PPAR
The peroxisome proliferator-activated receptors (PPARs), belonging to the nuclear receptor superfamily, are a group of nuclear receptor proteins that are composed of three isoforms, including PPARγ, PPARα and PPARδ, encoded by separate genes. PPARs have a modular structure characterized by the presence of two highly conserved domains, including the DNA binding domain (DBD) of two zinc fingers and the ligand binding domain (LBD) of 13 α-helices and a small 4-stranded β-sheet. PPARs are ligand-regulated transcription factors controlling gene expression by binding to specific response elements (PPREs) within promoters, where PPARs bind as heterodimers with a retinoid X receptor and interact with cofactors upon binding leading to the increasing of rate of transcription initiation.
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A4305 WY-14643 (Pirinixic Acid)1 CitationTarget: PPARSummary: PPARα agonist,selective and highly potent
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A4306 CiprofibrateSummary: PPARα agonist
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A4307 GW0742Summary: PPARδ/β agonist,potent and selective
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A4309 GW5015161 CitationSummary: PPARδ agonist,selective and potent
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A4310 Rosiglitazone HClSummary: PPARγ agonist
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A4324 Pioglitazone HClSummary: PPARγ agonist
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A3216 BalaglitazoneSummary: PPAR-γ partial agonist
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B2117 PioglitazoneSummary: PPAR agonist
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B1943 Fenofibrate1 CitationSummary: PPARα agonist
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B1947 GemfibrozilSummary: PPARα activator