC5=CC=C(NC6=NC(C)(C)CO6)C=C45",4.744,7,2,6]
["S8380","YM-58483 (BTP2)","b7","L1700-53","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","YM-58483/BTP2 is a blocker of store-operated Ca2+ entry (SOCE), which regulates the activation of non-excitable cells such as lymphocytes.",421.32,"223499-30-7",{"v":84,"d":"84.00"},199.37,"<1","N/A","http://selleckchem.com/products/ym-58483-btp2.html","C15H9F6N5OS","free base","N/A","CC1=C(SN=N1)C(=O)NC2=CC=C(C=C2)[N]3N=C(C=C3C(F)(F)F)C(F)(F)F",4.564,4,1,5]
["S8403","MX69","c8","L1700-53","in 10mM DMSO","MDM2/MDMX","Apoptosis","MX69 is a MDM2/XIAP inhibitor that binds to MDM2 RING protein with binding Kd values of 2.34 μM. It is used for cancer treatment.",474.57,"1005264-47-0",{"v":95,"d":"95.00"},200.18,"<1","N/A","http://selleckchem.com/products/mx69.html","C27H26N2O4S","free base","N/A","CC1=C(C)C=C(N[S](=O)(=O)C2=CC3=C(NC(C4CC=CC34)C5=CC=C(C=C5)C(O)=O)C=C2)C=C1",5.082,3,2,5]
["S8433","NS-398 (NS398)","g9","L1700-53","in 10mM DMSO","COX","Neuronal Signaling","NS-398 (N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide) is a selective inhibitor of cyclooxygenase-2 (COX-2). The IC50 values for human recombinant COX-1 and -2 are 75 and 1.77 μM, respectively.",314.36,"123653-11-2",{"v":62,"d":"62.00"},197.23,"<1","N/A","http://selleckchem.com/products/ns-398-ns398.html","C13H18N2O5S","free base","N-(2-cyclohexyloxy-4-nitrophenyl)methane sulfonamide","C[S](=O)(=O)NC1=C(OC2CCCCC2)C=C(C=C1)[N+]([O-])=O",2.477,3,1,5]
["S8457","UK-371804 HCl","c11","L1700-53","in 10mM DMSO","Serine Protease","Proteases","UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin).",422.29,"256476-36-5",{"v":30,"d":"30.00"},71.04,"<1","N/A","http://selleckchem.com/products/uk-371804-hcl.html","C14H16ClN5O4S.HCl","hydrochloride","UK-371804 HCl","Cl.CC(C)(N[S](=O)(=O)C1=CC2=C(C=C1)C(=CN=C2NC(N)=N)Cl)C(O)=O",1.326,4,3,6]
["S8474","LF3","a2","L1700-54","in 10mM DMSO","Wnt/beta-catenin","Stem Cells & Wnt","LF3 is a specific inhibitor of canonical Wnt signaling by disrupting the interaction between β-catenin and TCF4 with an IC50 less than 2 μM.",416.56,"664969-54-4",{"v":83,"d":"83.00"},199.25,"<1","N/A","http://selleckchem.com/products/lf3.html","C20H24N4O2S2","free base","N/A","N[S](=O)(=O)C1=CC=C(NC(=S)N2CCN(CC2)C\\C=C\\C3=CC=CC=C3)C=C1",3.762,2,2,7]
["S8518","AD80","g3","L1700-54","in 10mM DMSO","c-RET,S6 Kinase,Src","Protein Tyrosine Kinase","AD80, a multikinase inhibitor, shows strong activity against human RET (c-RET), BRAF, S6K, and SRC but were much less active than either AD57 or AD58 against mTOR. The IC50 value for RET is 4 nM.",473.43,"1384071-99-1",{"v":94,"d":"94.00"},198.55,"<1","N/A","http://selleckchem.com/products/ad80.html","C22H19F4N7O","free base","N/A","CC(C)[N]1N=C(C2=CC=C(NC(=O)NC3=CC(=CC=C3F)C(F)(F)F)C=C2)C4=C(N)N=CN=C14",4.406,4,3,5]
["S8538","Ritlecitinib (PF-06651600)","f4","L1700-54","in 10mM DMSO","JAK","JAK/STAT","Ritlecitinib (PF-06651600) is a potent and irreversible JAK3-selective inhibitor with an IC50 of 33.1 nM but without activity (IC50 > 10 000 nM) against JAK1, JAK2, and TYK2.",285.34,"1792180-81-4",{"v":57,"d":"57.00"},199.76,"N/A","N/A","http://selleckchem.com/products/pf-06651600.html","C15H19N5O","free base","N/A","CC1CCC(CN1C(=O)C=C)NC2=C3C=C[NH]C3=NC=N2",1.854,3,2,3]
["S8558","Tofogliflozin(CSG 452)","f5","L1700-54","in 10mM DMSO","SGLT","GPCR & G Protein","Tofogliflozin (CSG 452) is a novel sodium-glucose co-transporter 2(SGLT2) inhibitor with IC50 values of 2.9 nM and 8444 nM for hSGLT2 and hSGLT1, respectively.",404.45,"1201913-82-7",{"v":84,"d":"84.00"},207.69,{"v":4,"d":"4.00"},9.89,"http://selleckchem.com/products/tofogliflozin-csg-452.html","C22H26O6.H2O","hydrate","N/A","O.CCC1=CC=C(CC2=CC3=C(COC34OC(CO)C(O)C(O)C4O)C=C2)C=C1",{"v":1.92,"d":"1.920"},2,4,4]
["S8570","RXDX-106 (CEP-40783)","f6","L1700-54","in 10mM DMSO","Axl,c-Met,Mertk,Tyro3","Protein Tyrosine Kinase","RXDX-106 (CEP-40783) is an orally-available, potent and selective TAM(TYRO3, AXL, MER)/Met (c-Met) inhibitor displaying low nanomolar biochemical activity and slow (T1/2 >120 min) inhibitor off-rate in peptide phosphorylation assays and in vitro kinase binding assays, respectively.",588.56,"1437321-24-8",{"v":10,"d":"10.00"},16.99,"<1","N/A","http://selleckchem.com/products/rxdx-106-cep-40783.html","C31H26F2N4O6","free base","N/A","COC1=CC2=C(C=C1OC)C(=CC=N2)OC3=C(F)C=C(NC(=O)C4=CN(C(C)C)C(=O)N(C4=O)C5=CC=C(F)C=C5)C=C3",4.572,7,1,8]
["S8581","Serabelisib (TAK-117)","e7","L1700-54","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","Serabelisib (TAK-117, INK-1117, MLN-1117) is a potent and selective oral PI3Kα isoform inhibitor (IC50 of 21 nmol/L against PI3Kα) that has demonstrated > 100-fold selectivity relative to other class I PI3K family members (PI3Kβ/γ/δ) and mTOR, and a high degree of selectivity against many other kinase.",363.37,"1268454-23-4",{"v":16,"d":"16.00"},44.03,"<1","N/A","http://selleckchem.com/products/tak-117-ink-1117-mln-1117.html","C19H17N5O3","free base","INK-1117, MLN-1117","NC1=NC2=C(O1)C=CC(=C2)C3=C[N]4C(=NC=C4C(=O)N5CCOCC5)C=C3",0.939,5,1,2]
["S8607","JQ-EZ-05 (JQEZ5)","a9","L1700-54","in 10mM DMSO","EZH1/2,Histone Methyltransferase","Epigenetics","JQ-EZ-05 (JQEZ5) is a specific and reversible EZH1/2 inhibitor.",542.68,"1913252-04-6",{"v":24,"d":"24.00"},44.22,"N/A","N/A","http://selleckchem.com/products/jq-ez-05-jqez5.html","C30H38N8O2","free base","N/A","CCCC1=C(CNC(=O)C2=CC(=NC3=C2C=N[N]3C(C)C)C4=CC=C(N=C4)N5CCN(C)CC5)C(=O)NC(=C1)C",3.379,5,2,8]
["S8616","PKM2 inhibitor(compound 3k)","g9","L1700-54","in 10mM DMSO","PKM","Metabolism","PKM2 inhibitor(Compound 3K, PKM2-IN-1) displays PKM2 inhibitory activity with the IC50 value of 2.95 μM. The IC50 value for PKM1 is 4-5-fold higher than that for PKM2.",345.48,"94164-88-2",{"v":6,"d":"6.00"},17.37,"<1","N/A","http://selleckchem.com/products/pkm2-inhibitor-compound-3k.html","C18H19NO2S2","free base","PKM2-IN-1","CC1=C(CSC(=S)N2CCCCC2)C(=O)C3=CC=CC=C3C1=O",5.039,2,0,4]
["S8648","ACY-738","e11","L1700-54","in 10mM DMSO","HDAC","Epigenetics","ACY-738 inhibits HDAC6 with low nanomolar potency (IC50=1.7 nM) and a selectivity of 60- to 1500-fold over class I HDACs.",270.29,"1375465-91-0",{"v":54,"d":"54.00"},199.79,"<1","N/A","http://selleckchem.com/products/acy-738.html","C14H14N4O2","free base","N/A","ONC(=O)C1=CN=C(NC2(CC2)C3=CC=CC=C3)N=C1",1.325,3,2,4]
["S8672","Tenalisib (RP6530)","a3","L1700-55","in 10mM DMSO","PI3K","PI3K/Akt/mTOR","Tenalisib (RP6530) is a potent and selective dual PI3Kδ/γ inhibitor with IC50 values of 24.5 nM and 33.2 nM for PI3Kδ and PI3Kγ, respectively. Its selectivity over α and β isoforms are more than 300-fold and 100-fold, respectively.",415.42,"1639417-53-0",{"v":75,"d":"75.00"},180.54,"<1","N/A","http://selleckchem.com/products/tenalisib-rp6530.html","C23H18FN5O2","free base","N/A","CCC(NC1=C2N=C[NH]C2=NC=N1)C3=C(C(=O)C4=CC=CC=C4O3)C5=CC=CC(=C5)F",{"v":4.07,"d":"4.070"},5,2,5]
["S8686","PHTPP","b4","L1700-55","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","PHTPP is an ERβ selective antagonist with 36-fold selective for ER βover ERα.",423.31,"805239-56-9",{"v":50,"d":"50.00"},118.12,"<1","N/A","http://selleckchem.com/products/phtpp.html","C20H11F6N3O","free base","N/A","OC1=CC=C(C=C1)C2=C3N=C(C=C([N]3N=C2C4=CC=CC=C4)C(F)(F)F)C(F)(F)F",6.068,2,1,4]
["S8690","RAF709","d4","L1700-55","in 10mM DMSO","Raf","MAPK","RAF709 is a potent inhibitor of B/C RAF kinase with almost equivalent IC50 values of 0.4 nM for B-RAF and C-RAF, showing a high level of selectivity, demonstrating greater than 99% on-target binding to BRAF, BRAFV600E, and CRAF at 1 μM and very few off-targets with DDR1 (>99%), DDR2 (86%), FRK (92%), and PDGFRb (96%), the only kinases with binding >80% at 1 μM.",542.55,"1628838-42-5",{"v":100,"d":"100.00"},184.31,"<1","N/A","http://selleckchem.com/products/raf709.html","C28H29F3N4O4","free base","N/A","CC1=NC=C(NC(=O)C2=CC=CC(=C2)C(F)(F)F)C=C1C3=CC(=C(OC4CCOCC4)N=C3)N5CCOCC5",{"v":3.27,"d":"3.270"},6,1,7]
["S8711","Nemtabrutinib (ARQ 531)","h5","L1700-55","in 10mM DMSO","BTK","Angiogenesis","Nemtabrutinib (ARQ 531, MK-1026) is an ATP-competitive tyrosine kinase inhibitor designed to target BTK with an IC50 of 0.85 nM. It also has a distinct kinase selectivity profile with strong inhibitory activity against several key oncogenic drivers from TEC, Trk and Src family kinases.",478.93,"2095393-15-8",{"v":95,"d":"95.00"},198.36,"<1","N/A","https://www.selleckchem.com/products/arq531.html","C25H23ClN4O4","free base","MK-1026","OCC1CCC(CO1)NC2=C3C(=NC=N2)[NH]C=C3C(=O)C4=CC=C(OC5=CC=CC=C5)C=C4Cl",4.368,5,3,7]
["S8728","PK11000","g6","L1700-55","in 10mM DMSO","p53","Apoptosis","PK11000 stabilizes the DBD of both WT and mutant p53 proteins by covalent cysteine modification without compromising DNA binding and effective in inducing cell death.",236.63,"38275-34-2",{"v":47,"d":"47.00"},198.62,{"v":47,"d":"47.00"},198.62,"https://www.selleckchem.com/products/pk11000.html","C6H5ClN2O4S","free base","N/A","C[S](=O)(=O)C1=NC=C(Cl)C(=N1)C(O)=O",{"v":0.82,"d":"0.820"},5,0,2]
["S8747","BAY-8002","c8","L1700-55","in 10mM DMSO","MCT","Transmembrane Transporters","BAY-8002 is a novel MCT1 inhibitor and potently suppress bidirectional lactate transport. BAY-8002 significantly increases intratumor lactate levels and transiently modulates pyruvate levels.",415.85,"724440-27-1",{"v":83,"d":"83.00"},199.59,"<1","N/A","http://www.selleck.cn/products/bay-8002.html","C20H14ClNO5S","Free Base","N/A","OC(=O)C1=C(NC(=O)C2=C(Cl)C=CC(=C2)[S](=O)(=O)C3=CC=CC=C3)C=CC=C1",4.011,4,1,5]
["S8757","Ripretinib (DCC-2618)","c9","L1700-55","in 10mM DMSO","c-Kit,PDGFR","Protein Tyrosine Kinase","DCC-2618 is an orally bioavailable switch pocket control inhibitor of wild-type and mutated forms of the tumor-associated antigens (TAA) mast/stem cell factor receptor (SCFR) Kit (c-Kit) and PDGFR-alpha, with IC50 values of 4 nM, 8 nM, 18 nM, 5 nM and 14 nM for WT Kit (c-Kit), V654A Kit (c-Kit), T670I Kit (c-Kit), D816H Kit (c-Kit) and D816V Kit (c-Kit), respectively.",510.36,"1442472-39-0",{"v":100,"d":"100.00"},195.94,"<1","N/A","http://www.selleckchem.com/products/ripretinib-dcc-2618.html","C24H21BrFN5O2","Free Base","N/A","CCN1C(=O)C(=CC2=C1C=C(NC)N=C2)C3=C(Br)C=C(F)C(=C3)NC(=O)NC4=CC=CC=C4",4.129,3,3,5]
["S8773","TH34","g10","L1700-55","in 10mM DMSO","HDAC","Epigenetics","TH34 is a HDAC inhibitor that shows pronounced selectivity for HDACs 6, 8 and 10 over HDACs 1, 2 and 3.  In a NanoBRET assay, TH34 strongly binds HDAC6, 8 and 10 with low-micromolar IC50 concentrations (HDAC6: 4.6 µM, HDAC8: 1.9 µM, HDAC10: 7.7 µM).",{"v":256.3,"d":"256.30"},"2196203-96-8",{"v":51,"d":"51.00"},198.99,"<1","N/A","http://www.selleckchem.com/products/th34.html","C15H16N2O2","Free Base","N/A","CC1=CC=C(C=C1NCC2=CC=CC=C2)C(=O)NO",2.723,1,2,4]
["S8793","ULK-101","c2","L1700-56","in 10mM DMSO","Autophagy,ULK","Autophagy","ULK-101 is a potent and selective ULK1 inhibitor with IC50 values of 8.3 nM and 30 nM for ULK1 and ULK2, respectively.",460.45,"2443816-45-1",{"v":92,"d":"92.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://www.selleck.cn/products/ulk-101.html","C22H16F4N4OS","Free Base","N/A","FC1=CC=C(C=C1)C2=C[N]3N=CC(=C3N=C2)C4=CSC(=C4)C(=O)NC(C5CC5)C(F)(F)F",4.363,3,1,6]
["S8810","SPHINX31","b3","L1700-56","in 10mM DMSO","Serine/threonin kinase","Protein Tyrosine Kinase","SPHINX31 is a SRPK1 inhibiror with an IC50 of 5.9 nM with highly selectivity for SRPK1 over SRPK2 (50-fold) and CLK1 (100-fold).",507.51,"1818389-84-2",{"v":25,"d":"25.00"},49.26,"<1","N/A","http://www.selleck.cn/products/sphinx31.html","C27H24F3N5O2","free base","N/A","FC(F)(F)C1=CC(=C(C=C1)N2CCN(CC2)CC3=CC=CC=N3)NC(=O)C4=CC=C(O4)C5=CC=NC=C5",4.378,4,1,7]
["S8821","GSK3179106","f3","L1700-56","in 10mM DMSO","c-RET","Apoptosis","GSK3179106 is a potent, selective, and gut-restricted pyridone hinge binder small molecule RET (c-RET) kinase inhibitor with a RET IC50 of 0.3 nM and is efficacious in vivo.",467.41,"1627856-64-7",{"v":93,"d":"93.00"},198.97,"<1","N/A","http://www.selleck.cn/products/gsk3179106.html","C22H21F4N3O4","Free Base","N/A","CCOC1=CC(=O)NC=C1C2=CC=C(CC(=O)NC3=NOC(=C3)C(C)(C)C(F)(F)F)C(=C2)F",3.357,5,2,8]
["S8873","Letermovir (AIC246)","b5","L1700-56","in 10mM DMSO","CMV","Microbiology","Letermovir (AIC246, MK-8228) is a novel anti-CMV compound which targets the viral terminase complex and remains active against virus resistant to DNA polymerase inhibitors.",572.55,"917389-32-3",{"v":100,"d":"100.00"},174.66,"<1","N/A","http://www.selleck.cn/products/letermovir.html","C29H28F4N4O4","free base","MK-8228","COC1=CC(=CC=C1)N2CCN(CC2)C3=NC4=C(C=CC=C4F)C(CC(O)=O)N3C5=CC(=CC=C5OC)C(F)(F)F",5.451,4,0,8]
["S9020","Dihydrotanshinone I","g6","L1700-56","in 10mM DMSO","Others","Others","Dihydrotanshinone I (15,16-dihydrotanshinone I) is a naturally occurring compound extracted from Salvia miltiorrhiza Bunge, also known as Chinese sage, red sage root, and the Chinese herbal Dan Shen. It is a potent inhibitor of the HuR:RNA interaction, active in the low nanomolar range, mainly by limiting the association rate of HuR with RNA.",{"v":278.3,"d":"278.30"},"87205-99-0",{"v":10,"d":"10.00"},35.93,"N/A","N/A","https://www.selleckchem.com/products/dihydrotanshinone-i.html","C18H14O3","free base","15,16-dihydrotanshinone I","CC1COC2=C1C(=O)C(=O)C3=C2C=CC4=C3C=CC=C4C",3.184,3,0,0]
["S9033","Incensole acetate","f7","L1700-56","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Incensole acetate, isolated from Boswellia Resin, is a novel anti-inflammatory compound that inhibits NF-κB activation.",348.52,"34701-53-6","N/A","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","https://www.selleckchem.com/products/incensole-acetate.html","C22H36O3","free base","FI145245","CC(C)C12CCC(C)(O1)C(CC/C(=C/CC\\C(=C\\C2)C)C)OC(C)=O",{"v":0,"d":"0.000"},0,0,0]
["S9041","Corosolic acid","e8","L1700-56","in 10mM DMSO","NF-κB","NF-κB","Corosolic acid (Glucosol, Colosic acid, 2α-Hydroxyursolic acid) is one of the pentacyclic triterpenoids isolated from Lagerstroemia speciose and has been reported to exhibit anti-cancer and anti-proliferative activities in various cancer cells.",{"v":472.7,"d":"472.70"},"4547-24-4",{"v":95,"d":"95.00"},200.97,"N/A","N/A","https://www.selleckchem.com/products/corosolic-acid.html","C30H48O4","free base","Glucosol, Colosic acid, 2α-Hydroxyursolic acid","CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(C)C5CCC34C)C2C1C)C(O)=O",5.525,1,2,1]
["S9057","Sinigrin","a10","L1700-56","in 10mM DMSO","Fungal,Immunology & Inflammation related","Microbiology","Sinigrin (Allylglucosinolate, 2-Propenylglucosinolate) is a glucosinolate found in some plants of the Brassicaceae family and exerts various activities including anticancer, anti-inflammatory, antibacterial, antifungal, antioxidant, and wound healing effects.",397.46,"3952-98-5",{"v":10,"d":"10.00"},25.16,"N/A","N/A","https://www.selleckchem.com/products/sinigrin.html","C10H16KNO9S2","free base","Allylglucosinolate, 2-Propenylglucosinolate","[K+].OCC1OC(S\\C(CC=C)=N\\O[S]([O-])(=O)=O)C(O)C(O)C1O",-3.447,3,4,7]
["S9065","Songorine","h10","L1700-56","in 10mM DMSO","ADC Cytotoxin,GABA Receptor","Neuronal Signaling","Songorine, a ubiquitous alkaloid in the genus Aconitum, is a novel antagonist of the GABAA receptor in rat brain and has antiarrhythmic, antinociceptive, anti-inflammatory, regenerative and CNS-modulating properties.",357.49,"509-24-0",{"v":10,"d":"10.00"},27.97,"N/A","N/A","https://www.selleckchem.com/products/songorine.html","C22H31NO3","free base","FS145273","CCN1CC2(C)CCC(O)C34C1C(CC23)C56CC(C(=C)C5O)C(=O)CC46",1.035,1,2,1]
["S9082","Manninotriose","e2","L1700-57","in 10mM DMSO","Others","Others","Manninotriose, found in many foods, is a novel and important player in the RFO metabolism of red dead deadnettle.",504.44,"13382-86-0",{"v":10,"d":"10.00"},19.82,"N/A","N/A","https://www.selleckchem.com/products/manninotriose.html","C18H32O16","free base","N/A","OCC1OC(OCC2OC(OCC(O)C(O)C(O)C(O)C=O)C(O)C(O)C2O)C(O)C(O)C1O",-6.285,5,11,11]
["S9085","Corynoline","h2","L1700-57","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Corynoline is one of the major active components of many ethnopharmacological plants and exhibits anti-tumor, anti-inflammatory and hepatoprotective activities, etc.",{"v":367.4,"d":"367.40"},"18797-79-0",{"v":10,"d":"10.00"},27.22,"N/A","N/A","https://www.selleckchem.com/products/corynoline.html","C21H21NO5","free base","N/A","CN1CC2=C(C=CC3=C2OCO3)C4(C)C(O)CC5=C(C=C6OCOC6=C5)C14",2.732,4,1,0]
["S9106","Eleutheroside E","h4","L1700-57","in 10mM DMSO","Immunology & Inflammation related,NF-κB","NF-κB","Eleutheroside E, a principal component of Eleutherococcus senticosus (ES), has anti-inflammatory effects by inhibiting NF-κB and protecting against myocardial infarction.",742.72,"39432-56-9",{"v":10,"d":"10.00"},13.46,"N/A","N/A","https://www.selleckchem.com/products/eleutheroside-e.html","C34H46O18","free base","N/A","COC1=C(OC2OC(CO)C(O)C(O)C2O)C(=CC(=C1)C3OCC4C3COC4C5=CC(=C(OC6OC(CO)C(O)C(O)C6O)C(=C5)OC)OC)OC",-1.709,10,8,12]
["S9115","Wogonoside","g5","L1700-57","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Wogonoside (Oroxindin, Wogonin 7-O-glucuronide, Glychionide B), the main flavonoid component derived from the root of Scutellaria baicalensis Georgi, displays anti-inflammatory, anti-angiogenic, and anticancer chemotherapeutic activities.",460.39,"51059-44-0",{"v":38,"d":"38.00"},82.54,"N/A","N/A","https://www.selleckchem.com/products/wogonoside.html","C22H20O11","free base","Oroxindin, Wogonin 7-O-glucuronide, Glychionide B","COC1=C(OC2OC(C(O)C(O)C2O)C(O)=O)C=C(O)C3=C1OC(=CC3=O)C4=CC=CC=C4",0.833,6,4,5]
["S9129","20(S)-Ginsenoside Rh1","h6","L1700-57","in 10mM DMSO","Immunology & Inflammation related,Interleukins,PPAR,TNF-alpha","Immunology & Inflammation","20(S)-Ginsenoside Rh1 (Prosapogenin A2, Sanchinoside B2, Sanchinoside Rh1) is one of major bioactive compounds extracted from red ginseng, which has been increasingly used for enhancing cognition and physical health worldwide. It exhibits potent characteristics of anti-inflammatory, antioxidant, immunomodulatory effects, and positive effects on the nervous system. Ginsenoside Rh1 inhibits the expression of PPAR-γ, TNF-α, IL-6, and IL-1β.",638.87,"63223-86-9",{"v":100,"d":"100.00"},156.53,"N/A","N/A","https://www.selleckchem.com/products/20-s-ginsenoside-rh1.html","C36H62O9","free base","Prosapogenin A2, Sanchinoside B2, Sanchinoside Rh1","CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC3C4(C)CCC(O)C(C)(C)C4C(CC23C)OC5OC(CO)C(O)C(O)C5O",2.873,2,6,7]
["S9137","Erianin","g7","L1700-57","in 10mM DMSO","IDO/TDO","Metabolism","Erianin, a natural product derived from Dendrobium chrysotoxum, has been used as an analgesic in traditional Chinese medicine and is a potential anti-tumor agent. Erianin can inhibit IDO-induced tumor angiogenesis.",318.36,"95041-90-0",{"v":63,"d":"63.00"},197.89,"N/A","N/A","https://www.selleckchem.com/products/erianin.html","C18H22O5","free base","N/A","COC1=C(O)C=C(CCC2=CC(=C(OC)C(=C2)OC)OC)C=C1",3.953,4,1,7]
["S9154","Chelidonine","d9","L1700-57","in 10mM DMSO","AChR","Neuronal Signaling","Chelidonine (Stylophorin, Helidonine), a major bioactive, isoquinoline alkaloid ingredient in Chelidonium majus, exhibits anti-inflammatory properties and acetylcholinesterase and butyrylcholinesterase inhibitory activity.",353.37,"476-32-4",{"v":5,"d":"5.00"},14.15,"N/A","N/A","https://www.selleckchem.com/products/chelidonine.html","C20H19NO5","free base","Stylophorin, Helidonine","CN1CC2=C(C=CC3=C2OCO3)C4C(O)CC5=C(C=C6OCOC6=C5)C14",2.329,4,1,0]
["S9174","Xanthotoxol","h10","L1700-57","in 10mM DMSO","5-HT Receptor,Immunology & Inflammation related","Neuronal Signaling","Xanthotoxol (8-Hydroxypsoralen, 8-Hydroxypsoralene, 8-Hydroxyfuranocoumarin, Psoralen), a biologically active linear furocoumarin found in a large number of plants, shows strong pharmacological activities as anti-inflammatory, antioxidant, 5-HT antagonistic, and neuroprotective effects.",202.16,"2009-24-7",{"v":40,"d":"40.00"},197.86,"N/A","N/A","https://www.selleckchem.com/products/xanthotoxol.html","C11H6O4","free base","8-Hydroxypsoralen, 8-Hydroxypsoralene, 8-Hydroxyfuranocoumarin, Psoralen","OC1=C2OC(=O)C=CC2=CC3=C1OC=C3",1.961,3,1,0]
["S9184","Forsythoside B","g11","L1700-57","in 10mM DMSO","Immunology & Inflammation related,Interleukins,IκB/IKK,NF-κB,TNF-alpha","Immunology & Inflammation","Forsythoside B is a phenylethanoid glycoside isolated from the leaves of Lamiophlomis rotata Kudo, a Chinese folk medicinal plant. Forsythoside B has potent neuroprotective effects and has anti-inflammation, antioxidant, and antisepsis properties. Forsythoside B could inhibit TNF-alpha, IL-6, IκB and modulate NF-κB.",{"v":756.7,"d":"756.70"},"81525-13-5",{"v":100,"d":"100.00"},132.15,"N/A","N/A","https://www.selleckchem.com/products/forsythoside-b.html","C34H44O19","free base","N/A","CC1OC(OC2C(O)C(OCCC3=CC=C(O)C(=C3)O)OC(COC4OCC(O)(CO)C4O)C2OC(=O)/C=C/C5=CC(=C(O)C=C5)O)C(O)C(O)C1O",-0.925,8,10,14]
["S9188","Magnoflorine chloride","b2","L1700-58","in 10mM DMSO","Others","Others","Magnoflorine (Escholine, Thalictrine, Corytuberine methochloride), isolated from the rhizome of Sinomenium acutum and from Pachygone ovata, is usually used as an anxiolytic chemical with anti-oxidant, α-tyrosinase inhibitory and anti-inflammationary activities.",377.86,"6681-18-1",{"v":76,"d":"76.00"},201.13,"N/A","N/A","https://www.selleckchem.com/products/magnoflorinechloride.html","C20H24ClNO4","free base","Escholine chloride, Thalictrine chloride, Corytuberine methochloride","[Cl-].COC1=C(O)C2=C(CC3C4=C2C(=C(OC)C=C4CC[N+]3(C)C)O)C=C1",-0.946,2,2,2]
["S9221","Ferulaldehyde","c4","L1700-58","in 10mM DMSO","Heme Oxygenase","Immunology & Inflammation","Ferulaldehyde (Coniferaldehyde, Ferulyl aldehyde) is a natural intermediate of polyphenol metabolism of intestinal microflora.",178.18,"458-36-6",{"v":35,"d":"35.00"},196.43,"N/A","N/A","https://www.selleckchem.com/products/ferulaldehyde.html","C10H10O3","free base","Coniferaldehyde, Ferulyl aldehyde","COC1=CC(=CC=C1O)\\C=C\\C=O",1.691,2,1,3]
["S9225","Santalol","f4","L1700-58","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Santalol is a naturally occuring sesquiterpene that has antibacterial, anti-hyperglycaemic, anti inflammatory and antioxidant effects.",220.35,"11031-45-1","N/A","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","https://www.selleckchem.com/products/santalol.html","C15H24O","free base","N/A","CC(\\CO)=C/CCC1(C)C2CCC(C2)C1=C",3.662,0,1,4]
["S9240","Isofraxidin","b6","L1700-58","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Isofraxidin (6,8-Dimethoxyumbelliferone), a bioactive coumarin compound isolated from the functional foods Siberian ginseng and Apium graveolens, is an anti-bacterial, anti-oxidant, and anti-inflammatory agent.",222.19,"486-21-5",{"v":44,"d":"44.00"},198.03,"N/A","N/A","https://www.selleckchem.com/products/isofraxidin.html","C11H10O5","free base","6,8-Dimethoxyumbelliferone","COC1=CC2=C(OC(=O)C=C2)C(=C1O)OC",1.625,4,1,2]
["S9251","Oxypeucedanin","a7","L1700-58","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","Oxypeucedanin is a major coumarin aglycone that can be extracted from Ostericum koreanum. It is a kind of open-channel blocker of the hKv1.5 channel.",286.28,"737-52-0",{"v":24,"d":"24.00"},83.83,"N/A","N/A","https://www.selleckchem.com/products/oxypeucedanin.html","C16H14O5","free base","N/A","CC1(C)OC1COC2=C3C=CC(=O)OC3=CC4=C2C=CO4",2.485,5,0,3]
["S9267","Epimedin A","d8","L1700-58","in 10mM DMSO","Others","Others","Epimedin A is a major component of Herba Epimedii with bioactivities.",{"v":838.8,"d":"838.80"},"110623-72-8",{"v":100,"d":"100.00"},119.22,"N/A","N/A","https://www.selleckchem.com/products/epimedin-a.html","C39H50O20","free base","N/A","COC1=CC=C(C=C1)C2=C(OC3OC(C)C(O)C(O)C3OC4OC(CO)C(O)C(O)C4O)C(=O)C5=C(O)C=C(OC6OC(CO)C(O)C(O)C6O)C(=C5O2)CC=C(C)C",-0.764,9,11,12]
["S9291","Isopimpinellin","b10","L1700-58","in 10mM DMSO","Others","Metabolism","Isopimpinellin (5,8-Dimethoxypsoralen) is a natural product synthesized by numerous plant species. It may acts as an anticarcinogen.",246.22,"482-27-9",{"v":49,"d":"49.00"},199.01,"N/A","N/A","https://www.selleckchem.com/products/isopimpinellin.html","C13H10O5","free base","5,8-Dimethoxypsoralen","COC1=C2OC(=O)C=CC2=C(OC)C3=C1OC=C3",{"v":2.17,"d":"2.170"},5,0,2]
["S9301","Verbenalin","a11","L1700-58","in 10mM DMSO","Others","Others","Verbenalin (Verbenalol β-D-glucopyranoside, Verbenalol glucoside, Cornin), an iridoid glycoside found in Verbena officinalis, has been reported to exhibit uterine stimulant activity and demonstrated cardioprotection against experimental myocardial ischemic injury.",388.37,"548-37-8",{"v":78,"d":"78.00"},200.84,"N/A","N/A","https://www.selleckchem.com/products/verbenalin.html","C17H24O10","free base","Verbenalol β-D-glucopyranoside, Verbenalol glucoside, Cornin","COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C3C(C)CC(=O)C13",-1.937,6,4,5]
["S9313","Atractylenolide III","a2","L1700-59","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Atractylenolide III, a major component of Atractylodes rhizome, has anti-inflammatory and anti-angiogenesis activities.",248.32,"73030-71-4",{"v":50,"d":"50.00"},201.36,"N/A","N/A","https://www.selleckchem.com/products/atractylenolide-iii.html","C15H20O3","free base","N/A","CC1=C2CC3C(=C)CCCC3(C)CC2(O)OC1=O",2.924,2,0,0]
["S9328","5,6,7-Trimethoxyflavone","e3","L1700-59","in 10mM DMSO","Antiviral,Bacterial","Microbiology","5,6,7-Trimethoxyflavone (Baicalein Trimethyl Ether), methylations of the hydroxyl groups of oroxylin A or baicalein, has various pharmacological activities including antiviral, anticancer and antibacterial.",312.32,"973-67-1",{"v":10,"d":"10.00"},32.02,"N/A","N/A","https://www.selleckchem.com/products/trimethoxyflavone.html","C18H16O5","free base","Baicalein Trimethyl Ether","COC1=CC2=C(C(=O)C=C(O2)C3=CC=CC=C3)C(=C1OC)OC",3.087,5,0,4]
["S9331","7-Hydroxy-4-methyl-8-nitrocoumarin","h3","L1700-59","in 10mM DMSO","Casein Kinase","Cell Cycle","7-Hydroxy-4-methyl-8-nitrocoumarin is a chemical.",221.17,"19037-69-5",{"v":44,"d":"44.00"},198.95,"N/A","N/A","https://www.selleckchem.com/products/7-hydroxy-4-methyl-8-nitrocoumarin.html","C10H7NO5","free base","N/A","CC1=CC(=O)OC2=C1C=CC(=C2[N+]([O-])=O)O",1.998,2,1,1]
["S9348","D-(+)-Trehalose Anhydrous","d5","L1700-59","in 10mM DMSO","Others","Others","Trehalose is a non-reducing sugar. It is thought to provide plants and animals with the ability to withstanding periods of dehydration.",{"v":342.3,"d":"342.30"},"99-20-7",{"v":68,"d":"68.00"},198.66,"N/A","N/A","https://www.selleckchem.com/products/d-trehalose-anhydrous.html","C12H22O11","free base","N/A","OCC1OC(OC2OC(CO)C(O)C(O)C2O)C(O)C(O)C1O",-4.261,3,8,4]
["S9363","Coumarin 151","h6","L1700-59","in 10mM DMSO","Others","Others","Coumarin 151 (7-Amino-4-(trifluoromethyl)coumarin) is a fluorescent tracer used for the detection of proteinases.",229.16,"53518-15-3",{"v":46,"d":"46.00"},200.74,"N/A","N/A","https://www.selleckchem.com/products/coumarin-151.html","C10H6F3NO2","free base","7-Amino-4-(trifluoromethyl)coumarin","NC1=CC2=C(C=C1)C(=CC(=O)O2)C(F)(F)F",2.055,2,1,1]
["S9374","2',5'-Dihydroxyacetophenone","h7","L1700-59","in 10mM DMSO","ERK,Interleukins,NF-κB,NOS,TNF-alpha","Immunology & Inflammation","2',5'-Dihydroxyacetophenone (DHAP, 2-Acetylhydroquinone, Quinacetophenone) is a mixture of dihydroxyacetophenone isomers is used in food flavouring. 2',5'-Dihydroxyacetophenone significantly inhibits NO production via the suppression of iNOS expression. 2',5'-Dihydroxyacetophenone significantly decreases levels of the pro-inflammatory cytokines TNF-α and IL-6 by blocking the ERK1/2 and NF-κB signaling pathways.",152.15,"490-78-8",{"v":30,"d":"30.00"},197.18,"N/A","N/A","https://www.selleckchem.com/products/2-5-dihydroxyacetophenone.html","C8H8O3","free base","DHAP, 2-Acetylhydroquinone, Quinacetophenone","CC(=O)C1=C(O)C=CC(=C1)O",1.085,1,2,1]
["S9381","5-Methyl furfural","g8","L1700-59","in 10mM DMSO","Others","Others","5-Methyl furfural is an important chemical intermediate.",110.11,"620-02-0","N/A","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","https://www.selleckchem.com/products/5-methyl-furfural.html","C6H6O2","free base","N/A","CC1=CC=C(O1)C=O",{"v":1.13,"d":"1.130"},2,0,1]
["S9403","Ecliptasaponin A","e10","L1700-59","in 10mM DMSO","Others","Others","Ecliptasaponin A, a natural triterpenoid glucoside, has protective effects against the pulmonary fibrosis induced by bleomycin via reducing the oxidative stress, lung tissue inflammation, and the subsequent epithelial-mesenchymal transition.",634.84,"78285-90-2",{"v":100,"d":"100.00"},157.52,"N/A","N/A","https://www.selleckchem.com/products/ecliptasaponin-a.html","C36H58O9","free base","N/A","CC1(C)CCC2(C(O)CC3(C)C(=CCC4C5(C)CCC(OC6OC(CO)C(O)C(O)C6O)C(C)(C)C5CCC34C)C2C1)C(O)=O",3.598,3,5,4]
["S9405","Sesamoside","g10","L1700-59","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Sesamoside, a main chemical ingredient iridoid glycoside from Lamiophlomic rotata, has analgesic and anti-inflammatory effects in animal studies.",420.37,"117479-87-5",{"v":84,"d":"84.00"},199.83,"N/A","N/A","https://www.selleckchem.com/products/sesamoside.html","C17H24O12","free base","N/A","COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C3C4(C)OC4C(O)C13O",-3.893,6,5,5]
["S9424","Liensinine diperchlorate","g2","L1700-60","in 10mM DMSO","Autophagy,Mitophagy","Autophagy","Liensinine, a major isoquinoline alkaloid, inhibits late-stage autophagy/mitophagy through blocking autophagosome-lysosome fusion. It is a novel autophagy/mitophagy inhibitor.",811.66,"5088-90-4",{"v":50,"d":"50.00"},{"v":61.6,"d":"61.60"},"N/A","N/A","https://www.selleckchem.com/products/liensinine-diperchlorate.html","C37H44Cl2N2O14","free base","N/A","COC1=CC2=C(C=C1OC)C(CC3=CC(=C(O)C=C3)OC4=C(OC)C=C5CCN(C)C(CC6=CC=C(O)C=C6)C5=C4)N(C)CC2.O[Cl](=O)(=O)=O.O[Cl](=O)(=O)=O",7.669,4,2,9]
["S9428","Brazilin","b3","L1700-60","in 10mM DMSO","Beta Amyloid","Neuronal Signaling","Brazilin (Natural Red 24) is a red pigment obtained from the wood of the brazilwood family. It is used to dye fabric and has diverse biological activities, including neuroprotective, anti-inflammatory, antibacterial, and antioxidant properties.",286.28,"474-07-7",{"v":57,"d":"57.00"},199.11,"N/A","N/A","https://www.selleckchem.com/products/brazilin.html","C16H14O5","free base","Natural Red 24","OC1=CC2=C(C=C1)C3C4=CC(=C(O)C=C4CC3(O)CO2)O",1.933,1,3,0]
["S9442","Bergaptol","f4","L1700-60","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Bergaptol (5-Hydroxypsoralen, 5-Hydroxyfuranocoumarin) is a natural furanocoumarin found in the essential oils of citrus including lemon and bergamot.Bergaptol  is a potent inhibitors of debenzylation activity of CYP3A4 enzyme with an IC50 value of 24.92 μM.",202.16,"486-60-2",{"v":40,"d":"40.00"},197.86,"N/A","N/A","https://www.selleckchem.com/products/bergaptol.html","C11H6O4","free base","5-Hydroxypsoralen, 5-Hydroxyfuranocoumarin","OC1=C2C=COC2=CC3=C1C=CC(=O)O3",1.961,3,1,0]
["S9452","10-Undecenoic acid","f5","L1700-60","in 10mM DMSO","Others","Others","10-Undecenoic acid, a natural or synthetic fungistatic fatty acid, is used for the preparation of active pharmaceutical ingredients, cosmetics, perfumes, antidandruff shampoos and antimicrobial powders.",184.28,"112-38-9","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleckchem.com/products/10-undecenoic-acid.html","C11H20O2","Free Base","N/A","OC(=O)CCCCCCCCC=C",3.721,1,0,9]
["S9470","Penbutolol Sulfate","b7","L1700-60","in 10mM DMSO","Adrenergic Receptor","GPCR & G Protein","Penbutolol sulfate ((-)-Terbuclomine) is an effective beta-adrenergic receptor blocker and diuretic that is used as an antihypertensive agent.",680.94,"38363-32-5",{"v":15,"d":"15.00"},22.03,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/penbutolol-sulfate.html","C18H29NO2.1/2H2O4S","Sulfate","(-)-Terbuclomine","CC(C)(C)NCC(O)COC1=C(C=CC=C1)C2CCCC2.CC(C)(C)NCC(O)COC3=C(C=CC=C3)C4CCCC4.O[S](O)(=O)=O",6.536,2,4,14]
["S9480","Raspberry Ketone","a8","L1700-60","in 10mM DMSO","PPAR","Metabolism","Raspberry ketone (p-Hydroxybenzyl acetone, Frambinone, Oxyphenylon, Rheosmin, Rasketone) is a natural phenolic compound that is the primary aroma compound of red raspberries. Raspberry ketone shows cardioprotective action against isoproterenol-induced myocardial infarction in rats, and the effects may be due to its PPAR-α agonistic activity.",{"v":164.2,"d":"164.20"},"5471-51-2",{"v":33,"d":"33.00"},200.97,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/raspberry-ketone.html","C10H12O2","Free Base","p-Hydroxybenzyl acetone, Frambinone, Oxyphenylon, Rheosmin, Rasketone","CC(=O)CCC1=CC=C(O)C=C1",1.809,1,1,3]
["S9503","Fraxetin","e9","L1700-60","in 10mM DMSO","Heme Oxygenase","Apoptosis","Fraxetin (7,8-dihydroxy-6-methoxy coumarin), found in Fraxinus rhynchophylla, shows potent antioxidant activity.fraxetin alleviates lipid peroxidation, enhances hepatic antioxidant capabilities, inhibits CYP2E1 activity, and reduced the inflammatory mediators, including TNF-α and IL-1β via up-regulation of hemeoxygenase-1 (HO-1) protein.",208.17,"574-84-5",{"v":42,"d":"42.00"},201.76,"N/A","N/A","https://www.selleckchem.com/products/fraxetin.html","C10H8O5","free base","7,8-dihydroxy-6-methoxy coumarin","COC1=CC2=C(OC(=O)C=C2)C(=C1O)O","N/A","N/A","N/A","N/A"]
["S9509","Tiapride Hydrochloride","a10","L1700-60","in 10mM DMSO","Dopamine Receptor","Neuronal Signaling","Tiapride is a drug that selectively blocks D2 and D3 dopamine receptors in the brain and is used to treat a variety of neurological and psychiatric disorders.",364.89,"51012-33-0",{"v":35,"d":"35.00"},95.92,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/tiapride-hydrochloride.html","C15H25ClN2O4S","hydrochloride","N/A","Cl.CCN(CC)CCNC(=O)C1=CC(=CC=C1OC)[S](C)(=O)=O",1.766,4,1,8]
["S2931","Aurora Kinase Inhibitor III","a2","L1700-61","in 10mM DMSO","Aurora Kinase","Cell Cycle","Aurora kinase inhibitor III is a potent inhibitor of Aurora A kinase with an IC50 of 42 nM and has high selectivity for Aurora A over BMX, BTK, IGF-1R, c-Src, TRKB, SYK, and EGFR (IC50s = 386, 3,550, 591, 1,980, 2,510, 887, and >10,000 nM, respectively).",{"v":413.4,"d":"413.40"},"879127-16-9",{"v":83,"d":"83.00"},200.77,"<1","N/A","http://www.selleck.cn/products/aurora-kinase-inhibitor-iii.html","C21H18F3N5O","Free Base","N/A","FC(F)(F)C1=CC(=CC=C1)NC2=CC=NC(=N2)NC3=CC(=CC=C3)NC(=O)C4CC4",5.032,3,3,7]
["S6530","EBE-A22","b3","L1700-61","in 10mM DMSO","EGFR","Protein Tyrosine Kinase","EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.",374.23,"229476-53-3",{"v":9,"d":"9.00"},24.05,"<1","N/A","http://www.selleck.cn/products/ebe-a22.html","C17H16BrN3O2","Free Base","N/A","COC1=CC2=NC=NC(=C2C=C1OC)N(C)C3=CC=CC(=C3)Br",4.398,4,0,4]
["S6552","CYM5541","a4","L1700-61","in 10mM DMSO","S1P Receptor","GPCR & G Protein","CYM5541 (ML249) is a selective, allosteric agonist of S1P3 with an EC50 of between 72 and 132 nM and exhibits exquisite selectivity over other S1P receptor subtypes in vitro: S1P1 EC50 > 10 μM, S1P2 EC50 > 50 μM, S1P4 EC50 > 50 μM, and S1P5 EC50 > 25 μM.",316.44,"945128-26-7",{"v":32,"d":"32.00"},101.13,"<1","N/A","http://www.selleck.cn/products/cym5541.html","C19H28N2O2","Free Base","ML249","O=C(N(C1CCCCC1)C2CCCCC2)C3=NOC(=C3)C4CC4",4.746,3,0,4]
["S6579","RCGD423","h4","L1700-61","in 10mM DMSO","Interleukins","Transmembrane Transporters","RCGD-423 is a modulator of Glycoprotein 130 (gp130, IL6ST, IL6-beta, CD130) signalling that regulates cartilage growth and differentiation.",331.23,"108237-91-8",{"v":66,"d":"66.00"},199.26,"<1","N/A","http://www.selleck.cn/products/rcgd423.html","C15H11BrN2S","Free Base","N/A","BrC1=CC=C(NC2=NC(=CS2)C3=CC=CC=C3)C=C1",5.072,1,1,3]
["S6616","ETC-159","d6","L1700-61","in 10mM DMSO","PORCN","Stem Cells & Wnt","ETC-159 (ETC-1922159) is an orally available, potent porcupine inhibitor with an IC50 of 2.9 nM for inhibiting β-catenin reporter activity in STF3A cells.",391.38,"1638250-96-0",{"v":78,"d":"78.00"},199.29,"<1","N/A","http://www.selleck.cn/products/etc-159.html","C19H17N7O3","Free Base","ETC-1922159","CN1C(=O)N(C)C2=C([N](CC(=O)NC3=NN=C(C=C3)C4=CC=CC=C4)C=N2)C1=O",1.404,6,1,4]
["S6633","AM 095","a8","L1700-61","in 10mM DMSO","LPA Receptor","GPCR & G Protein","AM095 is an antagonist of the LPA type 1 receptor with IC50 values of 0.98 and 0.73 μM for recombinant human and mouse LPA1, respectively.",456.49,"1228690-36-5",{"v":91,"d":"91.00"},199.35,"<1","N/A","http://www.selleck.cn/products/am-095.html","C27H24N2O5","Free Base","N/A","CC(OC(=O)NC1=C(ON=C1C)C2=CC=C(C=C2)C3=CC=C(CC(O)=O)C=C3)C4=CC=CC=C4",5.284,5,1,8]
["S6646","Ciforadenant (CPI-444)","h8","L1700-61","in 10mM DMSO","Adenosine Receptor","GPCR & G Protein","Ciforadenant (CPI-444, V81444) is a potent and selective Adenosine A2A receptor antagonist. It binds to A2A receptors with a Ki of 3.54 nmol/L and demonstrates a greater than 50-fold selectivity for the A2A receptor over other adenosine receptor subtypes.",407.43,"1202402-40-1",{"v":81,"d":"81.00"},198.81,"<1","N/A","http://www.selleck.cn/products/cpi-444.html","C20H21N7O3","Free Base","V81444","CC1=CC=C(O1)C2=C3N=N[N](CC4=NC(=CC=C4)COC5CCOC5)C3=NC(=N2)N",1.769,8,1,6]
["S6710","SGC-GAK-1","c9","L1700-61","in 10mM DMSO","Serine/threonin kinase","Metabolism","SGC-GAK-1 is a potent, selective, and cell-active inhibitor of cyclin G-associated kinase (GAK) with Ki value of 3.1 nM and >50-fold selectivity over nearest kinase.",389.24,"2226517-76-4",{"v":78,"d":"78.00"},200.39,"<1","N/A","http://www.selleck.cn/products/sgc-gak-1.html","C18H17BrN2O3","Free Base","N/A","COC1=CC(=CC(=C1OC)OC)NC2=C3C=C(Br)C=CC3=NC=C2",4.265,4,1,5]
["S6729","Besifovir","c11","L1700-61","in 10mM DMSO","HBV","Microbiology","Besifovir is novel and potent acyclic nucleotide phosphonate used to treat hepatitis B virus (HBV) infection.",299.22,"441785-25-7",{"v":60,"d":"60.00"},200.52,{"v":60,"d":"60.00"},200.52,"http://www.selleck.cn/products/besifovir.html","C10H14N5O4P","Free Base","N/A","NC1=NC=C2N=C[N](CC3(CC3)OC[P](O)(O)=O)C2=N1",-0.821,4,1,5]
["S6739","MN 64","b2","L1700-62","in 10mM DMSO","PARP","DNA Damage/DNA Repair","MN-64 is a potent inhibitor of TNKS1 and TNKS2 with IC50 value of 6 and 72 nM, respectively.",264.32,"92831-11-3",{"v":53,"d":"53.00"},200.51,"<1","N/A","http://www.selleck.cn/products/mn-64.html","C18H16O2","Free Base","N/A","CC(C)C1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=CC=C3",{"v":4.33,"d":"4.330"},2,0,2]
["S6754","S1RA","g3","L1700-62","in 10mM DMSO","Sigma Receptor","GPCR & G Protein","S1RA (E-52862) is a selective sigma-1 receptor (σ1R) antagonist with a reported binding affinity of Ki = 17.0 ± 7.0 nM for human σ1 receptor , selective over the sigma-2 receptor and against a panel of other 170 receptors, enzymes, transporters and ion channels.",337.42,"878141-96-9",{"v":67,"d":"67.00"},198.57,{"v":67,"d":"67.00"},198.57,"http://www.selleck.cn/products/s1ra.html","C20H23N3O2","Free Base","E-52862","CC1=CC(=N[N]1C2=CC=C3C=CC=CC3=C2)OCCN4CCOCC4",3.459,3,0,5]
["S8455","Talabostat (PT-100)","b4","L1700-62","in 10mM DMSO","DPP","Proteases","Talabostat (Val-boroPro, PT-100) is a dipeptidyl peptidase inhibitor with IC50 values of <4 nM, 4 nM, 11 nM, 310 nM, 560 nM and 390 nM for DPP-IV, DPP8, DPP9, QPP, FAP and PEP respectively. It has antineoplastic and hematopoiesis- stimulating activities.",310.18,"150080-09-4",{"v":62,"d":"62.00"},199.88,{"v":62,"d":"62.00"},199.88,"http://www.selleck.cn/products/talabostat.html","C10H23BN2O6S","Free Base","Val-boroPro","CC(C)C(N)C(=O)N1CCCC1B(O)O.C[S](O)(=O)=O",{"v":0.33,"d":"0.330"},1,1,3]
["S8862","PDD00017273","g5","L1700-62","in 10mM DMSO","PARG","Metabolism","PDD00017273 is a potent and selective poly (ADP ribose) glycohydrolase (PARG) inhibitor with an IC50 of 26 nM. PDD00017273 exhibits >350-fold selectivity for PARG over a panel of ion channels, enzymes and receptors, including PARP1 and ARH3.",514.62,"1945950-21-9",{"v":100,"d":"100.00"},194.32,"<1","N/A","http://www.selleck.cn/products/pdd00017273.html","C23H26N6O4S2","Free Base","N/A","C[N]1N=C(C)C=C1CN2C(=O)N(CC3=CN=C(C)S3)C(=O)C4=CC(=CC=C24)[S](=O)(=O)NC5(C)CC5",1.554,6,1,7]
["S8899","FF-10101","f6","L1700-62","in 10mM DMSO","FLT3","Angiogenesis","FF-10101 is a novel irreversible FLT3 inhibitor with ic50 of 0.20 nM and 0.16 nM for FLT3 (WT) and FLT3(D835Y), respectively.",530.66,"1472797-69-5",{"v":100,"d":"100.00"},188.44,"<1","N/A","http://www.selleck.cn/products/ff-10101.html","C29H38N8O2","Free Base","N/A","CCCNC1=NC(=NC=C1C#CCCCNC(=O)C(C)N(C)C(=O)\\C=C\\CN(C)C)NC2=CC=C(C=C2)C#N",4.153,4,3,15]
["S9123","Eriodictyol","b8","L1700-62","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Eriodictyol, a flavonoid extracted from yerba santa, has anti-inflammatory and antioxidant activities and taste-modifying properties.",288.25,"552-58-9",{"v":57,"d":"57.00"},197.74,"N/A","N/A","https://www.selleckchem.com/products/eriodictyol.html","C15H12O6","free base","N/A","OC1=CC2=C(C(=O)CC(O2)C3=CC(=C(O)C=C3)O)C(=C1)O",2.131,2,4,1]
["S9192","Vitexin","e8","L1700-62","in 10mM DMSO","Others","Others","Vitexin (Apigenin-8-C-glucoside), an naturally occuring apigenin flavone glycoside, acts as a platelet aggregation and alpha-glucosidase inhibitor and shows antineoplastic activity.",432.38,"3681-93-4",{"v":47,"d":"47.00"},{"v":108.7,"d":"108.70"},"N/A","N/A","https://www.selleckchem.com/products/vitexin.html","C21H20O10","free base","Apigenin-8-C-glucoside","OCC1OC(C(O)C(O)C1O)C2=C(O)C=C(O)C3=C2OC(=CC3=O)C4=CC=C(O)C=C4",0.018,3,7,3]
["S1058","BI-1347","f10","L1700-62","in 10mM DMSO","CDK","Cell Cycle","BI-1347 is a small molecule inhibitor of Cyclin-dependent kinase 8(CDK8) with IC50 of 1.1 nM.",356.42,"2163056-91-3",{"v":71,"d":"71.00"},{"v":199.2,"d":"199.20"},"<1","N/A","http://www.selleck.cn/products/bi-1347.html","C22H20N4O","Free Base","N/A","CN(C)C(=O)C[N]1C=C(C=N1)C2=CC=C(C=C2)C3=CN=CC4=CC=CC=C34",{"v":2.54,"d":"2.540"},3,0,4]
["S1074","Poliumoside","a11","L1700-62","in 10mM DMSO","Aldose Reductase","Metabolism","Poliumoside exhibits significant inhibition of advanced glycation end product formation with IC50 values of 19.69  µM. In the rat lens aldose reductase assay.Poliumoside exhibits greater inhibitory effects on rat lens aldose reductase(RLAR) with IC50 values of 8.47 µM.",770.73,"94079-81-9",{"v":100,"d":"100.00"},129.75,{"v":100,"d":"100.00"},129.75,"http://www.selleck.cn/products/poliumoside.html","C35H46O19","Free Base","N/A","CC1OC(OCC2OC(OCCC3=CC(=C(O)C=C3)O)C(O)C(OC4OC(C)C(O)C(O)C4O)C2OC(=O)/C=C/C5=CC(=C(O)C=C5)O)C(O)C(O)C1O",-0.375,8,11,13]
["S2307","Roquinimex","a3","L1700-63","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Roquinimex (FCF 89, Linomide, LS 2616) is a novel immunomodulator augmenting natural killer (NK) cell activity and T-lymphocyte related effector functions. Roquinimex is a potent oral active tumor antiangiogenic agent. Roquinimex inhibits the secretion of TNF-α.",308.33,"84088-42-6",{"v":62,"d":"62.00"},201.08,"<1","N/A","http://www.selleck.cn/products/roquinimex.html","C18H16N2O3","Free Base","FCF 89, Linomide, LS 2616","CN(C1=CC=CC=C1)C(=O)C2=C(O)C3=C(C=CC=C3)N(C)C2=O",1.871,2,1,2]
["S2421","PF-04457845","d3","L1700-63","in 10mM DMSO","FAAH","Metabolism","PF-04457845 (PF-4457845) is a potent, favorable selective inhibitor of Fatty acid amide hydrolase (FAAH) with IC50 of 7.2 nM and 7.4 nM for hFAAH and rFAAH, respectively. PF-04457845 covalently modifies the active-site serine nucleophile of FAAH with exquisite selectivity relative to other members of the serine hydrolase superfamily.",455.43,"1020315-31-4",{"v":91,"d":"91.00"},199.81,"<1","N/A","https://www.selleckchem.com/products/pf-04457845.html","C23H20F3N5O2","Free Base","PF-4457845","FC(F)(F)C1=CN=C(OC2=CC(=CC=C2)C=C3CCN(CC3)C(=O)NC4=NN=CC=C4)C=C1",4.371,5,1,5]
["S2644","Lerisetron","g4","L1700-63","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","Lerisetron (F 0930, F 0930RS) is a 5-HT3 receptor antagonist with IC50 of 0.81μM.",292.38,"143257-98-1",{"v":58,"d":"58.00"},198.37,"<1","N/A","http://www.selleck.cn/products/lerisetron.html","C18H20N4","Free Base","F 0930, F 0930RS","C1CN(CCN1)C2=NC3=C(C=CC=C3)[N]2CC4=CC=CC=C4",{"v":3.26,"d":"3.260"},1,1,3]
["S6651","G15 (GRB-G15)","h5","L1700-63","in 10mM DMSO","Estrogen/progestogen Receptor,GPR,GPR","Endocrinology & Hormones","G15 is a cell-permeable high affinity and selective  G-protein coupled estrogen receptor 1 (GPER, GPR30)  antagonist with an affinity of approximately 20 nM that displays no affinity for ERα and ERβ at concentrations up to 10 μM.",370.24,"1161002-05-6",{"v":74,"d":"74.00"},199.87,"<1","N/A","http://www.selleck.cn/products/g15.html","C19H16BrNO2","Free Base","N/A","BrC1=CC2=C(OCO2)C=C1C3NC4=C(C=CC=C4)C5C=CCC35",4.509,2,1,1]
["S6667","STING inhibitor C-178","d7","L1700-63","in 10mM DMSO","STING","Immunology & Inflammation","C-178 is a covalent inhibitor of STING,covalently bind to Cys91.",322.27,"329198-87-0",{"v":32,"d":"32.00"},{"v":99.3,"d":"99.30"},"<1","N/A","http://www.selleck.cn/products/c-178.html","C17H10N2O5","Free Base","N/A","[O-][N+](=O)C1=CC=C(O1)C(=O)NC2=CC3=C(C=C2)C4=CC=CC=C4O3",3.532,3,1,3]
["S6674","Cytosporone B","h7","L1700-63","in 10mM DMSO","Nur77","Cell Cycle","Cytosporone B  is a naturally occurring agonist for nuclear orphan receptor Nur77(NR4A1) with an EC50 of 0.278nM.",{"v":322.4,"d":"322.40"},"321661-62-5",{"v":64,"d":"64.00"},198.51,"<1","N/A","http://www.selleck.cn/products/cytosporone-b.html","C18H26O5","Free Base","N/A","CCCCCCCC(=O)C1=C(O)C=C(O)C=C1CC(=O)OCC",4.272,3,2,11]
["S8909","UBCS039","h9","L1700-63","in 10mM DMSO","Sirtuin","Epigenetics","UBCS039 is the first synthetic SIRT6 activator with EC50 of 38 μM,induces a time-dependent activation of autophagy in several human tumor cell lines.",247.29,"358721-70-7",{"v":49,"d":"49.00"},198.15,"<1","N/A","http://www.selleck.cn/products/ubcs039.html","C16H13N3","Free Base","N/A","N1C(C2=CN=CC=C2)C3=CC=C[N]3C4=CC=CC=C14",2.914,1,1,1]
["S8949","Olutasidenib (FT-2102)","c10","L1700-63","in 10mM DMSO","Dehydrogenase","Metabolism","Olutasidenib is a potent, orally bioavailable, brain penetrant and selective mutant IDH1 (mIDH1) inhibitor with IC50 of 21.1 nM, 114 nM for IDH1-R132H, IDH1-R132C, respectively.",354.79,"1887014-12-1",{"v":71,"d":"71.00"},200.12,"<1","N/A","http://www.selleck.cn/products/olutasidenib-ft-2102.html","C18H15ClN4O2","Free Base","N/A","CC(NC1=CC=C(C#N)N(C)C1=O)C2=CC3=C(NC2=O)C=CC(=C3)Cl",1.234,2,2,3]
["S0103","ML327","c2","L1700-64","in 10mM DMSO","Apoptosis related,Myc","Cell Cycle","ML327 is an isoxazole compound that blocks MYC expression and tumor formation in neuroblastoma. ML327 also restores E-cadherin expression with In-Cell Western EC50 of 1.0 μM. ML327 induces apoptosis.",366.37,"1883510-31-3",{"v":50,"d":"50.00"},136.47,"<1","N/A","http://www.selleckchem.com/products/ml327.html","C19H18N4O4","Free Base","N/A","O=C(NCCCNC(=O)C1=CC=CNC1=O)C2=NOC(=C2)C3=CC=CC=C3",0.455,5,3,7]
["S0184","XY1","c3","L1700-64","in 10mM DMSO","PRMT","Methylation","XY1 is an inactive, close analog of SGC707 that can be used as the negative control for SGC707. SGC707 is a potent, selective and cell-active allosteric inhibitor of protein arginine methyltransferase 3 (PRMT3) with IC50 and Kd of 31 nM and 53 nM, respectively.",297.35,"1624117-53-8",{"v":59,"d":"59.00"},198.42,"˂1","N/A","http://www.selleckchem.com/products/xy1.html","C17H19N3O2","Free Base","N/A","O=C(NCC(=O)N1CCCC1)NC2=CC=C3C=CC=CC3=C2",1.581,2,2,3]
["S0302","F1063-0967","c4","L1700-64","in 10mM DMSO","phosphatase","Metabolism","F1063-0967 is an inhibitor of Dual-specificity phosphatase 26 (DUSP26) with IC50 of 11.62 μM.",484.59,"613225-56-2",{"v":100,"d":"100.00"},206.36,"˂1","N/A","http://www.selleckchem.com/products/f1063-0967.html","C24H24N2O5S2","Free Base","N/A","CC1=CC=C(C=C1)\\C=C2/SC(=S)N(CCCCCC(=O)NC3=CC(=C(C=C3)C(O)=O)O)C2=O",5.039,3,2,9]
["S0462","NS-1619","b5","L1700-64","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","NS-1619 is a selective activator of large conductance Ca2+-activated K+-channels.",362.23,"153587-01-0",{"v":72,"d":"72.00"},198.77,"˂1","N/A","http://www.selleckchem.com/products/ns-161.html","C15H8F6N2O2","Free Base","N/A","OC1=CC=C(C=C1N2C(=O)NC3=CC(=CC=C23)C(F)(F)F)C(F)(F)F",4.117,1,2,3]
["S2427","Triglycidyl Isocyanurate (Teroxirone)","h6","L1700-64","in 10mM DMSO","DNA/RNA Synthesis,p53","Apoptosis","Triglycidyl Isocyanurate (Teroxirone, Tris(2,3-epoxypropyl) Isocyanurate, TGI, TGIC) is a triazene triepoxide with antineoplastic activity. It inhibits growth of human non-small cell lung cancer cells by activating p53. Triglycidyl Isocyanurate alkylates and cross-links DNA, thereby inhibiting DNA replication. Triglycidyl Isocyanurate is also used in various polyester powder coatings in the metal finishing industry.",297.26,"2451-62-9",{"v":59,"d":"59.00"},198.48,"<1","N/A","http://www.selleckchem.com/products/triglycidyl-isocyanurat.html","C12H15N3O6","Free Base","Tris(2,3-epoxypropyl) Isocyanurate, TGI, TGIC","O=C1N(CC2CO2)C(=O)N(CC3CO3)C(=O)N1CC4CO4",-0.894,6,0,6]
["S2595","FK-3311","f7","L1700-64","in 10mM DMSO","COX","Immunology & Inflammation","FK-3311 (COX-2 Inhibitor V) is a selective, cell-permeable and orally available inhibitor of cyclooxygenase-2 (COX-2) with antiinflammatory. FK-3311 has protective effects against hepatic warm ischemia-reperfusion injury by marked inhibition of TxA2.",341.33,"116686-15-8",{"v":68,"d":"68.00"},199.22,"<1","N/A","http://www.selleckchem.com/products/fk-3311.html","C15H13F2NO4S","Free Base","COX-2 Inhibitor V","CC(=O)C1=CC=C(N[S](C)(=O)=O)C(=C1)OC2=CC=C(F)C=C2F",2.452,4,1,5]
["S6759","TC-G-1008 (GPR39-C3)","b9","L1700-64","in 10mM DMSO","GPR","Endocrinology & Hormones","TC-G-1008 (GPR39-C3) is a potent and orally bioavailable agonist of GPR39 with EC50 of 0.4nM and 0.8nM for rat and human receptor, respectively.",{"v":418.9,"d":"418.90"},"1621175-65-2",{"v":84,"d":"84.00"},200.53,"<1","N/A","http://www.selleckchem.com/products/gpr39-c3.html","C18H19ClN6O2S","Free Base","N/A","CNC1=NC(=CC(=N1)NCC2=C(Cl)C=C(N[S](C)(=O)=O)C=C2)C3=CC=CC=N3",3.112,5,3,7]
["S6775","TUG-891","e9","L1700-64","in 10mM DMSO","Others","Others","TUG-891 is a potent and selective agonist of the long chain free fatty acid (LCFA) receptor 4 (FFA4/GPR120), which demonstrates both potential opportunity and possible challenges to therapeutic agonism.",364.41,"1374516-07-0",{"v":23,"d":"23.00"},63.12,"<1","N/A","http://www.selleckchem.com/products/tug-891.html","C23H21FO3","Free Base","N/A","CC1=CC=C(C=C1)C2=CC=C(F)C=C2COC3=CC=C(CCC(O)=O)C=C3",5.728,2,0,7]
