天然产物研究与开发 ›› 2022, Vol. 34 ›› Issue (6): 987-995.doi: 10.16333/j.1001-6880.2022.6.011

• 研究简报 • 上一篇    下一篇

黑面神乙酸乙酯部位化学成分研究

江   程1,2*,顾   琼2*   

  1. 1深圳技师学院,深圳 518116;2中山大学药学院药物分子设计研究中心,广州 510006
  • 出版日期:2022-06-28 发布日期:2022-06-30
  • 基金资助:
    国家自然科学基金(81173470)

Chemical constituents from the ethyl acetate fraction of Breynia fruticosa

JIANG Cheng1,2*,GU Qiong2*   

  1. 1Shenzhen Institute of Technology,Shenzhen 518116,China;2Research Center for Drug Discovery,School of Pharmaceutical Sciences,Sun Yat-sen University,Guangzhou 510006,China
  • Online:2022-06-28 Published:2022-06-30

摘要:

为研究黑面神(Breynia fruticosa)地上部分化学成分及其抗Epstein-Barr病毒(EBV)活性。本研究采用硅胶等柱色谱和制备液相色谱等手段对黑面神地上部分95%醇水提物乙酸乙酯萃取部位进行分离纯化,并根据理化性质和谱学数据对化合物结构进行鉴定,鉴定后化合物进行抗EBV活性测试。从黑面神95%乙醇提取物乙酸乙酯萃取部分离得到24个化合物,分别鉴定为(-)-丁香树脂酚(1)、(+)-表丁香脂素(2)、(+)-丁香树脂酚(3)、(+)-(8′R,8R,7′S)-南烛木树脂酚(4)、(+)-5-甲氧基-异落叶松树脂酚(5)、表南烛木树脂酚(6)、burselignan(7)、(-)-异落叶松树脂酚(8)、(-)-(7S,7′S,8R,8′R)-3,3′,5,5′- tetramethoxy-7,7′-epoxylignane-4,4′,9,9′-tetraol(9)、(7S,7′R,8S,8′S)-3,3′-dimethoxy-7,7′-epoxylignane-4,4′,9,9′-tetraol(10)、(+)-大木姜子素(11)、1,2-methylene-dioxy-4-methoxy-secopterocarpan(12)、2-[4-(3-hydroxy-propyl)-2-methoxyphenoxy]-propane-1,3-diol(13)、shepherdine(14)、4-甲氧基异虎耳草素(15)、5-甲氧基异虎耳草素(16)、马尼拉二醇(17)、olean-12-ene-3β,22β-diol(18)、taxaxerol(19)、曼陀罗萜二醇(20)、二氢菜子甾醇(21)、β-谷甾醇(22)、(E)-6-methoxyl-decylcaffeate(23)、(8E,10Z,15E)-7-hydroxyoctadeca-8,10,15-trieno-icacid(24),化合物除了134822外均为首次从该植物中获得。将24个化合物均测试其体外抗EBV活性,结果显示在30 μmol/L浓度下,共有2个化合物抑制EB病毒裂解复制达到50%以上,其中化合物1214抑制EB病毒裂解复制IC50分别为16.4 μmol/L与5.7 μmol/L。

关键词: 黑面神, 大戟科, 木脂素, 抗EBV活性

Abstract:

To study the chemical constituents and explore the anti-Epstein-Barr virus (anti-EBV) bioactive compound from the aerial part of Breynia fruticosa.The compounds were separated by column chromatography such as silica gel,MCI gel CHP-20,ODS,and Sephadex LH-20 and purified by preparative HPLC method.The structures of all the isolated compounds were identified by combination of spectroscopic methods (MS,1H NMR,13C NMR) with the literature data,then all compounds assay through anti-EBV.As a result,chemical investigation on the aerial part of Breynia fruticosa led to the isolation of 24 compounds.Here,including (-)-syringaresinol (1),(+)-epi-syringaresinol (2),(+)-syringaresinol (3),(+)-(7R,8R,7′S)-lyoniresinol (4),(+)-5-methoxy-isolariciresinol (5),epi-lyoniresinol (6),burselignan (7),(-)-isolariciresinol (8),(-)-(7S,7′S,8R,8′R)-3,3′,5,5′-tetramethoxy- 7,7′-ep-oxylignane-4,4′,9,9′-tetraol (9),(7S,7′R,8S,8′S)-3,3′-dimethoxy-7,7′-epoxy-ligna-ne-4,4′,9,9′-tetraol (10),(+)-grandisin (11),1,2-methylene-dioxy-4-methoxy-secopterocarpan (12),2-[4-(3-hydroxypropyl)-2-methoxy- phenoxy]-propane-1,3-diol (13),shepherdine (14),4-O-methylnorbergenin (15),5-O-methylnorb-ergenin (16),maniladiol (17),olean-12-ene-3β,22β-diol (18),taxaxerol (19),daturadiol (20),dihydrobrassicasterol (21),β-sitosterol (22),(E)-6-methoxyl-decylcaffeate (23),(8E,10Z,15E)-7-hydroxyoctadeca-8,10,15-trieno-icacid (24) were reported in this paper.Except 1,3,4,8,22,all the compounds were obtained from this plant for the first time.The results showed that two compounds inhibited more than 50% cleavage and replication of EB virus with concentrations of 30 μmol/L.The IC50 of compounds 12 and 14 were 16.4 μmol/L and 5.7 μmol/L,respectively.

Key words: Breynia fruticosa, Euphorbiaceae, lignan, anti-EBV

中图分类号:  R284.2