研究简报

川西獐牙菜中两个新的链状单萜类化合物

  • 曹团武 ,
  • 何康 ,
  • 耿长安 ,
  • 张雪梅 ,
  • 周俊 ,
  • 陈纪军
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  • a 中国科学院昆明植物研究所 植物化学与西部植物资源持续利用国家重点实验室 昆明 650201;
    b 长江师范学院化学化工学院 武陵山天然药物研究与开发实验室 涪陵 408100

收稿日期: 2016-03-23

  修回日期: 2016-04-29

  网络出版日期: 2016-06-01

基金资助

国家杰出青年科学基金(No.81025023)资助项目.

Two New Linear Monoterpenoids from Swertia mussotii

  • Cao Tuanwu ,
  • He Kang ,
  • Geng Chang'an ,
  • Zhang Xuemei ,
  • Zhou Jun ,
  • Chen Jijun
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  • a State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201;
    b Laboratory of Natural Medicine Research and Development in Wuling Mountain, School of Chemistry and Chemical Engineering, Yangtze Normal University, Fuling 408100

Received date: 2016-03-23

  Revised date: 2016-04-29

  Online published: 2016-06-01

Supported by

Project supported by the National Science Foundation of China for Distinguished Young Scholar (No.81025023).

摘要

利用多种色谱分离方法对川西獐牙菜的化学成分进行研究,从其全草的乙醇提取物中分离得到四个化合物,应用HR-ESIMS,1D和2D NMR,IR,UV等多种现代波谱技术确定了这些化合物的化学结构,经鉴定分别为(S,2E,6E)-2,6-二甲基-4,8-二羟基辛烷-2,6-二烯酸(1),(S,2E,6E)-2,6-二甲基-4-羟基-8-甲酰氧基辛烷-2,6-二烯酸(2),swerimilegenins B和C(34).化合物12为两个新的链状单萜类化合物,分别命名为川西獐牙菜酸C和D,化合物34是两个不常见的C9骨架的环烯醚萜,为首次从该植物中分离得到.

本文引用格式

曹团武 , 何康 , 耿长安 , 张雪梅 , 周俊 , 陈纪军 . 川西獐牙菜中两个新的链状单萜类化合物[J]. 有机化学, 2016 , 36(9) : 2216 -2219 . DOI: 10.6023/cjoc201603038

Abstract

Investigation on Swertia mussotii resulted in four compounds by means of various chromatographic techniques (silica gel, Sephadex LH-20, RP-LC and Pre-HPLC). Their structures were determined as (S,2E,6E)-4,8-dihydroxy-2,6-dime-thylocta-2,6-dienoic acid (1), (S,2E,6E)-8-(formyloxy)-4-hydroxy-2,6-dimethylocta-2,6-dienoic acid (2), swerimilegenins B and C (3 and 4) on the basis of extensive spectroscopic analyses including MS, IR, UV, 1D- and 2D-NMR. Among them, compounds 1 and 2 are two new linear monoterpenoids named as swerimusic acids C (1) and D (2), compounds 3 and 4 are two unusual known secoiridoid aglycones of C9-skeleton obtained for the first time from this plant. Compounds 1~4 were evaluated for their anti-Hepatitis B Virus (HBV) activities on HepG2.2.15 cells line in vitro, but these compounds showed no anti-HBV activity at the maximal tesing concentration. Herin, we only report the isolation and structure elucidation of these compounds.

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