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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
CR2380	212844-54-7	Purvalanol B Purvalanol B, also known as NG 95, is a potent and selective CDK inhibitor that most potently inhibits Cdk2/cyclin A, Cdk2/cyclin ..
CR2378	1594094-64-0	CW069 CW069 is an allosteric inhibitor of HSET. CW069 showed marked activity against HSET in vitro. The inhibitor induced multipolar mit..
CR2374	309271-94-1	Inauhzin INZ Inauhzin is a potent SIRT inhibitor, which effectively reactivates p53 by inhibiting SIRT1 activity, promotes p53-dependent apopto..
CR2348	639052-78-1	LH846 LH846 is a selective inhibitor of casein kinase. IC50 values of LH846 are 290 nM, 1.3 μM and 2.5 μM for CK1δ, ε and α). LH 84..
CR2328	743420-02-2	Chidamide impurity Chidamide, also known as Tucidinostat , CS055 and HBI-8000 , is a n orally bioavailable benzamide type inhibitor of histone deacet..
CR2325	1233948-35-0	ELR510444 ELR510444 is a potent microtube disruptor with potential anticancer activity. ELR510444 has potent microtubule-disrupting activity..
CR2315	1337531-36-8	GSK2606414 GSK2606414 is an orally available, potent, and selective PERK inhibitor. GSK2606414 inhibits PERK activation in cells and inhibits..
CR2313	934353-76-1	ENMD-2076 ENMD-2076 is an orally-active, Aurora A/angiogenic kinase inhibitor with a unique kinase selectivity profile and multiple mechanis..
CR2305	52214-84-3	Ciprofibrate Ciprofibrate is a peroxisome proliferator-activated receptor agonist. Target: PPAR Ciprofibrate is a hypolipidemic compound that c..
CR2299	1314890-29-3	TMP269 TMP269 has no impact on the mitochondrial activity and/or the viability of human CD4+ T cells at 10 μM, and may be used as tools ..

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