Mazoudji Ajouan, Ecker Gerhard F
Department of Pharmaceutical Sciences, University of Vienna, Josef-Holaubek-Platz 2 (UZA II), 1090 Vienna, Austria.
Molecules. 2025 May 16;30(10):2179. doi: 10.3390/molecules30102179.
Inhibitors of the Sodium/Glucose co-transporter 2 (SGLT2) have been evolving into an important contribution to the treatment of diabetes mellitus. As the inhibition of SGLT2 is sensitive to the structural configuration at the sugar moiety of the inhibitors, it is of high interest to provide in silico-based methods for the prediction of the activity of potential SGLT2 inhibitors that take three-dimensional information into account. To attain this objective, a classification model based on the docking scores obtained from the best-performing docking-based virtual screening was created. Furthermore, the impact of ensemble docking using docking results from five SGLT2 structures and the incorporation of structural similarity information was assessed by creating classification models using these approaches. Taking a combined approach of docking score and structural similarity modelling led to the best performance with a Matthews Correlation Coefficient (MCC) of 0.64. Finally, to explore the ability of the used docking algorithms to correctly predict the influence of different three-dimensional information, a library of molecules with a negatively contributing configuration was created and docked, showing decreased docking scores for the molecule library with a disadvantaged configuration.
钠/葡萄糖协同转运蛋白2(SGLT2)抑制剂在糖尿病治疗中发挥着越来越重要的作用。由于SGLT2的抑制作用对抑制剂糖部分的结构构型敏感,因此提供基于计算机模拟的方法来预测潜在SGLT2抑制剂的活性并考虑三维信息具有很高的研究价值。为实现这一目标,基于从表现最佳的基于对接的虚拟筛选中获得的对接分数创建了一个分类模型。此外,通过使用这些方法创建分类模型,评估了使用来自五个SGLT2结构的对接结果进行的集成对接以及结构相似性信息的纳入的影响。采用对接分数和结构相似性建模相结合的方法,马修斯相关系数(MCC)达到0.64,性能最佳。最后,为了探索所使用的对接算法正确预测不同三维信息影响的能力,创建并对接了一个具有负贡献构型的分子库,结果显示具有不利构型的分子库对接分数降低。