dc.creatorArdiles, Alejandro
dc.creatorBarrientos, Ruth
dc.creatorSimirgiotis, Mario J.
dc.creatorBórquez, Jorge
dc.creatorSepúlveda, Beatriz
dc.creatorAreche, Carlos
dc.date.accessioned2018-12-20T14:22:54Z
dc.date.available2018-12-20T14:22:54Z
dc.date.created2018-12-20T14:22:54Z
dc.date.issued2018
dc.identifierMolecules, Volumen 23, Issue 9, 2018,
dc.identifier14203049
dc.identifier10.3390/molecules23092361
dc.identifierhttps://repositorio.uchile.cl/handle/2250/155793
dc.description.abstract© 2018 MDPI AG. All rights reserved. Forty-three metabolites including several methoxylated flavonoids, tremetones, and ent-clerodane diterpenes were accurately identified for the first time in the ethanolic extract of P. quadrangularis by means of hyphenated UHPLC-quadrupole Orbitrap mass spectrometry, and seven isolated compounds were tested regarding gastroprotective activity using the HCl/EtOH-induced lesion model in mice. A new tremetone (compound 6) is reported based on spectroscopic evidence. The isolated clerodanes and tremetones showed gastroprotective activity in a mouse model, evidenced by compound 7 (p-coumaroyloxytremetone), which showed the highest gastroprotective activity (76%), which was higher than the control drug lansoprazole (72%). Our findings revealed that several constituents of this plant have gastroprotective activity, and particularly, p-coumaroyloxytremetone could be considered as a lead molecule to explore new gastroprotective agents. This plant is a rich s
dc.languageen
dc.publisherMDPI AG
dc.rightshttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
dc.sourceMolecules
dc.subjectClerodanes
dc.subjectEndemic plants
dc.subjectGastric ulcer
dc.subjectGastroprotective
dc.subjectLC-MS/MS
dc.subjectTremetones
dc.titleGastroprotective activity of Parastrephia quadrangularis (Meyen), cabrera from the atacama desert
dc.typeArtículos de revistas


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