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ID: ALA1156855
Journal: Bioorg Med Chem Lett
Title: Identification of potent and selective VEGFR receptor tyrosine kinase inhibitors having new amide isostere headgroups.
Authors: Gaudette F, Raeppel S, Nguyen H, Beaulieu N, Beaulieu C, Dupont I, Macleod AR, Besterman JM, Vaisburg A.
Abstract: A novel series of malonamide-type dual VEGFR2/c-Met inhibitors in which one of the amide bonds was replaced by an amide isostere-a trifluoroethylamine unit, was designed, synthesized, and evaluated for their enzymatic and cellular inhibition of VEGFR2 and c-Met enzymes. Optimization of these molecular entities resulted in identification of potent and selective inhibitors of VEGFR2 enzyme.
CiteXplore: 20071170