Discovery of pyrimidine benzimidazoles as Src-family selective Lck inhibitors. Part II

A series of 4-amino-6-benzimidazole-pyrimidines was designed to target lymphocyte-specific tyrosine kinase (Lck), a member of the Src-family kinases (SFKs). These type II inhibitors were optimized using a cellular Lck-dependent proliferation assay and are capable of inhibiting Lck at single-digit nanomolar concentrations. This scaffold is likely to serve a valuable template for developing potent inhibitors of a number of SFKs.

A series of 4-amino-6-benzimidazole-pyrimidines were designed and synthesized as potent Lck inhibitors.Figure optionsDownload as PowerPoint slide