English  |  正體中文  |  简体中文  |  Items with full text/Total items : 12145/12927 (94%)
Visitors : 854000      Online Users : 1392
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/5328


    Title: Synthesis and biological evaluation of 7-arylindoline-1-benzenesulfonamides as a novel class of potent anticancer agents
    Authors: Chang, JY;Lai, MJ;Chang, YT;Lee, HY;Cheng, YC;Kuo, CC;Su, MC;Chang, CY;Liou, JP
    Contributors: National Institute of Cancer Research
    Abstract: A series of 7-arylindoline-1-benzenesulfonamides were prepared and evaluated for anticancer activity 7-(4'-Cyanophenyl)indoline-1-benzenesulfonamide 15 exhibited substantial antiproliferative activity with IC50 values ranging from 17-32 nM against a variety of human cancer cell lines, including MDR resistant line Compound 15 (IC50 = 1 5 mu M) also showed more potent inhibition of tubulin polymerization than 4a (combretastatin A-4. IC50 = 2 0 mu M) and displayed strong binding to the colchicine binding site of the tubulin
    Date: 2010-08
    Relation: MedChemComm. 2010 Aug;1(2):152-155.
    Link to: http://dx.doi.org/10.1039/c0md00052c
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000284979800008
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=79952514549
    Appears in Collections:[郭靜娟] 期刊論文
    [張俊彥] 期刊論文

    Files in This Item:

    File Description SizeFormat
    ISI000284979800008.pdf125KbAdobe PDF567View/Open


    All items in NHRI are protected by copyright, with all rights reserved.

    Related Items in TAIR

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback