期刊
MEDICINAL CHEMISTRY RESEARCH
卷 22, 期 2, 页码 615-624出版社
SPRINGER BIRKHAUSER
DOI: 10.1007/s00044-012-0053-7
关键词
SGLT2; N-beta-D-Xylosylindole derivatives; Type 2 diabetes; 3D QSAR; PHASE
Sodium-dependent glucose cotransporter 2 (SGLT2) have emerged as a novel drug target for hyperglycemia, a major complication of type 2 diabetes, with a multitude of therapeutic potential for their inhibitors. A series of N-beta-d-xylosylindole derivatives has been reported as SGLT2 inhibitors. Therefore, to determine the structural requisite of these SGLT2 inhibitors, 3D pharmacophore models and atom-based 3D QSAR models have been developed using the PHASE module of Schrodinger. The best six-featured pharmacophore hypothesis with two hydrogen bond acceptors, two hydrogen bond donors, one hydrophobic features, and one aromatic ring yielded a 3D QSAR model. The derived model have significant PLS values as R (2) = 0.9527, correlation coefficient of training set, and Q (2) = 0.9045, correlation coefficient of test set, indicating the model have good predictive power. The results provide detailed insights of N-beta-d-xylosylindole derivatives which can afford guidance for rational drug design of novel potent SGLT2 inhibitors.
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