An update on the recent advances and discovery of novel tubulin colchicine binding inhibitors

被引:12
|
作者
Weng, Haoxiang [1 ,2 ]
Li, Jinlong [1 ,2 ]
Zhu, Huajian [1 ,2 ]
Wong, Kei Fung Carver [3 ]
Zhu, Zheying [3 ]
Xu, Jinyi [1 ,2 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, 24 Tong Jia Xiang, Nanjing 210009, Peoples R China
[2] China Pharmaceut Univ, Dept Med Chem, 24 Tong Jia Xiang, Nanjing 210009, Peoples R China
[3] Univ Nottingham, Sch Pharm, Univ Pk Campus, Nottingham NG7 2RD, England
基金
中国国家自然科学基金;
关键词
antiproliferative effect; colchicine binding site; SARs; structure modification; tubulin polymerization inhibitors; BIOLOGICAL EVALUATION; PHASE-I; ANTICANCER AGENTS; POLYMERIZATION; DERIVATIVES; POTENT; SITE; MICROTUBULES; DOCKING; ANALOGS;
D O I
10.4155/fmc-2022-0212
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Microtubules, formed by alpha- and beta-tubulin heterodimer, are considered as a major target to prevent the proliferation of tumor cells. Microtubule-targeted agents have become increasingly effective anticancer drugs. However, due to the relatively sophisticated chemical structure of taxane and vinblastine, their application has faced numerous obstacles. Conversely, the structure of colchicine binding site inhibitors (CBSIs) is much easier to be modified. Moreover, CBSIs have strong antiproliferative effect on multidrug-resistant tumor cells and have become the mainstream research orientation of microtubule-targeted agents. This review focuses mainly on the recent advances of CBSIs during 2017-2022, attempts to depict their biological activities to analyze the structure-activity relationships and offers new perspectives for designing next generation of novel CBSIs.
引用
收藏
页码:73 / 95
页数:23
相关论文
共 50 条
  • [31] Discovery of potent tubulin inhibitors targeting the colchicine binding site via structure-based lead optimization and antitumor evaluation
    Liu, Wei
    He, Youyou
    Guo, Zhongjie
    Wang, Miaomiao
    Han, Xiaodong
    Jia, Hairui
    He, Jin
    Miao, Shanshan
    Wang, Shengzheng
    [J]. JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2023, 38 (01)
  • [32] SYNTHESIS AND TUBULIN BINDING OF NOVEL C-10 ANALOGS OF COLCHICINE
    STARETZ, ME
    HASTIE, SB
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 1993, 36 (06) : 758 - 764
  • [33] SYNTHESIS AND TUBULIN BINDING OF NOVEL C-10 COLCHICINE ANALOGS
    STARETZ, ME
    HASTIE, SB
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1991, 202 : 16 - MEDI
  • [34] THE SYNTHESIS AND TUBULIN BINDING OF NOVEL PHOTOAFFINITY-LABELING DERIVATIVES OF COLCHICINE
    STARETZ, ME
    HASTIE, SB
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1991, 201 : 31 - BIOT
  • [35] BINDING OF VINCRISTINE, VINBLASTINE AND COLCHICINE TO TUBULIN
    OWELLEN, RJ
    OWENS, AH
    DONIGIAN, DW
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1972, 47 (04) : 685 - &
  • [36] HALOTHANE MODIFIES COLCHICINE BINDING TO TUBULIN
    VERGARA, GA
    LIVINGSTON, A
    [J]. PHARMACOLOGY, 1981, 23 (05) : 264 - 270
  • [37] NEW COLCHICINE BINDING ASSAY FOR TUBULIN
    SHERLINE, P
    BODWIN, CK
    KIPNIS, DM
    [J]. ANALYTICAL BIOCHEMISTRY, 1974, 62 (02) : 400 - 407
  • [38] EFFECT OF HALOTHANE ON COLCHICINE BINDING BY TUBULIN
    VERGARA, GA
    LIVINGSTON, A
    [J]. BRITISH JOURNAL OF PHARMACOLOGY, 1980, 70 (01) : P123 - P124
  • [39] BINDING OF A BICYCLIC COLCHICINE DERIVATIVE TO TUBULIN
    DECKER, H
    LEE, JC
    [J]. FRESENIUS ZEITSCHRIFT FUR ANALYTISCHE CHEMIE, 1985, 321 (07): : 636 - 636
  • [40] Recent Development and SAR Analysis of Colchicine Binding Site Inhibitors
    Chen, Jing
    Liu, Tao
    Dong, Xiaowu
    Hu, Yongzhou
    [J]. MINI-REVIEWS IN MEDICINAL CHEMISTRY, 2009, 9 (10) : 1174 - 1190