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Cas Index 1

• 1256580-46-7 | Alectinib(CH5424802) (Catalog# : 51907)Alectinibis a second-generation, orally active, potent and highly selective inhibitor
• 1173900-33-8 | AZD6482 (Catalog# : 51603)AZD6482 is aPI3Kinhibitor withIC50of 10 nM, 8-, 87- and 109-fold more selective to PI
• 1204144-28-4 | AZD1208 (Catalog# : 51702)AZD1208 is a potent, highly selective, and orally available Pim kinase inhibitor that
• 1124329-14-1 | AZ3146 (Catalog# : 51903)AZ3146 is a selectiveMps1inhibitor withIC50of ~35 nM, contributes to recruitment of C
• 1056901-62-2 | AT13148 (Catalog# : 51902)AT13148, a first-in-class multi-AGC kinase inhibitor, against gastric cancer cells. A
• 1990504-34-1 | Bomedemstat (Catalog# : 24001)Bomedemstat is anorally available, irreversible inhibitor of lysine-specific demethyl
• 1809010-52-3 | Berotralstat HCl (Catalog# : 20619)Berotralstat HCl is a novel selective inhibitor of plasma kallikrein, blocking the en
• 1672668-24-4 | Belzutifan (Catalog# : 20606)Belzutifan, also known as PT2977 and MK-6482, is HIF-2alpha inhibitor. PT2977 binds t
• 1478364-68-9 | BI-1467335 HCl (Catalog# : 20601)BI-1467335, also known as PXS-4728A, is a SSAO/VAP inhibitor potentially for the trea
• 1440964-89-5 | Bozitinib (Catalog# : 20599)Bozitinib is a highly selective c-MET kinase inhibitor with blood-brain barrier perme
• 1815613-42-3 | BMS-986176 (Catalog# : 20597)BMS-986176, also known as LX9211, is a highly selective, CNS penetrant, potent AAK1 i
• 120533-76-8 | BML-278 (Catalog# : 20554)BML-278 is an activator of sirtuin 1 (SIRT1) that has an EC150 value (effective conce
• 1478712-37-6 | BMS-986120 (Catalog# : 20519)BMS-986120 is a potent and selective oral antagonist of protease-activated receptor-4
• 1478711-48-6 | BMS-986141 (Catalog# : 20518)BMS-986141 is an Orally-Active Small-Molecule Antagonist of the Platelet Protease-Act
• 1423719-30-5 | BI 1015550 ( Nerandomilast ) (Catalog# : 230402)BI 1015550 ( Nerandomilast )is an oral, preferential inhibitor of phosphodiesterase 4
• 1883299-62-4 | Brepocitinib ( PF-06700841 ) (Catalog# : 232251)Brepocitinib is a potential first-in-class dual, selective inhibitor of TYK2 and JAK1
• 1798787-27-5 | BIIB068 (Catalog# : 20453)
• 1428652-17-8 | Baxdrostat (Catalog# : 20451)Baxdrostat is an aldosterone synthase inhibitor.
• 1912445 -55-6 | BMS-986195 (Catalog# : 20444)
• 1912445-55-6 | Branebrutinib (Catalog# : 20428)Branebrutinib, also known as BMS-986195, is a potent, covalent, irreversible inhibito
• 1060810-24-3 | 1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one (Catalog# : 171454)1-(4-Bromo-6- methylpyridin-2- yl)ethan-1-one, CAS 1060810-24-3.
• 195615-84-0 | Blarcamesine HCl (Catalog# : 6111905)Anavex2-73 is a muscarinic/σ1 ligand. ANAVEX2-73 (0.01-3.0 mg/kg i.p.) alleviated th
• 1055-55-6 | Bunamidine hydrochloride (Catalog# : 20271)Bunamidine is a anti-parasitic drug, which was approved by FDA for the treatment of t
• 1303515-32-3 | BI-187004 (Catalog# : 21224)BI-187004, also known as VTP-34072, is an 11β-hydroxysteroid dehydrogenase 1 inhibit
• 1207853-23-3 | Benzyl(2S,5R)-5-amino-2-methylpiperidine-1-carboxylatehydrochloride (Catalog# : 20103006)
• 1333714-43-4 | Benpyrine racemate (Catalog# : 2091907)(Rac)-Benpyrine is a racemate of Benpyrine. (Rac)-Benpyrine is a potent and orally ac
• 1660117-38-3 | BI-894999 (Catalog# : 2091902)BI-894999 is a potent and selective BET inhibitor potentially useful for the Treatmen
• 1628264-07-2 | 6-bromo-2-ethyl-N,8-dimethylimidazo[1,2-a]pyridin-3-amine (Catalog# : 2091201)
• 1818314-88-3 | BMS-1166 (Catalog# : 2073102)BMS-1166is a potent PD-1/PD-L1 interaction inhibitor with an IC50 of 1.4 nM, antagoni
• 1891087-61-8 | BAY-1816032 (Catalog# : 2071615)BAY-1816032 is a potent and oral available BUB1 (budding uninhibited by benzimidazole