Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1378485 | Bioorganic & Medicinal Chemistry Letters | 2007 | 7 Pages |
Abstract
We have identified and synthesized a series of diaryl substituted pyrazoles as potent antagonists of the chemokine receptor subtype 2. Structure–activity relationship studies directed toward improving the potency led to the discovery of 23 (IC50 = 6 nM).
Graphical abstractWe have identified and synthesized a series of diaryl substituted pyrazoles as potent antagonists of the chemokine receptor subtype 2b. Structure–activity relationship studies directed toward improving the potency led to the discovery of 23 (IC50 = 6 nM).Figure optionsDownload full-size imageDownload as PowerPoint slide
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Anthony B. Pinkerton, Dehua Huang, Rowena V. Cube, John H. Hutchinson, Mary Struthers, Julia M. Ayala, Pasquale P. Vicario, Sima R. Patel, Thomas Wisniewski, Julie A. DeMartino, Jean-Michel Vernier,