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[大鼠肝脏微粒体中对-450细胞色素对磺胺苯吡唑的结合及其对细胞色素-P-450还原酶的影响]

[Sulfaphenazole binding by p-450 cytochrome of liver microsomes of rats and its effect of cytochrome-p-450-reductase].

作者信息

Miuller D, Liubbe G, Khoang-Tikh K, Klinger V

出版信息

Farmakol Toksikol. 1976 May-Jun;39(3):331-2.

PMID:16775
Abstract

Tests set up "in vitro" on the rats' liver microsomes showed that sulfaphenazol, which in an inhibitor of the mixed type N-and O-demethylation, is bound as a substrate of the II type (aniline type). It attenuates spectral changes caused by aniline and vice versa. Sulfaphenazol inhibits the activity of the ADPH cytochrome-P-450-reductase.

摘要

在大鼠肝脏微粒体上进行的“体外”试验表明,作为N-和O-混合类型去甲基化抑制剂的磺胺苯唑,作为II型(苯胺型)底物被结合。它减弱了由苯胺引起的光谱变化,反之亦然。磺胺苯唑抑制ADPH细胞色素P-450还原酶的活性。

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