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首页> 外文期刊>Asian Journal of Chemistry: An International Quarterly Research Journal of Chemistry >Synthesis, Characterization and Urease Inhibiting Derivatives of 5-(3,4-Methylenedioxyphenyl)-l,3,4-Oxadiazol-2-thiol
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Synthesis, Characterization and Urease Inhibiting Derivatives of 5-(3,4-Methylenedioxyphenyl)-l,3,4-Oxadiazol-2-thiol

机译:5-(3,4-亚甲基二氧苯基)-1,3,4-恶二唑-2-硫醇的合成,表征和脲酶抑制剂

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摘要

In the present work, the urease inhibition activity of 1,3,4-oxadiazole bearing molecules was evaluated and were found to be potential inhibitors. 3,4-(Methylenedioxy)benzoic acid (1) was employed to synthesize 5-(3,4-methylenedioxyphenyl)-l,3,4-oxadiazol-2-thiol (4) via a series of steps. It was further stepped to yield S-substituted-5-(3,4-methylenedioxyphenyl)-l,3,4-oxadiazoIe derivatives (6a-h) on action with alkyl/aralkyl halides (Sa-h) in DMF using LiH as an activator. All the synthesized compounds were well supported by IR, H NMR and EIMS spectral analysis. The enzyme inhibition activity against urease enzyme showed these molecules as potent inhibitors of this enzyme.
机译:在目前的工作中,评估了带有1,3,4-恶二唑的分子的脲酶抑制活性,发现它们是潜在的抑制剂。通过一系列步骤,使用3,4-(亚甲基二氧基)苯甲酸(1)合成5-(3,4-亚甲基二氧基苯基)-1,3,4-恶二唑-2-硫醇(4)。使用LiH作为溶剂,进一步与DMF中的烷基/芳烷基卤化物(Sa-h)作用,得到S-取代的5-(3,4-亚甲二氧基苯基)-1,3,4-恶二唑衍生物(6a-h)。激活剂。 IR,1 H NMR和EIMS光谱分析均很好地支持了所有合成的化合物。对脲酶的酶抑制活性表明这些分子是该酶的有效抑制剂。

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