Rana Monika, Terpstra Karna, Gutierrez Citlali, Xu Kerui, Arya Hemant, Bhatt Tarun K, Mirica Liviu M, Sharma Anuj K
Department of Chemistry, Central University of Rajasthan, Bandarsindri, Ajmer, 305817, India.
Department of Chemistry, University of Illinois at Urbana-Champaign, 600 S. Mathews Avenue, Urbana, Illinois, 61801, USA.
Chemistry. 2025 Jan 9;31(2):e202402748. doi: 10.1002/chem.202402748. Epub 2024 Nov 18.
Inhibition of amyloid β (Aβ) aggregation and cholinesterase activity are two major therapeutic targets for Alzheimer's disease (AD). Multifunctional Molecules (MFMs) specifically designed to address other contributing factors, such as metal ion induced abnormalities, oxidative stress, toxic Aβ aggregates etc. are very much required. Several multifunctional molecules have been developed using different molecular scaffolds. Reported herein is a new series of four MFMs based on ThT, Azo-stilbene and metal ion chelating pockets. The synthesis, characterization, and metal chelation ability for [Cu and Zn] are presented herein. Furthermore, we explored their multifunctionality w.r.t. to their (i) recognition of Aβ aggregates and monomeric form, (ii) utility in modulating the aggregation pathways of both metal-free and metal-bound amyloid-β, (iii) ex-vivo staining of amyloid plaques in 5xFAD mice brain sections, (iv) ability to scavenge free radicals and (v) ability to inhibit cholinesterase activity. Molecular docking studies were also performed with Aβ peptides and acetylcholinesterase enzyme to understand the observed inhibitory effect on activity. Overall, the studies presented here establish the multifunctional nature of these molecules and qualify them as promising candidates for furthermore investigation in the quest for finding Alzheimer's disease treatment.
抑制淀粉样β蛋白(Aβ)聚集和胆碱酯酶活性是阿尔茨海默病(AD)的两个主要治疗靶点。迫切需要专门设计用于解决其他促成因素的多功能分子(MFMs),例如金属离子诱导的异常、氧化应激、有毒Aβ聚集体等。已经使用不同的分子支架开发了几种多功能分子。本文报道了一系列基于硫黄素T(ThT)、偶氮芪和金属离子螯合口袋的新型多功能分子,共四种。本文介绍了它们的合成、表征以及对[铜和锌]的金属螯合能力。此外,我们还探索了它们在以下方面的多功能性:(i)识别Aβ聚集体和单体形式;(ii)调节无金属和金属结合的淀粉样β蛋白聚集途径的效用;(iii)对5xFAD小鼠脑切片中淀粉样斑块的体外染色;(iv)清除自由基的能力;(v)抑制胆碱酯酶活性的能力。还对Aβ肽和乙酰胆碱酯酶进行了分子对接研究,以了解观察到的对活性的抑制作用。总体而言,本文的研究确定了这些分子的多功能性质,并使其有资格作为寻找阿尔茨海默病治疗方法的进一步研究中有希望的候选物。