New cholinesterase inhibiting bisbenzylisoquinoline alkaloids from Abuta grandifolia

被引:24
作者
Cometa, Maria Francesca [2 ]
Fortuna, Stefano [2 ]
Palazzino, Giovanna [2 ]
Volpe, Maria Teresa [2 ]
Rengifo Salgado, Elsa [3 ]
Nicoletti, Marcello [1 ]
Tomassini, Lamberto [1 ]
机构
[1] Univ Roma La Sapienza, Dept Environm Biol, I-00185 Rome, Italy
[2] Ist Super Sanita, Dept Therapeut Res & Med Evaluat, I-00161 Rome, Italy
[3] Ctr Invest Allpahuayo, IIAP, Maynas, Loreto, Peru
关键词
Abuta grandifolia; Menispermaceae; Bisbenzylisoquinoline alkaloids; AChE inhibitor; BChE inhibitor; Alzheimer's disease; ALZHEIMERS-DISEASE; SENILE-DEMENTIA; ACETYLCHOLINESTERASE; BUTYRYLCHOLINESTERASE; PLANTS;
D O I
10.1016/j.fitote.2011.12.015
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The phytochemical study of the stem bark and wood of Abuta grandifolia (Mart.) Sandwith led to the identification of four bisbenzylisoquinoline alkaloids (BBIQs), namely (R,S)-2 N-norberbamunine (1), (R,R)-isochondodendrine (2), (S-S)-O4 ''-methyl, Nb-nor-O6 '-demethyl-(+)-curine (3), and (S-S)-O4 ''-methyl, O6 '-demethyl-(+)-curine (4), together with the aporphine alkaloid R-nomuciferine (5), all obtained by countercurrent distribution separation (CCD) and identified on the basis of their spectroscopic data. Alkaloids 3 and 4 were new. All the isolated compounds were tested for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibitory activities. 1 was the most active against AChE, whereas 3 and 4 were the most potent against BChE. interestingly, all tested alkaloids are more potent against BChE than against AChE. This selectivity of cholinesterase (ChE) inhibition could be important in order to speculate on their potential therapeutic relevance. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:476 / 480
页数:5
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