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Data set of activity cliffs with single-atom modification and associated X-ray structure information for medicinal and computational chemistry applications

机译:具有单原子修改的活动悬崖的数据集和用于药用和计算化学应用的相关X射线结构信息

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摘要

Activity cliffs (ACs) are defined as pairs of structurally similar or analogous active compounds with large potency differences [1]. As such, they provide important information for the exploration of structure-activity relationships (SARs) and chemical optimization. We have introduced a new category of ACs capturing minimal (single-atom) chemical modifications and identified more than 1500 of such ACs in compounds with activity against a variety of target proteins [2]. ACs with single-atom modifications (sam_ACs) include “atom-replacement ACs” (ar_ACs) that contain a single-atom replacement (N to C (N-C), O-C, N-O, or S-O) at a given position and “atom-walk ACs” (aw_ACs), in which two analogs are only distinguished by the position of a single heteroatom (non-carbon atom). For a number of sam_ACs, X-ray structures of complexes between AC targets and AC compounds were identified, which made it possible to explore the formation of sam_ACs on the basis of well-defined ligand-target interactions [2]. Our collection of sam_ACs including associated chemical and X-ray structure information, as described herein, is made freely available.
机译:活性悬崖(ACS)定义为具有大效力差异的结构上类似或类似的活性化合物[1]。因此,它们提供了探索结构 - 活动关系(SARS)和化学优化的重要信息。我们已经介绍了一种新的ACS捕获最小(单颗粒)化学修饰,并在具有针对各种靶蛋白的活性的化合物中鉴定了超过1500种的这种AC [2]。具有单原子修改的ACS(SAM_AC)包括在给定位置的单个原子替换(N到C(NC),OC,NO,OF)的“原子替换ACS”(AR_ACS)。 ACS“(AW_ACS),其中两个类似物仅通过单个杂原子(非碳原子)的位置来区分。对于许多SAM_ACS,鉴定了AC靶和AC化合物之间的复合物的X射线结构,这使得在明确定义的配体 - 靶相互作用的基础上可以探讨SAM_AC的形成[2]。我们的SAM_AC集合包括如本文所述的相关化学和X射线结构信息,是自由的。

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