Dual-target anti-Alzheimer's disease agents with both iron ion chelating and monoamine oxidase-B inhibitory activity

被引:30
作者
Mi, Zhisheng [1 ]
Gan, Bing [1 ,2 ]
Yu, Sihang [3 ]
Guo, Jianan [1 ]
Zhang, Changjun [1 ]
Jiang, Xiaoying [1 ]
Zhou, Tao [4 ]
Su, Jing [4 ]
Bai, Renren [1 ]
Xie, Yuanyuan [1 ,5 ]
机构
[1] Zhejiang Univ Technol, Coll Pharmaceut Sci, Hangzhou 310014, Zhejiang, Peoples R China
[2] Guiyang Inst Food & Drug Control, Guiyang, Guizhou, Peoples R China
[3] Jilin Univ, Coll Basic Med Sci, Dept Pathophysiol, Changchun, Jilin, Peoples R China
[4] Zhejiang Gongshang Univ, Sch Food Sci & Biotechnol, Hangzhou, Zhejiang, Peoples R China
[5] Zhejiang Univ Technol, Collaborat Innovat Ctr Yangtze River Delta Reg Gr, Hangzhou, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; iron ion chelation; MAO-B; coumarin derivatives; hydroxypyridinone; COUMARIN HYBRIDS; ACETYLCHOLINESTERASE; CHOLINESTERASE; DESIGN; SERIES; COPPER;
D O I
10.1080/14756366.2019.1634703
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MAO-B leads to an increase in the levels of hydrogen peroxide and oxidative free radicals, which contribute to the aetiology of the AD. Thus, both iron ion chelators and MAO-B inhibitors can be used to treat AD. Taking the coumarin derivatives and hydroxypyridinones as the lead compounds, a series of dual-target hybrids were designed and synthesised by Click Chemistry. The compounds were biologically evaluated for their iron ion chelating and MAO-B inhibitory activity. Most of the compounds displayed excellent iron ion chelating activity and moderate to good anti-MAO-B activity. Compounds 27b and 27j exhibited the most potent MAO-B inhibitory activity, with IC50 values of 0.68 and 0.86 mu M, respectively. In summary, these dual-target compounds have the potential anti-AD activity.
引用
收藏
页码:1489 / 1497
页数:9
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