Dimova Dilyana, Bajorath Jürgen
Department of Life Science Informatics, B-IT, LIMES Program Unit Chemical Biology and Medicinal Chemistry, Rheinische Friedrich-Wilhelms-Universität, Bonn, Germany.
Methods Mol Biol. 2018;1825:327-337. doi: 10.1007/978-1-4939-8639-2_10.
Scaffolds were originally introduced to delineate core structures of active compounds. They are also used to assess the ability of computational methods to identify structurally diverse active compounds. Biological activities of compound series are often mapped to scaffolds. This is done to better understand activity distributions over different structural classes or search for core structures of compounds that are preferentially active against target families of interest. Herein, we describe in detail how such scaffold activity profiles are generated and compare profiles for differently defined scaffolds. As an exemplary application, scaffolds of currently available kinase inhibitors covering the human kinome are analyzed.
支架最初被引入以描绘活性化合物的核心结构。它们还用于评估计算方法识别结构多样的活性化合物的能力。化合物系列的生物活性通常映射到支架上。这样做是为了更好地理解不同结构类别的活性分布,或寻找对感兴趣的靶标家族具有优先活性的化合物的核心结构。在此,我们详细描述了如何生成此类支架活性图谱,并比较不同定义支架的图谱。作为一个示例性应用,分析了覆盖人类激酶组的现有激酶抑制剂的支架。