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Identification of a novel series of potent RON receptor tyrosine kinase inhibitors
Authors:Stéphane Raeppel  Frédéric Gaudette  Michael Mannion  Stephen Claridge  Oscar Saavedra  Ljubomir Isakovic  Robert Déziel  Normand Beaulieu  Carole Beaulieu  Isabelle Dupont  Hannah Nguyen  James Wang  A. Robert Macleod  Christiane Maroun  Jeffrey M. Besterman  Arkadii Vaisburg
Affiliation:1. Department of Medicinal Chemistry, MethylGene Inc., 7220 rue Frederick-Banting, Montréal, QC, Canada H4S 2A1;2. Department Cell Biology and Pharmacology, MethylGene Inc., 7220 rue Frederick-Banting, Montréal, QC, Canada H4S 2A1;3. Department PK/Analytical Chemistry, MethylGene Inc., 7220 rue Frederick-Banting, Montréal, QC, Canada H4S 2A1
Abstract:A novel series of N-(3-fluoro-4-(2-substituted-thieno[3,2-b]pyridin-7-yloxy)phenyl)-1-phenyl-5-(trifluoromethyl)-1H-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.
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