Synthesis and structure-activity relationships of 1,2,4-triazoles as a novel class of potent tubulin polymerization inhibitors

被引:67
|
作者
Ouyang, XH
Chen, XL
Piatnitski, EL
Kiselyov, AS
He, HY
Mao, YY
Pattaropong, V
Yu, Y
Kim, KH
Kincaid, J
Smith, L
Wong, WC
Lee, SP
Milligan, DL
Malikzay, A
Fleming, J
Gerlak, J
Deevi, D
Doody, JF
Chiang, HH
Patel, SN
Wang, Y
Rolser, RL
Kussie, P
Labelle, M
Tuma, MC
机构
[1] ImClone Syst, Dept Chem, Brooklyn, NY 11226 USA
[2] ImClone Syst, Dept Prot Sci, New York, NY 10014 USA
[3] ImClone Syst, Dept Expt Therapeut, New York, NY 10014 USA
关键词
tubulin inhibitor; tubulin polymerization; 1,2,4-triazole; vascular disrupting agent; tumor vasculature; antimitotic;
D O I
10.1016/j.bmcl.2005.08.056
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A novel triazole-containing chemical series was shown to inhibit tubulin polymerization and cause cell cycle arrest in A431 cancer cells with EC50 values in the single digit nanomolar range. Binding experiments demonstrated that representative active compounds of this class compete with colchicine for its binding site on tubulin. The syntheses and structure-activity relationship studies for the triazole derivatives are described herein. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5154 / 5159
页数:6
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