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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
CR1636	927880-90-8	RAF265 (CHIR-265) CHIR-265 is an orally bioavailable small molecule with potential antineoplastic activity.CHIR-265 binds and inhibits Raf kinases, ..
CR1635	905281-76-7	GDC-0879 GDC-0879 is a highly selective, potent, and orally bioavailable RAF small-molecule inhibitor. In GDC-0879 -treated mice, both cell..
CR1634	923564-51-6	Navitoclax ABT-263 Navitoclax, also known as ABT-263, is an orally bioavailable, synthetic small-molecule antagonist of a subset of the B-cell leukem..
CR1632	1194044-20-6	LY2811376 LY2811376 is a potent and selective BACE1 inhibitor (IC50 = 239 nM for the synthetic peptide) that demonstrates ~10-fold selectivi..
CR1631	1210344-57-2	Ertugliflozin (PF-04971729) Ertugliflozin, also known as also known as PF-04971729, is a potent and selective inhibitor of the sodium-dependent glucose cotran..
CR1630	808118-40-3	Roxadustat FG-4592 Roxadustat, also known as ASP1517 and FG-4592, is an HIF α prolyl hydroxylase inhibitor in a cell-free assay. It stabilizes HIF-2..
CR1629	905586-69-8	AZ960 AZ960 is a novel inhibitor of Jak2 kinase. AZ960 inhibits JAK2 kinase with a K(i) of 0.00045 microm in vitro and treatment of TEL-..
CR1628	1030825-20-7	Canagliflozin INT4 2-[(5-Bromo-2-methylphenyl)methyl]-5-(4-fluorophenyl)-thiophene can be used to prepare Canagliflozin as sodium-dependent glucose c..
CR1627	81058-27-7	Canagliflozin intermediate 2,3,3-Trimethyl-5-Chloro-3H-Indole was used in the preparation of glucosylated monoterpenoids rhodiolosides A and D. Synonyms: ..
CR1626	842133-18-0	Canagliflozin Canagliflozin (INN, trade name Invokana) is a drug for the treatment of type 2 diabetes. It was developed by Mitsubishi Tanabe Pha..

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