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pubmed-article:11354358pubmed:abstractTextAs a continuation of our work with 1,4,5 substituted imidazole inhibitors of p38alpha, we report a series of 1-(4-piperidinyl)-4-(4-fluorophenyl)-5-(2-phenoxy-4-pyrimidinyl) imidazoles related to 7. The compounds have IC50's for inhibition of p38alpha ranging from 6.0 to 650nM. Statistical analysis of the p38beta inhibitor potencies shows a correlation of IC50's with the electron donating strength of low molecular weight substituents.lld:pubmed
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pubmed-article:11354358pubmed:authorpubmed-author:AdamsJ LJLlld:pubmed
pubmed-article:11354358pubmed:authorpubmed-author:BoehmJ CJClld:pubmed
pubmed-article:11354358pubmed:authorpubmed-author:BrownB TBTlld:pubmed
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pubmed-article:11354358pubmed:dateRevised2009-11-19lld:pubmed
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pubmed-article:11354358pubmed:articleTitlePhenoxypyrimidine inhibitors of p38alpha kinase: synthesis and statistical evaluation of the p38 inhibitory potencies of a series of 1-(piperidin-4-yl)-4-(4-fluorophenyl)-5-(2-phenoxypyrimidin-4-yl) imidazoles.lld:pubmed
pubmed-article:11354358pubmed:affiliationDepartment of Medicinal Chemistry , GlaxoSmithKline Pharmaceuticals, King of Prussia, PA 19406, USA. jeffrey_c_boehm@sbphrd.comlld:pubmed
pubmed-article:11354358pubmed:publicationTypeJournal Articlelld:pubmed
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