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3D-QSAR and Surflex Docking Studies of a Series of Alkaline Phosphatase Inhibitors 被引量:10

3D-QSAR and Surflex Docking Studies of a Series of Alkaline Phosphatase Inhibitors
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摘要 Alkaline phosphatases(APs) include the placental AP(PLAP), germ cell AP(GCAP), intestinal AP(IAP) and tissue nonspecific AP(TNAP). Over expression of TNAP in smooth muscle cells of kidney and vessels provokes the progress of such serious diseases as end-stage renal disease, idiopathic infantile arterial calcification, ankylosis, osteoarthritis and diabetes. In order to design and optimize the potent TNAP inhibitors, comparative molecular field analysis(CoMFA) and comparative molecular similarity indices analysis(CoMSIA) were used to analyze 3D structure-activity relationships(3D-QSAR) of TNAP inhibitors. The 3D-QSAR model(CoMFA with q^2 = 0.521, r^2 = 0.930; CoMSIA with q^2 = 0.529, r^2 = 0.933) had a good predictability. Surflex-dock was used to reveal the binding mode between the inhibitors and TNAP protein. CoMFA, CoMSIA and docking results provide guidance for the discovery of TNAP inhibitors. Finally, eight new compounds as potential TNAP inhibitors were designed. Alkaline phosphatases(APs) include the placental AP(PLAP), germ cell AP(GCAP), intestinal AP(IAP) and tissue nonspecific AP(TNAP). Over expression of TNAP in smooth muscle cells of kidney and vessels provokes the progress of such serious diseases as end-stage renal disease, idiopathic infantile arterial calcification, ankylosis, osteoarthritis and diabetes. In order to design and optimize the potent TNAP inhibitors, comparative molecular field analysis(CoMFA) and comparative molecular similarity indices analysis(CoMSIA) were used to analyze 3D structure-activity relationships(3D-QSAR) of TNAP inhibitors. The 3D-QSAR model(CoMFA with q^2 = 0.521, r^2 = 0.930; CoMSIA with q^2 = 0.529, r^2 = 0.933) had a good predictability. Surflex-dock was used to reveal the binding mode between the inhibitors and TNAP protein. CoMFA, CoMSIA and docking results provide guidance for the discovery of TNAP inhibitors. Finally, eight new compounds as potential TNAP inhibitors were designed.
作者 舒茂 武涛 王必武 李静 徐春媚 林治华 SHU Mao;WU Tao;WANG Bi-Wu;LI Jing;XU Chun-Mei;LIN Zhi-Hua
出处 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2019年第1期7-16,1,共11页 结构化学(英文)
基金 supported by the Key Project of Natural Science Foundation of Chongqing(No.cstc2015jcyjBX0080) Science and Technology project of Chongqing Education Commission(KJ1600907)
关键词 3D-QSAR surflex-dock ALKALINE PHOSPHATASE INHIBITORS 3D-QSAR surflex-dock alkaline phosphatase inhibitors
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