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Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity
The use of herbal medicinal preparations in dementia therapy has been studied based on experience from traditional medicine. A dichloromethane extract of gum ammoniacum, the gum-resin from Dorema ammoniacum D. Don had shown acetylcholinesterase (AChE) inhibitory activity in a previous study. The aim...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Österreichische Apotheker-Verlagsgesellschaft
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791940/ https://www.ncbi.nlm.nih.gov/pubmed/24106674 http://dx.doi.org/10.3797/scipharm.1306-16 |
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author | Adhami, Hamid-Reza Lutz, Johannes Kählig, Hanspeter Zehl, Martin Krenn, Liselotte |
author_facet | Adhami, Hamid-Reza Lutz, Johannes Kählig, Hanspeter Zehl, Martin Krenn, Liselotte |
author_sort | Adhami, Hamid-Reza |
collection | PubMed |
description | The use of herbal medicinal preparations in dementia therapy has been studied based on experience from traditional medicine. A dichloromethane extract of gum ammoniacum, the gum-resin from Dorema ammoniacum D. Don had shown acetylcholinesterase (AChE) inhibitory activity in a previous study. The aim of this study was the isolation and characterization of the active compounds from this resin. The extract was investigated by a respective colorimetric microplate assay and the active zones were identified via TLC bioautography and isolated using several chromatographic techniques. The structures of the active components were characterized by one- and two-dimensional (1)H and (13)C NMR spectroscopy and mass spectrometry as (2′S,5′S)-2′-ethenyl-5′-(3-hy-droxy-6-methyl-4-oxohept-5-en-2-yl)-7-methoxy-2′-methyl-4H-spiro[chromene-3,1′-cyclopentane]-2,4-dione (1), which is an analogue of doremone A and a new natural compound, and as (2′S,5′R)-2′-ethenyl-5′-[(2R,4R)-4-hydroxy-6-methyl-3-oxohept-5-en-2-yl]-7-methoxy-2′-methyl-4H-spiro[chromene-3,1′-cyclo-pentane]-2,4-dione (2 = doremone A), (4E,8E)-1-(2,4-dihydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one (3 = dshamirone), and 4,7-dihydroxy-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-2H-chromen-2-one (4 = am-moresinol). Dshamirone turned out to be the most active compound with an IC(50) value for AChE inhibitory activity of 23.5 μM, whereas the other substances showed weak activity. The concentrations of the analytes in the resin were determined by HPLC as 3.1%, 4.6%, 1.9%, and 9.9%, respectively. |
format | Online Article Text |
id | pubmed-3791940 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Österreichische Apotheker-Verlagsgesellschaft |
record_format | MEDLINE/PubMed |
spelling | pubmed-37919402013-10-08 Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity Adhami, Hamid-Reza Lutz, Johannes Kählig, Hanspeter Zehl, Martin Krenn, Liselotte Sci Pharm Research Article The use of herbal medicinal preparations in dementia therapy has been studied based on experience from traditional medicine. A dichloromethane extract of gum ammoniacum, the gum-resin from Dorema ammoniacum D. Don had shown acetylcholinesterase (AChE) inhibitory activity in a previous study. The aim of this study was the isolation and characterization of the active compounds from this resin. The extract was investigated by a respective colorimetric microplate assay and the active zones were identified via TLC bioautography and isolated using several chromatographic techniques. The structures of the active components were characterized by one- and two-dimensional (1)H and (13)C NMR spectroscopy and mass spectrometry as (2′S,5′S)-2′-ethenyl-5′-(3-hy-droxy-6-methyl-4-oxohept-5-en-2-yl)-7-methoxy-2′-methyl-4H-spiro[chromene-3,1′-cyclopentane]-2,4-dione (1), which is an analogue of doremone A and a new natural compound, and as (2′S,5′R)-2′-ethenyl-5′-[(2R,4R)-4-hydroxy-6-methyl-3-oxohept-5-en-2-yl]-7-methoxy-2′-methyl-4H-spiro[chromene-3,1′-cyclo-pentane]-2,4-dione (2 = doremone A), (4E,8E)-1-(2,4-dihydroxyphenyl)-5,9,13-trimethyltetradeca-4,8,12-trien-1-one (3 = dshamirone), and 4,7-dihydroxy-3-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trien-1-yl]-2H-chromen-2-one (4 = am-moresinol). Dshamirone turned out to be the most active compound with an IC(50) value for AChE inhibitory activity of 23.5 μM, whereas the other substances showed weak activity. The concentrations of the analytes in the resin were determined by HPLC as 3.1%, 4.6%, 1.9%, and 9.9%, respectively. Österreichische Apotheker-Verlagsgesellschaft 2013 2013-08-12 /pmc/articles/PMC3791940/ /pubmed/24106674 http://dx.doi.org/10.3797/scipharm.1306-16 Text en © Adhami et al.; licensee Österreichische Apotheker-Verlagsgesellschaft m. b. H., Vienna, Austria. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Adhami, Hamid-Reza Lutz, Johannes Kählig, Hanspeter Zehl, Martin Krenn, Liselotte Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title | Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title_full | Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title_fullStr | Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title_full_unstemmed | Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title_short | Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity |
title_sort | compounds from gum ammoniacum with acetylcholinesterase inhibitory activity |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3791940/ https://www.ncbi.nlm.nih.gov/pubmed/24106674 http://dx.doi.org/10.3797/scipharm.1306-16 |
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