| Literature DB >> 20128594 |
Barry G Shearer1, Robert W Wiethe, Adam Ashe, Andrew N Billin, James M Way, Thomas B Stanley, Craig D Wagner, Robert X Xu, Lisa M Leesnitzer, Raymond V Merrihew, Todd W Shearer, Michael R Jeune, John C Ulrich, Timothy M Willson.
Abstract
4-Chloro-N-(2-{[5-trifluoromethyl)-2-pyridyl]sulfonyl}ethyl)benzamide 3 (GSK3787) was identified as a potent and selective ligand for PPARdelta with good pharmacokinetic properties. A detailed binding study using mass spectral analysis confirmed covalent binding to Cys249 within the PPARdelta binding pocket. Gene expression studies showed that pyridylsulfone 3 antagonized the transcriptional activity of PPARdelta and inhibited basal CPT1a gene transcription. Compound 3 is a PPARdelta antagonist with utility as a tool to elucidate PPARdelta cell biology and pharmacology.Entities:
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Year: 2010 PMID: 20128594 DOI: 10.1021/jm900464j
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446