["S6784","STAT5-IN-1","e10","L1700-64","in 10mM DMSO","STAT","JAK/STAT","STAT5-IN-1 is a potent and selective STAT5 inhibitor with IC50 of 47 μM for STAT5β isoform.",293.28,"285986-31-4",{"v":20,"d":"20.00"},68.19,"<1","N/A","http://www.selleckchem.com/products/stat-in-1.html","C16H11N3O3","Free Base","N/A","O=C(N\\N=C\\C1=COC2=C(C=CC=C2)C1=O)C3=CC=CN=C3",0.943,5,1,3]
["S6799","DIM-C-pPhOH","a2","L1700-65","in 10mM DMSO","Nur77","Cell Cycle","DIM-C-pPhOH (C-DIM8, CDIM8) is a nuclear receptor 4A1 (NR4A1)(Nur77) antagonist. DIM-C-pPhOH inhibits tumor growth and mTOR signaling, induces apoptosis and cellular stress. DIM-C-pPhOH reduces cell proliferation with IC50 of 13.6 μM and 13.0 μM for ACHN cells and 786-O cells, respectively.",{"v":338.4,"d":"338.40"},"151358-47-3",{"v":68,"d":"68.00"},200.95,"<1","N/A","http://www.selleckchem.com/products/dim-c-pphoh.html","C23H18N2O","Free Base","C-DIM8, CDIM8","OC1=CC=C(C=C1)C(C2=C[NH]C3=C2C=CC=C3)C4=C[NH]C5=C4C=CC=C5",5.433,0,3,3]
["S6820","X-GAL","e3","L1700-65","in 10mM DMSO","Dyes","Others","X-GAL (BCIG) is a widely used chromogenic β-galactosidase substrate. β-galactosidase cleaves X-gal and produce an insoluble detectable blue compound. X-Gal is applied in blue-white selection of recombinant bacterial colonies with the lac+ genotype.",408.63,"7240-90-6",{"v":82,"d":"82.00"},200.67,"<1","N/A","http://www.selleckchem.com/products/x-gal.html","C14H15BrClNO6","Free Base","BCIG","OCC1OC(OC2=C[NH]C3=C2C(=C(Br)C=C3)Cl)C(O)C(O)C1O",1.364,2,5,3]
["S6832","MC-VC-PAB-PNP","d4","L1700-65","in 10mM DMSO","ADC Linker","Others","MC-Val-Cit-PAB-PNP (Mc-Val-Cit-PABC-PNP) is a cathepsin cleavable ADC peptide linker that is applicable to the synthesis of antibody-drug conjugates (ADCs).",737.76,"159857-81-5",{"v":100,"d":"100.00"},135.55,"<1","N/A","http://www.selleckchem.com/products/mc-vc-pab-pnp.html","C35H43N7O11","Free Base","Maleimidocaproyl-L-valine-L-citrulline-p-aminobenzyl alcohol p-nitrophenyl carbonate, Mc-Val-Cit-PABC-PNP","CC(C)C(NC(=O)CCCCCN1C(=O)C=CC1=O)C(=O)NC(CCCNC(N)=O)C(=O)NC2=CC=C(COC(=O)OC3=CC=C(C=C3)[N+]([O-])=O)C=C2",3.025,9,5,22]
["S7821","Bufalin","h5","L1700-65","in 10mM DMSO","ATPase,Others","Transmembrane Transporters","Bufalin (BF) is a potent inhibitor of steroid receptor coactivator SRC-3, SRC-1 and Na+/K+-ATPase. Bufalin binds to the subunit α1, α2 and α3 of Na+/K+-ATPase with Kd of 42.5 nM, 45 nM and 40 nM, respectively. Bufalin is a major digoxin-like immunoreactive component isolated from the Chinese medicine Chan Su with anti-cancer activity.",386.52,"465-21-4",{"v":78,"d":"78.00"},{"v":201.8,"d":"201.80"},"˂1","N/A","http://www.selleckchem.com/products/bufalin.html","C24H34O4","Free Base","BF","CC12CCC(O)CC1CCC3C2CCC4(C)C(CCC34O)C5=COC(=O)C=C5",3.313,2,1,1]
["S8888","GMB-475","h6","L1700-65","in 10mM DMSO","Bcr-Abl,E3 Ligase ,PROTAC","Angiogenesis","GMB-475 is a proteolysis-targeting chimera (PROTAC) that allosterically targets BCR-ABL1 protein and recruit the E3 ligase Von Hippel-Lindau (VHL), resulting in ubiquitination and subsequent degradation of the oncogenic fusion protein.",861.93,"2490599-18-1",{"v":100,"d":"100.00"},116.02,"<1","N/A","http://www.selleckchem.com/products/gmb-475.html","C43H46F3N7O7S","Free Base","N/A","CC1=C(SC=N1)C2=CC=C(CNC(=O)C3CC(O)CN3C(=O)C(NC(=O)COCCOC4=CC=C(C=C4)C5=CC(=NC=N5)NC6=CC=C(OC(F)(F)F)C=C6)C(C)(C)C)C=C2",6.683,9,4,18]
["S8947","SX-682","d8","L1700-65","in 10mM DMSO","CXCR","Immunology & Inflammation","SX-682 is an orally bioavailable small-molecule allosteric inhibitor of CXCR1 and CXCR2 that blocks tumor MDSC recruitment and enhances T cell activation and antitumor immunity.",{"v":467.2,"d":"467.20"},"1648843-04-2",{"v":93,"d":"93.00"},199.06,"˂1","N/A","http://www.selleckchem.com/products/sx-682.html","C19H14BF4N3O4S","Free Base","N/A","OB(O)C1=CC=C(OC(F)(F)F)C=C1CSC2=NC=C(C=N2)C(=O)NC3=CC=C(F)C=C3",5.761,4,1,8]
["S8980","SBI-797812","e9","L1700-65","in 10mM DMSO","NAMPT","Metabolism","SBI-797812 is a NAMPT activator which is structurally similar to active-site directed NAMPT inhibitors and blocks binding of these inhibitors to NAMPT. SBI-797812 turns NAMPT into a \"super catalyst\" that more efficiently generates NMN.",402.47,"2237268-08-3",{"v":80,"d":"80.00"},198.77,"<1","N/A","http://www.selleckchem.com/products/sbi-797812.html","C19H22N4O4S","Free Base","N/A","O=C(NCC1=CC=NC=C1)NC2=CC=C(C=C2)[S](=O)(=O)N3CC4CCC(C3)O4",0.702,5,2,5]
["S0085","BMS-813160","h10","L1700-65","in 10mM DMSO","CCR","Immunology & Inflammation","BMS-813160 is a potent, well-absorbed dual CCR2 and CCR5 chemokine antagonist. BMS-813160 inhibits inflammatory processes, angiogenesis, tumor cell migration, tumor cell proliferation and invasion.",484.64,"1286279-29-5",{"v":97,"d":"97.00"},200.15,"<1","N/A","http://www.selleckchem.com/products/bms813160.html","C25H40N8O2","free base","N/A","CC(=O)NC1CC(CCC1N2CCC(NC3=NC=NC4=CC(=N[N]34)C(C)(C)C)C2=O)NC(C)(C)C",1.774,5,3,7]
["S0095","VL285","c11","L1700-65","in 10mM DMSO","E3 Ligase ,E3 ligase Ligand,PROTAC","Ubiquitin","VL285 is a potent VHL ligand that degrades HaloTag7 fusion proteins. Cotreatment with excess VL285, the core VHL ligand from which HaloPROTAC3 is derived, is able to significantly reduce HaloPROTAC3 mediated activity to 50% degradation.",532.65,"1448188-57-5",{"v":100,"d":"100.00"},187.74,"<1","N/A","http://www.selleckchem.com/products/vl285.html","C29H32N4O4S","free base","N/A","CC(C)C(N1CC2=CC=CC=C2C1=O)C(=O)N3CC(O)CC3C(=O)NCC4=CC=C(C=C4)C5=C(C)N=CS5",2.287,4,2,7]
["S0156","CID 1375606","b2","L1700-66","in 10mM DMSO","GPR","Endocrinology & Hormones","CID 1375606 (2,4-Dichloro-N-(phenylcarbamoyl)phenylbenzamide) is an orphan G protein-coupled receptor GPR27 agonist.",385.24,"313493-80-0",{"v":77,"d":"77.00"},199.88,"<1","N/A","http://www.selleckchem.com/products/cid1375606.html","C20H14Cl2N2O2","free base","2,4-Dichloro-N-(phenylcarbamoyl)phenylbenzamide","ClC1=CC(=C(C=C1)C(=O)NC2=CC=C(C=C2)C(=O)NC3=CC=CC=C3)Cl",4.728,2,2,4]
["S0305","RO1138452","d4","L1700-66","in 10mM DMSO","Prostaglandin Receptor","Immunology & Inflammation","RO1138452 (CAY10441) is a potent and selective antagonist of IP (prostacyclin, PGI2) receptor with pKi of 9.3 and 8.7 in human platelets and a recombinant IP receptor system, respectively.",309.41,"221529-58-4",{"v":62,"d":"62.00"},200.38,"<1","N/A","https://www.selleckchem.com/products/ro1138452-cay10441.html","C19H23N3O","free base","CAY10441","CC(C)OC1=CC=C(CC2=CC=C(NC3=NCCN3)C=C2)C=C1",3.709,2,2,6]
["S0405","AF-353","c5","L1700-66","in 10mM DMSO","P2 Receptor","Neuronal Signaling","AF-353 (Ro-4) is a potent, selective and orally bioavailable antagonist of P2X3 receptor and P2X2/3 receptor with pIC50 of 8.06, 8.05 and 7.41 for human P2X3, rat P2X3 and human P2X2/3, respectively.",400.21,"865305-30-2",{"v":100,"d":"100.00"},249.87,"<1","N/A","http://www.selleckchem.com/products/af353.html","C14H17IN4O2","free base","Ro-4","COC1=C(I)C=C(OC2=CN=C(N)N=C2N)C(=C1)C(C)C",2.934,4,2,4]
["S0475","GC376","b6","L1700-66","in 10mM DMSO","3C-Like Protease","Proteases","GC376 is a 3CLpro (3C-like protease) inhibitor with IC50 of ~ 1.11 μM for the PEDV 3CLpro. GC376 is active against the 3CLpro of multiple coronaviruses, including SARS-CoV.",507.53,"1416992-39-6",{"v":100,"d":"100.00"},197.03,{"v":100,"d":"100.00"},197.03,"http://www.selleckchem.com/products/gc376-sodium.html","C21H30N3NaO8S","free base","N/A","[Na+].CC(C)CC(NC(=O)OCC1=CC=CC=C1)C(=O)NC(CC2CCNC2=O)C(O)[S]([O-])(=O)=O",-1.095,4,4,12]
["S0777","Isuzinaxib (APX-115 free base)","f7","L1700-66","in 10mM DMSO","CCR,Interleukins,NADPH-oxidase,TNF-alpha","Immunology & Inflammation","Isuzinaxib (APX-115 free base, Ewha-18278 free base) is a potent, orally active inhibitor of pan NADPH oxidase (pan-Nox) with Ki of 1.08 μM, 0.57 μM, and 0.63 μM for Nox1, Nox2 and Nox4, respectively. APX-115 free base (Ewha-18278 free base) significantly suppresses the expression of inflammatory molecules including MCP-1/CCL2, IL-6, and TNFα in the diabetic kidney.",279.34,"1270084-92-8",{"v":56,"d":"56.00"},200.47,"<1","N/A","http://www.selleckchem.com/products/apx-115-free-base.html","C17H17N3O","free base","Ewha-18278 free base","CCCC1=C(NN(C1=O)C2=CC=CC=N2)C3=CC=CC=C3",2.994,2,1,4]
["S0906","6-Methoxydihydrosanguinarine","e8","L1700-66","in 10mM DMSO","Bacterial","Immunology & Inflammation","6-Methoxydihydrosanguinarine is an lkaloid isolated from the fruits of M.cordata. 6-Methoxydihydrosanguinarine shows strong cytotoxicity against MCF-7 and SF-268 cell lines with IC50 values of 0.61 μM and 0.54 μM, respectively.",363.36,"72401-54-8",{"v":73,"d":"73.00"},{"v":200.9,"d":"200.90"},"<1","N/A","https://www.selleckchem.com/products/6-methoxydihydroavicine.html","C21H17NO5","free base","6-Methoxy Dihydrosanguinarine","COC1N(C)C2=C(C=CC3=C2C=C4OCOC4=C3)C5=CC6=C(OCO6)C=C15",3.777,5,0,1]
["S3210","3'-Hydroxy-4'-methoxyacetophenone","b10","L1700-66","in 10mM DMSO","Anti-infection","Immunology & Inflammation","3'-Hydroxy-4'-methoxyacetophenone (Acetoisovanillone, Isoacetovanillone, Diosmin EP Impurity A) is an active P. spinosa extract with anti-inflammatory potential.",166.17,"6100-74-9",{"v":33,"d":"33.00"},198.59,"<1","N/A","http://www.selleckchem.com/products/3-hydroxy-4-methoxyacetophenone.html","C9H10O3","free base","Acetoisovanillone, Isoacetovanillone, Diosmin EP Impurity A","COC1=C(O)C=C(C=C1)C(C)=O",1.311,2,1,2]
["S3215","2-O-α-D-Glucopyranosyl-L-ascorbic acid","e10","L1700-66","in 10mM DMSO","Others","Others","2-O-α-D-Glucopyranosyl-l-ascorbic acid (AA-2G), which is a glucoside derivative of ascorbic acid (AA), shows vitamin C activity after enzymatic hydrolysis to ascorbic acid. The antitumor activity of AA-2G is caused by ROS generated by AA released by rapid hydrolysis of AA-2G.",338.26,"129499-78-1",{"v":68,"d":"68.00"},201.03,{"v":68,"d":"68.00"},201.03,"http://www.selleckchem.com/products/2-o-a-d-glucopyranosyl-l-ascorbic-acid.html","C12H18O11","free base","AA-2G, 2-OaD-Glucopyranosyl-L-ascorbic acid, 2-O-alpha-D-Glucopyranosyl-L-ascorbic Acid, Ascorbic acid 2-glucoside, Ascorbyl glucoside","OCC(O)C1OC(=O)C(=C1O)OC2OC(CO)C(O)C(O)C2O",-3.639,4,7,5]
["S3230","L-Fucitol","f11","L1700-66","in 10mM DMSO","Others","Microbiology","L-Fucitol (1-Deoxy-D-galactitol), a galactitol analogue isolated from Myristica fragrans (Nutmeg), inhibits galactitol-positive strains of Escherichia coli K12.",166.17,"13074-06-1",{"v":10,"d":"10.00"},60.18,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/l-fucitol.html","C6H14O5","free base","1-Deoxy-D-galactitol","CC(O)C(O)C(O)C(O)CO",-2.052,0,5,4]
["S3247","Icariside I","a3","L1700-67","in 10mM DMSO","Others","Others","Icariside I (Icarisid I) is one of the main components in Epimedii Folium that significantly stimulates cell proliferation and osteoblasts differentiation.",530.52,"56725-99-6",{"v":100,"d":"100.00"},188.49,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/icariside-i.html","C27H30O11","free base","Icarisid I","COC1=CC=C(C=C1)C2=C(O)C(=O)C3=C(O2)C(=C(OC4OC(CO)C(O)C(O)C4O)C=C3O)CC=C(C)C",2.025,5,6,7]
["S3262","Scopolin","e4","L1700-67","in 10mM DMSO","Sirtuin","DNA Damage/DNA Repair","Scopolin,  a coumarin isolated from Arabidopsis thaliana (Arabidopsis), attenuates hepatic steatosis through activation of SIRT1-mediated signaling cascades, a potent regulator of lipid homeostasis.",354.31,"531-44-2",{"v":100,"d":"100.00"},282.24,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/scopolin.html","C16H18O9","free base","N/A","COC1=CC2=C(OC(=O)C=C2)C=C1OC3OC(CO)C(O)C(O)C3O",-0.289,5,4,4]
["S3271","Caudatin","d5","L1700-67","in 10mM DMSO","Apoptosis related","Apoptosis","Caudatin (Cauldatin), one species of C‑21 steroidal from Cynanchum auriculatum (C. auriculatum), effectively inhibits human glioma growth in vitro and in vivo through triggering cell cycle arrest and apoptosis.",490.63,"38395-02-7",{"v":100,"d":"100.00"},203.82,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/caudatin.html","C28H42O7","free base","Cauldatin","CC(C)/C(C)=C/C(=O)OC1CC2C3(C)CCC(O)CC3=CCC2(O)C4(O)CCC(O)(C(C)=O)C14C",{"v":2.46,"d":"2.460"},3,1,5]
["S3285","Dihydrolycorine","a7","L1700-67","in 10mM DMSO","Others","Others","Dihydrolycorine is a derivative of lycorine, an alkaloid isolated from Lycoris radiata Herb. Dihydrolycorine blocks protein synthesis in ascites cells and stabilize HeLa cell polysomes in vivo. Dihydrolycorine exhibits antihypertensive and neuroprotective activities.",289.33,"6271-21-2",{"v":100,"d":"100.00"},345.63,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/dihydrolycorine.html","C16H19NO4","free base","N/A","OC1CC2CCN3CC4=C(C=C5OCOC5=C4)C(C1O)C23",0.761,2,2,0]
["S3291","Myristicin","d7","L1700-67","in 10mM DMSO","MAO,P450 (e.g. CYP17)","Metabolism","Myristicin (Myristicine), a terpene-like active component in Nutmeg which is the seed of Myristica fragrans, is a weak inhibitor of monamine oxidase (MAO) and a mechanism-based inhibitor of CYP1A2.",192.21,"607-91-0","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleckchem.com/products/myristicin.html","C11H12O3","free base","Myristicine","COC1=C2OCOC2=CC(=C1)CC=C",2.589,3,0,3]
["S6186","3-Methylxanthine","d9","L1700-67","in 10mM DMSO","PDE","Metabolism","3-Methylxanthine (3-MX), a 3-alkylxanthine, is an inhibitor of cyclic guanosine monophosphate (GMP) phosphodiesterase (PDE) with IC50 of 920 μM on guinea-pig isolated trachealis muscle.",166.14,"1076-22-8",{"v":8,"d":"8.00"},48.15,"<1","N/A","http://www.selleckchem.com/products/3-methylxanthine.html","C6H6N4O2","free base","3-MX","CN1C(=O)NC(=O)C2=C1N=C[NH]2",-0.512,3,2,0]
["S6597","TLR2-IN-C29","g9","L1700-67","in 10mM DMSO","TLR","Immunology & Inflammation","TLR2-IN-C29 (C29) is a Toll-like receptor 2 (TLR2) inhibitor that inhibits TLR2/1 and TLR2/6 signaling.",285.29,"363600-92-4",{"v":57,"d":"57.00"},{"v":199.8,"d":"199.80"},"<1","N/A","http://www.selleckchem.com/products/tlr2-in-c29.html","C16H15NO4","free base","C29","COC1=CC=CC(=C1O)C=NC2=CC=CC(=C2C)C(O)=O",3.284,3,1,4]
["S6803","1-BCP","f10","L1700-67","in 10mM DMSO","GluR","Neuronal Signaling","1-BCP (Piperonylic acid piperidide) is a memory-enhancing agent that enhances AMPA-induced currents.",233.26,"34023-62-6",{"v":47,"d":"47.00"},201.49,{"v":6,"d":"6.00"},25.72,"http://www.selleckchem.com/products/1-bcp.html","C13H15NO3","free base","Piperonylic acid piperidide","O=C(N1CCCCC1)C2=CC=C3OCOC3=C2",1.929,3,0,1]
["S6873","Thioflavin T","c2","L1700-68","in 10mM DMSO","Dyes","Others","Thioflavin T (ThT, Thioflavine T, Basic Yellow 1) is a benzothiazole dye that exhibits enhanced fluorescence upon binding to amyloid fibrils and is commonly used to diagnose amyloid fibrils.",318.86,"2390-54-7",{"v":64,"d":"64.00"},200.72,{"v":3,"d":"3.00"},9.41,"http://www.selleckchem.com/products/thioflavin-t.html","C17H19ClN2S","free base","ThT, Thioflavine T, Basic Yellow 1","[Cl-].CN(C)C1=CC=C(C=C1)C2=[N+](C)C3=C(S2)C=C(C)C=C3",{"v":2.25,"d":"2.250"},0,0,2]
["S6906","Capric acid","g3","L1700-68","in 10mM DMSO","GluR,PPAR","Neuronal Signaling","Capric acid (DA, Decanoic acid, Decylic acid), a component of medium-chain triclycerides occurring naturally in coconut oil and palm kernel oil, contributes to seizure control through direct AMPA receptor inhibition. Capric acid is also a modulating ligand for PPARs. Due to its specific melting range the product may be solid, liquid, a solidified melt or a supercooled melt.",172.26,"334-48-5",{"v":34,"d":"34.00"},197.38,{"v":34,"d":"34.00"},197.38,"http://www.selleckchem.com/products/capric-acid.html","C10H20O2","free base","DA, Decanoic acid, Decylic acid","CCCCCCCCCC(O)=O",3.655,1,0,8]
["S7394","MDL-28170","c4","L1700-68","in 10mM DMSO","Cysteine Protease","Proteases","MDL-28170 (Calpain Inhibitor III) is a potent and selective calpain inhibitor of calpain that penetrates the blood-brain barrier and inhibits brain cysteine protease activity after systemic administration. MDL-28170 is also an inhibitor of γ-secretase.",382.45,"88191-84-8",{"v":76,"d":"76.00"},198.72,"<1","N/A","http://www.selleckchem.com/products/mdl-28170.html","C22H26N2O4","free base","Calpain Inhibitor III","CC(C)C(NC(=O)OCC1=CC=CC=C1)C(=O)NC(CC2=CC=CC=C2)C=O",3.531,4,2,10]
["S8916","BI-3406","c6","L1700-68","in 10mM DMSO","Ras","Cell Cycle","BI-3406 (compound I-13) is a potent, selective and orally active inhibitor of the interaction between KRAS and Son of Sevenless 1 (SOS1) with IC50 of 5 nM. BI-3406 reduces the formation of GTP-loaded KRAS, and inhibits MAPK pathway signaling. BI-3406 exhibits anti-tumor activities.",462.46,"2230836-55-0",{"v":92,"d":"92.00"},198.94,"<1","N/A","http://www.selleckchem.com/products/bi-3406.html","C23H25F3N4O3","free base","N/A","COC1=C(OC2CCOC2)C=C3C(=NC(=NC3=C1)C)NC(C)C4=CC(=CC(=C4)N)C(F)(F)F",3.594,5,2,7]
["S8975","Mezigdomide (CC-92480)","b7","L1700-68","in 10mM DMSO","E3 Ligase","Ubiquitin","Mezigdomide (CC-92480) is a novel protein degrader and a cereblon E3 ligase modulator (CELMoD) that has anti-myeloma activity.",567.61,"2259648-80-9",{"v":100,"d":"100.00"},176.18,"<1","N/A","http://www.selleckchem.com/products/cc-92480.html","C32H30FN5O4","free base","N/A","FC1=CC(=CC=C1N2CCN(CC2)CC3=CC=C(COC4=CC=CC5=C4CN(C6CCC(=O)NC6=O)C5=O)C=C3)C#N",3.586,4,1,7]
["S9611","ABTL-0812","f8","L1700-68","in 10mM DMSO","Akt,Autophagy,mTOR,ROS","PI3K/Akt/mTOR","ABTL0812 (α-Hydroxylinoleic acid, LP-10218, SCLN-0812) inhibits Akt/mTOR axis by inducing the overexpression of TRIB3 and activating autophagy in lung squamous carcinoma cell lines. ABTL0812 also induces AMPK activation and ROS accumulation.",296.44,"57818-44-7","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleckchem.com/products/abtl-0812.html","C18H32O3","free base","α-Hydroxylinoleic acid","CCCCC\\C=C/C\\C=C/CCCCCCC(O)C(O)=O",5.629,1,1,14]
["S9660","Remibrutinib (LOU064)","f9","L1700-68","in 10mM DMSO","BTK,Interleukins","Angiogenesis","Remibrutinib (LOU064) is a potent, highly selective covalent inhibitor of bruton tyrosine kinase (BTK) with IC50 of 1.3 nM, 2.5 nM and 18 nM for BTK, FcγR-induced IL8 and anti-IgM/IL4-induced CD69, respectively. Remibrutinib (LOU064) exhibits an exquisite kinase selectivity due to binding to an inactive conformation of BTK and has the potential for the treatment of autoimmune diseases.",507.53,"1787294-07-8",{"v":100,"d":"100.00"},197.03,"<1","N/A","http://www.selleckchem.com/products/remibrutinib-lou064.html","C27H27F2N5O3","free base","N/A","CN(CCOC1=C(N=CN=C1N)C2=C(C)C(=CC(=C2)F)NC(=O)C3=C(F)C=C(C=C3)C4CC4)C(=O)C=C",4.374,5,2,9]
["S9694","MLi-2","a10","L1700-68","in 10mM DMSO","LRRK2","Autophagy","MLi-2 is an orally active and highly selective inhibitor of LRRK2. MLi-2 exhibits exceptional potency in a purified LRRK2 kinase assay in vitro with IC50 of 0.76 nM, a cellular assay monitoring dephosphorylation of LRRK2 pSer935 LRRK2 with IC50 of 1.4 nM, and a radioligand competition binding assay with IC50 of 3.4 nM.",379.46,"1627091-47-7",{"v":76,"d":"76.00"},200.28,{"v":76,"d":"76.00"},200.28,"http://www.selleckchem.com/products/mli-2.html","C21H25N5O2","free base","N/A","CC1CN(CC(C)O1)C2=CC(=NC=N2)C3=N[NH]C4=CC=C(OC5(C)CC5)C=C34",3.892,5,1,4]
["S0140","KS176","e11","L1700-68","in 10mM DMSO","BCRP","Transmembrane Transporters","KS176 (compound 9) is a potent and selective inhibitor of the breast cancer resistance protein (BCRP, ABCG2) multidrug transporter with IC50 of 1.39 μM and 0.59 μM in Hoechst 33342 assay and Pheo A assay, respectively.",{"v":405.4,"d":"405.40"},"1253452-78-6",{"v":81,"d":"81.00"},{"v":199.8,"d":"199.80"},"<1","N/A","https://www.selleckchem.com/products/ks176.html","C22H19N3O5","Free Base","N/A","OCCC1=CC=C(NC(=O)C2=CC=CC=C2NC(=O)C3=CC=C(C=C3)[N+]([O-])=O)C=C1",{"v":3.01,"d":"3.010"},2,3,7]
["S0175","DMU2105","c3","L1700-69","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","DMU2105 is a potent and specific inhibitor of CYP1B1 with IC50 of 10 nM.",{"v":259.3,"d":"259.30"},"1031063-36-1",{"v":25,"d":"25.00"},96.41,"<1","N/A","https://www.selleckchem.com/products/dmu2105.html","C18H13NO","Free Base","N/A","O=C(/C=C/C1=CC2=CC=CC=C2C=C1)C3=CN=CC=C3",3.459,2,0,3]
["S0256","Ehp-inhibitor-1","a4","L1700-69","in 10mM DMSO","Ephrin receptor","Protein Tyrosine Kinase","Ehp-inhibitor-1 (Ehp inhibitor 2) is an Eph family tyrosine kinase inhibitor that targets Eph receptors.",317.34,"861249-59-4",{"v":40,"d":"40.00"},126.05,"<1","N/A","https://www.selleckchem.com/products/ehp-inhibitor.html","C18H15N5O","Free Base","Ehp inhibitor 2","COC1=CC(=CC=C1)C2=C(N)[N]3N=CC(=C3N=C2)C4=CN=CC=C4",1.765,4,1,3]
["S0354","Alsterpaullone","e5","L1700-69","in 10mM DMSO","Apoptosis related,Caspase,CDK,GSK-3","Cell Cycle","Alsterpaullone (Alp, 9-Nitropaullone, NSC 705701) is a potent inhibitor of CDK with IC50 of 35 nM, 15 nM, 200 nM and 40 nM for CDK1/cyclin B, CDK2/cyclin A, CDK2/cyclin E and CDK5/p35, respectively. Alsterpaullone also acts as a potent inhibitor of glycogen synthase kinase-3 (GSK-3) with IC50 of both 4 nM for GSK-3α and GSK-3β. Alsterpaullone induces apoptosis by activation of caspase-9. Alsterpaullone has antitumor activity and possesses potential for the treatment of neurodegenerative and proliferative disorders.",293.28,"237430-03-4",{"v":25,"d":"25.00"},85.24,"<1","N/A","https://www.selleckchem.com/products/alsterpaullone.html","C16H11N3O3","Free Base","Alp, 9-Nitropaullone, NSC 705701","[O-][N+](=O)C1=CC2=C([NH]C3=C2CC(=O)NC4=CC=CC=C34)C=C1",2.817,1,2,1]
["S0412","Bay 59-3074","d6","L1700-69","in 10mM DMSO","Cannabinoid Receptor","GPCR & G Protein","Bay 59-3074 is a selective cannabinoid CB1/CB2 receptor partial agonist with Ki of 55.4 nM, 48.3 nM and 45.5 nM at rat and human CB1 and human CB2 receptors, respectively. Bay 59-3074 displays analgesic properties.",453.36,"406205-74-1",{"v":91,"d":"91.00"},200.72,"<1","N/A","https://www.selleckchem.com/products/bay-59-3074.html","C18H13F6NO4S","Free Base","N/A","FC(F)(F)CCC[S](=O)(=O)OC1=CC=CC(=C1)OC2=CC=CC(=C2C#N)C(F)(F)F",5.354,2,0,9]
["S0464","AU1235","h6","L1700-69","in 10mM DMSO","MmpL3","Immunology & Inflammation","AU1235, an adamantyl urea, is a potent inhibitor of Mycobacterium tuberculosis protein MmpL3.",324.34,"1338780-86-1",{"v":10,"d":"10.00"},30.83,"<1","N/A","https://www.selleckchem.com/products/au1235.html","C17H19F3N2O","Free Base","N/A","FC1=C(F)C(=C(NC(=O)NC23CC4CC(CC(C4)C2)C3)C=C1)F",3.705,1,2,2]
["S0533","TLX agonist 1","d8","L1700-69","in 10mM DMSO","Others","Others","TLX agonist 1 (CCRP2, SUN23314) is a modulator of orphan nuclear receptor tailless (TLX, NR2E1) with EC50 of 1.0 μM and Kd of 650 nM. TLX agonist 1 (CCRP2, SUN23314) binds to recombinant TLX protein and enhances TLX transcriptional repressive activity.",374.48,"958323-31-4",{"v":40,"d":"40.00"},106.81,"<1","N/A","https://www.selleckchem.com/products/tlx-agonist-1.html","C23H26N4O","Free Base","CCRP2, SUN23314","C[N]1N=C(C=C1C)C(=O)N2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4",{"v":3.62,"d":"3.620"},2,0,4]
["S0729","TP0463518","c9","L1700-69","in 10mM DMSO","HIF","Angiogenesis","TP0463518 is a potent hypoxia-inducible factor prolyl hydroxylases (PHDs) inhibitor with Ki of 5.3 nM for human PHD2. TP0463518 inhibits human PHD1, human PHD3 and monkey PHD2 with IC50 of 18 nM, 63 nM and 22 nM, respectively.",431.83,"1558021-37-6",{"v":40,"d":"40.00"},92.63,"<1","N/A","https://www.selleckchem.com/products/tp0463518.html","C20H18ClN3O6","Free Base","N/A","OC(=O)CNC(=O)C1=C(O)CCN(CC2=CN=C(OC3=CC=C(Cl)C=C3)C=C2)C1=O",1.317,5,2,7]
["S0782","VU0238441","g10","L1700-69","in 10mM DMSO","AChR","Neuronal Signaling","VU0238441 is a pan muscarinic acetylcholine receptor (mAChR) positive allosteric modulator (PAM) with EC50 of 2.1 μM, 2.2 μM, 2.8 μM, 3.2 μM and >10 μM for M5, M3, M2, M1 and M4, respectively.",{"v":339.7,"d":"339.70"},"85511-68-8",{"v":50,"d":"50.00"},147.19,"<1","N/A","https://www.selleckchem.com/products/vu0238441.html","C16H9ClF3NO2","Free Base","N/A","FC(F)(F)C1=CC=C(CN2C(=O)C(=O)C3=C2C(=CC=C3)Cl)C=C1",4.066,2,0,3]
["S0856","KM91104","g11","L1700-69","in 10mM DMSO","ATPase","Transmembrane Transporters","KM 91104 is a cell-permeable inhibitor of V-ATPase that specifically targets the interaction between V-ATPase subunit a3 and subunit B2.",272.26,"304481-60-5",{"v":54,"d":"54.00"},198.34,"<1","N/A","https://www.selleckchem.com/products/km91104.html","C14H12N2O4","Free Base","N/A","OC1=C(O)C=C(C=C1)C(=O)NN=CC2=CC=CC=C2O",1.957,2,4,3]
["S1027","FL-411","c3","L1700-70","in 10mM DMSO","Autophagy,Epigenetic Reader Domain","Epigenetics","FL-411 (BRD4-IN-1) is a potent and selective inhibitor of Bromodomain-containing protein 4 (BRD4) with IC50 of 0.43 μM for BRD4(1). FL-411 induces ATG5-dependent autophagy-associated cell death (ACD) by blocking BRD4-AMPK interaction.",341.43,"2118944-88-8",{"v":10,"d":"10.00"},29.29,"<1","N/A","https://www.selleckchem.com/products/fl-411.html","C18H19N3O2S","Free Base","BRD4-IN-1","CN1CCC2=C(C1)SC3=C2C(=O)NC(=N3)C4=CC(=C(O)C(=C4)C)C",3.236,2,2,1]
["S2837","BCI","h4","L1700-70","in 10mM DMSO","phosphatase","Metabolism","BCI ((E)-BCI, compound 1) is an allosteric dual specificity phosphatase (DUSP) inhibitor with EC50 of 13.3 μM and 8.0 μM in cells for DUSP6 and DUSP1, respectively.",317.42,"1245792-51-1",{"v":63,"d":"63.00"},198.48,"<1","N/A","https://www.selleckchem.com/products/bci.html","C22H23NO","Free Base","(E)-BCI","O=C1\\C(=C\\C2=CC=CC=C2)C(NC3CCCCC3)C4=C1C=CC=C4",{"v":4.84,"d":"4.840"},1,1,3]
["S2964","HA-100 dihydrochloride","e5","L1700-70","in 10mM DMSO","MLCK,PKA,PKC,PKG","GPCR & G Protein","HA-100 dihydrochloride is an inhibitor of cGMP-dependent protein kinase (PKG), cAMP-dependent protein kinase (PKA), protein kinase C (PKC) and MLC-kinase with IC50 of 4 μM, 8 μM, 12 μM and 240 μM, respectively.",350.26,"210297-47-5",{"v":20,"d":"20.00"},{"v":57.1,"d":"57.10"},{"v":70,"d":"70.00"},199.85,"https://www.selleckchem.com/products/ha-100.html","C13H17Cl2N3O2S","Dihydrochloride","N/A","Cl.Cl.O=[S](=O)(N1CCNCC1)C2=CC=CC3=C2C=CN=C3",{"v":0.89,"d":"0.890"},3,1,2]
["S3088","(±)-Methyl Jasmonate","d7","L1700-70","in 10mM DMSO","Caspase","Apoptosis","(&plusmn;)-Methyl Jasmonate (MeJA, Methyl jasmonate, Methyl 2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate), a phytohormone that acts as a vital cell regulator in plants, is a new candidate for the treatment of Inflammatory bowel diseases (IBDs), modulating the expression of the major classes of caspase-type protease families.",{"v":224.3,"d":"224.30"},"39924-52-2","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","https://www.selleckchem.com/products/methyl-jasmonate.html","C13H20O3","Free Base","MeJA, Methyl jasmonate, Methyl 2-(3-oxo-2-(pent-2-en-1-yl)cyclopentyl)acetate","CC/C=C/CC1C(CCC1=O)CC(=O)OC",2.356,3,0,6]
["S3091","Methyl acetoacetate","g7","L1700-70","in 10mM DMSO","Others","Others","Methyl acetylacetate (MAA, Acetoacetate methyl ester, Methyl 3-oxobutanoate, Methyl 3-oxobutyrate, Methyl acetoacetate, Methyl acetylacetate), an endogenous metabolite, is used as a chemical reagent used in the synthesis of pharmaceuticals.",116.12,"105-45-3","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","https://www.selleckchem.com/products/methyl-acetoacetate.html","C5H8O3","Free Base","MAA, Acetoacetate methyl ester, Methyl 3-oxobutanoate, Methyl 3-oxobutyrate, Methyl acetoacetate, Methyl acetylacetate","COC(=O)CC(C)=O",-0.068,3,0,3]
["S3099","δ-Valerolactone","f8","L1700-70","in 10mM DMSO","Others","Others","δ-Valerolactone (Tetrahydro-2H-pyran-2-one, 5-Valerolactone, oxan-2-one) is an endogenous metabolite.",100.12,"542-28-9","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","https://www.selleckchem.com/products/5-valerolactone.html","C5H8O2","Free Base","Tetrahydro-2H-pyran-2-one, 5-Valerolactone, oxan-2-one","O=C1CCCCO1",0.732,2,0,0]
["S3157","3-Hydroxybenzaldehyde","h10","L1700-70","in 10mM DMSO","Others","Others","3-Hydroxybenzaldehyde (3-HBA), one of the benzaldehydes commonly found in nature, is produced by 3-hydroxybenzyl-alcohol dehydrogenase, and is a substrate of aldehyde dehydrogenase (ALDH) in rats and humans (ALDH2). 3-Hydroxybenzaldehyde exhibits vasculoprotective effects.",122.12,"100-83-4",{"v":24,"d":"24.00"},196.53,"<1","N/A","https://www.selleckchem.com/products/3-hydroxybenzaldehyde.html","C7H6O2","Free Base","3-HBA","OC1=CC=CC(=C1)C=O",1.347,1,1,1]
["S3169","2'-Deoxyuridine 5'-monophosphate disodium salt","b11","L1700-70","in 10mM DMSO","Thymidylate Synthase","Apoptosis","2'-Deoxyuridine 5'-monophosphate disodium salt (dUMP) is a substrate for thymidylate synthase and is converted to deoxythymidine monophosphate (dTMP). The inhibition of dUMP to dTMP at the methylation step is a key in controlling bacterial and eukaryotic cell growth.",352.15,"42155-08-8",{"v":20,"d":"20.00"},56.79,{"v":70,"d":"70.00"},198.78,"https://www.selleckchem.com/products/2-deoxyuridine-5-monophosphate-disodium-salt.html","C9H11N2Na2O8P","Disodium salt","dUMP","[Na+].[Na+].OC1CC(OC1CO[P]([O-])([O-])=O)N2C=CC(=O)NC2=O",-3.933,4,2,4]
["S3318","N-Acetyl-L-arginine dihydrate","f2","L1700-71","in 10mM DMSO","Others","Others","N-Acetyl-L-arginine (Ac-Arg-OH) dihydrate is an endogenous metabolite.",252.27,"210545-23-6",{"v":50,"d":"50.00"},{"v":198.2,"d":"198.20"},{"v":50,"d":"50.00"},{"v":198.2,"d":"198.20"},"https://www.selleckchem.com/products/n-acetyl-l-arginine-dihydrate.html","C8H20N4O5","Dihydrate","Ac-Arg-OH dihydrate","O.O.CC(=O)NC(CCCNC(N)=N)C(O)=O",-1.745,2,3,7]
["S3333","(2R,3R)-(-)-2,3-Butanediol","b4","L1700-71","in 10mM DMSO","Others","Others","(2R,3R)-(-)-2,3-Butanediol ((2R,3R)-Butane-2,3-diol) is an endogenous metabolite.",90.12,"24347-58-8","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","https://www.selleckchem.com/products/2r-3r-2-3-butanediol.html","C4H10O2","Free Base","(2R,3R)-Butane-2,3-diol","CC(O)C(C)O",-0.143,0,2,1]
["S3337","L-Histidinol dihydrochloride","e4","L1700-71","in 10mM DMSO","Others","Metabolism","L-Histidinol dihydrochloride, a structural analogue of the essential amino acid L-histidine, is a reversible inhibitor of protein biosynthesis which evokes disparate responses from non-tumorigenic and tumorigenic cells in culture.",214.09,"1596-64-1",{"v":43,"d":"43.00"},200.85,{"v":43,"d":"43.00"},200.85,"https://www.selleckchem.com/products/l-histidinol-dihydrochloride.html","C6H13Cl2N3O","Dihydrochloride","N/A","Cl.Cl.NC(CO)CC1=CN=C[NH]1",-0.598,1,3,3]
["S3365","(S)-(-)-1-Phenylethanol","f6","L1700-71","in 10mM DMSO","Others","Others","(S)-(-)-1-Phenylethanol ((S)-1-Phenylethanol, (S)-(-)-Phenylethanol) is an enantiomer of 1-Phenylethanol with flavor properties.",122.16,"1445-91-6","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","https://www.selleckchem.com/products/s-1-phenylethanol.html","C8H10O","Free Base","(S)-1-Phenylethanol, (S)-(-)-Phenylethanol","CC(O)C1=CC=CC=C1",1.603,0,1,1]
["S3371","N-Acetyl-D-mannosamine","a7","L1700-71","in 10mM DMSO","Others","Others","N-Acetyl-D-mannosamine (ManNAc, N-acetyl-beta-mannosamine), a precursor of a sialic acid, improves the age-dependent attenuation of synaptic transmission and long-term potentiation (LTP). N-Acetyl-D-mannosamine treatment is a potential therapeutic application for cognitive dysfunction.",221.21,"7772-94-3",{"v":44,"d":"44.00"},198.91,{"v":44,"d":"44.00"},198.91,"https://www.selleckchem.com/products/n-acetyl-d-mannosamine.html","C8H15NO6","Free Base","ManNAc, N-acetyl-beta-mannosamine","CC(=O)NC1C(O)OC(CO)C(O)C1O",-2.782,2,4,2]
["S6362","N-Acetyl-L-phenylalanine","b8","L1700-71","in 10mM DMSO","Others","Others","N-Acetyl-L-phenylalanine is a hazardous amphipathic metabolite of phenylalanine.",207.23,"2018-61-3",{"v":41,"d":"41.00"},197.85,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/n-acetyl-l-phenylalanine.html","C11H13NO3","Free Base","N/A","CC(=O)NC(CC1=CC=CC=C1)C(O)=O",0.895,2,1,4]
["S6908","DOTAP chloride","e9","L1700-71","in 10mM DMSO","Others","Others","DOTAP chloride (1,2-Dioleoyl-3-trimethylammonium-propane chloride) is an effective cationic lipid widely used as a liposomal transfection reagent. DOTAP is also a strong activator of the innate immune system in animal cells and a good candidate as an elicitor for the study of plant immunity.",698.54,"132172-61-3",{"v":100,"d":"100.00"},143.16,"<1","N/A","https://www.selleckchem.com/products/dotap-chloride.html","C42H80ClNO4","Chloride","1,2-Dioleoyl-3-trimethylammonium-propane chloride","[Cl-].CCCCCCCC\\C=C/CCCCCCCC(=O)OCC(C[N+](C)(C)C)OC(=O)CCCCCCC\\C=C/CCCCCCCC",{"v":10.13,"d":"10.130"},4,0,37]
["S6934","AMG-9810","d10","L1700-71","in 10mM DMSO","TLR,TRP Channel","Transmembrane Transporters","AMG-9810 is a potent, competitive and selective vanilloid receptor 1 (TRPV1) antagonist and inhibits capsaicin activation with IC50 of 24.5 nM and 85.6 nM for human TRPV1 and rat TRPV1, repectively. AMG-9810 blocks all known modes of TRPV1 activation, including protons-, heat-, and endogenous ligands, such as anandamide, N-arachidonyl dopamine, and oleoyldopamine. AMG-9810 significantly reduces the mRNA expression of TLR2 and TLR4. AMG-9810 also promotes mouse skin tumorigenesis mediated through EGFR/Akt/mTOR signaling.",337.41,"545395-94-6",{"v":67,"d":"67.00"},198.57,"<1","N/A","https://www.selleckchem.com/products/amg-9810.html","C21H23NO3","Free Base","N/A","CC(C)(C)C1=CC=C(/C=C/C(=O)NC2=CC=C3OCCOC3=C2)C=C1",4.268,3,1,4]
["S8914","2-NBDG","h11","L1700-71","in 10mM DMSO","Others","Others","2-NBDG, a fluorescent deoxyglucose derivative, is a a marker for detecting glucose uptake and an indicaotr of cell viability.",342.26,"186689-07-6",{"v":68,"d":"68.00"},198.68,{"v":2,"d":"2.00"},5.84,"https://www.selleckchem.com/products/2-nbdg.html","C12H14N4O8","Free Base","N/A","OCC(O)C(O)C(O)C(NC1=CC=C(C2=NON=C12)[N+]([O-])=O)C=O",{"v":-1.33,"d":"-1.330"},4,5,8]
["S9128","Isoacteoside","e3","L1700-72","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Isoacteoside, a phenylethanoid isolated from Monochasma savatieri Franch. ex Maxim., is an anti‐inflammatory herb widely used in traditional Chinese medicine.",624.59,"61303-13-7",{"v":100,"d":"100.00"},160.11,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/isoacteoside.html","C29H36O15","Free Base","N/A","CC1OC(OC2C(O)C(COC(=O)/C=C/C3=CC=C(O)C(=C3)O)OC(OCCC4=CC=C(O)C(=C4)O)C2O)C(O)C(O)C1O",0.484,6,9,11]
["S9198","Obtusifolin","d4","L1700-72","in 10mM DMSO","Aldose Reductase","Metabolism","Obtusifolin is anthraquinone found in the seeds of Cassia obtusifolia, has inhibitory effects on platelet aggregation and aldose reductase.",284.26,"477-85-0",{"v":25,"d":"25.00"},87.95,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/obtusifolin.html","C16H12O5","Free Base","N/A","COC1=C2C(=O)C3=C(C=CC=C3O)C(=O)C2=CC(=C1O)C",2.794,3,2,1]
["S9266","Ginsenoside Rc","h5","L1700-72","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Ginsenoside Rc, isolated from Panax ginseng, may exert various activities including anti-cancer, anti-inflammatory, antiobesity, and anti-diabetic effects.",1079.27,"11021-14-0",{"v":100,"d":"100.00"},92.66,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/ginsenoside-rc.html","C53H90O22","Free Base","N/A","CC(C)=CCCC(C)(OC1OC(COC2OC(CO)C(O)C2O)C(O)C(O)C1O)C3CCC4(C)C3C(O)CC5C6(C)CCC(OC7OC(CO)C(O)C(O)C7OC8OC(CO)C(O)C(O)C8O)C(C)(C)C6CCC45C",-0.688,8,14,16]
["S9300","Methylprotodioscin","g6","L1700-72","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Methyl protodioscin, a bioactive natural compound isolated from Dioscorea collettii Makino (Dioscoreaceae), has numerous pharmacological activities, including anti-inflammation, lipid-lowering, and\n\nanticancer activities.",1063.23,"54522-52-0",{"v":100,"d":"100.00"},94.05,{"v":100,"d":"100.00"},94.05,"https://www.selleckchem.com/products/methylprotodioscin.html","C52H86O22","Free Base","N/A","COC1(CCC(C)COC2OC(CO)C(O)C(O)C2O)OC3CC4C5CC=C6CC(CCC6(C)C5CCC4(C)C3C1C)OC7OC(CO)C(OC8OC(C)C(O)C(O)C8O)C(O)C7OC9OC(C)C(O)C(O)C9O",-0.936,10,12,15]
["S9316","Polyphyllin II","b7","L1700-72","in 10mM DMSO","Others","Others","Polyphyllin II, a natural compound extracted from Rhizoma of Paris polyphyllin, shows hemolytic activity.",855.02,"76296-72-5",{"v":100,"d":"100.00"},116.96,{"v":-1,"d":"-1.00"},"N/A","https://www.selleckchem.com/products/polyphyllin-ii.html","C44H70O16","Free Base","N/A","CC1CCC2(OC1)OC3CC4C5CC=C6CC(CCC6(C)C5CCC4(C)C3C2C)OC7OC(CO)C(OC8OC(CO)C(O)C8O)C(OC9OC(C)C(O)C(O)C9O)C7O",0.792,8,8,8]
["S9645","CBR-5884","g8","L1700-72","in 10mM DMSO","Dehydrogenase","Metabolism","CBR-5884 is a selective inhibitor of phosphoglycerate dehydrogenase (PHGDH) with IC50 of 33 μM. CBR-5884 inhibits de novo serine synthesis in cancer cells and was selectively toxic to cancer cell lines with high serine biosynthetic activity.",336.39,"681159-27-3",{"v":67,"d":"67.00"},199.17,"<1","N/A","https://www.selleckchem.com/products/cbr-5884.html","C14H12N2O4S2","Free Base","N/A","CCOC(=O)C1=C(C)C(=C(NC(=O)C2=CC=CO2)S1)SC#N",3.252,4,1,6]
["S9686","NBQX (FG9202)","f9","L1700-72","in 10mM DMSO","GluR","Neuronal Signaling","NBQX (FG9202, NNC 079202) is a highly selective and competitive antagonist of AMPA receptor (AMPAR) with anti-epileptic effect.",336.28,"118876-58-7",{"v":67,"d":"67.00"},199.24,"<1","N/A","https://www.selleckchem.com/products/nbqx.html","C12H8N4O6S","Free Base","NNC 079202","N[S](=O)(=O)C1=C2C(=CC=C1)C3=C(NC(=O)C(=O)N3)C=C2[N+]([O-])=O",-0.441,4,3,2]
["S9712","Fluzoparib (SHR-3162)","g10","L1700-72","in 10mM DMSO","PARP","DNA Damage/DNA Repair","Fluzoparib (SHR3162, HS10160) is a potent Poly (ADP-ribose) polymerase (PARP) inhibitor that shows anti-tumor activity, with an IC50 of 1.46±0.72 nM for PARP1.",{"v":472.4,"d":"472.40"},"1358715-18-0",{"v":94,"d":"94.00"},198.98,"<1","N/A","https://www.selleckchem.com/products/fluzoparib.html","C22H16F4N6O2","Free Base","HS10160","FC1=CC=C(CC2=NNC(=O)C3=C2C=CC=C3)C=C1C(=O)N4CC[N]5N=C(N=C5C4)C(F)(F)F",2.757,5,1,4]
["S0316","MPO-IN-28","g2","L1700-73","in 10mM DMSO","Peroxidases","Metabolism","MPO-IN-28 (Compound 28) is an inhibitor of myeloperoxidase (MPO) with IC50 of 44 nM.",231.25,"37836-90-1",{"v":46,"d":"46.00"},198.92,"<1","N/A","http://www.selleckchem.com/products/mpo-in-28.html","C11H13N5O","Free Base","N/A","COC1=CC2=NC(=NC(=C2C=C1)C)N=C(N)N",{"v":1.14,"d":"1.140"},4,2,2]
["S0626","DSP Crosslinker","f3","L1700-73","in 10mM DMSO","ADC Linker","Others","DSP Crosslinker is a cleavable ADC linker applied into the synthesis of antibody-drug conjugates (ADCs).",404.42,"57757-57-0",{"v":81,"d":"81.00"},200.29,"<1","N/A","http://www.selleckchem.com/products/dsp-crosslinker.html","C14H16N2O8S2","Free Base","N/A","O=C(CCSSCCC(=O)ON1C(=O)CCC1=O)ON2C(=O)CCC2=O",-0.659,8,0,11]
["S0839","ACP-105","b5","L1700-73","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","ACP-105 is an orally available and potent selective androgen receptor modulator (SARM) with pEC50 of 9.0 and 9.4 for AR wild type and AR mutation T877A, respectively.",290.79,"899821-23-9",{"v":58,"d":"58.00"},199.46,"<1","N/A","http://www.selleckchem.com/products/acp-105.html","C16H19ClN2O","Free Base","N/A","CC1=C(C=CC(=C1Cl)C#N)N2C3CCC2CC(C)(O)C3",3.177,0,0,1]
["S1711","Crotamiton","f5","L1700-73","in 10mM DMSO","Others","Angiogenesis","Crotamiton is a drug that is used as a scabicidal (for treating scabies) and an antipruritic",203.28,"483-63-6","The physical form of the compound is liquid, which can be dissolved in any proportion.","N/A","N/A","N/A","http://www.selleckchem.com/products/Crotamiton.html","C13H17NO","Free Base","N/A","CCN(C(=O)\\C=C\\C)C1=CC=CC=C1C",3.091,1,0,3]
["S2995","4-Hydroxyphenylpyruvic acid","e6","L1700-73","in 10mM DMSO","COX","Immunology & Inflammation","4-Hydroxyphenylpyruvic acid (4-HPPA), an abundant colon metabolite of polyphenols, is a potent scavenger that suppresses levels of free radicals and cyclooxygenase-2 (COX-2) and contributes to reduced risk of colon cancer development.",180.16,"156-39-8",{"v":36,"d":"36.00"},199.82,"<1","N/A","http://www.selleckchem.com/products/4-hydroxyphenylpyruvic-acid.html","C9H8O4","Free Base","4-HPPA","OC(=O)C(=O)CC1=CC=C(O)C=C1",1.128,2,1,3]
["S3498","Ecamsule.2Na","a8","L1700-73","in 10mM DMSO","Others","Others","Ecamsule.2Na is the Sodium salt form of Ecamsule. Ecamsule is an active ingredient of sunscreens that protects the skin from sunburn and erythema.",606.66,"90458-75-6",{"v":100,"d":"100.00"},164.84,{"v":100,"d":"100.00"},164.84,"http://www.selleckchem.com/products/ecamsule-2na.html","C28H32Na2O8S2","Free Base","N/A","[Na+].[Na+].CC1(C)C2CCC1(C[S]([O-])(=O)=O)C(=O)C2=CC3=CC=C(C=C3)C=C4C5CCC(C[S]([O-])(=O)=O)(C4=O)C5(C)C",-0.638,2,0,6]
["S3587","Mebrofenin","c9","L1700-73","in 10mM DMSO","Others","Others","Mebrofenin (SQ 26962) is a type of iminodiacetic acid (IDA) that is available as a ready to use the kit for radio-labeling with Technetium-99m (Tc-99m). Tc-99m Mebrofenin is used clinical for hepatobiliary scintigraphy.",387.23,"78266-06-5",{"v":77,"d":"77.00"},198.85,"<1","N/A","http://www.selleckchem.com/products/mebrofenin.html","C15H19BrN2O5","Free Base","SQ 26962","CC1=C(Br)C(=C(NC(=O)CN(CC(O)=O)CC(O)=O)C(=C1)C)C",-0.909,3,1,7]
["S3599","Resazurin sodium","e10","L1700-73","in 10mM DMSO","Dyes","Others","Resazurin sodium (Resazurin sodium salt, Diazoresorcinol sodium) is commonly used to measure bacterial and eukaryotic cell viability through its reduction to the fluorescent product resorufin.",251.17,"62758-13-8",{"v":50,"d":"50.00"},199.07,{"v":50,"d":"50.00"},199.07,"http://www.selleckchem.com/products/resazurin-sodium.html","C12H6NNaO4","Sodium","Resazurin sodium salt, Diazoresorcinol sodium","[Na+].[O-]C1=CC2=C(C=C1)[N+](=C3C=CC(=O)C=C3O2)[O-]",0.085,2,0,0]
["S4426","Sacubitril hemicalcium salt","d11","L1700-73","in 10mM DMSO","Neprilysin","Proteases","Sacubitril (AHU-377) hemicalcium salt, a component of the heart failure medicine LCZ696, is a potent inhibitor of neprilysin (neutral endopeptidase, NEP).",861.04,"1369773-39-6",{"v":100,"d":"100.00"},116.14,"<1","N/A","http://www.selleckchem.com/products/sacubitril-hemicalcium-salt.html","C48H56CaN2O10","Hemicalcium salt","AHU-377 hemicalcium salt","[Ca++].CCOC(=O)C(C)CC(CC1=CC=C(C=C1)C2=CC=CC=C2)NC(=O)CCC([O-])=O.CCOC(=O)C(C)CC(CC3=CC=C(C=C3)C4=CC=CC=C4)NC(=O)CCC([O-])=O",4.569,6,2,24]
["S4440","2-Phenylacetamide","h2","L1700-74","in 10mM DMSO","Estrogen/progestogen Receptor,GPR","Endocrinology & Hormones","2-Phenylacetamide, the main compound isolated from the seeds of Lepidium apetalum Willd (LA) with estrogenic activities, increases the expression of Estrogen receptorα (ERα), ERβ and GPR30 in the uterus and MCF-7 cells.",135.16,"103-81-1",{"v":27,"d":"27.00"},199.76,{"v":27,"d":"27.00"},199.76,"http://www.selleckchem.com/products/2-phenylacetamide.html","C8H9NO","Free Base","N/A","NC(=O)CC1=CC=CC=C1",0.866,1,1,2]
["S4447","Pipobroman","d3","L1700-74","in 10mM DMSO","DNA alkylator","DNA Damage/DNA Repair","Pipobroman (PB, Vercyte), a neutral amide of piperazine, acts as an alkylating agent with antiproliferative activity.",356.05,"54-91-1",{"v":71,"d":"71.00"},199.41,"<1","N/A","http://www.selleckchem.com/products/pipobroman.html","C10H16Br2N2O2","Free Base","PB, Vercyte","BrCCC(=O)N1CCN(CC1)C(=O)CCBr",0.647,2,0,4]
["S4611","TCEP Hydrochloride","d5","L1700-74","in 10mM DMSO","NF-κB","NF-κB","TCEP (Tris(2-carboxyethyl)phosphine) hydrochloride, a non-thiol reducing agent, promotes NF-κB-DNA binding in a dose-related manner.",286.65,"51805-45-9",{"v":57,"d":"57.00"},198.85,{"v":57,"d":"57.00"},198.85,"http://www.selleckchem.com/products/tcep-hydrochloride.html","C9H16ClO6P","Hydrochloride","Tris(2-​carboxyethyl)​phosphine Hydrochloride","Cl.OC(=O)CCP(CCC(O)=O)CCC(O)=O",0.548,3,0,9]
["S4713","Atropine","g5","L1700-74","in 10mM DMSO","AChR","Neuronal Signaling","Atropine (Atropen, Atnaa, Tropine tropate, DL-Hyoscyamine) is a competitive muscarinic acetylcholine receptor (mAChR) antagonist with anti-myopia effect.",289.37,"51-55-8",{"v":58,"d":"58.00"},200.44,"<1","N/A","http://www.selleckchem.com/products/atropine.html","C17H23NO3","Free Base","N/A","CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3",1.721,2,1,5]
["S5008","Ciprofloxacin hydrochloride","c7","L1700-74","in 10mM DMSO","Antibiotics,Antineoplastic and Immunosuppressive Antibiotics,Bacterial,Topoisomerase","Microbiology","Ciprofloxacin (CPX, Cetraxal, Ciloxan, Cipro, Bay-09867) hydrochloride, a fluorinated quinolone, is a β-diketone antibiotic with a broad spectrum antibacterial activity. Ciprofloxacin is an inhibitor of bacterial DNA gyrase (a subclass of Type II topoisomerases).",{"v":367.8,"d":"367.80"},"93107-08-5",{"v":7,"d":"7.00"},19.03,{"v":74,"d":"74.00"},{"v":201.2,"d":"201.20"},"http://www.selleckchem.com/products/ciprofloxacin-hydrochloride.html","C17H19ClFN3O3","Hydrochloride","CPX, Cetraxal, Ciloxan, Cipro, Bay-09867 hydrochloride","Cl.OC(=O)C1=CN(C2CC2)C3=CC(=C(F)C=C3C1=O)N4CCNCC4",-0.888,2,1,3]
["S5188","Ribociclib succinate","c8","L1700-74","in 10mM DMSO","CDK","Cell Cycle","Ribociclib (LEE011) succinate (Kisqali) is a highly specific dual inhibitor of CDK4 and CDK6 with IC50 of 10 nM and 39 nM, respectively.",552.63,"1374639-75-4",{"v":100,"d":"100.00"},180.95,"<1","N/A","http://www.selleckchem.com/products/ribociclib-succinate.html","C27H36N8O5","Succinate","LEE011 succinate, Kisqali","CN(C)C(=O)C1=CC2=CN=C(NC3=NC=C(C=C3)N4CCNCC4)N=C2[N]1C5CCCC5.OC(=O)CCC(O)=O",-0.164,6,2,8]
["S5300","Trometamol hydrochloride","g9","L1700-74","in 10mM DMSO","Others","Others","Trometamol (THAM, Tromethamine, TRIS-HCL) hydrochloride, a proton acceptor, is a biologically inert amino alcohol of low toxicity, which buffers carbon dioxide and acids in vitro and in vivo. Trometamol rapidly restores pH and acid-base regulation in acidaemia.",{"v":157.6,"d":"157.60"},"1185-53-1",{"v":32,"d":"32.00"},203.05,{"v":32,"d":"32.00"},203.05,"http://www.selleckchem.com/products/trometamol-hydrochloride.html","C4H12ClNO3","Hydrochloride","THAM, Tromethamine hydrochloride, TRIS-HCL","Cl.NC(CO)(CO)CO",-1.999,0,4,3]
["S5738","Megestrol","f10","L1700-74","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones","Megestrol, a synthetic progestin, is approved for the treatment of anorexia, cachexia, or an unexplained significant weight loss in patients with an acquired immunodeficiency syndrome diagnosis. Megestrol acetate (Megace) is one of the first progestational agents to be evaluated for use in the hormonal therapy of advanced breast cancer.",342.47,"3562-63-8",{"v":68,"d":"68.00"},198.56,"<1","N/A","http://www.selleckchem.com/products/megestrol.html","C22H30O3","Free Base","Megace","CC(=O)C1(O)CCC2C3C=C(C)C4=CC(=O)CCC4(C)C3CCC12C",3.126,2,0,1]
["S5922","L-Carnitine hydrochloride","h11","L1700-74","in 10mM DMSO","Leukotriene","Metabolism","L-Carnitine ((R)-Carnitine, Levocarnitine) hydrochloride improves oxygen saturation, and inhibits leukotriene synthesis. L-Carnitine hydrochloride functions to transport long chain fatty acyl-CoAs into the mitochondria for degradation by β-oxidation.",197.66,"6645-46-1",{"v":40,"d":"40.00"},202.37,{"v":40,"d":"40.00"},202.37,"http://www.selleckchem.com/products/l-carnitine-hydrochloride.html","C7H16ClNO3","Hydrochloride","(R)-Carnitine hydrochloride, Levocarnitine hydrochloride","[Cl-].C[N+](C)(C)CC(O)CC(O)=O",{"v":-4.49,"d":"-4.490"},1,1,4]
["S5966","Amlodipine maleate","g3","L1700-75","in 10mM DMSO","Calcium Channel","Transmembrane Transporters","Amlodipine (Amvaz, UK-48340) maleate is a long-acting calcium channel blocker, used to lower blood pressure and prevent chest pain.",524.95,"88150-47-4",{"v":100,"d":"100.00"},190.49,"<1","N/A","http://www.selleckchem.com/products/amlodipine-maleate.html","C24H29ClN2O9","Maleate","Amvaz, UK-48340 maleate","CCOC(=O)C1=C(COCCN)NC(=C(C1C2=CC=CC=C2Cl)C(=O)OC)C.OC(=O)\\C=C/C(O)=O",-0.864,7,2,12]
["S5979","2',3'-Dideoxyadenosine","f4","L1700-75","in 10mM DMSO","HBV,HIV","Microbiology","2',3'-Dideoxyadenosine (ddA, ddAdo) is an anti-human immunodeficiency virus agent against human immunodeficiency virus (HIV) and human hepatitis B virus (HBV) replication.",235.24,"4097-22-7",{"v":47,"d":"47.00"},{"v":199.8,"d":"199.80"},{"v":47,"d":"47.00"},{"v":199.8,"d":"199.80"},"http://www.selleckchem.com/products/2-3-dideoxyadenosine.html","C10H13N5O2","Free Base","ddA, ddAdo","NC1=C2N=C[N](C3CCC(CO)O3)C2=NC=N1",-0.476,4,2,2]
["S6437","Oxolamine Citrate","a5","L1700-75","in 10mM DMSO","P450 (e.g. CYP17)","Metabolism","Oxolamine (SKF-9976, AF-438) citrate, a cough suppressant, is an inhibitor of CYP2B1/2. Oxolamine citrate also exhibits anti-inflammatory effect.",437.44,"1949-20-8",{"v":87,"d":"87.00"},198.88,{"v":43,"d":"43.00"},{"v":98.3,"d":"98.30"},"http://www.selleckchem.com/products/oxolamine-citrate.html","C20H27N3O8","Citrate","SKF-9976 citrate, AF-438 citrate","CCN(CC)CCC1=NC(=NO1)C2=CC=CC=C2.OC(=O)CC(O)(CC(O)=O)C(O)=O",-1.921,6,0,11]
["S8948","SRX3207","c7","L1700-75","in 10mM DMSO","Epigenetic Reader Domain,PI3K,Syk","Angiogenesis","SRX3207 is an orally active dual inhibitor of Syk-PI3K with IC50 of 39.9 nM, 31200 nM, 3070 nM, 3070 nM, 244 nM, 388 nM, 9790 nM for Syk, Zap70, BRD41, BRD42, PI3K alpha, PI3K delta, PI3K gamma, respectively. SRX3207 blocks tumor immunosuppression and increases anti-tumor immunity.",555.65,"2254693-15-5",{"v":33,"d":"33.00"},59.39,"<1","N/A","http://www.selleckchem.com/products/srx3207.html","C29H29N7O3S","Free Base","N/A","CC1=N[N](C=C1CN2CCC2)C3=CC=NC(=N3)NC4=CC=C(C=C4)C5=CSC6=C5OC(=CC6=O)N7CCOCC7",{"v":4.59,"d":"4.590"},6,1,7]
["S8988","Rhosin hydrochloride","e7","L1700-75","in 10mM DMSO","Apoptosis related,Rho","Cell Cycle","Rhosin (G04) hydrochloride (HCl) is a potent, specific inhibitor of RhoA subfamily Rho GTPases with Kd of ~ 0.4 uM. Rhosin hydrochloride induces cell apoptosis.",394.86,"1281870-42-5",{"v":93,"d":"93.00"},235.53,{"v":93,"d":"93.00"},235.53,"http://www.selleckchem.com/products/rhosin-hydrochloride.html","C20H19ClN6O","Hydrochloride","G04 hydrochloride, Rhosin HCl","Cl.NC(CC1=C[NH]C2=CC=CC=C12)C(=O)N\\N=C\\C3=CC4=NC=CN=C4C=C3",2.237,4,3,5]
["S9721","Farudodstat","a9","L1700-75","in 10mM DMSO","AP-1,Apoptosis related,Dehydrogenase","Metabolism","Farudodstat(LAS 186323,ASLAN003) is a potent and orally active inhibitor of DHODH (Dihydroorotate dehydrogenase) with IC50 of 35 nM for human DHODH enzyme activity. ASLAN003 impairs protein synthesis and induces the differentiation and apoptosis transcriptional program in acute myeloid leukemia (AML) cells via activation of AP-1 transcription factors.",356.32,"1035688-66-4",{"v":71,"d":"71.00"},199.26,"<1","N/A","http://www.selleckchem.com/products/aslan003.html","C19H14F2N2O3","Free Base","LAS 186323,ASLAN003","COC1=CC=CC(=C1)C2=CC(=C(NC3=NC=CC=C3C(O)=O)C(=C2)F)F",4.311,3,1,5]
