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Extending the activity cliff concept: Structural categorization of activity cliffs and systematic identification of different types of cliffs in the ChEMBL database

机译:扩展活动悬崖概念:ChEMBL数据库中活动悬崖的结构分类和不同类型悬崖的系统识别

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Activity cliffs are generally understood as pairs or groups of similar compounds with large differences in potency. The study of activity cliffs is of high interest for the characterization of activity landscapes of compound data sets and the identification of SAR determinants, given the "small chemical change(s)-large potency effect" phenotype of cliffs. Herein, we introduce a new structural classification scheme for activity cliffs and introduce new cliff types. Activity cliffs are divided into five different classes dependent on whether the participating compounds are only distinguished by chirality, topology, R-group sets, core structures (scaffolds), or core structures and R-group topology. All cliff types are frequently detected in the ChEMBL database. R-group cliffs occur with higher propensity than other cliff types, as one might expect. However, many scaffold and R-group cliffs are not identified on the basis of whole-molecule similarity calculations, although they are often chemically intuitive. This makes the activity cliff classification attractive for medicinal chemistry analysis, independent of similarity calculations. Assignment of activity cliffs on the basis of well-defined structural criteria complements and further extends current approaches to identify and represent cliffs.
机译:活性悬崖通常被理解为在效能上有很大差异的成对或相似化合物的组合。鉴于悬崖的“小化学变化-大效能效应”表型,对活动悬崖的研究对于复合数据集活动景观的表征和SAR决定因素的识别具有很高的兴趣。在此,我们介绍了活动悬崖的一种新的结构分类方案,并介绍了新的悬崖类型。根据是否仅通过手性,拓扑,R-基集,核心结构(骨架)或核心结构和R-基拓扑区分参与化合物,将活性悬崖分为五类。 ChEMBL数据库中经常检测到所有悬崖类型。正如人们所期望的那样,R型悬崖比其他悬崖类型具有更高的倾向。但是,尽管基于化学直觉通常无法根据全分子相似性计算确定许多脚手架和R-group悬崖。这使得活动悬崖分类对于药物化学分析具有吸引力,而与相似度计算无关。在定义明确的结构标准的基础上分配活动悬崖的方法补充并扩展了当前识别和表示悬崖的方法。

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