Crene Biotechnology,API,pharmaceutical intermediates,small molecules,prostaglandins,chemicals

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- Prostaglandins - Custom Synthesis - PARP Inhibitors - PI3K Inhibitors - FAK Inhibitors - AKT Inhibitors - C-Kit Inhibitors - VEGFR Inhibitors - c-Met Inhibitors - CDK Inhibitors - CYP17 Inhibitors - DNA/RNA Inhibitors - mTOR Inhibitors - SRC Inhibitors - Others - Veterinary APIs

Catalog No	CAS NO	Product name
CR1383	1004316-88-4	Cobicistat Cobicistat, also known as GS9350, is an approved drug for use in the treatment of infection with the human immunodeficiency virus ..
CR1382	394730-60-0	Boceprevir Boceprevir (EBP 520) is a potent, highly selective, orally bioavailable HCV NS3 protease inhibitor with a Ki of 14 nM in both enzy..
CR1380	1370261-96-3	PRT062607 P505-15 P505-15, also known as PRT2607, PRT062607, and BIIB057, is a novel, highly selective, and orally bioavailable small molecule SYK i..
CR1377	185991-07-5	AMD 3465 hexahydrobromide AMD 3465 hexahydrobromide (GENZ-644494 hexahydrobromide) is a potent antagonist of CXCR4, inhibits binding of 12G5 mAb and CXCL12A..
CR3260	313493-80-0	CID 1375606 CID 1375606 (N-[4-(Anilinocarbonyl)phenyl]-2,4-dichlorobenzamide) is a specific and potent surrogate agonist of GPR27 (SREB1) that..
CR1376	314245-33-5	IU1 IU1 is a selective USP14 inhibitor. IU1 prevents ventilator-induced lung injury in rats. IU1 inhibits the catalytic activity of pr..
CR1375	1097917-15-1	ASP3026 ASP3026 is a novel and selective inhibitor for the ALK kinase. ASP3026 potently inhibited ALK kinase activity and was more selecti..
CR1374	1000413-72-8	TAK-875 Fasiglifam Fasiglifam, also known as TAK-875, is a potent, selective, and orally bioavailable GPR40 agonist, with a pharmacokinetic profile e..
CR1373	1146699-66-2	BMS-708163 Avagacestat Avagacestat, also known as BMS-708163, is an oral GSI designed for selective inhibition of Aβ synthesis currently in development ..
CR3259	953778-58-0	Suvecaltamide (MK-8998) MK-8998 is a T type calcium channel antagonist potentially for the treatment of schizophrenia. MK-8998 was not effective in treati..

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