淀粉样蛋白(真菌学)
神经科学
磺胺
路径(计算)
神经退行性变
疾病
计算生物学
化学
生物
医学
计算机科学
内科学
病理
立体化学
程序设计语言
作者
Joana Smirnovienė,Daumantas Matulis
出处
期刊:ChemMedChem
[Wiley]
日期:2025-09-01
卷期号:20 (19): e202500324-e202500324
被引量:1
标识
DOI:10.1002/cmdc.202500324
摘要
Protein amyloid aggregation is a critical pathological process implicated in nearly 50 amyloid-related diseases, including Alzheimer's and Parkinson's diseases. This review highlights the potential of sulfonamides, a versatile class of compounds recognized for their diverse pharmacological properties, as modulators of protein aggregation. We provide an overview of studies examining the efficacy of sulfonamide derivatives in inhibiting the aggregation of various amyloidogenic proteins, including amyloid-beta, tau, alpha-synuclein, insulin, and transthyretin. In vitro assays, such as Thioflavin T fluorescence and high-resolution imaging techniques, have shown that certain sulfonamides can significantly inhibit fibril formation and promote the stabilization of non-aggregated protein states. The potential for sulfonamides to serve as multi-target agents offers new avenues for therapeutic development. By integrating findings from current research, we support a proposal that sulfonamide-based compounds could play a pivotal role in addressing the multifaceted nature of amyloid-related neurodegenerative diseases, paving the way for innovative therapeutic strategies.
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