细胞周期蛋白依赖激酶
细胞生物学
蛋白质水解
生物
CDK抑制剂
转录因子
抄写(语言学)
药物发现
激酶
小分子
计算生物学
化学
生物化学
细胞周期
酶
细胞
基因
语言学
哲学
作者
Bin Yu,Zekun Du,Yuming Zhang,Zhiyu Li,Jinlei Bian
出处
期刊:Future Medicinal Chemistry
[Newlands Press Ltd]
日期:2021-12-23
卷期号:14 (3): 167-185
被引量:8
标识
DOI:10.4155/fmc-2021-0154
摘要
Proteolysis-targeting chimeras are a new modality of chemical tools and potential therapeutics involving the induction of protein degradation. Cyclin-dependent kinase (CDK) protein, which is involved in cycles and transcription cycles, participates in regulation of the cell cycle, transcription and splicing. Proteolysis-targeting chimeras targeting CDKs show several advantages over traditional CDK small-molecule inhibitors in potency, selectivity and drug resistance. In addition, the discovery of molecule glues promotes the development of CDK degraders. Herein, the authors describe the existing CDK degraders and focus on the discussion of the structural characteristics and design of these degraders.
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