Acetylcholinesterase-inhibitory activity of Iranian plants: Combined HPLC/bioassay-guided fractionation, molecular networking and docking strategies for the dereplication of active compounds

被引:36
作者
Abbas-Mohammadi, Mandi [1 ,2 ]
Farimani, Mandi Moridi [1 ]
Salehi, Peyman [1 ]
Ebrahimi, Samad Nejad [1 ]
Sonboli, Ali [1 ]
Kelso, Celine [2 ]
Skropeta, Danielle [2 ]
机构
[1] Shahid Beheshti Univ, GC, Med Plants & Drugs Res Inst, Dept Phytochem, Tehran, Iran
[2] Univ Wollongong, Sch Chem, Wollongong, NSW 2500, Australia
关键词
Acetylcholinesterase inhibitors; Ellman assay; Molecular networking; HPLC-ESI-QToF-MS/MS; Molecular docking; Prangos ferulacea; ALZHEIMERS-DISEASE; NATURAL-PRODUCTS; ANGELICA-DAHURICA; PRANGOS-FERULACEA; COUMARINS; EXTRACTS; DATABASE; ROOTS; CHOLINESTERASE;
D O I
10.1016/j.jpba.2018.06.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In order to search for discovery of acetylcholinesterase (AChE) inhibitors, as a therapeutic strategy for treatment of the Alzheimer's disease, twenty-five Iranian plants have been evaluated by an in vitro enzymatic Ellman method and molecular docking study. Each plant was successively extracted by n-hexane, ethyl acetate and methanol to obtain a total of 75 extracts. The inhibiting effect of extracts was measured by a colorimetric assay in 96-well microplates. The n-hexane extract of Prangos ferulacea showed the highest AChE inhibitory activity with 75.6% inhibition at a concentration of 50 mu g/mL. The chemical composition of this extract was investigated in detail based on a combination of HPLC/bioassay-guided fractionation and molecular networking techniques. The results led to the identification of seventeen compounds, one of them was a fatty acid derivative, two compounds had flavonoid structure and others were furanocoumarin type compounds. In vitro analysis showed that the subfraction F-10f was the most potent inhibitor against the activity of AChE with an IC50 value of 25.2 mu g/mL and good docking scores of its constituents confirming its high activity. (C) 2018 Elsevier B.V. All rights reserved.
引用
收藏
页码:471 / 479
页数:9
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