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dc.rights.licenseopenen_US
dc.contributor.authorGHRIBI, Lotfi
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorWAFFO TEGUO, Pierre
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorCLUZET, Stephanie
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMARCHAL, Axel
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMARQUES, Jessica
hal.structure.identifierUnité de Recherche Oenologie [Villenave d'Ornon] [OENO]
dc.contributor.authorMERILLON, Jean-Michel
dc.contributor.authorBEN JANNET, Hichem
dc.date.accessioned2021-05-21T16:05:41Z
dc.date.available2021-05-21T16:05:41Z
dc.date.issued2015-09-15
dc.identifier.issn1464-3405en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/78601
dc.description.abstractEnA phytochemical investigation of the roots of Ononis angustissima L. (Fabaceae) offered to the bio-guided isolation of new isoflavone 3-(4-(glucopyranosyloxy)-5-hydroxy-2-methoxyphenyl)-7-hydroxy-4H-chromen-4-one 1, together with nine known compounds, ononin 2, formononetin 3, (+)-puerol A-2'-O-β-D-glucose 4, (-)-puerol B-2'-O-β-D-glucopyranose ((-)-sophoraside A) 5, (+)-puerol A 6, (-)-trifolirhizin 7, (-)-trifolirhizin-6'-O-malonate 8, (-)-maackiain 9 and (-)-medicarpin 10. Compounds 2-10 were isolated and identified for the first time in Ononis angustissima. We investigated antioxidant capacities of isolated molecules and results showed that compound 6 exhibited the highest antioxidant activity with IC50 values of 19.53 μg/mL, 28.29 μg/mL and 38.53 μg/mL by DPPH radical, ABTS radical cation and reducing power assay, respectively, and an interesting IC50 (20.45 μg/mL) of 1 against DPPH. In addition, the neuroprotective activity of six isolated molecules (4-7, 9, 10) were evaluated. Following the exposure of PC12 cells to Aβ25-35, compounds 9 and 10 triggered a significant increase of cell viability and in a dose dependent manner.
dc.language.isoENen_US
dc.subject.enAnimals
dc.subject.enAntioxidants
dc.subject.enBenzothiazoles
dc.subject.enBiphenyl Compounds
dc.subject.enCell Survival
dc.subject.enDose-Response Relationship
dc.subject.enDrug
dc.subject.enFree Radicals
dc.subject.enMolecular Structure
dc.subject.enOnonis
dc.subject.enPC12 Cells
dc.subject.enPicrates
dc.subject.enPlant Extracts
dc.subject.enPlant Roots
dc.subject.enRats
dc.subject.enStructure-Activity Relationship
dc.subject.enSulfonic Acids
dc.subject.enTunisia
dc.title.enIsolation and structure elucidation of bioactive compounds from the roots of the Tunisian Ononis angustissima L.
dc.title.alternativeBioorg Med Chem Letten_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1016/j.bmcl.2015.07.076en_US
dc.subject.halSciences du Vivant [q-bio]/Biologie végétaleen_US
dc.identifier.pubmed26248805en_US
bordeaux.journalBioorganic and Medicinal Chemistry Lettersen_US
bordeaux.page3825-30en_US
bordeaux.volume25en_US
bordeaux.hal.laboratoriesUnité de Recherche Oenologie - EA 4577en_US
bordeaux.issue18en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.institutionBordeaux INPen_US
bordeaux.institutionINRAEen_US
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
bordeaux.import.sourcepubmed
hal.exportfalse
workflow.import.sourcepubmed
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