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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >RADICAL SCAVENGING ACTIVITY OF ASCORBIC ACID ANALOGS CONTAINING A CARBONYL CONJUGATED ENE-DIOL STRUCTURE
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RADICAL SCAVENGING ACTIVITY OF ASCORBIC ACID ANALOGS CONTAINING A CARBONYL CONJUGATED ENE-DIOL STRUCTURE

机译:含羰基共轭二烯结构的抗坏血酸类似物的自由基清除活性

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摘要

Small molecule antioxidants such as ascorbic acid (AscH(2)) prevent the oxidative damage of biological molecules by scavenging reactive oxygen species. A carbonyl-conjugated ene-diol structure is essential for the antioxidant activity of AscH(2). As such, we synthesized novel AscH(2) analogs containing a carbonyl conjugated ene-diol structure and evaluated their radical scavenging activities. When the 1,2-dihydroxyethyl group was removed, radical scavenging activity equal to AscH(2) was observed. Analogs containing an endocyclic nitrogen atom instead of a ring oxygen displayed higher radical scavenging activities than AscH(2). Therefore, the electron donating effect of the carbonyl conjugated ene-diol structure greatly increased the radical scavenging activity of AscH(2) analogs.
机译:小分子抗氧化剂,例如抗坏血酸(AscH(2))通过清除活性氧来防止生物分子的氧化损伤。羰基共轭烯二醇结构对于AscH(2)的抗氧化活性至关重要。因此,我们合成了新型AscH(2)类似物,其中包含羰基共轭烯二醇结构,并评估了其自由基清除活性。当1,2-二羟乙基被除去时,观察到的自由基清除活性等于AscH(2)。包含环内氮原子而不是环氧的类似物显示出比AscH(2)高的自由基清除活性。因此,羰基共轭烯-二醇结构的电子给体作用大大提高了AscH(2)类似物的自由基清除活性。

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