首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis, characterization and antimicrobial studies of 2-(4-methoxy-phenyl)-5-methyl-4-(2-arylsulfanyl-ethyl)-2,4-dihydro-(1,2,4) triazolo-3-ones and their corresponding sulfones.
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Synthesis, characterization and antimicrobial studies of 2-(4-methoxy-phenyl)-5-methyl-4-(2-arylsulfanyl-ethyl)-2,4-dihydro-(1,2,4) triazolo-3-ones and their corresponding sulfones.

机译:2-(4-甲氧基-苯基)-5-甲基-4-(2-芳基硫烷基-乙基)-2,4-二氢-(1,2,4)三唑并-3-酮的合成,表征和抗菌研究它们相应的砜。

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摘要

In the present investigation, a series of novel 2-(4-methoxy-phenyl)-5-methyl-4-(2-arylsulfanyl-ethyl)-2,4-dihydro-[1,2,4] triazolo-3-ones and their corresponding sulfones were prepared with the objective of developing better antimicrobial agents. The chemical structures of the newly synthesized compounds were characterized by spectral (IR, (1)H NMR, (13)C NMR and LCMS) methods. The newly synthesized compounds (4a-i) and (5a-e, 5h) were screened for their antimicrobial activity against Bacillus subtilis, Staphylococcus aureus, Staphylococcus epidermidis, Escherichia coli and Pseudomonas aeruginosa. The antifungal activity was tested against Rhizopus oryzae, Aspergillus niger, Aspergillus flavus, Candida albicans and Saccharomyces cerevisiae. Among all the compounds synthesized, compounds 4d and 5b exhibited significant antibacterial activity.
机译:在本研究中,一系列新型的2-(4-甲氧基-苯基)-5-甲基-4-(2-芳基硫烷基-乙基)-2,4-二氢-[1,2,4]三唑-3-为了开发更好的抗菌剂,制备了它们和它们相应的砜。通过光谱(IR,(1)H NMR,(13)C NMR和LCMS)方法表征了新合成的化合物的化学结构。筛选了新合成的化合物(4a-i)和(5a-e,5h)对枯草芽孢杆菌,金黄色葡萄球菌,表皮葡萄球菌,大肠埃希氏菌和铜绿假单胞菌的抗菌活性。测试了对米根霉,黑曲霉,黄曲霉,白色念珠菌和酿酒酵母的抗真菌活性。在所有合成的化合物中,化合物4d和5b表现出显着的抗菌活性。

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