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新型肉桂酰胺-二苄基胺杂合体:具有抗氧化、胆碱能和神经保护特性的强效神经生成剂,可作为治疗阿尔茨海默病的创新药物。

Novel cinnamamide-dibenzylamine hybrids: Potent neurogenic agents with antioxidant, cholinergic, and neuroprotective properties as innovative drugs for Alzheimer's disease.

机构信息

Jiangsu Key Laboratory of Bioactive Natural Product Research, State Key Laboratory of Natural Medicines, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, People's Republic of China.

Jiangsu Key Laboratory of Bioactive Natural Product Research, State Key Laboratory of Natural Medicines, China Pharmaceutical University, 24 Tong Jia Xiang, Nanjing 210009, People's Republic of China.

出版信息

Eur J Med Chem. 2017 Oct 20;139:68-83. doi: 10.1016/j.ejmech.2017.07.077. Epub 2017 Aug 1.

Abstract

By using fragments endowed with interesting and complementary properties for the treatment of Alzheimer's disease (AD), a novel series of cinnamamide-dibenzylamine hybrids have been designed, synthesized, and evaluated biologically. In vitro assay indicated that most of the target compounds exhibited a significant ability to inhibit ChEs, strong potency inhibitory of self-induced β-amyloid (Aβ) aggregation and to act as potential antioxidants and biometal chelators. A Lineweaver-Burk plot and molecular modeling study showed that compound 7f targeted both the CAS and PAS of AChE. In addition, compound 7f could chelate metal ions, reduce PC12 cells death induced by oxidative stress and penetrate the blood-brain barrier (BBB). Overall, all of these outstanding in vitro results in combination with promising in vivo outcomes highlighted derivative 7f as the lead structure worthy of further investigation.

摘要

通过利用具有治疗阿尔茨海默病(AD)的有趣和互补性质的片段,设计、合成并对一系列新型肉桂酰胺-二苄基胺杂合体进行了生物学评估。体外试验表明,大多数目标化合物具有显著抑制 ChE 的能力,强烈抑制自身诱导的β-淀粉样蛋白(Aβ)聚集的能力,以及作为潜在抗氧化剂和生物金属螯合剂的能力。Lineweaver-Burk 作图和分子建模研究表明,化合物 7f 靶向 AChE 的 CAS 和 PAS。此外,化合物 7f 可以螯合金属离子,减少氧化应激诱导的 PC12 细胞死亡,并穿透血脑屏障(BBB)。总的来说,所有这些出色的体外结果以及有前景的体内结果突出了衍生物 7f 作为值得进一步研究的先导结构。

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