Izquierdo-Ferrer Javier, Bellizzi Mary E, Tu Noah, Bogdan Andrew, Wang Ying
AbbVie, Inc., North Chicago, Illinois 60064, United States.
ACS Med Chem Lett. 2025 Jun 2;16(6):916-924. doi: 10.1021/acsmedchemlett.5c00175. eCollection 2025 Jun 12.
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.
用于高级复杂分子后期氧化(LSO)的化学方法仍然是一个高度相关的课题,每年都有新的和改进的方法被报道。尽管方法的数量不断增加,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尚不清楚。我们基于经过验证的LSO方法设计了一种高通量实验(HTE)板,能够仅使用几毫克化合物进行筛选,以增强我们的后期功能化(LSF)平台。艾伯维的各个项目都从该板中受益,为项目生成了重要数据,并为全面的构效关系(SAR)分析创建了新的类似物。我们通过筛选九种知名药物并分析氧化衍生物,展示了这种方法的变革能力。本报告强调了这种被忽视的转化如何能够成为药物化学的一种有效合成工具。