ML786 dihydrochloride is a potent and orally bioavailable Raf inhibitor, with IC 50 s of 2.1, 4.2, and 2.5 nM for V600E ΔB-Raf , wt B-Raf , and C-Raf , respectively. ML786 dihydrochloride also inhibits Abl-1 , DDR2 , EPHA2 , KDR , and RET ( IC 50 =<0.5, 7.0, 11, 6.2, 0.8 nM). ML786 dihydrochloride can be used for the research of cancers.
Products | Products > Disease Areas > Cancer | Products > Signaling Pathways > MAPK/ERK Pathway | Products > Signaling Pathways > Protein Tyrosine Kinase/RTK | Products > Research Areas > Cancer | Products > Research Areas > Cancer > Cancer Targeted Therapy | Products > Research Areas > Cancer > Cancer Metabolism and Metastasis | Products > Signaling Pathways > Raf | Products > Signaling Pathways > Bcr-Abl | Products > Signaling Pathways > Discoidin Domain Receptor | Products > Signaling Pathways > VEGFR | Products > Signaling Pathways > RET | Products > Signaling Pathways > Ephrin Receptor
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