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Arundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties

dc.rights.licenseopenen_US
dc.contributor.authorAUBERON, Florence
dc.contributor.authorOLATUNJI, Opeyemi Joshua
hal.structure.identifierUnité de Recherche Œnologie [Villenave d'Ornon] [OENO]
dc.contributor.authorWAFFO-TEGUO, Pierre
dc.contributor.authorOLATUNDE, Oladipupo Odunayo
dc.contributor.authorSINGH, Sudarshan
dc.contributor.authorBONTÉ, Frédéric
hal.structure.identifierUnité de Recherche Œnologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMÉRILLON, Jean-Michel
dc.contributor.authorLOBSTEIN, Annelise
dc.date.accessioned2023-11-28T13:10:06Z
dc.date.available2023-11-28T13:10:06Z
dc.date.issued2023-02
dc.identifier.issn0031-9422en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/186198
dc.description.abstractEnPhytochemical investigation of the underground parts of Arundina graminifolia D.Don Hochr was conducted leading to the isolation of nine new glucosyloxybenzyl 2R-benzylmalate and two new glucosyloxybenzyl 2R-isobutylmalate derivatives. The compounds were purified using chromatographic techniques and their structures were deduced based on spectroscopic techniques including nuclear magnetic resonance and high-resolution mass spectrometry as well as comparing with previous literature. The antioxidant activities of the isolated compounds were also evaluated. The compounds showed potent antioxidant activities in the ABTS radical scavenging, DPPH radical scavenging and FRAP activities. Furthermore, the isolated compounds were observed to exert minimal cytotoxic effects against RAW 264.7 cell, suggesting biocompatibility as well as cytoprotective effects against hydrogen peroxide induced cell toxicity.
dc.language.isoENen_US
dc.subject.enArundina graminifolia D.Don Hochr
dc.subject.enOrchidaceae
dc.subject.enGlucosyloxybenzyl 2R-benzylmalate derivatives
dc.subject.enGlucosyloxybenzyl 2R-isobutylmalate derivatives
dc.subject.enArundinosides I-IX
dc.subject.enGraminifolosides A-B
dc.title.enArundinosides I-IX and graminifolosides A-B: 2R-benzylmalate and 2R-isobutylmalates derivatives from Arundina graminifolia (D.Don) Hochr. with antioxidant, cytocompatibility and cytoprotective properties
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.phytochem.2022.113504en_US
dc.subject.halSciences du Vivant [q-bio]en_US
bordeaux.journalPhytochemistryen_US
bordeaux.page113504en_US
bordeaux.volume206en_US
bordeaux.hal.laboratoriesOenologie - UMR 1366en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcehal
hal.identifierhal-04114557
hal.version1
hal.popularnonen_US
hal.audienceInternationaleen_US
hal.exportfalse
workflow.import.sourcehal
dc.rights.ccPas de Licence CCen_US
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Phytochemistry&rft.date=2023-02&rft.volume=206&rft.spage=113504&rft.epage=113504&rft.eissn=0031-9422&rft.issn=0031-9422&rft.au=AUBERON,%20Florence&OLATUNJI,%20Opeyemi%20Joshua&WAFFO-TEGUO,%20Pierre&OLATUNDE,%20Oladipupo%20Odunayo&SINGH,%20Sudarshan&rft.genre=article


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