P450

1.The present drug2013drug interaction can be attributed to a strong inhibitory effect on cytochrome P450-3A4 activity by voriconazole.究其原因，是因为伏立康唑对细胞色素P450-3A4活性有强大的抑制作用。

2.The Cytochrome P450 superfamily participated in at least 16 key enzyme reactions in phenylpropanoid pathway.细胞色素P450超家族参与苯丙烷途径的至少16种关键酶反应。

3.METHODS The ultraviolet spectrophotometric method was used to measure P450 concentration of hepatic microsomes.方法紫外分光光度法测定大鼠肝微粒体P450含量；

4.This included characterization of an enzyme, cytochrome P450, that always introduces the epoxide in the desired beta configuration.还有细胞色素P450这个酶的鉴定，经常在想得到β-构型时引入这个环氧化物。

5.This review provides a better understanding of the cytochrome P450 system with a focus on those enzymes most involved in drug metabolism.这次综述提供了一个对大多数药物代谢有关的酶为重点的细胞色素P450系统的了解。

6.Azole and triazole drugs are cytochrome P450 inhibitors widely used as fungal antibiotics and possessing potent antimycobacterial activity.唑类和三氮唑类药物作为细胞色素P450抑制剂广泛被作为抗真菌药物和抗微生物药物使用。

7.Compound lipophilicity is of key importance to P450 binding affinity and enzyme selectivity.复合脂是至为重要的细胞色素P450酶结合亲和力和选择性。

8.OBJECTIVE To introduce the research status of cytochrome P450 and its new applications in clinical pharmacy.目的介绍细胞色素P450的研究进展及其在临床药学工作实践中的指导意义。

9.Objective: To investigate the expression of the aromatase P450 in breast hypertrophy and discuss its significance.目的：观察芳香化酶P450在肥大乳房乳腺组织中的表达状况，并探讨其意义。

10.An example of a flavoprotein undergoing a one-electron transfer is with the microsomal NADPH-cytochrome P450 reductase.的一个经历一个单电子转移黄素蛋白的例子是与微粒NADPH-细胞色素P450还原酶。