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Pravastatin, Simvastatin, Atorvastatin, Rosuvastatin

Kuhnil Pharmaceutical Co., Ltd. · FDA-approved active Small molecule

These statins inhibit HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, thereby reducing LDL cholesterol levels.

These statins inhibit HMG-CoA reductase, the rate-limiting enzyme in cholesterol synthesis, thereby reducing LDL cholesterol levels. Used for Hypercholesterolemia and dyslipidemia, Primary and secondary prevention of cardiovascular disease, Reduction of risk of myocardial infarction and stroke.

At a glance

Generic namePravastatin, Simvastatin, Atorvastatin, Rosuvastatin
SponsorKuhnil Pharmaceutical Co., Ltd.
Drug classHMG-CoA reductase inhibitor (statin)
TargetHMG-CoA reductase
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved

Mechanism of action

Statins competitively inhibit 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, which catalyzes the conversion of HMG-CoA to mevalonate, an early and rate-limiting step in cholesterol biosynthesis. By reducing hepatic cholesterol production, statins upregulate LDL receptors on hepatocytes, increasing clearance of LDL particles from the bloodstream. This leads to decreased plasma LDL cholesterol and reduced cardiovascular risk.

Approved indications

Common side effects

Key clinical trials

Primary sources

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SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

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