孕烷X受体
雄激素受体
药物代谢
异型生物质的
细胞色素P450
药品
药理学
药物发现
核受体
生物
计算生物学
新陈代谢
生物信息学
生物化学
转录因子
基因
酶
作者
Timothy M. Willson,Steven A. Kliewer
摘要
Mechanisms that protect the body from a diverse array of harmful chemicals are also involved in drug metabolism, and can cause adverse drug-drug interactions. Two closely related orphan nuclear hormone receptors--the pregnane X receptor (PXR) and the constitutive androstane receptor (CAR)--have recently emerged as transcriptional regulators of cytochrome P450 expression that couple xenobiotic exposure to oxidative metabolism. In this review, we provide an examination of the roles of PXR and CAR as xenobiotic sensors, and discuss the application of this knowledge to toxicological screening in drug discovery.
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