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 About 11 results found for searched term "51-83-2" (0.075 seconds)

Cat.No.  Name Target
M1867 PAC-1 Caspase
Procaspase activating compound 1
PAC-1 is a procaspase-activating compound; activates procaspase-3 to produce caspase-3 (EC50 = 0.22 μM).
M2489 Carbachol chloride AChR/AChE
Carbamylcholine
Carbachol is a cholinomimetic compound that binds and activates the acetylcholine receptor.
M2717 Galeterone Androgen Receptor
TOK-001
Galeterone is a selective CYP17 inhibitor and androgen receptor (AR) antagonist with IC50 of 300 nM and 384 nM, respectively, and is a potent inhibitor of human prostate tumor growth.
M5226 UMI-77 Bcl-2
UMI-77 is a selective Mcl-1 inhibitor with Ki of 490 nM, showing selectivity over other members of Bcl-2 family.
M5318 Zoligratinib EGFR/HER2
CH5183284;Debio 1347
CH5183284 is a selective and orally available FGFR inhibitor with IC50 of 9.3 nM, 7.6 nM, 22 nM, and 290 nM for FGFR1, FGFR2, FGFR3, and FGFR4, respectively. Phase 1.
M6338 3-MATIDA GluR
3-MATIDA is a potent, selective mGlu 1 antagonist.
M8353 SPA0355 Others
SPA0355 inhibits cytokine and LPS-induced activation of NF-kB in cell-based assays, blocking IKK-2 phosphorylation, degradation, and p65 binding to DNA.
M11529 Temuterkib ERK
LY3214996
Temuterkib (LY3214996) is a selective, novel erK1/2 inhibitor with an IC50 of 5 nM against ERK1 and ERK2. It can effectively inhibit intracellular P-RSK1 in cancer cell lines with BRAF and RAS mutations. Temuterkib has strong antitumor activity in cancer models with altered MAPK pathways.
M13923 CCR2-RA-[R] CCR
CCR2-RA-[R] is an allosteric antagonist of the C-C chemokine receptor type 2 (CCR2) with an IC50 of 103 nM.
M39160 Xanthopurpurin MMP
Xanthopurpurin, an anthraquinone glycoside, isolated from the roots of Rubia akane, shows mainly strong inhibition of collagen-induced platelet aggregation.
M50777 Angiotensin A Others
Angiotensin A is a renin–angiotensin system (RAS) peptide that causes a vasoconstrictive effect dependent on AT1 receptors.



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