有机化学 ›› 2013, Vol. 33 ›› Issue (06): 1284-1290.DOI: 10.6023/cjoc201303041 上一篇    下一篇

研究论文

棠梨枝叶的化学成分研究

赵冕a, 蔡乐a, 何健民a,b, 尹田鹏a, 隋迎春a, 罗梦婷a, 丁中涛a   

  1. a 教育部自然资源药物化学重点实验室 云南大学化学科学与工程学院 昆明 650091;
    b 保山学院资源环境学院 保山 678000
  • 收稿日期:2013-03-26 修回日期:2013-04-25 发布日期:2013-05-06
  • 通讯作者: 丁中涛 E-mail:ztding@ynu.edu.cn
  • 基金资助:

    国家自然科学基金(No.21002084)和云南省自然科学基金(No.2010CD017)资助项目.

Chemical Constituents from the Branches and Leaves of Pyrus pashia Buch.-Ham.ex D.Don

Zhao Miana, Cai Lea, He Jianmina,b, Yin Tianpenga, Sui Yingchuna, Luo Mengtinga, Ding Zhongtaoa   

  1. a Key Laboratory of Medicinal Chemistry for Nature Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091;
    b College of Resource and Environment, Baoshan University, Baoshan 678000
  • Received:2013-03-26 Revised:2013-04-25 Published:2013-05-06
  • Supported by:

    Project supported by the National Natural Science Foundation of China (No.21002084), and the Natural Science Foundation of China of Yunnan Province (No.2010CD017).

从棠梨枝叶(Pyrus pashia Buch.-Ham.ex D.Don)的甲醇提取物中分离得到了17个化合物, 采用高分辨质谱、一维和二维核磁共振等现代波谱技术, 鉴定上述化合物的结构分别为: pashinin A (1), 天麻苷-7-O-顺式咖啡酸酯(2), 天麻苷-7-O-反式咖啡酸酯(3), 山奈酚-3-O-β-D-(6"-O-对香豆酸酯)吡喃葡萄糖苷(4), 山奈酚-3-O-β-D-(6"-O-顺式对香豆酰)吡喃葡萄糖苷(5), 天麻苷-7-O-对羟基苯甲酸酯(6), 熊果苷(7), robustaside B (8), 委陵菜酸(9), 蔷薇酸(10), 槲皮素3-O-β-D-吡喃葡萄糖苷(11), 2R,3R-二氢槲皮素(12), 木犀草素-4'-O-β-D-吡喃葡萄糖苷(13), 芹黄素-4'-O-β-D-吡喃葡萄糖苷(14), 5,7,4'-三羟基异黄酮-7-O-β-D-吡喃葡萄糖苷(15), 染料木素(16), 咖啡酸(17), 其中化合物12为新化合物, 化合物3为新的天然产物.除化合物17外, 其余化合物均首次从该植物中分离得到.化合物13的抗肿瘤细胞活性实验表明其没有体外肿瘤细胞生长抑制活性(IC50 >40 μmol·L-1); 抗HIV病毒(HIV-1IIIB)实验显示: 化合物1有极弱的抗HIV-1的活性, 化合物4有弱的抗HIV-1的活性.

关键词: 棠梨, 枝叶, pashinin A, 天麻苷-7-O-顺式咖啡酸酯, 抗HIV-1活性

Seventeen compounds were isolated from the branches and leaves of Pyrus pashia Buch.-Ham.ex D.Don.On the basis of spectroscopic methods (HR-ESIMS, 1D- and 2D-NMR), their structures were identified as pashinin A (1), gastrodin-7-O-cis-caffeoyl ester (2), gastrodin-7-O-trans-caffeoyl ester (3), kaempferol-3-β-D-(6-O-trans-p-coumaroyl)glu- copyranoside (4), kaempferol-3-β-D-(6-O-cis-p-coumaroyl)glucopyranoside (5), gastrodin-7-O-p-hydroxybenzoyl ester (6), arbutin (7), robustaside B (8), tormentic acid (9), euscaphic acid (10), quercetin-3-O-β-D-glucopyranoside (11), 2R,3R-dihydyoquercetin (12), luteolin-4'-O-β-D-glucopyranoside (13), apigenin-4'-O-β-D-glucopyranoside (14), 5,7,4'-trihy- droxyisoflavone-7-O-β-D-glucopyranoside (15), genistein (16), caffeic acid (17).Among them, 1 and 2 were new compounds, 3 was a new natural product, 416 were isolated from this plant for the first time.Compounds 13 showed no cytotoxic effects on tumor cell (IC50 >40 μmol·L-1).1 and 4 exhibited weak anti-HIV-1 activities.

Key words: Pyrus pashia, branches and leaves, pashinin A, gastrodin-7-O-cis-caffeoyl ester, anti-HIV-1 activities