ZM 306416 hydrochloride 100mg 100mg | Purity Not Available
Adooq Bioscience
ZM 306416 is a VEGF receptor tyrosine kinase inhibitor that inhibits KDR (IC50 = 100 nM) and Flt (IC50 = 2 uM) tyrosine kinases.
More Information Supplier PageZM 306416 is a VEGF receptor tyrosine kinase inhibitor that inhibits KDR (IC50 = 100 nM) and Flt (IC50 = 2 uM) tyrosine kinases.
More Information Supplier PageZM 306416 is a VEGF receptor tyrosine kinase inhibitor that inhibits KDR (IC50 = 100 nM) and Flt (IC50 = 2 uM) tyrosine kinases.
More Information Supplier PageZM 323881 is a potent and selective inhibitor of the kinase activity of the human vascular endothelial growth factor receptor 2 (VEGFR2/KDR).
More Information Supplier PageTG 100713 is an inhibitor of PI3-kinase that inhibits endothelial cell proliferation.
More Information Supplier PageBay 11-7821 is an irreversible inhibitor of TNF-??-stimulated I??B?? phosphorylation.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageGW2580 is a small-molecule, ATP-competitive inhibitor of cFMS kinase.
More Information Supplier PageMoxalactam is a synthetically derived, structurally unique beta-lactam antibiotic. Its antimicrobial activity encompasses a wide spectrum and includes some strains of pseudomonal species.
More Information Supplier PageMoxalactam is a synthetically derived, structurally unique beta-lactam antibiotic. Its antimicrobial activity encompasses a wide spectrum and includes some strains of pseudomonal species.
More Information Supplier Page