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
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