化学
蛋白质降解
计算生物学
蛋白质水解
药物发现
小分子
降级(电信)
药物开发
组合化学
药品
药理学
生物化学
酶
计算机科学
生物
电信
医学
作者
Qindi He,Xiaofei Zhao,Donglin Wu,Siming Jia,Canlin Liu,Zitian Cheng,Fei Huang,Yadong Chen,Tao Lu,Shuai Lü
标识
DOI:10.1016/j.ejmech.2023.115741
摘要
Targeted protein degradation (TPD) has emerged as a promising approach for drug development, particularly for undruggable targets. TPD technology has also been instrumental in overcoming drug resistance. While some TPD molecules utilizing proteolysis-targeting chimera (PROTACs) or molecular glue strategies have been approved or evaluated in clinical trials, hydrophobic tag-based protein degradation (HyT-PD) has also gained significant attention as a tool for medicinal chemists. The increasing number of reported HyT-PD molecules possessing high efficiency in degrading protein and good pharmacokinetic (PK) properties, has further fueled interest in this approach. This review aims to present the design rationale, hydrophobic tags in use, and diverse mechanisms of action of HyT-PD. Additionally, the advantages and disadvantages of HyT-PD in protein degradation are discussed. This review may help inspire the development of more HyT-PDs with superior drug-like properties for clinical evaluation.
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