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丁苯酞-野黄芩苷杂合体的合成与评价:一种用于治疗阿尔茨海默病的多功能药物。

Synthesis and evaluation of butylphthalide-scutellarein hybrids as multifunctional agents for the treatment of Alzheimer's disease.

机构信息

Department of Medicinal Chemistry, Key Laboratory of Drug-Targeting and Drug Delivery System of the Education Ministry and Sichuan Province, Central Nervous System Drug Key Laboratory of Sichuan Province, 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

Eur J Med Chem. 2024 Feb 5;265:116099. doi: 10.1016/j.ejmech.2023.116099. Epub 2023 Dec 26.

Abstract

A series of butylphthalide and scutellarein hybrids 3-(alkyl/alkenyl) hydroxyphthalide derivatives were designed, synthesized and evaluated as multifunctional agents against Alzheimer's disease. In vitro bioactivity assays indicated that most of the compounds displayed excellent antioxidant activity and moderate to good inhibition activities of self-induced Aβ aggregation. Among them, compound 7c was demonstrated as a potential and balanced multifunctional candidate displaying the best inhibitory effects on self- and Cu-induced Aβ aggregation (90.2 % and 35.4 %, respectively) and moderate activity for disaggregation of Aβ aggregation (42.5 %). In addition, 7c also displayed excellent antioxidant (2.42 Trolox equivalents), metal ions chelating, oxidative stress alleviation, neuroprotective and anti-neuroinflammatory activities. Furthermore, in vivo study demonstrated that 7c could ameliorate the learning and memory impairment induced by sodium nitrite and Aβ in the step-down passive avoidance test. These balanced multifunctional profiles supporting compound 7c as a novel potential candidate for the treatment of AD.

摘要

一系列丁基苯酞和野黄芩苷的杂合体 3-(烷基/烯基)羟苯酞衍生物被设计、合成并评估为治疗阿尔茨海默病的多功能药物。体外生物活性测定表明,大多数化合物表现出优异的抗氧化活性和适度至良好的自诱导 Aβ聚集抑制活性。其中,化合物 7c 被证明是一种具有潜力和平衡多功能的候选药物,对自诱导和 Cu 诱导的 Aβ聚集具有最佳的抑制作用(分别为 90.2%和 35.4%),对 Aβ聚集的解聚具有适度的活性(42.5%)。此外,7c 还表现出优异的抗氧化(2.42 Trolox 当量)、金属离子螯合、氧化应激缓解、神经保护和抗神经炎症活性。此外,体内研究表明,7c 可改善亚硝酸钠和 Aβ在跳下被动回避试验中引起的学习和记忆障碍。这些平衡的多功能特性支持化合物 7c 作为一种新型的潜在候选药物用于治疗 AD。

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