期刊文献+

抗阿尔茨海默病的胆碱酯酶抑制剂研究进展 被引量:13

Advances in the Researches on Cholinesterase Inhibitors for the Treatment of Alzheimer′s Disease
下载PDF
导出
摘要 目前抗阿尔茨海默病的新策略之一是设计具有多靶向的药物。综述抗阿尔茨海默病的胆碱酯酶抑制剂研究的新进展,分类介绍乙酰胆碱酯酶和丁酰胆碱酯酶双重抑制剂、可抑制β-淀粉样蛋白聚集的胆碱酯酶抑制剂、具有抗氧化作用的胆碱酯酶抑制剂、可拮抗H3受体的胆碱酯酶抑制剂以及NO供体型胆碱酯酶抑制剂等多靶向药物,并讨论了各类药物的设计和优化。 One of the current strategies to combat Alzheimer's disease (AD) is to design multi-targe- ting drugs. The advances in the researches on eholinesterase inhibitors with multi functions to treat AD were reviewed in this article. These drugs including dual inhibitors of acetyleholinesterase/butyroeholines- terase, dual binding site acetylcholinesterase inhibitors targeting 13-amyloid aggregation, eholinesterase inhibitors with antioxidant functions, dual inhibitor of eholinesterase and H3 receptor and NO-donating cholinesterase inhibitors were introduced, and the design and optimization strategies were also discussed.
出处 《药学进展》 CAS 2009年第7期289-296,共8页 Progress in Pharmaceutical Sciences
基金 国家基础科学人才培养基金资助项目(No.J0630858)
关键词 阿尔茨海默病 胆碱酯酶抑制剂 多靶向 药物设计 Alzheimer's disease cholinesterase inhibitor multi targets drug design
  • 相关文献

参考文献2

二级参考文献49

  • 1Kathryn Z G, Ron Brookmeyer, Elizabeth J, et al. Worldwide variation in the doubling time of Alzheimer' s disease incidencerates. Alzheimer' s and Dementia [ J ] ,2007,3 (3) : S168 - S169.
  • 2Cavalli A, Bolognesi M L, Minarini, et al. Multi-target-directed ligands to combat neurodegenerative diseases [ J ]. J Med Chem, 2008,51(3) :347 -72.
  • 3Wang H,Carlier P R,Ho W L,et al. Effects of bis(7)-tacrine, a novel anti-Alzheimer' s agent, on rat brain AChE [ J ]. NeuroReport, 1999, 10(4):789-93.
  • 4Pan S Y,Han Y F,Carlier P R,et al. Schisandrin B protects against tacrine- and bisC7 )-tacrine-indueed hepatotoxicity and enhances cognitive function in mice [J]. Planta Med, 2002, 68 (3) :217 -20.
  • 5Li W, Pi R B, Chan H H, et al, Novel dimeric acetylcholinesterase inhibitor bis7-tacrine, but not donepezil, prevents glutamate-induced neuronal apoptosis by blocking N-methyl-D-aspartate receptors[J]. J Biol Chem, 2005,280(18): 79-88.
  • 6Luo J, Li W, Liu Y, et al. Novel dimeric bis (7) -tacrine protondependently inhibits NMDA-activated currents [ J ]. Biochem Biophys Res Commum, 2007,361 (2) :505 - 9.
  • 7Fu H J, Li Win, Luo J L, et al. Promising anti-Alzheimer' s dimer bis(7 )-tacrine reduces beta-amyloid generation by directly inhibiting BACE-1 activity [ J ]. Biochem Biophys Res Commum, 2008 15,366(3) :631 -6.
  • 8Hu M K, Wu L J, Hsiao G,et al. Homodimeric tacrine congeners as acetylcholinesterase inhibitors [ J ]. J Med Chem, 2002, 45 (11) : 2277 -82.
  • 9Savini L, Campian G, Gaeta A,et al Novel and potent tacrine-related hetero- and homobivalent ligands for aeetylcholinesterase and butyryleholinesterase[ J]. Bioorg Med Chem Lett, 2001, 11 ( 13 ) : 1779 - 82.
  • 10Carlier P R, Du D M, Han Y, et al. Potent, easily synthesized huperzine A-tacrine hybrid acetylcholinesterase inhibitors[J].Bioorg Med Chem Let,1999, 9(16) : 2335 -8.

共引文献13

同被引文献137

引证文献13

二级引证文献85

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部