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Minor structural modifications convert a selective PPARalpha agonist into a potent, highly selective PPARdelta agonist
Authors:Weigand Stefan  Bischoff Hilmar  Dittrich-Wengenroth Elke  Heckroth Heike  Lang Dieter  Vaupel Andrea  Woltering Michael
Institution:BAYER Health Care AG, Pharma Research, D-42096 Wuppertal, Germany. stefan.weigand@roche.com
Abstract:We report the solid-phase synthesis and pharmacological evaluation of a new series of small-molecule agonists of the human peroxisome proliferator-activated receptor delta (PPARdelta) based on a lead structure from our PPARalpha program. Compound 33 showed good pharmacokinetics.
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