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具有胆碱能、抗氧化、生物金属螯合和神经保护特性的多功能灯盏花乙素-卡巴拉汀杂合物用于治疗阿尔茨海默病。

Multifunctional scutellarin-rivastigmine hybrids with cholinergic, antioxidant, biometal chelating and neuroprotective properties for the treatment of Alzheimer's disease.

作者信息

Sang Zhipei, Li Yan, Qiang Xiaoming, Xiao Ganyuan, Liu Qiang, Tan Zhenghuai, Deng Yong

机构信息

Department of Medicinal Chemistry, Key Laboratory of Drug Targeting and Drug Delivery System of the Education Ministry, West China School of Pharmacy, Sichuan University, Chengdu 610041, China.

Institute of Traditional Chinese Medicine Pharmacology and Toxicology, Sichuan Academy of Chinese Medicine Sciences, Chengdu 610041, China.

出版信息

Bioorg Med Chem. 2015 Feb 15;23(4):668-80. doi: 10.1016/j.bmc.2015.01.005. Epub 2015 Jan 8.

Abstract

To discover multifunctional agents for the treatment of Alzheimer's disease (AD), a series of scutellarein carbamate derivatives were designed and synthesized based on the multitarget-directed ligand strategy. Their acetylcholinesterase and butyrylcholinesterase inhibitory activities, antioxidant activities, metal-chelating properties and neuroprotective effects against hydrogen peroxide induced PC12 cell injury were evaluated in vitro. The results showed that most of the synthetic compounds exhibited good multifunctional activities. In particular, compound 15c exhibited dual inhibitory potency on acetylcholinesterase and butyrylcholinesterase with IC50 values of 0.57 and 22.6μM, respectively, and good antioxidative activity, with a value 1.3-fold of Trolox. In addition, 15c acted as a selective biometal chelator and possessed neuroprotective effects. Furthermore, 15c could cross the blood-brain barrier (BBB) in vitro and had significant neuroprotective effects in scopolamine-induced cognitive impairment in mice. Taken together, these results suggest that compound 15c might be a potential multifunctional agent for the treatment of AD.

摘要

为了发现用于治疗阿尔茨海默病(AD)的多功能药物,基于多靶点导向配体策略设计并合成了一系列黄芩素氨基甲酸酯衍生物。在体外评估了它们的乙酰胆碱酯酶和丁酰胆碱酯酶抑制活性、抗氧化活性、金属螯合特性以及对过氧化氢诱导的PC12细胞损伤的神经保护作用。结果表明,大多数合成化合物表现出良好的多功能活性。特别是,化合物15c对乙酰胆碱酯酶和丁酰胆碱酯酶具有双重抑制效力,IC50值分别为0.57和22.6μM,并且具有良好的抗氧化活性,其值为曲洛昔芬的1.3倍。此外,15c作为一种选择性生物金属螯合剂,具有神经保护作用。此外,15c在体外可穿过血脑屏障(BBB),并对东莨菪碱诱导的小鼠认知障碍具有显著的神经保护作用。综上所述,这些结果表明化合物15c可能是一种治疗AD的潜在多功能药物。

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