新型3-取代1-(2-甲基-5-硝基苯基)-5-氧吡咯烷衍生物的合成及抗菌活性研究

Benas Balandis, K. Anusevičius, V. Mickevičius, M. Stasevych, V. Novikov
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引用次数: 0

摘要

-在1-(2-甲基-5-硝基苯基)-5-氧吡咯烷-3-碳肼的化学转化过程中合成了新的唑衍生物。合成的化合物的结构通过核磁共振和红外光谱进行了表征。大多数合成的化合物对金黄色葡萄球菌、单核增生乳杆菌、大肠杆菌和铜绿假单胞菌的抑菌活性进行了筛选。以金黄色葡萄球菌、大肠杆菌、铜绿假单胞菌和单核细胞增生乳杆菌为对照。
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 antibacterial activity of novel 3-substituted 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine derivatives
– The synthesis of novel azole derivatives has been accomplished during chemical transformations of the 1-(2-methyl-5-nitrophenyl)-5-oxopyrrolidine-3-carbohydrazide. The structure of the synthesized compounds was determined by NMR and IR spectroscopies. Most of the synthesized compounds were screened for their antibacterial activity against S. aureus, L. monocytogenes, E. coli, and P. aeruginosa bacteria strains. was used as a control for S. aureus, E. coli , P. aeruginosa , and L. monocytogenes .
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