脱甲基酶
组蛋白
基因亚型
翻译(生物学)
细胞生物学
生物
计算生物学
化学
生物化学
合理设计
酶
药物开发
药物发现
生物信息学
蛋白质-蛋白质相互作用
膜蛋白
作者
Xiaolong Yang,Yuyan Han,Lei Yu,Shilin Xu
标识
DOI:10.1080/13543776.2026.2614491
摘要
Significant progress has been achieved in the development of KDM4 inhibitors; however, most current compounds continue to face major challenges, including poor membrane permeability, limited cellular potency, and low isoform specificity. Strategies such as designing inhibitors with novel scaffolds, developing covalent inhibitors, advancing protein degraders, and targeting non-catalytic domains may provide viable solutions to these limitations. In addition, the physiological and pathological roles of KDM4 remain insufficiently characterized. Further in-depth investigations into the biological functions of KDM4 will be essential to guide the rational design and facilitate the clinical translation of KDM4-targeted therapeutics.
科研通智能强力驱动
Strongly Powered by AbleSci AI