药效团
秋水仙碱
微管蛋白
癌症
癌细胞系
化学
计算生物学
药理学
癌细胞
生物
癌症研究
生物化学
微管
细胞生物学
遗传学
作者
Lorelei Johnson,Ing Swie Goping,Aja M. Rieger,Jonathan Y. Mane,Torin Huzil,Asok Banerjee,Richard F. Ludueña,Bashar Hassani,Philip Winter,Jack A. Tuszyński
标识
DOI:10.2174/1568026617666170104143618
摘要
In this paper we provide an overview of the status of various colchicine derivatives in preclinical development with special focus on their anti-cancer activity. We discuss several groups of compounds that have been designed to differentially bind with specific affinities for tubulin β isotypes, especially in regard to βIII, which is commonly over-expressed in cancer. Computational prediction, protein-based and cell-based assays are summarized as well as some animal tests conducted on these compounds. It is concluded that an untapped potential exists for exploiting the colchicine scaffold as a pharmacophore with the possibility of increasing its affinity for tubulin isotypes overexpressed in cancer and decreasing it for normal cells thereby widening the therapeutic window. Keywords: Anti-cancer, Tubulin β isotypes, Colchicine Scaffold, Pharmacophore, Animal tests
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