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pubmed-article:15780613pubmed:abstractTextStarting from a PDE IV inhibitor hit derived from high throughput screening of the compound collection, a key pyrrolidine cyanamide pharmacophore was identified. Modifications of the pyrrolidine ring produced enhancements in cathepsin K inhibition. An X-ray co-crystal structure of a cyanamide with cathepsin K confirmed the mode of inhibition.lld:pubmed
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pubmed-article:15780613pubmed:articleTitleNovel and potent cyclic cyanamide-based cathepsin K inhibitors.lld:pubmed
pubmed-article:15780613pubmed:affiliationDepartment of Medicinal Chemistry, GlaxoSmithKline, Research Triangle Park, NC 27709, USA. david.n.deaton@gsk.comlld:pubmed
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