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
CR2296	717906-29-1	PF-431396 PF-431396 is dual focal adhesion kinase (FAK) and proline-rich tyrosine kinase 2 (PYK2) inhibitor (IC50 values are 2 and 11 nM res..
CR2295	896705-16-1	BMH-21 BMH-21 is a potent small molecule DNA intercalator. BMH-21 binds ribosomal DNA and inhibits RNA polymerase I (Pol I) transcription..
CR2294	151636-76-9	FL118 FL118 is an inhibitor of human survivin expression, activating tumor suppressor p53 as a novel MOA in p53 wild-type cancer cells.
CR2293	377090-84-1	SU9516 SU-9516 is a 3-substituted indolinone CDK inhibitor with IC50 of 22 nM, 40 nM, and 200 nM for CDK2, CDK1, and CDK4, respectively. ..
CR2292	1234708-04-3	SAR191801 hPGDS-IN-1 hPGDS-IN-1 is a hPGDS inhibitor ,with IC50 of 12 nM in the Fluorescence Polarization Assay or the EIA assay. IC50 value: 12 nM Tar..
CR2291	944842-54-0	Decernotinib (VX-509) Decernotinib, also known as VX-509 or VRT-831509 or adelatinib, is an oral, selective Janus kinase 3 (JAK3) inhibitor being develo..
CR2290	951319-59-8	16-phenoxy Prostaglandin F2α ethyl amide Synonyms: (Z)-7-((1R,2R,3R,5S)-3,5-dihydroxy-2-((R,E)-3-hydroxy-4-phenoxybut-1-enyl)cyclopentyl)-N-ethylhept-5-enamide;16-phenoxy ..
CR2289	1598426-03-9	2-(1-Phenyl-cyclopropylamino)-pyrimidine-5-carboxylic acid ethyl ester Synonyms:5-Pyrimidinecarboxylic acid, 2-[(1-phenylcyclopropyl)amino]-, ethyl ester;2-(1-Phenyl-cyclopropylamino)-pyrimidine-5-carb..
CR2288	35853-55-5	[2,8-Bis(trifluoromethyl)-4-quinolinyl]-2-pyridinylmethanone Properties:Density: 1.501g/cm3Boiling Point: 709.3ºC at 760mmHgFlash Point: 382.8ºCRefractive Index: 1.54
CR2287	1375465-91-0	ACY-738 ACY-738 is a potent and selective HDAC6 inhibitor with improved brain bioavailability. ACY-738 inhibits HDAC6 with low nanomolar p..

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