["S9786","BDTX-189","h9","L1700-75","in 10mM DMSO","EGFR,HER2,RIP kinase","Protein Tyrosine Kinase","BDTX-189 is a potent and selective inhibitor of allosteric EGFR and HER2 oncogenic mutations with Kd of 0.2 nM, 0.76 nM, 13 nM and 1.2 nM for EGFR, HER2, BLK and RIPK2, reapectively. BDTX-189 exhibits anticancer activity.",561.03,"2414572-47-5",{"v":100,"d":"100.00"},178.24,"<1","N/A","http://www.selleckchem.com/products/bdtx-189.html","C29H29ClN6O4","Free Base","N/A","ClC1=C(OCC2=NC=CC=C2)C=CC(=C1)NC3=NC=NC4=C3C=C(NC(=O)C=C)C(=C4)OCCN5CCOCC5",4.401,7,2,11]
["P1083","ZIP","h10","L1700-75","in 10mM DMSO","PKM","Metabolism","ZIP is a novel, cell-permeable protein kinase Mζ(PKMζ) inhibitor that blocks PKMζ-mediated synaptic potentiation.",1928.38,"863987-12-6",{"v":88,"d":"88.00"},45.63,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/peptide/ZIP.html","C90H154N30O17","Free Base","myristoyl-Ser-Ile-Tyr-Arg-Arg-Gly-Ala-Arg-Arg-Trp-Arg-Lys-Leu-OH","CCCCCCCCCCCCCC(=O)NC(CO)C(=O)NC(C(C)CC)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(C)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCNC(N)=N)C(=O)NC(CC2=C[NH]C3=C2C=CC=C3)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCCN)C(=O)NC(CC(C)C)C(O)=O",-2.031,14,27,76]
["S0778","LC3-mHTT-IN-AN1","a3","L1700-76","in 10mM DMSO","LC3","Autophagy","LC3-mHTT-IN-AN1 is a mHTT-LC3 linker compound that interacts with both mutant huntingtin protein (mHTT) and LC3B. LC3-mHTT-IN-AN1 reduces the levels of mHTT in an allele-selective manner in cultured Huntington disease (HD) mouse neurons.",411.04,"486443-73-6",{"v":82,"d":"82.00"},199.49,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/lc3-mhtt-in-an1.html","C15H9Br2NO3","Free Base","N/A","OC1=C(O)C(=CC(=C1)/C=C/2C(=O)NC3=C2C=C(Br)C=C3)Br",3.743,1,3,1]
["S0982","m-3M3FBS","h3","L1700-76","in 10mM DMSO","Phospholipase (e.g. PLA)","Metabolism","m-3M3FBS is a potent activator of phospholipase C (PLC) that stimulates a transient intracellular calcium concentration increase in neutrophils. m-3M3FBS induces apoptosis in monocytic leukemia cells.",343.36,"200933-14-8",{"v":69,"d":"69.00"},200.96,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/m-3m3fbs.html","C16H16F3NO2S","Free Base","N/A","CC1=CC(=C(C(=C1)C)[S](=O)(=O)NC2=CC=CC(=C2)C(F)(F)F)C",4.718,2,1,4]
["S1976","LCH-7749944","e4","L1700-76","in 10mM DMSO","PAK","Cytoskeletal Signaling","LCH-7749944 (GNF-PF-2356) is a novel and potent p21-activated kinase 4 (PAK4) inhibitor with an IC50 of 14.93 μM and has less potently inhibitory effect against PAK1, PAK5 and PAK6. LCH-7749944 causes successful inhibition of EGFR activity due to its inhibitory effect on PAK4.",350.41,"796888-12-5",{"v":70,"d":"70.00"},199.77,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/lch-7749944.html","C20H22N4O2","Free Base","GNF-PF-2356","COC1=CC=CC(=C1)NC2=NC3=CC=CC=C3C(=N2)NCC4CCCO4",4.149,4,2,6]
["S4485","Olodaterol (BI 1744)","d6","L1700-76","in 10mM DMSO","Adrenergic Receptor","Endocrinology & Hormones","Olodaterol (BI 1744) is a long-acting β2-adrenergic receptor agonist that is used as a component of an inhalation (Tiotropium/Olodaterol) for treating patients with chronic obstructive pulmonary disease (COPD).",386.44,"868049-49-4",{"v":77,"d":"77.00"},199.25,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/olodaterol-bi-1744-.html","C21H26N2O5","Free Base","N/A","COC1=CC=C(CC(C)(C)NCC(O)C2=C3OCC(=O)NC3=CC(=C2)O)C=C1",1.875,3,4,7]
["S5980","Losartan Carboxylic Acid (EXP-3174)","g6","L1700-76","in 10mM DMSO","Angiotensin Receptor","GPCR & G Protein","Losartan Carboxylic Acid (E-3174, EXP-3174), an active carboxylic acid metabolite of Losartan, is a non-peptide angiotensin II (AT1) receptor antagonist. Losartan Carboxylic Acid inhibits the specific binding of [125I]-angiotensin II to VSMC with IC50 of 1.1 nM.",436.89,"124750-92-1",{"v":87,"d":"87.00"},199.13,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/losartan-carboxylic-acid-exp-3174-.html","C22H21ClN6O2","Free Base","E-3174","CCCCC1=NC(=C([N]1CC2=CC=C(C=C2)C3=CC=CC=C3C4=N[NH]N=N4)C(O)=O)Cl",5.129,5,1,8]
["S6383","1-NM-PP1","c8","L1700-76","in 10mM DMSO","Bcr-Abl,CaMK,CDK,Src","Angiogenesis","1-NM-PP1 (PP1 Analog II, 1NM-PP1, analogue 9) is a potent inhibitor of Src family kinases with IC50 of 4.3 nM and 3.2 nM for v-Src-as1 and c-Fyn-as1, respectively. 1-NM-PP1 also inhibits CDK2-as1, CAMKII-as1 and c-Abl-as2 with IC50 of 5.0 nM, 8.0 nM and 120 nM, respectively.",331.41,"221244-14-0",{"v":66,"d":"66.00"},199.15,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/1-nm-pp1.html","C20H21N5","Free Base","PP1 Analog II, 1NM-PP1","CC(C)(C)[N]1N=C(CC2=CC=CC3=CC=CC=C23)C4=C(N)N=CN=C14",3.713,3,1,3]
["S6884","LY3405105","d9","L1700-76","in 10mM DMSO","CDK","Cell Cycle","LY3405105 is an orally active CDK7 inhibitor with an IC50 of 92.8 nM. LY3405105 shows potential antineoplastic activity.",497.63,"2326428-25-3",{"v":99,"d":"99.00"},198.94,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/ly3405105.html","C26H39N7O3","Free Base","N/A","CC(C)C1=C2N=C(C)C=C(NC3CCN(CC3)C(=O)OC4CCN(C4)C(=O)\\C=C\\CN(C)C)[N]2N=C1",1.936,5,1,8]
["S6981","Glycerol phenylbutyrate","g10","L1700-76","in 10mM DMSO","Sigma Receptor","GPCR & G Protein","Glycerol phenylbutyrate (GT4P, HPN-100M, Ravicti) is a nitrogen-binding agent and acts as a sigma-2 (σ2) receptor ligand with a pKi of 8.02. Glycerol phenylbutyrate is a prodrug in which phenylbutyrate (PBA) is released from the glycerol backbone by lipases in the gastrointestinal tract.",530.65,"611168-24-2","The physical form of the compound is liquid, which can be dissolved in any proportion.",{"v":0,"d":"0.00"},{"v":0,"d":"0.00"},{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/glycerol-phenylbutyrate.html","C33H38O6","Free Base","GT4P, HPN-100M, Ravicti","O=C(CCCC1=CC=CC=C1)OCC(COC(=O)CCCC2=CC=CC=C2)OC(=O)CCCC3=CC=CC=C3",7.563,6,0,20]
["S9477","AH7614","c2","L1700-77","in 10mM DMSO","GPR","GPCR & G Protein","AH7614 (compound 39) is a selective FFA4 (GPR120) antagonist with pIC50s of 7.1 for human FFA4 and 8.1 for mouse FFA4.",351.42,"6326-06-3",{"v":70,"d":"70.00"},199.19,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/ah7614.html","C20H17NO3S","Free Base","N/A","CC1=CC=C(C=C1)[S](=O)(=O)NC2C3=CC=CC=C3OC4=CC=CC=C24",4.153,3,1,3]
["S9737","Nor-NOHA acetate","b3","L1700-77","in 10mM DMSO","Arginase","Immunology & Inflammation","Nor-NOHA acetate (Nω-Hydroxy-nor-L-Arginine acetate, N-OMega-hydroxy-L-norarginine acetate, N-Hydroxy-nor-L-arginine acetate) is a reversible, competitive inhibitor of arginase. Nor-NOHA inhibits arginase activity in aorta with an IC50 of less than 1 μM, that is, similar to its effects on liver arginase (IC50 = 0.5 μM).",296.28,"1140844-63-8",{"v":50,"d":"50.00"},168.76,{"v":50,"d":"50.00"},168.76,"http://www.selleckchem.com/products/nor-noha-dihydrochloride.html","C9H20N4O7","acetate","Nω-Hydroxy-nor-L-Arginine acetate salt, N-OMega-hydroxy-L-norarginine acetate, N-Hydroxy-nor-L-arginine acetate","CC(O)=O.CC(O)=O.NC(CCN/C(N)=N/O)C(O)=O",-4.807,4,3,5]
["S9779","Emavusertib (CA-4948)","e3","L1700-77","in 10mM DMSO","FLT3,IRAK","Immunology & Inflammation","Emavusertib (CA-4948) is a potent and orally bioavailable inhibitor of interleukin-1 receptor-associated kinase 4/FMS-like Tyrosine Kinase 3 (IRAK4/FLT3) with anti-tumor activity.",{"v":491.5,"d":"491.50"},"1801344-14-8",{"v":49,"d":"49.00"},99.69,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/ca-4948.html","C24H25N7O5","Free Base","N/A","CC1=NC=CC(=C1)C2=NC(=CO2)C(=O)NC3=C(N=C4N=C(OC4=C3)N5CCOCC5)N6CCC(O)C6",1.031,8,2,5]
["S9874","4-Aminobenzohydrazide","f5","L1700-77","in 10mM DMSO","Peroxidases","Metabolism","4-Aminobenzohydrazide (4-Aminobenzhydrazide, 4-aminobenzoic acid hydrazide, 4-ABAH, Myeloperoxidase Inhibitor I, NSC 640) is an inhibitor of MPO (Myeloperoxidase) enzyme that enhances iNOS induction in MPO-positive cells, but not in MPO-KO cells.",151.17,"5351-17-7",{"v":30,"d":"30.00"},198.45,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/4-aminobenzohydrazide.html","C7H9N3O","Free Base","4-Aminobenzhydrazide, 4-aminobenzoic acid hydrazide, 4-ABAH, Myeloperoxidase Inhibitor I, NSC 640","NNC(=O)C1=CC=C(N)C=C1",-0.407,1,3,1]
["S9885","MYLS22","a6","L1700-77","in 10mM DMSO","Others","Others","MYLS22  is a first-in-class and selective inhibitor of optic atrophy 1 (OPA1) with anti-angiogenesis and anti-cancer activity.",443.52,"306959-01-3",{"v":81,"d":"81.00"},182.63,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/myls22.html","C24H21N5O2S","Free Base","N/A","CN1N(C(=O)C(=C1C)NC(=O)C2=CC3=C(S2)[N](N=C3C)C4=CC=CC=C4)C5=CC=CC=C5",3.247,3,1,4]
["E0001","DCPIB","b7","L1700-77","in 10mM DMSO","Potassium Channel,VRAC","Transmembrane Transporters","DCPIB is a specific and potent inhibitor of volume-regulated anion channels (VRAC). DCPIB potently inhibits several K2P channels with no voltage dependence, including TRESK, TASK1, and TASK3. DCPIB displayed superior selectivity toward TRESK with an IC50 of 0.14 μM, demonstrating at least 100-fold higher affinity over TREK1/TRAAK channels. DCPIB is also a novel selective blocker of I(Cl,swell), which blocks native I(Cl,swell) of calf bovine pulmonary artery endothelial (CPAE) cells with an IC(50) of 4.1 μM.",427.36,"82749-70-0",{"v":85,"d":"85.00"},{"v":198.9,"d":"198.90"},"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/dcpib.html","C22H28Cl2O4","Free Base","N/A","CCCCC1(CC2=CC(=C(Cl)C(=C2C1=O)Cl)OCCCC(O)=O)C3CCCC3",6.755,3,0,9]
["E0022","Ophiopogonin D","e8","L1700-77","in 10mM DMSO","AMPK,Immunology & Inflammation related,NF-κB","PI3K/Akt/mTOR","Ophiopogonin D (OJV-VI, Deacetylophiopogonin C) is a steroidal glycoside isolated from Chinese herb Radix ophiopogonis and shows anti-tumor property. Ophiopogonin D could suppress TGF-β1-mediated metastatic behavior of MDA-MB-231 cells by regulating ITGB1/FAK/Src/AKT/β-catenin/MMP-9 signaling axis. Ophiopogonin D attenuates PM2.5-induced inflammation via suppressing the AMPK/NF-κB pathway in mouse pulmonary epithelial cells.",855.02,"945619-74-9",{"v":100,"d":"100.00"},116.96,"<1",{"v":0,"d":"0.00"},"http://www.selleckchem.com/products/ophiopogonin-d.html","C44H70O16","Free Base","OJV-VI, Deacetylophiopogonin C","CC1CCC2(OC1)OC3CC4C5CC=C6CC(O)CC(OC7OC(C)C(O)C(OC8OCC(O)C(O)C8O)C7OC9OC(C)C(O)C(O)C9O)C6(C)C5CCC4(C)C3C2C",0.454,8,8,6]
["S0186","TA-01","a10","L1700-77","in 10mM DMSO","Casein Kinase,p38 MAPK","Stem Cells & Wnt","TA-01 is a potent inhibitor of CK1δ/ε and p38 MAPK with IC50 of 6.4 nM, 6.8 nM and 6.7 nM for CK1ε, CK1δ and p38 MAPK, respectively.",351.32,"1784751-18-3",{"v":20,"d":"20.00"},56.93,"<1","N/A","http://www.selleckchem.com/products/ta-01.html","C20H12F3N3","Free Base","N/A","FC1=CC=C(C=C1)C2=C([NH]C(=N2)C3=C(F)C=CC=C3F)C4=CC=NC=C4",{"v":4.86,"d":"4.860"},2,1,3]
["S0727","KUN50259 (DAAO inhibitor-1)","e11","L1700-77","in 10mM DMSO","Others","Metabolism","KUN50259 (DAAO inhibitor-1, Compound 35) is a potent inhibitor of D-amino acid oxidase (DAAO) with an IC50 of 0.12 μM.",152.13,"2065250-25-9",{"v":30,"d":"30.00"},{"v":197.2,"d":"197.20"},"<1","N/A","http://www.selleckchem.com/products/daao-inhibitor-1.html","C7H5FN2O","Free Base","Compound 35","FC1=CC2=C(C=C1)C(=O)NN2",{"v":1.01,"d":"1.010"},1,2,0]
["S0897","Cyclizine","a2","L1700-78","in 10mM DMSO","Histamine Receptor","Neuronal Signaling","Cyclizine is a piperazine first-generation antagonist of histamine 1 receptor.",266.38,"82-92-8",{"v":53,"d":"53.00"},198.96,"<1","N/A","http://www.selleckchem.com/products/cyclizine.html","C18H22N2","Free Base","N/A","CN1CCN(CC1)C(C2=CC=CC=C2)C3=CC=CC=C3",{"v":3.47,"d":"3.470"},0,0,3]
["S3383","RS102895","h2","L1700-78","in 10mM DMSO","CCR","Immunology & Inflammation","RS 102895 is a small molecule antagonist of CCR2 with an IC50 of 360 nM.",{"v":390.4,"d":"390.40"},"300815-41-2",{"v":85,"d":"85.00"},217.73,"<1","N/A","http://www.selleckchem.com/products/rs102895.html","C21H21F3N2O2","Free Base","N/A","FC(F)(F)C1=CC=C(CCN2CCC3(CC2)OC(=O)NC4=CC=CC=C34)C=C1",{"v":4.16,"d":"4.160"},2,1,4]
["S6709","Obatoclax (GX15-070)","h4","L1700-78","in 10mM DMSO","Bcl-2","Apoptosis","Obatoclax (GX15-070) is an antagonist of Bcl-2 with an Ki of 0.22 μM in a cell-free assay, can assist in overcoming MCL-1 mediated resistance to apoptosis.",317.38,"803712-67-6",{"v":63,"d":"63.00"},{"v":198.5,"d":"198.50"},"<1","N/A","http://www.selleckchem.com/products/obatoclax-gx15-070.html","C20H19N3O","Free Base","N/A","COC1=CC(=NC1=CC2=C(C)C=C(C)[NH]2)C3=CC4=C([NH]3)C=CC=C4",{"v":4.17,"d":"4.170"},2,2,3]
["S6946","Gap19","f5","L1700-78","in 10mM DMSO","Gap-Junction","Cytoskeletal Signaling","Gap19 is a nonapeptide derived from the cytoplasmic loop (CL) of Cx43 and acts as a selective connexin 43 (Cx43) hemichannel blocker. Gap19 blocks Cx43 hemichannels without inhibiting gap junctions (GJs) at IC50 of 6.5 μM when applied intracellulary.",1161.44,"1507930-57-5",{"v":100,"d":"100.00"},{"v":86.1,"d":"86.10"},{"v":100,"d":"100.00"},{"v":86.1,"d":"86.10"},"http://www.selleckchem.com/products/gap19.html","C55H96N14O13","Free Base","N/A","CCC(C)C(NC(=O)C(CCC(O)=O)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(N)CCCCN)C(C)CC)C(=O)NC(CCCCN)C(=O)NC(CCCCN)C(=O)NC(CC1=CC=CC=C1)C(=O)NC(CCCCN)C(O)=O",{"v":-6.67,"d":"-6.670"},11,14,45]
["S9782","Sulfopin","h6","L1700-78","in 10mM DMSO","Others","Metabolism","Sulfopin (PIN1-3) is a highly selective covalent inhibitor of Pin1 with a Ki of 17 nM in the FP assay. Sulfopin blocks Myc-driven tumor initiation and growth in vivo.",{"v":281.8,"d":"281.80"},"2451481-08-4",{"v":56,"d":"56.00"},198.72,{"v":3,"d":"3.00"},10.65,"http://www.selleckchem.com/products/sulfopin.html","C11H20ClNO3S","Free Base","PIN1-3","CC(C)(C)CN(C1CC[S](=O)(=O)C1)C(=O)CCl",{"v":1.09,"d":"1.090"},3,0,4]
["S9903","NRD167","g7","L1700-78","in 10mM DMSO","Sirtuin","DNA Damage/DNA Repair","NRD167 is a potent and selective SIRT5 inhibitor.",666.83,"2166487-23-4",{"v":100,"d":"100.00"},149.96,"<1","N/A","http://www.selleckchem.com/products/nrd167.html","C34H46N6O6S","Free Base","N/A","CCOC(=O)CCNC(=S)NCCCCC(NC(=O)OCC1=CC=CC=C1)C(=O)NC(CC2=C[NH]C3=C2C=CC=C3)C(=O)NC(C)C",{"v":4.79,"d":"4.790"},6,6,22]
["E0031","RN-1747","c9","L1700-78","in 10mM DMSO","TRP Channel","Transmembrane Transporters","RN-1747 is a selective TRPV4 agonist with EC50s of 0.77 μM, 4.0 μM and 4.1 μM for hTRPV4, mTRPV4 and rTRPV4, respectively. RN-1747 also antagonizes TRPM8 with IC50 of 4 μM.",395.86,"1024448-59-6",{"v":79,"d":"79.00"},199.57,"<1","N/A","http://www.selleckchem.com/products/rn-1747.html","C17H18ClN3O4S","Free Base","N/A","[O-][N+](=O)C1=C(C=CC(=C1)Cl)[S](=O)(=O)N2CCN(CC2)CC3=CC=CC=C3",{"v":3.05,"d":"3.050"},2,0,5]
["E0069","DFHBI","e10","L1700-78","in 10mM DMSO","Dyes","Others","DFHBI is a mimic of green fluorescent protein (GFP) fluorophore and binds to RNA aptamers. DFHBI can be used for imaging RNA in living cells.",252.22,"1241390-29-3",{"v":50,"d":"50.00"},198.24,"<1","N/A","http://www.selleckchem.com/products/dfhbi.html","C₁₂H₁₀F₂N₂O₂","Free Base","N/A","CN1C(=N\\C(=C/C2=CC(=C(O)C(=C2)F)F)C1=O)C",{"v":1.38,"d":"1.380"},2,1,1]
["E0120","2-Bromohexadecanoic acid","g11","L1700-78","in 10mM DMSO","Transferase","Metabolism","2-Bromohexadecanoic acid (2-BP, 2-bromopalmitate) is a nonmetabolisable analogue of palmitate and acts as a palmitoylation inhibitor, which inhibits multiple palmitoyl-acyl transferase (PAT) activity towards MyrGCK(NBD) and FarnCNRas(NBD) with identical IC50s of approx. 4 µM. 2-Bromohexadecanoic acid can directly and irreversibly inhibit the palmitoyltransferase activity of all DHHC (Asp-His-His-Cys) proteins.",335.32,"18263-25-7",{"v":67,"d":"67.00"},199.81,"<1","N/A","http://www.selleckchem.com/products/2-bromohexadecanoic-acid.html","C16H31BrO2","Free Base","2-BP, 2-bromopalmitate","CCCCCCCCCCCCCCC(Br)C(O)=O",{"v":6.95,"d":"6.950"},1,0,14]
["E0127","C-170","b2","L1700-79","in 10mM DMSO","STING","Immunology & Inflammation","C-170 is a covalent small-molecule inhibitor of STING. C-170 efficiently inhibits both hsSTING and mmSTING through the same covalent modification with C-171.",{"v":288.3,"d":"288.30"},"346691-38-1",{"v":58,"d":"58.00"},201.18,"<1","N/A","http://www.selleckchem.com/products/c-170.html","C15H16N2O4","Free Base","N/A","CCCCC1=CC=C(NC(=O)C2=CC=C(O2)[N+]([O-])=O)C=C1",{"v":3.88,"d":"3.880"},2,1,6]
["E0153","Lithium Chloride","b4","L1700-79","in 10mM DMSO","Antiviral","Microbiology","Lithium Chloride (LiCl) inhibits the replication of type 1 and type 2 Herpes simplex virus at concentrations which permitted host cell replication. Lithium chloride also prevents glucocorticoid-induced osteonecrosis of femoral heads and strengthens mesenchymal stem cell activity in rats.",42.39,"7447-41-8",{"v":8,"d":"8.00"},188.72,{"v":8,"d":"8.00"},188.72,"http://www.selleckchem.com/products/lithium-chloride.html","ClLi","Free Base","LiCl","[Li+].[Cl-]",{"v":-2.67,"d":"-2.670"},0,0,0]
["E0158","N-Nitroso-N-methylurea","f4","L1700-79","in 10mM DMSO","Others","Others","N-Nitroso-N-methylurea (NMU, MNU, NMH, 1-Methyl-1-nitrosourea, N-Methyl-Nnitrosourea, Methylnitrosourea) is a highly reliable carcinogen, mutagen, and teratogen.",103.08,"684-93-5",{"v":21,"d":"21.00"},203.73,{"v":10,"d":"10.00"},97.01,"http://www.selleckchem.com/products/n-nitroso-n-methylurea.html","C2H5N3O2","Free Base","NMU, MNU, NMH, 1-Methyl-1-nitrosourea, N-Methyl-Nnitrosourea, Methylnitrosourea","CN(N=O)C(N)=O",{"v":-0.34,"d":"-0.340"},2,1,1]
["E0197","2-Acetamidofluorene","b6","L1700-79","in 10mM DMSO","Others","Others","2-Acetamidofluorene (2-AAF, 2-Acetaminofluorene, N-2-Fluorenylacetamide, N-Acetyl-2-aminofluorene) is a carcinogenic and mutagenic compound.",223.27,"53-96-3",{"v":45,"d":"45.00"},201.55,"<1","N/A","http://www.selleckchem.com/products/2-acetamidofluorene.html","C15H13NO","Free Base","2-AAF, 2-Acetaminofluorene, N-2-Fluorenylacetamide, N-Acetyl-2-aminofluorene","CC(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C2",{"v":2.61,"d":"2.610"},1,1,1]
["E0362","BiP Inducer X (BIX)","a7","L1700-79","in 10mM DMSO","HSP (HSP90)","Cytoskeletal Signaling","BiP Inducer X (BIX) is a selective GRP78 (BiP, HSPA5) inducer. BIX induces BiP only, in a dose-dependent manner, without induction of other molecules involved in the ER stress response.",209.22,"101714-41-4",{"v":42,"d":"42.00"},200.75,"<1","N/A","http://www.selleckchem.com/products/bip-inducer-x-bix.html","C9H7NO3S","Free Base","N/A","OC1=C(O)C=C(C=C1)C(=O)CSC#N",{"v":1.5,"d":"1.500"},1,2,3]
["E1099","Ceapin-A7","c8","L1700-79","in 10mM DMSO","ATF-6","ER stress & UPR","Ceapin-A7 is a selective and highly potent inhibitor of the ATF6α, which can activate the response to ER stress, with IC50 of 0.59 μM.",470.32,"2323027-38-7",{"v":100,"d":"100.00"},212.62,"<1","N/A","http://www.selleckchem.com/products/ceapin-a7.html","C20H12F6N4O3","Free Base","N/A","FC(F)(F)C1=CC=C(C[N]2C=C(NC(=O)C3=NOC(=C3)C4=CC=CO4)C=N2)C(=C1)C(F)(F)F",{"v":4.82,"d":"4.820"},5,1,7]
["S0057","N-Succinimidyl-S-acetylthioacetate (SATA)","e9","L1700-79","in 10mM DMSO","Others","Others","N-Succinimidyl-S-acetylthioacetate (SATA) is a protein modification agent which introduces thiol-groups into protein molecules. N-Succinimidyl-S-acetylthioacetate (SATA) adds sulfhydryl groups to proteins and other amine-containing molecules in a protected form.",231.23,"76931-93-6",{"v":46,"d":"46.00"},198.94,"<1","N/A","http://www.selleckchem.com/products/n-succinimidyl-s-acetylthioacetate-sata.html","C8H9NO5S","free base","N/A","CC(=O)SCC(=O)ON1C(=O)CCC1=O",-0.692,5,0,5]
["S0282","YL 0919","a11","L1700-79","in 10mM DMSO","5-HT Receptor,5-HT Receptor","Neuronal Signaling","YL0919, a novel structure compound, exerts dual effect on the serotonergic system, as both 5-hydroxytryptamine receptor 1A (5-HT1A) agonist and 5-HT uptake blocker, showing remarkable antidepressant effects in animal models.",334.84,"1339058-04-6",{"v":67,"d":"67.00"},{"v":200.1,"d":"200.10"},"<1","N/A","http://www.selleckchem.com/products/yl-0919.html","C18H22N2O2.ClH","hydrochloride","N/A","Cl.OC1(CCN(CC1)CC2=CC=CC=C2)CN3C=CC=CC3=O",1.275,1,0,4]
["S0311","SKA-31","d11","L1700-79","in 10mM DMSO","Potassium Channel","Transmembrane Transporters","SKA-31(Naphtho[1,2-d]thiazol-2-ylamine) is a potent potassium channel activator with EC50s of 260 nM, 1.9 μM, 2.9 μM, and 2.9 μM for KCa3.1, KCa2.2, KCa2.1 and KCa2.3, respectively.",200.26,"40172-65-4",{"v":40,"d":"40.00"},199.74,"<1","N/A","http://www.selleckchem.com/products/ska-31.html","C11H8N2S","free base","Naphtho[1,2-d]thiazol-2-ylamine","NC1=NC2=C3C=CC=CC3=CC=C2S1",2.617,1,1,0]
["S0521","PNU-282987 S enantiomer free base","b3","L1700-80","in 10mM DMSO","AChR","Neuronal Signaling","PNU-282987 S enantiomer free base is the S-enantiomer of PNU-282987 free base, which is an α7 nicotinic acetylcholine receptor (α7 nAChR) agonist.",264.75,"737727-12-7",{"v":53,"d":"53.00"},200.19,"<1","N/A","http://www.selleckchem.com/products/pnu-282987-s-enantiomer-free-base.html","C14H17ClN2O","free base","N/A","ClC1=CC=C(C=C1)C(=O)NC2CN3CCC2CC3",2.238,1,1,2]
["S0712","Endoxifen E-isomer","h3","L1700-80","in 10mM DMSO","Others","Endocrinology & Hormones","Endoxifen E-isomer (E-Endoxifen), an E-isomer of Endoxifen and impurity in Endoxifen Z-isomer drug substance, exhibits antiestrogenic effects.",373.49,"114828-90-9",{"v":75,"d":"75.00"},200.81,"<1","N/A","http://www.selleckchem.com/products/endoxifen-e-isomer.html","C25H27NO2","free base","E-Endoxifen","CC\\C(C1=CC=CC=C1)=C(C2=CC=C(O)C=C2)/C3=CC=C(OCCNC)C=C3",5.541,1,2,8]
["S0871","Gusacitinib (ASN-002)","h5","L1700-80","in 10mM DMSO","JAK,Syk","Angiogenesis","Gusacitinib (ASN-002) is a novel and potent dual inhibitor of spleen tyrosine kinase (SYK) and Janus kinases (JAK) with IC50 values of 5-46 nM in biochemical assays.",460.53,"1425381-60-7",{"v":92,"d":"92.00"},199.77,"<1","N/A","http://www.selleckchem.com/products/gusacitinib.html","C24H28N8O2","free base","N/A","OC1CCN(CC1)C2=CC=C(NC3=NC(=NC4=C3C(=O)NN=C4)N5CCC(CC5)CC#N)C=C2",2.467,4,3,5]
["S0889","Dixanthogen","c6","L1700-80","in 10mM DMSO","Anti-infection","Microbiology","Dixanthogen is an ectoparasiticide.",242.41,"502-55-6",{"v":48,"d":"48.00"},198.01,"<1","N/A","http://www.selleckchem.com/products/dixanthogen.html","C6H10O2S4","free base","N/A","CCOC(=S)SSC(=S)OCC",4.736,2,0,7]
["S1246","NH2-PEG3-C2-NH-Boc","c7","L1700-80","in 10mM DMSO","PROTAC Linker","Others","NH2-PEG3-C2-Boc (PROTAC Linker 15) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.",292.37,"101187-40-0","The physical form of the compound is liquid, which can be dissolved in any proportion","The physical form of the compound is liquid, which can be dissolved in any proportion","N/A","N/A","http://www.selleckchem.com/products/nh2-peg3-c2-nh-boc.html","C13H28N2O5","free base","PROTAC Linker 15","CC(C)(C)OC(=O)NCCOCCOCCOCCN",-0.274,5,2,13]
["S2917","Cutamesine Dihydrochloride","g8","L1700-80","in 10mM DMSO","Sigma Receptor","GPCR & G Protein","Cutamesine dihydrochloride (SA4503 dihydrochloride,AGY94806 dihydrochloride) is a potent Sigma-1 receptor agonist with an IC50 of 17.4 nM in guinea pig brain membranes.",441.43,"165377-44-6",{"v":22,"d":"22.00"},49.84,{"v":88,"d":"88.00"},199.35,"http://www.selleckchem.com/products/sa-4503.html","C23H32N2O2.2HCl","Dihydrochloride","SA4503 dihydrochloride, AGY94806 dihydrochloride","Cl.Cl.COC1=C(OC)C=C(CCN2CCN(CCCC3=CC=CC=C3)CC2)C=C1",5.274,2,0,9]
["S3532","AN-2718","c10","L1700-80","in 10mM DMSO","Fungal","Microbiology","AN-2718, an inhibitor of fungal growth that blocks protein synthesis via the oxaborole tRNA trapping (OBORT) mechanism.",168.39,"174672-06-1",{"v":34,"d":"34.00"},201.91,"<1","N/A","http://www.selleckchem.com/products/an-2718.html","C7H6BClO2","free base","N/A","OB1OCC2=CC(=CC=C12)Cl",2.764,1,0,0]
["S3547","Bractoppin","h10","L1700-80","in 10mM DMSO","Others","DNA Damage/DNA Repair","Bractoppin, a drug-like inhibitor of phosphopeptide recognition by the human BRCA1 tandem (t)BRCT domain, which selectively inhibits substrate binding with nanomolar activity (IC50 = 0.074 μM) in vitro.",414.48,"2290527-07-8",{"v":83,"d":"83.00"},200.25,"<1","N/A","http://www.selleckchem.com/products/bractoppin.html","C25H23FN4O","free base","N/A","FC1=CC=CC=C1CN2CCN(CC2)C(=O)C3=CC=C4N=C([NH]C4=C3)C5=CC=CC=C5",{"v":4.43,"d":"4.430"},2,1,4]
["S6641","GW284543 (UNC10225170)","g2","L1700-81","in 10mM DMSO","MEK","MAPK","GW284543 (UNC10225170), a MEK5-selective inhibitor, inhibits MEK5 in a dose-dependently way as determined by reductions in pERK5, and decreases endogenous MYC protein.",372.42,"790186-68-4",{"v":9,"d":"9.00"},24.17,"<1","N/A","http://www.selleckchem.com/products/gw284543.html","C23H20N2O3","free base","N/A","COC1=CC2=C(C=C1OC)C(=CC=N2)NC3=CC(=CC=C3)OC4=CC=CC=C4",5.093,4,1,6]
["S6973","TJ191","b3","L1700-81","in 10mM DMSO","Others","Apoptosis","TJ191 is a selective anti-cancer small molecule that targets low TβRIII-expressing malignant T-cell leukemia/lymphoma cells.",255.38,"1522415-97-9",{"v":51,"d":"51.00"},{"v":199.7,"d":"199.70"},"<1","N/A","http://www.selleckchem.com/products/tj191.html","C13H21NO2S","free base","N/A","CCCCCCCC1=CC(=C(N)S1)C(=O)OC",3.818,2,1,8]
["S9849","5-(N-Ethyl-N-isopropyl)-Amiloride (EIPA)","b5","L1700-81","in 10mM DMSO","Sodium Channel","Transmembrane Transporters","5-(N-Ethyl-N-isopropyl)-Amiloride (EIPA) acts as an inhibitor of macropinocytosis and sodium-hydrogen exchangers(NHE)  (IC50=0.033μg/mL). EIPA blocks the activity of Na(+)/H(+) exchanger, which are plasma membrane proteins implicated in all forms of macropinocytosis.",299.76,"1154-25-2",{"v":60,"d":"60.00"},200.16,{"v":2,"d":"2.00"},6.67,"http://www.selleckchem.com/products/5-n-ethyl-n-isopropyl-amiloride-eipa.html","C11H18ClN7O","free base","N/A","CCN(C(C)C)C1=C(Cl)N=C(C(=N1)N)C(=O)NC(N)=N",1.236,3,3,5]
["S9929","VB124","g5","L1700-81","in 10mM DMSO","MCT","Transmembrane Transporters","VB124, a potent and selective MCT4 inhibitor, specifically inhibits lactate efflux/import in MDA-MB-231 cells expressing MCT4, and is used for the research of cardiac hypertrophy, heart failure, and metabolism.",426.89,"2230186-18-0",{"v":85,"d":"85.00"},199.11,"<1","N/A","http://www.selleckchem.com/products/vb124.html","C23H23ClN2O4","free base","N/A","CC(C)(OCC1=N[N](C2=C(Cl)C=CC=C2)C(=C1)C3=CC(=CC=C3)OC4CC4)C(O)=O",{"v":5.3,"d":"5.300"},4,0,8]
["E0070","4F 4PP oxalate","b7","L1700-81","in 10mM DMSO","5-HT Receptor","Neuronal Signaling","4F 4PP oxalate is an antagonist of the serotonin (5-HT) receptor subtype 5-HT2A (Ki = 5.3 nM), which is selective for 5-HT2A receptors over 5-HT1C receptors (Ki = 620 nM).",429.48,"144734-36-1",{"v":11,"d":"11.00"},25.61,"<1","N/A","http://www.selleckchem.com/products/4f-4pp-oxalate.html","C22H26FNO.C2H2O4","oxalate","N/A","OC(=O)C(O)=O.FC1=CC=C(C=C1)C(=O)C2CCN(CCCCC3=CC=CC=C3)CC2",2.489,3,0,8]
["E0101","AZD-6280","a8","L1700-81","in 10mM DMSO","GABA Receptor","Transmembrane Transporters","AZD-6280 is a selective GABAA (α2/3) receptor modulator, used for treatment of generalized anxiety disorder.",366.41,"942436-93-3",{"v":73,"d":"73.00"},199.23,"<1","N/A","http://www.selleckchem.com/products/azd-6280.html","C20H22N4O3","free base","N/A","CCCNC(=O)C1=C(N)C2=C(N=N1)C(=CC=C2)C3=C(OC)C=CC(=C3)OC",2.797,5,2,6]
["E0211","Dihydroberberine","e9","L1700-81","in 10mM DMSO","Immunology & Inflammation related,NF-κB","NF-κB","Dihydroberberine, a hydrogenated derivative of Berberine (BBR), exerts anti-inflammatory effect via dual modulation of NF-κB and MAPK signaling pathways.",337.37,"483-15-8",{"v":34,"d":"34.00"},100.78,{"v":-1,"d":"-1.00"},-2.96,"http://www.selleckchem.com/products/dihydroberberine.html","C20H19NO4","free base","N/A","COC1=CC=C2C=C3N(CCC4=C3C=C5OCOC5=C4)CC2=C1OC",{"v":3.15,"d":"3.150"},4,0,2]
["E0246","β-Anhydroicaritin","h9","L1700-81","in 10mM DMSO","Others","Endocrinology & Hormones","β-Anhydroicaritin is isolated from Boswellia carterii Birdware, has antiosteoporosis, estrogen regulation and antitumor properties.",368.38,"38226-86-7",{"v":9,"d":"9.00"},24.43,{"v":-1,"d":"-1.00"},-2.71,"http://www.selleckchem.com/products/beta-anhydroicaritin.html","C21H20O6","free base","N/A","COC1=CC=C(C=C1)C2=C(O)C(=O)C3=C(O)C=C4OC(C)(C)CCC4=C3O2",3.437,4,2,2]
["E0380","Hepln-13","a2","L1700-82","in 10mM DMSO","Serine/threonin kinase","Metabolism","Hepln-13 is a potent and orally active Hepsin inhibitor with an IC50 of 0.33 µM, can be used for the research of metastatic prostate cancer.",{"v":325.2,"d":"325.20"},"64369-13-7",{"v":65,"d":"65.00"},199.88,"<1","N/A","http://www.selleckchem.com/products/hepln-13.html","C17H13BrN2","free base","N/A","BrC1=CC=C(C=C1)C2NC3=CC=CC4=CC=CC(=C34)N2",4.706,0,2,1]
["E0389","DUBs-IN-2","d2","L1700-82","in 10mM DMSO","DUB","Ubiquitin","DUBs-IN-2 is a potent inhibitor of USP7 and USP8 deubiquitinating enzymes.",275.26,"924296-19-5",{"v":13,"d":"13.00"},47.23,"<1","N/A","http://www.selleckchem.com/products/dubs-in-2.html","C15H9N5O","free base","N/A","CCON=C1C2=CC=CC=C2C3=NC(=C(N=C13)C#N)C#N",3.282,4,0,2]
["E0462","Pyrintegrin","c4","L1700-82","in 10mM DMSO","Integrin","Cytoskeletal Signaling","Pyrintegrin is an β1-integrin agonist and a 2,4-disubstituted pyrimidine that promotes embryonic stem cells survival, also enhances cell-extracellular matrix (ECM) adhesion-mediated integrin signaling.",451.54,"1228445-38-2",{"v":45,"d":"45.00"},99.66,"<1","N/A","http://www.selleckchem.com/products/pyrintegrin.html","C23H25N5O3S","free base","N/A","OC1=CC=C2N(CCCC2=C1)C3=NC(=NC=C3)NC4=CC=C(C=C4)[S;v6](=O)(=O)NCC5CC5",4.437,4,3,7]
["E0473","CUDA","h4","L1700-82","in 10mM DMSO","Epoxide Hydrolase,PPAR","Metabolism","CUDA is a potent inhibitor of soluble epoxide hydrolase (sEH), with IC50s of 11.1 nM and 112 nM for mouse sEH and human sEH, respectively, also selectively increases peroxisome proliferator-activated receptor (PPAR) alpha activity.",{"v":340.5,"d":"340.50"},"479413-68-8",{"v":34,"d":"34.00"},99.85,"<1","N/A","http://www.selleckchem.com/products/cuda.html","C19H36N2O3","free base","N/A","OC(=O)CCCCCCCCCCCNC(=O)NC1CCCCC1",4.928,2,2,13]
["E0502","Metrizoic acid","d6","L1700-82","in 10mM DMSO","Others","Others","Metrizoic acid(Metrizoate) is a diagnostic radiopaque. The mechanism of action of metrizoic acid is as a X-Ray contrast activity.",627.94,"1949-45-7",{"v":100,"d":"100.00"},159.25,"<1","N/A","http://www.selleckchem.com/products/metrizoic-acid.html","C12H11I3N2O4","free base","Metrizoate","CN(C(C)=O)C1=C(I)C(=C(I)C(=C1I)NC(C)=O)C(O)=O",1.641,3,1,3]
["E0530","Prednicarbate","c7","L1700-82","in 10mM DMSO","Others","Endocrinology & Hormones","Prednicarbate (Dermatop) is a medium potency topical corticosteroid used to manage pruritus and inflammation associated with responsive skin conditions.",488.57,"73771-04-7",{"v":98,"d":"98.00"},200.59,"<1","N/A","http://www.selleckchem.com/products/prednicarbate.html","C27H36O8","free base","Dermatop","CCOC(=O)OC1(CCC2C3CCC4=CC(=O)C=CC4(C)C3C(O)CC12C)C(=O)COC(=O)CC",3.677,7,1,9]
["E0614","AWL-II-38.3","d8","L1700-82","in 10mM DMSO","Ephrin receptor","Protein Tyrosine Kinase","AWL-II-38.3 is a potent Ephrin type-A receptor 3 (EphA3) kinase inhibitor.",469.42,"1135205-94-5",{"v":94,"d":"94.00"},200.25,"<1","N/A","http://www.selleckchem.com/products/awl-ii-38-3.html","C23H18F3N5O3","free base","N/A","CC1=C[N](C=N1)C2=CC(=CC(=C2)C(F)(F)F)C(=O)NC3=CC(=C(C)C=C3)NC(=O)C4=CC=NO4",3.525,5,2,6]
["E0671","Deacetylasperulosidic acid","g9","L1700-82","in 10mM DMSO","Antioxidant,SOD","Immunology & Inflammation","Deacetylasperulosidic acid, a major phytochemical constituent of Morinda citrifolia fruit, has antioxidant activity by increasing superoxide dismutase (SOD) activity, as well as anticlastogenic activity by suppressing the induction of chromosome aberrations in Chinese hamster ovary cells and mice.",390.34,"14259-55-3",{"v":78,"d":"78.00"},199.83,{"v":19,"d":"19.00"},48.68,"http://www.selleckchem.com/products/deacetylasperulosidic-acid.html","C16H22O11","free base","N/A","OCC1OC(OC2OC=C(C3C(O)C=C(CO)C23)C(O)=O)C(O)C(O)C1O",-3.326,4,6,5]
["E0777","Z944","c11","L1700-82","in 10mM DMSO","Calcium Channel","Neuronal Signaling","Z944 is a highly selective antagonist for T-type calcium channel with IC50s of 50, 160, 110 nM for hCaV3.1, hCaV3.2, and hCaV3.3.",383.89,"1199236-64-0",{"v":19,"d":"19.00"},49.49,"<1","N/A","http://www.selleckchem.com/products/z944.html","C19H27ClFN3O2","free base","N/A","CC(C)(C)NC(=O)CN1CCC(CC1)CNC(=O)C2=CC(=CC(=C2)Cl)F",2.587,2,2,6]
["E0783","SM-7368","a2","L1700-83","in 10mM DMSO","MMP,NF-κB","NF-κB","SM-7368 is a potent NF-κB inhibitor that targets downstream of MAPK p38 activation, also inhibits TNF-α-induced MMP-9 upregulation.",328.69,"380623-76-7",{"v":66,"d":"66.00"},{"v":200.8,"d":"200.80"},"<1","N/A","http://www.selleckchem.com/products/sm-7368.html","C10H5ClN4O5S","free base","N/A","[O-][N+](=O)C1=CN=C(NC(=O)C2=CC=C(C(=C2)Cl)[N+]([O-])=O)S1",2.189,2,1,4]
["E0798","WAY-119064","g3","L1700-83","in 10mM DMSO","GSK-3","PI3K/Akt/mTOR","WAY-119064 is a potent glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 value of 80.5 nM.",{"v":264.3,"d":"264.30"},"1198098-03-1",{"v":13,"d":"13.00"},49.19,"<1","N/A","http://www.selleckchem.com/products/way-119064.html","C12H12N2O3S","free base","N/A","COC1=CC=C(C=C1OC)\\C=C2/SC(=NC2=O)N",1.964,4,1,3]
["E0809","Timapiprant Sodium","b4","L1700-83","in 10mM DMSO","Prostaglandin Receptor","GPCR & G Protein","Timapiprant sodium (OC000459 sodium), a potent, selective, and orally active D prostanoid receptor 2 (DP2, also known as CRTH2) antagonist, potently displaces [3H]PGD2 from human recombinant DP2, rat recombinant DP2, and human native DP2 with Ki values of 13, 3 and 4 nM, respectively.",371.36,"950688-14-9",{"v":74,"d":"74.00"},199.27,"<1","N/A","http://www.selleckchem.com/products/timapiprant-sodium.html","C21H17FN2O2.Na","Sodium salt","OC000459 sodium","[NaH].CC1=C(CC2=NC3=C(C=CC=C3)C=C2)C4=CC(=CC=C4[N]1CC(O)=O)F",4.329,2,0,4]
["E0834","7,8-Dimethoxy-4H-chromen-4-one","f5","L1700-83","in 10mM DMSO","Others","Others","7,8-Dimethoxy-4H-chromen-4-one is a bioactive compound.",206.19,"59887-97-7",{"v":41,"d":"41.00"},198.85,{"v":3,"d":"3.00"},14.55,"http://www.selleckchem.com/products/7-8-dimethoxy-4h-chromen-4-one.html","C11H10O4","free base","N/A","COC1=CC=C2C(=O)C=COC2=C1OC",1.355,4,0,2]
["E0947","Iu1-248","h6","L1700-83","in 10mM DMSO","DUB","Ubiquitin","Iu1-248, a derivative of IU1, is a potent and selective ubiquitin specific peptidase 14 (USP14) inhibitor with an IC50 of 0.83 μM.",337.42,"2307472-03-1",{"v":67,"d":"67.00"},198.57,"<1","N/A","http://www.selleckchem.com/products/iu1-248.html","C20H23N3O2","free base","N/A","CC1=CC(=C(C)[N]1C2=CC=C(C=C2)C#N)C(=O)CN3CCC(O)CC3",2.054,1,1,4]
["E1047","NAV-2729","b8","L1700-83","in 10mM DMSO","Ras","Cell Cycle","NAV-2729, an inhibitor of Arf6 activation which directly binds to Arf6, also inhibits all Arf guanine nucleotide exchange factors (ArfGEFs) with a strongest effect against BRAG2 and Arf1 .",456.88,"419547-11-8",{"v":91,"d":"91.00"},199.18,"<1","N/A","http://www.selleckchem.com/products/nav-2729.html","C25H17ClN4O3","free base","N/A","ClC1=CC=C(C=C1)C2=C3NC(=CC(=O)[N]3N=C2CC4=CC=CC=C4)C5=CC=C(C=C5)[N;v5](=O)=O",5.839,2,1,5]
["E1065","SBP-3264","a9","L1700-83","in 10mM DMSO","Serine/threonin kinase","Metabolism","SBP-3264 is a valuable chemical probe for understanding the roles of STK3 and STK4 in acute myeloid leukemia (AML).",369.85,"N/A",{"v":74,"d":"74.00"},200.08,"<1","N/A","http://www.selleckchem.com/products/sbp-3264.html","N/A","free base","N/A","CC(=O)NC1CCN(CC1)C2=C3C(=NC=N2)[NH]C=C3C4=CC(=CC=C4)Cl",2.592,3,2,3]
["E1136","SKLB-197","e10","L1700-83","in 10mM DMSO","ATM/ATR","DNA Damage/DNA Repair","SKLB-197 exerts selectively inhibition against ataxia telangiectasia mutated and Rad3-related (ATR) kinase with IC50 of 0.013 μM, also displays potent antitumor activity against ATM-deficent tumors both in vitro and in vivo.",{"v":424.5,"d":"424.50"},"2713577-16-1",{"v":85,"d":"85.00"},200.24,"<1","N/A","http://www.selleckchem.com/products/sklb-197.html","C25H24N6O","free base","N/A","CC1COCCN1C2=NC(=NC3=C2C=C(C=C3)C4=CC=N[N]4C)C5=C6C=C[NH]C6=CC=C5",4.527,4,1,3]
["E1146","CHD1Li 6.11","a11","L1700-83","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","CHD1Li 6.11, a potent oncogenic chromodomain helicase DNA binding protein 1 like (CHD1L) inhibitor and an orally bioavailable antitumor agent, shows the enzymatic inhibition of the catalytic CHD1L (cat-CHD1L) recombinant protein with IC50 of 3.3 µM, and significantly reduces the tumor volume of colorectal cancer (CRC) xenografts generated from isolated quasi mesenchymal cells (M-Phenotype).",{"v":472.4,"d":"472.40"},"2716890-91-2",{"v":94,"d":"94.00"},198.98,"<1","N/A","http://www.selleckchem.com/products/chd1li-6-11.html","C21H22BrN5OS","free base","N/A","CC1=CC(=NC(=N1)N2CCCC2)NC3=CC=C(NC(=O)CC4=CC(=CS4)Br)C=C3",5.088,3,2,6]
["E1235","NF-56-EJ40","a3","L1700-84","in 10mM DMSO","GPR","GPCR & G Protein","NF-56-EJ40 is a potent, high-affinity, and highly selective human SUCNR1 (GPR91) antagonist with an IC50 of 25 nM and a Ki of 33 nM, has high affinity for humanized rat SUCNR1 with a Ki value of 17.4 nM.",443.54,"2380230-73-7",{"v":5,"d":"5.00"},11.27,{"v":22,"d":"22.00"},{"v":49.6,"d":"49.60"},"http://www.selleckchem.com/products/nf-56-ej40.html","C27H29N3O3","free base","N/A","CN1CCN(CC1)CC2=CC=C(C=C2)C3=CC(=CC=C3)C(=O)NC4=C(CC(O)=O)C=CC=C4",0.793,2,1,7]
["E1281","Dimethyl itaconate","d3","L1700-84","in 10mM DMSO","NLRP3,Nrf2","Immunology & Inflammation","Dimethyl itaconate can reprogram neurotoxic to neuroprotective primary astrocytes through the regulation of LPS-induced Nod-like receptor protein 3 (NLRP3) inflammasome and nuclear factor 2/heme oxygenase-1 (NRF2/HO-1) pathways.",158.15,"617-52-7",{"v":32,"d":"32.00"},202.34,{"v":32,"d":"32.00"},202.34,"http://www.selleckchem.com/products/dimethyl-itaconate.html","C7H10O4","free base","N/A","COC(=O)CC(=C)C(=O)OC",0.569,4,0,5]
["E2250","IBT6A","f4","L1700-84","in 10mM DMSO","Others","Others","IBT6A is an impurity of Ibrutinib, which is a selective, irreversible Bruton tyrosine kinase (Btk) inhibitor with an IC50 of 0.5 nM.",386.45,"1022150-12-4",{"v":77,"d":"77.00"},199.25,"<1","N/A","http://www.selleckchem.com/products/ibt6a.html","C22H22N6O","free base","N/A","NC1=C2C(=NC=N1)[N](N=C2C3=CC=C(OC4=CC=CC=C4)C=C3)C5CCCNC5",3.492,4,2,4]
["E2374","PI-273","h5","L1700-84","in 10mM DMSO","Apoptosis related,PI4K","PI3K/Akt/mTOR","PI-273, the first reversibly and specific phosphatidylinositol 4-kinase (PI4KIIα) inhibitor with an IC50 of 0.47 μM, can inhibit breast cancer cell proliferation, block the cell cycle and induce cell apoptosis.",{"v":381.9,"d":"381.90"},"925069-34-7",{"v":6,"d":"6.00"},15.71,"<1","N/A","http://www.selleckchem.com/products/pi-273.html","C16H16ClN3O2S2","free base","N/A","CCC1=C(C)SC(=C1C(N)=O)NC(=S)NC(=O)C2=CC=C(Cl)C=C2",4.307,2,3,6]
["E2400","1A-116","d7","L1700-84","in 10mM DMSO","Rho","Cell Cycle","1A-116 is a Rac1 inhibitor, with antitumoral and antimetastatic effects in several types of cancer, such as breast cancer, prevents Rac1-regulated processes involved in the primary tumorigenesis and metastastic processes.",307.31,"1430208-73-3",{"v":61,"d":"61.00"},{"v":198.5,"d":"198.50"},"<1","N/A","http://www.selleckchem.com/products/1a-116.html","C16H16F3N3","free base","N/A","CC1=CC(=CC(=C1)NC(=N)NC2=C(C=CC=C2)C(F)(F)F)C",4.492,0,2,5]
["E2511","ZINC05007751","c8","L1700-84","in 10mM DMSO","Others","Cell Cycle","ZINC05007751 is a potent NIMA-related kinase NEK6 inhibitor with an IC50 of 3.4 μM, shows antiproliferative activity against a panel of human cancer cell lines and displays a synergistic effect with Cisplatin and Paclitaxel in a BRCA2 mutated ovarian cancer cell line.",{"v":304.3,"d":"304.30"},"591239-68-8",{"v":61,"d":"61.00"},200.46,"<1","N/A","http://www.selleckchem.com/products/zinc05007751.html","C18H12N2O3","free base","N/A","CC\\1=C(C#N)C(=O)NC(=O)C1=C\\C2=CC=C(O2)C3=CC=CC=C3",3.042,3,1,2]
["E2548","N-(p-Coumaroyl) Serotonin","e9","L1700-84","in 10mM DMSO","PDGFR","Protein Tyrosine Kinase","N-(p-Coumaroyl) Serotonin (p-coumaroylserotonin) is a polyphenol isolated from the seeds of safflower and has antioxidative, anti-atherogenic and anti-inflammatory properties, can inhibits PDGF-induced on phosphorylation of PDGF receptor and Ca2+ release from sarcoplasmic reticulum.",322.36,"68573-24-0",{"v":64,"d":"64.00"},198.54,"<1","N/A","http://www.selleckchem.com/products/n--p-coumaroyl--serotonin.html","C19H18N2O3","free base","p-coumaroylserotonin","NA","NA","NA","NA","NA"]
["E2636","EDC hydrochloride","c10","L1700-84","in 10mM DMSO","Others","Others","EDC hydrochloride (1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, EDC·HCl) is a carbodiimide reagent that can form nucleic acid and compounds with amide bonds.",{"v":191.7,"d":"191.70"},"25952-53-8",{"v":38,"d":"38.00"},198.23,{"v":38,"d":"38.00"},198.23,"http://www.selleckchem.com/products/edc-hydrochloride.html","C8H17N3.ClH","hydrochloride","1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, EDC·HCl","Cl.CCN=C=NCCCN(C)C",1.306,2,0,5]
["E2683","Ursodeoxycholic acid sodium","c2","L1700-85","in 10mM DMSO","Others","Others","Ursodeoxycholic acid sodium is a sodium salt of a naturally occurring bile acid that is used to treat a variety of hepatic and gastrointestinal diseases.",414.55,"2898-95-5",{"v":83,"d":"83.00"},200.22,{"v":83,"d":"83.00"},200.22,"http://www.selleckchem.com/products/ursodeoxycholic-acid-sodium.html","C24H40O4.Na","Sodium salt","N/A","[Na+].CC(CCC([O-])=O)C1CCC2C3C(O)CC4CC(O)CCC4(C)C3CCC12C",{"v":2.54,"d":"2.540"},0,2,4]
["E2687","Iodonitrotetrazolium chloride","f2","L1700-85","in 10mM DMSO","Dyes","Others","Iodonitrotetrazolium chloride (INT) on reduction gets converted to iodonitrotetrazolium formazan, a water insoluble violet colored dye or indicator, hence INT can be used for the colorimetric assay of various dehydrogenases.",{"v":505.7,"d":"505.70"},"146-68-9",{"v":100,"d":"100.00"},197.75,"<1","N/A","http://www.selleckchem.com/products/iodonitrotetrazolium-chloride.html","C19H13IN5O2.Cl","Chloride","INT","[Cl-].[O-][N+](=O)C1=CC=C(C=C1)[N+]2=NC(=N[N]2C3=CC=C(I)C=C3)C4=CC=CC=C4",2.559,2,0,4]
["E2829","Alkannin","d4","L1700-85","in 10mM DMSO","PKM","Metabolism","Alkannin is a potent and specific inhibitor of tumor-specific pyruvate kinase-M2 (PKM2), without inhibiting PKM1 and pyruvate kinase-L (PKL).",289.37,"517-88-4",{"v":100,"d":"100.00"},345.58,"<1","N/A","http://www.selleckchem.com/products/alkannin.html","C16H16O5","free base","N/A","CC(C)=CCC(O)C1=CC(=O)C2=C(O)C=CC(=C2C1=O)O",2.444,2,3,3]
["E2850","ORM-15341","b5","L1700-85","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","ORM-15341 is a potent and full antagonist for human AR (hAR) with IC50 value of 38 nM and the inhibition constant (Ki) value of 8 nM.",396.83,"1297537-33-7",{"v":79,"d":"79.00"},199.08,"<1","N/A","http://www.selleckchem.com/products/orm-15341.html","C19H17ClN6O2","free base","N/A","CC(C[N]1C=CC(=N1)C2=CC=C(C#N)C(=C2)Cl)NC(=O)C3=N[NH]C(=C3)C(C)=O",3.108,4,2,6]
["P1153","PKG inhibitor peptide","f6","L1700-85","in 10mM DMSO","PKG","GPCR & G Protein","PKG inhibitor peptide is an ATP-competitive inhibitor of cGMP-dependent protein kinase (PKG), with a Ki of 86 μM.",943.11,"82801-73-8",{"v":100,"d":"100.00"},106.03,{"v":100,"d":"100.00"},106.03,"http://www.selleckchem.com/products/pkg-inhibitor-peptide.html","C38H74N18O10","free base","N/A","CC(NC(=O)C(CCCNC(N)=N)NC(=O)C(CCCCN)NC(=O)C(N)CCCNC(N)=N)C(=O)NC(CCCNC(N)=N)C(=O)NC(CCCCN)C(=O)NC(CCC(O)=O)C(O)=O",-10.841,8,15,39]
["P1216","Box5","a8","L1700-85","in 10mM DMSO","Wnt/beta-catenin","Stem Cells & Wnt","Box5, a Wnt5a-derived N-butyloxycarbonyl hexapeptide (t-Boc-Met-Asp-Gly-Cys-Glu-Leu), acts as an Wnt5a antagonist, inhibits the basal migration and invasion of Wnt5a-expressing HTB63 melanoma cells, antagonizes the effects of Wnt5a on melanoma cell migration and invasion by directly inhibiting Wnt5a-induced PKC and Ca(2+) signaling.",666.76,"881188-48-3",{"v":100,"d":"100.00"},149.98,{"v":2,"d":"2.00"},{"v":3,"d":"3.00"},"http://www.selleckchem.com/products/box5.html","C25H42N6O11S2","free base","N/A","CSCCC(N)C(=O)NC(CC(O)=O)C(=O)NCC(=O)NC(CS)C(=O)NC(CCC(O)=O)C(=O)NC(CC(C)C)C(O)=O",{"v":-5.2,"d":"-5.200"},8,6,22]
["S3290","Procyanidin B2","b9","L1700-85","in 10mM DMSO","NLRP3,PPAR","Metabolism","Procyanidin B2 (PCB2), a natural flavonoid found in commonly consumed foods, possess anti-inflammatory, anti-oxidant and anti-cancer activities. Procyanidin B2 activates PPARγ to induce M2 polarization in mouse macrophages. Procyanidin B2 significantly suppresses the activation of NLRP3 inflammasome in the lung tissue induced by paraquat in the rat model.",578.52,"29106-49-8",{"v":100,"d":"100.00"},172.85,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/procyanidin-b2.html","C30H26O12","free base","PCB2","OC1CC2=C(OC1C3=CC(=C(O)C=C3)O)C(=C(O)C=C2O)C4C(O)C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(O)C=C6)O",3.565,2,10,3]
["S7048","Talazoparib (BMN 673)","e9","L1700-85","in 10mM DMSO","PARP","DNA Damage/DNA Repair","Talazoparib (BMN 673, LT-673) is a novel PARP inhibitor with IC50 of 0.57 nM for PARP1 in a cell-free assay. It is also a potent inhibitor of PARP-2, but does not inhibit PARG and is highly sensitive to PTEN mutation. Phase 3.",380.35,"1207456-01-6",{"v":38,"d":"38.00"},99.91,"<1","N/A","http://www.selleckchem.com/products/bmn-673.html","C19H14F2N6O","free base","LT-673","C[N]1N=CN=C1C2C(NC3=CC(=CC4=C3C2=NNC4=O)F)C5=CC=C(F)C=C5",2.467,4,2,2]
["S8832","Branebrutinib (BMS-986195)","e11","L1700-85","in 10mM DMSO","BTK","Protein Tyrosine Kinase","Branebrutinib (BMS-986195) is a potent inhibitor of BTK with IC50 values of 0.1 nM, 0.9 nM, 1.5 nM, 5 nM for BTK, TEC, BMX, TXK, respectively.",370.42,"1912445-55-6",{"v":74,"d":"74.00"},199.77,"<1","N/A","http://www.selleckchem.com/products/branebrutinib.html","C20H23FN4O2","free base","N/A","CC#CC(=O)NC1CCCN(C1)C2=C3C(=C(C)[NH]C3=C(C=C2F)C(N)=O)C",3.029,2,3,4]
["S9213","Jujuboside A","b2","L1700-86","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Jujuboside A, isolated from Semen Ziziphi Spinosae, exerts anti-oxidant, anti-inflammatory activities, and reduces the cell apoptosis.",1207.35,"55466-04-1",{"v":100,"d":"100.00"},82.83,{"v":-1,"d":"-1.00"},"N/A","http://www.selleckchem.com/products/jujuboside-a.html","C58H94O26","free base","N/A","CC1OC(OC2C(OCC(O)C2OC3OC(COC4OC(CO)C(O)C(O)C4O)C(O)C(O)C3OC5OCC(O)C(O)C5O)OC6CCC7(C)C(CCC8(C)C7CCC9C%10C(C)(O)CC(OC%10%11CC89CO%11)C=C(C)C)C6(C)C)C(O)C(O)C1O",-2.433,12,13,13]
["E2232","Guvacine hydrochloride","h2","L1700-86","in 10mM DMSO","GABA Receptor","Transmembrane Transporters","Guvacine hydrochloride is an alkaloid from the nut of Areca catechu, acts as an inhibitor of GABA transporter, and displays modest selectivity for cloned GABA transporters with IC50s of 14 μM (human GAT-1), 39 μM (rat GAT-1), 58 μM (rat GAT-2), 119 μM (human GAT-3), 378 μM (rat GAT-3), and 1870 μM (human BGT-3).",{"v":163.6,"d":"163.60"},"6027-91-4",{"v":16,"d":"16.00"},{"v":97.8,"d":"97.80"},{"v":33,"d":"33.00"},201.71,"http://www.selleckchem.com/products/guvacine-hydrochloride.html","C6H10ClNO2","hydrochloride","N/A","Cl.OC(=O)C1=CCCNC1",-1.607,1,1,1]
["S0054","D-I03","d4","L1700-86","in 10mM DMSO","DNA/RNA Synthesis","DNA Damage/DNA Repair","D-I03 is a selective inhibitor of RAD52 with Kd of 25.8 µM. D-I03 inhibits ssDNA annealing by RAD52 and D-loop formation with IC50 of 5 µM and 8 µM, respectively.",428.64,"688342-78-1",{"v":86,"d":"86.00"},200.63,"<1","N/A","http://www.selleckchem.com/products/d-i03.html","C23H36N6S","Free base","N/A","CCN(CC)CCNC(=S)NC1=CC2=C(C=C1)N=C(C=C2C)N3CCN(CC)CC3",5.028,1,2,10]
["S0308","AMZ30","h5","L1700-86","in 10mM DMSO","PP2A","PI3K/Akt/mTOR","AMZ30 (ML136, CS-2122) is a selective and covalent inhibitor of protein phosphatase methylesterase-1(PME-1) with IC50 of 0.60 μM. AMZ30 reduces the demethylated form of PP2A in living cells.",461.44,"1313613-09-0",{"v":86,"d":"86.00"},186.37,"<1","N/A","http://www.selleckchem.com/products/amz30.html","C19H12FN3O6S2","Free base","ML136, CS-2122","[O-][N+](=O)C1=CC(=CC=C1)[S](=O)(=O)[N]2C=CC=C2\\C=C(C#N)\\[S](=O)(=O)C3=CC=C(F)C=C3",3.825,4,0,6]
["S0403","LY2562175","a7","L1700-86","in 10mM DMSO","FXR","Metabolism","LY2562175 is a potent and selective agonist of FXR. LY2562175 promotes transcriptional activation of human FXR in a cell-based cotransfection assay with EC50 of 193 nM.",540.44,"1103500-20-4",{"v":100,"d":"100.00"},185.03,"<1","N/A","http://www.selleckchem.com/products/ly2562175.html","C28H27Cl2N3O4","Free base","N/A","C[N]1C=C(C(O)=O)C2=CC=C(C=C12)N3CCC(CC3)OCC4=C(ON=C4C5=C(Cl)C=CC=C5Cl)C6CC6",6.179,4,0,7]
["S0733","Tegatrabetan (BC-2059)","d8","L1700-86","in 10mM DMSO","Wnt/beta-catenin","Stem Cells & Wnt","Tegatrabetan (BC2059) is an antagonist of β-Catenin. Tegatrabetan (BC2059) treatment disrupts the binding of β-catenin with the scaffold protein transducin β-like 1 (TBL1) and proteasomal degradation and declines in the nuclear levels of β-catenin.",588.74,"1227637-23-1",{"v":100,"d":"100.00"},169.85,{"v":100,"d":"100.00"},169.85,"http://www.selleckchem.com/products/tegatrabetan.html","C28H36N4O6S2","Free base","N/A","CC1CC(C)CN(C1)[S](=O)(=O)C2=CC3=C(C=C2)C(N=O)C4=C(C=C(C=C4)[S](=O)(=O)N5CC(C)CC(C)C5)C3N=O",5.076,6,0,6]
["S0842","SP-13786","c9","L1700-86","in 10mM DMSO","PREP","Metabolism","SP-13786 (UAMC-1110)(compound 60) is a potent and selective inhibitor of fibroblast activation protein (FAP) and prolyl oligopeptidase (PREP) with IC50 of 3.2 nM and 1.8 μM, respectively.",344.32,"1448440-52-5",{"v":69,"d":"69.00"},200.39,"<1","N/A","http://www.selleckchem.com/products/sp-13786.html","C17H14F2N4O2","Free base","UAMC-1110","FC1(F)CC(C#N)N(C1)C(=O)CNC(=O)C2=CC=NC3=CC=CC=C23",0.921,3,1,3]
["S1522","Tosedostat (CHR2797)","f10","L1700-86","in 10mM DMSO","Aminopeptidase","Metabolism","Tosedostat (CHR2797) is an aminopeptidase inhibitor for LAP, PuSA and Aminopeptidase N with IC50 of 100 nM, 150 nM and 220 nM, respectively, and does not effectively inhibit either PILSAP, MetAP-2, LTA4 hydrolase, or MetAP-2. Phase 2.",406.47,"238750-77-1",{"v":51,"d":"51.00"},125.47,"<1","N/A","http://www.selleckchem.com/products/CHR-2797(Tosedostat).html","C21H30N2O6","Free base","N/A","CC(C)CC(C(O)C(=O)NO)C(=O)NC(C(=O)OC1CCCC1)C2=CC=CC=C2",2.406,4,3,10]
