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

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 o...

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Main Authors: Zhisheng Mi (Author), Bing Gan (Author), Sihang Yu (Author), Jianan Guo (Author), Changjun Zhang (Author), Xiaoying Jiang (Author), Tao Zhou (Author), Jing Su (Author), Renren Bai (Author), Yuanyuan Xie (Author)
Format: Book
Published: Taylor & Francis Group, 2019-01-01T00:00:00Z.
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Summary: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 μM, respectively. In summary, these dual-target compounds have the potential anti-AD activity.
Item Description:1475-6366
1475-6374
10.1080/14756366.2019.1634703