Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1369402 | Bioorganic & Medicinal Chemistry Letters | 2013 | 5 Pages |
Abstract
A novel series of potent benzoxazole mPGES-1 inhibitors has been derived from a hit from a high throughput screen. Compound 37 displays mPGES-1 inhibition in an enzyme assay (0.018 μM) and PGE-2 inhibition in a cell-based assay (0.034 μM). It demonstrates 500- and 2500-fold selectivity for mPGES-1 over COX-2 and 6-keto PGF-1α, respectively. In vivo PK studies in dogs demonstrate 55% oral bioavailability and an 7 h half-life.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Natasha Kablaoui, Snahel Patel, Jay Shao, Douglas Demian, Keith Hoffmaster, Francioise Berlioz, Michael L. Vazquez, William M. Moore, Richard A. Nugent,