Cytotoxic sesquiterpenoids from Ligularia pleurocaulis

被引:13
作者
Xie, Guang-Bo [1 ]
Xie, Ya [1 ]
Hu, Yang-Zhirong [1 ]
Zhu, Zhi-Xiang [2 ]
机构
[1] Univ Elect Sci & Technol China, Sch Life Sci & Technol, 4,Sect 2,North Jianshe Rd, Chengdu 610054, Peoples R China
[2] Beijing Univ Chinese Med, Modern Res Ctr Tradit Chinese Med, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Ligularia pleurocaulis; Compositae; Sesquiterpenoid; Biligupleurolide; Cytotoxicity; Cu K alpha X-ray crystallography; EREMOPHILANE-TYPE SESQUITERPENOIDS; OCCURRING TERPENE DERIVATIVES; KANGTINGENSIS; RHIZOMES;
D O I
10.1016/j.phytochem.2016.02.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phytochemical investigation of whole plants of Ligularia pleurocaulis led to isolation of five sesquiter-penoids, including an eremophilenolide dimer named biligupleurolide, along with eight known sesquiterpenoids. Their structures were determined by spectroscopic methods including 2D NMR techniques, and the structures of biligupleurolide and ligupleurolide were confirmed by X-ray diffraction analysis. All of the isolated compounds were tested for their cytotoxic activity against three cancer cell lines (HepG2, A549 and MCF-7), and biligupleurolide showed moderate inhibitory activities, with IC50 values of 5.2, 5.6 and 8.4 mu M against MCF-7, HepG2 and A549, respectively. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 50 条
  • [31] Songaricalarins A-E, Cytotoxic Oplopane Sesquiterpenes from Ligularia songarica
    Wang, Qi
    Chen, Tzu-Hsuan
    Bastow, Kenneth F.
    Morris-Natschke, Susan L.
    Lee, Kuo-Hsiung
    Chen, Dao-Feng
    JOURNAL OF NATURAL PRODUCTS, 2013, 76 (03): : 305 - 310
  • [32] Two Eremophilane-type Sesquiterpenoids from the Rhizomes of Ligularia veitchiana(Hemsl.) Greenm
    WANG Cai-fang1
    2.School of Pharmacy
    3.Mclean Hospital/Harvard Medical School
    Chemical Research in Chinese Universities, 2009, 25 (04) : 480 - 482
  • [33] New weakly cytotoxic eremophilane sesquiterpenes from the roots of Ligularia virgaurea
    Zhang, Zhan-Xin
    Lin, Chang-Jun
    Li, Ping-Lin
    Jia, Zhong-Jian
    PLANTA MEDICA, 2007, 73 (06) : 585 - 590
  • [34] Anti-allergic and Cytotoxic Effects of Sesquiterpenoids and Phenylpropanoids Isolated from Magnolia biondii
    Thi Tuyet Mai Nguyen
    Thi Thu Nguyen
    Lee, Hyun-Su
    Lee, Bomi
    Min, Byung Sun
    Kim, Jeong Ah
    NATURAL PRODUCT COMMUNICATIONS, 2017, 12 (10) : 1543 - 1545
  • [35] Sesquiterpenoids from Ainsliaea spicata and their cytotoxic and NO production inhibitory activities
    Shi, Zhi-Ran
    Zhang, Xian-Yuan
    Zeng, Ren-Tao
    Zhuo, Zhi-Guo
    Feng, Feng
    Shen, Yun-Heng
    Zhang, Wei-Dong
    PHYTOCHEMISTRY LETTERS, 2016, 18 : 87 - 94
  • [36] Cytotoxic and Apoptogenic Sesquiterpenoids from the Petroleum Ether Extract of Artemisia aucheri Aerial Parts
    Hosseinzadeh, Leila
    Shokoohinia, Yalda
    Arab, Mehri
    Allahyari, Elnaz
    Mojarrab, Mahdi
    IRANIAN JOURNAL OF PHARMACEUTICAL RESEARCH, 2019, 18 (01): : 391 - 399
  • [37] Three new sesquiterpenoids from Solanum septemlobum with cytotoxic activities
    Zhang, Lei
    Li, Gui-Sheng
    Yao, Fang
    Yue, Xi-Dian
    Dai, Sheng-Jun
    PHYTOCHEMISTRY LETTERS, 2015, 11 : 173 - 176
  • [38] Two New Sesquiterpenoids from Solanum lyratum with Cytotoxic Activities
    Ren, Yan
    Shen, Li
    Zhang, De-Wu
    Dai, Sheng-Jun
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2009, 57 (04) : 408 - 410
  • [39] Two new cytotoxic eudesmane sesquiterpenoids from Artemisia anomala
    Zan, Ke
    Chen, Xiao-Qing
    Chai, Xing-Yun
    Wu, Qing
    Fu, Qiang
    Zhou, Si-Xiang
    Tu, Peng-Fei
    PHYTOCHEMISTRY LETTERS, 2012, 5 (02) : 313 - 315
  • [40] Natural Sesquiterpenoids as Cytotoxic Anticancer Agents
    Chen, Q. -F.
    Liu, Z. -P.
    Wang, F. -P.
    MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2011, 11 (13) : 1153 - 1164