Drug intelligence / Profile preview

MHY2013

Development stage
Preclinical
Lead developer
부산대학교
Modality
Small Molecules
Administration
Intraperitoneal
01

Overview

MHY2013 is a potent small molecule peroxisome proliferator-activated receptor (PPAR) pan-agonist that targets all three isoforms: PPARα, PPARβ/δ, and PPARγ. It was synthesized and characterized by researchers at Pusan National University for the treatment of metabolic and fibrotic disorders. In preclinical models, MHY2013 has demonstrated significant anti-fibrotic and anti-inflammatory effects in the kidneys, specifically reducing tubule damage, myofibroblast activation, and pro-inflammatory cytokine production. Its mechanism of action involves the direct inhibition of TGF-β/SMAD signaling in fibroblasts via PPARγ and the suppression of NF-κB activation in epithelial cells via PPARβ/δ.

02

Targets

PPARD (Peroxisome proliferator–activated receptor delta)PPARG (Peroxisome proliferator-activated receptor gamma)PPARA (Peroxisome proliferator-activated receptor alpha)

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