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Synthesis, activity evaluation and 3D-QSAR study of some novel derivatives of 4, 5, 6, 7-tetrahydrothieno [3,2-c] pyridine
作者姓名:Die Cheng  Deng Ke Liu  Mo Liu  Ying Liu  Wei Ren Xu  Chang Xiao Liu
作者单位:a Department of Pharmaceutical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, People's Republic of China;b Tianjin Key Laboratory of Molecular Design and Drug Discovery, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, People's Republic of China;c State Key Laboratory of Pharmacokinetics and Pharmacodynamics, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, People's Republic of China
摘    要:A series of novel derivatives of 4, 5, 6, 7-tetrahydrothieno 3,2-c] pyridine were synthesized and structurally characterized by 1H NMR and MS. Their in vivo anti-platelet aggregation activities were evaluated. A 3D-QSAR was performed using the CoMFA and the CoMSIA. This model provided useful guidelines for novel anti-platelet thienopyridines design.

关 键 词:合成  活度评估  P2Y12感受器  3D-QSAR

Synthesis, activity evaluation and 3D-QSAR study of some novel derivatives of 4, 5, 6, 7-tetrahydrothieno [3,2-c] pyridine
Die Cheng,Deng Ke Liu,Mo Liu,Ying Liu,Wei Ren Xu,Chang Xiao Liu.Synthesis, activity evaluation and 3D-QSAR study of some novel derivatives of 4, 5, 6, 7-tetrahydrothieno [3,2-c] pyridine[J].Chinese Chemical Letters,2008,19(9):1075-1079.
Authors:Die Cheng  Deng Ke Liu  Mo Liu  Ying Liu  Wei Ren Xu  Chang Xiao Liu
Institution:a Department of Pharmaceutical Engineering, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, People's Republic of China;b Tianjin Key Laboratory of Molecular Design and Drug Discovery, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, People's Republic of China;c State Key Laboratory of Pharmacokinetics and Pharmacodynamics, Tianjin Institute of Pharmaceutical Research, Tianjin 300193, People's Republic of China
Abstract:A series of novel derivatives of 4, 5, 6, 7-tetrahydrothieno 3,2-c] pyridine were synthesized and strucmrally characterized by 1H NMR and MS. Their in vivo anti-platelet aggregation activities were evaluated. A 3D-QSAR was performed using the CoMFA and the CoMSIA. This model provided useful guidelines for novel anti-platelet thienopyridines design.
Keywords:Thienopyfidines  Anti-platelet aggregation activities  P2Y12 receptors  3D-QSAR
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