CYP3A4: Difference between revisions

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[[Category:Pharmacology]]
[[Category:Pharmacology]]
[[Category:Drug metabolism]]
[[Category:Drug metabolism]]
== CYP3A4 ==
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File:Hydroxylation_Mechanisms_of_Cytochrome_P450_Enzymes.png|Hydroxylation Mechanisms of Cytochrome P450 Enzymes
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Latest revision as of 22:02, 16 February 2025

CYP3A4 is a member of the cytochrome P450 superfamily of enzymes. These enzymes are responsible for the metabolism of a variety of substances, including drugs and endogenous compounds. CYP3A4 is one of the most important enzymes in this family, as it is involved in the metabolism of approximately half of all marketed drugs.

Function[edit]

CYP3A4 is an enzyme that is found in the liver and intestines. It plays a crucial role in the body's ability to metabolize drugs and other xenobiotics. This enzyme is responsible for the oxidation of a wide range of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics.

Clinical significance[edit]

Due to its role in drug metabolism, variations in the activity of CYP3A4 can have significant clinical implications. For example, individuals with low CYP3A4 activity may be at risk of drug toxicity, while those with high activity may require higher doses of medication to achieve therapeutic effects. Furthermore, certain drugs can inhibit or induce the activity of CYP3A4, potentially leading to drug-drug interactions.

Interactions[edit]

CYP3A4 has been shown to interact with a number of drugs and other substances. Some of these interactions can lead to changes in the metabolism of the substances involved, potentially affecting their efficacy or toxicity.

See also[edit]

References[edit]

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CYP3A4[edit]