摘要
CYP2C9是人类肝脏中含量丰富的一种CYP450酶,它能代谢和/或活化许多种药物、前致癌物、前毒物和致突变剂。CYP2C9基因具有遗传多态性,在人类存在几种等位基因的突变体。本文从基因结构、底物和探针药、影响其活性的因素、遗传多态性的分子机制等方面综述CYP2C9的研究进展。
As an abundant CYP450 form in human liver, CYP2C9 can metabolize and/or activate a large variety of drugs, pre-carcinogens, pre-toxins and mutagens. CYP2C9 gene has several mutant alleles leading to genetic polymorphisms in humans. In the present article, the CYP2C9 gene structure, the underlying molecular mechanisms for its genetic polymorphisms, the substrates and probe drugs toward CYP2C9, and factors affecting its enzyme activity are reviewed.
出处
《中国临床药理学杂志》
CAS
CSCD
北大核心
2000年第5期381-385,共5页
The Chinese Journal of Clinical Pharmacology
基金
国家自然科学基金重点项目!(No. F39330230)
美国中华医学基金项目!(No.92-568
No.99-697)