Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1378684 | Bioorganic & Medicinal Chemistry Letters | 2006 | 6 Pages |
Abstract
A series of C-2, C-8, and N-9 trisubstituted purine based inhibitors of TNF-α production are described. The most potent analogs showed low nanomolar activity against LPS-induced TNF-α production in a THP-1 cell based assay. The SAR of the series was optimized with the aid of X-ray co-crystal structures of these inhibitors bound with mutated p38 (mp38).
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Related Topics
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Chemistry
Organic Chemistry
Authors
Mark Sabat, John C. VanRens, Michael P. Clark, Todd A. Brugel, Jennifer Maier, Roger G. Bookland, Matthew J. Laufersweiler, Steven K. Laughlin, Adam Golebiowski, Biswanath De, Lily C. Hsieh, Richard L. Walter, Marlene J. Mekel, Michael J. Janusz,