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OBESITY RESEARCH SOLUTIONSPioglitazone-d4 is intended for use as an internal standard for the quantification of pioglitazone (Item Nos. 71745 | 10028 | 22263) by GC- or LC-MS. Pioglitazone is an agonist of the peroxisome proliferator-activated receptor γ (PPARγ; EC50 = ~500-600 nM for both human and murine PPARγ).1,2 It is selective for PPARγ over PPARα, exhibiting low level activation of PPARα at 1 µM and 5.4-fold activation at a concentration of 10 µM.1 Pioglitazone inhibits pyruvate oxidation and glucose production in hepatocytes when used at a concentration of 10 μM.3 In vivo, pioglitazone (0.3-3 mg/kg per day) reduces hyperglycemia, hyperlipidemia, and hyperinsulinemia in a dose-dependent manner in male Wistar fatty rats.4 It reduces the number of lesions in a transgenic rat adenocarcinoma of prostate (TRAP) model.5 Pioglitazone (2.5 mg/kg) also decreases production of neuroinflammatory cytokines and reduces immobility in the forced swim and tail suspension tests in a mouse model of chronic mild stress, indicating antidepressant-like activity that can be reversed by the PPARγ antagonist GW 9662 (Item No. 70785).6
WARNING This product is not for human or veterinary use.
1. Activation of human peroxisome proliferator-
2. The PPARs: From orphan receptors to drug discovery. J. Med. Chem. 43(4), 527-550 (2000).
3. Pioglitazone inhibits mitochondrial pyruvate metabolism and glucose production in hepatocytes. FEBS J. 284(3), 451-465 (2017).
4. Effects of pioglitazone on glucose and lipid metabolism in Wistar fatty rats. Arzneimittelforschung. 40(3), 263-267 (1990).
5. Pioglitazone, a peroxisome proliferator-
6. The antidepressant-