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Cas号索引 8

• 877387-37-6 (free base) | GSK5182 (Catalog# : 20375)GSK5182 is a specific inverse agonist for estrogen-related receptor γ.
• 881639-98-1 | G-1 (Catalog# : 206103)G-1 is a selective agonist for GPER. It acts by blocking tubulin polymerization.
• 827319-43-7 | GW-870086 (Catalog# : 1811263)GW-870086是一种糖皮质激素受体激动剂，有望用于哮喘和特应性皮炎
• 880635-03-0 | GW6471 (Catalog# : 181151)GW6471是一种PPARα拮抗剂(IC50 = 0.24μM)。GW6471提高SMRT和NCoR的蛋白质亲
• 817194-38-0 | GSK180736A (GSK180736) (Catalog# : 178901)GSK180736A是一种有效的、具有选择性的IC50 0.77 M25的GRK2抑制剂，比其
• 844903-58-8 | GSK163090 (Catalog# : 6111015)GSK163090 is a potent, selective, and orally active 5-HT1A/B/D receptor antagonist wi
• 863513-91-1 | GRT-6005 (Catalog# : 16071110)Cebranopadol is a potent nociceptin/orphanin FQ peptide (NOP) and opioid receptor ago
• 873652-48-3 | GDC-0152 (Catalog# : 16071101)GDC-0152 is a second mitochondrial activator of caspases (Smac) mimetic inhibitor of
• 839706-07-9 | GNF-7 (Catalog# : 16060604)BenzaMide
• 870483-87-7 | GW2580 (Catalog# : 122524)GW2580 is an orally bioavailable inhibitor of c-FMS kinase; completely inhibited huma
• 850664-21-0 | GSK269962A (Catalog# : 102206)GSK269962A(CAS 850664-21-0) is a potent ROCK inhibitor (IC50 values are 1.6 and 4 nM
• 851983-85-2 | Galeterone (Catalog# : 62003)Galeterone(VN/124-1,TOK001) is a highly selective, multi-targeted, oral small molecul
• 864082-47-3 | GSK429286A (Catalog# : 52629)GSK429286A is a selective inhibitor of ROCK1 and ROCK2 with IC50 of 14 nM and 63 nM,
• 888216-25-9 | Ganetespib(STA-9090) (Catalog# : 52021)Ganetespib blocked the ability of HSP90 to bind to biotinylated geldanamycin and disr
• 86227-47-6 | Icosapent ethyl (Catalog# : 24045)Icosapent ethyl is used for the treatment of hypertriglyceridemia.
• 851870-24-1 | 4-iodo-2-isopropyl-1-Methyl-1H-iMidazole (Catalog# : 2062023)
• 887401-93-6 | INCB3284甲磺酸盐 (Catalog# : 191143)INCB3284是一种有效的、选择性的、可口服的hCCR2拮抗剂。
• 835619-41-5 | Indeglitazar (Catalog# : 1812131)Indeglitazar，也称为PPM-204和PLX-204，是一个可口服的过氧化物酶体增
• 832115-62-5 | ISX-9 (Catalog# : 17022713)ISX-9 is a neurogenic agent. Isx-9 promotes neurogenesis in vivo, enhancing the proli
• 873225-46-8 | IKK-16 (Catalog# : 16123017)IKK-16 is a potent and slective inhibitor of IB kinase (IKK) (IC50 values are 40, 70
• 866927-10-8 | IC87201 (Catalog# : 16122820)IC87201 is a nNOS-PDZ/PSD-95-PDZ inhibitor. IC87201 showed great promise in cellular
• 851870-28-5 | 5-Iodo-2-isopropyl-1-methyl-1H-imidazole (Catalog# : 021701)Coming soon!
• 857679-55-1 | INCB8761 (PF-4136309) (Catalog# : 92210)INCB8761(PF-4136309) is a potent, selective, and orally bioavailable CCR2 antagonist.
• 879-37-8 | Indole-3-Acetamide (Catalog# : 81920)Coming soon!
• 873054-44-5 | Ivacaftor (Catalog# : 52805)Ivacaftor (VX-770) is a potentiator of CFTR targeting G551D-CFTR and F508del-CFTR wit
• 878489-28-2 | JNJ 303 (Catalog# : 122938)Coming soon!
• 881202-45-5 | JNJ-26854165 (Serdemetan) (Catalog# : 52522)JNJ-26854165 (Serdemetan) acts as a HDM2 ubiquitin ligase antagonist and also induces
• 888032-58-4 | KPI-10 (Catalog# : 20277)KPI-10 is a new compound currently being studied for its efficacy in the treatment of
• 845932-30-1 | KU59403 (Catalog# : 19123)KU59403是一种有效的选择性ATM(共济失调毛细血管扩张突变)抑制剂，
• 853299-07-7 | K03861 (Catalog# : 611921)K03861 is a type II CDK2 inhibitor with Kd of 8.2 nM.K03861 inhibits CDK2 activity by