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pubmed-article:14698147pubmed:abstractTextThe serine protease tryptase has been associated with a broad range of allergic and inflammatory diseases and, in particular, has been implicated as a critical mediator of asthma. The inhibition of tryptase therefore has the potential to be a valuable therapy for asthma. The synthesis, employing solution phase parallel methods, and SAR of a series of novel 2-azepanone tryptase inhibitors are presented. A member of this series, 8t, was identified as a potent inhibitor of human tryptase (IC(50)=38 nM) with selectivity >/=330-fold versus related serine proteases (trypsin, plasmin, uPA, tPA, APC, alpha-thrombin, and FXa) [corrected].lld:pubmed
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pubmed-article:14698147pubmed:authorpubmed-author:KwonChetClld:pubmed
pubmed-article:14698147pubmed:authorpubmed-author:ZhaoGuohuaGlld:pubmed
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pubmed-article:14698147pubmed:authorpubmed-author:BisacchiGrego...lld:pubmed
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pubmed-article:14698147pubmed:pagination309-12lld:pubmed
pubmed-article:14698147pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:14698147pubmed:year2004lld:pubmed
pubmed-article:14698147pubmed:articleTitleSynthesis of potent and selective 2-azepanone inhibitors of human tryptase.lld:pubmed
pubmed-article:14698147pubmed:affiliationThe Bristol-Myers Squibb Pharmaceutical Research Institute, PO Box 5400, Princeton, NJ 08543-5400, USA. guohua.zhao@bms.comlld:pubmed
pubmed-article:14698147pubmed:publicationTypeJournal Articlelld:pubmed
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