Information provided in the product description is from published literature. Due to the nature of scientific experimentation, your results (e.g., selectivity and effective concentrations) or specific application for this product may differ. If you have questions about how this product fits your application, please contact our technical support staff.
Visit our FAQ
Toll Free Phone (USA and Canada Only): (888) 526-5351
Direct Phone: (734) 975-3888
Product Categories
Provide batch numbers separated by commas to download or request available product inserts, QC sheets, certificates of analysis, data packs, and GC-MS data.

Discover high-quality research tools to investigate GLP-1 mechanisms and next-generation metabolic targets.
OBESITY RESEARCH SOLUTIONSMevastatin is a competitive HMG-CoA reductase inhibitor (Ki = 0.1 µM).1 In vivo, mevastatin (50 mg/kg) inhibits cholesterogenesis in the liver and ileum of normolipidemic rats, as well as enhances suppression of cholesterogenesis in cholesterol-fed rats or rats administered cholestyramine.2 Mevastatin also suppresses TNF-induced NF-κB activation (IC50 = ~17 µM) and potentiates apoptosis in human myeloid leukemia cells.3 It also suppresses induced ferroptosis in HT-1080 cells.4 Formulations containing mevastatin have been used in the treatment of familial hypercholesterolemia.5
WARNING This product is not for human or veterinary use.
1. Competitive inhibition of 3-
2. The effect of compactin, a potent inhibitor of 3-
3. Reversal of chemoresistance and enhancement of apoptosis by statins through down-
4. A compendium of kinetic modulatory profiles identifies ferroptosis regulators. Nat. Chem. Biol. (2021).
5. The discovery and development of HMG-