Target intelligence / Profile preview

Cytochrome P450 family 2 subfamily C member 9 (CYP2C9)

Target
CYP2C9
Molecular classification
Enzyme, Monooxygenase, Cytochrome P450
01

Overview

Cytochrome P450 2C9 (CYP2C9) is a member of the cytochrome P450 superfamily of enzymes. It functions as a phase I drug-metabolizing enzyme, primarily catalyzing the oxidation of both xenobiotic substances (such as drugs) and endogenous compounds (such as fatty acids and steroid hormones). The enzyme is encoded by the CYP2C9 gene, which is highly polymorphic—meaning genetic variations can significantly affect its metabolic activity. Genetic variants in CYP2C9 can lead to altered metabolism rates for many drugs. This has significant implications for dosing requirements—especially for medications with narrow therapeutic indices like warfarin—and risk assessment for adverse drug reactions or toxicity.

02

Mechanism of action

Monooxygenase that introduces an oxygen atom into substrates using electrons from NADPH via cytochrome P450 reductase

03

Biological functions

Xenobiotic metabolismDrug metabolismFatty acid metabolismSteroid hormone metabolism
04

Disease associations

Adverse drug reactionsDrug toxicityOrgan failure syndromes
05

Safety considerations

Altered drug metabolism rates due to genetic variantsDosing adjustments required for drugs with narrow therapeutic indicesRisk of adverse drug reactions or toxicityDrug-drug interactions due to enzyme inhibition or induction
06

Interacting drugs

Warfarin

9 more in the full profile.

07

Biomarkers

CYP2C9 polymorphisms

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