乙二醛衍生的一些新的硝基化合物的抗菌评价

Husam Hamza Salman
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引用次数: 2

摘要

目的:以乙二醛为原料与取代芳基羟胺缩合反应合成硝基化合物,并评价其抗菌效果。材料与方法:合成芳基羟胺衍生物,然后与乙二醛(40%)反应合成硝基酮化合物。结果:本研究合成的硝基化合物的结构经傅里叶变换红外光谱和核磁共振光谱及元素分析确证。结果支持了硝基酮类化合物的结构。结论:合成的硝基酮纯度高,收率好。研究了合成的氮酮对革兰氏阳性(金黄色葡萄球菌,ATCC 25923)和革兰氏阴性(大肠杆菌,ATCC 25922)细菌和真菌(黑曲霉和黄曲霉)的抑菌效果。研究证明,合成的氮酮具有显著的抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antimicrobial evaluation of some new nitrone compounds derived from glyoxal
Objective: The aim of this work includes the synthesis of nitrone compounds derived from glyoxal by a condensation reaction with substituted arylhydroxylamines and evaluation of their antimicrobial efficacy. Materials and Methods: The present work concerned the synthesis of arylhydroxylamine derivatives and subsequently reacted with glyoxal (40%) to synthesize the nitrone compounds. Results: The synthesized nitrones in our study, their structures identified with Fourier-transform infrared and 1H-Nuclear magnetic resonance spectroscopies in addition to elemental analysis (C.H.N.). The results support the structures of nitrone compounds. Conclusion: Synthesized nitrones obtained in high purity and an excellent yield. The synthesized nitrones investigated for evaluation of their antimicrobial efficacy against Gram-positive (Staphylococcus aureus, ATCC 25923) and Gram-negative (Escherichia coli, ATCC 25922) bacteria and fungus (Aspergillus niger and Aspergillus flavus). The study proved that the synthesized nitrones exhibited significant antimicrobial activity.
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