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首页> 外文期刊>European Journal of Medicinal Chemistry: Chimie Therapeutique >Aurone Mannich base derivatives as promising multifunctional agents with acetylcholinesterase inhibition, anti-beta-amyloid aggragation and neuroprotective properties for the treatment of Alzheimer's disease
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Aurone Mannich base derivatives as promising multifunctional agents with acetylcholinesterase inhibition, anti-beta-amyloid aggragation and neuroprotective properties for the treatment of Alzheimer's disease

机译:Aurone Mannich基础衍生物作为具有乙酰胆碱酯酶抑制,抗β-淀粉样蛋白的抑制作用和神经保护性的抗β-淀粉样蛋白的疾病,治疗阿尔茨海默病

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A series of aurone Mannich base derivatives were designed, synthesized and evaluated as multifunctional agents for the treatment of Alzheimer's disease. in vitro assays demonstrated that most of the derivatives were selective AChE inhibitors with good multifunctional properties. Among them, compound 7d exhibited outstanding inhibitory activity for RatAChE, EeAChE and HuAChE (IC50 = 0.00878 +/- 0.0002 mu M, 0.0212 +/- 0.006 mu M and 0.0371 +/- 0.004 mu M, respectively). Moreover, 7d displayed high antioxidant activity and could confer significant neuroprotective effect against H2O2-induced PC-12 cell injury. In addition, 7d also showed biometal chelating abilities, good self- and Cu2+-induced A beta(1-42) aggregation inhibitory potency and high BBB permeability. These multifunctional properties highlight 7d as promising candidate for further studies directed to the development of novel drugs against AD. (C) 2016 Elsevier Masson SAS. All rights reserved.
机译:设计,合成和评估了一系列Aurone Mannich基础衍生物,用于治疗阿尔茨海默病的多功能药物。 体外测定证明,大多数衍生物是具有良好多功能性质的选择性疼痛抑制剂。 其中,化合物7D表现出对大鼠的突出抑制活性,eeache和Huache(IC50 = 0.00878 +/- 0.0212Mu m,0.0212 +/- 0.006 mu m和0.0371 +/- 0.004 mu m)。 此外,7D显示出高抗氧化活性,并且可以赋予H2O2诱导的PC-12细胞损伤的显着神经保护作用。 此外,7d还显示出生物螯合能力,良好的自我和Cu2 + - 诱导β(1-42)聚集抑制效力和高BBB渗透性。 这些多功能特性突出显示7D作为进一步研究的承诺候选者,用于针对广告的新药的发展。 (c)2016年Elsevier Masson SAS。 版权所有。

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