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设计、合成并评价氟比洛芬-氯碘喹啉杂合体作为抗阿尔茨海默病的多靶标导向配体。

Design, synthesis and evaluation of flurbiprofen-clioquinol hybrids as multitarget-directed ligands against 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, Sichuan Engineering Laboratory for Plant-Sourced Drug and Sichuan Research Center for Drug Precision Industrial Technology, West China School of Pharmacy, Sichuan University, Chengdu 610041, PR China.

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

出版信息

Bioorg Med Chem. 2020 Apr 1;28(7):115374. doi: 10.1016/j.bmc.2020.115374. Epub 2020 Feb 13.

Abstract

A series of novel flurbiprofen-clioquinol hybrids were designed and synthesized as multifunctional agents for Alzheimer's disease therapy, and their potential was evaluated through various biological experiments. In vitro studies showed that most target compounds exhibited significant ability to inhibit self- and Cu-induced β-amyloid aggregation. Furthermore, some target compounds, especially 7i and 7r, also showed biometal chelating abilities, antioxidant activity, anti-neuroinflammatory activity and appropriate BBB permeability. These biological activities indicated that the representative compound 7i and 7r might be promising multifunctional agents for AD treatment.

摘要

设计并合成了一系列新型氟比洛芬-氯碘喹啉杂合体作为治疗阿尔茨海默病的多功能药物,并通过各种生物学实验评估了它们的潜力。体外研究表明,大多数目标化合物具有显著抑制自身和 Cu 诱导的β-淀粉样蛋白聚集的能力。此外,一些目标化合物,特别是 7i 和 7r,还表现出生物金属螯合能力、抗氧化活性、抗神经炎症活性和适当的 BBB 通透性。这些生物学活性表明,代表性化合物 7i 和 7r 可能是治疗 AD 的有前途的多功能药物。

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