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山国论文在线 http://www [7] ter Haar, E: Coll, J. T: Austen, D. A; et al, Structure of GSK3beta reveals a primed phosphorylation mechanism[J]. Nat Struct Biol 2001, 8,(7), 593-6. [8] Martinez, A: Alonso, M: Castro, A:et al, First non-ATP competitive glycogen synthase kinase 3 beta(GSK-3beta) inhibitors: thiadiazolidinones (TDzD)as potential drugs for the treatment of Alzheimer's disease [J]. Med Chem 2002, 45, (6),1292-9. [9] Doman, T. N: McGovern, S. L: Witherbee, B. J:et al, Molecular Docking and High-Throughput Screening for Novel Inhibitors of Protein Tyrosine Phosphatase-lBLJ. Journal of Medicina Chemistry2002,45,(11),2213-2221. [10] Polgar, T: Baki, A: Szendrei, G. I: et al, Comparative Virtual and Experimental High-Throughput Screening for Glycogen Synthase Kinase-3&#x03B2: Inhibitors[J]. Journal of Medicinal Chenistry 2005, 4 7946-7959 [11] New, J. S: Christopher, W. L: Yevich, J. P; et al, The thieno[3, 2-c]pyridine and furo[3, 2-c]pyridine rings: new pharmacophores with potential antipsychotic activity [j]. Journal of Medicinal Chemistry 1989, 32,(6), 1147-1156 [12] Lancelot, J.-C. L, Bertrand: Saturnino, Carmela; Caprariis, Paolo De: Robba, Max, A Novel Synthesis of 2, 3-Dihydro[1, 5]benzothiazepin-4(5H)-ones[J] Organic Preparations and Procedures nternational1992,24,(2),204-208 [13]A. Lvai H. Duddeck, Oxazepines and Thiazepines [j. Pharmazie 1983, 38, 827 [14] Meijer, L: Skaltsounis, A. L: Magiatis, P et al, GSK-3-selective inhibitors derived from Tyrian purple indirubins[J]. Chem Bio1. 2003, 10,(12),1255-12669 [7] ter Haar, E.; Coll, J. T.; Austen, D. A.; et al, Structure of GSK3beta reveals a primed phosphorylation mechanism[J]. Nat Struct Biol 2001, 8, (7), 593-6. [8] Martinez, A.; Alonso, M.; Castro, A.;et al, First non-ATP competitive glycogen synthase kinase 3 beta (GSK-3beta) inhibitors: thiadiazolidinones (TDZD) as potential drugs for the treatment of Alzheimer's disease[J]. J Med Chem 2002, 45, (6), 1292-9. [9] Doman, T. N.; McGovern, S. L.; Witherbee, B. J.;et al, Molecular Docking and High-Throughput Screening for Novel Inhibitors of Protein Tyrosine Phosphatase-1B[J]. Journal of Medicinal Chemistry 2002, 45, (11), 2213-2221. [10] Polgar, T.; Baki, A.; Szendrei, G. I.; et al, Comparative Virtual and Experimental High-Throughput Screening for Glycogen Synthase Kinase-3β Inhibitors[J]. Journal of Medicinal Chemistry 2005, 48, (25), 7946-7959. [11] New, J. S.; Christopher, W. L.; Yevich, J. P.; et al, The thieno[3,2-c]pyridine and furo[3,2-c]pyridine rings: new pharmacophores with potential antipsychotic activity[J]. Journal of Medicinal Chemistry 1989, 32, (6), 1147-1156. [12] Lancelot, J.-C. L., Bertrand; Saturnino, Carmela; Caprariis, Paolo De; Robba, Max, A Novel Synthesis of 2,3-Dihydro[1,5]benzothiazepin-4(5H)-ones[J].Organic Preparations and Procedures International 1992, 24, (2), 204 - 208. [13] A. Lvai ; H. Duddeck, Oxazepines and Thiazepines[J]. Pharmazie 1983, 38, 827. [14] Meijer, L.; Skaltsounis, A. L.; Magiatis, P.et al, GSK-3-selective inhibitors derived from Tyrian purple indirubins[J]. Chem. Biol. 2003, 10, (12), 1255-1266. 中国科技论文在线 http://www.paper.edu.cn
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