Laboratory of Organic Chemistry, Department of Chemistry, National and Kapodistrian University of Athens, Athens, Greece.
Department of Pharmacy, "G. D'Annunzio" University of Chieti-Pescara, 66100, Chieti Scalo, CH, Italy.
Eur J Med Chem. 2020 Jan 15;186:111880. doi: 10.1016/j.ejmech.2019.111880. Epub 2019 Nov 12.
To date, drugs that hit a single target are inadequate for the treatment of neurodegenerative diseases, such as Alzheimer's or Parkinson's diseases. The development of multitarget ligands, able to interact with the different pathways involved in the progession of these disorders, represents a great challenge for medicinal chemists. In this context, we report here the synthesis and biological evaluation of phenol-lipoyl hybrids (SV1-13), obtained via a linking strategy, to take advantage of the synergistic effect due to the antioxidant portions and anti-amyloid properties of the single constituents present in the hybrid molecule. Biological results showed that SV5 and SV10 possessed the best protective activity against Aβ induced neurotoxicity in differentiated SH-SY5Y cells. SV9 and SV10 showed remarkable antioxidant properties due to their ability to counteract the damage caused by HO in SHSY-5Y-treated cells. Hovewer, SV5, showing moderate antioxidant and good neuroprotective activities, resulted the best candidate for further experiments since it also resulted stable both simulated and plasma fluids.
迄今为止,针对阿尔茨海默病或帕金森病等神经退行性疾病,单一靶点药物的治疗效果并不理想。因此,开发能够与这些疾病进展过程中涉及的不同途径相互作用的多靶标配体,对药物化学家来说是一个巨大的挑战。在这种情况下,我们报告了酚酰基杂合体(SV1-13)的合成和生物学评价,这些杂合体是通过连接策略获得的,以利用存在于杂合体分子中的单个成分的抗氧化部分和抗淀粉样蛋白特性所产生的协同作用。生物学结果表明,SV5 和 SV10 对分化的 SH-SY5Y 细胞中 Aβ 诱导的神经毒性具有最佳的保护活性。SV9 和 SV10 由于能够抵抗 HO 在 SHSY-5Y 处理细胞中造成的损伤,因此具有显著的抗氧化特性。然而,SV5 表现出适度的抗氧化和良好的神经保护活性,是进一步实验的最佳候选者,因为它在模拟和血浆流体中也表现出稳定性。