Article ID Journal Published Year Pages File Type
1367188 Bioorganic & Medicinal Chemistry Letters 2006 4 Pages PDF
Abstract

A series of novel pyridine-2-propanoic acids was synthesized. A structure–activity relationship study of these compounds led to the identification of potent dual PPARα/γ agonists with varied isoform selectivity. Based on the results of efficacy studies in diabetic (db/db) mice, and the desired pharmacokinetic parameters, compound (S)-13 was selected for further profiling.

Graphical abstractA novel series of potent dual PPARα/γ agonists was identified. SAR studies led to the identification of a multitude of compounds with varied isoform selectivity.Figure optionsDownload full-size imageDownload as PowerPoint slide

Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Authors
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