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Novel, potent and selective anilinoquinazoline and anilinopyrimidine inhibitors of p38 MAP kinase
Authors:Cumming John G  McKenzie Caroline L  Bowden Stuart G  Campbell Douglas  Masters David J  Breed Jason  Jewsbury Philip J
Institution:AstraZeneca, Mereside, Alderley Park, Macclesfield, Cheshire, SK10 4TG, UK. john.cumming@astrazeneca.com
Abstract:SAR studies led to the identification of 4-(3-benzoylamino-6-methyl-anilino)quinazolines as potent and selective inhibitors of p38 MAP kinase. Further optimisation led to the identification of a series of 4-(3-benzoylamino-6-methyl-anilino)pyrimidines as potent inhibitors of the p38 MAP kinase signalling pathway in vitro and in vivo.
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