["S2221","Apatinib (YN968D1) mesylate","c11","L1700-86","in 10mM DMSO","VEGFR","Protein Tyrosine Kinase","Apatinib mesylate (YN968D1, Rivoceranib) is a potent inhibitor of the VEGF signaling pathway with IC50 values of 1 nM, 13 nM, 429 nM and 530 nM for VEGFR-2, Ret (c-Ret), c-Kit and c-Src, respectively. Apatinib mesylate induces both autophagy and apoptosis.",493.58,"1218779-75-9",{"v":22,"d":"22.00"},44.57,"<1","N/A","http://www.selleckchem.com/products/Apatinib-YN968D1.html","C25H27N5O4S","Mesylate","YN968D1, Rivoceranib","C[S](O)(=O)=O.O=C(NC1=CC=C(C=C1)C2(CCCC2)C#N)C3=CC=CN=C3NCC4=CC=NC=C4",3.164,3,2,6]
["S2846","ML359","b2","L1700-87","in 10mM DMSO","PDI","ER stress & UPR","ML359 is a small molecule inhibitor of protein disulfide isomerase （PDI).",417.93,"1069858-99-6",{"v":84,"d":"84.00"},200.99,"<1","N/A","http://www.selleckchem.com/products/ml359.html","C23H28ClNO4","Free base","N/A","CCOC(=O)C1(CCOC2=CC=CC=C2)CCN(CC1)CC3=CC=C(O)C(=C3)Cl",4.821,3,1,9]
["S3494","Vicriviroc maleate","f3","L1700-87","in 10mM DMSO","CCR,HIV Protease","GPCR & G Protein","Vicriviroc maleate(SCH-417690 maleate,SCH-D maleate) is a potent, selective, oral bioavailable and CNS penetrated antagonist of CCR5, with a Ki of 2.5 nM, and also inhibits HIV-1 in PBMC cells.",{"v":649.7,"d":"649.70"},"599179-03-0",{"v":100,"d":"100.00"},153.92,{"v":50,"d":"50.00"},76.96,"http://www.selleckchem.com/products/vicriviroc-maleate.html","C32H42F3N5O6","Maleate","SCH-417690 maleate, SCH-D maleate","COCC(N1CCN(CC1C)C2(C)CCN(CC2)C(=O)C3=C(C)N=CN=C3C)C4=CC=C(C=C4)C(F)(F)F.OC(=O)\\C=C/C(O)=O",-2.926,6,0,9]
["S4455","iGOT1-01","g4","L1700-87","in 10mM DMSO","GOT","Metabolism","iGOT1-01, a potent aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1; GOT1) inhibitor, possesses anti-cancer activity.",320.39,"882256-55-5",{"v":100,"d":"100.00"},312.12,"<1","N/A","http://www.selleckchem.com/products/igot1-01.html","C19H20N4O","Free base","N/A","O=C(NC1=CC=CC=C1)N2CCN(CC2)C3=C4C=C[NH]C4=CC=C3",3.075,1,2,2]
["S6248","Fasnall","b6","L1700-87","in 10mM DMSO","Fatty Acid Synthase","Metabolism","Fasnall, a thiophenopyrimidine, is a selective fatty acid synthase (FASN) inhibitor that shows potent anti-tumor activity.",338.47,"929978-58-5",{"v":13,"d":"13.00"},38.41,"<1","N/A","http://www.selleckchem.com/products/fasnall.html","C19H22N4S","Free base","N/A","CC1=C(C)C2=C(NC3CCN(C3)CC4=CC=CC=C4)N=CN=C2S1",3.723,2,1,4]
["S6731","Eliprodil (SL-820715)","f7","L1700-87","in 10mM DMSO","NMDAR","Neuronal Signaling","Eliprodil (SL-820715) is a non-competitive NR2B-selective NMDA antagonist with IC50 value of 1 μM and is less potent for NR2A- and NR2C-containing receptors with IC50 > 100 μM.",347.85,"119431-25-3",{"v":15,"d":"15.00"},43.12,"<1","N/A","http://www.selleckchem.com/products/eliprodil.html","C20H23ClFNO","Free base","N/A","OC(CN1CCC(CC1)CC2=CC=C(F)C=C2)C3=CC=C(Cl)C=C3",{"v":4.92,"d":"4.920"},0,1,5]
["S6767","GSK805","h7","L1700-87","in 10mM DMSO","Others","Others","GSK805 (JNJ 56914845, GSK-2336805) is a potent and orally bioavailable RORγt inhibitor.",532.36,"1426802-50-7",{"v":100,"d":"100.00"},187.84,"<1","N/A","http://www.selleckchem.com/products/gsk805.html","C23H18Cl2 F3NO4S","Free base","JNJ 56914845, GSK-2336805","CC[S](=O)(=O)C1=CC=C(CC(=O)NC2=CC(=C(C(=C2)Cl)C3=CC=CC=C3OC(F)(F)F)Cl)C=C1",7.491,4,1,8]
["S7554","Ravoxertinib (GDC-0994)","b10","L1700-87","in 10mM DMSO","ERK","MAPK","Ravoxertinib (GDC-0994) is a potent, orally available  and highly selective ERK1/2 inhibitor with IC50 of 1.1 nM and 0.3 nM, respectively. Phase 1.",439.85,"1453848-26-4",{"v":87,"d":"87.00"},197.79,"<1","N/A","http://www.selleckchem.com/products/gdc-0994.html","C21H18ClFN6O2","Free base","N/A","C[N]1N=CC=C1NC2=NC=CC(=N2)C3=CC(=O)N(C=C3)C(CO)C4=CC(=C(Cl)C=C4)F",2.798,4,2,6]
["S7710","R-268712","e10","L1700-87","in 10mM DMSO","TGF-beta/Smad","TGF-beta/Smad","R-268712 is a potent and selective inhibitor of ALK5 with an IC50 of 2.5 nM.",363.39,"879487-87-3",{"v":73,"d":"73.00"},200.89,"<1","N/A","http://www.selleckchem.com/products/r-268712.html","C20H18FN5O","Free base","N/A","CC1=NC(=CC=C1)C2=N[NH]C=C2C3=CC(=C(F)C=C3)C4=C[N](CCO)N=C4",3.134,3,2,5]
["S7926","Lifirafenib (BGB-283)","d11","L1700-87","in 10mM DMSO","EGFR,Raf","MAPK","Lifirafenib (BGB-283, Beigene-283) potently inhibits RAF family kinases and EGFR activities in biochemical assays with IC50 values of 23, 29 and 495 nM for the recombinant BRAFV600E kinase domain, EGFR and EGFR T790M/L858R mutant.",478.42,"1446090-79-4",{"v":95,"d":"95.00"},198.57,"<1","N/A","http://www.selleckchem.com/products/bgb-283-bgb283.html","C25H17F3N4O3","Free base","Beigene-283","FC(F)(F)C1=CC=C2N=C([NH]C2=C1)C3C4OC5=CC=C(OC6=C7CCC(=O)N=C7NC=C6)C=C5C34",3.338,5,2,4]
["S8377","ND646","c3","L1700-88","in 10mM DMSO","Acetyl-CoA carboxylase","Metabolism","ND-646 is an allosteric inhibitor of the ACC (Acetyl-coA carboxylase) enzymes that prevents ACC subunit dimerization to suppress fatty acid synthesis with IC50 of 3.5 nM and 4.1 nM for hACC1 and hACC2, respectively.",568.64,"1434639-57-2",{"v":100,"d":"100.00"},175.86,"<1","N/A","http://www.selleckchem.com/products/nd646.html","C28H32N4O7S","Free base","N/A","COC1=CC=CC=C1C(CN2C(=O)N(C(=O)C3=C2SC(=C3C)C4=NC=CO4)C(C)(C)C(N)=O)OC5CCOCC5",2.318,8,1,9]
["S8600","Elenbecestat","e4","L1700-88","in 10mM DMSO","BACE","Neuronal Signaling","Elenbecestat (E2609) is a novel BACE1 inhibitor, demonstrating prolonged reductions in plasma beta-amyloid levels after single dosing.",437.44,"1388651-30-6",{"v":87,"d":"87.00"},198.88,"<1","N/A","http://www.selleckchem.com/products/elenbecestat.html","C19H18F3N5O2S","Free base","E2609","CC1OCC2(N=C(N)SCC12)C3=C(F)C=CC(=C3)NC(=O)C4=CN=C(C=N4)C(F)F",2.037,5,2,4]
["S8718","RMC-4550","d5","L1700-88","in 10mM DMSO","phosphatase","Metabolism","RMC-4550 is a potent SHP-2inhibitor with an IC50 of 1.55 nM and it has no significant activity vs. 468 kinases, the catalytic domain of 15 phosphatases and other cellular targets including GPCRs, transporters and ion channels.",437.36,"2172651-73-7",{"v":100,"d":"100.00"},228.64,"<1","N/A","http://www.selleckchem.com/products/rmc-4550.html","C21H26Cl2N4O2","Free base","N/A","CC1OCC2(CCN(CC2)C3=C(CO)N=C(C(=N3)C)C4=C(Cl)C(=CC=C4)Cl)C1N",2.936,3,2,3]
["S8858","GSK3368715 (EPZ019997) 3HCl","h6","L1700-88","in 10mM DMSO","PRMT","Methylation","GSK3368715 is a potent inhibitor of type I protein arginine methyltransferases (PRMT) that inhibits PRMT1, 3, 4, 6 and 8 with Kiapp vaules ranging from 1.5 to 81 nM.",475.92,"2227587-26-8",{"v":81,"d":"81.00"},{"v":170.2,"d":"170.20"},{"v":81,"d":"81.00"},{"v":170.2,"d":"170.20"},"http://www.selleckchem.com/products/gsk3368715.html","C20H41Cl3N4O2","Trihydrochloride","N/A","Cl.Cl.Cl.CCOCC1(CCC(CC1)C2=N[NH]C=C2CN(C)CCNC)COCC",3.296,3,2,12]
["S8925","Simurosertib","b8","L1700-88","in 10mM DMSO","CDK","Cell Cycle","Simurosertib (TAK-931), an oral cell division cycle 7 (CDC7)-selective inhibitor with an IC50<0.3 nM, induces S phase delay and replication stress and causes mitotic aberrations through centrosome dysregulation and chromosome missegregation, resulting in irreversible antiproliferative effects in cancer cells.",341.43,"1330782-76-7",{"v":68,"d":"68.00"},199.16,"<1","N/A","http://www.selleckchem.com/products/simurosertib.html","C17H19N5OS","Free base","TAK-931","CC1=N[NH]C=C1C2=CC3=C(S2)C(=O)NC(=N3)C4CC5CCN4CC5",2.218,3,2,2]
["S8966","T-5224","d9","L1700-88","in 10mM DMSO","Interleukins,MMP","Proteases","T-5224 is a selective inhibitor of transcription factor c-Fos/activator protein (AP)-1 with anti-inflammatory effects. T-5224 specifically inhibits the DNA binding activity of c-Fos/c-Jun and the IL-1β-induced up-regulation of Mmp-3, Mmp-13 and Adamts-5 transcription.",517.53,"530141-72-1",{"v":100,"d":"100.00"},193.23,"<1","N/A","http://www.selleckchem.com/products/t-5224.html","C29H27NO8","Free base","N/A","OC(=O)CCC1=CC(=CC=C1OCC2=CC3=C(C=C2)C(=NO3)O)C(=O)C4=CC=C(OC5CCCC5)C=C4O",6.016,6,2,10]
["S8987","TNO155","g9","L1700-88","in 10mM DMSO","phosphatase","Metabolism","TNO155 is an inhibitor of protein tyrosine phosphatase (PTP) non-receptor type 11 (SHP2 /src homology region 2 domain phosphatase /PTPN11) with IC50 of 0.011 µM. TNO155 has potential antineoplastic activity.",421.95,"1801765-04-7",{"v":84,"d":"84.00"},199.08,"<1","N/A","http://www.selleckchem.com/products/tno155.html","C18H24ClN7OS","Free base","N/A","CC1OCC2(CCN(CC2)C3=CN=C(SC4=C(Cl)C(=NC=C4)N)C(=N3)N)C1N",1.523,4,3,3]
["S9726","Rimiducid (AP1903)","g11","L1700-88","in 10mM DMSO","FKBP","Apoptosis","Rimiducid (AP1903) is a chemical protein dimerizer and binds tightly to the target FKBP fusion protein while binding minimally to the abundant natural FKBP. Rimiducid elicites potent and dose-dependent apoptosis of cells in culture expressing dimerizer-dependent Fas constructs, with an EC50 of ≈0.1 nM.",1411.63,"195514-63-7",{"v":100,"d":"100.00"},70.84,"<1","N/A","http://www.selleckchem.com/products/rimiducid-ap1903.html","C78H98N4O20","Free base","N/A","CCC(C(=O)N1CCCCC1C(=O)OC(CCC2=CC(=C(OC)C=C2)OC)C3=CC(=CC=C3)OCC(=O)NCCNC(=O)COC4=CC=CC(=C4)C(CCC5=CC(=C(OC)C=C5)OC)OC(=O)C6CCCCN6C(=O)C(CC)C7=CC(=C(OC)C(=C7)OC)OC)C8=CC(=C(OC)C(=C8)OC)OC",11.602,20,2,39]
["S9829","BVT-948","c2","L1700-89","in 10mM DMSO","phosphatase","Metabolism","BVT 948 is a irreversible, noncompetitive and cell-permeable protein tyrosine phosphatase（PTP） inhibitor with IC50s of 0.9 μM, 1.7 μM, 0.09 μM, 1.5 μM and 0.7 μM for PTP1B, TCPTP, SHP-2, LAR and YopH respectively.",241.24,"39674-97-0",{"v":48,"d":"48.00"},198.97,"<1","N/A","http://www.selleckchem.com/products/alc-0315-offline.html","C14H11NO3","Free base","N/A","CC1(C)C(=O)N=C2C3=CC=CC=C3C(=O)C(=C12)O",1.973,3,1,0]
["S9944","PRN1008","b3","L1700-89","in 10mM DMSO","BTK","Angiogenesis","PRN1008 (Rilzabrutinib) is a reversible covalent, selective and oral active inhibitor of Bruton’s Tyrosine Kinase (BTK), with an IC50 of 1.3 nM.",665.76,"1575596-29-0",{"v":100,"d":"100.00"},{"v":150.2,"d":"150.20"},"<1","N/A","http://www.selleckchem.com/products/prn-008.html","C36H40FN9O3","Free base","Rilzabrutinib","CC(C)(/C=C(C#N)/C(=O)N1CCC(CC1)[N]2N=C(C3=C(F)C=C(OC4=CC=CC=C4)C=C3)C5=C2N=CN=C5N)N6CCN(CC6)C7COC7",3.758,6,1,8]
["E0116","PF-06446846 hydrochloride","f4","L1700-89","in 10mM DMSO","PCSK9","Metabolism","PF-06446846 (PF846) Hydrochloride is an orally bioavailable and specific inhibitor of PCSK9 with an IC50 of 0.3 µM in Huh7 cells.",470.35,"1632250-50-0",{"v":94,"d":"94.00"},199.85,{"v":94,"d":"94.00"},199.85,"http://www.selleckchem.com/products/pf-06446846-hydrochloride.html","C₂₂H₂₁Cl₂N₇O","Hydrochloride","PF846","Cl.ClC1=C(N=CC=C1)N(C2CCCNC2)C(=O)C3=CC=C(C=C3)[N]4N=NC5=C4N=CC=C5",3.783,5,1,4]
["E0326","S18-000003","h5","L1700-89","in 10mM DMSO","ROR","Metabolism","S18-000003, a potent, selective and orally active inhibitor of retinoic acid receptor-related orphan receptor-gamma-t (RORγt), with an IC50 of <30 μM towards human RORγt in competitive binding assays.",518.55,"2068119-11-7",{"v":100,"d":"100.00"},192.85,"<1","N/A","http://www.selleckchem.com/products/s18-000003.html","C26H25F3N2O4S","Free base","N/A","CC[S](=O)(=O)C1=CC=C(CC(=O)NC2=CC(=C(C=C2)C(C)(C)C(=O)NC3=C(F)C=C(F)C=C3)F)C=C1",4.839,4,2,8]
["E0636","GSK-1520489A","b7","L1700-89","in 10mM DMSO","Others","Others","GSK-1520489A(EX-A5430) is an active Protein Kinase, Membrane Associated Tyrosine/Threonine 1 (PKMYT1) inhibitor.",{"v":425.5,"d":"425.50"},"1042433-41-9",{"v":11,"d":"11.00"},25.85,"<1","N/A","http://www.selleckchem.com/products/gsk-1520489a.html","C21H23N5O3S","Free base","EX-A5430","CNC(=O)C1=CC=CC=C1NC2=NC(=NC=C2C)NC3=CC=CC(=C3)C[S](C)(=O)=O",3.438,5,3,7]
["E1078","Emvododstat (PTC299)","f8","L1700-89","in 10mM DMSO","Dehydrogenase,VEGFR","Protein Tyrosine Kinase","Emvododstat(PTC299), a post-transcriptional inhibitor of pathogenic VEGF and dihydroorotate dehydrogenase(DHODH), inhibits VEGFA mRNA translation and abnormal cell proliferation. In HeLa cells PTC299 inhibits hypoxia-induced VEGFA protein production with an EC50 of 1.64 nM.",467.34,"1256565-36-2",{"v":93,"d":"93.00"},{"v":199,"d":"199.00"},"<1","N/A","http://www.selleckchem.com/products/emvododstat-ptc299.html","C25H20Cl2N2O3","Free base","N/A","COC1=CC=C(C=C1)C2N(CCC3=C2[NH]C4=C3C=C(Cl)C=C4)C(=O)OC5=CC=C(Cl)C=C5",{"v":6.86,"d":"6.860"},3,1,4]
["E1088","TP-064","a9","L1700-89","in 10mM DMSO","PRMT","Methylation","TP-064 is a potent and selective small molecule inhibitor of PRMT4 with IC50 < 10 nM, >100 fold more selective for PRMT4 than other PRMTs.",{"v":458.6,"d":"458.60"},"2080306-20-1",{"v":92,"d":"92.00"},200.61,{"v":92,"d":"92.00"},200.61,"http://www.selleckchem.com/products/tp-064.html","C28H34N4O2","Free base","N/A","CNCCN1CCC(CC1)C2=NC=CC(=C2)CN(C)C(=O)C3=CC(=CC=C3)OC4=CC=CC=C4",3.749,3,1,9]
["E1179","EZM0414","g10","L1700-89","in 10mM DMSO","SETD","Methylation","EZM0414 is a potent, selective, and orally bioavailable inhibitor of Histone-lysine N-methyltransferase SETD2.",400.49,"2411748-50-8",{"v":40,"d":"40.00"},99.88,"<1","N/A","http://www.selleckchem.com/products/ezm0414.html","C22H29FN4O2","Free base","N/A","CC(=O)N1CCN(CC1)C2CCCC(C2)NC(=O)C3=CC4=C(F)C=CC(=C4[NH]3)C",2.707,2,2,3]
["E1205","BAY 2666605","e11","L1700-89","in 10mM DMSO","PDE","Metabolism","BAY 2666605 is an orally active phosphodiesterase 3A (PDE3A) and phosphodiesterase 3B (PDE3B) inhibitor with IC50s of 87 nM and 50 nM, respectively.",352.28,"2275774-60-0",{"v":70,"d":"70.00"},198.71,"<1","N/A","http://www.selleckchem.com/products/bay-2666605.html","C17H12F4N2O2","Free base","N/A","CC1OC(=O)NN=C1C2=CC=C(C3=CC=C(F)C=C3)C(=C2)C(F)(F)F",4.479,3,1,3]
["E1247","SR95531","d2","L1700-90","in 10mM DMSO","GABA Receptor","Neuronal Signaling","Gabazine(SR95531) is a potent competitive and allosteric antagonist of the GABAA receptor, with an IC50 for the GABA receptor of 9 µM.",368.23,"104104-50-9",{"v":74,"d":"74.00"},200.96,{"v":74,"d":"74.00"},200.96,"https://www.selleckchem.com/products/sr95531.html","C15H18BrN3O3","Free base","Gabazine","Br.COC1=CC=C(C=C1)C2=NN(CCCC(O)=O)C(=N)C=C2",2.233,3,0,6]
["E2382","(Rac)-IBT6A","d4","L1700-90","in 10mM DMSO","Others","Others","(Rac)-IBT6A (BTK inhibitor 1) is a racemate of IBT6A and an impurity of Ibrutinib, which is a Btk inhibitor (IC50=0.5 nM), and can be used in the synthesis of IBT6A Ibrutinib dimer and IBT6A adduct.",386.45,"1412418-47-3",{"v":77,"d":"77.00"},199.25,"<1","N/A","http://www.selleckchem.com/products/-rac--ibt6a.html","C22H22N6O","Free base","BTK inhibitor 1","NC1=C2C(=NC=N1)[N](N=C2C3=CC=C(OC4=CC=CC=C4)C=C3)C5CCCNC5",3.492,4,2,4]
["E2438","Ginsenoside Rg3","e5","L1700-90","in 10mM DMSO","Others","Others","Ginsenoside Rg3 is a ginsenoside found in Panax japonicus var. and Panax ginseng, mainly used for the study of tumor diseases.",{"v":785,"d":"785.00"},"11019-45-7",{"v":100,"d":"100.00"},127.39,"<1","N/A","http://www.selleckchem.com/products/ginsenoside-rg3.html","C42H72O13","Free base","N/A","CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC3C4(C)CCC(OC5OC(CO)C(O)C(O)C5OC6OC(CO)C(O)C(O)C6O)C(C)(C)C4CCC23C",2.295,4,8,10]
["E2655","Terevalefim","d6","L1700-90","in 10mM DMSO","c-Met","Protein Tyrosine Kinase","Terevalefim (ANG-3777), a small molecule hepatocyte growth factor (HGF) mimetic, induces c-MET dimerization and phosphorylation, reducing apoptosis and increasing cellular proliferation.",176.24,"1070881-42-3",{"v":35,"d":"35.00"},198.59,"<1","N/A","http://www.selleckchem.com/products/terevalefim.html","C9H8N2S","Free base","ANG-3777","[NH]1C=CC(=N1)\\C=C\\C2=CC=CS2",2.642,1,1,2]
["E2811","WAY-328133","h7","L1700-90","in 10mM DMSO","Others","Others","WAY-328133 is a bioactive compound.",310.32,"912790-04-6",{"v":20,"d":"20.00"},64.45,"<1","N/A","https://www.selleckchem.com/products/way-328133.html","C18H15FN2O2","Free base","N/A","FC1=CC=C(C=C1)C2=CC(=NO2)C(=O)NCCC3=CC=CC=C3",{"v":3.84,"d":"3.840"},3,1,5]
["E2813","SR 11237","a8","L1700-90","in 10mM DMSO","Retinoid Receptor","Metabolism","SR 11237, a retinoid X receptor (RXR)-specific agonist, can cause RXR/RXR homodimers to form and transactivate a reporter gene containing a RXR-response element.",380.48,"146670-40-8",{"v":38,"d":"38.00"},99.87,"<1","N/A","http://www.selleckchem.com/products/sr-11237.html","C24H28O4","Free base","N/A","CC1(C)CCC(C)(C)C2=CC(=CC=C12)C3(OCCO3)C4=CC=C(C=C4)C(O)=O",5.142,3,0,3]
["E2839","Bisindolylmaleimide VIII (acetate)","c9","L1700-90","in 10mM DMSO","PKC","TGF-beta/Smad","Bisindolylmaleimide VIII (acetate) (Ro 31-7549 acetate) is a potent and selective protein kinase C (PKC) inhibitor with an IC50 of 158 nM for rat brain PKC, also exerting IC50s of 53, 195, 163, 213, and 175 nM for PKC-α, PKC-βI, PKC-βII, PKC-γ, PKC-ε, respectively.",458.51,"138516-31-1",{"v":92,"d":"92.00"},200.65,"<1","N/A","http://www.selleckchem.com/products/bisindolylmaleimide-8--acetate-.html","C24H22N4O2.C2H4O2","Acetate","Ro 31-7549 acetate","C[N]1C=C(C2=CC=CC=C12)C3=C(C(=O)NC3=O)C4=C[N](CCCN)C5=CC=CC=C45.CC(O)=O",0.846,3,2,5]
["P1150","Saralasin Acetate","g10","L1700-90","in 10mM DMSO","RAAS","Endocrinology & Hormones","Saralasin Acetate, an octapeptide analog of angiotensin II, is a highly specific competitive inhibitor of angiotensin II that is used in the diagnosis of hypertension.",990.11,"39698-78-7",{"v":100,"d":"100.00"},{"v":101,"d":"101.00"},{"v":100,"d":"100.00"},{"v":101,"d":"101.00"},"http://www.selleckchem.com/products/saralasin-acetate.html","C44H71N13O13","Acetate","N/A","O.CNCC(=O)NC(CCCNC(N)=N)C(=O)NC(C(C)C)C(=O)NC(CC1=CC=C(O)C=C1)C(=O)NC(C(C)C)C(=O)NC(CC2=CN=C[NH]2)C(=O)N3CCCC3C(=O)NC(C)C(O)=O.CC(O)=O",-4.947,10,11,26]
["E4049","Taurodeoxycholate (sodium salt)","f11","L1700-90","in 10mM DMSO","Endogenous Metabolite","Metabolism","Taurodeoxycholate sodium salt is a bile salt-related anionic detergent used for isolation of membrane proteins including inner mitochondrial membrane proteins. and it inhibits various inflammatory responses",521.68,"1180-95-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/taurodeoxycholate-sodium-salt.html","C26H44NNaO6S","Sodium Salt","Taurodeoxycholate sodium salt","[Na;v0].CC(CCC(=O)NCC[S](O)(=O)=O)C1CCC2C3CCC4CC(O)CCC4(C)C3CC(O)C12C",3.065,1,3,7]
["E4090","Isoborneol","d3","L1700-91","in 10mM DMSO","HSV","Microbiology&virology","Isoborneol is a monoterpene alcohol, with neuroprotective and antiviral activities",154.25,"124-76-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/isoborneol.html","C10H18O","free base","Isoborneol","CC1(C)C2CCC1(C)C(O)C2",1.975,0,1,0]
["E4112","Menthol","g4","L1700-91","in 10mM DMSO","Others","Others","Menthyl alcohol is an organic compound made synthetically or obtained from peppermint or mint oils with flavoring and local anesthetic properties.",156.26,"1490-04-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/menthol.html","C10H20O","free base","Menthyl alcohol","CC(C)C1CCC(C)CC1O",2.779,0,1,1]
["E4125","3-Hydroxy-2-methylpyridine","f5","L1700-91","in 10mM DMSO","Others","Others","3-Hydroxy-2-methylpyridine could as a promising molecular scaffold for the future development of novel fibrillization inhibitors.",109.13,"1121-25-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/3-hydroxy-2-methylpyridine.html","C6H7NO","free base","3-Hydroxy-2-methylpyridine","CC1=C(O)C=CC=N1",{"v":0.72,"d":"0.720"},1,1,0]
["E4149","5-Methoxyindole-3-acetic acid","a7","L1700-91","in 10mM DMSO","Endogenous Metabolite","Metabolic Enzyme/Protease","5-Methoxyindole-3-acetic acid is a metabolite of Melatonin and is isolated from pineal tissue.",205.21,"3471-31-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/5-methoxyindole-3-acetic-acid.html","C11H11NO3","free base","5-Methoxyindole-3-acetic acid","COC1=CC=C2[NH]C=C(CC(O)=O)C2=C1",1.771,2,1,3]
["E4177","2′-O-Methyluridine","b8","L1700-91","in 10mM DMSO","Others","Others","2′-O-Methyluridine is a natural product that found in RNA such as rRNA, snRNA, snoRNA and tRNA in Archaea, Bacteria, and Eukaryota.",258.23,"2140-76-3","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/2-o-methyluridine.html","C10H14N2O6","free base","2′-O-Methyluridine","COC1C(O)C(CO)OC1N2C=CC(=O)NC2=O",-2.042,4,3,3]
["E4182","Ethyl 3-hydroxybutyrate","e8","L1700-91","in 10mM DMSO","Others","Others","Ethyl 3-hydroxybutyrate is a fragrance found in wine and Tribolium castaneum.",132.16,"5405-41-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/ethyl-3-hydroxybutyrate.html","C6H12O3","free base","Ethyl 3-hydroxybutyrate","CCOC(=O)CC(C)O",0.323,2,1,4]
["E4215","Ac-DL-Trp-OH","a10","L1700-91","in 10mM DMSO","Others","Others","N-Acetyl-tryptophan was study for its possible anti-​inflammatory and antinociceptive activities from the extraction of a Turkish plant, Salsola grandis.",246.26,"87-32-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/ac-dl-trp-oh.html","C13H14N2O3","free base","N-Acetyl-DL-tryptophan","CC(=O)NC(CC1=C[NH]C2=CC=CC=C12)C(O)=O",1.188,2,2,4]
["E4265","Pyrimidine","h11","L1700-91","in 10mM DMSO","Others","Others","Pyrimidines are heterocyclic, six-membered, nitrogen-containing carbon ring structures, with uracil, cytosine and thymine being the basal structures of ribose-containing nucleosides (uridine, cytidine, and thymidine respectively), or deoxyribose-containing deoxynucleosides, and their corresponding ribonucleotides or deoxyribonucleotides. Pyrimidines serve essential functions in human metabolism as ribonucleotide bases in RNA (uracil and cytosine), and as deoxyribonucleotide bases in DNA (cytosine and thymine), and are linked by phosphodiester bridges to purine nucleotides in double-stranded DNA, in both the nucleus and the mitochondria. Pyrimidine activated sugars are also involved in polysaccharide and phospholipid synthesis, glucuronidation in detoxification processes, glycosylation of proteins and lipids and in the recently identified novel endothelium-derived vasoactive dinucleotides.",80.09,"289-95-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/pyrimidine.html","C4H4N2","free base","Pyrimidine","C1=CN=CN=C1",0.051,2,0,0]
["E4283","2-Hydroxybenzothiazole","e2","L1700-92","in 10mM DMSO","Others","Others","2-Hydroxybenzothiazole is a natural product found in Cucumis sativus, Micrococcus, and other organisms with data available.",151.19,"934-34-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/2-hydroxybenzothiazole.html","C7H5NOS","free base","2-Hydroxybenzothiazole","O=C1NC2=CC=CC=C2S1",1.898,1,1,0]
["E4300","Dicyclo hexyl Phthalate","a4","L1700-92","in 10mM DMSO","Others","Others","NA",330.42,"84-61-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/dicyclo-hexyl-phthalate.html","C20H26O4","free base","Dicyclo hexyl Phthalate","O=C(OC1CCCCC1)C2=C(C=CC=C2)C(=O)OC3CCCCC3",5.257,4,0,6]
["E4307","1,4-Anthraquinone","c4","L1700-92","in 10mM DMSO","Others","Others","1,4-Anthraquinone is an anticancer drug that blocks nucleoside transport, inhibits macromolecule synthesis, induces DNA fragmentation, and decreases the growth and viability of L1210 leukemic cells in the same nanomolar range as daunorubicin in vitro.1,4-Anthraquinone is proposed as a novel pre-column reagent for high performance liquid chromatography (HPLC) determination of N-acetylcysteine (NAC) and captopril (CAP) in pharmaceutical formulations.",{"v":208.2,"d":"208.20"},"635-12-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/1-4-anthraquinone.html","C14H8O2","free base","1,4-Anthraquinone","O=C1C=CC(=O)C2=CC3=CC=CC=C3C=C12",2.666,2,0,0]
["E4326","2,4-Dihydroxypyridine","e6","L1700-92","in 10mM DMSO","Others","Others","2,4-Dihydroxypyridine is a chemical compound.",{"v":111.1,"d":"111.10"},"626-03-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/2-4-dihydroxypyridine.html","C5H5NO2","free base","2,4-Dihydroxypyridine","OC1=CC(=O)NC=C1",-0.862,1,2,0]
["E4335","ATMP","d7","L1700-92","in 10mM DMSO","Others","Others","ATMP is a phosphonic acid with chelating properties. It is an antiscalant.",299.05,"6419-19-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/atmp.html","C3H12NO9P3","free base","ATMP","O[P](O)(=O)CN(C[P](O)(O)=O)C[P](O)(O)=O",-2.026,0,0,6]
["E4338","N-BENZYLFORMAMIDE","g7","L1700-92","in 10mM DMSO","Others","Others","N-BENZYLFORMAMIDE is a natural product from Lepidium meyenii Walp.",149.19,"588-46-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/n-benzylformamide.html","C9H11NO","free base","N-BENZYLFORMAMIDE","CC(=O)NCC1=CC=CC=C1",0.957,1,1,2]
["E4359","Methyl L-pyroglutamate","f9","L1700-92","in 10mM DMSO","Others","Others","Methyl L-pyroglutamate shows anti-inflammatory activity. Methyl L-pyroglutamate is isolated from Portulaca oleracea L..",143.14,"4931-66-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/methyl-l-pyroglutamate.html","C6H9NO3","free base","Methyl L-pyroglutamate","COC(=O)C1CCC(=O)N1",-0.529,3,1,2]
["E4375","Menthofuran","c10","L1700-92","in 10mM DMSO","Others","Others","Menthofuran is a natural product.",150.22,"494-90-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/menthofuran.html","C10H14O","free base","Menthofuran","CC1CCC2=C(C1)OC=C2C",3.054,1,0,0]
["E4391","Methyl benzoin","g11","L1700-92","in 10mM DMSO","Others","Others","Methyl benzoin is a biochemical.",226.27,"3524-62-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/methyl-benzoin.html","C15H14O2","free base","Methyl benzoin","COC(C(=O)C1=CC=CC=C1)C2=CC=CC=C2",3.025,2,0,4]
["E4399","16a,17a-Epoxy-4-Pregnen-3,20-Dione","f2","L1700-93","in 10mM DMSO","Others","Others","16a,17a-Epoxy-4-Pregnen-3,20-Dione is a chemical compound.",{"v":328.4,"d":"328.40"},"1097-51-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/16alpha-17alpha-epoxy-4-pregnen-3-20-dione.html","C21H28O3","free base","16a,17a-Epoxy-4-Pregnen-3,20-Dione","CC(=O)C12OC1CC3C4CCC5=CC(=O)CCC5(C)C4CCC23C",2.924,3,0,1]
["E4029","Tyramine hydrochloride","e4","L1700-93","in 10mM DMSO","Others","Others","Tyramine hydrochloride is a biogenic trace amine that is generated via the decarboxylation of the amino acid tyrosine, exhibiting neuromodulatory properties as well as cardiovascular and immunological effects.",173.64,"60-19-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/tyramine-hydrochloride.html","C8H12ClNO","Hydrochloride salt","Tyramine hydrochloride","Cl.NCCC1=CC=C(O)C=C1",1.397,0,2,2]
["E4496","Cinnamoylglycine","g5","L1700-93","in 10mM DMSO","Endogenous Metabolite","Metabolism","Cinnamoylglycine is a glycine conjugate of cinnamic acid and a urinary metabolite in humans. It is used as a potential urinary biomarker.",205.21,"16534-24-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/cinnamoylglycine.html","C11H11NO3","free base","Cinnamoylglycine","OC(=O)CNC(=O)C=CC1=CC=CC=C1",0.987,2,1,4]
["E1552","Oleoylethanolamide","f6","L1700-93","in 10mM DMSO","Endogenous Metabolite;PPAR","Metabolism; DNA Damage/DNA Repair","Oleoylethanolamide is a high affinity endogenous agonist of PPAR-α.",325.53,"111-58-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/oleoylethanolamide.html","C20H39NO2","Free base","Oleoylethanolamide","CCCCCCCC\\C=C/CCCCCCCC(=O)NCCO",5.899,1,2,17]
["E4538","Aegeline","b8","L1700-93","in 10mM DMSO","Others","Others","Aegeline is an alkaloidal-amide, isolated from the leaves of Aegle marmelos and have shown antihyperglycemic as well as antidyslipidemic activities in the validated animal models of type 2 diabetes mellitus.",{"v":297.3,"d":"297.30"},"456-12-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/aegeline.html","C18H19NO3","Free base","Aegeline","COC1=CC=C(C=C1)C(O)CNC(=O)\\C=C\\C2=CC=CC=C2",2.562,2,2,6]
["E4543","4,7-Dihydroxycoumarin","f8","L1700-93","in 10mM DMSO","Others","Others","4, 7-DIHYDROXYCOUMARIN is a bioactive natural compound.",178.14,"1983-81-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/4-7-dihydroxycoumarin.html","C9H6O4","free base","4,7-DIHYDROXYCOUMARIN","OC1=CC=C2C(=CC(=O)OC2=C1)O",{"v":1.12,"d":"1.120"},2,2,0]
["E4555","7-Hydroxyisoflavone","e9","L1700-93","in 10mM DMSO","Others","Others","7-Hydroxyisoflavone against Enterovirus 71 in vitro.",238.24,"13057-72-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/7-hydroxyisoflavone.html","C15H10O3","Free base","7-Hydroxyisoflavone","OC1=CC=C2C(=O)C(=COC2=C1)C3=CC=CC=C3",2.624,2,1,1]
["E4563","7-Ethoxy-4-Methylcoumarin","a11","L1700-93","in 10mM DMSO","Others","Others","7-Ethoxy-4-Methylcoumarin is a natural organic compound",204.22,"87-05-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/7-ethoxy-4-methylcoumarin.html","C12H12O3","Free base","7-Ethoxy-4-Methylcoumarin","CCOC1=CC=C2C(=CC(=O)OC2=C1)C",2.678,3,0,2]
["E4572","5,7-Dihydroxy-4-phenylcoumarin","g11","L1700-93","in 10mM DMSO","Antibacterial","Microbiology&virology","5,7-dihydroxy-4-phenyl coumarin is found in the plant Passiflora serratodigitata with the antibacterial activity.",254.24,"7758-73-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/5-7-dihydroxy-4-phenylcoumarin.html","C15H10O4","Free base","5,7-Dihydroxy-4-phenylcoumarin","OC1=CC(=C2C(=C1)OC(=O)C=C2C3=CC=CC=C3)O",2.894,2,2,1]
["E4058","Xylan","e3","L1700-94","in 10mM DMSO","Others","Metabolism","Xylan is the main hemicellulose component in the secondary plant cell walls of flowering plants. It is a major source of renewable energy especially for second generation biofuels and can be used for feedstuff raw materials.",166.13,"9014-63-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/xylan.html","C5H10O6","Free base","Xylan","COC1=CC=C2C(=CC1=O)C(CCC3=CC(=C(OC)C(=C23)OC)OC)NC(C)=O",2.044,6,1,5]
["E4079","Benzyl salicylate","a5","L1700-94","in 10mM DMSO","Others","Natural Products","Benzyl salicylate is a salicylic acid benzyl ester. It can be used as a fragrance additive or UV light absorber.",228.24,"118-58-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/benzyl-salicylate.html","C14H12O3","Free base","Benzyl 2-hydroxybenzoate","OC1=C(C=CC=C1)C(=O)OCC2=CC=CC=C2",3.026,2,1,4]
["E4101","Pyrrole-2-carboxaldehyde","h5","L1700-94","in 10mM DMSO","Others","Natural Products","Pyrrole-2-carboxaldehyde is a member of pyrroles and a 1,3-thiazole-2-carbaldehyde. It has vibrational and electronic characteristics used to establish the existence of dimeric form in solid phase and monomeric form in solution phase.",{"v":95.1,"d":"95.10"},"1003-29-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/pyrrole-2-carboxaldehyde.html","C5H5NO","Free base","Pyrrole-2-carboxaldehyde","O=CC1=CC=C[NH]1",0.974,1,1,1]
["E4128","4-Methoxyphenethyl alcohol","b7","L1700-94","in 10mM DMSO","DNA/RNA Synthesis","Cell Cycle","4-Methoxyphenethyl alcohol is an aromatic alcohol, the major component in the anise-like odour produced by Amorphophallus. It can inhibits the protein, RNA and DNA synthesis in Escherichia coli.",152.19,"702-23-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/4-methoxyphenethyl-alcohol.html","C9H12O2","Free base","p-Methoxyphenethyl alcohol","COC1=CC=C(CCO)C=C1",{"v":1.53,"d":"1.530"},1,1,3]
["E4148","4-Methyl-1-pentanol","h7","L1700-94","in 10mM DMSO","Others","Natural Products","4-Methyl-1-pentanol (Isohexanol) is a volatile aroma compound of red wine from cv. Kalecik Karasι, a native grape variety of Vitis vinifera.",102.18,"626-89-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/4-methyl-1-pentanol.html","C6H14O","Free base","Isohexanol","CC(C)CCCO",1.678,0,1,3]
["E4162","Dibenzoylmethane","g8","L1700-94","in 10mM DMSO","Nrf2","NF-κB","Dibenzoylmethane (DBM) is a minor ingredient in licorice that activates Nrf2 and prevents various cancers and oxidative damage.It is also an analog of curcumin, results in dissociation from Keap1 and nuclear translocation of Nrf2.",224.26,"120-46-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/dibenzoylmethane.html","C15H12O2","Free base","1,3-Diphenylpropane-1,3-dione","O=C(CC(=O)C1=CC=CC=C1)C2=CC=CC=C2",3.154,2,0,4]
["E4199","1,4-Dimethoxybenzene","g10","L1700-94","in 10mM DMSO","Others","Others","1,4-Dimethoxybenzene is a dimethoxybenzene that is used as a pharmaceutical intermediate. It is used as a diazo dye and as a floral scent compound in willows that attracts an oligolectic bee.",138.16,"150-78-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/1-4-dimethoxybenzene.html","C8H10O2","Free base","N/A","COC1=CC=C(OC)C=C1",1.797,2,0,2]
["E4205","2-Heptanol","c11","L1700-94","in 10mM DMSO","Bacterial","Microbiology","2-Heptanol is one of the chemical constituents identified in the essential oil of the rhizome of Curcuma angustifolia and Curcuma zedoaria with good antimicrobial and antioxidant activity.. 2-Heptanol in combination with dimethyl sulfoxide forms a porogenic mixture that may be used to produce macroporous poly (acrylamide-co-N,N′-methylenebisacrylamide) Monolithics via copolymerization.",{"v":116.2,"d":"116.20"},"543-49-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/2-heptanol.html","C7H16O","Free base","s-Heptyl alcohol","CCCCCC(C)O",{"v":2.26,"d":"2.260"},0,1,4]
["E4232","Ethoxyacetic acid","g2","L1700-95","in 10mM DMSO","N/A","Metabolism","Ethoxyacetic acid is biomarker of exposure to widely used industrial chemicals such as alkyl-substituted ethylene glycols and other aliphatic ethers. Ethoxyacetic acid is metabolite of glycol ether alkoxy acid and is used to evaluate its toxicity in embryonic stem cell test in mouse.",{"v":104.1,"d":"104.10"},"627-03-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/ethoxyacetic-acid.html","C4H8O3","Free base","N/A","CCOCC(O)=O",{"v":-0.12,"d":"-0.120"},2,0,3]
["E4250","2-Methylpyrazine","c4","L1700-95","in 10mM DMSO","Others","Metabolism","2-Methylpyrazine is an alkyl-substituted pyrazine used as a key intermediate in the synthesis of pyrazineamide, an anti-tubercular drug.",94.11,"109-08-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/2-methylpyrazine.html","C5H6N2","Free base","N/A","CC1=NC=CN=C1",-0.189,2,0,0]
["E4251","(E)-Cinnamamide","d4","L1700-95","in 10mM DMSO","Others","Others","(E)-Cinnamamide, the less active isomer of cinnamamide, is a derivative of the plant secondary compound Cinnamic acid. Cinnamamide is effective as a non-lethal chemical repellent suitable for reducing avian pest damage.",147.17,"22031-64-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/e-cinnamamide.html","C9H9NO","Free base","N/A","NC(=O)/C=C/C1=CC=CC=C1",{"v":1.3,"d":"1.300"},1,1,2]
["E4268","Monomethyl phthalate","f5","L1700-95","in 10mM DMSO","Others","Metabolism","Monoethyl phthalate (2-(Methoxycarbonyl)benzoic acid) is a phthalic acid monoester resulting from the condensation of one of the carboxy groups of phthalic acid with ethanol, which has a role as a metabolite. Monomethyl phthalate acts as a urinary biomarker of phthalate exposure and is used as a standard for the determination of thyroid cancer and benign nodules.",180.16,"4376-18-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/monomethyl-phthalate.html","C9H8O4","Free base","2-(Methoxycarbonyl)benzoic acid","COC(=O)C1=C(C=CC=C1)C(O)=O",1.315,3,0,3]
["E4365","4-Methoxycinnamaldehyde","f7","L1700-95","in 10mM DMSO","RSV","Microbiology","4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde), is an active constituent of Agastache rugosa that exhibits cytoprotective activity against respiratory syncytial virus (RSV) in human larynx carcinoma cell line. 4-Methoxycinnamaldehyde effectively inhibits cytopathic effect of RSV.",162.19,"1963-36-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/4-methoxycinnamaldehyde.html","C10H10O2","Free base","p-Methoxycinnamaldehyde","COC1=CC=C(C=CC=O)C=C1",1.933,2,0,3]
["E4368","alpha-lactose monohydrate","a8","L1700-95","in 10mM DMSO","Others","Others","alpha-lactose monohydrate is the major sugar present in milk. Lactose exists in the form of two anomers, α and β. The α form normally crystallizes as a monohydrate.",{"v":342.3,"d":"342.30"},"5989-81-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/alpha-lactose.html","C12H22O11","Free base","α-D-Lactose","O.OCC1OC(OC2C(O)C(O)C(O)OC2CO)C(O)C(O)C1O",-4.468,3,7,4]
["E4426","Glucosamine (sulfate)","g9","L1700-95","in 10mM DMSO","Others","Metabolism","Glucosamine sulfate (D-Glucosamine sulfate) is an amino sugar and a prominent precursor in the biochemical synthesis of glycosylated proteins and lipids, and is used as a dietary supplement. Glucosamine sulfate also is a natural constituent of glycosaminoglycans in the cartilage matrix and synovial fluid, which when administered exogenously, exerts pharmacological effects on osteoarthritic cartilage and chondrocytes.",277.25,"14999-43-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/glucosamine-sulfate.html","C6H15NO9S","sulfate salt","D-Glucosamine sulfate","NC(C=O)C(O)C(O)C(O)CO.O[S](O)(=O)=O",-3.688,1,5,5]
["E4442","1,4-Dihydro-4-oxoquinoline-2-carboxylic acid","e10","L1700-95","in 10mM DMSO","NMDAR/ GluR/AChR","Neuronal Signaling","1,4-Dihydro-4-oxoquinoline-2-carboxylic acid (Kynurenic acid), an endogenous tryptophan metabolite, is a broad-spectrum antagonist targeting NMDA, glutamate, α7 nicotinic acetylcholine receptor. Kynurenic acid is also an agonist of GPR35/CXCR8.",189.17,"13593-94-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/1-4-dihydro-4-oxoquinoline-2-carboxylic-acid.html","C10H7NO3","Free base","Kynurenic acid, Quinurenic acid","OC(=O)C1=CC(=O)C2=CC=CC=C2N1",1.073,2,1,1]
["E4489","Thymopentin Acetate","a2","L1700-96","in 10mM DMSO","Others","Metabolism","Thymopentin acetate is a biologically active peptide secreted mainly by the epithelial cells of the thymic cortex and medulla. Thymopentin acetate is an effective immunomodulatory agent with a short plasma half-life of 30 seconds. Thymopentin acetate enhances the generation of T-cell lineage derived from human embryonic stem cells (hESCs).",739.82,"89318-88-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/thymopentin-acetate.html","C32H53N9O11","acetate salt","N/A","CC(C)C(NC(=O)C(CC(O)=O)NC(=O)C(CCCCN)NC(=O)C(N)CCCNC(N)=N)C(=O)NC(CC1=CC=C(O)C=C1)C(O)=O.CC(O)=O",-6.879,7,9,23]
["E4524","H-Val-Tyr-OH","d3","L1700-96","in 10mM DMSO","Others","Metabolism","H-Val-Tyr-OH is an endogenous metabolite and is an Antihypertensive dipeptide.",280.32,"3061-91-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/h-val-tyr-oh.html","C14H20N2O4","Free base","Valyl-tyrosine","CC(C)C(N)C(=O)NC(CC1=CC=C(O)C=C1)C(O)=O",{"v":-1.46,"d":"-1.460"},2,3,6]
["E4562","Tylosin Phosphate","e4","L1700-96","in 10mM DMSO","Anti-infection","Antibiotics","Tylosin phosphate is a macrolide antibiotic found naturally as a fermentation product of Streptomyces fradiae. Tylosin tartrate exerts potent antimicrobial activity against Gram-positive bacteria. Tylosin phosphate is widely used as a feed additive for promoting animal growth. Tylosin phosphate is used for veterinary purposes against bacterial dysentery and respiratory diseases in poultry, pigs and cattle.",{"v":1014.1,"d":"1014.10"},"1405-53-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/tylosin-phosphate.html","C46H80NO21P","Phosphate","N/A","CCC1OC(=O)CC(O)C(C)C(OC2OC(C)C(OC3CC(C)(O)C(O)C(C)O3)C(C2O)N(C)C)C(CC=O)CC(C)C(=O)\\C=C\\C(=C\\C1COC4OC(C)C(O)C(OC)C4OC)C.O[P](O)(O)=O",{"v":1.24,"d":"1.240"},12,4,13]
["E0099","GSK3987","h4","L1700-96","in 10mM DMSO","Liver X Receptor","Metabolism","GSK3987 is an agonist of pan LXRα/β with EC50s of 50 nM, 40 nM for LXRα-SRC1 and LXRβ-SRC1, respectively. GSK3987 increases the expression of ABCA1 and SREBP-1c and induces cellular cholesterol efflux and triglyceride accumulation.",384.43,"264206-85-1",{"v":77,"d":"77.00"},{"v":200.3,"d":"200.30"},"<1","N/A","https://www.selleckchem.com/products/gsk3987.html","C24H20N2O3","free base","N/A","COC1=CC=C(NC2=C(C(=O)N(CC3=CC=CC=C3)C2=O)C4=CC=CC=C4)C=C1",3.947,3,1,6]
["E1215","JQAD1","h6","L1700-96","in 10mM DMSO","Histone Acetyltransferase","Epigenetics","JQAD1 is a CRBN-dependent PROTAC that selectively targets EP300 for degradation.",932.95,"2417097-18-6",{"v":100,"d":"100.00"},107.19,"<1","N/A","https://www.selleckchem.com/products/jqad1.html","C48H52F4N6O9","free base","N/A","CC(N(CC1=CC=C(F)C=C1)C(=O)CN2C(=O)OC3(CCC4=CC(=CC=C34)NC(=O)CCCCCCCCCCCNC5=CC=C6C(=O)N(C7CCC(=O)NC7=O)C(=O)C6=C5)C2=O)C(F)(F)F",7.276,9,3,21]
["E1274","TH1760","c8","L1700-96","in 10mM DMSO","NUDIX","DNA Damage/DNA Repair","TH1760 (Compound 18) is a first-in-class, potent, selective and cell-active NUDT15 (MTH2) inhibitor with an IC50 value of 25 nM.",426.45,"2567914-01-4",{"v":7,"d":"7.00"},16.41,"<1","N/A","https://www.selleckchem.com/products/th1760.html","C20H18N4O5S","free base","Compound 18","O=C1NC2=CC=C(C=C2O1)[S](=O)(=O)N3CCN(CC3)C(=O)C4=CC5=C([NH]C=C5)C=C4",1.631,5,2,3]
["E1310","DPCPX","h8","L1700-96","in 10mM DMSO","Others","Others","DPCPX (PD 116948), a xanthine derivative, is a highly potent and selective adenosine A1 receptor (ADORA1) antagonist, with a Ki of 0.46 nM.",304.39,"102146-07-6",{"v":61,"d":"61.00"},{"v":200.4,"d":"200.40"},"<1","N/A","https://www.selleckchem.com/products/dpcpx.html","C16H24N4O2","free base","PD 116948","CCCN1C(=O)N(CCC)C2=C([NH]C(=N2)C3CCCC3)C1=O",{"v":3.37,"d":"3.370"},3,1,5]
["E1328","TP-1454","g9","L1700-96","in 10mM DMSO","PKM","Metabolism","TP-1454 is an activator of PKM2 with AC50 of 10 Nm in biochemical assays.TP-1454 modulates tumor-immune responses by destabilizing T-regulatory cells.",462.46,"2490276-04-3",{"v":92,"d":"92.00"},198.94,"<1","N/A","https://www.selleckchem.com/products/tp-1454.html","C19H22F4N4O3S","free base","N/A","NC1=CC=CC(=C1CN(CCC2CC[S](=O)(=O)CC2)C(=O)C3=CC(=N[NH]3)C(F)(F)F)F",2.929,4,2,7]
["E1339","HPPE","f10","L1700-96","in 10mM DMSO","Nrf2","Immunology & Inflammation","HPPE is a specific nonelectrophilic and physiological Bach1 inhibitor via heme-binding sites of Bach1 protein, derepresses Bach1-mediated repression.",479.48,"1325721-55-8",{"v":96,"d":"96.00"},200.22,"<1","N/A","https://www.selleckchem.com/products/hppe.html","C21H20F3N5O3S","free base","N/A","C[N]1C(=NC2=CC(=CC=C12)C(=O)NCCOCCO)NC3=NC4=CC=C(C=C4S3)C(F)(F)F",3.748,4,3,9]
["E1389","Eeyarestatin I","c2","L1700-97","in 10mM DMSO","Others","Ubiquitin","Eeyarestatin I is a potent inhibitor of endoplasmic reticulum-associated protein degradation (ERAD). Eeyarestatin I also inhibits Sec61 translocon.",630.44,"412960-54-4",{"v":85,"d":"85.00"},134.83,"<1","N/A","https://www.selleckchem.com/products/eeyarestatin-i.html","C27H25Cl2N7O7","free base","N/A","CC1(C)C(N(O)C(=O)NC2=CC=C(Cl)C=C2)N(C(=O)N1CC(=O)NN=CC=CC3=CC=C(O3)[N](=O)=O)C4=CC=C(Cl)C=C4",4.544,5,2,9]
["E1436","A2ti-2","g3","L1700-97","in 10mM DMSO","Anti-infection","Microbiology","A2ti-2 is a selective and low-affinity inhibitor of annexin A2/S100A10 heterotetramer (A2t)with an IC50 of 230 μM. It specifically disrupts the protein-protein interaction (PPI) between A2 and S100A10 and also prevents human papillomavirus type 16 (HPV16) infection.",354.43,"482646-13-9",{"v":71,"d":"71.00"},200.32,"<1","N/A","https://www.selleckchem.com/products/a2ti-2.html","C18H18N4O2S","free base","N/A","CC1=C(OCC2=NN=C(SCC(N)=O)[N]2C3=CC=CC=C3)C=CC=C1",{"v":3.16,"d":"3.160"},4,1,7]
["E1502","Deutenzalutamide","b4","L1700-97","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Deutenzalutamide (HC-1119, MDV3100) is an androgen receptor (AR) antagonist with an IC50 of 36 nM in LNCaP prostate cells. It can be used in a treatment of advanced prostate cancer.",467.46,"1443331-82-5",{"v":93,"d":"93.00"},198.95,"<1","N/A","https://www.selleckchem.com/products/deutenzalutamide.html","C21H13D3F4N4O2S","free base","HC-1119, MDV3100","C(NC(=O)C1=C(F)C=C(C=C1)N2C(=S)N(C(=O)C2(C)C)C3=CC(=C(C=C3)C#N)C(F)(F)F)([2H])([2H])[2H]",4.954,2,1,5]
["E2866","Sodium tetradecyl sulfate","e5","L1700-97","in 10mM DMSO","Others","Others","Sodium tetradecyl sulfate, a detergent sclerosant, is widely used agent for esophageal varices and varicose veins.",317.44,"1191-50-0 ",{"v":63,"d":"63.00"},198.46,{"v":63,"d":"63.00"},198.46,"https://www.selleckchem.com/products/sodium-tetradecyl-sulfate.html","C14H30O4S.Na","sodium tetradecyl sulfate","N/A","[Na;v0].CCCCCCCCCCCCCCO[S](O)(=O)=O",5.322,1,0,14]
["E2878","iothalamate sodium","f6","L1700-97","in 10mM DMSO","Others","Others","Iothalamate sodium is the sodium salt form of iothalamate, an organic iodine compound and a radiographic contrast medium.",{"v":636.9,"d":"636.90"},"1225-20-3",{"v":100,"d":"100.00"},157.01,"<1","N/A","https://www.selleckchem.com/products/iothalamate-sodium.html","C11H9I3N2O4.Na","sodium","N/A","[Na;v0].CNC(=O)C1=C(I)C(=C(I)C(=C1I)NC(C)=O)C(O)=O",1.522,3,2,3]
["E2905","DIRECT RED 80","b8","L1700-97","in 10mM DMSO","Others","Others","Direct Red 80 (Sirius Red) is a polyazo dye used principally in staining methods for collagen and amyloid. Direct Red 80 does not release benzidine upon degradation and is safer than many traditional direct dyes.",1379.13,"2610-10-8",{"v":100,"d":"100.00"},72.51,{"v":100,"d":"100.00"},72.51,"https://www.selleckchem.com/products/direct-red-80.html","C45H32N10O21S6.6Na","sodium","Sirius Red","[Na;v0].OC1=C(N=NC2=C(C=C(C=C2)N=NC3=CC=C(C=C3)[S](O)(=O)=O)[S](O)(=O)=O)C(=CC4=C1C=CC(=C4)NC(=O)NC5=CC6=C(C=C5)C(=C(N=NC7=C(C=C(C=C7)N=NC8=CC=C(C=C8)[S](O)(=O)=O)[S](O)(=O)=O)C(=C6)[S](O)(=O)=O)O)[S](O)(=O)=O",{"v":9.33,"d":"9.330"},9,4,16]
["E2915","Ovalbumin (257-264) chicken","a9","L1700-97","in 10mM DMSO","Others","Peptide products","Ovalbumin (257-264) Chicken (OVA Peptide(257-264) , SIINFEKL) is a class I (Kb)-restricted peptide epitope of ovalbumin (OVA) and has been used to trigger T cell activation in immunology studies.",963.13,"138831-86-4",{"v":100,"d":"100.00"},103.83,{"v":10,"d":"10.00"},10.38,"https://www.selleckchem.com/products/ovalbumin-257-264-chicken.html","C45H74N10O13","free base","OVA Peptide(257-264) , SIINFEKL","CCC(C)C(NC(=O)C(N)CO)C(=O)NC(C(C)CC)C(=O)NC(CC(N)=O)C(=O)NC(CC1=CC=CC=C1)C(=O)NC(CCC(O)=O)C(=O)NC(CCCCN)C(=O)NC(CC(C)C)C(O)=O",-5.958,10,11,33]
["E2942","MES","h10","L1700-97","in 10mM DMSO","Others","Others","MES (2-Morpholinoethanesulphonic acid) is a buffering agent in biology and biochemistry. It is one of the Good's buffers, the buffer capacity ranging pH 5.5-7.0. It is broadly used to regulate pH value for plants culture medium, reagent solution, and physiological experiments.",195.24,"4432-31-9",{"v":20,"d":"20.00"},102.44,{"v":39,"d":"39.00"},199.75,"https://www.selleckchem.com/products/mes.html","C6H13NO4S","free base","2-Morpholinoethanesulphonic acid","O[S](=O)(=O)CCN1CCOCC1",-0.588,1,0,3]
["E2948","β-Amyloid (25-35)","e11","L1700-97","in 10mM DMSO","Beta Amyloid","Neuronal Signaling","β-Amyloid (25-35) (Amyloid beta-peptide (25-35), Aβ25-35, β-Amyloid peptide (25-35)) , a sequence GSNKGAIIGLM, is a highly toxic synthetic derivative of Amyloid beta-peptide (Aβ-peptides) which forms fibrillary aggregates. β-Amyloid (25-35) is involved in the pathogenesis of Alzheimer's disease.",1060.27,"131602-53-4",{"v":100,"d":"100.00"},94.32,"<1","N/A","https://www.selleckchem.com/products/beta-amyloid-25-35.html","C45H81N13O14S","sulfate","Amyloid beta-peptide (25-35); Aβ25-35; β-Amyloid peptide (25-35), β-淀粉样蛋白 (25-35)","CCC(C)C(NC(=O)C(NC(=O)C(C)NC(=O)CNC(=O)C(CCCCN)NC(=O)C(CC(N)=O)NC(=O)C(CO)NC(=O)CN)C(C)CC)C(=O)NCC(=O)NC(CC(C)C)C(=O)NC(CCSC)C(O)=O",{"v":-7.23,"d":"-7.230"},12,14,37]
["E2968","Zinc sulfate heptahydrate","a3","L1700-98","in 10mM DMSO","Others","Others","Zinc sulfate heptahydrate is a hydrate that is the heptahydrate form of zinc sulfate. Zinc sulfate heptahydrate is a dietary supplement used for zinc deficiency and can also accelerate the rate of healing. It is also used in prepration of zinc tris(thiourea) sulphate (ZTS), a semiorganic nonlinear optic (NLO) material that may be useful in laser fusion experiments and in second-harmonic-generation (SHG) devices.",289.58,"7446-20-0",{"v":36,"d":"36.00"},124.32,{"v":36,"d":"36.00"},124.32,"https://www.selleckchem.com/products/zinc-sulfate-heptahydrate.html","H2O4S.7H2O.Zn","zinc sulfate","N/A","O.[Zn].O[S](O)(=O)=O",-0.815,0,0,0]
["E2998","Acetylthiocholine iodide","e4","L1700-98","in 10mM DMSO","Others","Others","Acetylthiocholine iodide(S-Acetylthiocholine iodide; ATCh iodide) is used as a substrate in the preparation of acetylcholine esterase (AChE) assay working solution for AChE activity assay. In addition, the compound is used in some medical research, for example in the fields of neuroscience and organ physiology.",289.18,"1866-15-5",{"v":58,"d":"58.00"},200.57,{"v":58,"d":"58.00"},200.57,"https://www.selleckchem.com/products/acetylthiocholine-iodide.html","C7H16NOS.I","iodide","S-Acetylthiocholine iodide; ATCh iodide","[I-].CC(=O)SCC[N+](C)(C)C",-3.749,1,0,4]
["E4012","4-Methylumbelliferyl beta-D-glucopyranoside","e5","L1700-98","in 10mM DMSO","Others","Others","4-Methylumbelliferyl beta-D-glucopyranoside(MUD) is a β-D-glucoside, is a fluorogenic substrate for β-glucosidase. It is utilized in the assay of beta-glucosidase activity.",338.31,"18997-57-4",{"v":68,"d":"68.00"},{"v":201,"d":"201.00"},{"v":2,"d":"2.00"},5.91,"https://www.selleckchem.com/products/4-methylumbelliferyl-beta-d-glucopyranoside.html","C16H18O8","free base","MUD","CC1=CC(=O)OC2=CC(=CC=C12)OC3OC(CO)C(O)C(O)C3O",0.174,4,4,3]
["E4015","4-Methylumbelliferyl N-acetyl-beta-D-glucosaminide","h5","L1700-98","in 10mM DMSO","Dye","Others","4-Methylumbelliferyl N-acetyl-beta-D-glucosaminide is a fluorogenic substrate used for assays of N-acetyl-β-D-glucosaminidase (NAGase).",379.36,"37067-30-4",{"v":76,"d":"76.00"},200.34,{"v":3,"d":"3.00"},7.91,"https://www.selleckchem.com/products/4-methylumbelliferyl-n-acetyl-beta-d-glucosaminide.html","C18H21NO8","free base","N/A","CC(=O)NC1C(O)C(O)C(CO)OC1OC2=CC=C3C(=CC(=O)OC3=C2)C",-0.094,5,4,4]
["S0886","SC-26196","d7","L1700-98","in 10mM DMSO","Others","Others","SC-26196 is a potent, orally active Delta6 desaturase (D6D, FADS2) inhibitor with an IC50 of 200nM.",423.55,"218136-59-5",{"v":8,"d":"8.00"},18.89,"<1","N/A","https://www.selleckchem.com/products/sc-26196.html","C27H29N5","free base","N/A","N#CC(CCCN1CCN(CC1)N=CC2=CN=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4",{"v":4.07,"d":"4.070"},2,0,8]
["S7354","Filanesib hydrochloride","b8","L1700-98","in 10mM DMSO","Kinesin","Cytoskeletal Signaling","Filanesib (ARRY-520) hydrochloride is a kinesin spindle protein (KSP) inhibitor that blocks the separation of centrosomes and assembly of spindles in the early stage of cell mitosis, and cell proliferation.",456.94,"1385020-40-5",{"v":91,"d":"91.00"},199.15,{"v":91,"d":"91.00"},199.15,"https://www.selleckchem.com/products/filanesib.html","C20H22F2N4O2S.ClH","hydrochloride","ARRY-520 hydrochloride","Cl.CON(C)C(=O)N1N=C(SC1(CCCN)C2=CC=CC=C2)C3=C(F)C=CC(=C3)F",3.854,3,1,6]
["E1217","PCLX-001 (DDD86481)","h9","L1700-98","in 10mM DMSO","Others","Others","PCLX-001 (DDD86481) is an orally active dual N-myristoyltransferase (NMT) inhibitor. It inhibits NMT1 and NMT2 with IC50 of 5 nM and 8 nM, respectively, in vitro. PCLX-001 inhibits early B-cell receptor (BCR) signalling, which can be used in B-cell malignancy research.",537.51,"1215011-08-7",{"v":13,"d":"13.00"},24.19,"<1","N/A","https://www.selleckchem.com/products/pclx-001-ddd86481.html","C24H30Cl2N6O2S","free base","DDD86481","CC(C)CC1=N[N](C)C(=C1N[S](=O)(=O)C2=C(Cl)C=C(C=C2Cl)C3=CC=NC(=C3)N4CCNCC4)C",4.589,4,2,7]
