一个小型化的化学高通量实验板,使后期氧化筛选和放大。

IF 4 3区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Medicinal Chemistry Letters Pub Date : 2025-06-02 eCollection Date: 2025-06-12 DOI:10.1021/acsmedchemlett.5c00175
Javier Izquierdo-Ferrer, Mary E Bellizzi, Noah Tu, Andrew Bogdan, Ying Wang
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引用次数: 0

摘要

化学方法用于高级复杂分子的后期氧化(LSO)仍然是一个高度相关的话题,每年都有新的和改进的方法被报道。尽管方法越来越多,但这些方法在生物活性分子中的范围和局限性在很大程度上是未知的。我们设计了一个基于经过验证的LSO方法的高通量实验(HTE)板,能够仅使用几毫克筛选化合物,以增强我们的后期功能化(LSF)平台。艾伯维的各种项目都受益于这个板块,为项目生成必要的数据,并为全面的结构-活性关系(SAR)分析创建新的类似物。我们通过筛选九种知名药物并分析氧化衍生物来证明这种方法的转化能力。本报告强调了这种被忽视的转化如何成为药物化学的有效合成工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Miniaturized Chemical High Throughput Experimentation Plate to Enable Late-Stage Oxidation Screening and Scale-up.

Chemical methods for Late-Stage Oxidation (LSO) of advanced and complex molecules remain a highly relevant topic, with new and improved methods being reported annually. Despite the growing number of methodologies, the scope and limitations of these methods in bioactive molecules is largely unknown. We have designed a High-Throughput Experimentation (HTE) plate based on validated LSO methods, capable of screening compounds using only a few milligrams, to enhance our Late-Stage Functionalization (LSF) platform. Various projects at AbbVie have benefited from this plate, generating essential data for programs and creating new analogs for comprehensive Structure-Activity Relationship (SAR) analysis. We demonstrated the transformative capabilities of this approach by screening nine well-known drugs and analyzed the oxidized derivatives. This report highlights how this overlooked transformation can be an effective synthetic tool for medicinal chemistry.

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来源期刊
ACS Medicinal Chemistry Letters
ACS Medicinal Chemistry Letters CHEMISTRY, MEDICINAL-
CiteScore
7.30
自引率
2.40%
发文量
328
审稿时长
1 months
期刊介绍: ACS Medicinal Chemistry Letters is interested in receiving manuscripts that discuss various aspects of medicinal chemistry. The journal will publish studies that pertain to a broad range of subject matter, including compound design and optimization, biological evaluation, drug delivery, imaging agents, and pharmacology of both small and large bioactive molecules. Specific areas include but are not limited to: Identification, synthesis, and optimization of lead biologically active molecules and drugs (small molecules and biologics) Biological characterization of new molecular entities in the context of drug discovery Computational, cheminformatics, and structural studies for the identification or SAR analysis of bioactive molecules, ligands and their targets, etc. Novel and improved methodologies, including radiation biochemistry, with broad application to medicinal chemistry Discovery technologies for biologically active molecules from both synthetic and natural (plant and other) sources Pharmacokinetic/pharmacodynamic studies that address mechanisms underlying drug disposition and response Pharmacogenetic and pharmacogenomic studies used to enhance drug design and the translation of medicinal chemistry into the clinic Mechanistic drug metabolism and regulation of metabolic enzyme gene expression Chemistry patents relevant to the medicinal chemistry field.
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