化学
药理学
CYP3A4型
医学
生物化学
细胞色素P450
酶
作者
Dong‐Zhu Tu,Xueyan Hu,J. Lei,Shuyan Liu,Z XIAO,Ling Yang,Guangbo Ge
标识
DOI:10.1080/13543776.2025.2470294
摘要
Introduction Cytochrome P450 3A4 (CYP3A4), one of the most important xenobiotic-metabolizing enzymes, plays a central role in drug metabolism and acts as a key mediator in drug-drug interactions. CYP3A4 inhibitors can potentiate the in vivo therapeutic effects of CYP3A4-substrate drugs via enhancing their systematic exposure levels. Two CYP3A4 inhibitors (ritonavir and cobicistat) have already been approved for modulating the exposure levels of CYP3A4-substrate drugs.
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