Identification and characterization of 4-chloro-N-(2-{[5-trifluoromethyl)-2-pyridyl]sulfonyl}ethyl)benzamide (GSK3787), a selective and irreversible peroxisome proliferator-activated receptor delta (PPARdelta) antagonist

4-氯-N-(2-{[5-三氟甲基)-2-吡啶基]磺酰基}乙基)苯甲酰胺 (GSK3787) 的鉴别和表征,一种选择性和不可逆的过氧化物酶体增殖激活受体 delta (PPARdelta) 拮抗剂

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作者:Barry G Shearer, 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.

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