化学
生物信息学
芹菜素
生物化学
体外
槲皮素
黄酮醇
迷迭香酸
药效团
姜黄素
虚拟筛选
类黄酮
药理学
生物
抗氧化剂
基因
作者
Alba Espargaró,Tiziana Ginex,Maria del Mar Vadell,Maria Antònia Busquets,Joan Estelrich,Diego Muñoz‐Torrero,F. Javier Luque,Raimon Sabaté
标识
DOI:10.1021/acs.jnatprod.6b00643
摘要
Alzheimer's disease (AD) is the main cause of dementia in people over 65 years. One of the major culprits in AD is the self-aggregation of amyloid-β peptide (Aβ), which has stimulated the search for small molecules able to inhibit Aβ aggregation. In this context, we recently reported a simple, but effective in vitro cell-based assay to evaluate the potential antiaggregation activity of putative Aβ aggregation inhibitors. In this work this assay was used together with docking and molecular dynamics simulations to analyze the anti-Aβ aggregation activity of several naturally occurring flavonoids and phenolic compounds. The results showed that rosmarinic acid, melatonin, and o-vanillin displayed zero or low inhibitory capacity, curcumin was found to have an intermediate inhibitory potency, and apigenin and quercetin showed potent antiaggregation activity. Finally, the suitability of the combined in vitro cell-based/in silico approach to distinguish between active and inactive compounds was further assessed for an additional set of flavonols and dihydroflavonols.
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