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

+ AII PRODUCTS

- 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
CR3096	1230487-00-9	Siponimod (BAF312) Siponimod, also known as BAF-312, is a a potent and orally selective S1P Receptor Modulator with EC50 value of 0.39nM for S1P1 rec..
CR3094	192705-79-6	PD166866 PD166866 is a selective inhibitor of the FGF-1 receptor tyrosine kinase (FGFR1) with IC50 = 55 nM, and no effect on c-Src, PDGFR-b..
CR3094	945526-43-2	ISCK03 ISCK03 is a potent c-kit inhibitor. ISCK03 inhibits SCF/c-kit signaling in 501mel human melanoma cells and abolishes melanin produ..
CR3093	298708-79-9	BAY41-4109 racemic BAY41-4109 racemic is a mixture of R-isomer of BAY41-4109 and S-isomer of BAY41-4109. BAY-41-4109 is a heteroaryldihydropyrimidine..
CR3092	1459687-96-7	GJ-103 sodium salt GJ103 sodium salt is an active analog of the read-through compound GJ072. Chemical-induced read through of premature stop codons m..
CR3091	1459687-89-8	GJ-103 free acid GJ-103 is an active analog of the read-through compound GJ072. Chemical-induced read through of premature stop codons might be exp..
CR3090	256477-09-5	UK-371804 UK-371804 is a potent and selective uPA inhibitor with excellent enzyme potency (Ki 10 nM) and selectivity profile (4000-fold vers..
CR3089	1429749-41-6	Thiomyristoyl Thiomyristoyl is a potent and specific SIRT2 inhibitor with an IC50 of 28 nM. IC50 & Target: IC50: 28 nM (SIRT2). Thiomyristoy..
CR3088	927871-76-9	S107 It is a benzothiazepine derivative that binds the RyR1 channel and enhances the binding affinity of Calstabin-1. By preventing the..
CR3087	413611-93-5	10074-G5 10074-G5 is a c-Myc/Max interaction inhibitor. 10074-G5, similarly to 10058-F4 (#F3680), specifically inhibits this interaction by..

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