某些微生物菌株对融合1,2,4-三唑衍生物的敏感性。

Krzysztof Sztanke, Anna Sidor-Wójtowicz, Janina Truchlińska, Kazimierz Pasternak, Małgorzata Sztanke
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引用次数: 0

摘要

1,2,4-三唑是许多具有不同药理活性的药物的结构元素。此外,从文献资料可知,1,2,4-三唑及其融合体系具有抗菌、抗真菌和抗炎活性。对得到的化合物进行了潜在的抗菌活性测试。对106株细菌、6株酵母菌样真菌和3株霉菌进行的微生物学试验表明,在检测浓度(100微克毫升(-1)和200微克毫升(-1))下,所有测试化合物对测试细菌和霉菌的生长没有影响。在咪唑三唑体系的各种取代衍生物中,化合物V在检测浓度下显著抑制了6株白色念珠菌的生长。其化学结构与文献中描述的新型抗真菌药物相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The susceptibility of certain microbial strains to fused 1,2,4-triazole derivatives.

1,2,4-Triazole is the structural element of many drugs that have different pharmacological spectrum of activity. Besides, from the literature data it follows that 1,2,4-triazoles and its fused systems show antibacterial, antifungal and anti-inflammatory activities. The obtained compounds were tested for their potential antimicrobial activity. Microbiological tests conducted on 106 strains of bacteria, 6 strains of yeast-like fungi and 3 strains of moulds have shown that all the tested compounds in the examined concentrations (100 microg ml(-1) and 200 microg ml(-1)) had no influence on the growth of the tested bacteria and moulds. It has been found that among variously substituted derivatives of imidazotriazole system compound V significantly inhibited the growth of 6 strains of Candida albicans in the examined concentrations. Its chemical structure was similar to novel antifungal agents described in the literature.

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