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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C5280 3-Thiatetradecanoic AcidSummary: activator of PPAR
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B5581 SR 1664Summary: inhibits Cdk5-mediated PPARγ phosphorylation, antidiabetic agent
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A8957 AUDASummary: Potent epoxide hydrolase inhibitor/PPARα activator
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B3610 ClofibrateSummary: PPAR agonist
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B7010 15-deoxy-Δ-12,14-Prostaglandin J2Target: PPARSummary: PPARγ agonist
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B7406 GSK 0660Summary: PPARδ antagonist
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B7471 S26948Summary: PPARγ agonist
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B7553 TesaglitazarSummary: Dual-specificity PPARα/γ agonist
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B7609 CP 775146Summary: PPARα agonist
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B6681 CiglitazoneSummary: PPARγ agonist