Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1376933 | Bioorganic & Medicinal Chemistry Letters | 2008 | 6 Pages |
Abstract
The biphenyl amides (BPAs) are a novel series of p38 MAP kinase inhibitors. The discovery of the series through structure-based focused screening is described, and the binding mode of the compounds is explained with reference to X-ray crystal structures.
Graphical abstractThe biphenyl amides (BPAs) are a novel series of p38α MAP kinase inhibitors. The discovery of the series through structure-based focused screening is described, and the binding mode of the compounds is explained with reference to X-ray crystal structures.Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Richard M. Angell, Paul Bamborough, Anne Cleasby, Stuart G. Cockerill, Katherine L. Jones, Christopher J. Mooney, Donald O. Somers, Ann L. Walker,