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用于药物重新利用的高通量体内表型筛选:发现MLR-1023,一种具有临床概念验证的新型胰岛素增敏剂和新型Lyn激酶激活剂。

High throughput in vivo phenotypic screening for drug repurposing: Discovery of MLR-1023 a novel insulin sensitizer and novel Lyn kinase activator with clinical proof of concept.

作者信息

Lipinski Christopher A, Reaume Andrew G

机构信息

Melior Discovery, Inc., 860 Springdale Drive, Exton, PA 19087, United States.

Melior Discovery, Inc., 860 Springdale Drive, Exton, PA 19087, United States.

出版信息

Bioorg Med Chem. 2020 May 1;28(9):115425. doi: 10.1016/j.bmc.2020.115425. Epub 2020 Mar 16.

Abstract

Drug discovery requires the combination of medicinal chemistry and biology. In this article Chris Lipinski, the medicinal chemist, describes the chemical origins at Pfizer of Tolimidone the starting point for the repurposed MLR-1023 (Ochman et al., 2012). Andrew Reaume, the biologist, describes his motivation to develop a high quality (i.e. in vivo model) phenotypic screening platform as an ideal drug repositioning platform.

摘要

药物研发需要药物化学与生物学相结合。在本文中,药物化学家克里斯·利平斯基描述了辉瑞公司托利米酮的化学起源,它是重新利用的MLR - 1023(奥赫曼等人,2012年)的起始点。生物学家安德鲁·雷姆描述了他开发一个高质量(即体内模型)表型筛选平台作为理想的药物重新定位平台的动机。

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