研究简报

海南暗罗根克罗烷型二萜化学成分研究

  • 李小宝 ,
  • 陈光英 ,
  • 邵泰明 ,
  • 宋小平 ,
  • 韩长日 ,
  • 余章昕
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  • a 海南师范大学化学与化工学院 热带药用植物化学教育部重点实验室 海口 571158;
    b 海南省药食同源植物资源重点实验室 海南科技职业学院化学与材料工程学院 海口 571126

收稿日期: 2017-05-23

  修回日期: 2017-06-10

  网络出版日期: 2017-06-23

基金资助

国家自然科学基金(Nos.81160391,21362009,81360478)、国家国际科技合作专项(No.2014DFA40850)、创新发展团队(No.IRT-16R19)、海南省自然科学基金创新研究团队(No.2016CXTD007)及海南省自然科学基金(No.20162031)资助项目.

Clerodane Diterpenes from the Roots of Polyalthia laui

  • Li Xiaobao ,
  • Chen Guangying ,
  • Shao Taiminga ,
  • Song Xiaoping ,
  • Han Changri ,
  • Yu Zhangxin
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  • a Key Laboratory of Tropical Medicinal Plant Chemistry of Ministry of Education, College of Chemistry and Chemical Engineering, Hainan Normal University, Haikou 571158;
    b Key Laboratory of Medicinal and Edible Plants Resources of Hainan Province, School of Chemical and Material Engineering, Hainan Institute of Science and Technology, Haikou 571126

Received date: 2017-05-23

  Revised date: 2017-06-10

  Online published: 2017-06-23

Supported by

Project supported by the National Natural Science Foundation of China (Nos.81160391,21362009,81360478),the International S&T Cooperation Program of China (No.2014DFA40850),the Program for Innovative Research Team in University (No.IRT-16R19),the Hainan Provincal Natural Science Foundation of Innovatie Research Team Project (No.2016CXTD007) and the Natural Science Foundation of Hainan Province (No.20162031).

摘要

对海南暗罗根化学成分进行系统研究,分离得到5个克罗烷型二萜类化合物.根据它们的NMR和HRMS数据,鉴定它们的结构分别为:(4→2)重排-2,13-二甲酰基-克罗烷-2,12E-二双键-15-甲酯(1)、克罗烷-3,12E-二双键-15,16-二甲酸(2)、14,15-降二碳克罗烷-3-双键-2,13-二酮(3)、克罗烷-3,13Z-二双键-15,16-内酯(4)、16-羟基克罗烷-3,13Z-二双键-15,16-内酯(5).其中化合物1~2为新化合物.化合物1~5的体外细胞毒活性筛选结果表明,它们对4种肿瘤细胞株(Hela、A549、MCF-7和HL-60)均显示出了一定的体外生长抑制活性,其IC50值范围为13.22~37.16 μmol/L.

本文引用格式

李小宝 , 陈光英 , 邵泰明 , 宋小平 , 韩长日 , 余章昕 . 海南暗罗根克罗烷型二萜化学成分研究[J]. 有机化学, 2017 , 37(10) : 2763 -2766 . DOI: 10.6023/cjoc201705035

Abstract

Five clerodane diterpenes were isolated from the roots of Polyalthia laui during a systematic phytochemical investigation. Their structures were elucidated by the NMR and HRMS data as methyl (4→2)-abeo-2,13-diformyl-cleroda-2,12E-dien-15-ate (1), (E)-ent-cleroda-3,12-diene-15,16-dioic acid (2), 14,15-dinorclerod-3-ene-2,13-dione (3), solidagolactone (4), and 16-hydroxy-3,13Z-kolavadien-16,15-olide (5). Among them, compounds 1~2 are new clerodane diterpenes. Biological evaluation of compounds 1~5 against human Hela, A549, MCF-7 and HL-60 human cancer cell lines showed that all com-pounds displayed moderate cytotoxicities against various human cancer cell lines with IC50 ranged from 13.22 to 37.16 μmol/L.

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