Chemical Structure : DN203316
Catalog No.: PC-26999Not For Human Use, Lab Use Only.
DN203316 is a potent, selective peroxisome proliferator-activated receptor delta (PPARδ) agonist with EC50 of 0.02 uM (hPPARδ).
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DN203316 is a potent, selective peroxisome proliferator-activated receptor delta (PPARδ) agonist with EC50 of 0.02 uM (hPPARδ).
DN203316 attenuates cholesterol-induced ferroptosis in hepatocytes, without detectable toxicity.
DN203316 restores expression of xCT and GPX4 at both the transcript and protein levels and increases GSH levels in cholesterol-exposed hepatocytes.
DN203316 reduces exosomal dsDNA release from ferroptotic hepatocytes and inhibits STING-driven fibrogenesis in MASH.
DN203316 (3 mg/kg/day, i.p.) alleviates MASH by suppressing ferroptosis and STING-driven fibrogenesis in HFHC-induced MASH mice.
| M.Wt | 440.46 | |
| Formula | C19H15F3N2O3S2 | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Kim YJ, et al. Exp Mol Med. 2026 Jun 5. doi: 10.1038/s12276-026-01740-0.

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