Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376936 | Bioorganic & Medicinal Chemistry Letters | 2008 | 8 Pages |
Abstract
Nitric oxide (NO), a mediator of various physiological and pathophysiological processes, is synthesized by three isozymes of nitric oxide synthase (NOS). Potential candidate clinical drugs should be devoid of inhibitory activity against endothelial NOS (eNOS), since eNOS plays an important role in maintaining normal blood pressure and flow. A new series of aminopiperidines as potent inhibitors of iNOS were identified from a HTS lead. From this study, we identified compound 33 as a potent iNOS inhibitor, with >25-fold selectivity over eNOS and 16-fold selectivity over nNOS.
Graphical abstractThe design and synthesis of a novel class of iNOS inhibitors are described.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Bertrand Le Bourdonnec, Lara K. Leister, Christopher A. Ajello, Joel A. Cassel, Pamela R. Seida, Heather O’Hare, Minghua Gu, Guo-Hua Chu, Paul A. Tuthill, Robert N. DeHaven, Roland E. Dolle,