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首页> 外文期刊>Neurochemical research >Multi-target Design Strategies in the Context of Alzheimer’s Disease: Acetylcholinesterase Inhibition and NMDA Receptor Antagonism as the Driving Forces
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Multi-target Design Strategies in the Context of Alzheimer’s Disease: Acetylcholinesterase Inhibition and NMDA Receptor Antagonism as the Driving Forces

机译:阿尔茨海默氏病背景下的多目标设计策略:乙酰胆碱酯酶抑制和NMDA受体拮抗作用为驱动力

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摘要

In recent years, the multi-target-directed ligand concept has been used to design a variety of molecules hitting different biological targets for Alzheimer’s disease. We have sought to combine, in the same molecule, the neuroprotective action of N-methyl-d-aspartate receptor antagonism with the symptomatic relief offered by cholinergic activity through acetylcholinesterase inhibition. This strategy could potentially maintain the positive outcomes of memantine–acetylcholinesterase inhibitor combinations, but with the benefits of a single molecule therapy. Herein, we discuss selected examples of multifunctional compounds, which we rationally designed to simultaneously modulate these targets. We also examine the intertwined relationship between acetylcholinesterase, N-methyl-d-aspartate receptors, and other active players in the neurotoxic cascade.
机译:近年来,多目标导向的配体概念已被用来设计各种分子,这些分子可以击中阿尔茨海默氏病的不同生物学靶标。我们试图在同一分子中将N-甲基-d-天冬氨酸受体拮抗作用的神经保护作用与通过乙酰胆碱酯酶抑制作用所产生的胆碱能活性所缓解的症状相结合。这种策略可能会保持美金刚-乙酰胆碱酯酶抑制剂组合的积极结果,但具有单分子疗法的益处。在本文中,我们讨论了多功能化合物的一些选定实例,我们对其进行合理设计以同时调节这些目标。我们还检查了神经毒性级联反应中乙酰胆碱酯酶,N-甲基-d-天冬氨酸受体和其他活跃分子之间的相互缠绕的关系。

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