化学
小分子
药物发现
双功能
计算生物学
组合化学
蛋白质降解
蛋白质工程
蛋白质水解
纳米技术
生物化学
酶
生物
催化作用
材料科学
作者
Shaowen Xie,Jingjie Zhu,Junda Li,Feiyan Zhan,Hong Yao,Jinyi Xu,Shengtao Xu
标识
DOI:10.1021/acs.jmedchem.3c00736
摘要
Targeted protein degradation (TPD) technologies have catalyzed a paradigm shift in therapeutic strategies and offer innovative avenues for drug design. Hydrophobic tags (HyTs) are bifunctional TPD molecules consisting of a ″lipophilic small-molecule tags″ group and a small-molecule ligand for the target protein. Despite the vast potential of HyTs, they have received relatively limited attention as a promising frontier. Leveraging their lower molecular weight and reduced numbers of hydrogen bond donors/acceptors (HBDs/HBAs) in comparison with proteolysis-targeting chimeras (PROTACs), HyTs present a compelling approach for enhancing druglike properties. In this Perspective, we explore the diverse range of HyT structures and their corresponding degradation mechanisms, thereby illuminating their broad applicability in targeting a diverse array of proteins, including previously elusive targets. Moreover, we scrutinize the challenges and opportunities entailed in developing this technology as a viable and fruitful strategy for drug discovery.
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