Recent advances in bioactivity-guided drug screening strategies for pre-clinical and clinical drug discovery

被引:1
|
作者
Chen, Simin [1 ]
Shen, Chenxiao [1 ]
Li, Wanyu [1 ]
Fan, Yu [1 ,2 ]
Yang, Dong-Hua [3 ]
Wang, Yitao [1 ,2 ]
Feng, Ruibing [1 ,2 ]
Li, Guodong [1 ,2 ]
Zhong, Zhangfeng [1 ]
机构
[1] Univ Macau, Inst Chinese Med Sci, Macao Ctr Res & Dev Chinese Med, State Key Lab Qual Res Chinese Med, Macau 999078, Peoples R China
[2] Zhuhai UM Sci & Technol Res Inst, Zhuhai 519031, Peoples R China
[3] New York Coll Tradit Chinese Med, New York, NY 11501 USA
基金
中国国家自然科学基金;
关键词
Bioactivity-guided drug screening; High-throughput screening; Natural products; Clinical drugs; ON-A-CHIP; NATURAL-PRODUCTS; CANCER; INHIBITOR; MODEL; DROSOPHILA; TOOLS; IDENTIFICATION; ORGANOIDS; PLATFORM;
D O I
10.1016/j.trac.2024.118042
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Over the past two decades, bioactivity-guided drug screening has become a pivotal approach in drug discovery, which could identify potential drug candidates with desirable therapeutic effects against specific disease phenotypes or targets. This strategy has led to the discovery of many clinical medications such as natural products, peptides, and antibody drugs, and become a mainstream method. Herein, we first systematically summarize the principles and applications of recent bioactivity-guided drug screening strategies through technological advances in in silico screening, cell model systems, organoid model systems, and animal model systems. We then provide an overview on the representative active compounds, pre-clinical drugs, and marketed drugs, and discuss the present challenges and future directions of bioactivity-guided drug screening methods for clinical drug development. Based on the research advancements, it is anticipated that more disease-relevant screening models and efficient methods can be developed to identify drugs with ideal therapeutic effects and favorable pharmacological properties.
引用
收藏
页数:19
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