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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >A facile, one-pot synthesis, characterization and antimicrobial activity of o-hydroxy anilide derivatives and 1-substituted-1,3-dicyclohexylurea analogs of long chain carboxylic acids.
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A facile, one-pot synthesis, characterization and antimicrobial activity of o-hydroxy anilide derivatives and 1-substituted-1,3-dicyclohexylurea analogs of long chain carboxylic acids.

机译:长链羧酸的邻羟基苯胺衍生物和1-取代-1,3-二环己基脲类似物的简便,一锅合成,表征和抗菌活性。

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摘要

A series of novel o-hydroxy anilide derivatives and 1-substituted-1,3-dicyclohexylurea analogs of long chain carboxylic acids have been synthesized. The structures of the synthesized compounds were elucidated by IR, (1)H NMR, (13)C NMR and mass spectral data. All the synthesized compounds were tested for their antimicrobial activity by disk diffusion assay with slight modifications against Gram-positive, Gram-negative strains of bacteria as well as fungal strains. After that minimum inhibitory concentrations (MICs), minimum bactericidal concentrations (MBCs) and minimum fungicidal concentrations (MFCs) of all the synthesized compounds were determined. The investigation of antimicrobial screening data revealed that all the tested compounds showed moderate to good microbial inhibitions. Compounds 3e, 4e, 3f and 4f were found to be the most potent antimicrobial agents.
机译:已经合成了一系列新颖的长链羧酸的邻羟基苯胺衍生物和1-取代的-1,3-二环己基脲类。通过IR,(1)H NMR,(13)C NMR和质谱数据阐明合成的化合物的结构。通过盘扩散测定法对所有合成的化合物的抗微生物活性进行了测试,对细菌的革兰氏阳性,革兰氏阴性菌株以及真菌菌株进行了轻微修饰。之后,确定所有合成化合物的最小抑菌浓度(MIC),最小杀菌浓度(MBC)和最小杀菌浓度(MFCs)。抗菌筛选数据的研究表明,所有测试化合物均显示出中度至良好的微生物抑制作用。发现化合物3e,4e,3f和4f是最有效的抗菌剂。

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