首页> 外文期刊>Natural product research >A new glycosidic antioxidant from Ranunculus muricatus L. (Ranunculaceae) exhibited lipoxygenasae and xanthine oxidase inhibition properties
【24h】

A new glycosidic antioxidant from Ranunculus muricatus L. (Ranunculaceae) exhibited lipoxygenasae and xanthine oxidase inhibition properties

机译:来自毛茛属Muricatus L.(毛茛科)的新糖苷抗氧化剂表现出脂氧合和黄嘌呤氧化酶抑制性质

获取原文
获取原文并翻译 | 示例
           

摘要

Phytochemical investigation of Ranunculus muricatus L. (Ranunculaceae) led to the isolation of a new metabolite named as ranuncoside from the ethyl acetate fraction of the plant. Structure of the novel compound was elucidated through detailed spectroscopic analyses, using UV, IR, 1 H, 13 C NMR and 2D NMR in combination with EIMS and HR EI-MS techniques. The compound was evaluated for antioxidant activity using the 1,1-diphenyl-2-picryl-hydrazyl (DPPH) free radical scavenging assay. Its inhibitory potential was tested against lipoxygenase and xanthine oxidase enzymes. Ranuncoside potently scavenged the DPPH free radicals (IC 50 = 56.7 ± 0.43 μM) and strongly inhibited the activities of lipoxygenase (IC 50 = 63.9 ± 0.17 μM) and xanthine oxidase (IC 50 = 43.3 ± 0.22 μM). ? 2016 Informa UK Limited, trading as Taylor & Francis Group.
机译:毛茛属Muricatus L.(毛茛科)的植物化学研究导致了从植物的乙酸乙酯分数中分离名为RanuncoSide的新代谢物。 通过详细的光谱分析,使用UV,IR,1 H,13 C NMR和2D NMR与EIMS和HR EI-MS技术组合来阐明新化合物的结构。 使用1,1-二苯基-2-Picryl-肼(DPPH)自由基清除测定评价该化合物进行抗氧化活性。 其抑制潜力针对脂氧合酶和黄嘌呤氧化酶进行测试。 ranuncoside易于清除Dpph自由基(Ic 50 = 56.7±0.43μm)并强烈抑制脂氧合酶(IC 50 = 63.9±0.17μm)和黄嘌呤氧化酶的活性(IC 50 = 43.3±0.22μm)。 还 2016年Informa UK Limited,贸易为泰勒&弗朗西斯集团。

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