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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
CR2422	1056901-62-2	AT13148 AT13148 is a novel oral multi-AGC kinase inhibitor with potent pharmacodynamic and antitumor activity, which shows a distinct mech..
CR2421	1401031-39-7	TRV130 hydrochloride Oliceridine HCl Oliceridine, also known as TRV130, is a µ- opioid receptor agonist, that is currently under evaluation in human clinical tria..
CR2420	1173900-33-8	AZD6482 KIN-193 AZD6482 is a potent, selective and ATP competitive PI3Kβ inhibitor (IC(50) 0.01 μm). AZD6482 inhibited insulin-induced human adi..
CR2419	900185-02-6	PIK-294 PIK-294 is a highly selective inihibitor of the phosphoinositide 3-kinase (PI3K) p110δ with an IC50 value of 10 nM compared to IC..
CR2418	1098189-15-1	GS-9451 Vedroprevir Vedroprevir, also known as GS9451, is a selective hepatitis C virus (HCV) NS3 protease inhibitor in development for the treatment ..
CR2417	939805-30-8	ACTB-1003 ACTB-1003 is an oral kinase inhibitor targeting cancer mutations (FGFR inhibition), angiogenesis (inhibition of VEGFR2 and Tie-2) ..
CR2416	1291074-87-7	ENMD-2076 Tartrate ENMD-2076 has selective activity against Aurora A and Flt3 with IC50 of 14 nM and 1.86 nM, 25-fold selective for Aurora A than ove..
CR2415	168110-44-9	Micafungin FR-179642 impurity acid FR 179642 is an impurity of Micafungin, a lipopeptide compound that acts as an antifungal agent with activity against Aspergillus ..
CR2414	1214265-58-3	WZ4003 WZ4003 is a selective inhibitors of the LKB1-tumour-suppressor-activated NUAK kinases. WZ4003 inhibits both NUAK isoforms (IC50 fo..
CR2413	1403254-99-8	EPZ-6438 Tazemetostat Tazemetostat, also known as EPZ-6438 and E7438, is a potent, selective, and orally bioavailable small-molecule inhibitor of EZH2 e..

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