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Cas号索引 1

• 168835-82-3 | SU-1498 (Catalog# : 17984)SU-1498是一种选择性的受体酪氨酸激酶抑制剂，血管内皮生长因子
• 1174428-47-7 | SF2523 (Catalog# : 17918)SF2523是一种高效、选择行的日常pan-PI3K/BRD4抑制剂。具有明显的选
• 1450881-55-6 | SAR-20347 (Catalog# : 1781101)SAR-20347是一种强力JAK1和酪氨酸激酶2的双抑制剂 (TYK2).
• 1523406-39-4 | SAR-405 (Catalog# : 2017882)SAR-405是一种有效且选择性的PIK3C3/Vps34抑制剂，防止自噬和协同MTO
• 148554-65-8 | 雷帕霉素(钠盐) (Catalog# : 20177313)雷帕霉素是第一个体内open-ring代谢物,不影响mTOR的雷帕霉素抑制Ch
• 1184843-57-9 | SAR-020106 (Catalog# : 17031004)SAR-020106是一种 ATP -竞争性、强效和选择性的CHK1抑制剂，其IC50为1
• 1456632-41-9 | SH5-07 (Catalog# : 17031002)SH5-07是一种健壮的氧肟抗酸的STAT3抑制剂，它能在体外诱导抗肿瘤
• 138794-73-7 | Sardomozide HCl (Catalog# : 17030306)Sardomozide，又名SAM486A或CGP48664，是第二代多胺合成抑制剂，它抑制
• 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