Target intelligence / Profile preview

3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase) (HMGCR)

Target
HMGCR
Molecular classification
Enzyme, Oxidoreductase
01

Overview

3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMG-CoA reductase) is the rate-limiting enzyme in the mevalonate pathway, which is the metabolic route for the endogenous synthesis of cholesterol and other isoprenoids (UniProt: P04035). Located primarily in the endoplasmic reticulum of hepatocytes, it catalyzes the conversion of HMG-CoA to mevalonate using NADPH as a reducing agent (PubMed: 11574408). Dysregulation or high activity of this enzyme leads to elevated levels of low-density lipoprotein cholesterol (LDL-C), a major risk factor for atherosclerosis and coronary heart disease (StatPearls: NBK430910). Rosuvastatin and other statins function as competitive inhibitors of HMG-CoA reductase, binding to the active site with higher affinity than the natural substrate (PubChem: CID 126457). This inhibition reduces intracellular cholesterol levels, prompting the liver to up-regulate LDL receptors, which enhances the clearance of LDL-C from the systemic circulation (NIH: LiverTox).

Other names
HMGCR3-hydroxy-3-methylglutaryl-CoA reductaseHMG-CoA reductase
02

Mechanism of action

Competitive inhibition of the HMG-CoA reductase enzyme, which catalyzes the rate-limiting step in cholesterol synthesis.

03

Biological functions

Cholesterol biosynthesisMevalonate pathwayIsoprenoid synthesis
04

Disease associations

HypercholesterolemiaCardiovascular diseaseAtherosclerosisDyslipidemia
05

Safety considerations

MyopathyRhabdomyolysisHepatotoxicityNew-onset diabetes mellitusCognitive impairment
06

Interacting drugs

Rosuvastatin

6 more in the full profile.

07

Biomarkers

Low-density lipoprotein cholesterol (LDL-C)Total cholesterolApolipoprotein BHigh-sensitivity C-reactive protein (hsCRP)

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