Suppr超能文献

嵌合体诱导蛋白降解:PROTAC 技术及其他。

Chimera induced protein degradation: PROTACs and beyond.

机构信息

School of Pharmaceutical Sciences, Guangzhou University of Chinese Medicine, 232 East Waihuan Road, 51006, Guangzhou, PR China.

出版信息

Eur J Med Chem. 2020 Nov 15;206:112494. doi: 10.1016/j.ejmech.2020.112494. Epub 2020 Jul 19.

Abstract

Ubiquitin-proteasome system, autophagy-lysosome pathway and N-end rule pathway are crucial protein quality control mechanisms in human body. Hijacking these endogenous protein degrading measures by chimera degraders could be a revolutionary strategy for the discovery of small-molecule drugs. As the most advanced chimera degraders, PROTACs have demonstrated the potential by delivering two drug candidates into clinical trials. The development of chimera degraders exploiting these three pathways are reviewed, a focus is given on the chemical structures and their influences on biological effects from a viewpoint of medicinal chemistry.

摘要

泛素-蛋白酶体系统、自噬-溶酶体途径和 N 端规则途径是人体内重要的蛋白质质量控制机制。通过嵌合体降解剂劫持这些内源性蛋白质降解措施可能是发现小分子药物的革命性策略。作为最先进的嵌合体降解剂,PROTACs 通过将两种候选药物递送至临床试验中已经证明了其潜力。本文综述了利用这三种途径开发嵌合体降解剂的研究进展,重点从药物化学的角度讨论了它们的化学结构及其对生物学效应的影响。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验