Drug intelligence / Profile preview

resveratrol + rosiglitazone

Development stage
Preclinical
Lead developer
Jupiter Neurosciences
Modality
Small Molecules
Administration
Oral (for Both Agents Individually; No Fixed-dose Combination Product Identified)
01

Overview

Resveratrol + rosiglitazone is a combination of two small molecules, resveratrol and rosiglitazone. Resveratrol is a natural polyphenolic compound found in grapes and other plants, known for its antioxidant properties and ability to activate SIRT1, PGC-1α, and JNK pathways. Rosiglitazone is a thiazolidinedione class antidiabetic agent that acts as an agonist of peroxisome proliferator-activated receptor gamma (PPAR-γ), improving insulin sensitivity in adipose tissue. The combination has been studied for synergistic effects on metabolic processes such as fatty acid re-esterification in adipose tissue from obese individuals, with evidence suggesting enhanced gene expression related to metabolism (PDK4 and PEPCK) compared to either agent alone[1]. Additionally, resveratrol may counteract some adverse effects of rosiglitazone on vascular mineralization by reducing oxidative stress and osteoblast-like differentiation in vascular smooth muscle cells[2].

02

Targets

PPARA (Peroxisome proliferator-activated receptor alpha)PPARG (Peroxisome proliferator-activated receptor gamma)

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