工程伦理学
药品
药理学
药物发现
药物开发
医学
化学
梅德林
生产力
治疗方法
基础(证据)
病毒灭活
机制(生物学)
重症监护医学
临床实习
管理科学
作者
Yujun Deng,S Wang,Lei Geng,Zhiwei Meng,Fangrong Chen,Xiaoxiao Yang,Feng Wang,Yuanli Chen,Zhiyu Li,Zhouling Xie
标识
DOI:10.1021/acs.jmedchem.6c00858
摘要
Previously drugged therapeutic targets have continued to attract substantial scientific and clinical interest, resulting in numerous FDA approvals for new chemical entities (NCEs) over the past 15 years. This sustained productivity demonstrates that these established therapeutic drug targets remain a central foundation of modern drug discovery, supporting not only incremental improvements in efficacy and safety but also the development of innovative medicinal chemistry strategies and novel mechanisms of action. In this Perspective, we provide a comprehensive analysis of the contributions of previously drugged therapeutic targets to FDA-approved small-molecule drugs between 2010 and 2025, with an emphasis on therapeutic innovation based on several representative therapeutic drug targets across central nervous system, infectious disease, and oncology indications. The design principles and translational insights derived from these paradigmatic cases highlight the enduring value of these "evergreen" therapeutic drug targets and may inform future efforts to develop more effective, differentiated, and resistance-resilient therapeutics.
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