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Cas号索引 1

• 1229236-86-5 | Gandotinib(LY2784544) (Catalog# : 91415)Gandotinib is an orally bioavailable imidazopyridazine and inhibitor of Janus kinase
• 1365888-06-7 | GDC-0810 ( Brilanestrant , ARN-810 ) (Catalog# : 90731)GDC-0810 (Brilanestrant, ARN-810, RG6046) is a selective estrogen receptor degrader (
• 1380672-07-0 | G007-LK (Catalog# : 62908)G007-LK is specific tankyrase 1/2 inhibitor.G007-LK (66) displayed high selectivity t
• 1207360-89-1 | GDC-0349 (Catalog# : 62702)GDC-0349 is a potent and selective ATP-competitive inhibitor of mTOR.
• 103766-25-2 | Gimeracil (Catalog# : 52804)Gimeracil(Gimestat) is an inhibitor of dihydropyrimidine dehydrogenase (DPYD), which
• 1260907-17-2 | GSK 525762A (Catalog# : 52745)GSK 525762A (I-BET 762) is an inhibitor for BET proteins with IC50 of ~35 nM.
• 1218942-37-0 | GKT137831 (Catalog# : 52627)GKT137831 is a novel and specific dual Nox1/Nox4 inhibitor with Ki of 14040 nM and 11
• 1372540-25-4 | GSK2636771 (Catalog# : 52618)GSK2636771 is a potent, orally bioavailable and selective inhibitor of PI3K (0.89 nM)
• 1047634-63-8 | GSK2110183 (Catalog# : 52584)GSK2110183 is an orally bioavailable, selective, ATP-competitive and potent pan-Akt i
• 1262618-39-2 | GS967 (Catalog# : 52216)GS967 is a novel, potent, and selective inhibitor of cardiac late sodium current(late
• 1346574-57-9 | GSK126 (Catalog# : 52208)GSK126 is a potent, highly selectiveEZH2 methyltransferaseinhibitor withIC50of 9.9 nM
• 1346572-63-1 | GSK503 (Catalog# : 51805)GSK-503 is a potent EZH2 inhibitor with potential anticancer activity. Reference: 1.
• 1394076-92-6 | GNE-317 (Catalog# : 52215)GNE-317 is a potent, brain-penetrantPI3Kinhibitor
• 188591-46-0 | GSK3787 (Catalog# : 52018)GSK3787 is as a selective and irreversible antagonist ofPPARwithpIC50of 6.6, with no
• 1337532-29-2 | GSK 2656157 (Catalog# : 52019)GSK2656157 is an ATP-competitive and highly selective inhibitor ofPERKwithIC50of 0.9
• 1644645-32-8 | HTL14242 (Catalog# : 24115)HTL14242 is a mGlu5 Negative Allosteric Modulator. Metabotropic glutamate receptors (
• 1441057-15-3 | 2(1H)-Pyridinone, 5,6-dihydro-4-(4-methylphenyl)-3-(2H-tetrazol-5-yl)-6-[4-(4,4,4-trifluorobutoxy)phenyl]-6-(trifluoromethyl)-, (6S)- (Catalog# : 20430)
• 182318-78-1 | 4-hydroxybiphenyl-4-carboxamide (Catalog# : 20404)
• 173933-40-9 | HISPOLON(P) (Catalog# : 210201)
• 1415792-84-5 | HMPL-523 (Catalog# : 20123101)HMPL-523 is a novel, highly selective and potent small molecule oral inhibitor target
• 1628291-95-1 | HC-070 (Catalog# : 206104)HC-070 is a potent inhibitor of TRPC4 and TRPC5, leading to anxiolytic and antidepres
• 155558-32-0 (HCl) | Hydroxyfasudil HCl (Catalog# : 204610)Hydroxyfasudil, aslo known as HA1100, is a cell-permeable hydroxylated metabolite of
• 1009734-33-1 | HZ-1157 (Catalog# : 19182)HZ-1157是一种丙肝病毒(HCV)抑制剂，对HCV NS3/4A蛋白酶有抑制作用。
• 173528-92-2 | HMN-154 (Catalog# : 184122)HMN-154是一种苯磺胺的抗癌剂。HMN-154通过剂量依赖性的方式抑制NF
• 1420290-99-8 | HJC0152 (Catalog# : 1710133)HJC0152是对人的头部和颈部鳞状细胞癌（鳞癌）的信号转导与转录
• 1702259-66-2 | H3B-6527 (Catalog# : 179822)H3B-6527是一个强有力的口服活性分子抑制剂，具有潜在的抗肿瘤活
• 130964-39-5 | H-89盐酸盐 (Catalog# : 178815)H-89是一种特殊的腺苷酸环酶抑制剂(DDA)，是一种循环的氨依赖性蛋
• 1448867-41-1 | HDM201 (Catalog# : 2017872)HDM201是一种口服生物利用率在人的同源基因(HDM2)抑制剂。具有潜在
• 1802181-20-9 | HM-61713 (BI-1482694) (Catalog# : 17022709)BI-1482694是布鲁顿酪氨酸激酶(BTK)的一种有效的小分子抑制剂。
• 1158279-20-9 | HLCL-61 HCl (Catalog# : 16122819)HLCL-61 is a potent and selective PRMT5 inhibitor for treatment of acute myeloid leuk