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dc.contributor.authorAssia, Khalfallah-
dc.date.accessioned2022-07-03T09:18:28Z-
dc.date.available2022-07-03T09:18:28Z-
dc.date.issued2017-07-
dc.identifier.citationscience biologieen_US
dc.identifier.issn1478-6419-
dc.identifier.urihttp://dspace.centre-univ-mila.dz/jspui/handle/123456789/1783-
dc.description.abstractThis is the first study on the phytochemistry and antioxidant activity of Ferula longipes Coss. ex Bonnier and Maury (Apiaceae). A new flavonoid quercetin-3-O-α-L-rhamnopyranoside-7-O-ß-D-[2-O-caffeoyl]- lucopyranoside (1), along with 10 known compounds kaempferol-3-O- α-L-rhamnopyranoside (2), quercetin-3-O-α-L-rhamnopyranoside (3), kaempferol-3-O-ß-D-glucopyranoside-7-O-α-L-rhamnopyranoside 4),isorhamnetin-3-O-α-L-rhamnopyranoside-7-O-ß-D-glucopyranoside (5), quercetin-3-O-α-L- amnopyranoside-7-O-ß-D-glucopyranoside (6), isorhamnetin-3,7-di-O-β-D-glucopyranoside (7), apigenin (8), apigenin-7-O-ß-D-glucopyranoside (9), 3,5-dicaffeoylquinic acid (10), deltoin (11) were isolated from the aerial parts of Ferula longipes Coss. Structures elucidation was performed by comprehensive 1D and 2D NMR analyses, mass spectrometry and by comparison with literature data. The compounds 1, 3, 4, 6, 7 and 10 were evaluated for their antioxidant activity, compound 1 exhibited the best antiradical activity potential and showed IC50 and A0.5 values 5.70, 7.25, 5.00, and 2.63 μg/mL towards DPPH free radical-scavenging, ABTS, CUPRAC, and reducing power assays, respectively compared with BHA, BHT and ascorbic acid which were used as positive controls.en_US
dc.language.isoenen_US
dc.publisherAbdelhafid boussouf university Centre milaen_US
dc.subjectFerula longipes Coss. ex Bonnier and Maury; Apiaceae; flavonoid; antioxidant activity; reducing power assaysen_US
dc.titleChemical composition and antioxidant activity of aerial parts of Ferula longipes Coss. ex Bonnier and Maury.en_US
dc.typeArticleen_US
Appears in Collections:Biological Sciences

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