部分镇痛活性咪唑[2,1-c]三嗪类药物抗菌活性的排除。

Krzysztof Sztanke, Anna Sidor-Wójtowicz, Janina Truchlińiska, Kazimierz Pasternak, Małgorzata Sztanke
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摘要

本研究的目的是排除某些镇痛活性咪唑[2,1-c]三嗪类药物的潜在抗菌活性。这些化合物在其化学结构中含有潜在的药效团形成和特征,类似于不含碱性氮原子的类吗啡镇痛药和阿片受体激动剂。这些化合物对实验动物的中枢神经系统显示出显著的抗伤性活性,且毒性值极低(LD50值在2000 mg kg(-1) bw以上)。对106株细菌、6株酵母样真菌和3株霉菌进行了微生物学试验。所检测的咪唑[2,1-c]三嗪浓度为100微克毫升(-1)和200微克毫升(-1)对所测微生物的生长没有影响。在镇痛活性化合物的情况下,缺乏这种影响是有益的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Exclusion of antimicrobial activity of some analgesic active imidazo[2,1-c]triazines.

The purpose of this study was to exclude the potential antimicrobial activity of certain analgesic active imidazo[2,1-c]triazines. These compounds contain in their chemical structure potential pharmacophore formations and features similar to those present in morphine - like analgesics and opioid receptor agonists containing no basic nitrogen atom. These compounds showed significant antinociceptive activity on the central nervous system of the tested animals, correlated with very low toxicity value (LD50 value of above 2000 mg kg(-1) b.w. via i. p.). Microbiological tests were conducted on 106 strains of bacteria, 6 strains of yeast-like fungi and 3 strains of moulds. The examined imidazo[2,1-c]triazines in concentrations of 100 microg ml(-1) and 200 microg ml(-1) had no influence on the growth of the microorganisms tested. Lack of this influence can be profitable in the case of analgesic active compounds.

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