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Cas号索引 6

• 603148-36-3 | Azeliragon (Catalog# : 25033)Azeliragon (TTP488) 是一种口服生物可利用的 AGE (RAGE) 受体小分子抑制
• 60186-21-2 | 2-Amino-6-fluoro-3-nitropyridine (Catalog# : 20389)
• 68844-77-9 | Astemizole (Catalog# : 2071552)Astemizole is a histamine H1-receptor antagonist. Astemizole competitively binds to h
• 634913-39-6 | AER-271 (Catalog# : 2071523)AER-271 is a potent aquaporin-4 (AQP4) inhibitor. AER-271 blocks acute cerebral edema
• 6308-22-1 | AKOS B018304 (Catalog# : 2051513)AKOS B018304 is a potent inhibitor of chikungunya virus with low micro molar activity.
• 677007-74-8 | Avatrombopag maleate (Catalog# : 5141902)Avatrombopag maleate 是一种口服生物可用的小分子血栓生成素受体激动
• 638213-98-6 | AGL-2263 (Catalog# : 1810175)AGL-2263是一种新型的胰岛素受体抑制剂。
• 630124-46-8 | AST487 (Catalog# : 186158)AST487, 也称为NVP- AST487, 是一种RET激酶抑制剂/FLT3抑制剂。
• 618913-30-7 | AZD-5904 (Catalog# : 181121)AZD5904是一个有效的口服生物利用率MPO抑制剂。在临床前研究中,AZ
• 620175-39-5 | AFN-1252 (Catalog# : 17021406)AFN-1252(Debio 1452) 是enoyl -酰基载体蛋白还原酶(FabI)的有效抑制剂。
• 6147-11-1 | Alpha-Mangostin (Catalog# : 16122802)Alpha-Mangostin is a natural xanthonoid, a type of organic compound isolated from var
• 66389-74-0 | (+)-Apogossypol (Catalog# : 61125)(+)-Apogossypol(Apogossypol; NSC736630) is a potent inhibitor of Bcl-2 family protein
• 612847-09-3 | AKT inhibitor VIII (Catalog# : 161009020)AKT inhibitor VIII suppresses hyperthermia-induced Ndrg2 phosphorylation in gastric c
• 648449-76-7 | AS-604850 (Catalog# : 160926014)Treatment with this PI3K inhibitor enhanced myelination and axon number in the spinal
• 648450-29-7 | AS-605240 (Catalog# : 160926007)Orally administration of AS605240 significantly prevented lung inflammation and reduc
• 659730-32-2 | AMG-517 (Catalog# : 16071001)AMG 517 is a potent and selective TRPV1 antagonist, and antagonizes capsaicin, proton
• 630420-16-5 | Asunaprevir (Catalog# : 16070810)Asunaprevir, also known as BMS-650032, is an inhibitor of the hepatitis C virus enzym
• 65678-07-1 | AG1024 (Catalog# : 010422)AG-1024 inhibits IGF-1R autophosphorylation with IC50 of 7 M, less potent to IR with
• 68302-57-8 | Amoxanox (Catalog# : 91411)Amlexanox inhibits mast cell release of allergic mediators, which is also an antialle
• 69975-65-1 | 6-Aminoindan-1-one (Catalog# : 81928)Coming soon!
• 612487-72-6 | AZD1080 (Catalog# : 52626)AZD1080 is a selective, orally active, brain permeable GSK3 inhibitor of GSK3 and GSK
• 602306-29-6 | AZD-5438 (Catalog# : 52577)AZD5438 is a potent inhibitor of CDK1/2/9 with IC50 of 16 nM/6 nM/20 nM. It is less p
• 663619-90-7 | 9-溴-2-羟基-7-甲基-4H-吡啶并[1,2-a]嘧啶-4-酮 (Catalog# : S-204156)
• 675103-36-3 | BAY 678 (Catalog# : 1812286)BAY 678是一种有效且具有选择性的人类中性粒细胞弹性蛋白酶(HNE)抑
• 66611-37-8 | BGP-15 (Catalog# : 17109003)BGP-15, 是一种带有PARP抑制活性的烟碱类胺肟衍生物。已经证明BGP-
• 6066-49-5 | Butylphthalide (Catalog# : 16122908)Butylphthalide, also known as 3-n-butylphthalide or NBP, is an antioxidant and one of
• 648903-57-5 | BAY-61-3606 (Catalog# : 6111415)BAY-61-3606 is a potent and selective inhibitor of Syk kinase (Ki = 7.5 nM).
• 623152-17-0 | BMS-582949 (Catalog# : 16062903)BMS-582949 is a potent and selective P38 mitogen-activated protein kinase (P38 MAPK)
• 65002-17-7 | Bucillamine (Catalog# : 011315)Bucillamine is an antirheumatic agent developed from tiopronin.
• 627530-84-1 | BMS-564929 (Catalog# : 122920)BMS-564929 is a novel, highly potent, orally active, nonsteroidal tissue selective an