Imidazo[4,5-b]pyridine inhibitors of B-Raf kinase

Abstract

This Letter details the synthesis and evaluation of imidazo[4,5-b]pyridines as inhibitors of B-Raf kinase. These compounds bind in a DFG-in, αC-helix out conformation of B-Raf, which is a binding mode associated with significant kinase selectivity. Structure-activity relationship studies involved optimization of the ATP-cleft binding region of these molecules, and led to compound 23, an inhibitor with excellent enzyme/cell potency, and kinase selectivity.

Keywords: B-Raf; DFG-in; Imidazopyridine; Scaffold hopping; αC-helix out.