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Cytochrome P450 2C19 (CYP2C19) is a key enzyme in the cytochrome P450 superfamily, primarily expressed in the liver. It metabolizes a wide range of clinically important drugs, including antiplatelet agents, proton pump inhibitors, antidepressants, and anticonvulsants. Genetic polymorphisms in CYP2C19 significantly affect drug metabolism, impacting efficacy and safety.
CYP2C19 catalyzes oxidation reactions that modify both endogenous compounds and xenobiotics (foreign substances such as drugs). This process typically increases water solubility for easier elimination from the body. For some drugs like clopidogrel (Plavix), CYP2C19 activates prodrugs into their active forms; for others like voriconazole or certain antidepressants, it deactivates them for excretion.
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