系留
药物发现
降级(电信)
化学
计算生物学
药品
蛋白质降解
纳米技术
计算机科学
细胞生物学
生物
生物化学
药理学
材料科学
电信
作者
Jieke Gao,Jiantao Zhang,Xiaoli Han,Jinming Zhou
标识
DOI:10.2174/0929867329666220930120328
摘要
Targeted protein degradation (TPD) strategies have become a new trend in drug discovery due to the capability of triggering the degradation of protein of interest (POI) selectively and effectively in recent decades. Particularly, the hydrophobic tag tethering degrader (HyTTD) has drawn a lot of attention and may offer a promising strategy for new drug research and development in the future. Herein, we will give an overview of the development of HyTTD, the structure-activity relationship (SAR) between HyTTD and linkers, HyTs, and ligand motifs, as well as the various HyTTDs targeting different targets, thus offering a rational strategy for the design of HyTTDs in further TPD drug discovery.
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