Cytochrome P 450 enzymes are very important for metabolism function in body.

细胞色素P450酶是体内代谢转换的重要酶系.

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Cytochrome P 450 enzyme system shown to activate many carcinogens.

细胞色素P450酶系统可以激活多种癌基因.

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CYP 450 gene has several mutant alleles leading to genetic polymorphisms in humans.

细胞色素P450氧化酶的基因具有遗传多态性,在人类存在等位基因的突变体.

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However, biricodar and valspodar are both substrates for the P 450 isoenzyme 3 A 4.

然而, 比立考达和伐司朴达都是P450同工酶3A4的底物.

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Objective : To study activity of cytochrome P 450 for human liver microsomes.

目的: 为测定人肝细胞微粒体细胞色素P450氧化酶的活性.

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Induction and inhibition of cytochrome P 450 ( CYP 450 ) catalytic activity has been concluded to be pharmacokinetic drug - drug interaction.

细胞色素P450酶 ( CYP450 ) 活性的诱导或抑制,是引起临床药物代谢性相互作用的主要作用机制.

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Cytochrome P 450 s are a large group of heme - binding enzymes and widely distribute in biology.

细胞色素P450是一种血红素结合蛋白,在生物界广泛存在.

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Cytochrome P 450 ( CYP 450 ) plays an important role in the cause and therapy of tumors.

细胞色素氧化酶 P450 在肿瘤的发病和治疗中起着不容忽视的作用.

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They also bind tightly to some of the TB P 450 enzymes and inactivate them.

氮杂茂可与结核菌内的一些P450酶类紧密结合使其失活.

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Azole and triazole drugs are cytochrome P 450 inhibitors widely used as fungal antibiotics and antimycobacterial actiity.

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.

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