Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1370469 | Bioorganic & Medicinal Chemistry Letters | 2011 | 5 Pages |
Abstract
Biphenylacetic acid (5) was identified through a library screen as an inhibitor of the prostaglandin D2 receptor DP2 (CRTH2). Optimization for potency and pharmacokinetic properties led to a series of selective CRTH2 antagonists. Compounds demonstrated potency in a human DP2 binding assay and a human whole blood eosinophil shape change assay, as well as good oral bioavailability in rat and dog, and efficacy in a mouse model of allergic rhinitis following oral dosing.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jill M. Scott, Christopher Baccei, Gretchen Bain, Alex Broadhead, Jilly F. Evans, Patrick Fagan, John H. Hutchinson, Christopher King, Daniel S. Lorrain, Catherine Lee, Peppi Prasit, Pat Prodanovich, Angelina Santini, Brian A. Stearns,