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Evaluation of New 2-N-tert-butyl-5-aryl-1, 3, 4-Oxadiazol-2-Amines for Antimicrobial Activity

机译:新型2-N-叔丁基-5-芳基-1,3,4-恶二唑-2-胺的抗菌活性评估

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A series of five membered heterocyclic oxadiazole derivatives synthesized by intramolecular cyclisation of N-tert-butyl-2-aroyl hydrazine carbothioamides (IIa-g) with iodine-pot.iodide in basic medium were tested for their biological activities against selected microorganisms. The newly synthesized compounds were investigated for their antimicrobial activities by Agar diffusion method. For antibacterial study, the bacterial strain used included both gram-positive strains like Ecoli and gram negative strain S.aureus. Antifungal activity was performed against the fungus A. niger. Among the synthesized compounds (IIIa-g), few compounds showed weak antimicrobial activities in comparison with standard drugs.
机译:测试了在碱性介质中通过N-叔丁基-2-芳酰基肼碳硫酰胺(IIa-g)分子内环化合成的一系列五元杂环恶二唑衍生物对选定微生物的生物学活性。通过琼脂扩散法研究了新合成的化合物的抗菌活性。为了进行抗菌研究,使用的细菌菌株包括革兰氏阳性菌株(如Ecoli)和革兰氏阴性菌株金黄色葡萄球菌。对真菌黑曲霉进行了抗真菌活性。在合成的化合物(IIIa-g)中,与标准药物相比,几乎没有化合物显示出较弱的抗菌活性。

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