微管蛋白
紫杉醇
秋水仙碱
微管
长春瑞滨
多重耐药
化学
计算生物学
结合位点
药理学
生物化学
生物
癌症
细胞生物学
抗药性
遗传学
化疗
顺铂
作者
Kewei Sun,Zhonghao Sun,Feng-Lan Zhao,Guangzhi Shan,Qingguo Meng
标识
DOI:10.4155/fmc-2020-0376
摘要
Microtubules have been a concerning target of cancer chemotherapeutics for decades, and several tubulin-targeted agents, such as paclitaxel, vincristine and vinorelbine, have been approved. The colchicine binding site is one of the primary targets on microtubules and possesses advantages compared with other tubulin-targeted agents, such as inhibitors of tumor vessels and overcoming P-glycoprotein overexpression-mediated multidrug resistance. This study reviews and summarizes colchicine binding site inhibitors reported in recent years with structural studies via the crystal structures of complexes or computer simulations to discover new lead compounds. We are attempting to resolve the challenge of colchicine site agent research.
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