一些新的硝基衍生物的合成、表征及生物活性的筛选

Jihad Haji Mohammed, Nabaz Abdulmajeed Mohammad Salih
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引用次数: 0

摘要

本文以硝基苯衍生物为原料,在氯化铵水溶液中以锌粉为还原剂,还原出相应的苯羟胺的吸电子和给电子基团,开始了几种新型硝基苯衍生物的合成研究。制备的苯羟胺衍生物与不同取代的苯甲醛反应得到硝基酮的目标衍生物。通过FT-IR、1H-NMR和13C NMR等波谱方法对合成的硝基化合物进行了结构表征。最后,对新合成的化合物在不同浓度下的微生物活性进行了筛选,并对革兰氏阴性大肠杆菌(E. coli)、革兰氏阳性金黄色葡萄球菌(S. aureus)和真菌(白色念珠菌)的生长进行了抑制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SYNTHESIS AND CHARACTERIZATION OF SOME NEW NITRONES DERIVATIVES AND SCREENING THEIR BIOLOGICAL ACTIVITIES
Synthetic approached towards the synthesis of some novel nitrones derivatives have been started with reduction of nitrobenzene derivatives as starting material bearing electron withdrawing and electron donating groups to corresponding phenylhydroxylamine in presence of zinc dust as reducing agent in aqueous solution of ammonium chloride (NH4Cl). The prepared phenylhydroxylamine derivatives were reacted with different substituted benzaldehydes to give the target derivatives of nitrone. The structures of the synthesized nitrones were characterized by spectroscopic methods FT-IR, 1H-NMR and 13C NMR. Finally, the newly synthesized compounds were screened for their microorganism activities at different concentration, and inhibited growth of Escherichia coli (E. coli) Gram negative, Staphylococcus aureus (S. aureus) Gram positive, and fungi (candida albicans).
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