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基于解吸电喷雾电离质谱的高通量药物衍生化及生物测定

High-Throughput Drug Derivatization and Bioassay by Desorption Electrospray Ionization Mass Spectrometry.

作者信息

Ghosh Jyotirmoy, Morato Nicolás M, Feng Yunfei, Cooks R Graham

机构信息

Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN, 47907, USA.

出版信息

Chempluschem. 2025 Jun;90(6):e202500164. doi: 10.1002/cplu.202500164. Epub 2025 Apr 30.

Abstract

Adapting high-throughput (HT) synthetic methods to the modification of drugs and to testing of their bioactivity should expedite drug discovery. Herein, the applicability of HT desorption electrospray ionization mass spectrometry (DESI MS) to achieve late-stage functionalization (LSF) and rapidly generate a modified opioid library is demonstrated. Specifically, aza-Michael addition and sulfur (VI) fluoride exchange reactions are used for functionalization. The modified drugs are both synthesized and characterized using an automated HT-DESI MS platform, with the reaction occurring during the droplet flight. Analysis by MS characterizes reaction products at a throughput of >1 reaction per second. With this platform, multiple nor-opioid scaffolds and functionalization reagents are screened and a selection of the hits obtained is subjected to HT label-free bioassays using the same DESI-MS platform. This combination of accelerated LSF reactions to rapidly create a diverse library of functionalized drugs with direct bioassays of the crude reaction mixtures for structure-activity relationship evaluation, both using the same platform, is anticipated to help expedite the early drug discovery process.

摘要

使高通量(HT)合成方法适用于药物修饰及其生物活性测试应能加快药物发现进程。本文展示了HT解吸电喷雾电离质谱(DESI MS)用于实现后期官能化(LSF)并快速生成修饰阿片样物质库的适用性。具体而言,氮杂迈克尔加成反应和六价硫氟交换反应用于官能化。使用自动化HT-DESI MS平台合成并表征修饰后的药物,反应在液滴飞行过程中发生。通过质谱分析以每秒>1个反应的通量表征反应产物。利用该平台,筛选了多种去甲阿片样物质支架和官能化试剂,并使用相同的DESI-MS平台对获得的部分命中化合物进行了无标记HT生物测定。这种加速LSF反应以快速创建多样化的官能化药物库,并使用同一平台对粗反应混合物进行直接生物测定以评估构效关系的组合,有望有助于加快早期药物发现进程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/435f/12143458/c774ed91c062/CPLU-90-e202500164-g001.jpg

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