药物发现
前药
药物开发
化学
毒性
药品
计算生物学
药理学
医学
生物
生物化学
有机化学
作者
Chuanjie Chen,Yiwen Yang,Zhe Wang,Huiwen Li,Chanjuan Dong,Xuan Zhang
标识
DOI:10.1021/acs.jmedchem.3c00302
摘要
Proteolysis-targeting chimera (PROTAC) technology represents a novel and promising modality for targeted protein degradation with transformative implications for the clinical management of various diseases. Despite notable advantages, the possibility of on-target off-tumor toxicity in healthy cells represents a critical challenge to clinical applications in cancer treatment. Researchers are currently exploring strategies to enhance targeted degradation activity in a cell-selective manner to minimize undesirable side effects. In this Perspective, we highlight innovative approaches for prodrug-based PROTACs (pro-PROTACs) that facilitate tumor-targeted release. The development of such approaches may further expand the range of potential applications of PROTAC technology within drug development.
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