PPARβ/δ Agonist
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PPARβ/δ Agonist (31)
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- Indeglitazar
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PPAR agonist 5
0 ImagesCat. No.: HY-163547CAS No.: 3059387-62-8PPAR agonist 5 (compound 4b) is a potent PPAR agonist with EC50 values of 3.20, 1.51, 1.92 µM for PPARα, PPARβ/δ, PPARγ, respectively. PPAR agonist 5 shows anti-inflammatory effect.
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Chiglitazar sodium
0 ImagesSynonyms: Carfloglitazar sodium -
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Pioglitazone potassium
0 ImagesCat. No.: HY-13956BCAS No.: 1266523-09-4Synonyms: U 72107 potassiumPioglitazone (U 72107) potassium is an orally active and selective PPARγ (peroxisome proliferator-activated receptor) agonist with high affinity binding to the PPARγ ligand-binding domain with EC50 of 0.93 μM and 0.99 μM for human and mouse PPARγ, respectively. Pioglitazone potassium can be used in diabetes research.
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- PPARα/δ agonist 2
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Pparδ agonist 1
0 ImagesCat. No.: HY-107901CAS No.: 1902161-12-9Pparδ agonist 1 is a PPAR-δ agonist, with an EC50 of 5.06 nM, used in the research of PPAR-delta related diseases, such as mitochondrial diseases, muscular diseases, vascular diseases, demyelinating diseases and metabolic diseases.
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Rac-Pemafibrate
0 ImagesCat. No.: HY-17618ACAS No.: 848258-31-1Synonyms: Rac-K13675Pemafibrate racemate (K13675 racemate) is the racemate of pemafibrate, and activates PPARα activity, with EC50s of 1 nM, >10 μM and 1.7 μM for h-PPARα, h-PPARγ and h-PPARδ, respectively.
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Fonadelpar
0 ImagesCat. No.: HY-17633CAS No.: 515138-06-4Synonyms: NPS-005; SJP-0035Fonadelpar is a PPARδ agonist, used in the research of neuroparalytic keratopathy.
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Pparδ agonist 2
0 ImagesCat. No.: HY-100120CAS No.: 870884-12-1Pparδ agonist 2 is a PPARδ agonist extracted from patent WO 2016057656 A1.
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KD-3010
0 ImagesCat. No.: HY-111068CAS No.: 934760-92-6KD-3010 is a potent, orally active, and selective PPARδ agonist.
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DN203316
0 ImagesCat. No.: HY-162963CAS No.: 2982696-04-6Synonyms: PPARδ agonist 11DN203316 (PPARδ agonist 11) is a potent, selective, orally active PPARδ agonist (EC50 = 20 nM) with high selectivity over PPARα and PPARγ. DN203316 suppresses NF-κB-mediated inflammatory signaling, inhibits ferroptosis by upregulating xCT and GPX4, and attenuates STING-TBK1-IRF3-driven fibrogenic responses. DN203316 is useful for research on inflammatory disorders, metabolic dysfunction-associated steatohepatitis (MASH), and liver fibrosis.
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