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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
CR2643	1380432-32-5	EHop-016 EHop-016 is a novel potent and selective inhibitor of RAC. EHop-016 inhibits Rac activity in the MDA-MB-435 metastatic cancer cell..
CR2642	1357389-11-7	RGFP966 RGFP966 is a selective HDAC3 inhibitor . S ystemic treatment with RGFP966 facilitates extinction in mice in a manner resistant to ..
CR2641	850664-21-0	GSK269962A GSK269962 is a selective ROCK inhibitor with IC50 values of 1.6 and 6 nM for ROCK-I and ROCK-II, respectively. GSK269962 can becom..
CR2640	1815589-51-5	NA. Synonyms: Benzamide, 2-fluoro-N-[(1S)-1-[[1-(1H-indazol-5-yl)-3-methyl-2,4-dioxo-1,3,8-triazaspiro[4.5]dec-8-yl]carbonyl]-2-methyl..
CR3395	1243243-89-1	Wnt-C59 Wnt-C59 is a potent porcupine (PORCN) inhibitor. Wnt-C59 inhibits PORCN activity in vitro at nanomolar concentrations, as assessed..
CR2639	351994-94-0	BDTH2 Emeramide Emeramide, also known as NBMI or N,N'-Bis(2-mercaptoethyl)isophthalamide, is a mercury/heavy metal chelator. Emeramide molecul..
CR2638	1374601-40-7	BRD4770 BRD4770 is a novel histone methyltransferase inhibitor. BRD4770 reduced cellular levels of di- and trimethylated H3K9 without indu..
CR2637	108852-90-0	PNU152243A Nemorubicin Nemorubicin, also known as PNU152243A, is a doxorubicin derivative that differs significantly from its parent drug in terms of spe..
CR2636	139504-50-0	Maytansinoid DM1 Mertansine Mertansine refers to the thiol-containing maytansinoid, DM1 (N2’-deacetyl-N2’-(3-mercapto-1-oxopropyl)maytansine) attached to a ..
CR2635	138148-68-2	DM1-Sme Mertansine DM1-SMe is a potent maytansinoid microtubular inhibitor and an unconjugated DM1 as a mixed disulfide with thiomethane to cap its s..

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