Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Adhami, Hamid-Reza, Lutz, Johannes, Kählig, Hanspeter, Zehl, Martin, Krenn, Liselotte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Österreichische Apotheker-Verlagsgesellschaft 2013
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
_version_ 1782286775617585152
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
work_keys_str_mv AT adhamihamidreza compoundsfromgumammoniacumwithacetylcholinesteraseinhibitoryactivity
AT lutzjohannes compoundsfromgumammoniacumwithacetylcholinesteraseinhibitoryactivity
AT kahlighanspeter compoundsfromgumammoniacumwithacetylcholinesteraseinhibitoryactivity
AT zehlmartin compoundsfromgumammoniacumwithacetylcholinesteraseinhibitoryactivity
AT krennliselotte compoundsfromgumammoniacumwithacetylcholinesteraseinhibitoryactivity