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Rosuvastatin is an inhibitor of HMG-CoA reductase (IC50 = 5 nM).1 It inhibits cholesterol synthesis in isolated rat hepatocytes with an IC50 value of 0.16 nM.2 Rosuvastatin (10 mg/kg) reduces plasma total cholesterol, triglyceride, LDL-C, and oxidized LDL-C levels in Ldlr-/- mice fed a high-fat diet.3 It decreases the area of aortic atherosclerotic lesions in the same model. Formulations containing rosuvastatin have been used in the treatment of dyslipidemias.
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1. Structural mechanism for statin inhibition of HMG-
2. Preclinical and clinical pharmacology of Rosuvastatin, a new 3-
3. Rosuvastatin inhibits MMP-