["E1507","Zilurgisertib fumarate","g10","L1700-98","in 10mM DMSO","ALK","Protein Tyrosine Kinase","Zilurgisertib fumarate(INCB-000928 fumarate, NBU-928 fumarate) is a selective ALK 2 inhibitor.It is under development for the treatment of heterotopic ossification and fibrodysplasia ossificans progressiva.",618.72,"2173390-30-0",{"v":100,"d":"100.00"},161.62,{"v":100,"d":"100.00"},161.62,"https://www.selleckchem.com/products/zilurgisertib-fumarate.html","C30H38N4O3.xC4H4O4","Fumarate salt","INCB-000928 fumarate, NBU-928 fumarate","NC1=NC=C(C=C1C(=O)NC23CCC(O)(CC2)CC3)C4=CC=C(C=C4)C56CC5CN(C6)C7CCOCC7.OC(=O)\\C=C\\C(O)=O",-1.094,5,2,7]
["E1598","VT103","c2","L1700-99","in 10mM DMSO","TEAD","Hippo","VT103 is an orally active and selective inhibitor of TEAD1 protein palmitoylation with anti-proliferative and anti-tumor activity. It also inhibits YAP/TAZ-TEAD promoted gene transcription, blocks TEAD auto-palmitoylation and disrupts interaction between YAP/TAZ and TEAD.",410.42,"2290608-13-6",{"v":82,"d":"82.00"},{"v":199.8,"d":"199.80"},"<1","N/A","https://www.selleckchem.com/products/vt103.html","C18H17F3N4O2S","free base","N/A","CN[S](=O)(=O)C1=CC(=C(NC2=CC=C(C=C2)C(F)(F)F)C=C1)C3=C[N](C)C=N3",3.273,3,2,6]
["E1651","CD532","e3","L1700-99","in 10mM DMSO","Aurora Kinase","Epigenetics","CD532 is a potent  Aurora A kinase inhibitor with an IC50 of 45 nM. It breaks the native conformation of Aurora-A, drives the degradation of  N-Myc in N-Myc-driven cancers, and also exhibits anti-proliferative effects.",522.53,"1639009-81-6",{"v":100,"d":"100.00"},191.38,"<1","N/A","https://www.selleckchem.com/products/cd532.html","C26H25F3N8O","free base","N/A","FC(F)(F)C1=CC=CC(=C1)NC(=O)NC2=CC=C(NC3=NC=CC(=N3)NC4=N[NH]C(=C4)C5CCCC5)C=C2",6.645,4,5,8]
["E1712","FM19G11","g4","L1700-99","in 10mM DMSO","HIF","Angiogenesis","FM19G11 is a  hypoxia-inducible factor-1-alpha (HIF-1α) inhibitor, and it inhibits hypoxia-induced luciferase activity with an IC50 of 80 nM in HeLa cells.",{"v":463.4,"d":"463.40"},"329932-55-0",{"v":93,"d":"93.00"},200.69,"<1","N/A","https://www.selleckchem.com/products/fm19g11.html","C23H17N3O8","free base","N/A","CC1=CC=C(C=C1)C(=O)COC(=O)C2=CC=CC(=C2)NC(=O)C3=C(C=C(C=C3)[N](=O)=O)[N](=O)=O",4.001,4,1,9]
["E1727","Pimicotinib","b5","L1700-99","in 10mM DMSO","CSF-1R","Protein Tyrosine Kinase","Pimicotinib (ABSK021) is an orally bioavailable inhibitor of colony stimulating factor 1 receptor (CSF1R). It enhances antitumor T-cell immune responses and inhibits the proliferation of tumor cells having potential immunomodulatory and antineoplastic activities.",420.47,"2253123-16-7",{"v":84,"d":"84.00"},199.78,"<1","N/A","https://www.selleckchem.com/products/pimicotinib.html","C22H24N6O3","free base","ABSK021","C[N]1C=C(C=N1)C2=CC(=CC=N2)OC3=C(C)N=C(NC(=O)N4CCC(C)(C)C4=O)C=C3",2.748,6,1,4]
["E1775","2,4-Thiazolidinedione","f6","L1700-99","in 10mM DMSO","PPAR","Metabolism","2,4-Thiazolidinedione (Thiazolidinedione), an insulin sensitizer, is a specific agonist of peroxisome proliferator-activated receptor (PPAR)γ. Thiazolidinedione treatment corrects impaired muscle insulin action in vivo.",117.13,"2295-31-0",{"v":23,"d":"23.00"},196.36,{"v":23,"d":"23.00"},196.36,"https://www.selleckchem.com/products/2,4-thiazolidinedione.html","C3H3NO2S","free base","Thiazolidinedione","O=C1CSC(=O)N1",0.045,2,1,0]
["E2981","PI4KIIIbeta-IN-10","f7","L1700-99","in 10mM DMSO","PI4K","PI3K/Akt/mTOR","PI4KIIIbeta-IN-10 is a potent inhibitor of PI4KIIIβ with an IC50 of 3.6 nM. It also exhibits weak inhibition of PI3KC2γ, PI3Kα, and PI4KIIIα, and <20% inhibition at concentrations up to 20 µM for PI4K2α, PI4K2β, and PI3Kβ.",475.58,"1881233-39-1",{"v":95,"d":"95.00"},199.76,"<1","N/A","https://www.selleckchem.com/products/pi4kiiibeta-in-10.html","C22H25N3O5S2","free base","N/A","COC1=C(C=C(C=C1)C2=C(C)N=C(NC(=O)C(C)(C)C)S2)[S](=O)(=O)NC3=CC=C(O)C=C3",3.815,5,3,7]
["E4445","3-Benzoylpropionic acid","b9","L1700-99","in 10mM DMSO","Others","Others","3-Benzoylpropionic acid is a carboxylate compound which can be used as a fungicide and an oligonucleotide synthesis reagent.",178.18,"2051-95-8",{"v":36,"d":"36.00"},202.04,{"v":4,"d":"4.00"},22.45,"https://www.selleckchem.com/products/3-benzoylpropionic-acid.html","C10H10O3","free base","N/A","OC(=O)CCC(=O)C1=CC=CC=C1",1.415,2,0,4]
["E4467","Temozolomide Acid","a10","L1700-99","in 10mM DMSO","Others","Others","Temozolomide acid is a carboxylic acid derivative of Temozolomide. It has an anticancer activity by causing breaks in DNA double strand, cell cycle arrest, and eventually cell death.",195.14,"113942-30-6",{"v":39,"d":"39.00"},199.86,"<1","N/A","https://www.selleckchem.com/products/temozolomide-acid.html","C6H5N5O3","free base","N/A","CN1N=NC2=C(N=C[N]2C1=O)C(O)=O",0.679,5,0,1]
["S2520","CD437(AHPN)","g10","L1700-99","in 10mM DMSO","Retinoid Receptor","Metabolism","CD437(AHPN), a synthetic retinoid, is a selective Retinoic acid Receptor γ ( RARγ) agonist. It exhibits an antiproliferative effect and induces apoptosis via activation of AP-1 in vitro.",398.49,"125316-60-1",{"v":80,"d":"80.00"},200.76,"<1","N/A","https://www.selleckchem.com/products/cd437.html","C27H26O3","free base","AHPN","OC(=O)C1=CC2=C(C=C1)C=C(C=C2)C3=CC=C(O)C(=C3)C45CC6CC(CC(C6)C4)C5",6.054,1,1,3]
["S9969","RMC-4630","a2","L1700-100","in 10mM DMSO","Microtubule Associated","Cytoskeletal Signaling","RMC-4630 (SSE15206) is an inhibitor of microtubule polymerization with a GI50 of 197 nM in HCT116 cells. It can overcome multidrug resistance and cause aberrant mitosis, resulting in G2/M arrest due to incomplete spindle formation in cancer cells.",450.99,"2172652-48-9",{"v":45,"d":"45.00"},99.78,"<1","N/A","https://www.selleckchem.com/products/rmc-4630.html","C20H27ClN6O2S","Chloride","SSE15206","CC1OCC2(CCN(CC2)C3=NC(=C(SC4=CC=NC(=C4Cl)N)N=C3CO)C)C1N",1.624,4,3,4]
["E1486","Zamaporvint (RXC004)","a4","L1700-100","in 10mM DMSO","Wnt/beta-catenin","Stem Cells & Wnt","Zamaporvint (RXC004) is an orally active and selective inhibitor of Wnt. It targets membrane-bound o-acyltransferase Porcupine and inhibits Wnt ligand palmitoylation, secretion, and pathway activation. RXC004 exhibits potent antiproliferative effects in Wnt ligand-dependent colorectal and pancreatic cell lines and possesses multiple antitumor mechanisms.",439.39,"1900754-56-4",{"v":88,"d":"88.00"},200.28,"<1","N/A","https://www.selleckchem.com/products/rxc004.html","C21H16F3N7O","free base","N/A","CC1=C(N=C[N]1CC(=O)NC2=CC=C(C=N2)C3=NC=CN=C3)C4=CC=NC(=C4)C(F)(F)F",1.906,6,1,6]
["E1517","ZEN-3694","d4","L1700-100","in 10mM DMSO","Epigenetic Reader Domain","Epigenetics","ZEN-3694 is an orally bioavailable  bromodomain extraterminal inhibitor (BETi)  that leads to down-regulation of expression of AR-signaling in metastatic castrationresistant prostate cancer (mCRPC) models.",333.39,"1643947-30-1",{"v":67,"d":"67.00"},200.97,"<1","N/A","https://www.selleckchem.com/products/zen-3694.html","C19H19N5O","free base","N/A","CNC1=NC2=NC=C(C=C2[N]1CC3=CC=CC=C3)C4=C(C)ON=C4C",{"v":2.93,"d":"2.930"},4,1,4]
["E4026","Poly(2-hydroxyethyl methacrylate)","f5","L1700-100","in 10mM DMSO","Others","Others","Poly(2-hydroxyethyl methacrylate) is one of the most important hydrogels in the world of biomaterials. It is the basic component of contact lenses and is also used in the implantation of soft tissues, synthetic transplant for gristle and bone, regeneration of neurotic tissue, transmission of agents, etc.",130.14,"25249-16-5",{"v":100,"d":"100.00"},{"v":768.4,"d":"768.40"},"<1","N/A","https://www.selleckchem.com/products/poly-2-hydroxyethyl-methacrylate.html","(C6H10O3)x","free base","N/A","CC(=C)C(=O)OCCO",0.625,2,1,4]
["S1634","Acetaminophen","h6","L1700-100","in 10mM DMSO","COX","Neuronal Signaling","Acetaminophen is a COX inhibitor for COX-1 and COX-2 with IC50 of 113.7 μM and 25.8 μM, respectively.",151.16,"103-90-2",{"v":30,"d":"30.00"},198.47,{"v":13,"d":"13.00"},{"v":86,"d":"86.00"},"https://www.selleckchem.com/products/acetaminophen.html","C8H9NO2","Free Base","Paracetamol, Tylenol, APAP","CC(=O)Nc1ccc(O)cc1",0.708,1,2,1]
["E0539","Apiopaeonoside","d8","L1700-100","in 10mM DMSO","anti-inflammatory","Immunology & Inflammation","Apiopaeonoside is a component of Moutan Cortex (Paenonia suffruticosa) with potential anti-inflammatory effects.",460.43,"100291-86-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/apiopaeonoside.html","C20H28O12","Free Base","NA","COC1=CC(=C(C=C1)C(C)=O)OC2OC(COC3OCC(O)(CO)C3O)C(O)C(O)C2O",-2.028,6,5,8]
["E0567","Tetrahydromagnolol","c9","L1700-100","in 10mM DMSO","cannabinoid CB2 receptor","GPCR & G Protein","Tetrahydromagnolol, a metabolite of magnolol,  is a potent and selective agonist of the cannabinoid CB2 receptor with an EC50 of 170 nM.",{"v":270.4,"d":"270.40"},"20601-85-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/tetrahydromagnolol.html","C18H22O2","Free Base","Magnolignan","CCCC1=CC=C(O)C(=C1)C2=CC(=CC=C2O)CCC",5.661,0,2,5]
["E0593","Polyporusterone B","h10","L1700-100","in 10mM DMSO","AAPH-induced hemolysis","Immunology & Inflammation","Polyporusterone B is a triterpene carboxylic acid isolated from Polyporus umbellatus (Chuling) with antioxidant properties. It effectively protects red blood cells from AAPH-induced hemolysis with a dose-dependent inhibitory effect. Polyporusterone B exhibits significant anti-hemolytic activity and enhances free-radical scavenging in rats.",476.65,"141360-89-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/polyporusterone-b.html","C28H44O6","free base","NA","CC(C)C(=C)CC(O)C(C)(O)C1CCC2(O)C3=CC(=O)C4CC(O)C(O)CC4(C)C3CCC12C",2.544,1,3,5]
["E0663","DESMETHYLBELLIDIFOLIN","g11","L1700-100","in 10mM DMSO","anti-inflammatory","Immunology & Inflammation","DESMETHYLBELLIDIFOLIN is a xanthone derived from Gentianella acuta with antispasmodic and anti-inflammatory properties. It inhibits trinitrobenzenesulfonic acid (TNBS)-induced ulcerative colitis (UC), reduces the inflammatory response and alleviates colon muscle spasms, with the potential to treat ulcerative colitis.",{"v":260.2,"d":"260.20"},"2980-32-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/tetrahydroxyxanthone.html","C13H8O6","Free Base","1,3,5,8-Tetrahydroxyxanthone","OC1=CC(=C2C(=O)C3=C(O)C=CC(=C3OC2=C1)O)O",1.996,2,4,0]
["E0689","Eudesmin","c3","L1700-101","in 10mM DMSO","S6K1","PI3K/Akt/mTOR","Eudesmin is a bicyclic lignan obtained from plants in the Magnoliaceae, Apiaceae, Ochnaceae, and Rutaceae families with anti-tumor, anti-inflammatory, and anti-bacterial activities. It inhibits mTOR-dependent activation of S6K1 and the nuclear localization of activated S6K1. Eudesmin also blocks adipogenesis by down-regulating the S6K1-H2BS36p axis, which in turn regulates genes involved in cell fate determination.",{"v":386.4,"d":"386.40"},"526-06-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/eudesmin.html","C22H26O6","Free Base","(-)-Eudesmin","COC1=C(OC)C=C(C=C1)C2OCC3C2COC3C4=CC(=C(OC)C=C4)OC",2.635,6,0,6]
["E0754","GL3","f4","L1700-101","in 10mM DMSO","Others","Others","GL3 is a major component of Osmanthus fragrans seeds, consisting of methyloleoside derivatives. These compounds are based on both phenylethanoid and methyloleoside structures.",1073.01,"60037-39-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/gl3.html","C48H64O27","free base","N/A","COC(=O)C1=COC(OC2OC(CO)C(O)C(O)C2O)C(=C/C)/C1CC(=O)OCC3OC(OCCC4=CC=C(OC(=O)CC5\\C(=C/C)C(OC=C5C(=O)OC)OC6OC(CO)C(O)C(O)C6O)C=C4)C(O)C(O)C3O",-2.604,16,11,23]
["E0773","Rhodojaponin III","g5","L1700-101","in 10mM DMSO","VGSCs","Transmembrane Transporters","Rhodojaponin III is a diterpenoid from the leaves of Rhododendron molle with anti-inflammatory and antinociceptive effects, acting through mild inhibition of voltage-gated sodium channels (VGSCs) to reduce nociceptive and neuropathic pain.",368.46,"26342-66-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/rhodojaponin-3.html","C20H32O6","free base","NA","CC1(O)CC23CC(O)C4(O)C(C5OC5C4(C)C)C(C)(O)C2CCC1C3O",-0.701,1,2,0]
["E0901","Pinosylvin","b6","L1700-101","in 10mM DMSO","COX-2, TNF-α, IL-6","Neuronal Signaling, Immunology & Inflammation","Pinosylvin is a stilbenoid primarly found in Pinus genus, with anti-inflammatory properties. It inhibits PGE2 production mediated by COX-2 in LPS-treated RAW 264.7 cells, with an IC50 value of 10.6 µM. It significantly reduces the release of pro-inflammatory cytokines (TNF-α and IL-6) and NO mediators in LPS-stimulated RAW 264.7 cells.",212.24,"22139-77-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/pinosylvin.html","C14H12O2","Free Base","trans-3,5-dihydroxystilbene","OC1=CC(=CC(=C1)\\C=C\\C2=CC=CC=C2)O",3.332,0,2,2]
["E0910","Swertisin","a7","L1700-101","in 10mM DMSO","adenosine A1 receptor, SGLT2","GPCR & G Protein","Swertisin is from a medicinal plant Enicostemma Littorale that acts as an antagonist of the adenosine A1 receptor and an inhibitor of SGLT2. It also exhibits anti-diabetic and antioxidant properties.",{"v":446.4,"d":"446.40"},"6991-10-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/swertisin.html","C22H22O10","free base","NA","COC1=C(C2OC(CO)C(O)C(O)C2O)C(=C3C(=O)C=C(OC3=C1)C4=CC=C(O)C=C4)O",0.244,4,6,4]
["E0927","Saikosaponin B3","f8","L1700-101","in 10mM DMSO","NOS, Interleukins, TNF-alpha, NF-κB, ROS","Immunology & Inflammation, Apoptosis, NF-κB","Saikosaponin B3 is isolated from the root of Bupleurum falcatum L, significantly reduce LPS-induced NO production, iNOS mRNA expression, and pro-inflammatory cytokine levels (IL-1β, IL-6, TNF-α). It also inhibited NF-κB activation and nuclear translocation while restoring mitochondrial integrity. It may be useful in research on reducing neuroinflammation-mediated neurodegeneration by suppressing NF-κB-mediated inflammatory pathways.",813.02,"58316-42-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/saikosaponin-b3.html","C43H72O14","free base","N/A","COC1C=C2C3CC(C)(C)CCC3(CO)C(O)CC2(C)C4(C)CCC5C(C)(CO)C(CCC5(C)C14)OC6OC(C)C(O)C(OC7OC(CO)C(O)C(O)C7O)C6O",0.788,5,9,8]
["E2008","7-Methoxyrosmanol","b10","L1700-101","in 10mM DMSO","PEPCK, G6Pase","Metabolism","7-Methoxyrosmanol is a phenolic diterpene extracted from rosemary that modulates the cAMP/PKA/CREB signaling pathway, which is essential for controlling gluconeogenesis in the liver. It suppresses the cAMP-induced activation of luciferase expression driven by the PEPCK-C and G6Pase gene promoters, which are vital for gluconeogenesis and leads to increased blood glucose levels in conditions such as type II diabetes.",{"v":360.4,"d":"360.40"},"113085-62-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/7-methoxyrosmanol.html","C21H28O5","Free base","7-O-Methylrosmanol","COC1C2OC(=O)C3(CCCC(C)(C)C23)C4=C(O)C(=C(C=C14)C(C)C)O",3.896,3,2,2]
["E2020","1-[2-Hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one","a11","L1700-101","in 10mM DMSO","SARS-CoV","Microbiology","1-[2-Hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-2-propen-1-one is a chalcone isolated from Psoralea corylifolia, inhibitor of severe acute respiratory syndrome coronavirus (SARS-CoV) papain-like protease (PLpro) activity, with an IC50 of 10.1 μM",{"v":338.4,"d":"338.40"},"20784-60-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/4-o-methylbavachalcone.html","C21H22O4","free base","4'-O-Methylbavachalcone","COC1=C(CC=C(C)C)C=C(C(=C1)O)C(=O)\\C=C\\C2=CC=C(O)C=C2",5.058,2,2,6]
["E2043","Atractyloside A","h11","L1700-101","in 10mM DMSO","influenza B virus, p38 MAPK","Microbiology, MAPK","Atractyloside A is a bioactive guaiane-type sesquiterpenoid glucoside isolated from Atractylodes lancea. It exhibits antiviral activity against the influenza B virus by inhibiting viral replication and suppressing the expression of essential viral proteins. It enhances gastrointestinal function through the modulation of the p38 MAPK pathway and plays nd plays a vital role in alleviating Spleen-Deficiency Syndrome (SDS) by enhancing gastrointestinal motility, promoting gut hormone secretion, and protecting the intestinal mucosal barrier.",{"v":448.5,"d":"448.50"},"126054-77-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/atractyloside-a.html","C21H36O10","Free base","NA","CC(C)(OC1OC(CO)C(O)C(O)C1O)C2CCC(O)(CO)C3CC(=O)C(C)(O)C3C2",-1.973,3,5,5]
["E2057","Methylnissolin","a3","L1700-102","in 10mM DMSO","ERK, PDGFR","MAPK, Protein Tyrosine Kinase","Methylnissolin is isolated from Astragalus membranaceus, an inhibitor of PDGF-BB-induced vascular smooth muscle cell proliferation and DNA synthesis with an IC50 of 10 µM. It inhibits PDGF-BB-induced phosphorylation of extracellular signal-regulated kinase 1/2 (ERIC1/2) mitogen-activated protein (MAP) kinase. It also inhibits PDGF-BB-induced vascular smooth muscle cell proliferation by inhibition of the ERK1/2 MAP kinase cascade.",300.31,"73340-41-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/methylnissolin.html","C17H16O5","free base","Astrapterocarpan","COC1=CC=C2C3COC4=CC(=CC=C4C3OC2=C1OC)O",2.666,4,1,2]
["E2094","Persicogenin","a5","L1700-102","in 10mM DMSO","Apoptosis","Apoptosis","Persicogenin is a flavanoned isolated from Rhus retinorrhoea acts as as an anti-mutagenic, anticancer, and anti-mycobacterial agent. It also induces concentration-dependent apoptosis in MCF-7, HeLa, and HT-29 cells.",{"v":316.3,"d":"316.30"},"28590-40-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/persicogenin.html","C17H16O6","Free Base","NA","COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC(=C(OC)C=C3)O)O",2.583,4,2,3]
["E2097","Furanodienone","d5","L1700-102","in 10mM DMSO","NOX4, PRDX1, MAPK/p53","Immunology & Inflammation, MAPK","Furanodienone is a biologically active sesquiterpene from Rhizome Curcumae that induces apoptosis in CRC cells through mitochondrial ROS generated by NOX4, leading to PRDX1 suppression and activation of the MAPKs/p53-mediated caspase-dependent signaling pathway.",{"v":230.3,"d":"230.30"},"24268-41-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/furanodienone.html","C15H18O2","Free Base","NA","N/A","N/A","N/A","N/A","N/A"]
["E2128","Corylifol A","c7","L1700-102","in 10mM DMSO","STAT3","JAK/STAT","Corylifol A is a flavonoid from Psoralea corylifolia that effectively inhibits IL-6-induced STAT3 activation and phosphorylation, with an IC50 of 0.81 µM. It also has potential for treating inflammatory diseases.",390.47,"775351-88-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/corylifol-a.html","C25H26O4","free base","Corylifol-A; Corylinin","CC(C)=CCC/C(C)=C/CC1=C(O)C=CC(=C1)C2=COC3=CC(=CC=C3C2=O)O",6.065,2,2,6]
["E2171","Senkyunolide H","h7","L1700-102","in 10mM DMSO","NF-κB, JNK, ERK","NF-κB, MAPK","Senkyunolide H is an active component from Ligusticum chuanxiong Hort that alleviates osteoclastogenesis and postmenopausal osteoporosis by inhibiting the NF-κB, JNK, and ERK signaling pathways.",224.25,"94596-27-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/senkyunolide-h.html","C12H16O4","Free Base","NA","CCC\\C=C\\1OC(=O)C2=C1CCC(O)C2O",1.316,2,2,2]
["E2205","Panasenoside","e9","L1700-102","in 10mM DMSO","alpha-glucosidase","Metabolism","Panasenoside is an acylated quercetin glycoside from Panax ginseng flower buds that inhibits alpha-glucosidase.",610.52,"31512-06-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/panasenoside.html","C27H30O16","Free Base","NA","OCC1OC(OC2C(O)C(O)C(CO)OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(O)C=C5)C(O)C(O)C1O",-1.804,6,10,7]
["E2216","Methyl caffeate","e10","L1700-102","in 10mM DMSO","Carbohydrate Metabolism, Antioxidant","Microbiology, Metabolism, Immunology & Inflammation","Methyl caffeate is a bioactive compound isolated from Solanum torvum Swartz. (Solanaceae) fruit, exhibits antimicrobial and antimycobacterial activities. It also shows α-glucosidase inhibition, oxidative stress reduction, anti-platelet effects, and anticancer activity in cervical, lung, and leukemia cell lines.",194.18,"3843-74-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/methyl-caffeate.html","C10H10O4","free base","N/A","COC(=O)C=CC1=CC(=C(O)C=C1)O",1.669,2,2,3]
["E2239","Methylophiopogonanone B","a2","L1700-103","in 10mM DMSO","Rho signaling","Cell Cycle","Methylophiopogonanone B is a homoisoflavonoid compound derived from Ophiopogon japonicus induces actin cytoskeletal reorganization, dendrite retraction and stress fiber formation by activating the Rho signaling pathway. It also induces microtubule destabilization and tubulin depolymerization.",{"v":328.4,"d":"328.40"},"74805-91-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/methylophiopogonanone-b.html","C19H20O5","Free Base","NA","COC1=CC=C(CC2COC3=C(C)C(=C(C)C(=C3C2=O)O)O)C=C1",{"v":3.91,"d":"3.910"},3,2,3]
["E2245","(-)-Zuonin A","d2","L1700-103","in 10mM DMSO","JNK","MAPK","(-)-Zuonin A is a potent small-molecule inhibitor of JNK, with IC₅₀ values of 1.7 μM for JNK1, 2.9 μM for JNK2, and 1.74 μM for JNK3. It also inhibits MKK4 and MKK7, preventing JNK phosphorylation and activation.",340.37,"84709-25-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/--zuonin-a.html","C20H20O5","free base","D-Epigalbacin","CC1C(C)C(OC1C2=CC=C3OCOC3=C2)C4=CC=C5OCOC5=C4",{"v":3.91,"d":"3.910"},5,0,2]
["E2300","8-Epidiosbulbin E acetate","d4","L1700-103","in 10mM DMSO","NA","Microbiology","8-Epidiosbulbin E acetate is a norditerpene isolated from Dioscorea bulbifera L. bulbs with broad-spectrum plasmid-curing activity against multidrug-resistant (MDR) bacteria. It effectively reverses antibiotic resistance by curing R-plasmids from clinical bacterial isolates.",388.41,"91095-48-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/8-epidiosbulbin-e-acetate.html","C21H24O7","free base","NA","CC(=O)OC1CC2C(=O)OC(CC2(C)C3CC4CC(C13)C(=O)O4)C5=COC=C5",1.695,7,0,3]
["E2306","Celosin H","f4","L1700-103","in 10mM DMSO","Others","Others","Celosin H is a triterpenoid saponin from Celosiae Semen, exhibits hepatoprotective properties. It helps protect the liver from damage.",957.06,"1623405-28-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/celosin-h.html","C47H72O20","free base","N/A","CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(OC6OC(C(O)C(OC7OCC(O)C(O)C7O)C6O)C(O)=O)C(C)(C=O)C5CCC34C)C2C1)C(=O)OC8OC(CO)C(O)C(O)C8O",{"v":-0.14,"d":"-0.140"},9,10,10]
["E2322","Dehydrocorydaline nitrate","g5","L1700-103","in 10mM DMSO","Trypanosoma cruzi, Plasmodium falciparum","Microbiology","Dehydrocorydaline nitrate is a protoberberine alkaloid that exhibits anti-parasitic activity against T. cruzi both in vitro and in vivo, with IC50 values of 3.47 μM for trypomastigotes and 4.98 μM for proliferative amastigotes. It also exhibits significant anti-malarial effects against Plasmodium falciparum, with IC50 values of < 50 nM for the 3D7 strain and < 200 nM for the Dd2 strain.",{"v":428.4,"d":"428.40"},"13005-09-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/dehydrocorydaline-nitrate-13-methylpalmatine-nitrate.html","C22H24N2O7","nitrate","13-Methylpalmatine nitrate","COC1=CC=C2C(=C3C4=CC(=C(OC)C=C4CC[N+]3=CC2=C1OC)OC)C.[O-][N](=O)=O",2.265,4,0,4]
["E2335","Dactylorhin A","c7","L1700-103","in 10mM DMSO","NOS","Immunology & Inflammation","Dactylorhin A is a glucoside isolated from Bletilla striata tubers. It acts as a moderate inhibitor of NO production in RAW 264.7 macrophages. It exhibits potential anti-inflammatory effects by suppressing macrophage activation.",888.86,"256459-34-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/dactylorhin-a.html","C40H56O22","free base","N/A","CC(C)CC(CC(=O)OCC1=CC=C(OC2OC(CO)C(O)C(O)C2O)C=C1)(OC3OC(CO)C(O)C(O)C3O)C(=O)OCC4=CC=C(OC5OC(CO)C(O)C(O)C5O)C=C4",-1.941,10,12,20]
["E2405","vexibinol","g8","L1700-103","in 10mM DMSO","Carbohydrate Metabolism, p38 MAPK, Caspase, Bcl-2","Metabolism, MAPK, Apoptosis","Vexibinol is a compound isolated from Sophora flavescens, an effective inhibitor of α-glucosidase and β-amylase. It exhibits anti-tumor and anti-inflammatory properties by promoting apoptosis in leukemia and breast adenocarcinoma cells through nuclear condensation, DNA fragmentation, ROS production, and activation of caspase-dependent pathways. Additionally, it suppresses cancer cell migration and invasion via MAPK pathway inhibition.",424.49,"97938-30-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/kushenol-f.html","C25H28O6","free base","Sophoraflavanone G, Kushenol F","CC(C)=CCC(CC1=C2OC(CC(=O)C2=C(O)C=C1O)C3=C(O)C=C(O)C=C3)C(C)=C",5.664,2,4,6]
["E2414","Sibiricaxanthone B","e9","L1700-103","in 10mM DMSO","NA","Neuronal Signaling","Sibiricaxanthone B is an active compound from Polygala–Acorus, strongly binds to EGFR and ALB, which are involved in brain development and cognitive function. It may contribute to the therapeutic effects of Polygala–Acorus in neurological disorders like ASD by modulating key signaling pathways.",538.45,"241125-81-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/sibiricaxanthone-b.html","C24H26O14","free base","NA","OCC1OC(C(OC2OCC(O)(CO)C2O)C(O)C1O)C3=C(O)C=C4OC5=CC=C(O)C=C5C(=O)C4=C3O",-1.562,5,8,5]
["E2450","AESCIN IB(SH)","c11","L1700-103","in 10mM DMSO","HIV Protease, TNF-alpha","Neuronal Signaling, Metabolism, Proteases,  Apoptosis, Immunology & Inflammation","AESCIN IB(SH) is a triterpenoid saponin isolated from Aesculus chinensis seeds, an inhibitor of HIV-1 protease with an IC₅₀ of 50 µM. It suppresses triple-negative breast cancer (TNBC) cell invasion by downregulating LOXL2, upregulating E-cadherin, and blocking TNF-α/TGF-β-induced migration of breast cancer cells. It also showed inhibitory effects on pancreatic lipase (PL) activity.",1131.26,"26339-90-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/escin-ib.html","C55H86O24","free base","Escin IB","C\\C=C(C)/C(=O)OC1C(OC(C)=O)C2(CO)C(O)CC3(C)C(=CCC4C5(C)CCC(OC6OC(C(OC7OC(CO)C(O)C(O)C7O)C(O)C6OC8OC(CO)C(O)C(O)C8O)C(O)=O)C(C)(CO)C5CCC34C)C2CC1(C)C",-0.723,11,12,16]
["E2457","Quercetin 3-gentiobioside","f11","L1700-103","in 10mM DMSO","aldose reductase, advanced glycation end-products","Metabolism","Quercetin-3-gentiobioside is a flavonoid glycoside that inhibits AR (aldose reductase) and AGEs (advanced glycation end-products) and exhibits antioxidant, anti-inflammatory, and antidiabetic properties.",{"v":626.5,"d":"626.50"},"7431-83-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/quercetin-3-o-beta-gentiobioside.html","C27H30O17","Free Base","NA","OCC1OC(OCC2OC(OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(O)C=C5)O)C(O)C(O)C2O)C(O)C(O)C1O",-2.046,6,11,7]
["E2537","N-trans-Feruloyltyramine","b3","L1700-104","in 10mM DMSO","Apoptosis, antioxidant, anti-inflammation","Apoptosis, Immunology & Inflammation","N-trans-Feruloyltyramine is an alkaloid found in Polyalthia suberosa, Tinospora tuberculata, Polygonum sachalinensis, and Allium sativum. It exhibits antioxidant, anti-inflammation and anti-cancer effects. It improves H2O2-induced intracellular ROS generation and decreases apoptosis.",{"v":313.3,"d":"313.30"},"66648-43-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/n-trans-feruloyltyramine.html","C18H19NO4","Free Base","Moupinamide","COC1=C(O)C=CC(=C1)\\C=C\\C(=O)NCCC2=CC=C(O)C=C2",{"v":2.91,"d":"2.910"},2,3,6]
["E2562","14-Deoxyandrographolide","b4","L1700-104","in 10mM DMSO","TNF-alpha, Calcium Channel","Apoptosis, Transmembrane Transporters","14-Deoxyandrographolide is a diterpene extracted from Andrographis paniculata, exhibits calcium channel-blocking activity and acts as a uterine smooth muscle relaxant. It also desensitizes hepatocytes to TNF-α-mediated apoptosis by inducing TNFRSF1A release.",334.45,"4176-97-0","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/14-deoxyandrographolide.html","C20H30O4","free base","N/A","CC1(CO)C(O)CCC2(C)C(CCC3=CCOC3=O)C(=C)CCC12",3.023,2,2,4]
["E2596","N-​Benzyllinolenamide","a5","L1700-104","in 10mM DMSO","FAAH","Metabolism","N-Benzyllinolenamide is a natural macamide extracted from Lepidium meyenii, an inhibitor of fatty acid amide hydrolase (FAAH). It exhibits an IC50 of 41.8 μM, suggesting potential regulatory effects on lipid signaling.",367.57,"883715-18-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/n-​benzyllinolenamide.html","C25H37NO","free base","N/A","CC\\C=C/C/C=C\\C\\C=C/CCCCCCCC(=O)NCC1=CC=CC=C1",7.133,1,1,15]
["E2715","Polygalaxanthone XI","e6","L1700-104","in 10mM DMSO","anti-inflammatory","Immunology & Inflammation","Polygalaxanthone XI is a bioactive compound found in P. tenuifolia root with anti-inflammatory, antioxidant, anticancer, and neuroprotective effects.",568.48,"857859-82-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/polygalaxanthone-xi.html","C25H28O15","Free Base","NA","COC1=C(O)C=C2OC3=CC(=C(C4OC(CO)C(O)C(O)C4OC5OCC(O)(CO)C5O)C(=C3C(=O)C2=C1)O)O",-1.579,6,8,6]
["E2737","Theaflavin-3-gallate","c7","L1700-104","in 10mM DMSO","singlet oxygen, hydrogen peroxide, superoxide, hydroxide radicals","Immunology & Inflammation","Theaflavin-3-gallate is a polyphenolic flavonoid found in black tea (C. sinensis) and effectively scavenges singlet oxygen, hydrogen peroxide, superoxide, and hydroxide radicals, with IC50 values of 0.86, 0.45, 21.7, and 32.49 µM, respectively.",{"v":716.6,"d":"716.60"},"30462-34-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/theaflavin-3-gallate.html","C36H28O16","Free Base","NA","OC1CC2=C(O)C=C(O)C=C2OC1C3=C4C=C(C=C(O)C(=O)C4=C(O)C(=C3)O)C5OC6=CC(=CC(=C6CC5OC(=O)C7=CC(=C(O)C(=C7)O)O)O)O",3.947,5,11,5]
["E5010","3-HYDROXY-3-METHYLGLUTARIC ACID","a9","L1700-104","in 10mM DMSO","HMG-CoA Reductase","Metabolism","3-HYDROXY-3-METHYLGLUTARIC ACID induces lipid peroxidation, oxidative protein damage, and reduces antioxidant defenses in the rat cerebral cortex. It is a competitive inhibitor of HMG-CoA reductase (HMGCoAR) and  strongly suppresses cholesterol biosynthesis and helps reduce bile cholesterol supersaturation and hypercholesterolemia.",162.14,"503-49-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/3-hydroxy-3-methylglutaric-acid.html","C6H10O5","free base","MEGLUTOL","CC(O)(CC(O)=O)CC(O)=O",-0.665,2,0,4]
["E5078","Forsythoside E","e10","L1700-104","in 10mM DMSO","AChR, BChE","Neuronal Signaling","Forsythoside E is a caffeoyl phenylethanoid glycoside from Forsythia suspensa fruits, an inhibitor of cholinesterase activity. It exhibits IC50 values of 1.08 mM for acetylcholinesterase (AChE) and 0.92 mM for butyrylcholinesterase (BChE).",462.45,"93675-88-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/forsythoside-e.html","C20H30O12","free base","N/A","CC1OC(OCC2OC(OCCC3=CC(=C(O)C=C3)O)C(O)C(O)C2O)C(O)C(O)C1O",-1.543,4,8,7]
["E5094","Erythrodiol","h10","L1700-104","in 10mM DMSO","Caspase","Apoptosis","Erythrodiol is a precursor of pentacyclic triterpenic acids in Olea europaea, promotes ChE production by stabilizing ABCA1. It inhibits human colorectal carcinoma cell growth with an EC50 of 48.8 µM, increases caspase-3-like activity, and exhibits antiproliferative and proapoptotic effects, making it a potential candidate for atherosclerosis therapy or prevention.",442.72,"545-48-2","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/erythrodiol.html","C30H50O2","free base","N/A","CC1(C)CCC2(CO)CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC34C)C2C1",6.213,0,2,1]
["E5122","Obtucarbamate A","b2","L1700-105","in 10mM DMSO","others","Others","Obtucarbamate A is extracted from Disporum cantoniense. It exhibits potent antitussive activity.",238.24,"6935-99-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/obtucarbamate-a.html","C11H14N2O4","free base","N/A","COC(=O)NC1=CC=C(C)C(=C1)NC(=O)OC",1.843,4,2,4]
["E5163","Glucovanillin","d3","L1700-105","in 10mM DMSO","Lipase","Metabolism","Glucovanilli is extracted from natural sources as Acinetobacter radioresistens, is a potent inhibitor of lipase with an IC50 of 13 mM. It has potential therapeutic applications in managing lipase-related diseases.",314.29,"494-08-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/glucovanillin.html","C14H18O8","free base","N/A","COC1=C(OC2OC(CO)C(O)C(O)C2O)C=CC(=C1)C=O",-0.599,4,4,5]
["E5182","Prosaikogenin D","c4","L1700-105","in 10mM DMSO","Apoptosis related","Apoptosis","Prosaikogenin D is a saponin isolated from the roots of Bupleurum bicaule (Apiaceae), exhibits potent anticancer activity. It targets cancer cell proliferation and survival pathways.",618.84,"103629-72-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/prosaikogenin-d.html","C36H58O8","free base","N/A","CC1OC(OC2CCC3(C)C(CCC4(C)C3C=CC5=C6CC(C)(C)CCC6(CO)C(O)CC45C)C2(C)CO)C(O)C(O)C1O",2.911,2,6,4]
["E5215","Pro-xylane","g5","L1700-105","in 10mM DMSO","Others","Others","Pro-xylane is a biologically active C-glycoside an activator of glycosaminoglycan (GAG) biosynthesis, promoting skin hydration and firmness. It has otent anti-aging properties, is biodegradable, eco-friendly, and widely used in cosmetic research.",192.21,"439685-79-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/pro-xylane.html","C8H16O5","free base","Hydroxypropyl tetrahydropyrantriol","CC(O)CC1OCC(O)C(O)C1O",-1.734,1,4,2]
["E5273","Eupalinolide A","d7","L1700-105","in 10mM DMSO","HSF1, tyrosinase","Metabolism, Proteases","Eupalinolide A is a sesquiterpene lactone from Eupatorium lindleyanum that induces HSP70 expression by interacting with HSP90, activating HSF1. It also suppresses melanin production in mouse melanoma cells under UVB-stimulated conditions by downregulating tyrosinase activity and expression.",462.49,"877822-40-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/eupalinolide-a.html","C24H30O9","Free Base","NA","N/A","N/A","N/A","N/A","N/A"]
["E5335","Beta-Eudesmol","c8","L1700-105","in 10mM DMSO","nAChR","Neuronal Signaling","Beta-Eudesmol is an uncharged alcohol found in Arractylodes lancea that blocks the nicotinic ACh receptor channel in open and closed conformations and accelerates the desensitization of the nicotinic ACh receptor. It can induce apoptosis and exhibit anti-inflammatory activities.",222.37,"473-15-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/beta-eudesmol.html","C15H26O","Free Base","NA","CC(C)(O)C1CCC2(C)CCCC(=C)C2C1",3.719,0,0,1]
["E5397","Puerarin 6''-O-Xyloside","g9","L1700-105","in 10mM DMSO","Apoptosis","Apoptosis","Puerarin 6″-O-xyloside is a bioactive flavonoid glycoside isolated from Pueraria lobata (Leguminosae) that exhibits potent antitumor activity against lung carcinoma by inducing apoptosis through caspase activation and Bax/Bcl-2 modulation.",548.49,"114240-18-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/puerarin-6-o-xyloside.html","C26H28O13","free base","NA","OC1COC(OCC2OC(C(O)C(O)C2O)C3=C4OC=C(C(=O)C4=CC=C3O)C5=CC=C(O)C=C5)C(O)C1O",-1.245,5,8,5]
["E5423","Iristectorin B","f10","L1700-105","in 10mM DMSO","ferroptosis","Metabolism","Iristectorin B is a natural isoflavone derived from Dried Shoot that protects against acute stroke-induced neuronal death by inhibiting ferroptosis.",492.43,"94396-09-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/iristectorin-b.html","C23H24O12","free base","NA","COC1=C(O)C=CC(=C1)C2=COC3=CC(=C(OC)C(=C3C2=O)O)OC4OC(CO)C(O)C(O)C4O",0.178,6,6,6]
["E5477","Qingyangshengenin A","c2","L1700-106","in 10mM DMSO","antiepileptic","Neuronal Signaling","Qingyangshengenin A is a C21 steroidal constituent isolated from the roots of Cynanchum otophyllum Schneid, exhibits antiepileptic activity and protects rats from audiogenic seizures.",{"v":933.1,"d":"933.10"},"106644-33-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/qingyangshengenin-a.html","C49H72O17","Free Base","NA","COC1CC(OC(C)C1O)OC2C(C)OC(CC2OC)OC3C(C)OC(CC3OC)OC4CCC5(C)C6CC(OC(=O)C7=CC=C(O)C=C7)C8(C)C(O)(CCC8(O)C6(O)CC=C5C4)C(C)=O",2.577,12,2,13]
["E5491","Notoginsenoside R2","f2","L1700-106","in 10mM DMSO","Apoptosis, c-Src","Apoptosis, Angiogenesis","Notoginsenoside R2 is a crucial active saponin in Panax notoginseng (Burk.) F. H. Chen exerts neuroprotective effects by reducing oxidative stress and inhibiting cell apoptosis. It ameliorates mitochondrial dysfunction and delays the progression of diabetic nephropathy (DN) partly through suppression of c-Src.",{"v":771,"d":"771.00"},"80418-25-3","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/notoginsenoside-r2.html","C41H70O13","Free Base","Ginsenoside Ng-R2","CC(C)=CCCC(C)(O)C1CCC2(C)C1C(O)CC3C4(C)CCC(O)C(C)(C)C4C(CC23C)OC5OC(CO)C(O)C(O)C5OC6OCC(O)C(O)C6O",1.637,4,8,9]
["E5559","Loganetin","c4","L1700-106","in 10mM DMSO","TLR4","Immunology & Inflammation","Loganetin, an iridoid monoterpenoid from cornus fruits, is a potential antagonist of TLR4 with EC50 of 25.4 nM, that regulates TLR4-related proteins and demonstrates anti-inflammatory and anti-apoptotic effects. It improves acute kidney injury (AKI) by inhibiting TLR4 and blocking the JNK/p38 pathway, with the potential to treat AKI.",228.24,"29748-10-5","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/loganetin.html","C11H16O5","Free Base","NA","COC(=O)C1=COC(O)C2C(C)C(O)CC12",-0.148,3,1,2]
["E5579","Asatone","b5","L1700-106","in 10mM DMSO","NF-κB, p38 MAPK, ERK, JNK","NF-κB, MAPK","Asatone is an active component isolated from Radix et Rhizoma Asari, with anti-inflammatory effect via activation of NF-κB and donwn regulation of p-MAPK (ERK, JNK and p38) pathways.",448.51,"38451-63-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/asatone.html","C24H32O8","free base","N/A","COC1=CC2(CC=C)C(C3C(=CC2(OC)C(=O)C3(OC)OC)CC=C)C(OC)(OC)C1=O",1.372,8,0,10]
["E5599","Euphorbia factor L7a","f6","L1700-106","in 10mM DMSO","Bacterial, Anti-infection, Antiviral, Immunology & Inflammation related, Antioxidant","Microbiology, Immunology & Inflammation","Euphorbia factor L7a is a diterpenoid isolated from Euphorbia lathyris (Caper spurge) exhibits anti-Multidrug resistance(MDR) properties by increasing anticancer drug accumulation and enhancing cytotoxicity in cancer cells. It also exhibits diuretic, anti-inflammatory, antiviral, anticancer, antioxidant, hepatoprotective, and neuroprotective activities.",548.67,"93550-94-8","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/euphorbia-factor-l7a.html","C33H40O7","free base","N/A","N/A","N/A","N/A","N/A","N/A"]
["E5614","Kaempferol 3-O-β-D-galactopyranoside","e7","L1700-106","in 10mM DMSO","PI3K, Akt, HIF, Caspase","PI3K/Akt/mTOR, Angiogenesis, Epigenetics, Apoptosis","Kaempferol 3-O-β-D-galactopyranoside is a galactose-conjugated flavonol with antifungal, anticancer, and cardioprotective effects. It regulates apoptosis through MAPK, PI3K/AKT, and HIF-1 signaling pathways, inducing mitochondrial outer membrane permeabilization (MOMP) and activating both death receptor-dependent and mitochondria-dependent apoptotic pathways, making it a potential therapeutic agent for human lung cancer.",448.38,"23627-87-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/kaempferol-3-o-beta-d-galactopyranoside.html","C21H20O11","free base","Trifolin","OCC1OC(OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(O)C=C4)C(O)C(O)C1O",-0.058,4,7,4]
["E5630","Rupestonic acid","d8","L1700-106","in 10mM DMSO","Influenza Virus","Microbiology","Rupestonic acid is a sesquiterpene isolated from Artemisia rupestris L., exhibits strong anti-influenza activity. It possesses multifunctional groups and shows high effectiveness against influenza virus B.",248.32,"115473-63-7","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/rupestonic-acid.html","C15H20O3","free base","N/A","CC1CCC(CC2=C(C)C(=O)CC12)C(=C)C(O)=O",3.135,2,0,2]
["E5720","Isocurcumenol","a10","L1700-106","in 10mM DMSO","Erα","Endocrinology & Hormones","Isocurcumenol is a sesquiterpenoid compound isolated from the rhizomes of Curcuma zedoaria (white turmeric) with anti-inflammatory, anticancer, and antioxidant effects. It inhibits activity against Estrogen Receptor α (ERα), with a binding affinity of 0.584 M.",234.33,"24063-71-6","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/isocurcumenol.html","C15H22O2","Free Base","NA","CC1CCC2C(=C)CC3(O)OC12CC3=C(C)C",2.928,1,0,0]
["S0703","DELTALINE","e11","L1700-106","in 10mM DMSO","Others","Others","DELTALINE is a diterpenoid alkaloid isolated from Delphinium delavayi Franch. It has analgesic properties and is used to treat rheumatic pain, stroke-related paralysis, and rheumatoid arthritis.",507.62,"6836-11-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/deltaline.html","C27H41NO8","free base","N/A","CCN1CC2(C)CCC(OC)C34C2C(OC(C)=O)C5(OCOC56CC(OC)C7CC3(O)C6C7OC)C14",-0.734,7,0,6]
["S0905","(-)-Syringaresnol-4-O-β-D-apiofuranosyl-(1→2)-β-D-glucopyranoside","h11","L1700-106","in 10mM DMSO","NA","NA","(-)-Syringaresnol-4-O-β-D-apiofuranosyl-(1→2)-β-D-glucopyranoside is a natural compound extracted from the bark of Albizia julibrissin.",712.69,"136997-64-3","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/syringaresnol-4-o-beta-d-apiofuranosy.html","C33H44O17","free base","NA","COC1=C(O)C(=CC(=C1)C2OCC3C2COC3C4=CC(=C(OC5OC(CO)C(O)C(O)C5OC6OCC(O)(CO)C6O)C(=C4)OC)OC)OC",-1.188,10,6,12]
["S0932","Baimaside","c3","L1700-107","in 10mM DMSO","ChAT, AChE, Ach","Neuronal Signaling","Baimaside is a flavonoid from Hibiscus rosa-sinensis, which exhibits neuroprotective effects by improving memory and preventing neuronal loss in SCOP-induced Alzheimer's mice through increasing ChAT levels, reducing AChE activity, and subsequently increasing ACh levels in the hippocampal CA1 region.",{"v":626.5,"d":"626.50"},"18609-17-1","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/quercetin-3-o-sophoroside.html","C27H30O17","Free Base","Quercetin-3-O-sophoroside","OCC1OC(OC2C(O)C(O)C(CO)OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(O)C=C5)O)C(O)C(O)C1O",-2.046,6,11,7]
["S0952","Benzoylhypaconine","d4","L1700-107","in 10mM DMSO","COX-2","Immunology & Inflammation","Benzoylhypaconine is a monoester diterpene alkaloid found in Aconitum that exhibits anti-inflammatory activity. It also inhibits COX-2 activity with an IC50 of 20.5 µM in a cell-free assay.",573.67,"63238-66-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/benzoylhypaconine.html","C31H43NO9","Free Base","Benzoylhypacoitine","COCC12CCC(OC)C34C5CC6(O)C(OC)C(O)C(O)(C5C6OC(=O)C7=CC=CC=C7)C(C(OC)C13)C4N(C)C2",-0.481,6,1,8]
["S0961","Isopsoralenoside","c5","L1700-107","in 10mM DMSO","anti-inflammatory","Immunology & Inflammation","Isopsoralenoside is a benzofuran glycoside isolated from the fruits of Psoralea corylifolia with anti-inflammatory, antioxidant, anticancer, and immunomodulatory effects.",{"v":366.3,"d":"366.30"},"905954-18-9","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/isopsoralenoside.html","C17H18O9","Free Base","NA","OCC1OC(OC2=C3C=COC3=CC=C2\\C=C/C(O)=O)C(O)C(O)C1O",0.059,4,4,5]
["S5470","(Z)-Ligustilide","h6","L1700-107","in 10mM DMSO","Estrogen/progestogen Receptor","Endocrinology & Hormones, Metabolism","(Z)-Ligustilide is extracted from Ligusticum chuanxiong Hort, is a bioactive compound with antimicrobial and antifungal properties. It also inhibits fatty acid uptake and esterification, making it a potential therapeutic for NAFLD, while exhibiting epigenetic regulation and ERα reactivation in tamoxifen-resistant breast cancer.",190.24,"81944-09-4","N/A",">10","N/A","N/A","https://www.selleckchem.com/products/z-ligustilide.html","C12H14O2","free base","N/A","CCC\\C=C\\1OC(=O)C2=C1CCC=C2",2.941,2,0,2]
["S1135","Pemetrexed (LY-231514) disodium","c2","L1700-108","in 10mM Water","Apoptosis related,Autophagy,DHFR,DNA/RNA Synthesis,Thymidylate Synthase","Metabolism","Pemetrexed (LY-231514) disodium is a novel antifolate and antimetabolite for TS, DHFR and GARFT with Ki of 1.3 nM, 7.2 nM and 65 nM in cell-free assays, respectively. Pemetrexed induces autophagy and apoptosis.",471.37,"150399-23-8","<1","N/A",{"v":94,"d":"94.00"},199.42,"http://selleckchem.com/products/Pemetrexed-disodium.html","C20H19N5Na2O6","Disodium salt","LY-231514 disodium","[Na+].[Na+].NC1=NC(=O)C2=C([NH]C=C2CCC3=CC=C(C=C3)C(=O)NC(CCC([O-])=O)C([O-])=O)N1",-1.804,3,4,9]
["S1375","Dorzolamide HCl","b3","L1700-108","in 10mM Water","Carbonic Anhydrase","Metabolism","Dorzolamide (MK-507, L-671152) HCl is a water-soluble, potent inhibitor of human carbonic anhydrase II and IV with Ki of 1.9 nM and 31 nM, respectively, used as anti-glaucoma agent.",{"v":360.9,"d":"360.90"},"130693-82-2","<1","N/A",{"v":14,"d":"14.00"},38.79,"http://selleckchem.com/products/Dorzolamide-HCL.html","C10H16N2O4S3.HCl","Hydrochloride","MK-507 (L-671152) HCl","Cl.CCNC1CC(C)[S](=O)(=O)C2=C1C=C(S2)[S](N)(=O)=O",0.527,4,2,3]
["S1749","L-Glutamine","f4","L1700-108","in 10mM Water","Others","Others","L-Glutamine (Gln) is one of the 20 amino acids encoded by the standard genetic code and also a major respiratory fuel and substrate for nucleic acid synthesis in mammalian intestinal cells.",146.14,"56-85-9","<1","N/A",{"v":29,"d":"29.00"},198.44,"http://selleckchem.com/products/Glutamine.html","C5H10N2O3","free base","N/A","NC(CCC(N)=O)C(O)=O",-4.087,2,2,4]
["S1853","Penicillamine","h4","L1700-108","in 10mM Water","Others","Others","Penicillamine (Dimethyl Cysteine) is used as an antirheumatic and as a chelating agent in Wilson’s disease.",149.21,"52-67-5","<1","N/A",{"v":30,"d":"30.00"},201.06,"http://selleckchem.com/products/Penicillamine(Cuprimine).html","C5H11NO2S","free base","Dimethyl Cysteine","CC(C)(S)C(N)C(O)=O",-2.496,1,1,2]
["S1999","Sodium butyrate","a6","L1700-108","in 10mM Water","Apoptosis related,Autophagy,HDAC","Epigenetics","Sodium butyrate (NaB, Butanoic acid sodium salt), sodium salt of butyric acid, is a histone deacetylase inhibitor and competitively binds to the zinc sites of class I and II histone deacetylases (HDACs). Sodium butyrate (NaB) inhibits cell cycle progression, promotes differentiation, and induces apoptosis and autophagy in several types of cancer cells.",110.09,"156-54-7","<1","N/A",{"v":22,"d":"22.00"},199.84,"http://selleckchem.com/products/Sodium-butyrate.html","C4H7NaO2","Sodium Salt","NaB, Butanoic acid sodium salt","[Na+].CCCC([O-])=O",-0.556,0,0,2]
["S2507","Salbutamol Sulfate","e7","L1700-108","in 10mM Water","Adrenergic Receptor","Neuronal Signaling","Salbutamol Sulfate (Albuterol, Ventolin, Aerolin, Ventorlin, Asthalin, Asthavent) is a short-acting β2-adrenergic receptor agonist with an IC50 of 8.93 µM.",337.39,"51022-70-9","<1","N/A",{"v":68,"d":"68.00"},201.55,"http://selleckchem.com/products/Salbutamol-sulfate(Albuterol).html","C13H21NO3.H2SO4","Sulfate","Albuterol, Ventolin, Aerolin, Ventorlin, Asthalin, Asthavent","CC(C)(C)NCC(O)C1=CC=C(O)C(=C1)CO.O[S](O)(=O)=O",0.334,0,4,5]
["S2568","Neomycin sulfate","d8","L1700-108","in 10mM Water","Antibiotics,Antibiotics for Mammalian Cell Culture,Antineoplastic and Immunosuppressive Antibiotics,Bacterial,Selection Antibiotics for Transfected Cell","Microbiology","Neomycin sulfate(Framycin sulfate) is an aminoglycoside antibiotic, used to treat bacteria infections.",712.72,"28002-70-2 ,1405-10-3","<1","N/A",{"v":143,"d":"143.00"},200.64,"http://selleckchem.com/products/Neomycin-sulfate.html","C23H46N6O13.H2SO4","Sulfate","Framycin sulfate","NCC1OC(OC2C(N)CC(N)C(O)C2OC3OC(CO)C(OC4OC(CN)C(O)C(O)C4N)C3O)C(N)C(O)C1O.O[S](O)(=O)=O",-9.566,6,13,9]
["S3056","Miltefosine","g9","L1700-108","in 10mM Water","Akt","PI3K/Akt/mTOR","Miltefosine (Hexadecylphosphocholine) inhibits PI3K/Akt activity with ED50 of 17.2 μM and 8.1 μM in carcinoma cell lines A431 and HeLa, first oral drug for Visceral leishmaniasis, effective against both promastigotes and amastigotes.",407.57,"58066-85-6","<1","N/A",{"v":81,"d":"81.00"},198.74,"http://selleckchem.com/products/miltefosine-hexadecylphosphocholine.html","C21H46NO4P","free base","Hexadecylphosphocholine","CCCCCCCCCCCCCCCCO[P]([O-])(=O)OCC[N+](C)(C)C",3.722,2,0,20]
["S3642","Cesium chloride","e11","L1700-108","in 10mM Water","Others","Others","Cesium chloride (CsCl) is the inorganic compound. It is widely used medicine structure in isopycnic centrifugation for separating various types of DNA and is a reagent in analytical chemistry.",168.36,"7647-17-8","<1","N/A",{"v":33,"d":"33.00"},196.01,"http://selleckchem.com/products/cesium-chloride.html","CsCl","inorganic salt","CsCl","Cl[Cs]",0.485,0,0,0]
["S3752","isoleucine","d2","L1700-109","in 10mM Water","Others","Others","Isoleucine (Ile) is a non-polar, uncharged (at physiological pH), aliphatic amino acid that is used in the biosynthesis of proteins.",131.17,"73-32-5","<1","N/A",{"v":26,"d":"26.00"},198.22,"http://selleckchem.com/products/isoleucine.html","C6H13NO2","free base","Ile","CCC(C)C(N)C(O)=O",{"v":0,"d":"0.000"},0,0,0]
["S3973","L-SelenoMethionine","d3","L1700-109","in 10mM Water","ROS","Immunology & Inflammation","L-SelenoMethionine (SeMet), a naturally occurring amino acid, is a major food-form of selenium. It has been used as a supplement, and exhibits some important functions like cancer prevention and antioxidative defense.",196.11,"3211-76-5","<1","N/A",{"v":39,"d":"39.00"},198.87,"http://selleckchem.com/products/l-selenomethionine.html","C5H11NO2Se","free base","N/A","C[Se]CCC(N)C(O)=O",{"v":0,"d":"0.000"},0,0,0]
["S4052","Netilmicin Sulfate","d4","L1700-109","in 10mM Water","Antibiotics,Antineoplastic and Immunosuppressive Antibiotics","Microbiology","Netilmicin Sulfate is a member of the aminoglycoside family of antibiotics.",1441.55,"56391-57-2","<1","N/A",{"v":288,"d":"288.00"},199.78,"http://selleckchem.com/products/netilmicin-sulfate.html","C21H41N5O7.2.5H2SO4","Sulfate","N/A","CCNC1CC(N)C(OC2OC(=CCC2N)CN)C(O)C1OC3OCC(C)(O)C(NC)C3O.CCNC4CC(N)C(OC5OC(=CCC5N)CN)C(O)C4OC6OCC(C)(O)C(NC)C6O.O[S](O)(=O)=O.O[S](O)(=O)=O.O[S](O)(=O)=O.O[S](O)(=O)=O.O[S](O)(=O)=O",-10.844,8,14,16]
["S4127","Terbutaline Sulfate","c5","L1700-109","in 10mM Water","Adrenergic Receptor","GPCR & G Protein","Terbutaline Sulfate(Terbutaline hemisulfate) is a selective β2-adrenergic receptor agonist with IC50 of 53 nM.",548.65,"23031-32-5","<1","N/A",{"v":100,"d":"100.00"},182.27,"http://selleckchem.com/products/terbutaline-sulfate.html","C24H38N2O6.H2SO4","Sulfate","Terbutaline hemisulfate","CC(C)(C)NCC(O)C1=CC(=CC(=C1)O)O.CC(C)(C)NCC(O)C2=CC(=CC(=C2)O)O.O[S](O)(=O)=O",2.001,0,8,8]
["S4236","Proflavine Hemisulfate","g6","L1700-109","in 10mM Water","Anti-infection,DNA/RNA Synthesis","Microbiology","Proflavine Hemisulfate is a topical antiseptic by interchelating DNA, thereby disrupting DNA synthesis and leading to high levels of mutation in the copied DNA strands.",258.25,"1811-28-5","<1","N/A",{"v":22,"d":"22.00"},85.19,"http://selleckchem.com/products/proflavine-hemisulfate.html","C13H11N3.1/2H2SO4","Sulfate","N/A","NC1=CC=C2C=C3C=CC(=CC3=NC2=C1)N.NC4=CC=C5C=C6C=CC(=CC6=NC5=C4)N.O[S](O)(=O)=O",3.113,2,4,0]
