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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >STRUCTURE-ACTIVITY RELATIONSHIPS OF SYNTHESIZED PROCYANIDIN OLIGOMERS: DPPH RADICAL SCAVENGING ACTIVITY AND MAILLARD REACTION INHIBITORY ACTIVITY
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STRUCTURE-ACTIVITY RELATIONSHIPS OF SYNTHESIZED PROCYANIDIN OLIGOMERS: DPPH RADICAL SCAVENGING ACTIVITY AND MAILLARD REACTION INHIBITORY ACTIVITY

机译:合成的脯氨酰胺低聚物的结构-活性关系:DPPH自由基清除活性和Maillard反应抑制活性

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摘要

Procyanidins are known as condensed tannins and/or oligomeric flavonoids, and are present in many edible plants and show interesting various biological activities. We previously developed and reported a simple and versatile method of synthesizing procyanidin oligomers consisting of (-)-epicatechin and (+)-catechin. Here, we report the structure-activity relationships (SAR) between the DPPH (1,1-diphenyl-2-picrylhydrazyl) radical scavenging activity and Maillard reaction inhibitory activities of various procyanidin oligomers synthesized, including dimers, trimers, tetramers, pentamers, 3-O-substituted oligomers, and other artificial oligomers.
机译:原花青素被称为缩合单宁和/或低聚类黄酮,存在于许多食用植物中,并表现出令人感兴趣的各种生物活性。我们先前开发并报道了一种简单而通用的合成由(-)-表儿茶素和(+)-儿茶素组成的原花青素低聚物的方法。在这里,我们报告的DPPH(1,1-二苯基-2-picylhydrazyl)自由基清除活性和合成的各种原花青素低聚物,包括二聚体,三聚体,四聚体,五聚体,3的美拉德反应抑制活性之间存在构效关系(SAR)。 -O-取代的低聚物和其他人工低聚物。

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