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从新开发的吲唑酮为重点的 DNA 编码文库中发现小分子 p300 抑制剂。

Discovery Small-Molecule p300 Inhibitors Derived from a Newly Developed Indazolone-Focused DNA-Encoded Library.

机构信息

State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, 501 Haike Road, Shanghai 201203, China.

University of Chinese Academy of Sciences, No. 19A Yuquan Road, Beijing 100049, China.

出版信息

Bioconjug Chem. 2024 Aug 21;35(8):1251-1257. doi: 10.1021/acs.bioconjchem.4c00307. Epub 2024 Aug 8.

Abstract

The DNA-encoded library (DEL) is a robust tool for chemical biology and drug discovery. In this study, we developed a DNA-compatible light-promoted reaction that is highly efficient and plate-compatible for DEL construction based on the formation of the indazolone scaffold. Employing this high-efficiency approach, we constructed a DEL featuring an indazolone core, which enabled the identification of a novel series of ligands specifically targeting E1A-binding protein (p300) after DEL selection. Taken together, our findings underscore the feasibility of light-promoted reactions in DEL synthesis and unveil promising avenues for developing p300-targeting inhibitors.

摘要

DNA 编码文库 (DEL) 是化学生物学和药物发现的强大工具。在这项研究中,我们开发了一种基于吲唑酮骨架形成的高效、板兼容的 DNA 兼容光促进反应,用于 DEL 构建。采用这种高效方法,我们构建了一个以吲唑酮为核心的 DEL,通过 DEL 选择,鉴定出了一系列专门针对 E1A 结合蛋白 (p300) 的新型配体。总之,我们的研究结果强调了光促进反应在 DEL 合成中的可行性,并为开发靶向 p300 的抑制剂开辟了有前途的途径。

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