杂环化合物的杂化合成及其抑菌活性研究

N. Desai, D. Vaja
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引用次数: 3

摘要

合成了一系列新的N-(1-(2-(1-苯基-3-(对苯基)- 1h -吡唑-4-基)-5-(吡啶-4-基)-1,3,4-恶二唑-3(2H)-基)乙基)芳基苯胺及其衍生物。用光谱技术对合成化合物的结构进行了表征。新合成的衍生物对革兰氏阳性菌(金黄色葡萄球菌和化脓性葡萄球菌)、革兰氏阴性菌(大肠杆菌和铜绿假单胞菌)和真菌(白色假单胞菌、黑单胞菌和clavatus假单胞菌)的抗菌活性进行了评价。其中,5f、5i、5l和5t具有较好的抑菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Hybrid Approach for Synthesis and Antimicrobial Activity of Heterocyclic Compounds
We have synthesized novel series of N-(1-(2-(1-phenyl-3-(p-tolyl)-1H-pyrazol-4-yl)-5-(pyridin-4-yl)-1,3,4-oxadiazol-3(2H)-yl)ethylidene)arylaniline and their derivatives. The structures of synthesized compounds were well characterized by spectroscopic techniques. Antimicrobial activity of the newly synthesized derivatives was evaluated against gram positive (S. aureus and S. pyogenes), gram negative bacteria (E. coli and P. aeruginosa), and strains of fungi (C. albicans, A. niger and A. clavatus). Among the screened derivatives 5c, 5f, 5i, 5l and 5t demonstrated superior antimicrobial activity against microbial strains.
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