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Discover high-quality research tools to investigate GLP-1 mechanisms and next-generation metabolic targets.
OBESITY RESEARCH SOLUTIONSPemafibrate is an orally bioavailable and selective agonist of peroxisome proliferator-activated receptor α (PPARα; EC50 = 1 nM for transcriptional activity), a transcription factor that is essential for regulation of lipid homeostasis.1 It is selective for PPARα over PPARδ and PPARγ (EC50s = 2,300 and 1,000 nM, respectively, for transcriptional activity). In human HepG2 hepatoma cells, pemafibrate is 1,000-fold more potent than the classical PPARα agonists fenofibrate (Item No. 10005368) and Wy 14643 (Item No. 70730) in activating PPARα transcriptional activity.2 Pemafibrate (0.001% w/w) reduces plasma triglyceride levels, non-esterified fatty acids, and total cholesterol in mice fed a moderate-fat diet, and, when administered at 0.00025%, it reduces liver lipid accumulation and improves prognosis in wild-type but not Ppara knockout mice in a model of diet-induced non-alcoholic fatty liver disease (NAFLD).2 In mouse models of non-alcoholic steatohepatitis (NASH), pemafibrate stimulates expression of PPARα, enhances lipid turnover, and reduces liver triglyceride levels and inflammation.3 It also dose-dependently reduces the area of atherosclerotic lesions in human apolipoprotein E2 (ApoE2) knock-in mice.4
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1. Selective peroxisome proliferator-
2. Selective peroxisome proliferator-
3. Pemafibrate, a novel selective peroxisome proliferator-
4. The novel selective PPARα modulator (SPPARMα) pemafibrate improves dyslipidemia, enhances reverse cholesterol transport and decreases inflammation and atherosclerosis. Atherosclerosis 249, 200-208 (2016).