Design, synthesis and biological evaluation of D-ring opened galantamine analogs as multifunctional anti-Alzheimer agents

被引:59
|
作者
Fang, Lei [1 ,2 ]
Fang, Xubin [1 ]
Gou, Shaohua [1 ]
Lupp, Amelie [3 ]
Lenhardt, Isabel [3 ]
Sun, Yanyan [1 ]
Huang, Zhangjian [2 ]
Chen, Yao [4 ]
Zhang, Yihua [2 ]
Fleck, Christian [3 ]
机构
[1] Southeast Univ, Jiangsu Prov Hitech Key Lab Biomed Res, Pharmaceut Res Ctr, Sch Chem & Chem Engn, Nanjing 211189, Jiangsu, Peoples R China
[2] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[3] Univ Jena, Inst Pharmacol & Toxicol, D-07743 Jena, Germany
[4] Univ Jena, Inst Pharm, Jena, Germany
基金
中国国家自然科学基金;
关键词
Anti-Alzheimer; AChE inhibitors; Neuroprotective agents; A beta aggregation inhibitors; Galantamine analogs; POTENT ACETYLCHOLINESTERASE INHIBITORS; DISEASE; GALANTHAMINE; AGGREGATION; PEPTIDE; SCOPOLAMINE; CYCLIZATION; RATS;
D O I
10.1016/j.ejmech.2014.02.035
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Facing the multifactorial nature of Alzheimer's disease, twelve dibenzofuran/carbazole derivatives, which can be considered as the D-ring opened analogs of galantamine, have been designed and synthesized as multifunctional anti-Alzheimer agents. In vitro tests revealed that compounds 3 and 5, which bear a nitrate moiety in the molecule, showed a potent inhibition activity towards AChE and compound 3 showed a good A beta 42 aggregation inhibitory activity. Moreover, 3 and 5 could also release a relative low concentration of NO in vitro and they did not show toxicity to neuronal cells, while exerted a neuroprotective effect against the A beta-induced toxicity. More importantly, compound 3 showed a significant spatial memory improving effect in vivo, and a good safety in the ex vivo toxicity study. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:376 / 386
页数:11
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