Torrey Pines Institute for Molecular Studies, Port St. Lucie, Florida 34987, United States.
J Chem Inf Model. 2011 Sep 26;51(9):2427-39. doi: 10.1021/ci200281v. Epub 2011 Aug 29.
Dual and triple activity-difference (DAD/TAD) maps are tools for the systematic characterization of structure-activity relationships (SAR) of compound data sets screened against two or three targets. DAD and TAD maps are two- and three- dimensional representations of the pairwise activity differences of compound data sets, respectively. Adding pairwise structural similarity information into these maps readily reveals activity cliff regions in the SAR for one, two, or three targets. In addition, pairs of compounds in the smooth regions of the SAR and scaffold hops are also easily identified in these maps. Herein, DAD and TAD maps are employed for the systematic characterization of the SAR of a benchmark set of 299 compounds screened against dopamine, norepinephrine, and serotonin transporters. To reduce the well-known dependence of the activity landscape on the structural representation, five selected 2D and 3D structure representations were used to characterize the SAR. Systematic analysis of the DAD and TAD maps reveals regions in the landscape with similar SAR for two or the three targets as well as regions with inverse SAR, i.e., changes in structure that increase activity for one target, but decrease activity for the other target. Focusing the analysis on pairs of compounds with high structure similarity revealed the presence of single-, dual-, and triple-target activity cliffs, i.e., small changes in structure with high changes in potency for one, two, or the three targets, respectively. Triple-target scaffold hops are also discussed. Activity cliffs and scaffold hops were also quantified and represented using two recently proposed approaches namely, mean Structure Activity Landscape Index (mean SALI) and Consensus Structure-Activity Similarity (SAS) maps.
双靶和三靶活性差异(DAD/TAD)图谱是用于系统表征针对两个或三个靶标筛选的化合物数据集结构活性关系(SAR)的工具。DAD 和 TAD 图谱分别是化合物数据集的成对活性差异的二维和三维表示。将成对的结构相似性信息添加到这些图谱中,很容易揭示 SAR 中针对一个、两个或三个靶标的活性悬崖区域。此外,SAR 中平滑区域和支架跳跃的化合物对也可以在这些图谱中轻松识别。在此,DAD 和 TAD 图谱用于系统表征针对多巴胺、去甲肾上腺素和 5-羟色胺转运体筛选的 299 个化合物的基准数据集的 SAR。为了降低众所周知的活性景观对结构表示的依赖性,使用了五种选定的 2D 和 3D 结构表示来表征 SAR。对 DAD 和 TAD 图谱的系统分析揭示了景观中具有相似 SAR 的两个或三个靶标区域,以及具有反向 SAR 的区域,即结构变化增加一个靶标活性,但降低另一个靶标活性。将分析重点放在具有高结构相似性的化合物对上,揭示了存在单靶、双靶和三靶活性悬崖,即结构的微小变化具有针对一个、两个或三个靶标的高效力变化。还讨论了三靶标支架跳跃。使用最近提出的两种方法,即平均结构活性景观指数(mean SALI)和共识结构-活性相似性(SAS)图谱,对活性悬崖和支架跳跃进行了量化和表示。