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抗结核异烟肼与结核分枝杆菌耐药性——综述

Antitubercular isoniazid and drug resistance of Mycobacterium tuberculosis--a review.

作者信息

Scior Thomas, Meneses Morales Iván, Garcés Eisele Solón Javier, Domeyer David, Laufer Stefan

机构信息

Department of Pharmacy, Benemérita Universidad Autónoma de Puebla, Puebla, Pue.72570, México.

出版信息

Arch Pharm (Weinheim). 2002;335(11-12):511-25. doi: 10.1002/ardp.200290005.

Abstract

Isoniazid is one of the most potent drugs available for tuberculosis treatment. As a pro-drug it requires activation, which is performed by catalase/peroxidase. The active principle, whose identity has not yet been determined unambiguously, then acts on at least one target molecule, the enoyl-acyl carrier protein, required for the synthesis of the vital mycolic acids present in the cell wall of the bacterium. Some other targets have been proposed in order to explain the unusual potency of isoniazid; however, the supporting data are still controversial. We thoroughly discuss the action of isoniazid, resistance mechanisms, and the possible active product, which includes an isonicotinic acid-NADH adduct as well as a meta-isomer of NADH. Both structures have been probed positively in a 3D modeling analysis.

摘要

异烟肼是可用于治疗结核病的最有效的药物之一。作为一种前体药物,它需要通过过氧化氢酶/过氧化物酶进行激活。其活性成分的身份尚未明确确定,然后作用于至少一种靶分子,即烯酰 - 酰基载体蛋白,这是细菌细胞壁中存在的重要分枝菌酸合成所必需的。为了解释异烟肼的非凡效力,还提出了一些其他靶点;然而,支持数据仍存在争议。我们深入讨论了异烟肼的作用、耐药机制以及可能的活性产物,其中包括异烟酸 - NADH加合物以及NADH的间位异构体。在三维建模分析中,这两种结构均得到了肯定的验证。

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