Novel polyacetylene derivatives and their inhibitory activities on acetylcholinesterase obtained from Panax ginseng roots

被引:22
作者
Murata, Kazuya [1 ]
Iida, Daiki [1 ]
Ueno, Yoshihiro [1 ]
Samukawa, Keiichi [2 ]
Ishizaka, Toshihiko [3 ]
Kotake, Takeshi [1 ]
Matsuda, Hideaki [1 ]
机构
[1] Kindai Univ, Fac Pharm, 3-4-1 Kowakae, Higashiosaka, Osaka 5778502, Japan
[2] Osaka City Univ, Fac Med, Abeno Ku, 1-4-3 Asahimachi, Osaka 5458585, Japan
[3] Sakai City Med Ctr, Nishi Ku, 1-1-1 Ebaraji Cho, Sakai, Osaka 5938304, Japan
关键词
Acetylcholinesterase; Butyrylcholinesterase; Panax ginseng; Polyacetylene; ALZHEIMERS-DISEASE;
D O I
10.1007/s11418-016-1036-7
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In our research program to identify cholinesterase and beta-secretase inhibitors, we investigated Ginseng (root of Panax ginseng), a crude drug described as a multifunctional drug in the ancient Chinese herbal book Shennong Ben Cao Jing. Results from hexane and methanol extracts showed moderate inhibitory activities. This suggests that ginseng roots may be effective for the prevention of and therapy for dementia. We then focused on hexane extracts of raw ginseng root and dried ginseng root since the determination of hexane extract constituents has not been studied extensively. Activity-guided fractionation and purification led to the isolation of 4 polyacetylene compounds; homopanaxynol, homopanaxydol, (9Z)-heptadeca-1, 9-diene-4,6-diyn-3-one, and (8E)-octadeca-1,8-diene-4,6-diyn-3,10-diol. The chemical structures of these compounds, including stereochemistry, were determined. This is the first study to identify the structure of homopanaxynol and homopanaxydol. Moreover, the modes of action of some compounds were characterized as competitive inhibitors. This study showed, for the first time, that polyacetylene compounds possess acetylcholinesterase inhibitory activities.
引用
收藏
页码:114 / 122
页数:9
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