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呋喃香豆素类化合物从当归根和果实中对丁酰胆碱酯酶抑制活性的生物活性导向分离。

Bioactivity-guided fractionation for the butyrylcholinesterase inhibitory activity of furanocoumarins from Angelica archangelica L. roots and fruits.

机构信息

Department of Pharmacognosy and Molecular Basis of Phytotherapy, Medical University of Warsaw, Banacha 1, 02-097, Warsaw, Poland.

出版信息

J Agric Food Chem. 2011 Sep 14;59(17):9186-93. doi: 10.1021/jf201971s. Epub 2011 Aug 9.

Abstract

Isolation and identification of the inhibitors of butyrylcholinesterase (BChE), obtained from the extracts of roots and fruits of Angelica archangelica L., are reported. Our results confirmed the weak inhibitory effect of Angelica roots on acetylcholinesterase activity. BChE inhibition was much more pronounced at a concentration of 100 μg/mL for hexane extracts and attained a higher rate than 50%. The TLC bioautography guided fractionation and spectroscopic analysis led to the isolation and identification of imperatorin from the fruit's hexane extract and of heraclenol-2'-O-angelate from the root's hexane extract. Both compounds showed significant BChE inhibition activity with IC(50) = 14.4 ± 3.2 μM and IC(50) = 7.5 ± 1.8 μM, respectively. Only C8-substituted and C5-unsubstituted furanocoumarins were active, which could supply information about the initial structures of specific BChE inhibitors.

摘要

本研究报告了从当归根和果实提取物中分离得到的丁酰胆碱酯酶(BChE)抑制剂。我们的结果证实了当归根对乙酰胆碱酯酶活性的弱抑制作用。在 100μg/mL 浓度下,正己烷提取物对 BChE 的抑制作用更为明显,抑制率超过 50%。TLC 生物自显影引导的分步分离和光谱分析导致从果实的正己烷提取物中分离鉴定出欧前胡素,从根的正己烷提取物中分离鉴定出白芷素-2'-O-当归酸酯。这两种化合物均表现出显著的 BChE 抑制活性,IC50 值分别为 14.4±3.2 μM 和 7.5±1.8 μM。只有 C8 取代和 C5 未取代的呋喃香豆素具有活性,这为特定 BChE 抑制剂的初始结构提供了信息。

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