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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Synthesis of some novel 2-substituted-5-(isopropylthiazole) clubbed 1,2,4-triazole and 1,3,4-oxadiazoles as potential antimicrobial and antitubercular agents.
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Synthesis of some novel 2-substituted-5-(isopropylthiazole) clubbed 1,2,4-triazole and 1,3,4-oxadiazoles as potential antimicrobial and antitubercular agents.

机译:一些新型的2-取代的5-(异丙基噻唑)棒状的1,2,4-三唑和1,3,4-恶二唑的合成作为潜在的抗微生物剂和抗结核剂。

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摘要

In the present study a series of 2-substituted-5-[isopropylthiazole] clubbed 1,2,4-triazole and 1,3,4-oxadiazole derivatives have been synthesized and characterized by IR, 1H NMR, 13C NMR and mass spectral analysis. Synthesized compounds were evaluated for their preliminary cytotoxicity, antimicrobial and antitubercular activity against Mycobacterium tuberculosis H37Rv strain by broth dilution assay method. Antimycobacterial activity tested against M. tuberculosis indicated that compounds 4b and 6g exhibited twofold enhanced potency than parent compound 1 and the results indicate that some of them exhibited promising activities and they deserve more consideration as potential antitubercular agents. Compound 3c, 4b and 6c exhibited good or moderate antibacterial inhibition and compounds 3h and 7c showed excellent antifungal activity.
机译:在本研究中,合成了一系列2-取代的5- [异丙基噻唑]棒状的1,2,4-三唑和1,3,4-恶二唑衍生物,并通过IR,1H NMR,13C NMR和质谱分析对其进行了表征。 。通过肉汤稀释测定法评价合成的化合物对结核分枝杆菌H37Rv菌株的初步细胞毒性,抗微生物和抗结核活性。测试的针对结核分枝杆菌的抗分枝杆菌活性表明,化合物4b和6g的效力比母体化合物1增强了两倍,结果表明,其中一些化合物表现出令人鼓舞的活性,作为潜在的抗结核剂,它们应得到更多的考虑。化合物3c,4b和6c表现出良好或中等的抗菌抑制作用,化合物3h和7c表现出优异的抗真菌活性。

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