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pubmed-article:15149645pubmed:abstractTextSeveral 8-substituted 2-naphthamidine-based inhibitors of the serine protease urokinase plasminogen activator (uPA) are described. Direct attachment of five-membered saturated or unsaturated rings improved inhibitor performance; substitution with sulfones further improved binding profiles. Combination of these substituents or of previously described NH-linked heteroaromatic rings with 6-phenyl amide substituents provided further enhancements to potency and selectivity.lld:pubmed
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pubmed-article:15149645pubmed:dateRevised2008-11-21lld:pubmed
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pubmed-article:15149645pubmed:articleTitleInteraction with the S1 beta-pocket of urokinase: 8-heterocycle substituted and 6,8-disubstituted 2-naphthamidine urokinase inhibitors.lld:pubmed
pubmed-article:15149645pubmed:affiliationCancer Research, Global Pharmaceutical R & D, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064-6101, USA. mike.d.wendt@abbott.comlld:pubmed
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