The cytotoxic activities of cardiac glycosides from Streptocaulon juventas and the structure-activity relationships

被引:20
|
作者
Xue, Rui [1 ]
Han, Na [1 ]
Ye, Chun [1 ]
Wang, Lihui [2 ]
Yang, Jingyu [2 ]
Wang, Yu [3 ]
Yin, Jun [1 ]
机构
[1] Shenyang Pharmaceut Univ, Sch Tradit Chinese Mat Med, Dev & Utilizat Key Lab Northeast Plant Mat, Shenyang 110016, Peoples R China
[2] Shenyang Pharmaceut Univ, Sch Life Sci & Biopharmaceut, Shenyang 110016, Peoples R China
[3] Peoples Liberat Army 463 Hosp, Shenyang 110042, Peoples R China
关键词
Cardiac glycosides; Streptocaulon juventas; Anti-tumor activity; A549; NCI-H460; MRC-5; CARDENOLIDE GLYCOSIDES; ANTIPROLIFERATIVE ACTIVITY; SIGNALING PATHWAYS; CANCER; DIGITOXIN; PROLIFERATION; APOPTOSIS; BUFALIN; DIGITALIS;
D O I
10.1016/j.fitote.2014.08.008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A series of cardiac glycosides were isolated and identified from the anti-tumor fraction of the root of Streptocaulon juventas in previous studies. In the present research, the cytotoxic activities of the 43 cardiac glycosides on three cell lines, human lung A549 adenocarcinoma cell, large cell lung cancer NCI-H460 cell and normal human fetal lung fibroblast MRC-5 cell, were evaluated in vitro. Most of the tested compounds showed potent inhibitory activities toward the three cell lines. Then, the structure-activity relationships were discussed in detail. It was indicated that hydroxyl and acetyl groups at C-16 increased the activity, whereas hydroxyl group at C-1 and C-5 can both increase and decrease the activity. Two glucosyl groups which were connected by C1' -> C6' showed better inhibitory activity against cancer cell lines, while the C1' -> C4' connection showed stronger inhibitory activity against the normal cell line. Also, this is the first report that the activities of these compounds exhibited different variation trends between A549 and NCI-H460 cell lines, which indicated that these compounds could selectively inhibit the cell growth. The results would lay a foundation for further research on new anti-tumor drug development. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:228 / 233
页数:6
相关论文
共 50 条
  • [41] Structure-Activity Relationships from Natural Evolution
    Bolboaca, Sorana D.
    Rosca, Daniela D.
    Jaentschi, Lorentz
    MATCH-COMMUNICATIONS IN MATHEMATICAL AND IN COMPUTER CHEMISTRY, 2014, 71 (01) : 149 - 172
  • [42] BATRACHOTOXIN ANALOGS ON CARDIAC-MUSCLE - STRUCTURE-ACTIVITY RELATIONSHIPS
    SHOTZBER.GS
    ALBUQUER.EX
    DALY, J
    WITKOP, B
    PHARMACOLOGIST, 1973, 15 (02): : 233 - 233
  • [43] THE STRUCTURE-ACTIVITY RELATIONSHIPS FROM DSC DATA
    Musuc, Adina Magdalena
    Oancea, Dumitru
    REVUE ROUMAINE DE CHIMIE, 2021, 66 (02) : 161 - 166
  • [44] Synthesis, cytotoxic activities and structure-activity relationships of topoisomerase I inhibitors: Indolizinoquinoline-5,12-dione derivatives
    Cheng, Yu
    An, Lin-Kun
    Wu, Ning
    Wang, Xiao-Dong
    Bu, Xian-Zhang
    Huang, Zhi-Shu
    Gu, Lian-Quan
    BIOORGANIC & MEDICINAL CHEMISTRY, 2008, 16 (08) : 4617 - 4625
  • [45] Structure-activity relationships within a family of selectively cytotoxic macrolide natural products
    Salomon, AR
    Zhang, YB
    Seto, H
    Khosla, C
    ORGANIC LETTERS, 2001, 3 (01) : 57 - 59
  • [46] Structure-activity relationships of novel heteroaryl-acrylonitriles as cytotoxic and antibacterial agents
    Saczewski, Franciszek
    Stencel, Agnieszka
    Bienczak, Andrzej M.
    Langowska, Karolina A.
    Michaelis, Martin
    Werel, Wladyslaw
    Halasa, Rafal
    Reszka, Przemyslaw
    Bednarski, Patrick J.
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2008, 43 (09) : 1847 - 1857
  • [47] Novel glitazones: glucose uptake and cytotoxic activities, and structure–activity relationships
    B. R. Prashantha Kumar
    S. Santhosh Kumar
    Patel Viral
    Ashish Wadhwani
    R. Vadivelan
    M. N. Satish Kumar
    K. Elango
    M. J. Nanjan
    Medicinal Chemistry Research, 2012, 21 : 2689 - 2701
  • [48] Synthesis, biological activities and structure-activity relationships for new avermectin analogues
    Zhang, Jian
    Nan, Xiang
    Yu, Hai-Tao
    Cheng, Pi-Le
    Zhang, Yan
    Liu, Ying-Qian
    Zhang, Shao-Yong
    Hu, Guan-Fang
    Liu, Huanxiang
    Chen, An-Liang
    EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 2016, 121 : 422 - 432
  • [49] Structure-activity relationships between antibacterial activities and physicochemical properties of sulfonamides
    Mengelers, MJB
    Hougee, PE
    Janssen, LHM
    VanMiert, ASJPAM
    JOURNAL OF VETERINARY PHARMACOLOGY AND THERAPEUTICS, 1997, 20 (04) : 276 - 283
  • [50] DPPH-Scavenging Activities and Structure-Activity Relationships of Phenolic Compounds
    Zheng, Cheng-Dong
    Li, Gang
    Li, Hu-Qiang
    Xu, Xiao-Jing
    Gao, Jin-Ming
    Zhang, An-Ling
    NATURAL PRODUCT COMMUNICATIONS, 2010, 5 (11) : 1759 - 1765