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Isolation and structure elucidation of bioactive compounds from the roots of the Tunisian Ononis angustissima L.
Ghribi, Lotfi; Waffo-Téguo, Pierre; Cluzet, Stéphanie; Marchal, Axel; Marques, Jessica; Mérillon, Jean-Michel; Ben Jannet, Hichem.
Afiliação
  • Ghribi L; Laboratory of Heterocyclic Chemistry, Natural Products and Reactivity, Team: Medicinal Chemistry and Natural Products, Faculty of Science of Monastir, University of Monastir, Avenue of Environment, 5019 Monastir, Tunisia.
  • Waffo-Téguo P; Univ. de Bordeaux, ISVV, EA 3675 GESVAB, 33140 Villenave d'Ornon, France.
  • Cluzet S; Univ. de Bordeaux, ISVV, EA 3675 GESVAB, 33140 Villenave d'Ornon, France.
  • Marchal A; Univ. de Bordeaux, ISVV, EA 4577, Unité de recherche OENOLOGIE, F-33882 Villenave d'Ornon, France.
  • Marques J; Univ. de Bordeaux, ISVV, EA 3675 GESVAB, 33140 Villenave d'Ornon, France.
  • Mérillon JM; Univ. de Bordeaux, ISVV, EA 3675 GESVAB, 33140 Villenave d'Ornon, France.
  • Ben Jannet H; Laboratory of Heterocyclic Chemistry, Natural Products and Reactivity, Team: Medicinal Chemistry and Natural Products, Faculty of Science of Monastir, University of Monastir, Avenue of Environment, 5019 Monastir, Tunisia. Electronic address: hich.benjannet@yahoo.fr.
Bioorg Med Chem Lett ; 25(18): 3825-30, 2015 Sep 15.
Article em En | MEDLINE | ID: mdl-26248805
ABSTRACT
A 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-ß-D-glucose 4, (-)-puerol B-2'-O-ß-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 Aß25-35, compounds 9 and 10 triggered a significant increase of cell viability and in a dose dependent manner.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Extratos Vegetais / Raízes de Plantas / Ononis / Antioxidantes Limite: Animals País/Região como assunto: Africa Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Tunísia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Extratos Vegetais / Raízes de Plantas / Ononis / Antioxidantes Limite: Animals País/Região como assunto: Africa Idioma: En Revista: Bioorg Med Chem Lett Assunto da revista: BIOQUIMICA / QUIMICA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: Tunísia