Next Article in Journal
Quantification of Sesquiterpene Lactones in Asteraceae Plant Extracts: Evaluation of their Allergenic Potential
Previous Article in Journal
Synthesis by Ring-Closing Metathesis and Cytotoxic Evaluation of Novel Thienylmacrolactones
 
 
Scientia Pharmaceutica is published by MDPI from Volume 84 Issue 3 (2016). Previous articles were published by another publisher in Open Access under a CC-BY (or CC-BY-NC-ND) licence, and they are hosted by MDPI on mdpi.com as a courtesy and upon agreement with Austrian Pharmaceutical Society (Österreichische Pharmazeutische Gesellschaft, ÖPhG).
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity

by
Hamid-Reza ADHAMI
1,*,
Johannes LUTZ
1,
Hanspeter KÄHLIG
2,
Martin ZEHL
1 and
Liselotte KRENN
1
1
Department of Pharmacognosy, University of Vienna, Althanstraße 14, 1090 Vienna, Austria
2
Institute of Organic Chemistry, University of Vienna, Währingerstraße 38, 1090 Vienna, Austria
*
Author to whom correspondence should be addressed.
Sci. Pharm. 2013, 81(3), 793-806; https://doi.org/10.3797/scipharm.1306-16
Submission received: 28 June 2013 / Accepted: 12 August 2013 / Published: 12 August 2013

Abstract

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 1H and 13C 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 IC50 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.
Keywords: Dorema ammoniacum; Acetylcholinesterase inhibition; Doremone A; Dshamirone; Ammoresinol; Spiro-sesquiterpenoidic chromane-2,4-dione Dorema ammoniacum; Acetylcholinesterase inhibition; Doremone A; Dshamirone; Ammoresinol; Spiro-sesquiterpenoidic chromane-2,4-dione

Share and Cite

MDPI and ACS Style

ADHAMI, H.-R.; LUTZ, J.; KÄHLIG, H.; ZEHL, M.; KRENN, L. Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity. Sci. Pharm. 2013, 81, 793-806. https://doi.org/10.3797/scipharm.1306-16

AMA Style

ADHAMI H-R, LUTZ J, KÄHLIG H, ZEHL M, KRENN L. Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity. Scientia Pharmaceutica. 2013; 81(3):793-806. https://doi.org/10.3797/scipharm.1306-16

Chicago/Turabian Style

ADHAMI, Hamid-Reza, Johannes LUTZ, Hanspeter KÄHLIG, Martin ZEHL, and Liselotte KRENN. 2013. "Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity" Scientia Pharmaceutica 81, no. 3: 793-806. https://doi.org/10.3797/scipharm.1306-16

APA Style

ADHAMI, H. -R., LUTZ, J., KÄHLIG, H., ZEHL, M., & KRENN, L. (2013). Compounds from Gum Ammoniacum with Acetylcholinesterase Inhibitory Activity. Scientia Pharmaceutica, 81(3), 793-806. https://doi.org/10.3797/scipharm.1306-16

Article Metrics

Back to TopTop