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Cas号索引 1

• 149690-05-1 | 钠盐沙库必曲 (Catalog# : 17030108)沙库必曲，也被称为AHU377，是血管紧张素受体神经内肽酶抑制剂被
• 1801747-42-1 | SHP099游离 (Catalog# : 17030107)<SHP099是强有力的,选择性,具有口服生物利用率,是一种IC50 = 0.07μM的
• 1431699-67-0 | 泰地唑胺杂质 A (Catalog# : 17021402)泰地唑胺杂质 A是磷酸四唑磷酸酯活跃的一部分，对革兰氏阳性菌
• 1265965-22-7 | S49076 (Catalog# : 17021309)S49076是一种新型的、能有效抑制IC50值低于20 nmol/ L的MET、AXL / MER和
• 1001908-89-9 | SRT2183 (Catalog# : 17021306)SRT2183是sirtuin子型SIRT1的小分子激活剂，目前由Sirtris制药公司开发
• 18883-66-4 | 链脲菌素 (Catalog# : 17011712)链脲菌素是一种从链球菌中分离出来的甲基亚硝基脲类抗肿瘤抗生
• 1018899-04-1 | Sotagliflozin (Catalog# : 17011711)Sotagliflozin,也称为LX4211,是一种口服活性和双SGLT1 / SGLT2抑制剂，在
• 127254-12-0 | 西他沙星 (Catalog# : 17011706)西他沙星是一种新型的广谱口服氟喹诺酮，它对许多革兰氏阳性、
• 1801747-11-4 | SHP099盐酸盐 (Catalog# : 17011704)SHP099是一个强有力的、选择性、口服生物利用率和有效的IC50 = 0.0
• 1687736-54-4 | SGC707 (Catalog# : 17011702)SGC707是一种强效、选择性和细胞活性的蛋白质精氨酸甲基转移酶3
• 1884220-36-3 | SBI0206965 (Catalog# : 71161)SBI0206965是一种有效的选择性自噬激酶ULK1抑制剂。许多肿瘤变得沉
• 149400-88-4 | Sardomozide (Catalog# : 17011607)Sardomozide，也叫SAM486A或CGP48664,是一种第二代聚胺合成抑制剂，抑制
• 1092539-44-0 | SAR131675 (Catalog# : 17011605)SAR131675是一种有效的选择性vegfr - 3抑制剂。
• 127373-66-4 | Sivelestat (ONO-5046) (Catalog# : 16122760)Sivelestat is a potent and selective inhibitor of neutrophil elastase with IC50 of 44
• 17318-31-9 | SQ22536 (Catalog# : 16122726)SQ22536 is an inhibitor of adenylyl cyclase with an IC50 of 1.4 M. It can inhibit PGE
• 111540-00-2 | STA-21 (Catalog# : 16122706)STA-21 is a selective STAT3 inhibitor.In cells, STA-21 inhibits Stat3 DNA binding act
• 1335106-03-0 | SR1001 (Catalog# : 6111522)SR1001 is a selective ROR and ROR inverse agonist; suppresses TH17 cell differentiati
• 1324003-64-6 | S1P1 Agonist III (Catalog# : 61119)S1P1 Agonist III is a potent and orally active S1P1 agonist with EC50 of 18 nM; no ac
• 1186222-89-8 | 4SC-202 (Catalog# : 611937)4SC-202 is an orally available potent HDACi specific for class I HDAC isoenzymes(NO H
• 1454585-06-8 | SR-3029 (Catalog# : 611915)SR 3029 is a potent and highly specific CK1/CK1 inhibitor with the IC50 of 97 nM.SR-3
• 1456632-40-8 | SH-4-54 (Catalog# : 16071406)SH-4-54 is a potent STAT inhibitor with KD of 300 nM and 464 nM for STAT3 and STAT5,
• 1230487-00-9 | Siponimod (Catalog# : 16071404)Siponimod, also known as BAF-312, is a a potent and orally selective S1P Receptor Mod
• 1116743-46-4 | SAR125844 (Catalog# : 16071023)SAR125844 is a potent and highly selective c-Met inhibitor with potential antineoplas
• 1093403-33-8 | SRT2104 (Catalog# : 16071014)SRT2104, also known as GSK2245840, is a novel, first-in-class, highly selective small
• 1359164-11-6 | SR-2211 (Catalog# : 16071002)SR-2211
• 1022150-57-7 | SGX-523 (Catalog# : 16070912)SGX523 is a novel, ATP-competitive kinase inhibitor remarkable for its exquisite sele
• 160162-42-5 | SR 11302 (Catalog# : 16070908)SR 11302
• 1239875-86-5 | SGI 7079 (Catalog# : 16070902)SGI 7079
• 125941-87-9 | SCH23390 (Catalog# : 16070103)SCH23390
• 130495-35-1 | SKF-96365 HCl (Catalog# : 16062905)SKF-96365 is a selective TRPC channel blocker. SKF-96365 activates cytoprotective aut