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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 - Gs-441524 - Vitamin D Analogs - Antibiotics

Catalog No	CAS NO	Product name
CR3269	1457983-28-6	G-749 G-749 is a novel FLT3 inhibitor that showed potent and sustained inhibition of the FLT3 wild type and mutants including FLT3-ITD, ..
CR3268	516480-79-8	BML-277 BML-277, also known as Chk2 Inhibitor II, is a Chk2 (checkpoint kinase 2) inhibitor. BML-277 protects T cells from apoptosis by co..
CR3267	837422-57-8	WH-4-023 WH-4-023 is a potent and selective dual Lck/Src inhibitor with IC50 of 2 nM/6 nM for Lck and Src kinase respectively. The lymphocy..
CR3266	1374828-69-9	GNE-0877 GNE-0877 is a highly potent and selective LRRK2 inhibitor. Leucine-rich repeat kinase 2 (LRRK2) has drawn significant interest in ..
CR3264	62717-42-4	SKF-38393 HCl SKF-38393, aslo known as (+/-)-SKF-38393, is a synthetic compound of the benzazepine chemical class which acts as a selective D1/D..
CR3263	20012-10-6	SKF-38393 HBr Synonyms: SKF 38393 hydrobromide;(±)-SKF 38393 hydrobromide;SKF 38393;(±)-1-phenyl-2,3,4,5-tetrahydro-(1H)-3-benzazepi..
CR1668	1374744-69-0	TG101348 Dihydrochloride Fedratinib, also known as TG101348 and SAR302503, is a JAK2 inhibitor, is also an orally bioavailable, small-molecule, ATP-competi..
CR1667	936091-26-8	TG101348 Fedratinib Fedratinib, also known as TG101348 and SAR302503, is a JAK2 inhibitor, is also an orally bioavailable, small-molecule, ATP-competi..
CR1666	939791-38-5	PF-00562271 Besylate PF-562271 Besylate, also known as PF-562,271 and PF-271, is an orally bioavailable small molecule and ATP-competitive focal adhesi..
CR1665	170364-57-5	Enzastaurin LY317615 Enzastaurin is a synthetic macrocyclic bisindolemaleimide with potential antineoplastic activity. Binding to the ATP-binding site,..

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