a Tumour Targeted Therapy and Chemical Biology Research Center, School of Pharmaceutical Sciences , Chongqing University , Chongqing , China.
b Department of Chemistry , The University of Hong Kong , Hong Kong SAR , China.
Expert Opin Drug Discov. 2019 Aug;14(8):735-753. doi: 10.1080/17460441.2019.1614559. Epub 2019 May 21.
: DNA-encoded chemical libraries (DELs) have come of age and emerged to become a powerful technology platform for ligand discovery in biomedical research and drug discovery. Today, DELs have been widely adopted in the pharmaceutical industry and employed in drug discovery programs worldwide. DELs are capable of interrogating drug targets with an extremely large number of compounds highly efficiently. : In this review, the authors introduce the history of DELs and provide an overview of the major technological components, including encoding methods, library synthesis, chemistry, selection methods, hit deconvolution strategy, and post-selection data analysis. A brief update on the hit compounds recently discovered from DEL selections against drug targets is also provided. Finally, the authors discuss their views on the present challenges and future directions for the development and application of DELs in drug discovery. : DELs have provided great opportunities for lead compound discovery at an unprecedented scale and efficiency in drug discovery. The key to the future success of DELs as true discovery modalities, rather than just 'a way to make many compounds,' is to go beyond physical binding to functional or even phenotypic assays with the capability to probe the biological system.
DNA 编码化合物库 (DEL) 已经成熟并成为生物医学研究和药物发现中配体发现的强大技术平台。如今,DEL 已在制药行业得到广泛应用,并在全球范围内用于药物发现计划。DEL 能够非常高效地用大量化合物来探究药物靶点。
在这篇综述中,作者介绍了 DEL 的历史,并概述了主要的技术组成部分,包括编码方法、文库合成、化学、选择方法、命中解卷积策略和选择后数据分析。还简要介绍了最近从针对药物靶点的 DEL 选择中发现的命中化合物。最后,作者讨论了他们对 DEL 在药物发现中的开发和应用的当前挑战和未来方向的看法。
DEL 为药物发现中的先导化合物发现提供了前所未有的规模和效率的巨大机会。DEL 作为真正的发现模式而不仅仅是“制造许多化合物的一种方式”的未来成功的关键是超越物理结合,采用具有探测生物系统能力的功能甚至表型测定方法。