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J Med Chem ; 53(4): 1857-61, 2010 Feb 25.
Article in English | MEDLINE | ID: mdl-20128594

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.


Subject(s)
Benzamides/chemical synthesis , PPAR delta/antagonists & inhibitors , Sulfones/chemical synthesis , Animals , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacokinetics , Antineoplastic Agents/pharmacology , Benzamides/pharmacokinetics , Benzamides/pharmacology , Binding Sites , Carnitine O-Palmitoyltransferase/biosynthesis , Carnitine O-Palmitoyltransferase/genetics , Cell Line, Tumor , Cysteine/metabolism , Drug Screening Assays, Antitumor , Genes, Reporter , Humans , Ligands , Male , Mass Spectrometry , Mice , Mice, Inbred C57BL , Muscle Fibers, Skeletal/drug effects , Muscle Fibers, Skeletal/enzymology , PPAR delta/agonists , PPAR delta/genetics , Protein Serine-Threonine Kinases/biosynthesis , Protein Serine-Threonine Kinases/genetics , Pyruvate Dehydrogenase Acetyl-Transferring Kinase , Structure-Activity Relationship , Sulfones/pharmacokinetics , Sulfones/pharmacology , Tissue Distribution , Transcription, Genetic/drug effects
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