...
首页> 外文期刊>Fitoterapia >New coumarins from the roots of Angelica dahurica var. formosana cv. Chuanbaizhi and their inhibition on NO production in LPS-activated RAW264.7 cells
【24h】

New coumarins from the roots of Angelica dahurica var. formosana cv. Chuanbaizhi and their inhibition on NO production in LPS-activated RAW264.7 cells

机译:当归的新香豆素。福尔摩萨纳简历川白芝及其对LPS激活的RAW264.7细胞NO生成的抑制作用

获取原文
获取原文并翻译 | 示例

摘要

A new linear pyranocoumarin named (-)-hydroxydecursinol (1) and a new biscoumarin named (+/-)-dahuribiscoumarin (2), together with six known compounds isoimperatorin (3), imperatorin (4), phellopterin (5), isodemethylfuropinarine (6), demethylfuropinarine (7), and (+)-decursinol (8) were isolated from the 75% ethanolic extract of the roots of Angelica dahurica var. formosana cv. Chuanbaizhi. Their structures were elucidated by extensive spectroscopic techniques, including 2D NMR spectroscopy and mass spectrometry, and the structure of 2 was confirmed by single-crystal X-ray diffraction. All of the isolated compounds were evaluated for the inhibition against nitric oxide (NO) production in the lipopolysaccharide (LPS)-activated RAW264.7 macrophage cell line, and exhibited the inhibitory activity on NO production in a concentration-dependent manner. Furthermore, real-time PCR analysis revealed that compounds 2, 5-8 could significantly suppress the expression levels of inducible nitric oxide synthase mRNA in a concentration-dependent manner. And their primary structure-activity relationships of NO inhibitory effects were also briefly discussed. These compounds are potential candidates for further bioassay studies to determine their suitability as drug leads. (C) 2015 Elsevier B.V. All rights reserved.
机译:一种新的线性吡喃香豆素,名为(-)-羟基去氢醇(1)和一种新的双香豆素,命名为(+/-)-dahuribiscoumarin(2),以及六种已知的化合物异欧前胡素(3),欧前胡素(4),鞘翅肽(5),异十二烷基呋喃丁林(6)从当归根部的75%乙醇提取物中分离出去甲基呋喃丁碱(7)和(+)-去氢醇(8)。福尔摩萨纳简历川白芝。通过包括2D NMR光谱和质谱在内的广泛光谱技术阐明了它们的结构,并通过单晶X射线衍射确认了2的结构。评价所有分离的化合物对脂多糖(LPS)激活的RAW264.7巨噬细胞系中一氧化氮(NO)产生的抑制作用,并以浓度依赖性的方式表现出对NO产生的抑制活性。此外,实时PCR分析显示化合物2、5-8可以浓度依赖性显着抑制诱导型一氧化氮合酶mRNA的表达水平。并简要讨论了它们对NO抑制作用的主要构效关系。这些化合物可能用于进一步的生物测定研究,以确定它们是否适合用作药物前导。 (C)2015 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 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