["S4523","Dihydrostreptomycin sulfate","c8","L1700-109","in 10mM Water","Antibiotics,Antibiotics for Mammalian Cell Culture,Bacterial,Selection Antibiotics for Transfected Cell","Microbiology","Dihydrostreptomycin sulfate is an aminoglycoside antibiotic, used to treat bacterial diseases in cattle, pigs and sheep. Dihydrostreptomycin is a derivative of streptomycin.",1461.42,"5490-27-7","<1","N/A",{"v":100,"d":"100.00"},68.43,"http://selleckchem.com/products/dihydrostreptomycin-sulfate.html","2C21H41N7O12.3H2SO4","Sulfate","N/A","CNC1C(O)C(O)C(CO)OC1OC2C(OC(C)C2(O)CO)OC3C(O)C(O)C(NC(N)=N)C(O)C3NC(N)=N.CNC4C(O)C(O)C(CO)OC4OC5C(OC(C)C5(O)CO)OC6C(O)C(O)C(NC(N)=N)C(O)C6NC(N)=N.O[S](O)(=O)=O.O[S](O)(=O)=O.O[S](O)(=O)=O",-14.916,8,24,22]
["S4671","Cefradine","c9","L1700-109","in 10mM Water","Antibiotics","Microbiology","Cefradine (Cephradine, Sefril, Anspor, Velosef) is a semi-synthetic cephalosporin antibiotic.",{"v":349.4,"d":"349.40"},"38821-53-3","<1","N/A",{"v":10,"d":"10.00"},28.62,"http://selleckchem.com/products/cefradine.html","C16H19N3O4S","free base","Cephradine, Sefril, Anspor, Cephradin, Velosef","CC1=C(N2C(SC1)C(NC(=O)C(N)C3=CCC=CC3)C2=O)C(O)=O",-2.277,3,2,4]
["S4811","VitaMin U","g10","L1700-109","in 10mM Water","Vitamin","Metabolism","Vitamin U (Methylmethioninesulfonium Chloride, Cabagin-U, Smethylmethionine) is a vitamin found in green vegetables. It is used in the treatment of peptic ulcers, colitis, and gastritis and has an effect on secretory, acid-forming, and enzymatic functions of the intestinal tract.",{"v":199.7,"d":"199.70"},"3493-12-7","<1","N/A",{"v":39,"d":"39.00"},195.29,"http://selleckchem.com/products/vitamin-u.html","C6H14NO2.Cl","chloride","Methylmethioninesulfonium Chloride, Cabagin-U, Smethylmethionine","[Cl-].C[S+](C)CCC(N)C(O)=O",{"v":0,"d":"0.000"},0,0,0]
["S4993","Timonacic","f11","L1700-109","in 10mM Water","Others","Others","Timonacic (Thiazolidine-4-carboxylic acid, Detoxepa, Hepalidine, 1,3-Thiazolidine-4-carboxylic acid) is a cyclic sulfur amino acid derivative with potential antineoplastic and antioxidant activities.",133.17,"444-27-9",{"v":1,"d":"1.00"},7.51,{"v":27,"d":"27.00"},202.75,"http://www.selleckchem.com/products/timonacic.html","C4H7NO2S","Free Base","Thiazolidine-4-carboxylic acid, Detoxepa, Hepalidine, 1,3-Thiazolidine-4-carboxylic acid","OC(=O)C1CSCN1",-2.889,1,1,1]
["S5124","DL-Citrulline","d2","L1700-110","in 10mM Water","Others","Others","L-Citrulline (Citrulline, Cit) is a naturally occurring nonessential amino acid which is the key intermediate in the urea cycle.",175.19,"627-77-0","<1","N/A",{"v":35,"d":"35.00"},199.78,"http://selleckchem.com/products/dl-citrulline.html","C6H13N3O3","free base","Citrulline","NC(CCCNC(N)=O)C(O)=O",{"v":0,"d":"0.000"},0,0,0]
["S5374","5'-Cytidylic acid","b4","L1700-110","in 10mM Water","DNA/RNA Synthesis","DNA Damage/DNA Repair","5'-Cytidylic acid (Cytidine monophosphate, Cytidine 5'-phosphate) is a nucleotide that is used as a monomer in RNA.",{"v":323.2,"d":"323.20"},"63-37-6","<1","N/A",{"v":64,"d":"64.00"},198.02,"http://selleckchem.com/products/5-cytidylic-acid.html","C9H14N3O8P","free base","Cytidine monophosphate, Cytidine 5'-phosphate","NC1=NC(=O)N(C=C1)C2OC(CO[P](O)(O)=O)C(O)C2O",-2.468,4,3,4]
["S5431","L-Homoarginine hydrochloride","e4","L1700-110","in 10mM Water","phosphatase","Metabolism","L-Homoarginine is a specific inhibitor of liver-type alkaline phosphatase.",224.69,"1483-01-8","<1","N/A",{"v":44,"d":"44.00"},195.83,"http://selleckchem.com/products/l-homoarginine-hydrochloride.html","C7H16N4O2.HCl","hydrochloride","N/A","Cl.NC(CCCCNC(N)=N)C(O)=O",-2.992,1,3,7]
["S5584","Citronellol","a6","L1700-110","in 10mM Water","Apoptosis related,Caspase,RIP kinase,ROS,TNF-alpha","Apoptosis","Citronellol (Dihydrogeraniol, (±)-β-Citronellol), a constituent of rose and geranium oils, is used in perfumes and insect repellents. Citronellol can cause necrotic apoptosis of NCI-H1299 cells by up-regulating TNF-α, RIP1 / RIP3 activities, and down-regulating caspase-3 / caspase-8 activities. Citronellol also results in a biphasic increase in ROS production at 1 h and at 12 h in NCI-H1299 cells.",156.27,"106-22-9","<1","N/A",{"v":31,"d":"31.00"},198.37,"http://selleckchem.com/products/citronellol.html","C10H20O","free base","Dihydrogeraniol, (±)-β-Citronellol","CC(CCO)CCC=C(C)C",3.049,0,1,5]
["S5632","L-aspartic Acid","a7","L1700-110","in 10mM Water","Others","Others","L-aspartic Acid is one of non-essential amino acids and may be a neurotransmitter.",{"v":133.1,"d":"133.10"},"56-84-8","<1","N/A",{"v":8,"d":"8.00"},60.11,"http://selleckchem.com/products/l-aspartic-acid.html","C4H7NO4","free base","N/A","NC(CC(O)=O)C(O)=O",{"v":-3.78,"d":"-3.780"},2,1,3]
["S5867","Bendazac L-lysine","e8","L1700-110","in 10mM Water","Others","Others","Bendazac L-lysine has a protective effect against lens protein denaturation both in vitro and in vivo. It is also a nonsteroidal anti-inflammatory drug (NSAID) used for joint and muscular pain.",428.48,"81919-14-4",{"v":3,"d":"3.00"},{"v":7,"d":"7.00"},{"v":86,"d":"86.00"},200.71,"https://www.selleckchem.com/products/bendazac-l-lysine.html","C22H28N4O5","Free Base","N/A","NCCCCC(N)C(O)=O.OC(=O)COC1=N[N](CC2=CC=CC=C2)C3=C1C=CC=C3",-2.452,4,2,10]
["S6103","Inosine 5′-triphosphate trisodium salt","a10","L1700-110","in 10mM Water","Others","Others","Inosine 5′-triphosphate (ITP) is used in studies on the impact of deamination of ATP and GTP by various enzymes and chemical processes.",574.11,"35908-31-7","N/A","N/A",{"v":114,"d":"114.00"},198.57,"http://www.selleck.cn/products/inosine-5-triphosphate-trisodium-salt.html","C10H12N4Na3O14P3","trisodium salt","N/A","[Na+].[Na+].[Na+].OC1C(O)C(OC1CO[P]([O-])(=O)O[P]([O-])(=O)O[P](O)([O-])=O)[N]2C=NC3=C2N=CNC3=O",-7.316,7,3,8]
["S6133","H-Gly-Pro-OH","h10","L1700-110","in 10mM Water","Others","Others","H-Gly-Pro-OH (Glycyl proline, Glycyl-L-proline) is a dipeptide composed of glycine and proline, and is an end product of collagen metabolism that is further cleaved by prolidase. The resulting proline molecules are recycled into collagen or other proteins.",172.18,"704-15-4","N/A","N/A",{"v":34,"d":"34.00"},197.47,"http://www.selleck.cn/products/h-gly-pro-oh.html","C7H12N2O3","free base","Glycyl proline, Glycyl-L-proline","NCC(=O)N1CCCC1C(O)=O",-3.783,2,1,2]
["S6270","2-Aminoisobutyric acid","e2","L1700-111","in 10mM Water","Fungal","Microbiology","2-Aminoisobutyric acid (NSC-16590, 2-Methylalanine, H-Aib-OH) is a rare, non-protein amino acid and end-product of pyrimidine metabolism, excreted in urine and found in some antibiotics of fungal origin.",103.12,"62-57-7","N/A","N/A",10.29,99.83,"http://www.selleck.cn/products/nsc-16590.html","C4H9NO2","free base","NSC-16590, 2-Methylalanine, H-Aib-OH","CC(C)(N)C(O)=O",-2.849,1,1,1]
["S6322","Pipecolic acid","d3","L1700-111","in 10mM Water","Immunology & Inflammation related","Immunology & Inflammation","Pipecolic acid (piperidine-2-carboxylic acid), a metabolite of lysine found in human physiological fluids such as urine, plasma and CSF, is an important regulator of immunity in plants and humans alike.",129.16,"535-75-1","N/A","N/A",25.83,{"v":200,"d":"200.00"},"http://www.selleck.cn/products/pipecolic-acid.html","C6H11NO2","free base","piperidine-2-carboxylic acid","OC(=O)C1CCCCN1",-2.387,1,1,1]
["S6592","Diquafosol Tetrasodium","e4","L1700-111","in 10mM Water","P2 Receptor","Neuronal Signaling","Diquafosol Tetrasodium (INS-365), a P2Y2 receptor agonist, is a pharmaceutical drug for the treatment of dry eye disease.",878.23,"211427-08-6","N/A","N/A",{"v":100,"d":"100.00"},113.87,"http://www.selleck.cn/products/diquafosol-tetrasodium.html","C18H22N4Na4O23P4","Tetrasodium","INS-365","[Na+].[Na+].[Na+].[Na+].OC1C(O)C(OC1CO[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)O[P]([O-])(=O)OCC2OC(C(O)C2O)N3C=CC(=O)NC3=O)N4C=CC(=O)NC4=O",-11.332,11,6,14]
["S7547","XL413 (BMS-863233)","d5","L1700-111","in 10mM Water","CDK","Cell Cycle","XL413 (BMS-863233) is a potent and selective cell division cycle 7 homolog (CDC7) kinase inhibitor with IC50 of 3.4 nM, showing 63-, 12- and 35-fold selectivity over CK2, Pim-1 and pMCM2, respectively. Phase 1/2.",326.18,"1169562-71-3","<1","N/A",{"v":46,"d":"46.00"},141.03,"http://selleckchem.com/products/xl413-bms-863233.html","C14H13Cl2N3O2","free base","N/A","Cl.ClC1=CC2=C(OC3=C2N=C(NC3=O)C4CCCN4)C=C1",2.537,3,2,1]
["S8199","Ruxotemitide (LTX 315)","c6","L1700-111","in 10mM Water","Bcl-2","Apoptosis","Ruxotemitide (LTX 315, Oncopore) is the oncolytic peptide that kills cancer cells through Bax/Bak-regulated mitochondrial membrane permeabilization.",1439.79,"1345407-05-7","N/A","N/A",{"v":100,"d":"100.00"},69.45,"http://selleckchem.com/products/ltx-315.html","C78H106N18O9","free base","Oncopore","NCCCCC(N)C(=O)NC(CCCCN)C(=O)NC(CC1=C[NH]C2=C1C=CC=C2)C(=O)NC(CC3=C[NH]C4=C3C=CC=C4)C(=O)NC(CCCCN)C(=O)NC(CCCCN)C(=O)NC(CC5=C[NH]C6=C5C=CC=C6)C(=O)NC(C(C7=CC=CC=C7)C8=CC=CC=C8)C(=O)NC(CCCCN)C(N)=O",3.102,9,18,46]
["S9367","Adenosine disodium triphosphate hydrate","g7","L1700-111","in 10mM Water","Others","Others","Adenosine disodium triphosphate hydrate(ATP disodium) is the sodium salt form of adenosine triphosphate (ATP), a complex organic chemical that provides energy to drive many processes in living cells., ,",551.14,"34369-07-8","N/A",{"v":0,"d":"0.00"},{"v":100,"d":"100.00"},181.44,"https://www.selleckchem.com/products/adenosine-disodium-triphosphate.html","C10H14N5Na2O13P3.xH2O","disodium triphosphate hydrate","ATP disodium","O[C@H]1([C@H](N2C3C(N=C2)=C(N)N=CN=3)O[C@H](CO[P](O[P](O[P](=O)(O)O)(=O)O)(=O)O)[C@@H](O)1).[Na].O",-5.474,7,3,8]
["P1034","Terlipressin Acetate","f8","L1700-111","in 10mM Water","5-alpha Reductase","Angiogenesis","Terlipressin Acetate is an analogue of vasopressin used as a vasoactive drug in the management of hypotension. It has been found to be effective when norepinephrine does not help.",1227.37,"14636-12-5","N/A","N/A","N/A",{"v":10,"d":"10.00"},"http://selleckchem.com/products/terlipressin-acetate.html","C52H74N16O15S2","Acetate","Gly-Gly-Gly-Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Lys-Gly-NH2(Cys4-Cys9)","NCCCCC(NC(=O)C1CCCN1C(=O)C2CSSCC(NC(=O)CNC(=O)CNC(=O)CN)C(=O)NC(CC3=CC=C(O)C=C3)C(=O)NC(CC4=CC=CC=C4)C(=O)NC(CCC(N)=O)C(=O)NC(CC(N)=O)C(=O)N2)C(=O)NCC(N)=O","N/A","N/A","N/A","N/A"]
["S2433","DL-Buthionine-Sulfoximine","c10","L1700-111","in 10mM Water","Glutathione","Metabolism","DL-Buthionine-Sulfoximine (BSO, DL-Buthionine-(S,R)-sulfoximine) is an inhibitor of glutathione (GSH) synthesis.",222.31,"5072-26-4","<1","N/A",{"v":44,"d":"44.00"},197.92,"http://www.selleckchem.com/products/dl-buthionine-sulfoximine.html","C8H18N2O3S","Free Base","BSO, DL-Buthionine-(S,R)-sulfoximine","CCCC[S](=N)(=O)CCC(N)C(O)=O",{"v":-2.18,"d":"-2.180"},2,1,7]
["P1088","Lanreotide acetate","g11","L1700-111","in 10mM Water","GHSR","Endocrinology & Hormones","Lanreotide (Laromustine, Angiopeptin, BIM 23014, Dermopeptin, Ipstyl, ITM-014, Somatulina, Somatuline, Lanreotidum) acetate, an analog of the native somatostatin peptide, is a physiological inhibitor of growth hormone (GH). Lanreotide also has antitumoral effects.",1156.38,"2378114-72-6",{"v":-1,"d":"-1.00"},"N/A",{"v":23,"d":"23.00"},19.89,"https://www.selleckchem.com/products/lanreotide-acetate.html","C56H73N11O12S2","Acetate","Laromustine, Angiopeptin, BIM 23014, BIM 23014C, BM 23014, Dermopeptin, Ipstyl, ITM-014, ITM-014T, Somatulina, Somatuline, Lanreotidum","CC(C)C1NC(=O)C(CCCCN)NC(=O)C(CC2=C[NH]C3=C2C=CC=C3)NC(=O)C(CC4=CC=C(O)C=C4)NC(=O)C(CSSCC(NC1=O)C(=O)NC(C(C)O)C(N)=O)NC(=O)C(N)CC5=CC6=CC=CC=C6C=C5.CC(O)=O",-0.979,9,13,17]
["S2996","L-DAB HBR","f2","L1700-112","in 10mM Water","GABA Receptor","Neuronal Signaling","L-DAB HBR (L-Dab Hydrobromide, L-2,4-Diaminobutyric acid hydrobromide) is an inhibitor of GABA (Gamma-aminobutyric acid) transaminase with IC50 of >500 μM. L-DAB HBR exhibits antitumor activity.",199.05,"73143-97-2","<1","N/A",{"v":23,"d":"23.00"},{"v":194.7,"d":"194.70"},"https://www.selleckchem.com/products/ldab-hbr.html","C4H11BrN2O2","Hydrobromide","L-Dab Hydrobromide, L-2,4-Diaminobutyric acid hydrobromide","Br.NCCC(N)C(O)=O",-3.786,1,2,3]
["S3142","Potassium sorbate","e3","L1700-112","in 10mM Water","Bacterial","Microbiology","Potassium sorbate (Sorbic acid potassium) is a nonpoisonous food preservative isolated from Sorbus aucuparia. Potassium sorbate is an effective inhibitor of most molds and yeasts and some bacteria.",150.22,"24634-61-5","<1","N/A",{"v":30,"d":"30.00"},199.71,"https://www.selleckchem.com/products/potassium-sorbate.html","C6H7KO2","Potassium","Sorbic acid potassium","[K+].C/C=C/C=C/C([O-])=O",-0.111,0,0,2]
["S3349","Phosphocholine chloride calcium salt tetrahydrate","f4","L1700-112","in 10mM Water","Others","Others","Phosphocholine (Phosphorylcholine) chloride calcium salt tetrahydrate is an active endogenous metabolite.",329.73,"72556-74-2","<1","N/A",{"v":66,"d":"66.00"},200.16,"https://www.selleckchem.com/products/phosphocholine-chloride-calcium-salt-tetrahydrate.html","C5H21CaClNO8P","Calcium salt tetrahydrate","Phosphorylcholine chloride calcium salt tetrahydrate","O.O.O.O.[Cl-].[Ca++].C[N+](C)(C)CCO[P]([O-])([O-])=O",-7.326,1,0,4]
["S9666","DX600","e5","L1700-112","in 10mM Water","ACE","Endocrinology & Hormones","DX600 is a specific inhibitor of angiotensin-converting enzyme 2 (ACE2) that does not cross-react with ACE.",3074.32,"478188-26-0",{"v":-1,"d":"-1.00"},"N/A",{"v":100,"d":"100.00"},32.53,"https://www.selleckchem.com/products/dx600.html","C141H185N35O40S2","Free Base","N/A","CC(C)CC1NC(=O)C2CCCN2C(=O)C(CO)NC(=O)C(CSSCC(NC(=O)C(CCCCN)NC(=O)C(CC3=C[NH]C4=C3C=CC=C4)NC(=O)C(CC5=C[NH]C6=C5C=CC=C6)NC(=O)C7CCCN7C(=O)C(CC8=CC=C(O)C=C8)NC(=O)C(CC9=CC=C(O)C=C9)NC(=O)C(CCCNC(N)=N)NC1=O)C(=O)NC(C(C)O)C(=O)NC(CC%10=CC=C(O)C=C%10)C(=O)N%11CCCC%11C(=O)NC(CC(O)=O)C(=O)N%12CCCC%12C(=O)NC(CCC(O)=O)C(=O)NCC(=O)NCC(=O)NCC(N)=O)NC(=O)C(CC%13=CN=C[NH]%13)NC(=O)C(CO)NC(=O)C(CC%14=CC=C(O)C=C%14)NC(=O)C(CC(O)=O)NC(=O)CNC(C)=O",-10.444,31,36,63]
["S4494","Methionine","b7","L1700-112","in 10mM Water","GABA Receptor","Neuronal Signaling","Methionine (MRX-1024, D-Methionine) is an activitor of GABAA receptor that modulates neuronal activity.",149.21,"348-67-4","<1","N/A",{"v":29,"d":"29.00"},194.36,"http://www.selleckchem.com/products/methionine.html","C5H11NO2S","Free Base","MRX-1024, D-Methionine","CSCCC(N)C(O)=O",-2.834,1,1,4]
["S5260","ATP","a8","L1700-112","in 10mM Water","Immunology & Inflammation related","Immunology & Inflammation","ATP (Adenosine-Triphosphate, Adenosine 5'-triphosphate) is a multifunctional nucleoside triphosphate and an important endogenous signaling molecule in immunity and inflammation.",507.18,"56-65-5","<1","N/A",{"v":100,"d":"100.00"},197.17,"http://www.selleckchem.com/products/atp.html","C10H16N5O13P3","Free Base","Adenosine-Triphosphate, Adenosine 5'-triphosphate","NC1=C2N=C[N](C3OC(CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)C(O)C3O)C2=NC=N1",-2.526,7,3,8]
["S6090","JFD01307SC","e9","L1700-112","in 10mM Water","Bacterial","Microbiology","JFD01307SC ([(1,1-dioxidotetrahydrothien-3-yl)amino]acetic acid) shows activity against M.tuberculosis with minimum inhibitory concentrations (MICs) in the range of 8 to 16 µg/ml. JFD01307SC may targets enzymes involved in glutamine biosynthesis.",193.22,"51070-56-5","<1",{"v":0,"d":"0.00"},{"v":3,"d":"3.00"},15.53,"http://www.selleckchem.com/products/jfd01307sc.html","C6H11NO4S","Free Base","[(1,1-dioxidotetrahydrothien-3-yl)amino]acetic acid","OC(=O)CNC1CC[S](=O)(=O)C1",-3.932,3,1,3]
["E0375","Ammonium ferric citrate","a11","L1700-112","in 10mM Water","Ferroptosis","Apoptosis","Ammonium ferric citrate (Ferric ammonium citrate, Ammonium iron(III) citrate, Iron ammonium citrate, FerriSeltz) induces ferroptosis in non-small-cell lung carcinoma through the inhibition of GPX4-GSS/GSR-GGT axis activity.",978.05,"1185-57-5","<1","N/A",{"v":53,"d":"53.00"},54.19,"http://www.selleckchem.com/products/ammonium-ferric-citrate.html","C24H32Fe3N3O28","Citrate","Ferric ammonium citrate, Ammonium iron(III) citrate, Iron ammonium citrate, FerriSeltz","[NH4+].[NH4+].[NH4+].[Fe+3].[Fe+3].[Fe+3].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.OC(CC([O-])=O)(CC([O-])=O)C([O-])=O.OC(CC([O-])=O)(CC([O-])=O)C([O-])=O",{"v":-28.54,"d":"-28.540"},0,0,20]
["E0532","Menotropin","a2","L1700-113","in 10mM Water","Estrogen/progestogen Receptor","Endocrinology & Hormones","Menotropin (Human Menopausal Gonadotrophin) is a hormonally active medication for the treatment of fertility disturbances, which are extracted from the urine of postmenopausal women.",142.24,"61489-71-2","<1","N/A",{"v":28,"d":"28.00"},196.85,"http://www.selleckchem.com/products/menotropin.html","C9H18O","free base","Human Menopausal Gonadotrophin","CC(C)(C)CCCCC=O",2.767,1,0,5]
["E2403","ζ-Stat (NSC37044)","d2","L1700-113","in 10mM Water","PKC","Cytoskeletal Signaling","ζ-Stat (NSC37044) is a specific and atypical protein kinase Cζ (PKCζ) inhibitor, with an IC50 of 5 μM.",384.36,"3316-02-7","<1","N/A",{"v":39,"d":"39.00"},101.47,"http://www.selleckchem.com/products/zeta-stat-nsc37044-.html","C10H8O10S3","free base","N/A","OC1=CC(=CC2=CC(=CC(=C12)[S](O)(=O)=O)[S](O)(=O)=O)[S](O)(=O)=O",0.494,0,1,3]
["S0833","EIDD-1931","h3","L1700-113","in 10mM Water","COVID-19,SARS-CoV","Microbiology","EIDD-1931 (Beta-d-N4-hydroxycytidine, β-d-N4-hydroxycytidine, NHC) is an active metabolite of EIDD-2801, a promising COVID-19 inhibitor. EIDD-1931 (NHC) has broad spectrum antiviral activity against SARS-CoV-2, MERS-CoV, SARS-CoV, and related zoonotic group 2b or 2c Bat-CoVs with average IC50 of 0.15 μM, as well as increased potency against a coronavirus bearing resistance mutations to the nucleoside analog inhibitor remdesivir.",259.22,"3258-02-4","<1","N/A",{"v":15,"d":"15.00"},57.87,"http://www.selleckchem.com/products/eidd-1931.html","C9H13N3O6","Free base","Beta-d-N4-hydroxycytidine, β-d-N4-hydroxycytidine, NHC","OCC1OC(C(O)C1O)N2C=C\\C(NC2=O)=N\\O",-2.384,3,4,2]
["S8416","PACAP 6-38","g4","L1700-113","in 10mM Water","cAMP","GPCR & G Protein","PACAP 6-38 is a PACAP (pituitary adenylate cyclase-activating polypeptide) non-stimulating competitive antagonist with an IC50 value of 2 nM. It also acts as a functional CARTp antagonist in vivo.",4024.74,"143748-18-9","<1","N/A",{"v":100,"d":"100.00"},24.85,"http://www.selleckchem.com/products/pacap-6-38.html","C182H300N56O45S","Free base","N/A","CSCCC(NC(=O)C(CCC(N)=O)NC(=O)C(CCCCN)NC(=O)C(CCCNC(N)=N)NC(=O)C(CC1=CC=C(O)C=C1)NC(=O)C(CCCNC(N)=N)NC(=O)C(CO)NC(=O)C(CC2=CC=C(O)C=C2)NC(=O)C(CO)NC(=O)C(CC(O)=O)NC(=O)C(NC(=O)C(N)CC3=CC=CC=C3)C(C)O)C(=O)NC(C)C(=O)NC(C(C)C)C(=O)NC(CCCCN)C(=O)NC(CCCCN)C(=O)NC(CC4=CC=C(O)C=C4)C(=O)NC(CC(C)C)C(=O)NC(C)C(=O)NC(C)C(=O)NC(C(C)C)C(=O)NC(CC(C)C)C(=O)NCC(=O)NC(CCCCN)C(=O)NC(CCCNC(N)=N)C(=O)NC(CC5=CC=C(O)C=C5)C(=O)NC(CCCCN)C(=O)NC(CCC(N)=O)C(=O)NC(CCCNC(N)=N)C(=O)NC(C(C)C)C(=O)NC(CCCCN)C(=O)NC(CC(N)=O)C(=O)NC(CCCCN)C(N)=O",{"v":-15.97,"d":"-15.970"},37,59,146]
["P1020","Argipressin acetate","b6","L1700-113","in 10mM Water","5-alpha Reductase","Angiogenesis","Argpressin Acetate  is a neurohypophysial hormone found in most mammals. It acts as a neurotransmitter at synapses in the brain, increases [Ca2+]i in cultured rat hippocampal neurons.",1084.23,"113-79-1","<1","N/A",{"v":100,"d":"100.00"},92.23,"http://www.selleckchem.com/peptide/argipressin-acetate.html","C46H65N15O12S2","Acetate","Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2(Cys1-Cys6)","NC1CSSCC(NC(=O)C(CC(N)=O)NC(=O)C(CCC(N)=O)NC(=O)C(CC2=CC=CC=C2)NC(=O)C(CC3=CC=C(O)C=C3)NC1=O)C(=O)N4CCCC4C(=O)NC(CCCNC(N)=N)C(=O)NCC(N)=O",{"v":-4.77,"d":"-4.770"},11,14,20]
["E4063","β-Glycerophosphate (disodium salt hydrate)","c7","L1700-113","in 10mM Water","Others","Others","β-Glycerophosphate is a classical serine-threonine phosphatase inhibitor used in kinase reaction buffers. BGP is often used in combination with other phosphatase/protease inhibitors for broad spectrum inhibition. It functions as an organic phosphate donor and has been used in culture media for mesenchymal stem cell differentiation to osteoblast-type cells. BGP is also used to buffer M17 media for Lactococcus culture in recombinant protein expression.",234.05,"154804-51-0","N/A","N/A","N/A","N/A","https://www.selleckchem.com/products/beta-glycerophosphate-disodium-salt-hydrate.html","C3H9Na2O7P","disodium phosphate","β-Glycerophosphate disodium salt hydrate","O.[Na;v0].OCC(CO)O[P](O)(O)=O",-1.687,1,2,4]
["E4288","DL-Valine","g8","L1700-113","in 10mM Water","Others","Others","DL-Valine is 2-amino-3-methylbutanoic acid.It is synthesized in plants via several steps starting from pyruvic acid.",117.15,"516-06-3","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/dl-valine.html","C5H11NO2","free base","DL-Valine","CC(C)C(N)C(O)=O",-2.318,1,1,2]
["E4491","α-D-Glucose 1-phosphate disodium salt hy","g9","L1700-113","in 10mM Water","Others","Others","α-D-Glucose 1-phosphate disodium salt is converted into D-glucose-6-phosphate by the enzyme phosphoglucomutase.",322.11,"56401-20-8","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/alpha-d-glucose-1-phosphate-disodium-salt-hydrate.html","C6H13Na2O10P","disodium salt","α-D-Glucose 1-phosphate disodium salt hy","[Na;v0].OCC1OC(O[P](O)(O)=O)C(O)C(O)C1O",-2.585,2,4,3]
["E4390","Aspartic acid (calcium)","c11","L1700-113","in 10mM Water","Others","Others","Aspartic acid calcium is a chelate where calcium is attached to L-Aspartic acid, an amino acid that is used in the biosynthesis of proteins.",171.16,"21059-46-1","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/aspartic-acid-calcium.html","C4H5CaNO4","Calcium","N/A","[Ca;v0].NC(CC(O)=O)C(O)=O",{"v":-3.78,"d":"-3.780"},2,1,3]
["E4431","D-Fructose-1,6-Diphosphate","f11","L1700-113","in 10mM Water","Others","Others","D-Fructose 1,6-Diphosphate, also known as Harden-Young ester, is fructose sugar phosphorylated on carbons 1 and 6 (i.e., is a fructosephosphate). The β-D-form of this compound is very common in cells.",340.12,"488-69-7","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/d-fructose-1-6-diphosphate.html","C6H14O12P2","Free base","D-fructose-1,6-bis(dihydrogen phosphate)","OC(CO[P](O)(O)=O)C(O)C(O)C(=O)CO[P](O)(O)=O",-3.017,3,3,9]
["E2895","Sodium Bicarbonate","f3","L1700-114","in 10mM Water","Others","Others","Sodium bicarbonate(Armex Blast Media Flow Formula XL, BI-CF 40E, BI-H 40E, Bakeshure 180, Sodium Hydrogen Carbonate, Sodium hydrogen carbonate) is a biochemical reagent used as a pH buffering agent, an electrolyte replenisher, systemic alkalizer and in topical cleansing solutions.",85.01,"144-55-8","<1","N/A",{"v":25,"d":"25.00"},294.08,"https://www.selleckchem.com/products/sodium-bicarbonate.html","CH2O3.Na","Free base","Armex Blast Media Flow Formula XL, BI-CF 40E, BI-H 40E, Bakeshure 180, Sodium Hydrogen Carbonate, Sodium hydrogen carbonate","[Na;v0].OC(O)=O",0.213,0,0,0]
["E5043","[(1aS,1bα,5aα,6aβ)-1a,1b,2,5a,6,6a-Hexahydro-6α-hydroxy-1aβ-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2α-yl]6-O-α-D-galactopyranosyl-β-D-glucopyranoside","f4","L1700-114","in 10mM Water","NF-κB, p38 MAPK,Immunology & Inflammation related","NF-κB, MAPK, Immunology & Inflammation","[(1aS,1bα,5aα,6aβ)-1a,1b,2,5a,6,6a-Hexahydro-6α-hydroxy-1aβ-(hydroxymethyl)oxireno[4,5]cyclopenta[1,2-c]pyran-2α-yl]6-O-α-D-galactopyranosyl-β-D-glucopyranoside is a neuroprotective compound extracted from Rehmanniae radix, exhibits low toxicity and anti-inflammatory properties. It inhibits pro-inflammatory mediator release, promotes M2 microglial polarization, and protects neurons from apoptosis by suppressing NF-κB and MAPK signaling, making it a potential candidate for spinal cord injury research.",524.47,"81720-05-0","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/rehmannioside-a.html","C21H32O15","free base","Rehmannioside A","OCC1OC(OCC2OC(OC3OC=CC4C(O)C5OC5(CO)C34)C(O)C(O)C2O)C(O)C(O)C1O",-5.328,6,9,7]
["E5450","Taurohyodeoxycholic acid","f5","L1700-114","in 10mM Water","anti-inflammatory","Immunology & Inflammation","Taurohyodeoxycholic acid is a natural taurine-conjugated hyodeoxycholic acid that promotes a biliary lecithin secretion and exhibits anti-inflammatory effects.",{"v":499.7,"d":"499.70"},"2958-04-5","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/taurohyodeoxycholic-acid.html","C26H45NO6S","Free Base","NA","CC(CCC(=O)NCC[S](O)(=O)=O)C1CCC2C3CC(O)C4CC(O)CCC4(C)C3CCC12C",2.997,1,3,7]
["S0929","Kukoamine B","e6","L1700-114","in 10mM Water","Antioxidant","Immunology & Inflammation","Kukoamine B is natural a spermine alkaloid, is a potent dual inhibitor of Lipopolysaccharides (LPS) and oligodeoxynucleotides containing CpG motifs (CpG DNA) with Kd values of 1.23 µM and 0.66 µM, respectively. It exhibits anti-inflammatory, anti-diabetic, antioxidant, anti-osteoporotic, and neuroprotective effects, making it a potential candidate for sepsis research.",530.66,"164991-67-7","N/A","N/A","N/A",">10","https://www.selleckchem.com/products/kukoamine-b.html","C28H42N4O6","free base","N/A","NCCCN(CCCCNCCCNC(=O)CCC1=CC(=C(O)C=C1)O)C(=O)CCC2=CC(=C(O)C=C2)O",1.655,2,7,18]
["S1327","Ellagic acid","c3","L1700-115","in 2mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Ellagic acid (Elagostasine, Gallogen) has antiproliferative and antioxidant property.",302.19,"476-66-4",{"v":3,"d":"3.00"},9.93,"<1","N/A","http://selleckchem.com/products/Ellagic-acid.html","C14H6O8","free base","Elagostasine, Gallogen","OC1=CC2=C3C(=C1O)OC(=O)C4=CC(=C(O)C(=C34)OC2=O)O",{"v":0,"d":"0.000"},0,0,0]
["S1464","Marbofloxacin","a4","L1700-115","in 2mM DMSO","Topoisomerase","DNA Damage/DNA Repair","Marbofloxacin is a potent antibiotic inhibiting bacterial DNA replication.",362.36,"115550-35-1",{"v":3,"d":"3.00"},8.28,"<1","N/A","http://selleckchem.com/products/Marbofloxacin.html","C17H19FN4O4","free base","N/A","CN1CCN(CC1)C2=C(F)C=C3C(=O)C(=CN4N(C)COC2=C34)C(O)=O",-2.038,3,0,2]
["S1986","Meclizine 2HCl","g5","L1700-115","in 2mM DMSO","CAR,Histamine Receptor","Neuronal Signaling","Meclizine (NSC 28728,Meclozine dihydrochloride) is a histamine H1 receptor antagonist used to treat nausea and motion sickness, has anti-histamine, anti-muscarinic and anti-oxidative phosphorylation properties, also an agonist ligand for mCAR (constitutive androstane receptor) and an inverse agonist for hCAR.",463.87,"1104-22-9",{"v":4,"d":"4.00"},8.62,"<1","N/A","http://selleckchem.com/products/meclizine-dihydrochloride.html","C25H27Cl2N2.2HCl","Dihydrochloride","NSC 28728,Meclozine dihydrochloride","Cl.Cl.CC1=CC(=CC=C1)CN2CCN(CC2)C(C3=CC=CC=C3)C4=CC=C(Cl)C=C4",{"v":0,"d":"0.000"},0,0,0]
["S2110","Vinpocetine","b6","L1700-115","in 2mM DMSO","Sodium Channel","Transmembrane Transporters","Vinpocetine (RGH-4405,Ethyl apovincaminate,AY 27255) is a selective inhibitor of voltage-sensitive sodium channel for the treatment of stroke, vascular dementia  and Alzheimer's disease.",350.45,"42971-09-5",{"v":3,"d":"3.00"},8.56,"<1","N/A","http://selleckchem.com/products/vinpocetine-cavinton.html","C22H26N2O2","free base","RGH-4405,Ethyl apovincaminate,AY 27255","CCOC(=O)C1=CC2(CC)CCCN3CCC4=C(C23)[N]1C5=CC=CC=C45",{"v":0,"d":"0.000"},0,0,0]
["S2735","MK-8776 (SCH 900776)","d8","L1700-115","in 2mM DMSO","CDK,Chk","Cell Cycle","MK-8776 (SCH 900776) is a selective Chk1 inhibitor with IC50 of 3 nM in a cell-free assay. It shows 500-fold selectivity against Chk2. Phase 2.",376.25,"891494-63-6",{"v":3,"d":"3.00"},7.97,"<1","N/A","http://selleckchem.com/products/sch-900776.html","C15H18BrN7","Free Base","N/A","C[N]1C=C(C=N1)C2=C3N=C(C4CCCNC4)C(=C(N)[N]3N=C2)Br",{"v":1.32,"d":"1.320"},3,2,2]
["S2788","Capmatinib (INCB28060)","f8","L1700-115","in 2mM DMSO","Apoptosis related,c-Met,Wnt/beta-catenin","Protein Tyrosine Kinase","Capmatinib (INCB28060, INC280, NVP-INC280) is a novel, ATP-competitive inhibitor of c-MET with IC50 of 0.13 nM in a cell-free assay, inactive against RONβ, as well as EGFR and HER-3. Capmatinib (INCB28060) inhibits Wnt/β-catenin and EMT signaling pathways and induces apoptosis in diffuse gastric cancer positive for c-MET amplification. Phase 1.",412.42,"1029712-80-8",{"v":2,"d":"2.00"},4.85,"<1","N/A","http://selleckchem.com/products/incb28060.html","C23H17FN6O","Free Base","INC280, NVP-INC280","CNC(=O)C1=CC=C(C=C1F)C2=N[N]3C(=CN=C3N=C2)CC4=CC=C5N=CC=CC5=C4",3.246,5,1,4]
["S3721","Bilastine","b10","L1700-115","in 2mM DMSO","Histamine Receptor","Neuronal Signaling","Bilastine is a new, well-tolerated, nonsedating H1 receptor antihistamine and has a rapid onset and prolonged duration of action.",463.61,"202189-78-4",{"v":1,"d":"1.00"},2.16,"<1","N/A","http://selleckchem.com/products/bilastine.html","C28H37N3O3","free base","N/A","CCOCC[N]1C(=NC2=C1C=CC=C2)C3CCN(CC3)CCC4=CC=C(C=C4)C(C)(C)C(O)=O",{"v":2.07,"d":"2.070"},3,0,10]
["S4142","Clopidol","a11","L1700-115","in 2mM DMSO","Anti-infection","Microbiology","Clopidol (WR 61112) is an antiprotozoal agent.",192.04,"2971-90-6",{"v":1,"d":"1.00"},5.21,"<1","N/A","http://selleckchem.com/products/clopidol.html","C7H7Cl2NO","free base","WR 61112","CC1=C(Cl)C(=C(Cl)C(=N1)C)O",2.331,1,1,0]
["S5170","Coumarin 6","e2","L1700-116","in 2mM DMSO","Others","Others","Coumarin 6 is a fluorescent dye frequently used to facilitate the traceability of drug delivery systems in vitro.",350.43,"38215-36-0",{"v":3,"d":"3.00"},8.56,"N/A","N/A","http://selleckchem.com/products/coumarin-6.html","C20H18N2O2S","free base","N/A","CCN(CC)C1=CC2=C(C=C1)C=C(C(=O)O2)C3=NC4=C(S3)C=CC=C4",4.728,3,0,4]
["S5908","Garenoxacin","b4","L1700-116","in 2mM DMSO","Anti-infection","Microbiology","Garenoxacin (T-3811ME, BMS-284756) is a novel des-F(6) quinolone that has been shown to be effective in vitro against a wide range of clinically important pathogens, including gram-positive and gram-negative aerobes and anaerobes.",426.41,"194804-75-6",{"v":2,"d":"2.00"},4.69,"<1","N/A","http://www.selleckchem.com/products/garenoxacin.html","C23H20F2N2O4","Free Base","T-3811ME, BMS-284756","CC1NCC2=C1C=CC(=C2)C3=C(OC(F)F)C4=C(C=C3)C(=O)C(=CN4C5CC5)C(O)=O",0.934,3,1,5]
["S7004","EPZ005687","a5","L1700-116","in 2mM DMSO","EZH1/2,Histone Methyltransferase","Epigenetics","EPZ005687 is a potent and selective inhibitor of EZH2 with Ki of 24 nM in a cell-free assay, 50-fold selectivity against EZH1 and 500-fold selectivity against 15 other protein methyltransferases.",539.67,"1396772-26-1",{"v":2,"d":"2.00"},3.71,"<1","N/A","http://selleckchem.com/products/epz005687.html","C32H37N5O3","Free Base","N/A","CC1=CC(=C(CNC(=O)C2=CC(=CC3=C2C=N[N]3C4CCCC4)C5=CC=C(CN6CCOCC6)C=C5)C(=O)N1)C",3.919,4,2,7]
["S7400","ISRIB (trans-isomer)","b6","L1700-116","in 2mM DMSO","PERK","Apoptosis","ISRIB (trans-isomer), the trans-isomer of ISRIB, is a potent and selective PERK inhibitor with IC50 of 5 nM and does not have global effects on translation, transcription, or mRNA stability in non-stressed cells.",451.34,"1597403-47-8",{"v":4,"d":"4.00"},8.86,"<1","N/A","http://selleckchem.com/products/isrib-trans-isomer.html","C22H24Cl2N2O4","Free Base","N/A","ClC1=CC=C(OCC(=O)NC2CCC(CC2)NC(=O)COC3=CC=C(Cl)C=C3)C=C1",4.055,4,2,8]
["S8113","BI-9564","f7","L1700-116","in 2mM DMSO","Epigenetic Reader Domain","Epigenetics","BI-9564 is a selective inhibitor of BRD9 and BRD7 bromodomains with the IC50 of 75 nM and 3.4 µM, respectively.",353.41,"1883429-22-8",{"v":3,"d":"3.00"},8.49,"<1","N/A","http://selleckchem.com/products/bi-9564.html","C20H23N3O3","Free Base","N/A","COC1=C(CN(C)C)C=C(OC)C(=C1)C2=CN(C)C(=O)C3=C2C=CN=C3",1.301,4,0,5]
["S8527","ROC-325","a8","L1700-116","in 2mM DMSO","Autophagy","Autophagy","ROC-325 is an orally available novel inhibitor of lysosomal-mediated autophagy which diminishes AML cell viability with the IC50 range of 0.7-2.2 μM.",503.06,"1859141-26-6",{"v":4,"d":"4.00"},7.95,"<1","N/A","http://selleckchem.com/products/roc-325.html","C28H27ClN4OS","free base","N/A","CN(CCNC1=CC=NC2=C1C=CC(=C2)Cl)CCNC3=CC=C(C)C4=C3C(=O)C5=CC=CC=C5S4",6.264,2,2,8]
["S9551","Uvaol","e9","L1700-116","in 2mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","Uvaol is a pentacyclic triterpene, found in the non-glyceride fraction of olive pomace oil, exhibiting both pro- and anti-inflammatory properties.",442.72,"545-46-0",{"v":3,"d":"3.00"},6.78,{"v":1,"d":"1.00"},2.26,"https://www.selleckchem.com/products/uvaol.html","C30H50O2","Free Base","N/A","CC1CCC2(CO)CCC3(C)C(=CCC4C5(C)CCC(O)C(C)(C)C5CCC34C)C2C1C",6.258,0,2,1]
["S6345","3-Nitro-L-tyrosine","b11","L1700-116","in 2mM DMSO","Adrenergic Receptor","Endocrinology & Hormones","3-Nitro-L-tyrosine (3-NT, N-Tyr, MNT), synthesized from L-tyrosine by peroxynitrite, is a product of nitric oxide and superoxide. 3-Nitro-L-tyrosine inhibits the hemodynamic responses to angiotensin II, possibly through the inhibition of alpha 1-adrenoceptor-mediated events.",226.19,"621-44-3",{"v":2,"d":"2.00"},8.84,{"v":1,"d":"1.00"},4.42,"http://www.selleckchem.com/products/3-nitro-l-tyrosine.html","C9H10N2O5","free base","3-NT, N-Tyr, MNT","NC(CC1=CC(=C(O)C=C1)[N+]([O-])=O)C(O)=O",-1.953,1,2,4]
["S5799","Potassium guaiacolsulfonate hemihydrate","a2","L1700-117","in 2mM DMSO","Others","Others","Potassium guaiacolsulfonate hemihydrate (Potassium Hydroxymethoxybenzenesulfonate, Sulfogaiacol) is used as an expectorant for relieving symptoms of cough and mucus in the chest due to respiratory infections, asthma, colds, or hay fever.",{"v":502.6,"d":"502.60"},"78247-49-1",{"v":5,"d":"5.00"},9.95,{"v":5,"d":"5.00"},9.95,"http://www.selleckchem.com/products/potassium-guaiacolsulfonate-hemihydrate.html","C14H16K2O11S2","Hemihydrate","Potassium Hydroxymethoxybenzenesulfonate, Sulfogaiacol","O.[K+].[K+].COC1=C(O)C=CC(=C1)[S]([O-])(=O)=O.COC2=C(O)C=CC(=C2)[S]([O-])(=O)=O",-2.889,2,2,4]
["E0335","4-MMPB","h2","L1700-117","in 2mM DMSO","Lipoxygenase","Metabolism","4-MMPB, a selective inhibitor of 15-lipoxygenase (15-LO) with an IC50 of 18 μM, shows IC50s of 19.5 μM and 19.1 μM for soybean 15-lipoxygenase (SLO) and human 15-lipoxygenase-1 (15-LOX-1), respectively.",313.42,"928853-86-5",{"v":3,"d":"3.00"},9.57,"<1","N/A","http://www.selleckchem.com/products/4-mmpb.html","C16H19N5S","free base","N/A","CN1CCN(CC1)C2=NC(=C3NC4=CC=CC=C4SC3=N2)C",3.352,2,1,1]
["S7089","SM-164","d4","L1700-117","in 2mM DMSO","IAP","Apoptosis","SM-164 is a potent, non-peptide, cell-permeable antagonist of XIAP that targets both the BIR2 and BIR3 domains with IC50 of 1.39 nM. SM-164 induces apoptosis and tumor regression.",1121.42,"957135-43-2",{"v":3,"d":"3.00"},2.68,"<1","N/A","http://www.selleckchem.com/products/sm-164.html","C62H84N14O6","Free base","N/A","CNC(C)C(=O)NC1CCCCC2CCC(N2C1=O)C(=O)NC(C3=CC=CC=C3)C4=C[N](CCCCC5=CC=C(CCCC[N]6C=C(N=N6)C(NC(=O)C7CCC8CCCCC(NC(=O)C(C)NC)C(=O)N78)C9=CC=CC=C9)C=C5)N=N4",6.779,10,6,24]
["E2818","MARK4 inhibitor 1","c5","L1700-117","in 2mM DMSO","AMPK","PI3K/Akt/mTOR","MARK4 inhibitor 1 is a potent microtubule affinity-regulating kinase 4 (MARK4) inhibitor, with an IC50 of 1.54 μM for MARK4 inhibition assay.",{"v":390.4,"d":"390.40"},"2271081-58-2",{"v":2,"d":"2.00"},5.12,"<1","N/A","http://www.selleckchem.com/products/mark4-inhibitor-1.html","C20H18N6O3","Free base","N/A","COC1=CC=C(C[N]2C=C(N=N2)C(=O)N\\N=C\\3C(=O)NC4=C(C)C=CC=C34)C=C1",2.428,6,2,5]
["E4552","1,2-dioleoyl-sn-glycero-3-phosphocholine","h6","L1700-117","in 2mM DMSO","Others","Others","1,2-dioleoyl-sn-glycero-3-phosphocholine is a phospholipid containing the unsaturated long-chain (18:1) oleic acid inserted at the sn-1 and sn-2 positions.",{"v":786.1,"d":"786.10"},"4235-95-4","N/A",">2","N/A","N/A","https://www.selleckchem.com/products/1-2-dioleoyl-sn-glycero-3-phosphocholine.html","C44H84NO8P","phosphatidylcholine","1,2-dioleoyl-sn-glycero-3-phosphocholine","CCCCCCCC\\C=C/CCCCCCCC(=O)OCC(CO[P]([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCCCCCC\\C=C/CCCCCCCC",10.758,6,0,42]
["E4180","DL-Tryptophan","c7","L1700-117","in 2mM DMSO","Others","Metabolism","DL-tryptophan exists as a zwitterion during crystallization. DL-tryptophan is used as an optimal medium supplement for culturing yeast.",204.23,"54-12-6","N/A",">2","N/A","N/A","https://www.selleckchem.com/products/dl-tryptophan.html","C11H12N2O2","free base","(±)-Tryptophan","NC(CC1=C[NH]C2=CC=CC=C12)C(O)=O",-1.312,1,2,3]
["E0223","Columbamine","h8","L1700-117","in 2mM DMSO","Wnt/β-catenin","Stem Cells & Wnt","Columbamine is a tetrahydroisoquinoline alkaloid derived from Rhizoma Coptidis and exerts anti-tumor effects in colon cancer cells by inhibiting the Wnt/β-catenin signaling pathway, leading to reducing proliferation, migration, and invasion while promoting apoptosis to suppress cancer progression.",{"v":338.4,"d":"338.40"},"3621-36-1","N/A",">2","N/A","N/A","https://www.selleckchem.com/products/columbamine.html","C20H20NO4+","Free Base","NA","COC1=C(O)C=C2C(=C1)CC[N+]3=CC4=C(OC)C(=CC=C4C=C23)OC",3.936,3,1,3]
["E2449","Daucosterol","g9","L1700-117","in 2mM DMSO","α-amylase, α-glucosidase, DPPH radical, Wnt/β-catenin","Metabolism, Stem Cells & Wnt","Daucosterol is a β-sitosterol glycoside isolated from Astragalus membranaceus (Leguminosae) that inhibits α-amylase, α-glucosidase and DPPH radical with IC50 of 46.4 μM, 17.0 μM, and 155 µM, respectively. It also inhibits cell migration and invasion in HCC cells via the Wnt/β-catenin signalling pathway.",{"v":576.8,"d":"576.80"},"474-58-8","N/A",">2","N/A","N/A","https://www.selleckchem.com/products/eleutheroside-a.html","C35H60O6","Free base","Eleutheroside A, β-Sitosterol β-D-glucoside","CCC(CCC(C)C1CCC2C3CC=C4CC(CCC4(C)C3CCC12C)OC5OC(CO)C(O)C(O)C5O)C(C)C",6.337,2,4,9]
["S3749","Calcium gluconate monohydrate","h2","L1700-118","in 2mM Water","Others","Others","Calcium gluconate (Calcarea gluconica, Calcium gluconate anhydrous, Calcium D-gluconate, Calciofon, Glucobiogen) is element or mineral necessary for normal nerve, muscle, and cardiac function. Calcium as the gluconate salt helps to maintain calcium balance and prevent bone loss when taken orally.",448.39,"66905-23-5","<1","N/A",{"v":4,"d":"4.00"},8.92,"http://selleckchem.com/products/calcium-gluconate.html","C12H22O14.Ca.H2O","monohydrate","Calcarea gluconica, Calcium gluconate anhydrous, Calcium D-gluconate, Calciofon, Glucobiogen","O.[Ca++].OCC(O)C(O)C(O)C(O)C([O-])=O.OCC(O)C(O)C(O)C(O)C([O-])=O",-8.781,0,10,10]
["S8030","Plerixafor (AMD3100)","g3","L1700-118","in 2mM Water","CXCR,HIV","GPCR & G Protein","Plerixafor (AMD3100, JM 3100, SID791) is a chemokine receptor antagonist for CXCR4 and CXCL12-mediated chemotaxis with IC50 of 44 nM and 5.7 nM in cell-free assays, respectively. Plerixafor inhibits human immunodeficiency virus (HIV) replication.",502.78,"110078-46-1","<1","N/A",{"v":3,"d":"3.00"},5.97,"http://selleckchem.com/products/plerixafor.html","C28H54N8","Free Base","JM 3100, SID791","C1CNCCNCCCN(CCNC1)CC2=CC=C(CN3CCCNCCNCCCNCC3)C=C2",{"v":-0.52,"d":"-0.520"},0,6,4]
["P2006","CL-278474","f2","L1700-120","in 10mM DMSO","ATP-utilizing enzyme","others","ATP-utilizing enzyme inhibitory activity",{"v":303.42244,"d":"303.42"},"58125-33-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H21N3OS","free base","N/A","O=C(CN1CCCCC1)NC2=C(C#N)C3=C(CCCC3)S2",2.922,1,1,3]
["P2009","CL-292502","a3","L1700-120","in 10mM DMSO","Anti-infection,Immunology & Inflammation related","Microbiology,Immunology & Inflammation,Neuronal Signaling","antimicrobial activity;\nantiinflammatory and antimicrobial activity;\nanti-Alzheimer's disease agent;\nneurite elongation stimulator;",{"v":305.37366,"d":"305.37"},"25111-96-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H19N3O","free base","N/A","CN(C)C1=CC=C(C=C1)\\C=C/2C(=NN(C3=CC=CC=C3)C2=O)C",3.196,2,0,3]
["P2025","CL-423530","a5","L1700-120","in 10mM DMSO","SERT","others","SERT inhibitor",{"v":302.7588,"d":"302.76"},"1095530-73-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H15ClN4O","free base","N/A","CCC1=C([O-])C2=[N+](C=N[N]2CC3=C(Cl)C=CC=C3)N=C1C",3.125,2,0,3]
["P2028","CL-47345","d5","L1700-120","in 10mM DMSO","glycogen phosphorylase","others","glycogen phosphorylase inhibitory activity",{"v":282.33702,"d":"282.34"},"111922-87-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H18N2O2","free base","N/A","CC1=CC=C(NC(=O)CC(=O)NC2=CC=C(C)C=C2)C=C1",2.888,2,2,4]
["P2045","WAY-114193","e7","L1700-120","in 10mM DMSO","DHODH","others","DHODH inhibitor",{"v":293.3382,"d":"293.34"},"853696-42-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H15NO4S","free base","N/A","CCOC(=O)C1=C(NC2=CC=C(OC)C=C2)SCC1=O",2.426,4,1,6]
["P2048","WAY-116749","h7","L1700-120","in 10mM DMSO","HIV-1","Microbiology","HIV-1 Integrase Inhibitors",{"v":413.49002,"d":"413.49"},"380872-69-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H23N3O4S","free base","N/A","CCOC(=O)C1=C(NC(=O)CC2NC3=C(NC2=O)C=CC=C3)SC4=C1CCCC4",2.838,4,3,6]
["P2060","WAY-226055","d9","L1700-120","in 10mM DMSO","p53-MDM2","Apoptosis","inhibitors of p53-MDM2 Protein-Protein Interaction;\ninhibitors of interaction of p53-MDM2/X protein.",{"v":421.8762,"d":"421.88"},"381717-91-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H20ClN3O3","free base","N/A","OC1=C(C(N(CCC[N]2C=CN=C2)C1=O)C3=CC=C(Cl)C=C3)C(=O)C4=CC=CC=C4",2.854,3,1,7]
["P2064","WAY-231484","h9","L1700-120","in 10mM DMSO","FKBP12","PI3K/Akt/mTOR","FKBP12 Inhibitors",{"v":255.69746,"d":"255.70"},"144501-98-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H14ClNO3","free base","N/A","ClC1=CC=CC(=C1)OCC(=O)N2CCOCC2",1.431,3,0,3]
["P2080","WAY-278488","h11","L1700-120","in 10mM DMSO","IDO","Metabolism & Immunology & Inflammation","IDO inhibitor",{"v":220.24772,"d":"220.25"},"314027-92-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C10H8N2O2S","free base","N/A","OC(=O)CSC1=C2C=CC=CC2=CN=N1",1.682,3,0,3]
["P2083","WAY-278742","c2","L1700-121","in 10mM DMSO","others","cancer","altering the lifespan of a eukaryotic organism;\ninhibit stimulation of cell proliferation of MDA-MB-231 human breast cancer cells by free fatty acids;",{"v":297.3748,"d":"297.37"},"956369-08-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H15N3OS","free base","N/A","CC1=CC=C(CC2SC(NC2=O)=NC3=NC=CC=C3)C=C1",3.797,3,1,3]
["P2100","WAY-298199","d4","L1700-121","in 10mM DMSO","Anti-infection","Microbiology","modulating bromodomains;\nmodulators of bromodomain activity（anti-viral）;\nmodulators of bromodomains;",{"v":232.30148,"d":"232.30"},"303093-76-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H12N2OS","free base","N/A","CC(=O)NC1=NC=C(CC2=CC=CC=C2)S1",1.792,2,1,3]
["P2108","WAY-299185","d5","L1700-121","in 10mM DMSO","TAOK2,pro-matrix metalloproteinase","others","TAOK2 inhibitor;\npro-matrix metalloproteinase inhibitors;",{"v":394.8989,"d":"394.90"},"333746-76-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H15ClN4O2S2","free base","N/A","COC1=CC=C(Cl)C=C1NC2=NC(=CS2)C3=C(C)N=C(NC(C)=O)S3",3.663,4,2,5]
["P2121","WAY-299862","a7","L1700-121","in 10mM DMSO","antiinflammatory","antiinflammatory","antiinflammatory activity",{"v":398.49852,"d":"398.50"},"303792-67-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H18N2O3S2","free base","N/A","OC1=C(NC(=O)CCCN2C(=S)SC(=C\\C3=CC=CC=C3)/C2=O)C=CC=C1",4.011,2,2,6]
["P2124","WAY-299914","d7","L1700-121","in 10mM DMSO","ubiquitin,acetyl-CoA carboxylase","Ubiquitin","ubiquitin-specific protease inhibitors;\nacetyl-CoA carboxylase inhibitor;\nacetyl-CoA carboxylase inhibitors;\nacetyl-CoA carboxylase (ACC) inhibitors;\ninhibitors of acetyl-CoA carboxylase;\nantiallergic agents;",{"v":236.29018,"d":"236.29"},"52505-51-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H12N2O2S","free base","N/A","CCOC(=O)C1=C(N)C2=C(S1)N=C(C)C=C2",1.771,3,1,3]
["P2136","WAY-300323","h8","L1700-121","in 10mM DMSO","others","Hedgehog","Hedgehog pathway antagonists;\nHedgehog pathway antagonists;",{"v":360.42894,"d":"360.43"},"111272-66-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H16N2O2S","free base","N/A","COC1=CC=C(C=C1)C(=O)NC2=CC=C(C=C2)C3=NC4=C(S3)C=CC=C4",4.607,3,1,4]
["P2148","WAY-300582","d10","L1700-121","in 10mM DMSO","ras","Cell Cycle","useful for the treatment of ras associated disorders;\nuseful for the treatment of ras associated disorders;",{"v":437.49312,"d":"437.49"},"306281-21-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H23N5O2","free base","N/A","CC1=CC=C(C=C1)C(=O)NC(=C/C2=C[N](N=C2C3=CC=CC=C3)C4=CC=CC=C4)/C(=O)NN",3.956,3,3,6]
["P2156","WAY-300916","d11","L1700-121","in 10mM DMSO","insulin-regulated aminopeptidase","others","inhibitors of insulin-regulated aminopeptidase",{"v":356.32944,"d":"356.33"},"374102-08-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H16N2O6","free base","N/A","CCOC(=O)C1=C(N)OC2=C(C=CC(=C2)O)C1C3=CC=C(C=C3)[N+]([O-])=O",2.839,3,2,5]
["P2159","WAY-301183","g11","L1700-121","in 10mM DMSO","cyclic nucleotide synthesis","others","inhibit cyclic nucleotide synthesis",{"v":436.25816,"d":"436.26"},"332382-63-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H14BrN3O3","free base","N/A","CN1C(=O)NC(=O)C2=C1NC3=C(C2C4=CC(=CC=C4)Br)C(=O)C5=C3C=CC=C5",2.826,3,2,1]
["P2177","WAY-301617","a4","L1700-122","in 10mM DMSO","11bHSD1","others","11b-hydroxysteroid dehydrogenase type 1 inhibitor",{"v":398.4009296,"d":"398.40"},"311773-87-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H13F3N2OS","free base","N/A","FC(F)(F)C1=C(NC(=O)C2=C(SC3=CC=CC=C3C#N)C=CC=C2)C=CC=C1",5.554,1,1,5]
["P2179","WAY-310331","c4","L1700-122","in 10mM DMSO","others","others","inhibiting mammalian S-nitrosoglutathione reductase",{"v":307.34318,"d":"307.34"},"625412-88-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17NO3","free base","N/A","OC(=O)CCC1=CC=C([N]1C2=CC=C(O)C=C2)C3=CC=CC=C3",4.264,1,1,5]
["P2195","WAY-311152-A","c6","L1700-122","in 10mM DMSO","Histamine Receptor","Neuronal Signaling,Immunology & Inflammation,GPCR & G Protein","antihistamine activity",{"v":285.3592032,"d":"285.36"},"160539-86-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H20FN3","free base","N/A","FC1=CC=C(CN2CCN(CC2)CC3=CN=CC=C3)C=C1",2.499,1,0,4]
["P2198","WAY-311207-A","f6","L1700-122","in 10mM DMSO","others","Neuronal Signaling","anesthetic effects",{"v":353.49774,"d":"353.50"},"58575-74-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H31NO2","free base","N/A","CC(C)OC1=CC=C(C=C1)C(O)C(CN2CCCCC2)C3=CC=CC=C3",4.563,1,1,7]
["P2211","WAY-311636","c8","L1700-122","in 10mM DMSO","others","others","antispasmodic activity",{"v":280.32114,"d":"280.32"},"7685-88-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H16N2O2","free base","N/A","O=C1CC(NCC2=CC=CC=C2)C(=O)N1C3=CC=CC=C3",2.063,2,1,4]
["P2219","WAY-311811","c9","L1700-122","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","integrin inhibitor for treating and preventing inflammatory diseases;\ninhibitors of solute transporters;\ninhibitors of urea transporter UT-B .",{"v":476.54746,"d":"476.55"},"376374-54-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H24N4O4S","free base","N/A","CC1=C(C=C(C=C1)C2=C3C=CC=CC3=C(NC4=CC=C(O)C=C4)N=N2)[S](=O)(=O)N5CCOCC5",4.205,5,2,5]
["P2231","WAY-312431","g10","L1700-122","in 10mM DMSO","others","others","modifying the acid content of citrus fruits",{"v":358.45458,"d":"358.45"},"73096-28-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H22N2O3S","free base","N/A","CC1=CC=C(NC(=O)C2CCCN2[S](=O)(=O)C3=CC=C(C)C=C3)C=C1",3.152,3,1,4]
["P2236","WAY-312522","d11","L1700-122","in 10mM DMSO","others","others","altering the lifespan of a eukaryotic organism",{"v":427.4983,"d":"427.50"},"381180-32-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H25N5O2","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)C\\C(C)=N\\NC(=O)C4=CC=CC=C4N",3.256,3,3,6]
["P2251","WAY-323237","c3","L1700-123","in 10mM DMSO","Cathepsin L","others","inhibitor for Cathepsin L",{"v":406.45762,"d":"406.46"},"853700-58-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H18N4O3S","free base","N/A","CCC1=CC=C(NC(=O)CSC2=NC(=C(N=N2)C3=CC=CO3)C4=CC=CO4)C=C1",4.909,6,1,7]
["P2254","WAY-323260","f3","L1700-123","in 10mM DMSO","lipoprotein oxidation","Neuronal Signaling","lipoprotein oxidation inhibitor (useful for treatment of neurological conditions)",{"v":314.17658,"d":"314.18"},"853710-07-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12BrNO","free base","N/A","BrC1=CC=C(OCC2=CC=CC=C2)C3=NC=CC=C13",4.331,2,0,3]
["P2272","WAY-323543","h5","L1700-123","in 10mM DMSO","soluble epoxide hydrolase","others","inhibitor of soluble epoxide hydrolase;\naltering the lifespan of a eukaryotic organism;",{"v":364.50222,"d":"364.50"},"854041-16-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H28N2O3S","free base","N/A","O=C(NC1CCCCCC1)C2CCN(CC2)[S](=O)(=O)C3=CC=CC=C3",2.941,3,1,4]
["P2281","WAY-323877","a7","L1700-123","in 10mM DMSO","Androgen Receptor,Anti-infection","Endocrinology & Hormones,Microbiology","Androgen Receptor modulator;\nantitubercular activity;\nantimycobacterial activity;",{"v":254.35006,"d":"254.35"},"167483-31-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H14N2S","free base","N/A","C(CC1=CC=CC=C1)SC2=NC3=C([NH]2)C=CC=C3",4.333,1,1,4]
["P2288","WAY-324034","h7","L1700-123","in 10mM DMSO","others","others","antioxidant and cytotoxic activities",{"v":404.3129,"d":"404.31"},"693234-15-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H15Cl2N3OS","free base","N/A","CC1=N[N](C2=CC=CC=C2)C3=C1C(SCC(=O)N3)C4=C(Cl)C=C(Cl)C=C4",4.759,2,1,2]
["P2295","WAY-324071","g8","L1700-123","in 10mM DMSO","PfDHODH","others","PfDHODH inhibitor",{"v":386.51104,"d":"386.51"},"372182-94-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H26N4O2S","free base","N/A","CC(C)CC1=NC2=C(C3=C1COC(C)(C)C3)C4=C(S2)C(=NC=N4)NCCO",3.516,4,2,5]
["P2307","WAY-324166","c10","L1700-123","in 10mM DMSO","others","wnt","wnt pathway antagonist;\nwnt pathway antagonist;",{"v":457.27408,"d":"457.27"},"663213-98-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H17BrN2O5","free base","N/A","COC1=CC(=CC(=C1OCC=C)Br)C2C3=C(OC(=C2C#N)N)C=C4OCOC4=C3",3.962,5,1,5]
["P2310","WAY-324216","f10","L1700-123","in 10mM DMSO","others","others","inhibitors of inhibitors of differentiation;\ninhibitors of inhibitors of differentiation;",{"v":341.40092,"d":"341.40"},"1146620-92-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H23NO4","free base","N/A","CC(C)COC(=O)C1C2OC3(CN(CC4=CC=CC=C4)C(=O)C13)C=C2",1.954,4,0,6]
["P2327","WAY-324512","g2","L1700-124","in 10mM DMSO","glucokinase","Others","glucokinase activator",{"v":297.73898,"d":"297.74"},"939052-77-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12ClN3O","free base","N/A","OC1=C(C=CC=C1)C2=NC(=N[NH]2)/C=C/C3=C(Cl)C=CC=C3",4.025,2,2,3]
