Identification of a novel series of potent RON receptor tyrosine kinase inhibitors

Abstract A novel series of N -(3-fluoro-4-(2-substituted-thieno[3,2- b ]pyridin-7-yloxy)phenyl)-1-phenyl-5-(trifluoromethyl)-1 H -pyrazole-4-carboxamides targeting RON receptor tyrosine kinase was designed and synthesized. SAR study of the series allowed us to identify compounds possessing either inhibitory activity of RON kinase enzyme in the low nanomolar range with low residual activity against the closely related c-Met or potent dual inhibitory activity against RON and c-Met, − with no significant activity against VEGFR2 in both cases.