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
CR3354	1073160-26-5	Defactinib hydrochloride Defactinib, also known as VS-6063 and PF-04554878, is an orally bioavailable, small-molecule focal adhesion kinase (FAK) inhibitor..
CR3353	1073154-85-4	Defactinib VS-6063 Defactinib, also known as VS-6063 and PF-04554878, is an orally bioavailable, small-molecule focal adhesion kinase (FAK) inhibitor..
CR3352	1884712-47-3	CPI-637 CPI-637 is a potent and selective CBP/ EP300 bromodomain inhibitor. The biochemical potency of CPI-637 translated well into cells ..
CR3351	55779-48-1	Coelenterazine Coelenterazine is the luciferin, the light-emitting molecule, found in many aquatic organisms across seven phyla. It is the substr..
CR3350	1265229-25-1	Debio-1347 CH5183284 Debio-1347, also known as FF284 and CH5183284, is an orally bioavailable inhibitor of the fibroblast growth factor receptor subtyp..
CR3349	1015474-32-4	Avadomide (CC-122) Avadomide, also known as CC-122, is an orally available pleiotropic pathway modulator with potential antineoplastic activity. CC-1..
CR3348	865783-99-9	ON-013105 Briciclib Briciclib, also known as ON 013105 or ON 014185, is a benzyl styryl sulfone analog, and a disodium phosphate ester prodrug of ON 0..
CR3347	321674-73-1	BIBR 1532 BIBR1532 is a selective telomerase inhibitor. BIBR1132 is highly selective for inhibition of telomerase, resulting in delayed grow..
CR3346	40665-94-9	Dimethyl 3-(3-chlorophenoxy)-2-oxopropylphosphonate Synonyms:DIMETHYL 3-(3-CHLOROPHENOXY)-2-OXOPROPYLPHOSPHONATE;Dimethyl 3-(3-chlorophenoxy)-2-oxopropylphosphonate, 98 %;3-(m-Chloro..
CR3345	1220646-23-0	AVN-492 AVN-492 is a potent and selective 5-HT6R Antagonist. The affinity of AVN-492 to bind to 5-HT6R (Ki = 91 pM) was more than three ..

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