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南欧大戟的化学成分研究

颜欣平 周兰婷 于静怡 李锦花 彭华勇 杨得坡

中草药2026,Vol.57Issue(10):3700-3708,9.
中草药2026,Vol.57Issue(10):3700-3708,9.DOI:10.7501/j.issn.0253-2670.2026.10.003

南欧大戟的化学成分研究

Chemical constituents of Euphorbia peplus

颜欣平 1周兰婷 1于静怡 1李锦花 1彭华勇 2杨得坡3

作者信息

  • 1. 吉首大学药学院,湖南 吉首 416000
  • 2. 吉首大学药学院,湖南 吉首 416000||中山大学药学院,广东 广州 510006
  • 3. 中山大学药学院,广东 广州 510006
  • 折叠

摘要

Abstract

Objective To investigate the terpenoid constituents of fruit shells of Euphorbia peplus and evaluate their anti-inflammatory activities.Methods Various chromatographic techniques were applied to isolate terpenoids from the petroleum ether-soluble fraction of the ethanol extract of E.peplus fruit shells.The chemical structures of all isolates were elucidated by comprehensive spectroscopic analyses(1D/2D NMR,HRMS)combined with single-crystal X-ray diffraction.Anti-inflammatory activities were assessed by measuring the inhibition of nitric oxide(NO)production in lipopolysaccharide(LPS)-induced RAW264.7 macrophages.Results A total of 13 terpenoids were isolated from the petroleum ether fraction of E.peplus fruit shells,including four paraliane-type diterpenoids(1-4),one pepluane-type diterpenoid(5),three jatrophane-type diterpenoids(6-8),two ingenane-type diterpenoids(9 and 10),one abietane-type diterpenoid(11),one ursane-type triterpenoid(12),and one dinor-monocyclic diterpenoid(13).They were respectively identified as(2S,3S,4R,5R,6R,8S,12S,13S,15R)-8β-acetyl-paralianone D(1),(1R,2R,3S,4R,5R,6R,8S,12S,13S,14R,15R)-1,5,8,14-tetraacetoxy-3-benzoyloxy-15-hydroxy-9-oxo-paraliane(2),(2S,3S,4R,5R,6R,8S,12S,13S,14R,15R)-5,8,14-triacetoxy-3-benzoyloxy-15-hydroxy-9-oxo-parapliane(3),paralianone A(4),(2S,3S,4R,5R,6R,8R,9R,10R,12S,13S,14R,15R)-5,8,9,10,14-pentaacetoxy-3-benzoyloxy-15-hydroxypepluane(5),euphpepluone A(6),euphpepluone D(7),(2S,3S,4R,5R,7S,8R,13S,15R)-5α,7β,8α-triacetoxy-3β-benzoyloxy-15β-hydroxyjatropha-6(17),11E-diene-9,14-dione(8),20-deoxyingenol(9),20-O-(2'E,4'Z-decadienoyl)ingenol(10),helioscopinolide D(11),ursolic acid(12)and(3R,6R,7E,9E,11E)-3-hydroxy-13-apo-α-caroten-13-one(13).The structure of compound 1 was confirmed by single-crystal X-ray diffraction.In the anti-inflammatory activity screening,only compound 2 exhibited inhibitory activity against NO production,with an IC50 value of(37.6±8.2)μmol/L.Conclusion Compounds 1,2,10,and 13 were isolated from E.peplus for the first time.Compound 2 demonstrated moderate anti-inflammatory activity.This study enriches the terpenoid chemical diversity of terpenoids from E.peplus and provides an experimental basis for further research on its anti-inflammatory substances.

关键词

大戟科/南欧大戟/二萜/抗炎/20-去氧巨大戟醇/熊果酸/(2S,3S,4R,5R,6R,8S,12S,13S,15R)-8β-acetyl-paralianone D

Key words

Euphorbiaceae/Euphorbia peplus Linn./diterpenoids/anti-inflammatory/20-deoxyingenol/ursolic acid/8β-acetyl-paralianone D/(2S,3S,4R,5R,6R,8S,12S,13S,15R)-8β-acetyl-paralianone D

分类

医药卫生

引用本文复制引用

颜欣平,周兰婷,于静怡,李锦花,彭华勇,杨得坡..南欧大戟的化学成分研究[J].中草药,2026,57(10):3700-3708,9.

基金项目

国家重点研发计划项目(2022YFD1600304) (2022YFD1600304)

湖南省教育厅项目(25C0336) (25C0336)

大学生创新创业训练计划项目(S202510531097) (S202510531097)

中草药

0253-2670

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