["P2330","WAY-324567","b3","L1700-124","in 10mM DMSO","Anti-infection","Microbiology","antibacterial activity;",{"v":460.52162,"d":"460.52"},"160591-50-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C27H28N2O5","free base","N/A","COC1=CC(=C(C=C1)\\C=C/2CCCC3=C2OC(=C(C#N)C3C4=CC=C(OC)C=C4OC)N)OC",4.413,5,1,6]
["P2340","WAY-324680","d4","L1700-124","in 10mM DMSO","11β-HSD1","Others","11β-HSD1 inhibitor",{"v":456.4635296,"d":"456.46"},"489410-54-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H23F3N6O","free base","N/A","CN(CC1=C(C)[N](C)N=C1C)C(=O)C2=C3N=C(C=C([N]3N=C2)C(F)(F)F)C4=CC=C(C)C=C4",3.982,4,0,5]
["P2351","WAY-324759","g5","L1700-124","in 10mM DMSO","others","cancer","antitumor agent",{"v":434.46442,"d":"434.46"},"444908-85-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H18N2O5S","free base","N/A","COC1=CC=CC2=C1OC(=O)C(=C2)C(=O)NC3=C(C(N)=O)C(=C(C)S3)C4=CC=CC=C4",{"v":3.08,"d":"3.080"},5,2,5]
["P2363","WAY-324977","c7","L1700-124","in 10mM DMSO","Anti-infection","Microbiology","antibacterial activity;\naltering the lifespan of a eukaryotic organism;",{"v":240.26058,"d":"240.26"},"129227-36-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H12N4O","free base","N/A","CC1=N[N](C(=C1)C)C2=C(O)N=C3C=CC=CC3=N2",2.784,3,1,1]
["P2370","WAY-325092","b8","L1700-124","in 10mM DMSO","Others","Others","inhibitors of differentiation;",{"v":421.44582,"d":"421.45"},"510764-00-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H23N3O5","free base","N/A","CC(N1C(=O)C2=C(C=CC=C2)C1=O)C(=O)N3CCN(CC3)CC4=CC5=C(OCO5)C=C4",1.921,5,0,4]
["P2383","WAY-325387","g9","L1700-124","in 10mM DMSO","Others","Others","high inhibition rate against osteoclast formation",{"v":368.25436,"d":"368.25"},"445254-59-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H19Cl2NO3","free base","N/A","ClC1=CC=C(Cl)C(=C1)OCC2=CC=C(O2)C(=O)N3CCCCCC3",4.986,3,0,4]
["P2390","WAY-325417","f10","L1700-124","in 10mM DMSO","Others","Others","controlling invertebrate pests",{"v":350.41098,"d":"350.41"},"834913-12-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H22N2O3","free base","N/A","CC(C)(C)C1=CC=C(OCC2=CC=C(O2)C(=O)NC3=CC=CN=C3)C=C1",3.904,4,1,6]
["P2402","WAY-325461","b2","L1700-125","in 10mM DMSO","Others","Others","high inhibition rate against osteoclast formation",{"v":343.37528,"d":"343.38"},"445285-28-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H17NO3","free base","N/A","O=C(NC1=CC=CC=C1)C2=CC=C(COC3=CC=C4C=CC=CC4=C3)O2",4.563,3,1,5]
["P2405","WAY-325472","e2","L1700-125","in 10mM DMSO","11β-HSD1","Others","11β-HSD1 inhibitor",{"v":343.4168,"d":"343.42"},"438471-96-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H25NO4","free base","N/A","CCOC1=CC=C(OCC2=CC=C(O2)C(=O)N3CCC(C)CC3)C=C1",3.785,4,0,6]
["P2422","WAY-325680","f4","L1700-125","in 10mM DMSO","α-synuclein","others","inhibiting α-synuclein toxicity",{"v":363.3451632,"d":"363.35"},"869356-38-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H14FN5O2","free base","N/A","CC1=C(C=NC(=N1)NC2=NC3=C(O2)C=CC=C3)C(=O)NC4=CC=C(F)C=C4",3.462,5,2,4]
["P2425","WAY-325748","a5","L1700-125","in 10mM DMSO","folate cycle","Others","folate cycle inhibitor",{"v":386.40332,"d":"386.40"},"869469-29-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H18N4O3","free base","N/A","COC1=CC=C(C=C1)C2=NC3=C(C=CC=C3)[N]4C=C5C(=O)N(C)C(=O)N(C)C5=C24",3.217,4,0,2]
["P2432","WAY-325875","h5","L1700-125","in 10mM DMSO","CK1","Metabolism","CK1 inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":327.40738,"d":"327.41"},"868963-65-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H17N7S","free base","N/A","C[N]1C=CN=C1SCC2=NC(=NC(=N2)NC3=CC=C(C)C=C3)N",2.925,4,2,5]
["P2441","WAY-326067","a7","L1700-125","in 10mM DMSO","11β-HSD1","Others","11β-hydroxysteroid dehydrogenase type 1 inhibitor;",{"v":370.3958064,"d":"370.40"},"869709-06-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H20F2N4O","free base","N/A","FC(F)C1=CC(=NC2=C(C=N[N]12)C(=O)N3CCCCCC3)C4=CC=CC=C4",3.719,3,0,3]
["P2457","WAY-326166","a9","L1700-125","in 10mM DMSO","11β-HSD1","Others","11β-hydroxysteroid dehydrogenase type 1 inhibitor;",{"v":414.4483664,"d":"414.45"},"869774-94-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H24F2N4O2","free base","N/A","CCC1CCCCN1C(=O)C2=C3N=C(C=C(C(F)F)[N]3N=C2)C4=CC=C(OC)C=C4",4.147,4,0,5]
["P2464","WAY-326275","h9","L1700-125","in 10mM DMSO","Others","Others","inhibitor of lethal toxin pathway;\nuseful for modulating hepatocyte growth factor/scatter factor activity;",{"v":333.43012,"d":"333.43"},"869873-21-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H23N5","free base","N/A","CC(NC1=NC(=NC2=CC=CC=C12)N3CCNCC3)C4=CC=CC=C4",3.801,2,2,4]
["P2476","WAY-326387","d11","L1700-125","in 10mM DMSO","Anti-infection","Microbiology","anti-osteosarcoma activity;\nantibacterial activities;",{"v":343.33068,"d":"343.33"},"870758-11-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H17NO6","free base","N/A","CCOC(=O)C1=C(N)OC2=C(OC(=CC2=O)CO)C1C3=CC=CC=C3",0.651,5,2,5]
["P2484","WAY-326448","d2","L1700-126","in 10mM DMSO","cathepsin B","Proteases","cathepsin B inhibitor",{"v":347.34582,"d":"347.35"},"870763-67-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H13N3O5S","free base","N/A","CC1=CC=C(C=C1)[S](=O)(=O)[N]2N=C(OC(=O)C3=CC=CO3)C=C2N",2.861,6,1,5]
["P2496","WAY-326792","h3","L1700-126","in 10mM DMSO","Serotonin Transporter","Others","Serotonin Transporter Compound",{"v":274.40114,"d":"274.40"},"1041098-30-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H26N2O","free base","N/A","CN(C)C(C(=O)NC1CCCCC1)C2=CC=C(C)C=C2",3.443,1,1,4]
["P2499","WAY-326813","c4","L1700-126","in 10mM DMSO","Hsp90","Cytoskeletal Signaling","Hsp90 C-terminal inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":392.4692032,"d":"392.47"},"442898-49-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H25FN4O","free base","N/A","CCN1CCN(CC1)C2=NC3=CC=C(NC(=O)C4=CC=CC=C4F)C=C3C(=C2)C",{"v":4.5,"d":"4.500"},2,1,4]
["P2506","WAY-326996","b5","L1700-126","in 10mM DMSO","Anti-infection","Microbiology","inhibitor of flavivirus replication",{"v":476.52102,"d":"476.52"},"685868-32-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C27H28N2O6","free base","N/A","COC1=CC=C(C=C1)C2C(C(=O)NC3=CC=CC(=C3)OC)C4=CC(=C(OC)C=C4C(=O)N2C)OC",3.339,6,1,7]
["P2524","WAY-327362","d7","L1700-126","in 10mM DMSO","calcium channel","Transmembrane Transporters","calcium channel antagonist",{"v":426.52854,"d":"426.53"},"687574-49-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H26N2O4S","free base","N/A","CC1CCN(CC1)[S](=O)(=O)C2=CC=C3OC(=C(C)C3=C2)C(=O)NCC4=CC=CC=C4",3.988,4,1,5]
["P2532","WAY-327443","d8","L1700-126","in 10mM DMSO","Others","Others","cytotoxic agent",{"v":280.32444,"d":"280.32"},"693233-52-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H16N4O","free base","N/A","OC1=C(C#N)C(=NC(=N1)N2CCCCC2)C3=CC=CC=C3",3.774,2,1,2]
["P2539","WAY-327500","c9","L1700-126","in 10mM DMSO","phosphodiesterase type 10A","Others","inhibitors of phosphodiesterase type 10A",{"v":373.44608,"d":"373.45"},"892266-03-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H27N3O4","free base","N/A","CCN1CCN(CC1)C(=O)C2=CN(CC)C(=O)C3=CC(=C(OC)C=C23)OC",0.929,4,0,5]
["P2553","WAY-327951","a11","L1700-126","in 10mM DMSO","caspase","Apoptosis & Proteases","caspase enzyme inhibitor",{"v":473.97236,"d":"473.97"},"687590-53-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H24ClN3O4S","free base","N/A","ClC1=CC=C(CCNC(=O)C2=CC(=O)NC3=CC=C(C=C23)[S](=O)(=O)N4CCCCC4)C=C1",3.024,4,2,6]
["P2559","WAY-327958","g11","L1700-126","in 10mM DMSO","caspase","Apoptosis & Proteases","caspase enzyme inhibitor",{"v":441.50012,"d":"441.50"},"687591-25-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H23N3O5S","free base","N/A","COC1=CC=CC(=C1)CNC(=O)C2=CC(=O)NC3=CC=C(C=C23)[S](=O)(=O)N4CCCC4",1.565,5,2,6]
["P2574","WAY-328226","f3","L1700-127","in 10mM DMSO","CFTR","Transmembrane Transporters","modulating CFTR activity",{"v":345.39292,"d":"345.39"},"688050-45-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H23N3O4","free base","N/A","COC1=CC=C(C=C1)C2=CC(=NO2)C(=O)NCCCN3CCOCC3",1.602,5,1,7]
["P2577","WAY-328260","a4","L1700-127","in 10mM DMSO","CFTR","Transmembrane Transporters","modulating CFTR activity;\naltering the lifespan of a eukaryotic organism;",{"v":298.29336,"d":"298.29"},"909861-78-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H14N2O4","free base","N/A","COC1=CC=CC(=C1)C2=CC(=NO2)C(=O)NCC3=CC=CO3",2.479,5,1,5]
["P2585","WAY-329601","a5","L1700-127","in 10mM DMSO","others","kinase","kinase inhibitory activity",{"v":377.438,"d":"377.44"},"956964-95-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H15N3O4S2","free base","N/A","CCOC1=CC=C(NC(=O)C[S](=O)(=O)C2=CC=CC3=NSN=C23)C=C1",2.452,6,1,6]
["P2597","WAY-329762","e6","L1700-127","in 10mM DMSO","anti-infection","Microbiology","antitubercular activity",{"v":364.4358832,"d":"364.44"},"901224-47-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H17FN2OS","free base","N/A","CCN(C(=O)C1=CC2=CC3=CC=C(C)C=C3N=C2S1)C4=C(F)C=CC=C4",5.399,2,0,3]
["P2609","WAY-330337","a8","L1700-127","in 10mM DMSO","Others","Neuronal Signaling","neuroprotective effects;\naltering the lifespan of a eukaryotic organism;",{"v":310.34712,"d":"310.35"},"956204-00-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H18N2O3","free base","N/A","COC1=CC2=CC3=C(OC(=C3)C(=O)N4CCCCC4)N=C2C=C1",3.125,4,0,2]
["P2614","WAY-330540","f8","L1700-127","in 10mM DMSO","others","Microbiology","preventing norovirus infection",{"v":396.39814,"d":"396.40"},"956695-97-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H16N4O3","free base","N/A","OC(=O)C1=CC=C(C=C1)N2C(C3=CC=CN=C3)C4=C([NH]N=C4C5=CC=CC=C5)C2=O",3.347,4,1,4]
["P2629","WAY-331967","e10","L1700-127","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":358.49764,"d":"358.50"},"902585-05-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H26N2O2S","free base","N/A","CC1=C(CSCC(=O)NC2CCCCC2)N=C(O1)C3=C(C)C=CC=C3",3.966,3,1,6]
["P2636","WAY-331975","d11","L1700-127","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":392.9427,"d":"392.94"},"901721-67-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H25ClN2O2S","free base","N/A","CC1CCCCC1NC(=O)CSCC2=C(C)OC(=N2)C3=CC=CC=C3Cl",4.463,3,1,6]
["P2648","WAY-331989","h2","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":404.8855232,"d":"404.89"},"902585-95-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H18ClFN2O2S","free base","N/A","CC1=C(CSCC(=O)NCC2=C(Cl)C=CC=C2)N=C(O1)C3=C(F)C=CC=C3",4.074,3,1,7]
["P2657","WAY-332000","a4","L1700-128","in 10mM DMSO","beta-catenin","Wnt/beta-catenin","beta-catenin modulator;",{"v":372.52422,"d":"372.52"},"902168-10-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H28N2O2S","free base","N/A","CC1CCCCC1NC(=O)CSCC2=C(C)OC(=N2)C3=CC(=CC=C3)C",4.285,3,1,6]
["P2659","WAY-332002","c4","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":449.60824,"d":"449.61"},"901751-79-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H31N3O2S","free base","N/A","CC1CN(CCN1C2=CC=CC(=C2)C)C(=O)CSCC3=C(C)OC(=N3)C4=CC=C(C)C=C4",4.806,3,0,6]
["P2671","WAY-332023","g5","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":404.52302,"d":"404.52"},"1053086-89-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H28N2O4S","free base","N/A","COC1=CC=C(C=C1)C2=NC(=C(C)O2)C[S](=O)CC(=O)NC3CCCCC3C",{"v":2.67,"d":"2.670"},5,1,7]
["P2683","WAY-332035","c7","L1700-128","in 10mM DMSO","beta-catenin","Wnt/beta-catenin","beta-catenin modulator;",{"v":416.92104,"d":"416.92"},"1015858-20-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21ClN2O3S","free base","N/A","CC1=CC=CC(=C1)C2=NC(=C(C)O2)C[S](=O)CC(=O)NCC3=C(Cl)C=CC=C3",3.243,4,1,7]
["P2686","WAY-332038","f7","L1700-128","in 10mM DMSO","beta-catenin","Wnt/beta-catenin","beta-catenin modulator;",{"v":396.50256,"d":"396.50"},"958503-24-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H24N2O3S","free base","N/A","CC1=CC=C(CNC(=O)C[S](=O)CC2=C(C)OC(=N2)C3=CC(=CC=C3)C)C=C1",3.065,4,1,7]
["P2703","WAY-332060","g9","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":446.90396,"d":"446.90"},"1015858-82-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H19ClN2O5S","free base","N/A","CC1=C(C[S](=O)CC(=O)NCC2=CC3=C(OCO3)C=C2)N=C(O1)C4=CC=C(Cl)C=C4",2.525,6,1,7]
["P2710","WAY-332068","f10","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":360.47046,"d":"360.47"},"1015864-69-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H24N2O3S","free base","N/A","CC1=C(C[S](=O)CC(=O)NC2CCCC2)N=C(O1)C3=C(C)C=CC=C3",2.398,4,1,6]
["P2715","WAY-332074","c11","L1700-128","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":416.92104,"d":"416.92"},"1015865-20-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21ClN2O3S","free base","N/A","CC1=CC=C(CNC(=O)C[S](=O)CC2=C(C)OC(=N2)C3=CC=CC=C3Cl)C=C1",3.243,4,1,7]
["P2726","WAY-332088","f2","L1700-129","in 10mM DMSO","beta-catenin","Stem Cells & Wnt","beta-catenin modulator;",{"v":432.92044,"d":"432.92"},"902588-17-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21ClN2O4S","free base","N/A","CC1=C(C[S](=O)(=O)CC(=O)NCC2=CC=CC(=C2)Cl)N=C(O1)C3=CC=CC=C3C",3.339,5,1,7]
["P2733","WAY-343996","e3","L1700-129","in 10mM DMSO","Anti-infection","Microbiology","analgesics;\naltering the lifespan of a eukaryotic organism;\nantinociceptive properties;\nantifungal activity.",{"v":257.31094,"d":"257.31"},"346464-59-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H11N3OS","free base","N/A","CC1=C(C=CO1)C2=NN=C(S)[N]2C3=CC=CC=C3",3.052,3,0,2]
["P2745","WAY-345171","a5","L1700-129","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":294.4156,"d":"294.42"},"956140-65-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H10N2OS3","free base","N/A","CSCC1=NC2=C(C(=O)N1)C(=CS2)C3=CC=CS3",2.568,2,1,3]
["P2755","WAY-348941","c6","L1700-129","in 10mM DMSO","CD4 D1","others","a novel nonpeptide organic ligand of CD4 D1;\nimmunosuppressives;",{"v":269.32164,"d":"269.32"},"113143-13-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H11N3OS","free base","N/A","O=C(N\\N=C\\C1=C[NH]C2=C1C=CC=C2)C3=CC=CS3",{"v":2.93,"d":"2.930"},2,2,3]
["P2766","WAY-353603","f7","L1700-129","in 10mM DMSO","soluble epoxide hydrolase","others","Inhibitors for the soluble epoxide hydrolase",{"v":247.33274,"d":"247.33"},"340221-20-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H21NO2","free base","N/A","COC1=CC=C(NC(=O)CC2CCCCC2)C=C1",3.305,2,1,4]
["P2778","WAY-357996","b9","L1700-129","in 10mM DMSO","ERK1/2","MAPK","inhibitors of ERK1/2",{"v":274.3134,"d":"274.31"},"39582-95-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C10H10O5S2","free base","N/A","O=[S]1(=O)CC(O[S](=O)(=O)C2=CC=CC=C2)C=C1",0.582,3,0,3]
["P2786","WAY-359288-A","b10","L1700-129","in 10mM DMSO","others","cancer","anticancer",{"v":311.3750232,"d":"311.38"},"327975-20-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H18FN3O2S","free base","N/A","FC1=CC=C(C=C1)C(=O)NC(=S)NCCN2CCOCC2",1.943,2,2,6]
["P2799","WAY-381602","g11","L1700-129","in 10mM DMSO","phosphatidylcholine transfer protein","others","phosphatidylcholine transfer protein inhibitors",{"v":477.9593832,"d":"477.96"},"379696-86-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H17ClFN3O3S2","free base","N/A","CC1=C(NC(=S)NC(=O)C2=CC=C(F)C=C2)C=C(C=C1)[S](=O)(=O)NC3=CC=CC(=C3)Cl",{"v":5.61,"d":"5.610"},3,3,7]
["P2802","WAY-381644","b2","L1700-130","in 10mM DMSO","phosphatidylcholine transfer protein","others","phosphatidylcholine transfer protein inhibitors;\naltering the lifespan of eukaryotic organisms;",{"v":477.9593832,"d":"477.96"},"379713-58-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H17ClFN3O3S2","free base","N/A","CC1=CC=C(NC(=S)NC(=O)C2=CC=C(F)C=C2)C=C1[S](=O)(=O)NC3=CC=CC=C3Cl",{"v":5.61,"d":"5.610"},3,3,7]
["P2810","WAY-382534","b3","L1700-130","in 10mM DMSO","Pin1","others","altering the lifespan of a eukaryotic organism;\nPin1 peptidyl prolyl isomerase-modulating compounds;",{"v":332.399,"d":"332.40"},"1008487-75-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H20N4O","free base","N/A","CC1=CC=C(C=C1)[N]2C(=CC(=C2C)/C=N/NC(=O)C3=CC=NC=C3)C",3.186,3,1,4]
["P2820","WAY-388279","d4","L1700-130","in 10mM DMSO","Anti-infection","Microbiology","antimitotic activity;\naltering the lifespan of a eukaryotic organism;",{"v":323.32112,"d":"323.32"},"615282-41-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H13NO6S","free base","N/A","COC1=CC=C2C=C(SC(=O)C2=C1OC)C(=O)NCC(O)=O",0.819,5,1,5]
["P2831","WAY-604499","g5","L1700-130","in 10mM DMSO","Anti-infection","Microbiology","antifungal activity",{"v":197.25744,"d":"197.26"},"354542-00-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C8H11N3OS","free base","N/A","CCC1=NN=C(NC(=O)C2CC2)S1",1.109,3,1,3]
["P2843","WAY-604968","c7","L1700-130","in 10mM DMSO","Anti-infection","Microbiology","bactericidal and fungicidal activity",{"v":266.321,"d":"266.32"},"182199-66-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H10N4S","free base","N/A","CC1=NN=C2[N]1C=NC3=C2C(=CS3)C4=CC=CC=C4",2.532,3,0,1]
["P2855","WAY-605650","g8","L1700-130","in 10mM DMSO","Anti-infection","Microbiology","Inhibitors of bacterial type III secretion system",{"v":347.79282,"d":"347.79"},"380543-06-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H18ClNO4","free base","N/A","CC(C)(OC1=CC=C(Cl)C=C1)C(=O)NCC2=CC3=C(OCO3)C=C2",3.685,4,1,5]
["P2859","WAY-606012","c9","L1700-130","in 10mM DMSO","p53","Apoptosis","stabilizing p53 mutants",{"v":378.44752,"d":"378.45"},"380314-37-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H18N4O2S","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)CSC4=NC(=CC=N4)O",4.095,3,2,5]
["P2875","WAY-606816","c11","L1700-130","in 10mM DMSO","IDE,PHOSPHO1,CTP synthase","Others","extracellular IDE inhibitor;\ninhibitor of PHOSPHO1;\nbacterial PyrG (CTP synthase) inhibitor;\nmodulating RNA-binding proteins;",{"v":426.46556,"d":"426.47"},"521318-69-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H14N2O5S2","free base","N/A","OC(=O)C1=C(N[S](=O)(=O)C2=CC(=CC=C2)N3SC4=C(C=CC=C4)C3=O)C=CC=C1",3.275,4,1,5]
["P2882","WAY-607145","b2","L1700-131","in 10mM DMSO","Anti-infection","Microbiology","altering the lifespan of a eukaryotic organism;\nanti-hepatitis B activity;",{"v":411.54034,"d":"411.54"},"380471-87-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21N3O2S2","free base","N/A","O=C1CSC(N1CC2CCCO2)C3=C[N](N=C3C4=CC=CS4)C5=CC=CC=C5",4.148,3,0,5]
["P2885","WAY-607289-A","e2","L1700-131","in 10mM DMSO","σ1 receptor","Others","σ1 receptor radioligands",{"v":273.33026,"d":"273.33"},"385371-21-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H19N3O2","free base","N/A","N#CCCN1CCN(CC1)CC2=CC3=C(OCO3)C=C2",1.607,2,0,4]
["P2902","WAY-607882","f4","L1700-131","in 10mM DMSO","retroviral","Microbiology","antiretroviral activity",{"v":488.4853864,"d":"488.49"},"455300-59-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C27H22F2N4O3","free base","N/A","FC1=CC=C(C=C1)\\C=C\\2CCCC3C(N(N=C23)C(=O)COC(=O)C4=NC=CN=C4)C5=CC=C(F)C=C5",4.113,6,0,6]
["P2905","WAY-608046","a5","L1700-131","in 10mM DMSO","Others","Others","altering the lifespan of a eukaryotic organism;\ninhibitor of cholesterol absorption;",{"v":330.3815,"d":"330.38"},"452278-67-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H10N2O3S2","free base","N/A","O=C1N(CC2=NC3=C(S2)C=CC=C3)[S](=O)(=O)C4=C1C=CC=C4",2.425,4,0,2]
["P2918","WAY-608333","f6","L1700-131","in 10mM DMSO","Others","cancer","altering the lifespan of a eukaryotic organism;\nanti-cancer;",{"v":347.41364,"d":"347.41"},"882222-22-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H21N5O","free base","N/A","CN1CCN(CC1)C(=O)C2=C[N](N=C2C3=CN=CC=C3)C4=CC=CC=C4",2.224,3,0,3]
["P2932","WAY-620124","d8","L1700-131","in 10mM DMSO","NDH-2","Others","NDH-2 inhibitor",{"v":299.36754,"d":"299.37"},"626222-52-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H21N3O2","free base","N/A","O=C(CCC1=NC2=C(C=CC=C2)C(=O)N1)NC3CCCCC3",2.111,3,2,4]
["P2938","WAY-620252","b9","L1700-131","in 10mM DMSO","p53","Apoptosis","stabilizing p53 mutants;",{"v":454.52034,"d":"454.52"},"956357-71-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C27H26N4O3","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)CN4C(=O)NC(C)(C4=O)C5=CC=C(C)C=C5",4.246,3,2,5]
["P2950","WAY-620537","f10","L1700-131","in 10mM DMSO","tubulin","Cytoskeletal Signaling","bind to tubulin and activate GEF-H1",{"v":414.3837632,"d":"414.38"},"733000-36-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H19FN2O6","free base","N/A","[O-][N+](=O)C1=CC(=CC=C1)C(=O)NC(=O)COC(=O)C2(CCCC2)C3=CC(=CC=C3)F",3.748,4,1,7]
["P2958","WAY-620929","f11","L1700-131","in 10mM DMSO","NADPH,Myeloperoxidase","Immunology & Inflammation","inhibitor of NADPH-oxidase;\nMyeloperoxidase (MPO) inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":305.39526,"d":"305.40"},"146381-57-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H19N3O2S","free base","N/A","O=C1N(CCCN2CCOCC2)C(=S)NC3=C1C=CC=C3",{"v":2.03,"d":"2.030"},2,1,4]
["P2962","WAY-621057","b2","L1700-132","in 10mM DMSO","USP14","Proteases","USP14 inhibitor",{"v":312.40606,"d":"312.41"},"301683-65-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H24N2O2","free base","N/A","CC1=CC=C(C=C1)[N]2C(=CC(=C2C)C(=O)CN3CCOCC3)C",2.917,2,0,4]
["P2974","WAY-621733","f3","L1700-132","in 10mM DMSO","DNA Topoisomerase Iia","Others","Inhibitor of the Human DNA Topoisomerase Iia;\naltering the lifespan of a eukaryotic organism;",{"v":351.37758,"d":"351.38"},"745070-17-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H17N3O5S","free base","N/A","CN(C1CC[S](=O)(=O)C1)C(=O)COC(=O)C2=N[NH]C3=C2C=CC=C3",0.531,6,1,5]
["P2981","WAY-621848","e4","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","anti-fungi",{"v":235.32204,"d":"235.32"},"34967-98-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H21NO2","free base","N/A","CN(C1CCCCC1)C(=O)C2=C(C)OC(=C2)C",2.497,2,0,2]
["P2991","WAY-622134","g5","L1700-132","in 10mM DMSO","11β-HSD1","Others","11β-HSD1 inhibitor",{"v":448.57712,"d":"448.58"},"409356-56-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H28N2O3S","free base","N/A","CC1=C(C)C=C(C=C1)N(CC2=CC=C(C=C2)C(=O)N3CCC4=C(C3)C=CC=C4)[S](C)(=O)=O",4.575,3,0,5]
["P2999","WAY-624876","g6","L1700-132","in 10mM DMSO","anti-infection","Microbiology","antileishmanial ;\naltering the lifespan of a eukaryotic organism;",{"v":427.49668,"d":"427.50"},"745033-86-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H17N3O4S2","free base","N/A","COC1=CC=C(C=C1)C2=NCC(CSC3=NN=C(O3)C4=CC5=C(OCO5)C=C4)S2",4.134,7,0,6]
["P3000","WAY-636782","h6","L1700-132","in 10mM DMSO","mPTP","others","mPTP modulators",{"v":354.40122,"d":"354.40"},"792957-74-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H18N2O2","free base","N/A","OC1=NC2=C(C=CC=C2)C(=C1)C(=O)NC3=C(CC4=CC=CC=C4)C=CC=C3",5.072,2,2,4]
["P3001","WAY-636833","a7","L1700-132","in 10mM DMSO","others","others","increasing stress tolerance in plants",{"v":329.84704,"d":"329.85"},"792960-68-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H16ClN3S","free base","N/A","CC(SC1=NN=C([N]1C)C2=CC=C(Cl)C=C2)C3=CC=CC=C3",5.033,2,0,4]
["P3002","WAY-636839","b7","L1700-132","in 10mM DMSO","11b-HSD1","others","11b-HSD1 inhibitor",{"v":340.5271,"d":"340.53"},"792960-91-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H20N2OS3","free base","N/A","CSC1=NN=C(SCC(=O)[C]23C[CH]4[CH2]C([CH2][CH](C4)C2)C3)S1",4.066,3,0,5]
["P3003","WAY-637017","c7","L1700-132","in 10mM DMSO","AKT,NF-kB","PI3K/Akt/mTOR,NF-kB","Dual AKT/NF-kB Inhibitor",{"v":386.87844,"d":"386.88"},"695204-60-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H11ClN4OS2","free base","N/A","NC1=NN=C(S1)SC2=C(C3=CC=CC=C3)C4=C(NC2=O)C=CC(=C4)Cl",3.487,3,2,3]
["P3004","WAY-637061","d7","L1700-132","in 10mM DMSO","KLF5","Others","altering the lifespan of a eukaryotic organism;\nKLF5 inhibitor;",{"v":364.4823,"d":"364.48"},"793722-28-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H20N2O3S2","free base","N/A","CCOC(=O)C1=C(C)N=C(NC(=O)C2=CC3=C(CCC(C)C3)S2)S1",3.978,4,1,5]
["P3005","WAY-637184-A","e7","L1700-132","in 10mM DMSO","vanilloid receptor subtype 1","others","antagonists of vanilloid receptor subtype 1;\ninsecticides and acaricides;",{"v":232.3214,"d":"232.32"},"70505-90-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H20N2O","free base","N/A","CN1CCC2(CC1)CC(N)C3=C(O2)C=CC=C3",0.796,1,1,0]
["P3006","WAY-637193","f7","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","antibacterial activity;\ninhibition of protein glycosylation;",{"v":141.13128,"d":"141.13"},"52553-11-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C4H7N5O","free base","N/A","CC1=NN=C(N)N(N)C1=O",-1.352,3,2,0]
["P3007","WAY-637195","g7","L1700-132","in 10mM DMSO","others","others","inhibition of protein glycosylation",{"v":199.16736,"d":"199.17"},"197793-89-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C6H9N5O3","free base","N/A","NN1C(=NN=C(CCC(O)=O)C1=O)N",-1.507,4,2,3]
["P3008","WAY-637196","h7","L1700-132","in 10mM DMSO","others","others","inhibition of protein glycosylation",{"v":209.22838,"d":"209.23"},"197793-86-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C7H7N5OS","free base","N/A","NN1C(=NN=C(C2=CC=CS2)C1=O)N",0.275,3,2,1]
["P3009","WAY-637221-A","a8","L1700-132","in 10mM DMSO","p38","MAPK","p38 MAPK inhibitor",{"v":186.2099,"d":"186.21"},"52855-74-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H10N2O","free base","N/A","O=C(CC1=NC=C[NH]1)C2=CC=CC=C2",1.562,2,1,3]
["P3010","WAY-637300","b8","L1700-132","in 10mM DMSO","LXR","Others","LXR modulators",{"v":230.26246,"d":"230.26"},"956411-90-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H14N2O2","free base","N/A","CC1(NC(=O)NC1=O)C2=CC3=C(CCC3)C=C2",1.927,2,2,1]
["P3011","WAY-637379","c8","L1700-132","in 10mM DMSO","Bcl-2","Apoptosis","altering the lifespan of a eukaryotic organism;\nBcl-2 inhibitor;",{"v":448.29926,"d":"448.30"},"791598-98-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H19Cl2N3O4","free base","N/A","CN(CC(=O)NC1=C(Cl)C=CC=C1Cl)C(=O)CCCN2C(=O)C3=C(C=CC=C3)C2=O",2.662,4,1,7]
["P3012","WAY-637471","d8","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","antitubercular activity",{"v":344.3203632,"d":"344.32"},"793729-44-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H9FN4O3S","free base","N/A","FC1=CC=C(C=C1)C2=NN=C(CSC3=NN=C(O3)C4=CC=CO4)O2",2.889,7,0,5]
["P3013","WAY-637475","e8","L1700-132","in 10mM DMSO","PDE4B,P-glycoprotein","others","PDE4B inhibitor;\nP-glycoprotein inhibitor;",{"v":348.35204,"d":"348.35"},"793729-54-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H16N2O4","free base","N/A","[O-][N+](=O)C1=CC=C(C=C1)C2=CC=C(O2)C(=O)N3CCCC4=C3C=CC=C4",{"v":4.45,"d":"4.450"},2,0,3]
["P3014","WAY-637476","f8","L1700-132","in 10mM DMSO","gonadotropin-releasing hormone","others","gonadotropin-releasing hormone antagonists",{"v":288.32168,"d":"288.32"},"793729-55-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H12N2O3S","free base","N/A","[O-][N+](=O)C1=CC=C(S1)C(=O)N2CCCC3=C2C=CC=C3",3.323,1,0,2]
["P3015","WAY-637483","g8","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","Antibacterial activities;\nantiulcer agent;",{"v":309.3409,"d":"309.34"},"21013-92-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H15N3O4S","free base","N/A","CC1=CC=C(C=C1)[S](=O)(=O)NC(CC2=C[NH]C=N2)C(O)=O",0.778,4,2,6]
["P3016","WAY-637486","h8","L1700-132","in 10mM DMSO","alanyl aminopeptidase, dipeptidyl peptidase IV","others","Dual alanyl aminopeptidase and dipeptidyl peptidase IV inhibitor",{"v":383.5071,"d":"383.51"},"526188-81-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H25N3O2S","free base","N/A","CCOC(=O)N1CCN(CC1)C(C2=CC=CS2)C3=C(C)[NH]C4=C3C=CC=C4",{"v":4.01,"d":"4.010"},2,1,5]
["P3017","WAY-637570","a9","L1700-132","in 10mM DMSO","others","others","inhibit the prion protein conversion from PrPC to PrPSc",{"v":336.42746,"d":"336.43"},"1097624-48-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H24N2O2","free base","N/A","CCC(C)C(NC(=O)C1=CC=CC=C1)C(=O)N2CCC3=C2C=CC=C3",3.738,2,1,5]
["P3018","WAY-637574","b9","L1700-132","in 10mM DMSO","GPRC6A Receptor","others","GPRC6A Receptor",{"v":366.45996,"d":"366.46"},"794575-46-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H14N4OS2","free base","N/A","NC1=NN=C(SCC(=O)C2=C([NH]C3=C2C=CC=C3)C4=CC=CC=C4)S1",3.999,3,2,5]
["P3019","WAY-637658","c9","L1700-132","in 10mM DMSO","KLF5","others","KLF5 inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":367.48778,"d":"367.49"},"793731-79-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17N3OS2","free base","N/A","CC1=CC2=C(C=C1)N=C(NC(=O)CCCC3=NC4=C(S3)C=CC=C4)S2",4.742,3,1,5]
["P3020","WAY-637664","d9","L1700-132","in 10mM DMSO","InhA","others","InhA inhibitors;\naltering the lifespan of a eukaryotic organism;",{"v":336.3844,"d":"336.38"},"353522-37-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H20N2O3","free base","N/A","O=C(CCCC1=C[NH]C2=CC=CC=C12)NCC3=CC4=C(OCO4)C=C3",{"v":3.63,"d":"3.630"},3,2,6]
["P3021","WAY-637685","e9","L1700-132","in 10mM DMSO","PfDHODH","others","active against PfDHODH resistant mutants",{"v":247.72006,"d":"247.72"},"790719-57-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H14ClNO","free base","N/A","CC(=O)C1=C(C)[NH]C=C1CC2=C(Cl)C=CC=C2",3.448,1,1,3]
["P3022","WAY-637686","f9","L1700-132","in 10mM DMSO","PfDHODH","others","active against PfDHODH resistant mutants",{"v":281.2729696,"d":"281.27"},"790719-58-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H14F3NO","free base","N/A","CC(=O)C1=C(C)[NH]C=C1CC2=CC(=CC=C2)C(F)(F)F",3.725,1,1,4]
["P3023","WAY-637921","g9","L1700-132","in 10mM DMSO","others","Neuronal Signaling","neuroprotective effects (useful in the treatment of neurodegenerative diseases)",{"v":330.40142,"d":"330.40"},"794583-45-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H18N2O3S","free base","N/A","O=C(NC1=NC(=CS1)C2=CC3=C(OCCO3)C=C2)C4CCCC4",{"v":3.35,"d":"3.350"},4,1,3]
["P3024","WAY-637936","h9","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","altering the lifespan of a eukaryotic organism;\nparamyxovirus inhibitor;",{"v":346.4422032,"d":"346.44"},"795282-68-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H15FN2OS2","free base","N/A","FC1=CC=C(C=C1)C2=CSC(=N2)NC(=O)CCCC3=CC=CS3",4.243,2,1,6]
["P3025","WAY-637940","a10","L1700-132","in 10mM DMSO","HIV","Microbiology","Inhibit HIV-1 Entry",{"v":347.38888,"d":"347.39"},"795282-95-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H17N3O4S","free base","N/A","N[S](=O)(=O)C1=CC=C(NC(=O)CNC(=O)CC2=CC=CC=C2)C=C1",0.414,4,3,6]
["P3026","WAY-638082","b10","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","anti-infective agent;\nmethionine aminopeptidase inhibitor;",{"v":255.29506,"d":"255.30"},"313687-86-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H9N3OS","free base","N/A","O=C(NC1=NC=CS1)C2=NC3=C(C=CC=C3)C=C2",2.226,3,1,2]
["P3027","WAY-638088","c10","L1700-132","in 10mM DMSO","others","Neuronal Signaling","neuroprotective effects (useful in the treatment of neurodegenerative diseases)",{"v":243.32412,"d":"243.32"},"332055-83-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H13NOS","free base","N/A","O=C(NC1=CC2=C(CCC2)C=C1)C3=CC=CS3",3.625,1,1,2]
["P3028","WAY-638103","d10","L1700-132","in 10mM DMSO","tubulin","Cytoskeletal Signaling","antitubulin agent",{"v":281.26284,"d":"281.26"},"793712-73-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H11NO4","free base","N/A","O=C(NC1=CC2=C(OCO2)C=C1)C3=CC4=C(O3)C=CC=C4",2.977,4,1,2]
["P3029","WAY-638106","e10","L1700-132","in 10mM DMSO","others","others","antiarrhythmic agent;\nantiarrhythmic agent;",{"v":450.48704,"d":"450.49"},"92084-79-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H26N4O5","free base","N/A","CCOC(=O)N1CCN(CC1)C(=O)CN2C(=O)NC(C2=O)(C3=CC=CC=C3)C4=CC=CC=C4",1.785,5,1,6]
["P3030","WAY-638127","f10","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","antitubercular activity",{"v":276.24478,"d":"276.24"},"313981-44-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H12N2O5","free base","N/A","COC1=CC=CC=C1CNC(=O)C2=CC=C(O2)[N+]([O-])=O",2.019,3,1,5]
["P3031","WAY-638137","g10","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","antibacterial activities",{"v":368.471,"d":"368.47"},"793713-92-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H20N2O4S2","free base","N/A","CC1=CC=CC(=C1)[S](=O)(=O)NCCN[S](=O)(=O)C2=CC=CC(=C2)C",2.273,4,2,7]
["P3032","WAY-638178-A","h10","L1700-132","in 10mM DMSO","others","Neuronal Signaling","antidepressant",{"v":340.41616,"d":"340.42"},"691008-82-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H24N2O3","free base","N/A","OC(CN1CCN(CC1)CC2=CC3=C(OCO3)C=C2)C4=CC=CC=C4",2.701,2,1,5]
["P3033","WAY-638199","a11","L1700-132","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator;\nAndrogen Receptor modulator;",{"v":292.35344,"d":"292.35"},"1351369-16-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H16N2O3S","free base","N/A","COC1=CC(=CC=C1)CN2C(=O)NC3(CCSC3)C2=O",1.205,3,1,3]
["P3034","WAY-638311","b11","L1700-132","in 10mM DMSO","abscisic acid receptor","others","abscisic acid receptor agonist",{"v":321.3385096,"d":"321.34"},"612042-35-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H10F3NO2S2","free base","N/A","FC(F)(F)C1=CC(=CC=C1)[S](=O)(=O)NCC2=CC=CS2",3.006,2,1,5]
["P3035","WAY-638358","c11","L1700-132","in 10mM DMSO","carbonic anhydrase","Metabolism","carbonic anhydrase inhibitor",{"v":305.3522,"d":"305.35"},"78659-11-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H15N3O3S","free base","N/A","N[S](=O)(=O)C1=CC=C(CCNC(=O)C2=NC=CC=C2)C=C1",0.925,4,2,5]
["P3036","WAY-638359","d11","L1700-132","in 10mM DMSO","glucocorticoid receptor","Endocrinology & Hormones","glucocorticoid receptor modulator",{"v":319.8009632,"d":"319.80"},"794560-57-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H19ClFNO","free base","N/A","CC(CCC1=CC=CC=C1)NC(=O)CC2=C(Cl)C=CC=C2F",4.681,1,1,6]
["P3037","WAY-638394","e11","L1700-132","in 10mM DMSO","others","others","treating bone deficit conditions",{"v":333.38376,"d":"333.38"},"190437-83-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H19N3O2","free base","N/A","O=C(NC1=CC=C(C=C1)N2CCOCC2)C3=NC4=CC=CC=C4C=C3",3.079,3,1,3]
["P3038","WAY-638400","f11","L1700-132","in 10mM DMSO","carbonic anhydrase","Metabolism","carbonic anhydrase inhibitory activity",{"v":243.34404,"d":"243.34"},"794557-15-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H21NO","free base","N/A","O=C(NC1CCCC2=C1C=CC=C2)C3CCCC3",3.643,1,1,2]
["P3039","WAY-638430","g11","L1700-132","in 10mM DMSO","Anti-infection","Microbiology","antimycobacterial and antiplasmodial agent",{"v":282.3204,"d":"282.32"},"794563-45-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H10N4OS","free base","N/A","O=C(NC1=NC(=CS1)C2=NC=CC=C2)C3=CN=CC=C3",1.686,4,1,3]
["P3040","WAY-638440","h11","L1700-132","in 10mM DMSO","type I MetAPs,Anti-infection","Microbiology","Inhibitor of methionine aminopeptidases (MetAPs);\nantiviral activities;\ntype I MetAPs inhibitor;",{"v":205.23638,"d":"205.24"},"301208-58-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C9H7N3OS","free base","N/A","O=C(NC1=NC=CS1)C2=CC=CC=N2",0.889,3,1,2]
["P3041","WAY-638449","a2","L1700-133","in 10mM DMSO","HpNikR","others","inhibitor for HpNikR",{"v":470.52304,"d":"470.52"},"794563-97-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H26N6O3","free base","N/A","O=C(CN1C(=O)NC2(CCC3=C2C=CC=C3)C1=O)NC4=CC=C(C=C4)C5=NN=C6CCCCC[N]56",2.818,5,2,4]
["P3042","WAY-638459","b2","L1700-133","in 10mM DMSO","p53","Apoptosis","stabilizing p53 mutants;\nstabilizing p53 mutants;",{"v":421.40276,"d":"421.40"},"794553-31-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H19N3O6","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)C(C)OC(=O)C4=CC=C(O4)[N+]([O-])=O",4.268,4,1,7]
["P3043","WAY-638487","c2","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","anti negative-sense ssRNA virus infections",{"v":378.87306,"d":"378.87"},"796067-84-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H19ClN2O3S","free base","N/A","COC1=C(O)C(=CC(=C1)C(=S)N2CCN(CC2)C3=C(Cl)C=CC=C3)O",4.461,1,2,4]
["P3044","WAY-638544","d2","L1700-133","in 10mM DMSO","MCL-1","Apoptosis","modulation of MCL-1",{"v":340.3747232,"d":"340.37"},"796065-72-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H13FN4OS","free base","N/A","FC1=C(OCCSC2=NC3=C(N=N2)C4=C([NH]3)C=CC=C4)C=CC=C1",4.605,4,1,5]
["P3045","WAY-638575","e2","L1700-133","in 10mM DMSO","Other","cancer","antitumor agent",{"v":289.31304,"d":"289.31"},"401936-27-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H11N5O2S","free base","N/A","C[N]1N=NN=C1SCCN2C(=O)C3=C(C=CC=C3)C2=O",0.904,5,0,4]
["P3046","WAY-638584","f2","L1700-133","in 10mM DMSO","neuropeptide Y","Neuronal Signaling","neuropeptide Y antagonist",{"v":436.52336,"d":"436.52"},"289700-48-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H24N2O4S","free base","N/A","O=C(NC1=CC=C(C=C1)[S](=O)(=O)N2CCOCC2)C(C3=CC=CC=C3)C4=CC=CC=C4",2.948,4,1,6]
["P3047","WAY-638592","g2","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","for treating, ameliorating, or preventing disease conditions caused by a viral infection with neg.-sense ssRNA viruses",{"v":359.37798,"d":"359.38"},"796053-09-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H17N3O3","free base","N/A","OCC[N]1N=C(C2=CC=CC=C2)C3=C1N=CC(=C3)C(=O)C4=C(O)C=CC=C4",3.297,3,2,5]
["P3048","WAY-638666","h2","L1700-133","in 10mM DMSO","Others","Neuronal Signaling","neuroprotective effects",{"v":271.37728,"d":"271.38"},"794563-32-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H17NOS","free base","N/A","CCC1=C(C)C=C(S1)C(=O)N2CCC3=C2C=CC=C3",4.147,1,0,2]
["P3049","WAY-638697","a3","L1700-133","in 10mM DMSO","α7β1 integrin","Others","α7β1 integrin modulatory agent;",{"v":414.53944,"d":"414.54"},"796083-16-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H26N2O5S2","free base","N/A","CCCN(C1CC[S](=O)(=O)C1)C(=O)C2=CC=C(C=C2)[S](=O)(=O)N3CCCC3",1.202,5,0,6]
["P3050","WAY-638700","b3","L1700-133","in 10mM DMSO","PPAR","Metabolism","PPAR modulator",{"v":354.42612,"d":"354.43"},"686770-29-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H18N4O2S","free base","N/A","CC(=O)NCCNC(=O)C1=C[N](N=C1C2=CC=CS2)C3=CC=CC=C3",2.357,3,2,6]
["P3051","WAY-638741","c3","L1700-133","in 10mM DMSO","glucocerebrosidase","Others","Glucocerebrosidase Inhibitor",{"v":400.4961,"d":"400.50"},"796085-51-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H20N4OS","free base","N/A","O=C(N1CCN(CC1)C2=C3C=CC=CC3=NC(=N2)C4=CC=CS4)C5=CC=CC=C5",4.544,3,0,3]
["P3052","WAY-638774","d3","L1700-133","in 10mM DMSO","pyruvate kinase M2","Metabolism","pyruvate kinase M2 activator;",{"v":442.4816632,"d":"442.48"},"796092-26-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H19FN2O6S2","free base","N/A","FC1=CC(=CC=C1)[S](=O)(=O)N2CCN(CC2)[S](=O)(=O)C3=CC4=C(OCCO4)C=C3",1.522,6,0,4]
["P3053","WAY-638778","e3","L1700-133","in 10mM DMSO","SHP2","others","inhibition of SHP2 phosphatase",{"v":298.35956,"d":"298.36"},"343618-41-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H14N2O2S","free base","N/A","COC1=CC=C(CN2C(=S)NC3=C(C=CC=C3)C2=O)C=C1",3.709,2,1,3]
["P3054","WAY-638832","f3","L1700-133","in 10mM DMSO","Other","Immunology & Inflammation","antiulcer agent",{"v":260.35464,"d":"260.35"},"196797-05-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H16N2OS","free base","N/A","CC(=O)C1=C(C)N=C(NCCC2=CC=CC=C2)S1",2.854,2,1,5]
["P3055","WAY-638833","g3","L1700-133","in 10mM DMSO","Others","Neuronal Signaling","neuroprotective effects;\naltering the lifespan of a eukaryotic organism;",{"v":277.3172,"d":"277.32"},"794576-60-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H15NO2","free base","N/A","O=C(NC1=CC2=C(CCC2)C=C1)C3=CC4=C(O3)C=CC=C4",4.266,2,1,2]
["P3056","WAY-638847","h3","L1700-133","in 10mM DMSO","human methionine aminopeptidase 1","Others","inhibitor of human methionine aminopeptidase 1",{"v":218.2749,"d":"218.27"},"478257-65-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H10N2OS","free base","N/A","CC(=O)C1=C(C)N=C(S1)C2=NC=CC=C2",1.802,3,0,2]
["P3057","WAY-638857","a4","L1700-133","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator;\nurease inhibitor;",{"v":255.26862,"d":"255.27"},"1351446-58-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H13NO3","free base","N/A","OC(=O)C1CN(C(=O)C1)C2=C3C=CC=CC3=CC=C2",1.639,2,0,2]
["P3058","WAY-638861","b4","L1700-133","in 10mM DMSO","FXR,diacylglycerol acyltransferase","Metabolism","FXR inhibitor;\ndiacylglycerol acyltransferase inhibitor;",{"v":278.30526,"d":"278.31"},"905589-98-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14N2O2","free base","N/A","OC(=O)C1=C[N](CC2=CC=CC=C2)N=C1C3=CC=CC=C3",{"v":3.64,"d":"3.640"},2,0,4]
["P3059","WAY-638867","c4","L1700-133","in 10mM DMSO","NIK,FAK","Angiogenesis & Cytoskeletal Signaling","NIK inhibitor;\nFAK inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":180.25014,"d":"180.25"},"3524-30-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C9H16N4","free base","N/A","CN1CCC(CC1)[N]2N=CC=C2N",-0.032,1,1,1]
["P3060","WAY-638924","d4","L1700-133","in 10mM DMSO","Others","Others","including S1P for guiding pluripotent stem cells to an injury",{"v":341.43066,"d":"341.43"},"796093-87-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H19N5OS","free base","N/A","C[N]1N=NN=C1SCC(=O)C2=C(C)[N](CC3=CC=CC=C3)C(=C2)C",2.653,4,0,6]
["P3061","WAY-638934","e4","L1700-133","in 10mM DMSO","Others","cancer,Immunology & Inflammation","useful for the treatment of cancer and inflammatory disease;",{"v":314.36226,"d":"314.36"},"796083-72-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H14N4O2S","free base","N/A","CN(C)C(=O)C1=C(C)C2=C(S1)N=C(NC2=O)C3=NC=CC=C3",1.749,4,1,2]
["P3062","WAY-638944","f4","L1700-133","in 10mM DMSO","Others","Neuronal Signaling","potential antianxiety, antidepressant, and antipsychotic agent",{"v":242.27976,"d":"242.28"},"137448-39-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H14N6","free base","N/A","C1CN(CCN1C2=NC=CN=C2)C3=NC=CC=N3",0.601,4,0,2]
["P3063","WAY-638948","g4","L1700-133","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":294.36932,"d":"294.37"},"1351448-98-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H18N2O3S","free base","N/A","NC(=O)C1CCCN(C1)C(=O)CCC(=O)C2=CC=CS2",0.762,3,1,5]
["P3064","WAY-639009","h4","L1700-133","in 10mM DMSO","p38","MAPK","p38 inhibitor",{"v":339.81872,"d":"339.82"},"956323-98-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H18ClN3O","free base","N/A","CC1=N[N](C(=C1C(=O)NCCC2=CC=CC=C2)Cl)C3=CC=CC=C3",{"v":3.91,"d":"3.910"},2,1,5]
["P3065","WAY-639012","a5","L1700-133","in 10mM DMSO","Others","Others","increasing stress tolerance in plants",{"v":335.42278,"d":"335.42"},"618413-75-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17N3OS","free base","N/A","CC[N]1C(=NN=C1C2=CC=CO2)SCC3=C4C=CC=CC4=CC=C3",4.644,3,0,5]
["P3066","WAY-639019","b5","L1700-133","in 10mM DMSO","Bcl-2","Apoptosis","altering the lifespan of a eukaryotic organism;\nmodulate the function of anti-apoptotic proteins such as Bcl-2 and related Bcl-2 family members;",{"v":342.45518,"d":"342.46"},"793728-59-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H22N2O2S","free base","N/A","COC1=C(C=CC=C1)N2CCN(CC2)C(=O)C3=CC4=C(CCC4)S3",3.737,2,0,3]
["P3067","WAY-639024-A","c5","L1700-133","in 10mM DMSO","sodium channel","Transmembrane Transporters","useful for the treatment and/or prevention of sodium channel mediated diseases or conditions",{"v":370.48674,"d":"370.49"},"497228-34-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H26N2O","free base","N/A","CC1=CC(=CC=C1)C(=O)N2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4",4.883,1,0,4]
["P3068","WAY-639108","d5","L1700-133","in 10mM DMSO","Mcl-1","Apoptosis","inhibitor of Mcl-1",{"v":478.52028,"d":"478.52"},"790237-66-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H22N4O5S","free base","N/A","CC(=O)NC1=CC=C(C=C1)C2=CSC(=N2)NC(=O)C3CN(C(=O)C3)C4=CC5=C(OCCO5)C=C4",1.736,6,2,5]
["P3069","WAY-639117","e5","L1700-133","in 10mM DMSO","PKM2","Metabolism","PKM2 activator",{"v":290.31926,"d":"290.32"},"785809-41-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14N4O","free base","N/A","CC1=CN2C(=O)C=C(C[N]3C=NC4=C3C=CC=C4)N=C2C=C1",1.742,3,0,2]
["P3070","WAY-639228-A","f5","L1700-133","in 10mM DMSO","Others","Others","antithrombotic or anticoagulant agent",{"v":380.50316,"d":"380.50"},"179051-05-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H24N2O2S","free base","N/A","O=[S](=O)(NC1CCN(CC1)CC2=CC=CC=C2)C3=CC=C4C=CC=CC4=C3",3.343,2,1,5]
["P3071","WAY-639234","g5","L1700-133","in 10mM DMSO","cav2.2 calcium channel","Transmembrane Transporters","cav2.2 calcium channel blocking agent ;",{"v":449.4461296,"d":"449.45"},"796096-78-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H18F3N3O3S","free base","N/A","FC(F)(F)C1=C(C=CC=C1)[S](=O)(=O)N2CCN(CC2)C(=O)C3=NC4=C(C=CC=C4)C=C3",3.385,4,0,4]
["P3072","WAY-639251","h5","L1700-133","in 10mM DMSO","Aslfm","others","inhibitor of Aslfm",{"v":314.35896,"d":"314.36"},"796055-86-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H14N2O3S","free base","N/A","OC1=NC=C(C=C1)C(=O)N(CC2=CC=CO2)CC3=CC=CS3",2.479,3,1,5]
["P3073","WAY-639267","a6","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","antiviral activity",{"v":452.54766,"d":"452.55"},"796056-83-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H24N4O5S2","free base","N/A","O=[S](=O)(N1CCOCC1)C2=CC=C(C=C2)[S](=O)(=O)N3CCN(CC3)C4=NC=CC=C4",0.769,6,0,5]
["P3074","WAY-639284","b6","L1700-133","in 10mM DMSO","Mcl-1","Apoptosis","inhibitors of Mcl-1",{"v":350.19932,"d":"350.20"},"796058-45-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H13Cl2N3O2","free base","N/A","ClC1=C(Cl)C(=CC=C1)NC(=O)CN2CC(=O)NC3=C2C=CC=C3",2.763,2,2,3]
["P3075","WAY-639299","c6","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","altering the lifespan of a eukaryotic organism;\nparamyxovirus inhibitor;",{"v":385.50306,"d":"385.50"},"796059-20-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H19N3O2S2","free base","N/A","CC(=O)NC1=CC=C(C=C1)C2=CSC(=N2)NC(=O)CCCC3=CC=CS3",3.158,3,2,7]
["P3076","WAY-639359","d6","L1700-133","in 10mM DMSO","antiinflammatory","Immunology & Inflammation","antiinflammatory and antalgic activities",{"v":236.26858,"d":"236.27"},"58962-95-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H12N2O","free base","N/A","CC1=C([N]2C=CC=CC2=C1)C(=O)C3=CN=CC=C3",2.693,2,0,2]
["P3078","WAY-639446","f6","L1700-133","in 10mM DMSO","antiinflammatory","Immunology & Inflammation,cancer","anti-inflammatory and anti-cancer activity",{"v":319.38032,"d":"319.38"},"724746-07-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H13N3OS","free base","N/A","CC1=C(C2=CC=CC=C2)C3=C(S1)N=C(NC3=O)C4=NC=CC=C4",3.221,3,1,2]
["P3079","WAY-639461","g6","L1700-133","in 10mM DMSO","mGluR5","Neuronal Signaling","mGluR5 neg. allosteric modulator",{"v":292.12018,"d":"292.12"},"339103-05-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H7Cl2N3O","free base","N/A","ClC1=CC=C(C(=C1)Cl)C2=NC(=NO2)C3=NC=CC=C3",3.751,4,0,2]
["P3080","WAY-639483","h6","L1700-133","in 10mM DMSO","11β-HSD1","Others","11β-HSD1 inhibitor",{"v":382.52234,"d":"382.52"},"791125-94-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H26N4OS","free base","N/A","CC1=CC(=C(C)C=C1)[N]2N=NN=C2SCC(=O)[C]34C[CH]5[CH2]C([CH2][CH](C5)C3)C4",{"v":4.91,"d":"4.910"},4,0,5]
["P3081","WAY-639497","a7","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","altering the lifespan of a eukaryotic organism;\nantibacterial agent;",{"v":427.495,"d":"427.50"},"1031873-45-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H25N3O3","free base","N/A","CC1N(C(=O)N(CC(=O)NC(C2=CC=CC=C2)C3=CC=CC=C3)C1=O)C4=CC=C(C)C=C4",4.054,3,1,6]
["P3082","WAY-639549","b7","L1700-133","in 10mM DMSO","AChE,BuChE","Neuronal Signaling","AChE and BuChE enzyme inhibitor",{"v":372.45956,"d":"372.46"},"794579-71-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H24N2O2","free base","N/A","CC1=CC(=CC=C1)C(=O)NCCC(=O)NC(C2=CC=CC=C2)C3=CC=CC=C3",4.027,2,2,7]
["P3083","WAY-639621","c7","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","anti-Tuberculosis activity",{"v":327.42392,"d":"327.42"},"794582-71-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H13N3OS2","free base","N/A","O=C(CSC1=CC=CC=C1)NC2=NC(=CS2)C3=NC=CC=C3",{"v":3.23,"d":"3.230"},3,1,5]
["P3084","WAY-639698","d7","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","antitubercular activity",{"v":326.3299,"d":"326.33"},"476317-29-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H10N4O3S","free base","N/A","[O-][N+](=O)C1=C(C=CC=C1)C(=O)NC2=NC(=CS2)C3=NC=CC=C3",2.731,3,1,4]
["P3085","WAY-639715","e7","L1700-133","in 10mM DMSO","Others","Neuronal Signaling","neuroprotective effects",{"v":341.4058432,"d":"341.41"},"795285-30-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H16FN5S","free base","N/A","CC1=C(NC2=NC(=NC(=N2)N)CSC3=CC=C(F)C=C3)C=CC=C1",4.496,3,2,5]
["P3086","WAY-639717","f7","L1700-133","in 10mM DMSO","Mcl-1","Apoptosis","inhibitor of Mcl-1",{"v":431.53174,"d":"431.53"},"795285-35-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H21N5O3S2","free base","N/A","CN(C)[S](=O)(=O)C1=CC(=CC=C1)NC2=NN=C(CS2)C3=CC=C(NC(C)=O)C=C3",1.961,5,2,6]
["P3087","WAY-639729","g7","L1700-133","in 10mM DMSO","Others","Others","photoactive pesticide",{"v":257.37384,"d":"257.37"},"113214-30-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H11NS2","free base","N/A","CC1=C(N=C(S1)C2=CC=CS2)C3=CC=CC=C3",4.256,1,0,2]
["P3088","WAY-639760","h7","L1700-133","in 10mM DMSO","glucocerebrosidase,PDE-5,cGMP phosphodiesterase,TXA2 synthetase","Metabolism","glucocerebrosidase (GCase) modulator;\nβ-Glucocerebrosidase Modulator;\nPDE-5 inhibitor;\ninhibitor of cGMP phosphodiesterase and TXA2 synthetase;",{"v":312.36784,"d":"312.37"},"157862-79-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H16N4","free base","N/A","C(NC1=NC(=NC2=C1C=CC=C2)C3=CN=CC=C3)C4=CC=CC=C4",3.788,3,1,4]
["P3089","WAY-639807","a8","L1700-133","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":296.1233,"d":"296.12"},"791127-56-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C10H10BrN5O","free base","N/A","CC1=C(Br)C=CC(=C1)NC(=O)C[N]2C=NN=N2",1.011,4,1,3]
["P3090","WAY-639872","b8","L1700-133","in 10mM DMSO","NaV1.7","Others","NaV1.7 inhibitor",{"v":363.40974,"d":"363.41"},"796119-18-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21N3O3","free base","N/A","O=C(COC1=C2N=CC=CC2=CC=C1)NC3=C(C=CC=C3)N4CCOCC4",2.486,4,1,5]
