Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil
The purpose of this study was to investigate the chemical composition and anticholinesterase inhibitory activity of the essential oil obtained from Piper crassipes leaves collected from Malaysia. Twenty-two components were identified using gas chromatography-flame ionisation detection (GC-FID) and g...
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2024
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2-s2.0-85196320808 Rezod U.J.; Salleh W.M.N.H.W.; Salihu A.S.; Ab Ghani N. Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil 2024 Natural Product Research 10.1080/14786419.2024.2369225 https://www.scopus.com/inward/record.uri?eid=2-s2.0-85196320808&doi=10.1080%2f14786419.2024.2369225&partnerID=40&md5=320baeef16fb0c7dc895ada06481843b The purpose of this study was to investigate the chemical composition and anticholinesterase inhibitory activity of the essential oil obtained from Piper crassipes leaves collected from Malaysia. Twenty-two components were identified using gas chromatography-flame ionisation detection (GC-FID) and gas chromatography/mass spectrometry (GC-MS), which represent 97.8% of the essential oil. The identified major components included chavibetol (59.8%), chavibetol acetate (10.4%), γ-muurolene (5.4%), and germacrene D (4.6%). Anticholinesterase activity was assessed using Ellman’s method. A moderate inhibitory effect was observed for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes with IC50 values of 77.2 ± 0.2 and 89.2 ± 0.2 µg/mL, respectively. The molecular docking studies revealed that chavibetol acetate showed potent interactions with the cholinesterase target, while other compounds exhibited varied binding patterns, providing crucial insights into their potential as cholinesterase inhibitors. © 2024 Informa UK Limited, trading as Taylor & Francis Group. Taylor and Francis Ltd. 14786419 English Article All Open Access; Green Open Access |
author |
Rezod U.J.; Salleh W.M.N.H.W.; Salihu A.S.; Ab Ghani N. |
spellingShingle |
Rezod U.J.; Salleh W.M.N.H.W.; Salihu A.S.; Ab Ghani N. Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
author_facet |
Rezod U.J.; Salleh W.M.N.H.W.; Salihu A.S.; Ab Ghani N. |
author_sort |
Rezod U.J.; Salleh W.M.N.H.W.; Salihu A.S.; Ab Ghani N. |
title |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
title_short |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
title_full |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
title_fullStr |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
title_full_unstemmed |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
title_sort |
Chemical composition, anticholinesterase activity, and molecular docking studies of Piper crassipes Korth. ex Miq. essential oil |
publishDate |
2024 |
container_title |
Natural Product Research |
container_volume |
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container_issue |
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doi_str_mv |
10.1080/14786419.2024.2369225 |
url |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85196320808&doi=10.1080%2f14786419.2024.2369225&partnerID=40&md5=320baeef16fb0c7dc895ada06481843b |
description |
The purpose of this study was to investigate the chemical composition and anticholinesterase inhibitory activity of the essential oil obtained from Piper crassipes leaves collected from Malaysia. Twenty-two components were identified using gas chromatography-flame ionisation detection (GC-FID) and gas chromatography/mass spectrometry (GC-MS), which represent 97.8% of the essential oil. The identified major components included chavibetol (59.8%), chavibetol acetate (10.4%), γ-muurolene (5.4%), and germacrene D (4.6%). Anticholinesterase activity was assessed using Ellman’s method. A moderate inhibitory effect was observed for acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) enzymes with IC50 values of 77.2 ± 0.2 and 89.2 ± 0.2 µg/mL, respectively. The molecular docking studies revealed that chavibetol acetate showed potent interactions with the cholinesterase target, while other compounds exhibited varied binding patterns, providing crucial insights into their potential as cholinesterase inhibitors. © 2024 Informa UK Limited, trading as Taylor & Francis Group. |
publisher |
Taylor and Francis Ltd. |
issn |
14786419 |
language |
English |
format |
Article |
accesstype |
All Open Access; Green Open Access |
record_format |
scopus |
collection |
Scopus |
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1809678155529584640 |