首页> 外文期刊>Dhaka University Journal of Pharmaceutical Sciences >Studies of Biologically Active Heterocycles: Synthesis, Characterization and Antimicrobial Activity of Some 5-Substitutd-2-Amino-1,3,4-Oxadiazoles
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Studies of Biologically Active Heterocycles: Synthesis, Characterization and Antimicrobial Activity of Some 5-Substitutd-2-Amino-1,3,4-Oxadiazoles

机译:生物活性杂环的研究:某些5-取代的2-氨基-1,3,4-Oxadiazoles的合成,表征和抗菌活性

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In the present study, 5-substituted-2-amino-1,3,4-oxadiazoles (4a-k) have been synthesized by the electrochemical oxidation of semicarbazones (3a-k) using platinum anode at room temperature under controlled potential electrolysis in an undivided cell assembly. The structural assignment of these compounds (4a-k) has been made on the basis of elemental analysis, IR, 1H NMR and 13C NMR. The synthesized compounds were screened for their inhibiting activity against Klebsilla penumoniae, Escherichia coli, Bassilus subtilis and Streptococcus aureus and antifungal activity against Aspergillus niger and Crysosporium pannical and results have been compared with the standard antibacterial agents, Streptomycin and antifungal drug, Griseofulvin. The Compounds exhibited significant antibacterial activity and antifungal activity. Key words: Electrochemical oxidation; controlled potential; 5-substituted-2-amino-1,3,4-oxadiazole; semicarbazone; antimicrobial agents DOI: 10.3329/dujps.v9i1.7434 Dhaka Univ. J. Pharm. Sci. 9(1): 53-59 2010 (June)
机译:在本研究中,通过在室温下在受控电势下于室温下使用铂阳极对半咔唑酮(3a-k)进行电化学氧化,合成了5-取代的2-氨基-1,3,4-恶二唑(4a-k)。未分割的单元格组件。这些化合物(4a-k)的结构分配基于元素分析,IR,1H NMR和13C NMR进行。筛选了合成的化合物对肺炎克雷伯菌,大肠杆菌,枯草芽孢杆菌和金黄色链球菌的抑制活性以及对黑曲霉和宽孢子孢菌的抗真菌活性,并与标准抗菌剂,链霉素和抗真菌药Griseoful比较。该化合物表现出显着的抗菌活性和抗真菌活性。关键字:电化学氧化控制电位; 5-取代的2-氨基-1,3,4-恶二唑;氨基脲抗菌剂DOI:10.3329 / dujps.v9i1.7434达卡大学。 J.药物科学9(1):2010年6月53-59日

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