Caroguaianolide A-E, five new cytotoxic sesquiterpene lactones from Carpesium abrotanoides L.

被引:18
|
作者
Wang, Lei [1 ]
Qin, Wen [1 ]
Tian, Li [1 ]
Zhang, Xue-Xue [1 ]
Lin, Fang [1 ]
Cheng, Fan [1 ]
Chen, Jian-Feng [1 ]
Liu, Cheng-Xiong [1 ]
Guo, Zhi-Yong [1 ]
Proksch, Peter [2 ]
Zou, Kun [1 ]
机构
[1] China Three Gorges Univ, Hubei Key Lab Nat Prod Res & Dev, Coll Biol & Pharmaceut Sci, Yichang 443002, Peoples R China
[2] Heinrich Heine Univ Duesseldorf, Inst Pharmaceut Biol & Biotechnol, D-40225 Dusseldorf, Germany
关键词
Carpesium abrotanoides L; Sesquiterpene lactones; Structural elucidation; Cytotoxic activities; GUAIANOLIDE SESQUITERPENES; EUPATORIUM-CHINENSE; PULICARIA-CRISPA; CONSTITUENTS;
D O I
10.1016/j.fitote.2018.03.015
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Five new guaiane-type sesquiterpene lactones, caroguaianolide A-E (1-5), along with nine known sesquiterpene lactones (6-14) were isolated from the whole plant of Carpesium abrotanoides L. Their structures were elucidated on the basis of spectroscopic date, HRESIMS analysis, and comparison of experimental and calculated ECD data. All isolated compounds (1-14) were tested in vitro for their cytotoxic activities against the MDA-MB-231, HGC-27 cancer cell lines, of which compounds 1-3, 6, 7, 11 and 12 showed significant cytotoxic activities with IC50 values ranging from 2.67 to 12.34 mu M.
引用
收藏
页码:349 / 355
页数:7
相关论文
共 50 条
  • [31] Bioactivity-Guided Isolation of Antiproliferative Sesquiterpene Lactones from Centaurea solstitialis L. ssp solstitialis
    Erenler, Ramazan
    Sen, Ozkan
    Yaglioglu, Ayse Sahin
    Demirtas, Ibrahim
    COMBINATORIAL CHEMISTRY & HIGH THROUGHPUT SCREENING, 2016, 19 (01) : 66 - 72
  • [32] Antitumor agents.: 228.: Five new agarofurans, reissantins A-E, and cytotoxic principles from Reissantia buchananiii
    Chang, FR
    Hayashi, K
    Chen, IH
    Liaw, CC
    Bastow, KF
    Nakanishi, Y
    Nozaki, H
    Cragg, GA
    Wu, YC
    Lee, KH
    JOURNAL OF NATURAL PRODUCTS, 2003, 66 (11): : 1416 - 1420
  • [33] Schisphenlignans A-E: Five New Dibenzocyclooctadiene Lignans from Schisandra sphenanthera
    Liang, Cheng-Qin
    Hu, Jing
    Shi, Yi-Ming
    Shang, Shan-Zhai
    Du, Xue
    Zhan, Rui
    Xiong, Wen-Yong
    Zhang, Hong-Bin
    Xiao, Wei-Lie
    Sun, Han-Dong
    CHEMICAL & PHARMACEUTICAL BULLETIN, 2013, 61 (01) : 96 - 100
  • [34] Hysterolides A-I, dimeric or monomeric sesquiterpene lactones from Parthenium hysterophorus L.
    Li, Hua
    Lan, Qian
    Li, Hong-Xia
    Liang, Dong
    Zhang, Gui-Jie
    PHYTOCHEMISTRY, 2024, 219
  • [35] Use of Micellar Electrokinetic Chromatography to Analyze Sesquiterpene Lactones from Laurus nobilis L.
    S. P. Senchenko
    N. M. Nasukhova
    L. A. Agova
    D. A. Konovalov
    Pharmaceutical Chemistry Journal, 2016, 50 : 320 - 322
  • [36] Use of Micellar Electrokinetic Chromatography to Analyze Sesquiterpene Lactones from Laurus nobilis L.
    Senchenko, S. P.
    Nasukhova, N. M.
    Agova, L. A.
    Konovalov, D. A.
    PHARMACEUTICAL CHEMISTRY JOURNAL, 2016, 50 (05) : 320 - 322
  • [37] Biological Activity of Flavonoids and Rare Sesquiterpene Lactones Isolated From Centaurea ragusina L.
    Grienke, Ulrike
    Brkanac, Sandra Radic
    Vujcic, Valerija
    Urban, Ernst
    Ivankovic, Sinisa
    Stojkovic, Ranko
    Rollinger, Judith M.
    Kralj, Juran
    Brozovic, Anamaria
    Stojkovic, Marijana Radic
    FRONTIERS IN PHARMACOLOGY, 2018, 9
  • [38] Japonicones E-L, Dimeric Sesquiterpene Lactones from Inula japonica Thunb.
    Qin, Jiang Jiang
    Jin, Hui Zi
    Zhu, Jia Xian
    Fu, Jian Jun
    Hu, Xiao Jia
    Liu, Xiao Hua
    Zhu, Yan
    Yan, Shi Kai
    Zhang, Wei Dong
    PLANTA MEDICA, 2010, 76 (03) : 278 - 283
  • [39] Germacrane-Type Sesquiterpene Lactones from Achillea millefolium L. and Their Anti-Inflammatory Activity
    Li, Hongliang
    Aisa, Haji Akber
    Li, Jun
    CHEMISTRY & BIODIVERSITY, 2023, 20 (04)
  • [40] Screening of several biological activities induced by different sesquiterpene lactones isolated from Centaurea behen L. and Rhaponticum repens (L.) Hidalgo
    Shakeri, Abolfazl
    Amini, Elaheh
    Asili, Javad
    Masullo, Milena
    Piacente, Sonia
    Iranshahi, Mehrdad
    NATURAL PRODUCT RESEARCH, 2018, 32 (12) : 1436 - 1440