Description
An inhibitor of HMG-CoA reductase (Ki = 0.3 nM for the rat enzyme); binds to the HMG-CoA binding site; inhibits human CYP2C9 (IC50 = 100 nM); inhibits increases in serum cholesterol, triglycerides, phospholipids, and TBARS levels, as well as vascular ACE activity in rabbits fed a high-cholesterol diet at 2 mg/kg; increases survival in a mouse model of myocardial infarction at 10 mg/kg per day
Formal name: 7-[3-(4-fluorophenyl)-1-(1-methylethyl)-1H-indol-2-yl]-3,5-dihydroxy-6-heptenoic acid
Synonyms:
Molecular weight: 411.5
CAS: 93957-54-1
Purity: ≥98%
Formulation: A crystalline solid
Product Type|Biochemicals|Small Molecule Inhibitors|Cytochrome P450||Product Type|Biochemicals|Small Molecule Inhibitors|Sterol Biosynthesis||Research Area|Cardiovascular System|Cardiovascular Diseases|Myocardial Infarction||Research Area|Cardiovascular System|Lipids & Lipoproteins|Cholesterol Metabolism||Research Area|Cell Biology|Cell Death|Ferroptosis||Research Area|Endocrinology & Metabolism|Metabolic Diseases|Dyslipidemias