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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Multi-targeted ChEI-copper chelating molecules as neuroprotective agents
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Multi-targeted ChEI-copper chelating molecules as neuroprotective agents

机译:多针对的Chei-Copper Chelating分子作为神经保护剂

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The identification of a valid therapeutic treatment for Alzheimer's disease (AD) represents nowadays an urgent and still unmet medical need, since currently available anti-AD drugs only relieve symptoms and show a modest efficacy. Recent evidence indicates that multi-target-directed ligands (MTDLs) can potentially provide an effective strategy to develop innovative therapies directed towards the onset and progression of this multifactorial neurodegenerative disorder. In this work we designed, synthesized and evaluated a new series of MTDLs bearing the rivastigmine skeleton (ChE-inhibitor) linked to known metal-chelating moieties with linkers of different length. For all the novel derivatives, AChE/BuChE inhibitory activity, ROS scavenging activity and potential cytotoxicity have been assessed. For the best compound (4), copper chelating properties and neuroprotective effects were also evaluated. Our data demonstrated that hybrid derivative 4 is able to effectively inhibit AChE and BuChE and to chelate copper, showing a protective action on neurons. These results, although preliminary, indicate that compound 4 can be considered as a possible hit molecule for the development of new anti-AD MTDLs. (C) 2019 Elsevier Masson SAS. All rights reserved.
机译:有效治疗阿尔茨海默氏病(AD)的识别时下代表的一项紧迫而仍然未满足的医疗需求,因为目前可用的抗AD药物只能缓解症状,表现出适度的功效。最近的证据表明,多目标导向配体(MTDLs)有可能提供一种有效的战略来开发针对这种多因素的神经退行性疾病的发生和发展创新疗法。在这项工作中,我们设计,合成并评价了一系列新的MTDLs轴承连接到公知的金属螯合部分具有不同长度的连接体的利凡斯的明骨架(CHE-抑制剂)的。对于所有的新颖的衍生物,乙酰胆碱酯酶/ BuChE的抑制活性,ROS清除活性和细胞毒性潜力进行了评估。为了获得最佳的化合物(4),铜螯合性质和神经保护作用也进行了评价。我们的数据表明,混合衍生物4能够有效地抑制乙酰胆碱酯酶和丁酰胆碱酯酶和螯合铜,表现出对神经元的保护作用。这些的结果,尽管初步的,表明化合物4可以被认为是用于新的抗AD MTDLs发展的可能的命中分子。 (c)2019年Elsevier Masson SAS。版权所有。

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