Synthesis of Imperatorin Analogs and Their Evaluation as Acetylcholinesterase and Butyrylcholinesterase Inhibitors

被引:18
作者
Granica, Sebastian [1 ,2 ]
Kiss, Anna K. [2 ]
Jaronczyk, Malgorzata [3 ]
Maurin, Jan K. [3 ,4 ]
Mazurek, Aleksander P. [3 ]
Czarnocki, Zbigniew [1 ]
机构
[1] Univ Warsaw, Fac Chem, PL-02093 Warsaw, Poland
[2] Med Univ Warsaw, Fac Pharm, Dept Pharmacognosy & Mol Basis Phytotherapy, Warsaw, Poland
[3] Natl Med Inst, Warsaw, Poland
[4] Natl Ctr Nucl Res, Otwock, Poland
关键词
Acetylcholinesterase; Alzheimer's disease; Angelica archangelica; Butyrylcholinesterase; Furocoumarins; ANGELICA-DAHURICA; COUMARINS; FURANOCOUMARINS; DERIVATIVES; ROOTS; FUROCOUMARINS; CONSTITUENTS; COMPONENTS; SUBSTRATE; PSORALEN;
D O I
10.1002/ardp.201300259
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, we synthesized several imperatorin analogs using imperatorin and xanthotoxin as substrates. The anti-cholinesterase activities of all compounds were evaluated in in vitro experiments according to the modified Ellman's method. For each synthesized compound, IC50 values for both enzymes were established. Galantamine hydrobromide was used as a positive control in the enzymatic experiments. All active compounds showed selectivity toward butyrylcholinesterase (BuChE) rather than acetylcholinesterase. The most active ones were 8-(3-methylbutoxy)-psoralen and 8-hexoxypsoralen with IC50 values for BuChE of around 16.5 and 16.4 mu M, respectively. The results of our study may be considered as the beginning of a search for potential anti-Alzheimer's disease drugs based on the structure of natural furocoumarins.
引用
收藏
页码:775 / 782
页数:8
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