抗抑郁药物非莫西汀及其立体异构体类似物对腹泻肠杆菌科的抗生素作用。

J. Kristiansen, I. Mortensen, K. Gaarslev
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引用次数: 11

摘要

目前的研究是为了说明抗抑郁药物非莫西汀及其三种类似物对20种产生腹泻的肠杆菌科细菌的抗菌作用。研究表明,非莫西汀的立体异构体形式的活性是顺式形式的两倍以上,并抑制所有低于400微克/毫升(1.2毫米)的菌株。两种顺式化合物在100微克/毫升~ 800微克/毫升(0.3 mM ~ 2.4 mM)范围内对20株病原菌分别只有11株和9株的抑制作用。我们的研究指出,细菌细胞有一个目标的精神药理学活性药物。因此,已知的精神药物及其立体异构体类似物可能代表了一个潜在的新的抗菌药物池。此外,细菌模型可作为研究神经药理学药物和其他膜活性化合物与生物膜相互作用的模型系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The antibiotic effect of the anti-depressive drug femoxetine and its stereo-isomeric analogs on diarrhoea producing enterobacteriaceae.
The present investigation has been undertaken to illustrate the antibacterial effect on 20 diarrhoea producing enterobacteriaceae of an anti-depressive drug available as femoxetine and its three analogs. It has been shown that the stereo-isomeric trans forms of femoxetine are more than twice as active as the cis forms and inhibited all the strains below 400 microgram/ml (1.2 mM). The two cis compounds only inhibited 11 and 9 of the 20 strains respectively in the investigated area 100 microgram/ml - 800 microgram/ml (0.3 mM - 2.4 mM). Our investigations point out that the bacterial cell has a target for psychopharmacologically active agents. Thus the known psychopharmaca and their stereo-isomeric analogs may represent a pool of potentially new antimicrobial drugs. Furthermore the bacterial model may be useful as a model system in the study of the interaction of neuropharmacological agents and other membrane active compounds with biological membranes.
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