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(±)-:Pentatarget-导向配体,兼具胆碱酯酶、单胺氧化酶和糖原合成酶激酶 3β抑制作用,以及钙通道拮抗和抗聚集作用,可用于治疗阿尔茨海默病。

(±)-: Pentatarget-Directed Ligand combining Cholinesterase, Monoamine Oxidase, and Glycogen Synthase Kinase 3β Inhibition with Calcium Channel Antagonism and Antiaggregating Properties for Alzheimer's Disease.

机构信息

Neurosciences intégratives et cliniques EA 481, Univ. Bourgogne Franche-Comté, F-25000 Besançon, France.

Servicio de Farmacología Clínica, Instituto de Investigación Sanitaria, Hospital Universitario de la Princesa, C/Diego de León, 62, 28006 Madrid, Spain.

出版信息

ACS Chem Neurosci. 2021 Apr 21;12(8):1328-1342. doi: 10.1021/acschemneuro.0c00803. Epub 2021 Apr 2.

Abstract

Multitarget-directed ligands (MTDLs) are considered a promising therapeutic strategy to address the multifactorial nature of Alzheimer's disease (AD). Novel MTDLs have been designed as inhibitors of human acetylcholinesterases/butyrylcholinesterases, monoamine oxidase A/B, and glycogen synthase kinase 3β and as calcium channel antagonists via the Biginelli multicomponent reaction. Among these MTDLs, (±) was identified as a promising new hit compound showing balanced activities toward the aforementioned recognized AD targets. Additional studies demonstrated antioxidant effects and brain penetration, along with the ability to inhibit the aggregation of both τ protein and β-amyloid peptide. The studies have shown that (±) (10 mg/kg intraperitoneally) significantly reduces scopolamine-induced cognitive deficits.

摘要

多靶点配体(MTDLs)被认为是一种有前途的治疗策略,可以解决阿尔茨海默病(AD)的多因素性质。新型 MTDLs 被设计为人类乙酰胆碱酯酶/丁酰胆碱酯酶、单胺氧化酶 A/B 和糖原合酶激酶 3β的抑制剂,以及通过比格利尼多组分反应的钙通道拮抗剂。在这些 MTDLs 中,(±)被鉴定为一种有前途的新发现化合物,对上述公认的 AD 靶点表现出平衡的活性。进一步的研究表明,它具有抗氧化作用和脑穿透能力,以及抑制τ蛋白和β-淀粉样肽聚集的能力。研究表明,(±)(腹腔内 10mg/kg)显著减少东莨菪碱诱导的认知缺陷。

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