["P3091","WAY-639881","c8","L1700-133","in 10mM DMSO","T1R1/T1R3 or T1R2/T1R3 ligand","Others","taste receptor T1R1/T1R3 or T1R2/T1R3 ligand",{"v":331.2071,"d":"331.21"},"844900-78-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H15BrN2O","free base","N/A","BrC1=CC(=CN=C1)C(=O)NC2CCCC3=C2C=CC=C3",3.235,2,1,2]
["P3092","WAY-639889","d8","L1700-133","in 10mM DMSO","neuropeptide Y-5","Neuronal Signaling","neuropeptide Y-5 antagonist",{"v":413.51478,"d":"413.51"},"432506-24-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H27N5O","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)CN4CCN(CC4)C5=NC=CC=C5",4.022,2,1,5]
["P3093","WAY-639907","e8","L1700-133","in 10mM DMSO","L-CPT1","Others","L-CPT1 inhibitor",{"v":257.31094,"d":"257.31"},"851723-60-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H11N3OS","free base","N/A","O=C(NCC1=CC=CS1)C2=N[NH]C3=C2C=CC=C3",2.433,2,2,3]
["P3094","WAY-639917","f8","L1700-133","in 10mM DMSO","Others","Others","useful in the treatment and/or prevention of disorders of the dopamine system",{"v":277.3205,"d":"277.32"},"159305-08-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H15N3O","free base","N/A","O=C(N1CCC2=C(C1)C=CC=C2)C3=N[NH]C4=C3C=CC=C4",2.974,2,1,1]
["P3095","WAY-639921","g8","L1700-133","in 10mM DMSO","PDE-5,cGMP phosphodiesterase and TXA2 synthetase","Metabolism","PDE-5 inhibitor;\ninhibitors of cGMP phosphodiesterase and TXA2 synthetase;",{"v":318.39556,"d":"318.40"},"157862-84-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H14N4S","free base","N/A","C(NC1=C2C=CC=CC2=NC(=N1)C3=CN=CC=C3)C4=CC=CS4",3.528,3,1,4]
["P3096","WAY-640015","h8","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","antimycobacterial activity",{"v":343.76436,"d":"343.76"},"204651-69-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14ClN3O3","free base","N/A","CC(=O)NC1=CC=C(OCC2=NN=C(O2)C3=CC=C(Cl)C=C3)C=C1",2.674,5,1,5]
["P3097","WAY-640071","a9","L1700-133","in 10mM DMSO","antiinflammatory","Immunology & Inflammation","anti-inflammatory and analgesic activities",{"v":252.71996,"d":"252.72"},"796115-75-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H9ClN2OS","free base","N/A","ClC1=C(CC(=O)NC2=NC=CS2)C=CC=C1",2.311,2,1,3]
["P3098","WAY-640150","b9","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","inhibit the Mycobacterium tuberculosis PyrG enzyme activity;\nanti-Tuberculosis activity;",{"v":345.86636,"d":"345.87"},"956369-64-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H24ClN3O","free base","N/A","CC1=N[N](CC2=CC=CC=C2)C(=C1C(=O)NC3CCCCCC3)Cl",4.327,2,1,4]
["P3099","WAY-640166","c9","L1700-133","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":290.31596,"d":"290.32"},"796123-34-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H14N2O2","free base","N/A","CC1=CC(=NO1)C(=O)NC2=CC3=C(CC4=C3C=CC=C4)C=C2",3.305,3,1,2]
["P3100","WAY-640169","d9","L1700-133","in 10mM DMSO","GATA4-NKX2-5","Others","modulate the GATA4-NKX2-5 transcriptional synergy/modulate heart regeneration",{"v":346.34276,"d":"346.34"},"796123-56-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H14N6O2","free base","N/A","CC1=C(C(=O)NC2=CC=C(C=C2)[N]3C=NN=N3)C(=NO1)C4=CC=CC=C4",2.048,6,1,4]
["P3101","WAY-640257","e9","L1700-133","in 10mM DMSO","TcTS","Others","TcTS inhibitor (inhibitors of Trypanosoma cruzi trans-sialidase)",{"v":409.30796,"d":"409.31"},"796858-11-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H14Cl2N2O4S2","free base","N/A","COCCNC(=O)C1=CC=C(N[S](=O)(=O)C2=C(Cl)SC(=C2)Cl)C=C1",1.974,4,2,7]
["P3102","WAY-640327","f9","L1700-133","in 10mM DMSO","Others","Others","regulating insulin secretion;\naltering the lifespan of a eukaryotic organism;",{"v":413.46842,"d":"413.47"},"851184-73-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H23N3O3","free base","N/A","CC1=C(C)C(=CC=C1)NC(=O)CNC(=O)COC2=CC=C(C=C2)C3=CC=C(C=C3)C#N",3.879,3,2,7]
["P3103","WAY-640360","g9","L1700-133","in 10mM DMSO","TREK-2","Others","activate TREK-2;\naltering the lifespan of a eukaryotic organism;",{"v":441.56464,"d":"441.56"},"851400-21-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C28H31N3O2","free base","N/A","CC1CN(CCN1C2=CC(=CC=C2)C)C(=O)CC(NC(=O)C3=CC=CC=C3)C4=CC=CC=C4",4.657,2,1,6]
["P3104","WAY-640400","h9","L1700-133","in 10mM DMSO","K-Ras","Cell Cycle","inhibit interactions among activated K-Ras proteins and their upstream and downstream effectors",{"v":368.4527,"d":"368.45"},"791132-77-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H20N4O2S","free base","N/A","CC(=O)C1=CC=C(C=C1)N2CCN(CC2)CC3=CC(=O)N4C=CSC4=N3",1.554,3,0,4]
["P3105","WAY-640414","a10","L1700-133","in 10mM DMSO","dopamine receptor","Neuronal Signaling & GPCR & G Protein","dopamine receptor modulator",{"v":294.39078,"d":"294.39"},"748798-97-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H22N2O","free base","N/A","O=C(CN1CCCC1)NC2=C(CC3=CC=CC=C3)C=CC=C2",3.392,1,1,5]
["P3106","WAY-640426","b10","L1700-133","in 10mM DMSO","Others","Microbiology","inhibitors of Mycobacterium tuberculosis",{"v":302.3052,"d":"302.31"},"851278-26-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H10N2O4S","free base","N/A","C1OC2=C(O1)C=C(OCC3=NN=C(O3)C4=CC=CS4)C=C2",2.611,6,0,4]
["P3107","WAY-640486","c10","L1700-133","in 10mM DMSO","11β-HSD1","Others","11β-HSD1 inhibitor",{"v":381.4084,"d":"381.41"},"851282-35-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H15N5O3S","free base","N/A","CC1=CC=C(C=C1)[N]2N=NN=C2SCC(=O)C3=CC4=C(OCC(=O)N4)C=C3",2.332,6,1,5]
["P3108","WAY-640509","d10","L1700-133","in 10mM DMSO","glucocerebrosidase","Others","Glucocerebrosidase Inhibitor",{"v":489.54622,"d":"489.55"},"851185-20-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H23N5O4S","free base","N/A","O=[S](=O)(N1CCN(CC1)C2=C3C=CC=CC3=NC(=N2)C4=CN=CC=C4)C5=CC6=C(OCCO6)C=C5",2.928,7,0,4]
["P3109","WAY-640582","e10","L1700-133","in 10mM DMSO","neuropeptide Y5 receptor","Neuronal Signaling","neuropeptide Y5 receptor ligand",{"v":319.35718,"d":"319.36"},"322723-35-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17N3O2","free base","N/A","CC[N]1C2=C(C=CC=C2)C3=C1C=CC(=C3)NC(=O)C4=NOC(=C4)C",{"v":3.69,"d":"3.690"},3,1,3]
["P3110","WAY-640666","f10","L1700-133","in 10mM DMSO","advanced glycosylation end product receptor","Others","altering the lifespan of a eukaryotic organism;\nmodulators of advanced glycosylation end product receptor (RAGE) activity;",{"v":497.5304496,"d":"497.53"},"796082-31-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H26F3N3O4S","free base","N/A","FC(F)(F)C1=CC(=CC=C1)[S](=O)(=O)N2CCC(CC2)C(=O)NC3=C(C=CC=C3)N4CCOCC4",2.996,4,1,6]
["P3111","WAY-640674","g10","L1700-133","in 10mM DMSO","glucocerebrosidase","Others","glucocerebrosidase (GCase) modulator",{"v":338.40512,"d":"338.41"},"796079-91-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H18N4","free base","N/A","C1CC2=C(CN1C3=C4C=CC=CC4=NC(=N3)C5=CN=CC=C5)C=CC=C2",4.217,3,0,2]
["P3112","WAY-640783","h10","L1700-133","in 10mM DMSO","FLT3","Angiogenesis & Protein Tyrosine Kinase","FLT3 inhibitor",{"v":280.79626,"d":"280.80"},"851208-04-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H9ClN2S2","free base","N/A","CC1=C(C)C2=C(S1)N=C(N=C2Cl)C3=CC=CS3",{"v":4.19,"d":"4.190"},2,0,1]
["P3113","WAY-640810","a11","L1700-133","in 10mM DMSO","beta2 integrin","Others","beta2 integrin agonist;\naltering the lifespan of a eukaryotic organism;",{"v":386.46952,"d":"386.47"},"851206-31-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H18N4OS","free base","N/A","O=C(NC1=NC2=C(CCCC2)S1)C3=C4C=CC=CC4=NC(=C3)C5=CC=NC=C5",3.984,4,1,3]
["P3114","WAY-640817","b11","L1700-133","in 10mM DMSO","Anti-infection","Microbiology","altering the lifespan of a eukaryotic organism;\nparamyxovirus inhibitor;",{"v":358.47772,"d":"358.48"},"851206-59-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H18N2O2S2","free base","N/A","COC1=CC=C(C=C1)C2=CSC(=N2)NC(=O)CCCC3=CC=CS3",4.021,3,1,7]
["P3115","WAY-640833","c11","L1700-133","in 10mM DMSO","Others","Others","regulating insulin secretion",{"v":336.3844,"d":"336.38"},"851187-80-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H20N2O3","free base","N/A","CC1=CC=C(NC(=O)C2=CC=C(OCC3=C(C)ON=C3C)C=C2)C=C1",{"v":3.55,"d":"3.550"},4,1,5]
["P3116","WAY-640878","d11","L1700-133","in 10mM DMSO","KCNQ1 potassium channel","Transmembrane Transporters","KCNQ1 potassium channel activator;\naltering the lifespan of a eukaryotic organism;",{"v":457.56572,"d":"457.57"},"1008671-38-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H23N3O4S2","free base","N/A","COC1=CC=C(C=C1)C2=CSC(=N2)NC(=O)C3CCCCN3[S](=O)(=O)C4=CC=CC=C4",3.563,5,1,6]
["P3117","WAY-640879","e11","L1700-133","in 10mM DMSO","CB1 receptor","GPCR & G Protein","agonist for CB1 receptor",{"v":452.52276,"d":"452.52"},"851212-80-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H24N2O5S","free base","N/A","CC1=C(C=C(NC(=O)C2=C(OC3=CC=CC=C3)C=CC=C2)C=C1)[S](=O)(=O)N4CCOCC4",3.465,5,1,6]
["P3118","WAY-640898","f11","L1700-133","in 10mM DMSO","FPR1 receptor","Others","FPR1 receptor antagonist",{"v":379.47534,"d":"379.48"},"851453-95-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H21N3O2S","free base","N/A","CSCCC(NC(=O)C1=C(C)C2=C(O1)C=CC=C2)C3=NC4=C([NH]3)C=CC=C4",4.223,3,2,6]
["P3119","WAY-640957","g11","L1700-133","in 10mM DMSO","15-lipoxygenase","others","inhibitor of 15-lipoxygenase;\nantithrombotics;",{"v":368.3734096,"d":"368.37"},"120823-38-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H15F3N2O2S","free base","N/A","FC(F)(F)C1=CC(=CC=C1)[S](=O)(=O)NCCC2=C[NH]C3=C2C=CC=C3",3.881,2,2,6]
["P3120","WAY-641007","h11","L1700-133","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":289.3528,"d":"289.35"},"1351440-41-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H15N3O2S","free base","N/A","CC(O)CN1CC(=O)C(=C1N)C2=NC3=C(S2)C=CC=C3",1.324,2,2,3]
["P3121","WAY-641018","a2","L1700-134","in 10mM DMSO","FLT3","Angiogenesis & Protein Tyrosine Kinase","FLT3 inhibitor",{"v":262.3506,"d":"262.35"},"354562-75-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H10N2OS2","free base","N/A","CC1=C(C)C2=C(S1)N=C(NC2=O)C3=CC=CS3",2.865,2,1,1]
["P3122","WAY-641910","b2","L1700-134","in 10mM DMSO","Mcl-1","Apoptosis","inhibitor of Mcl-1;\naltering the lifespan of a eukaryotic organism;",{"v":365.49182,"d":"365.49"},"851687-22-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H23N3OS","free base","N/A","CC(SC1=NC2=C([NH]1)C=CC(=C2)C)C(=O)NC3CCCC4=C3C=CC=C4",5.058,2,2,4]
["P3123","WAY-642338","c2","L1700-134","in 10mM DMSO","Mcl-1","Apoptosis","inhibitor of Mcl-1;\naltering the lifespan of a eukaryotic organism;",{"v":321.3962,"d":"321.40"},"851458-34-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H15N3OS","free base","N/A","C(NC1=NN=C(CS1)C2=CC3=C(O2)C=CC=C3)C4=CC=CC=C4",4.325,3,1,4]
["P3124","WAY-642555","d2","L1700-134","in 10mM DMSO","Mcl-1","Apoptosis","inhibitors of Mcl-1;\naltering the lifespan of a eukaryotic organism;",{"v":415.46284,"d":"415.46"},"956780-46-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H21N3O5S","free base","N/A","CC1(NC(=O)N(CC(=O)NC2CC[S](=O)(=O)C2)C1=O)C3=C4C=CC=CC4=CC=C3",0.552,5,2,4]
["P3125","WAY-642938","e2","L1700-134","in 10mM DMSO","Others","Others","modulator of insect olfactory receptors;\naltering the lifespan of a eukaryotic organism;",{"v":471.574,"d":"471.57"},"851274-39-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H25N5O2S","free base","N/A","CCOC1=C(C=CC=C1)[N]2C(=NN=C2C3=CN=CC=C3)SCC(=O)N4CCCC5=C4C=CC=C5",{"v":4.54,"d":"4.540"},5,0,7]
["P3126","WAY-643053","f2","L1700-134","in 10mM DMSO","others","others","analgesic activities",{"v":401.50246,"d":"401.50"},"330555-46-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H19N3O3S2","free base","N/A","CCOC(=O)C1=C(NC(=O)CSC2=NC3=C([NH]2)C=CC=C3)SC4=C1CCC4",3.983,4,2,7]
["P3127","WAY-643198","g2","L1700-134","in 10mM DMSO","others","cancer","anti-cancer activity",{"v":320.36508,"d":"320.37"},"749220-49-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H12N2O2S","free base","N/A","O=C(CSC1=C2C=CC=CC2=NC=N1)C3=CC4=C(O3)C=CC=C4",{"v":4.32,"d":"4.320"},4,0,4]
["P3128","WAY-643578","h2","L1700-134","in 10mM DMSO","MCL-1","Apoptosis","modulation of MCL-1",{"v":395.7845296,"d":"395.78"},"956910-01-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H13ClF3N3O3S","free base","N/A","FC(F)(F)C1=CC(=C(SCC(=O)NC(=O)CN2CCCC2=O)N=C1)Cl",1.731,4,1,6]
["P3129","WAY-655778","a3","L1700-134","in 10mM DMSO","β3-adrenergic receptor,5-HT3 receptor,Anti-infection","Neuronal Signaling,\nGPCR & G Protein,Microbiology","enhance functional O-mannosyl glycans (FOG) of Alpha-dystroglycan (α-DG);\nantifungal agent;\nβ3-adrenergic receptor agonist;\n5-HT3 receptor agonist;",{"v":233.3326,"d":"233.33"},"232263-03-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H15N3S","free base","N/A","C1CN(CCN1)CC2=NC3=C(S2)C=CC=C3",1.602,1,1,2]
["P3130","WAY-655810","b3","L1700-134","in 10mM DMSO","PKM2","Metabolism","PKM2 modulator",{"v":418.46348,"d":"418.46"},"847840-70-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H22N2O6S","free base","N/A","O=C(COC1=CC=CC=C1)N2CCN(CC2)[S](=O)(=O)C3=CC4=C(OCCO4)C=C3",1.449,6,0,5]
["P3131","WAY-655821","c3","L1700-134","in 10mM DMSO","storeoperated calcium (SOC) channel","Transmembrane Transporters","storeoperated calcium (SOC) channels modulator",{"v":443.5639,"d":"443.56"},"847840-96-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H25N5OS","free base","N/A","CC1=CC(=C(C=C1)[N]2N=NN=C2SC(C(=O)NC3=C(C)C=CC(=C3)C)C4=CC=CC=C4)C",{"v":6.1,"d":"6.100"},4,1,6]
["P3132","WAY-655834","d3","L1700-134","in 10mM DMSO","proline transporter","others","proline transporter inhibitor",{"v":358.43628,"d":"358.44"},"796977-98-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H22N4O","free base","N/A","O=C(CC1=CC=C(C=C1)C2=CC=CC=C2)N3CCN(CC3)C4=NC=CC=N4",3.168,3,0,4]
["P3133","WAY-655953","e3","L1700-134","in 10mM DMSO","JAMM protease","proteases","JAMM protease inhibitor",{"v":338.44334,"d":"338.44"},"848249-35-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H26N2O2","free base","N/A","CCC1=C(OCC(=O)NC2=C(C)C=C(C=C2)N3CCCC3)C=CC=C1",4.501,2,1,6]
["P3134","WAY-656018","f3","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","anthelmintic activity",{"v":301.72768,"d":"301.73"},"107249-99-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H12ClN3O2","free base","N/A","ClC1=CC=CC=C1OCC(=O)NC2=NC3=C([NH]2)C=CC=C3",3.171,3,2,4]
["P3135","WAY-656021","g3","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","anthelmintic activity;\naltering the lifespan of a eukaryotic organism;",{"v":267.28262,"d":"267.28"},"107249-98-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H13N3O2","free base","N/A","O=C(COC1=CC=CC=C1)NC2=NC3=C([NH]2)C=CC=C3",2.507,3,2,4]
["P3136","WAY-656135","h3","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":294.36932,"d":"294.37"},"1351286-63-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H18N2O3S","free base","N/A","COC(=O)C1CN(CCS1)C(=O)NC2=CC=C(C)C=C2",1.913,3,1,3]
["P3137","WAY-656238","a4","L1700-134","in 10mM DMSO","others","others","analgesic activity",{"v":311.33518,"d":"311.34"},"107249-97-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H17N3O3","free base","N/A","COC1=C(OC)C=C(CC(=O)NC2=NC3=C([NH]2)C=CC=C3)C=C1",2.673,4,2,5]
["P3138","WAY-656416","b4","L1700-134","in 10mM DMSO","MAGL/FAAH","Metabolism","MAGL/FAAH inhibitor",{"v":416.47236,"d":"416.47"},"852828-17-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H24N4O3","free base","N/A","[O-][N+](=O)C1=CC=C(NC(=O)N2CCN(CC2)C(C3=CC=CC=C3)C4=CC=CC=C4)C=C1",4.199,1,1,5]
["P3139","WAY-656439","c4","L1700-134","in 10mM DMSO","MCL-1","Apoptosis","modulation of MCL-1",{"v":359.38128,"d":"359.38"},"852828-79-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H17N5O2","free base","N/A","CC1=CC=C(NC(=O)COC2=C3C=N[N](C4=CC=CC=C4)C3=NC=N2)C=C1",3.321,5,1,5]
["P3140","WAY-656494","d4","L1700-134","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","immune regulant",{"v":286.71634,"d":"286.72"},"852830-03-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H11ClN4O","free base","N/A","ClC1=CC(=CC=C1)NC(=O)NC2=NC3=C([NH]2)C=CC=C3",3.244,2,3,2]
["P3141","WAY-656520","e4","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":291.26426,"d":"291.26"},"852830-98-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H9N5O2","free base","N/A","[O-][N+](=O)C1=CC=C(C=C1)C2=N[N]3C=NC4=C(C=CC=C4)C3=N2",2.848,3,0,2]
["P3142","WAY-656522","f4","L1700-134","in 10mM DMSO","others","cancer","Anticancer activity;\nantioxidant;",{"v":294.37086,"d":"294.37"},"852831-10-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14N2OS","free base","N/A","CC1=NC2=C(C=CC=C2)C(=N1)SCC(=O)C3=CC=CC=C3",{"v":3.68,"d":"3.680"},3,0,4]
["P3143","WAY-656627","g4","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","antimalarial agent",{"v":388.84474,"d":"388.84"},"852845-92-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H21ClN2O4","free base","N/A","ClC1=CC(=C(C=C1)N2CCOCC2)NC(=O)CC3=CC4=C(OCCO4)C=C3",2.949,4,1,4]
["P3144","WAY-656661","h4","L1700-134","in 10mM DMSO","others","cancer","anti-proliferative effect",{"v":408.44706,"d":"408.45"},"852846-73-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H24N2O5","free base","N/A","CC1=C2OC(=O)C=C(CN3CCN(CC3)CC4=CC5=C(OCO5)C=C4)C2=CC=C1O",3.486,4,1,4]
["P3145","WAY-656665","a5","L1700-134","in 10mM DMSO","Androgen Receptor","Neuronal Signaling, Endocrinology & Hormones","neuroprotective effect;\nAndrogen Receptor modulator;\naltering the lifespan of a eukaryotic organism;",{"v":293.35966,"d":"293.36"},"852846-92-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H19NO2","free base","N/A","COC1=C(C=CC=C1)/C=C/C(=O)NC2=CC3=C(CCC3)C=C2",4.123,2,1,4]
["P3146","WAY-656903","b5","L1700-134","in 10mM DMSO","NMDA receptor","Neuronal Signaling","NMDAR modulator",{"v":353.43806,"d":"353.44"},"852902-01-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H19N3O2S","free base","N/A","CC1=C(C2=CC=CC=C2)C3=C(S1)N=CN(CC(=O)N4CCCC4)C3=O",2.133,3,0,3]
["P3147","WAY-656941","c5","L1700-134","in 10mM DMSO","others","wnt","Wnt signaling activator",{"v":360.4025832,"d":"360.40"},"852902-93-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H17FN2O3S","free base","N/A","COC1=C(OC)C=C(CCC(=O)NC2=NC3=C(S2)C=C(F)C=C3)C=C1",3.903,4,1,6]
["P3148","WAY-657003","d5","L1700-134","in 10mM DMSO","others","cancer","anti-proliferative effect;\naltering the lifespan of a eukaryotic organism;",{"v":406.47424,"d":"406.47"},"852905-13-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H26N2O4","free base","N/A","CC1=C(C)C2=C(C=C1)C(=CC(=O)O2)CN3CCN(CC3)CC4=CC5=C(OCO5)C=C4",4.214,4,0,4]
["P3149","WAY-657021","e5","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","fungicidal and bactericidal activities",{"v":264.23408,"d":"264.23"},"852906-23-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H12N2O5","free base","N/A","[O-][N+](=O)C1=C(OCC(=O)N2CCCC2=O)C=CC=C1",1.013,3,0,4]
["P3150","WAY-657095","f5","L1700-134","in 10mM DMSO","Immunology & Inflammation related","Immunology & Inflammation","anti-inflammatory and analgesic activities",{"v":324.28758,"d":"324.29"},"852917-90-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H12N2O5","free base","N/A","CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C3=CC=C(C=C3)[N+]([O-])=O",3.025,3,1,3]
["P3151","WAY-657136","g5","L1700-134","in 10mM DMSO","cathepsin B","Proteases","Cathepsin B Inhibitor",{"v":322.35452,"d":"322.35"},"852932-33-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H18O4","free base","N/A","CC1=C(OC2=C3C=CC=CC3=CC=C12)C(=O)OC4CCCCC4=O",{"v":4.56,"d":"4.560"},4,0,3]
["P3152","WAY-657191","h5","L1700-134","in 10mM DMSO","nitric oxide synthetase","others","Vascular endothelial nitric oxide production promoters and/or nitric oxide synthetase activators;\nnitrogen monoxide production accelerators and/or endothelial nitric oxide synthase activators;",{"v":244.2642232,"d":"244.26"},"852934-82-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H13FN2O","free base","N/A","FC1=CC=C(CCNC(=O)C2=CN=CC=C2)C=C1",1.997,2,1,4]
["P3153","WAY-657196","a6","L1700-134","in 10mM DMSO","cannabinoid receptor","GPCR & G Protein","cannabinoid receptor agonist",{"v":364.50222,"d":"364.50"},"852934-91-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H28N2O3S","free base","N/A","CC1=CC=C(C=C1[S](=O)(=O)N2CCCCC2)C(=O)NC3CCCCC3",3.416,3,1,4]
["P3154","WAY-657206","b6","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","anti-Tuberculosis activity",{"v":349.4063,"d":"349.41"},"852938-33-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H15N3O2S","free base","N/A","CC1=CC2=C(C=C1)C(=CO2)CC(=O)NC3=NC(=CS3)C4=NC=CC=C4",3.661,4,1,4]
["P3155","WAY-657249","c6","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","Antitubercular CTP Synthetase Inhibitor;\nanti-Tuberculosis activity;",{"v":329.3487832,"d":"329.35"},"852940-38-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12FN3O2S","free base","N/A","FC1=CC(=CC=C1)OCC(=O)NC2=NC(=CS2)C3=NC=CC=C3",2.877,4,1,5]
["P3156","WAY-657273","d6","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","Antibacterial and antifungal compound",{"v":452.4781032,"d":"452.48"},"852941-46-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H25FN4O4","free base","N/A","CC1COC2=C3N1C=C(C(=O)OCC4=NC=CC=C4)C(=O)C3=CC(=C2N5CCN(C)CC5)F",2.535,5,0,5]
["P3157","WAY-657541","e6","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","anti-Tuberculosis activity",{"v":329.3487832,"d":"329.35"},"853339-68-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12FN3O2S","free base","N/A","FC1=C(OCC(=O)NC2=NC(=CS2)C3=NC=CC=C3)C=CC=C1",2.877,4,1,5]
["P3158","WAY-657568","f6","L1700-134","in 10mM DMSO","Catalytic Inhibitor","others","Catalytic Inhibitors of the Human DNA Topoisomerase Iia",{"v":393.45732,"d":"393.46"},"853351-76-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H23N3O5S","free base","N/A","CC(C)CN(C1CC[S](=O)(=O)C1)C(=O)COC(=O)C2=N[NH]C3=C2C=CC=C3",1.722,6,1,7]
["P3159","WAY-657584","g6","L1700-134","in 10mM DMSO","Bcl-2","Apoptosis","altering the lifespan of a eukaryotic organism;\nBcl-2 inhibitor;",{"v":225.24594,"d":"225.25"},"853352-52-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H11N3O","free base","N/A","O=C(N1CCC2=C1C=CC=C2)C3=NC=CN=C3",1.022,3,0,1]
["P3160","WAY-657592","h6","L1700-134","in 10mM DMSO","calcium channel","Transmembrane Transporters,Neuronal Signaling","modulator of the activity of neuronal calcium channels",{"v":416.53372,"d":"416.53"},"853352-97-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H28N2O4S","free base","N/A","COC1=CC=C(CNC(=O)C2=CC=C(C=C2)[S](=O)(=O)N3CC(C)CC(C)C3)C=C1",3.278,4,1,6]
["P3161","WAY-657644","a7","L1700-134","in 10mM DMSO","CYP51","others","Trypanosoma cruzi CYP51 inhibitor",{"v":316.35324,"d":"316.35"},"853570-80-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H16N2O2","free base","N/A","O=C(CC1=COC2=C1C3=C(C=CC=C3)C=C2)NCC4=CN=CC=C4",2.717,3,1,4]
["P3162","WAY-657667","b7","L1700-134","in 10mM DMSO","others","others","increasing stress tolerance in plants",{"v":350.26552,"d":"350.27"},"853571-75-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H13Cl2N3S","free base","N/A","CC1=NN=C(SCC2=CC(=C(Cl)C=C2)Cl)[N]1C3=CC=CC=C3",5.233,2,0,4]
["P3163","WAY-658091","c7","L1700-134","in 10mM DMSO","Others","Others","increasing stress tolerance in plants",{"v":374.4076464,"d":"374.41"},"848340-38-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H16F2N4OS","free base","N/A","CCC[N]1C(=NN=C1C2=CC=NC=C2)SCC(=O)C3=CC(=C(F)C=C3)F",3.797,4,0,7]
["P3164","WAY-658118","d7","L1700-134","in 10mM DMSO","TRPA1","Transmembrane Transporters","TRPA1 antagonist;",{"v":444.89468,"d":"444.89"},"848341-57-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17ClN6O3S","free base","N/A","CN1C(=O)N(C)C2=C([N](CC(=O)NC3=NC(=C(C)S3)C4=CC=C(Cl)C=C4)C=N2)C1=O",{"v":2.29,"d":"2.290"},5,1,4]
["P3165","WAY-658230","e7","L1700-134","in 10mM DMSO","mGluR5","Neuronal Signaling","antagonists for mGluR5",{"v":282.29066,"d":"282.29"},"849128-64-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14O4","free base","N/A","COC(=O)C1=C(COC2=CC=CC=C2)C3=C(O1)C=CC=C3",3.847,4,0,5]
["P3166","WAY-658261","f7","L1700-134","in 10mM DMSO","Others","Others","increasing stress tolerance in plants",{"v":354.25422,"d":"354.25"},"849125-00-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H13Cl2N3OS","free base","N/A","C[N]1C(=NN=C1C2=C(C)OC=C2)SCC3=C(Cl)C=C(Cl)C=C3",{"v":4.57,"d":"4.570"},3,0,4]
["P3167","WAY-658262-A","g7","L1700-134","in 10mM DMSO","scavenger receptors SR-BI","Others","scavenger receptors SR-BI inhibitors;\nregulation of the scavenger receptor SR-BI;",{"v":235.30542,"d":"235.31"},"63236-62-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H13N3OS","free base","N/A","O=C(CSC1=NCCN1)NC2=CC=CC=C2",{"v":1.29,"d":"1.290"},2,2,4]
["P3168","WAY-658430-A","h7","L1700-134","in 10mM DMSO","Others","Others","antihypertensives, contraceptives, peripheral vasodilators, and drugs in the treatment of parkinsonism",{"v":218.29482,"d":"218.29"},"55745-69-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H18N2O","free base","N/A","C1CN(CCN1)CC2=CC3=C(OCC3)C=C2",1.383,1,1,2]
["P3169","WAY-658459","a8","L1700-134","in 10mM DMSO","antiinflammatory","Immunology & Inflammation","Antiplatelet Agent;\ncardiovascular, antiinflammatory, and antiallergy agents;",{"v":395.5178,"d":"395.52"},"130717-29-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H25N3O2S","free base","N/A","COC1=CC=C(C=C1)C2=C(N=C(S2)N3CCN(C)CC3)C4=CC=C(OC)C=C4",{"v":4.67,"d":"4.670"},3,0,5]
["P3170","WAY-658494","b8","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":295.37722,"d":"295.38"},"1351358-93-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H13NO3S2","free base","N/A","CCOC(=O)\\C=C1/NC(=O)\\C(S1)=C/C2=CC=C(C)S2",2.483,3,1,4]
["P3171","WAY-658542","c8","L1700-134","in 10mM DMSO","gamma-secretase,5-HT2A","Neuronal Signaling & Stem Cells & Wnt & Proteases","inhibitor of gamma-secretase;\n5-HT2A antagonist;",{"v":364.88954,"d":"364.89"},"867327-33-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H21ClN2O2S","free base","N/A","ClC1=CC=C(C=C1)[S](=O)(=O)N2CCN(CC2)CCC3=CC=CC=C3",3.473,2,0,5]
["P3172","WAY-658650","d8","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","cytotoxicity and anti-metastatic properties;\nanti-tubercular agent;\nantimycobacterial and antiplasmodial agent;\nantagonist for adenosine A1 and A3 receptors;",{"v":326.3299,"d":"326.33"},"476319-66-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H10N4O3S","free base","N/A","[O-][N+](=O)C1=CC=C(C=C1)C(=O)NC2=NC(=CS2)C3=NC=CC=C3",2.731,3,1,4]
["P3173","WAY-658674","e8","L1700-134","in 10mM DMSO","Others","Others","herbicides",{"v":284.76182,"d":"284.76"},"42310-54-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H13ClN2O2S","free base","N/A","CC1=C(OCC(=O)NC2=NCCS2)C=CC(=C1)Cl",3.088,3,1,4]
["P3174","WAY-658675","f8","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","insecticides or fungicides",{"v":316.78538,"d":"316.79"},"545382-94-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H17ClN4O","free base","N/A","ClC1=CC=C(CC(=O)N2CCN(CC2)C3=NC=CC=N3)C=C1",2.314,3,0,3]
["P3175","WAY-658691","g8","L1700-134","in 10mM DMSO","Others","Others","antiproliferative activity/inhibition of tubulin polymerization",{"v":410.48938,"d":"410.49"},"868233-37-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H22N4O3S","free base","N/A","CCOC(=O)C1=C(C)[NH]C(=C1C(=O)CSC2=NC3=C(C=CC=C3)C4CC=NN24)C",3.052,5,1,7]
["P3176","WAY-658725","h8","L1700-134","in 10mM DMSO","sAPPb,Ab","Others","inhibitors of sAPPb and Ab production",{"v":310.7775,"d":"310.78"},"857040-20-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H15ClN2O","free base","N/A","ClC1=C2C=CC=NC2=C3OCN(CC4=CC=CC=C4)CC3=C1",4.122,2,0,2]
["P3177","WAY-658784","a9","L1700-134","in 10mM DMSO","Canonical BMP signaling pathway","Others","Canonical BMP signaling pathway activator",{"v":427.47508,"d":"427.48"},"863416-56-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C24H17N3O3S","free base","N/A","CC1=CC2=C(C=C1)N=C(S2)C3=CC=C(NC(=O)COC(=O)C4=CC=C(C=C4)C#N)C=C3",4.695,4,1,6]
["P3178","WAY-658876","b9","L1700-134","in 10mM DMSO","epoxide hydrolase","Others","inhibitor of the human soluble epoxide hydrolase",{"v":327.4174,"d":"327.42"},"863558-02-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H25NO3","free base","N/A","COC(=O)C1=CC=C(CNC(=O)[C]23C[CH]4[CH2]C([CH2][CH](C4)C2)C3)C=C1",3.368,3,1,5]
["P3179","WAY-658941","c9","L1700-134","in 10mM DMSO","Others","Others","AceMIF-specific inhibitor",{"v":404.86728,"d":"404.87"},"863592-53-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H17ClN2O4S","free base","N/A","CN(C1=CC=CC=C1)[S](=O)(=O)C2=C(Cl)C=CC(=C2)C(=O)NCC3=CC=CO3",3.161,4,1,6]
["P3180","WAY-658979","d9","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","antibacterial activity",{"v":370.7864,"d":"370.79"},"863614-80-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H15ClN2O4","free base","N/A","CC1=CC(=O)C(C(=O)O1)C(=O)\\C=C\\C2=C(Cl)[N](N=C2C)C3=CC=CC=C3",3.087,5,0,4]
["P3181","WAY-659053","e9","L1700-134","in 10mM DMSO","Others","Others","glucose uptake activator",{"v":362.40506,"d":"362.41"},"848833-24-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H14N4O2S","free base","N/A","O=C(CC1=NNC(=O)C2=C1C=CC=C2)NC3=NC(=CS3)C4=CC=CC=C4",2.743,4,2,4]
["P3182","WAY-659095","f9","L1700-134","in 10mM DMSO","PDE9","Metabolism","Sialoadhesin ligand;\nPDE9 inhibitor;",{"v":300.33238,"d":"300.33"},"421562-28-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H12N2O3S","free base","N/A","CC1=C(SC2=C1C(=O)NC(=N2)CC3=CC=CC=C3)C(O)=O",2.722,3,1,3]
["P3183","WAY-659100","g9","L1700-134","in 10mM DMSO","hormone sensitive lipase,metalloprotease","Others","hormone sensitive lipase (HSL) inhibitor;\nmetalloprotease inhibitor;",{"v":388.3814296,"d":"388.38"},"308830-70-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H23F3N2O4","free base","N/A","CC(C)(C)OC(=O)N1CCC(CC1)C(=O)NC2=CC=C(OC(F)(F)F)C=C2",{"v":4.53,"d":"4.530"},4,1,6]
["P3184","WAY-659204","h9","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":289.37594,"d":"289.38"},"863763-20-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H11N3OS2","free base","N/A","CC1=CSC(=N1)SCC2=NN=C(O2)C3=CC=CC=C3",2.727,4,0,4]
["P3185","WAY-659490","a10","L1700-134","in 10mM DMSO","peroxidase system","Others","inhibit the peroxidase system",{"v":412.4292696,"d":"412.43"},"865279-64-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H19F3N4O2S","free base","N/A","CCCCN1C(=O)NC(=O)C2=C1N=C(CSC3=CC(=CC=C3)C(F)(F)F)[N]2C",4.283,3,1,7]
["P3186","WAY-659512","b10","L1700-134","in 10mM DMSO","Others","Others","increasing stress tolerance in plants",{"v":354.25422,"d":"354.25"},"865613-84-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H13Cl2N3OS","free base","N/A","C[N]1C(=NN=C1C2=C(C)OC=C2)SCC3=CC(=C(Cl)C=C3)Cl",{"v":4.57,"d":"4.570"},3,0,4]
["P3187","WAY-659590","c10","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":289.1809,"d":"289.18"},"867283-39-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H10Cl2N2OS","free base","N/A","ClC1=C(Cl)C=C(CC(=O)NC2=NCCS2)C=C1",3.466,2,1,3]
["P3188","WAY-659611","d10","L1700-134","in 10mM DMSO","mGluR2","Neuronal Signaling","modulator of mGluR2 receptors",{"v":439.8849632,"d":"439.88"},"867296-94-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H19ClFNO5S","free base","N/A","FC1=CC=C(C=C1)C(=O)COC(=O)C2=C(Cl)C=CC(=C2)[S](=O)(=O)N3CCCCC3",3.845,5,0,7]
["P3189","WAY-659677","e10","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator;\naltering the lifespan of a eukaryotic organism;",{"v":295.33248,"d":"295.33"},"867300-85-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H17NO3","free base","N/A","COC1=CC2=C(C=C1)C(=CC(=O)O2)CN(C)C3=CC=CC=C3",3.589,3,0,4]
["P3191","WAY-659746","g10","L1700-134","in 10mM DMSO","Others","cancer,Immunology & Inflammation,Microbiology","useful for treating cancer and inflammatory disease;\nanti-Tuberculosis activity;",{"v":328.3242632,"d":"328.32"},"867327-79-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H9FN6OS","free base","N/A","FC1=CC=C(C=C1)C2=N[N](CC3=CC(=O)N4C=CSC4=N3)N=N2",1.575,5,0,3]
["P3192","WAY-659763","h10","L1700-134","in 10mM DMSO","Others","Others","cytotoxic and antiproliferative activities gainst BMEC and HUVEC",{"v":273.32696,"d":"273.33"},"867329-47-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H19NO3","free base","N/A","CC1=CC=C(CNC(=O)C2CC=CCC2C(O)=O)C=C1",{"v":2.31,"d":"2.310"},2,1,4]
["P3193","WAY-659873","a11","L1700-134","in 10mM DMSO","S1PR2","Others","including S1P for guiding pluripotent stem cells to an injury;\nS1PR2 agonist;",{"v":388.3829696,"d":"388.38"},"868268-81-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C21H19F3N2O2","free base","N/A","CC1=CC(=C(C)[N]1CC2=CC=CC=C2)C(=O)CN3C=C(C=CC3=O)C(F)(F)F",3.214,2,0,6]
["P3194","WAY-659977","b11","L1700-134","in 10mM DMSO","Tankyrase","DNA Damage","Tankyrase Inhibitor;",{"v":442.46658,"d":"442.47"},"869474-43-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C25H22N4O4","free base","N/A","COC1=C(NC(=O)C2=CC=C(NC(=O)CCC3=NC4=C(C=CC=C4)C(=O)N3)C=C2)C=CC=C1",2.597,5,3,7]
["P3195","WAY-659989","c11","L1700-134","in 10mM DMSO","Anti-infection","Microbiology","anti-viral;",{"v":413.51148,"d":"413.51"},"869474-87-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C26H27N3O2","free base","N/A","CC1=CC=C(CNC(=O)C2=C(NC(=O)CN3CCC4=C(C3)C=CC=C4)C=CC=C2)C=C1",3.892,2,2,6]
["P3196","WAY-660211","d11","L1700-134","in 10mM DMSO","voltage-gated sodium channels","Transmembrane Transporters","inhibitor of voltage-gated sodium channels;",{"v":451.94692,"d":"451.95"},"587843-16-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H18ClN3O4S2","free base","N/A","CC(C)(OC1=CC=C(Cl)C=C1)C(=O)NC2=CC=C(C=C2)[S](=O)(=O)NC3=NC=CS3",3.395,5,2,7]
["P3197","WAY-660313","e11","L1700-134","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":291.36868,"d":"291.37"},"1351360-87-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H17N3O2S","free base","N/A","CN1CCN(CC1)C2=NC(=CS2)C3=CC(=C(O)C=C3)O",2.409,1,2,2]
["P3198","WAY-660319","f11","L1700-134","in 10mM DMSO","α7β1 integrin","Others","α7β1 integrin modulatory agent;\nmodulator of α7β1 integrins;",{"v":475.55786,"d":"475.56"},"849121-82-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H29N3O6S","free base","N/A","COC1=C(CC(=O)NC2=C(C=CC(=C2)[S](=O)(=O)N3CCOCC3)N4CCOCC4)C=CC=C1",1.287,6,1,7]
["P3199","WAY-660357","g11","L1700-134","in 10mM DMSO","Others","Others","increasing stress tolerance in plants",{"v":329.3736,"d":"329.37"},"871089-29-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H15N3O3S","free base","N/A","COC(=O)C1=CC=C(CSC2=NN=C([N]2C)C3=CC=CO3)C=C1",3.242,5,0,6]
["P3200","WAY-660418","h11","L1700-134","in 10mM DMSO","γ-secretase","Neuronal Signaling & Stem Cells & Wnt & Proteases","γ-secretase inhibitor",{"v":317.78844,"d":"317.79"},"871096-98-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H16ClNO4S","free base","N/A","ClC1=CC=C(C=C1)[S](=O)(=O)N2CCC3(CC2)OCCO3",1.676,4,0,2]
["P3202","WAY-660764","b2","L1700-135","in 10mM DMSO","Anti-infection","Microbiology","antiviral activity",{"v":401.50092,"d":"401.50"},"871262-32-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H23N3O5S2","free base","N/A","CC(=O)N1CCN(CC1)[S](=O)(=O)C2=CC=C(C=C2)[S](=O)(=O)N3CCCC3",-0.259,5,0,4]
["P3203","WAY-660770","c2","L1700-135","in 10mM DMSO","Ad5","Others","inhibitor of the Ad5 transduction",{"v":421.33132,"d":"421.33"},"871262-40-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H13BrN2O2S2","free base","N/A","BrC1=CC2=C(OC(OC2)C3=CC=CC=C3)C(=C1)CSC4=NN=CS4",4.567,4,0,4]
["P3204","WAY-660898","d2","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":289.28814,"d":"289.29"},"871797-45-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H11N3O2","free base","N/A","OC1=C(C=CC=C1)C(=O)C2=CC3=NC4=C(C=CC=C4)[N]3N=C2",{"v":3.03,"d":"3.030"},3,1,2]
["P3205","WAY-660959","e2","L1700-135","in 10mM DMSO","MAPK","MAPK","has affinity to the MAPK Phosphatase of Plasmodium falciparum",{"v":365.44876,"d":"365.45"},"872211-49-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H19N3O2S","free base","N/A","NC(=O)C1=C(NC(=O)CNC(C2=CC=CC=C2)C3=CC=CC=C3)SC=C1",2.404,2,3,7]
["P3206","WAY-660965","f2","L1700-135","in 10mM DMSO","TRPA1","Transmembrane Transporters","TRPA1 antagonist;",{"v":384.3892,"d":"384.39"},"872211-87-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H20N6O4","free base","N/A","CN1C(=O)N(C)C2=C([N](CC(=O)NC(=O)NC3=C(C)C=C(C)C=C3)C=N2)C1=O",1.288,5,2,3]
["P3207","WAY-661012","g2","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":291.34554,"d":"291.35"},"872319-20-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H21N3O3","free base","N/A","CC(NC1CC1)C(=O)N2CCN(CC2)C(=O)C3=CC=CO3",{"v":0.3,"d":"0.300"},3,1,4]
["P3208","WAY-661054","h2","L1700-135","in 10mM DMSO","Hsp90","Cytoskeletal Signaling","Hsp90 inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":415.46438,"d":"415.46"},"872457-88-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C23H17N3O3S","free base","N/A","O=C(CSC1=NN=C([N]1C2=CC=CC=C2)C3=CC=C4OCOC4=C3)C5=CC=CC=C5",5.008,5,0,6]
["P3209","WAY-661156","a3","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","antinociceptive activity;\nAndrogen Receptor modulator;",{"v":294.35102,"d":"294.35"},"875157-56-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H18N4O","free base","N/A","O=C(/C=C/C1=CC=CC=C1)N2CCN(CC2)C3=NC=CC=N3",2.083,3,0,3]
["P3210","WAY-661688","b3","L1700-135","in 10mM DMSO","tie2","Protein Tyrosine Kinase","tie2 inhibitor",{"v":336.37108,"d":"336.37"},"896687-93-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12N6OS","free base","N/A","C(SC1=NN=C([NH]1)C2=CC=NC=C2)C3=NN=C(O3)C4=CC=CC=C4",2.127,6,1,5]
["P3211","WAY-661708","c3","L1700-135","in 10mM DMSO","amyloid beta","Others","amyloid beta modulator",{"v":281.39378,"d":"281.39"},"896690-34-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H27N3O2","free base","N/A","CC1CCCC(NC(=O)NC(=O)CN2CCCC2)C1C",{"v":2.05,"d":"2.050"},2,2,3]
["P3212","WAY-661794","d3","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":290.31926,"d":"290.32"},"896797-43-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14N4O","free base","N/A","COC1=CC=C(C=C1)C2=C(C=N[NH]2)C3=NC4=C([NH]3)C=CC=C4",3.508,3,2,3]
["P3213","WAY-661798","e3","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":288.34644,"d":"288.35"},"896797-56-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H16N4","free base","N/A","C[N]1C=C(C2=NC3=C(C=CC=C3)[N]2C)C(=N1)C4=CC=CC=C4",4.073,2,0,2]
["P3214","WAY-661823","f3","L1700-135","in 10mM DMSO","Others","Others","promote sensory hair cell regeneration",{"v":292.74076,"d":"292.74"},"897765-06-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H9ClN2O2S","free base","N/A","CC1=C(OC2=C1C=CC=C2Cl)C(=O)NC3=NC=CS3",3.357,3,1,2]
["P3215","WAY-661874","g3","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":293.3199,"d":"293.32"},"897770-56-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H15N3O2","free base","N/A","CCC1=CC=C(C=C1)C(=O)CN2N=NC3=C(C=CC=C3)C2=O",{"v":4.03,"d":"4.030"},4,0,4]
["P3216","WAY-661957","h3","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":291.30072,"d":"291.30"},"899902-32-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H13NO3","free base","N/A","O=C1NC=C(C=C1)C(=O)OC2=CC=C(C=C2)C3=CC=CC=C3",2.586,3,1,4]
["P3217","WAY-662041","a4","L1700-135","in 10mM DMSO","serotonin 5-HT2 receptors","Neuronal Signaling & GPCR & G Protein","serotonin 5-HT2A receptor antagonist",{"v":399.3346,"d":"399.33"},"901023-89-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H20Cl2N2O2S","free base","N/A","ClC1=CC(=C(Cl)C=C1)[S](=O)(=O)N2CCN(CC2)CCC3=CC=CC=C3",4.137,2,0,5]
["P3218","WAY-662152","b4","L1700-135","in 10mM DMSO","SRPK","Protein Tyrosine Kinase","SRPK inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":335.3236496,"d":"335.32"},"902155-31-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H16F3N3O","free base","N/A","FC(F)(F)C1=CC(=C(C=C1)N2CCCC2)NC(=O)C3=CN=CC=C3",3.029,2,1,4]
["P3219","WAY-662162","c4","L1700-135","in 10mM DMSO","UDP-galactopyranose mutase","Others","Inhibitor of UDP-galactopyranose mutase;",{"v":477.76206,"d":"477.76"},"902471-48-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H14BrClN4O2S","free base","N/A","OC(=O)CC1SC2=NN=C(CC3=CC=C(Br)C=C3)[N]2N=C1C4=CC=C(Cl)C=C4",5.032,4,0,5]
["P3220","WAY-663086","d4","L1700-135","in 10mM DMSO","Androgen Receptor","Endocrinology & Hormones","Androgen Receptor modulator",{"v":292.31368,"d":"292.31"},"956731-22-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H12N4O3S","free base","N/A","CC1=CC(=O)NC(=C1C#N)SCC(=O)N2CCNC2=O",0.049,3,2,3]
["P3221","WAY-663641","e4","L1700-135","in 10mM DMSO","others","others","scavengers against the ABTS radical species",{"v":340.46244,"d":"340.46"},"329904-27-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H16N2OS2","free base","N/A","O=C(CSCC1=CC=CC=C1)NC2=NC(=CS2)C3=CC=CC=C3",3.959,2,1,6]
["P3222","WAY-663740","f4","L1700-135","in 10mM DMSO","HIV-1","Microbiology","inhibiting HIV-1 replication",{"v":332.4206,"d":"332.42"},"876934-56-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H20N4O2S","free base","N/A","CC1=CC=C(C=C1)[N]2C(=NN=C2SCC(=O)N3CCOCC3)C",{"v":1.76,"d":"1.760"},4,0,4]
["P3223","WL-149027","g4","L1700-135","in 10mM DMSO","Anti inflammatory,calcium channel","Neuronal Signaling,Immunology & Inflammation,Transmembrane Transporters","anticonvulsant, anti-inflammatory and antimicrobial agents;\nT-type calcium channel blockers.",{"v":287.7673,"d":"287.77"},"23711-34-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C14H10ClN3S","free base","N/A","SC1=NN=C([N]1C2=CC=CC=C2)C3=C(Cl)C=CC=C3",4.467,2,0,2]
["P3224","WL-309756","h4","L1700-135","in 10mM DMSO","others","cancer","antitumor activity",{"v":184.5831,"d":"184.58"},"3149-90-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C6H5ClN4O","free base","N/A","CC1=NC2=NC=N[N]2C(=C1Cl)O",1.484,3,1,0]
["P3225","WL-312474","a5","L1700-135","in 10mM DMSO","Anti-infection","Microbiology,Immunology & Inflammation","antibacterial activity/anti-inflammatory activity/analgesic activity",{"v":220.29078,"d":"220.29"},"909209-02-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C11H12N2OS","free base","N/A","CC1=NC2=C(C(=N1)O)C3=C(CCCC3)S2",2.748,2,1,0]
["P3226","WL-389539","b5","L1700-135","in 10mM DMSO","Others","Others","antioxidant activity",{"v":150.1745,"d":"150.17"},"909856-86-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C9H10O2","free base","N/A","C1COC2=CC=CC=C2OC1",1.678,2,0,0]
["P3227","WY-507","c5","L1700-135","in 10mM DMSO","Others","Others","binders to the extra-domain B of fibronectin;\nclass III antiarrhythmic agent;",{"v":225.32876,"d":"225.33"},"924069-79-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H19N","free base","N/A","C(CC1=CC=CC=C1)NCCC2=CC=CC=C2",3.593,0,1,6]
["P3228","WYE-122602","d5","L1700-135","in 10mM DMSO","Others","cancer","anti-cancer",{"v":279.29002,"d":"279.29"},"92595-45-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H13NO3","free base","N/A","OC1=CC=C(NC(=O)C2=C(O)C=C3C=CC=CC3=C2)C=C1",3.039,1,3,2]
["P3229","WYE-175761","e5","L1700-135","in 10mM DMSO","CTP","Others","CTP inhibitor;\nInhibitor of the mitochondrial citrate transport protein;",{"v":322.2933,"d":"322.29"},"92966-73-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H10N2O6S","free base","N/A","OC(=O)C1=CC(=CC=C1)[S](=O)(=O)NC2=CC=C(C=C2)[N+]([O-])=O",1.841,3,1,5]
["P3230","WYE-175768","f5","L1700-135","in 10mM DMSO","PPAR","Metabolism","PPAR agonist",{"v":383.41768,"d":"383.42"},"956236-52-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H17NO5S","free base","N/A","OC(=O)C1=CC(=CC=C1)[S](=O)(=O)NC2=CC=C(OCC3=CC=CC=C3)C=C2",3.514,4,1,7]
["P3231","WYE-175779","g5","L1700-135","in 10mM DMSO","mitochondrial citrate transport protein","Others","Mitochondrial and plasma membrane citrate transporters;\nInhibitors of the mitochondrial citrate transport protein: validation of the role of substrate binding residues and discovery of the first purely competitive inhibitor;\naltering the lifespan of a eukaryotic organism;",{"v":321.3483,"d":"321.35"},"956239-87-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H15NO5S","free base","N/A","COC1=CC=C(N[S](=O)(=O)C2=CC(=C(C)C=C2)C(O)=O)C=C1",2.417,4,1,5]
["P3232","WYE-175782","h5","L1700-135","in 10mM DMSO","Others","Others","anticholesteremic activity",{"v":351.80466,"d":"351.80"},"956256-67-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H14ClNO4S","free base","N/A","OC(=O)C1=C(Cl)C=CC(=C1)[S](=O)(=O)N2CCC3=C(C2)C=CC=C3",2.899,3,0,3]
["P3233","WYE-175819","a6","L1700-135","in 10mM DMSO","PPARα","Metabolism","PPARα activity;\nantimalarial agent;\nenhance the production of EPO;",{"v":309.316,"d":"309.32"},"956262-49-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C18H15NO4","free base","N/A","COC1=CC=C(C=C1OC)C2=NC3=CC=CC=C3C(=C2)C(O)=O",{"v":3.56,"d":"3.560"},4,0,4]
["P3234","WYE-175827","b6","L1700-135","in 10mM DMSO","IL-8 receptor,Gro-α","Others","IL-8 receptor antagonist/inhibitor of Gro-α",{"v":254.3286,"d":"254.33"},"182499-85-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C10H10N2O2S2","free base","N/A","NC1=C(N[S](=O)(=O)C2=CC=CS2)C=CC=C1",1.357,2,2,3]
["P3235","WYE-175839","c6","L1700-135","in 10mM DMSO","serine racemase,tubulin polymerization","N/A","serine racemase inhibitor;\ntubulin polymerization inhibitor;",{"v":266.2913432,"d":"266.29"},"216700-84-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C12H11FN2O2S","free base","N/A","NC1=C(N[S](=O)(=O)C2=CC=C(F)C=C2)C=CC=C1",1.776,2,2,3]
["P3236","WYE-176041","d6","L1700-135","in 10mM DMSO","Others","Others","hypolipidemic activity",{"v":354.31026,"d":"354.31"},"137988-21-7",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H14O7","free base","N/A","COC(=O)C1=CC=C(OC2=COC3=C(C=CC(=C3)OC(C)=O)C2=O)C=C1",2.275,7,0,6]
["P3237","WYE-176087","e6","L1700-135","in 10mM DMSO","Cdc25B,MKP-1","Others","inhibitors against Lpd activity, PDH activity, and/or the growth of tubercle bacillus;\nCdc25B inhibitor;\naltering the lifespan of a eukaryotic organism;\nMKP-1 inhibitor;",{"v":369.41916,"d":"369.42"},"302937-15-1",null,{"v":10,"d":"10.00"},null,null,"N/A","C22H19N5O","free base","N/A","CCCC[N]1C(=C(C#N)C2=NC3=CC=CC=C3N=C12)NC(=O)C4=CC=CC=C4",4.538,3,1,5]
["P3238","WYE-176114","f6","L1700-135","in 10mM DMSO","NS5B","Proteases","altering the lifespan of a eukaryotic organism;\nNS5B inhibitor;",{"v":314.28946,"d":"314.29"},"73868-66-3",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H14O6","free base","N/A","COC(=O)C1=CC(=C(C)O1)C2=C(C)OC3=C(C=CC(=C3)O)C2=O",2.534,5,1,3]
["P3239","WYE-176115","g6","L1700-135","in 10mM DMSO","NS5B","Proteases","NS5B inhibitor;\nantiblastic activity and stimulates heart activity;",{"v":300.26288,"d":"300.26"},"73486-45-0",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12O6","free base","N/A","COC(=O)C1=CC(=C(C)O1)C2=COC3=C(C=CC(=C3)O)C2=O",{"v":2.02,"d":"2.020"},5,1,3]
["P3240","WYE-176182","h6","L1700-135","in 10mM DMSO","ASBT,PPAR","Metabolism","inhibition effect on apical sodium-dependent bile acid transporter (ASBT) in cell level;\nPPAR agonist;",{"v":322.2933,"d":"322.29"},"59923-19-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H10N2O6S","free base","N/A","OC(=O)C1=CC=C(N[S](=O)(=O)C2=CC(=CC=C2)[N+]([O-])=O)C=C1",1.841,3,1,5]
["P3241","WYE-176204-A","a7","L1700-135","in 10mM DMSO","IDO","Metabolism","IDO inhibitor",{"v":192.21778,"d":"192.22"},"471917-75-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C9H12N4O","free base","N/A","NN1C(=N)N(CCO)C2=C1C=CC=C2",-0.078,0,2,2]
["P3242","WYE-176234","b7","L1700-135","in 10mM DMSO","Anti-infection","Microbiology","antivirulence agent;\nantimalarial HDP inhibitor;",{"v":286.32242,"d":"286.32"},"201284-86-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H18O4","free base","N/A","CC(C)C1=CC=C(OCC(=O)C2=CC=C(O)C=C2O)C=C1",3.779,2,2,5]
["P3243","WYE-176235","c7","L1700-135","in 10mM DMSO","SOD-1","Others","stabilize mutant superoxide dismutase-1 (SOD-1)",{"v":256.29644,"d":"256.30"},"302918-17-8",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H16O3","free base","N/A","CC1=CC=CC=C1CC(=O)C2=C(O)C(=C(O)C=C2)C",3.757,1,2,3]
["P3244","WYE-176237","d7","L1700-135","in 10mM DMSO","antimalarial HDP","Microbiology","antimalarial HDP inhibitor",{"v":258.26926,"d":"258.27"},"315233-87-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C15H14O4","free base","N/A","CC1=C(C(=O)COC2=CC=CC=C2)C(=CC(=C1)O)O",3.071,2,2,4]
["P3245","WYE-176238","e7","L1700-135","in 10mM DMSO","KLF10","Others","KLF10 inhibitor;",{"v":322.35452,"d":"322.35"},"315234-15-2",null,{"v":10,"d":"10.00"},null,null,"N/A","C20H18O4","free base","N/A","CCC1=CC(=C(O)C=C1O)C(=O)COC2=CC3=C(C=CC=C3)C=C2",4.436,2,2,5]
["P3246","WYE-176244","f7","L1700-135","in 10mM DMSO","PTP1B","Others","PTP1B inhibitor;\nbactericidal and fungicidal activity;",{"v":344.40808,"d":"344.41"},"86109-60-6",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H12N2O3S2","free base","N/A","OC(=O)C1=CC=C(NC(=O)CSC2=NC3=C(S2)C=CC=C3)C=C1",3.263,3,1,5]
["P3247","WYE-176249","g7","L1700-135","in 10mM DMSO","VEGF","Angiogenesis","VEGF inhibitor",{"v":351.37582,"d":"351.38"},"304881-10-5",null,{"v":10,"d":"10.00"},null,null,"N/A","C19H13NO4S","free base","N/A","COC1=CC=C(C=C1)C2=CSC(=N2)C3=CC4=C(OC3=O)C=C(O)C=C4",3.929,4,1,3]
["P3248","WYE-176270","h7","L1700-135","in 10mM DMSO","carnitine palmitoyltransferase","Metabolism","altering the lifespan of a eukaryotic organism;\ncarnitine palmitoyltransferase inhibitor;",{"v":290.31112,"d":"290.31"},"380173-60-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H18O5","free base","N/A","CCCC1=CC(=C(OCC2=CC=C(O2)C(O)=O)C=C1)OC",3.882,4,0,7]
["P3249","WYE-176272","a8","L1700-135","in 10mM DMSO","microbial heme oxygenase","Microbiology","inhibitor of microbial heme oxygenase,",{"v":288.29524,"d":"288.30"},"307548-90-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C16H16O5","free base","N/A","CC(OC1=C(C)C2=C(C=C1)C3=C(CCC3)C(=O)O2)C(O)=O",3.312,4,0,3]
["P3250","WYE-176392","b8","L1700-135","in 10mM DMSO","SOD dimers","Others","stabilize SOD dimers",{"v":318.3741,"d":"318.37"},"379697-13-9",null,{"v":10,"d":"10.00"},null,null,"N/A","C13H10N4O2S2","free base","N/A","O=C1NN=C(SCC2=CSC(=N2)C3=CC=CC=C3)C(=O)N1",1.948,4,2,4]
["P3251","WYE-179397","c8","L1700-135","in 10mM DMSO","Anti-infection","Microbiology","anthelmintic activity",{"v":326.34982,"d":"326.35"},"89790-87-4",null,{"v":10,"d":"10.00"},null,null,"N/A","C17H18N4O3","free base","N/A","NC1=C(C=C(C=C1)C(=O)N2CCN(CC2)C3=CC=CC=C3)[N+]([O-])=O",2.021,1,1,3]