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Biphenyl amide p38 kinase inhibitors 2: Optimisation and SAR
Authors:Angell Richard M  Angell Tony D  Bamborough Paul  Brown David  Brown Murray  Buckton Jacky B  Cockerill Stuart G  Edwards Chris D  Jones Katherine L  Longstaff Tim  Smee Penny A  Smith Kathryn J  Somers Don O  Walker Ann L  Willson Malcolm
Institution:GlaxoSmithKline R&D, Medicines Research Centre, Gunnels Wood Road, Stevenage, Hertfordshire SG1 2NY, UK.
Abstract:The biphenyl amides are a novel series of p38 MAP kinase inhibitors. Structure-activity relationships of the series against p38alpha are discussed with reference to the X-ray crystal structure of an example. The series was optimised rapidly to a compound showing oral activity in an in vivo disease model.
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