首页> 外文期刊>The Journal of Organic Chemistry >Stilbene oligomers from Parthenocissus laetevirens: Isolation, biomimetic synthesis, absolute configuration, and implication of antioxidative defense system in the plant
【24h】

Stilbene oligomers from Parthenocissus laetevirens: Isolation, biomimetic synthesis, absolute configuration, and implication of antioxidative defense system in the plant

机译:来自爬山虎爬山虎的Stilbene低聚物:分离,仿生合成,绝对构型以及植物抗氧化防御系统的意义

获取原文
获取原文并翻译 | 示例
       

摘要

Five new stilbene oligomers, laetevirenol A-E (4-8), were isolated from Parthenocissus laetevirens, together with three known stilbene oligomers (2, 3, and 9). The structures of the new compounds were elucidated by spectroscopic analysis, including 1D and 2D NMR experiments. Afterward the absolute configurations were determined. Biornimetic transformations revealed a possible biogenetic route, where stilbene trimers were enzymatically synthesized for the first time. In addition, their antioxidant activities were evaluated by 1,1-diphenyl-2-picrylhydrazyl (DPPH) assay. The results showed that stilbene oligomers with an unusual phenanthrene moiety exhibited much stronger antioxidant activities. Thus, the photocatalyzed cyclization of stilbenes was supposed to be an antioxidant activity promoting transformation, which was hypothesized to play a role in the antioxidative defense system of the plant.
机译:五种新的1,2-二苯乙烯低聚物,laetevirenol A-E(4-8),与三个已知的1,2-二苯乙烯低聚物(2,3,和9)分离自爬山虎爬山虎。通过光谱分析(包括1D和2D NMR实验)阐明了新化合物的结构。之后,确定绝对配置。生物仿制药的转化揭示了一种可能的生物遗传途径,其中首次酶促合成了二苯乙烯三聚体。另外,它们的抗氧化活性通过1,1-二苯基-2-吡啶并肼基(DPPH)测定来评估。结果表明,具有不寻常菲部分的1,2-二苯乙烯低聚物表现出更强的抗氧化活性。因此,据推测,对苯二酚的光催化环化是促进转化的抗氧化剂活性,据推测其在植物的抗氧化防御系统中起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号