ML239 10 mg | 99.54%
TargetMol

ML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM.
More Information Supplier PageML239 is a potent and selective inhibitor of breast cancer stem cells, with an IC50 of 1.16 μM.
More Information Supplier PageML-18 is a non-peptide bombesin receptor subtype-3 (BRS-3) antagonist with an IC50 of 4.8 μM.
More Information Supplier PageML-18 is a non-peptide bombesin receptor subtype-3 (BRS-3) antagonist with an IC50 of 4.8 μM.
More Information Supplier PageGSK461364(Ki=2.2 nM) inhibits purified Plk1 .The specificity of GSK461364 for Plk1 is more than 1000-fold over Plk2/3.
More Information Supplier PageCeftiofur Hydrochloride is the hydrochloride salt form of ceftiofur, a semisynthetic, beta-lactamase-stable, broad-spectrum, third-generation cephalosporin with antibacterial activity.
More Information Supplier PageElesclomol (STA-4783) is an effective oxidative stress inducer that elicits pro-apoptosis of tumor cells.
More Information Supplier PageLDN193189 hydrochloride is a selective BMP type I receptor kinases inhibitor.
More Information Supplier PageEntospletinib (IC50= 7.7 nM)is a specific Syk inhibitor, which is orally bioavailable.
More Information Supplier PageBatimastat (BB-94) is an effective, broad-spectrum matrix metalloprotease (MMP) inhibitor. Batimastat induces extracellular matrix degradation and inhibits angiogenesis, tumor growth and invasion, and metastasis.
More Information Supplier PageThis product is isolated and purified from the leaves of Phyllostachys heterocycla
More Information Supplier Page