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首页> 外文期刊>Turkish journal of chemistry >Synthesis and evaluation of antioxidant activities of novel 1,3,4-oxadiazole and imine containing 1H-benzimidazoles
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Synthesis and evaluation of antioxidant activities of novel 1,3,4-oxadiazole and imine containing 1H-benzimidazoles

机译:新型1,3,4-恶二唑和含1H-苯并咪唑的亚胺的合成及抗氧化活性评估

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摘要

Some novel 2-(substitutedbenzylthio)-5-((2- (4-substitutedpheny1)-1H-benzo[d]imidazol-1-yl)methyl)-1,3,4-oxadiazoles (5-12) and 2-(2-(4-chlorophenyl)-1H-benzo[d] imidazol-1-yl)-N'-(arylmethylene)acetohydrazide derivatives (13-22) were prepared and their in vitro antioxidant properties were investigated by determination of rat liver microsomal NADPH-dependent inhibition of lipid peroxidation (LP) levels and microsomal ethoxyresorufin O-deethylase (EROD) activity. Compound 18 was found to be the most active compound with 100% inhibition on LP level and 92% inhibition on EROD. Compounds 4b, 17, and 19 showed the strongest inhibitory effect (97%) on EROD. The free radical scavenging capacities of the compounds were also tested in vitro determining the interaction of the stable free radical 2,2,diphenyl-1-picrylhydrazyl (DPPH), and compounds 4a and 4b exhibited good antioxidant activities.
机译:一些新颖的2-(取代的苄硫基)-5-((2-(4-取代的苯基1)-1H-苯并[d]咪唑-1-基)甲基)-1,3,4-恶二唑(5-12)和2-制备了(2-(4-氯苯基)-1H-苯并[d]咪唑-1-基)-N'-(芳基亚甲基)乙酰肼衍生物(13-22),并通过测定大鼠肝的体外抗氧化性能进行了研究NADPH依赖微粒体对脂质过氧化(LP)水平的抑制和微粒体乙氧基间苯二酚O-脱乙基酶(EROD)活性。发现化合物18是最具活性的化合物,其对LP水平的抑制为100%,对EROD的抑制为92%。化合物4b,17和19对EROD表现出最强的抑制作用(97%)。还通过体外测试化合物的自由基清除能力来测定稳定的自由基2,2,2,二苯基-1-吡啶并肼基(DPPH)的相互作用,化合物4a和4b表现出良好的抗氧化活性。

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