Target intelligence / Profile preview

Cytochrome P450 Family (CYP450s or CYPs)

Target
CYP450s or CYPs
Molecular classification
Enzyme, Monooxygenase, Hemoprotein
01

Overview

Cytochromes P450 constitute an essential superfamily of hemoprotein monooxygenases responsible for metabolizing endogenous substrates and xenobiotics through oxidative biotransformation processes critical to pharmacology, toxicology, endocrinology, and physiology across species. They are involved in the metabolism of a wide array of substrates including drugs, steroids, and fatty acids. Genetic variability in CYP genes leads to differences in drug response and potential drug-drug interactions. They have a characteristic spectrophotometric absorption peak at 450 nm when reduced and complexed with carbon monoxide.

Other names
Cytochrome P450sP450sCYP enzymesCYPs
02

Mechanism of action

Catalyzes phase I oxidative reactions, including hydroxylation and epoxidation, leading to detoxification or activation of drugs. Acts as a monooxygenase, incorporating one atom of molecular oxygen into the substrate and the other into water.

03

Biological functions

Drug metabolismSteroid biosynthesisFatty acid metabolismMetabolism of vitaminsProstaglandin metabolismBile acid metabolismRetinoic acid metabolismXenobiotic metabolismOxidative biotransformation
04

Disease associations

Drug metabolism related diseasesToxicologyEndocrinology related diseasesPharmacology related diseases
05

Safety considerations

Drug-drug interactions due to CYP inhibition or inductionAdverse drug reactions due to genetic polymorphisms affecting CYP activityToxicity from drug metabolites produced by CYPs
06

Interacting drugs

Numerous drugs metabolized or affected by CYPs

2 more in the full profile.

07

Biomarkers

CYP genotypes (e.g., CYP2D6, CYP2C9) for predicting drug responseCYP enzyme activity levels

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