A potent cRAF1 kinase inhibitor (IC = 9 nM). Shows 100-fold selectivity for Raf kinase versus Cdk1, Cdk2, c-src, ERK2, MEK, p38, Tie2, VEGFR2, and c-Fms. cRAF1 inhibitors are predicted to be broad spectrum antitumor agents.
本公司网站所展示销售的产品仅供科研!
沪公网安备 31011202007337号