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dc.contributor.authorLabed, Amira
dc.contributor.authorFerhat, Maria
dc.contributor.authorLabed-Zouad, Ilhem
dc.contributor.authorKaplaner, Erhan
dc.contributor.authorZerizer, Sakina
dc.contributor.authorVoutquenne-Nazabadioko, Laurence
dc.contributor.authorÖztürk, Mehmet
dc.date.accessioned2020-11-20T15:01:53Z
dc.date.available2020-11-20T15:01:53Z
dc.date.issued2016
dc.identifier.issn1388-0209
dc.identifier.issn1744-5116
dc.identifier.urihttps://doi.org/10.1080/13880209.2016.1200632
dc.identifier.urihttps://hdl.handle.net/20.500.12809/2270
dc.descriptionWOS: 000389443300031en_US
dc.descriptionPubMed ID: 27431425en_US
dc.description.abstractContext: The phytochemical study and biological activities of Astragalus armatus Willd. subsp. numidicus (Fabaceae) pods, an endemic shrub of Maghreb, are reported. Objective: This study isolates the secondary metabolites and determines the bioactivities of Astragalus armatus pods. Materials and methods: The chloroform, ethyl acetate and n-butanol extracts of hydro-ethanolic extracts were studied. Antioxidant activity was investigated using DPPH and ABTS radical scavenging, CUPRAC and ferrous chelating assays at concentrations ranging from 3 to 200 mu g/mL. Anticholinesterase activity was determined against acetylcholinesterase and butyrylcholinesterase enzymes at 50, 100 and 200 mu g/mL. Antibacterial activity was performed according to minimum inhibitory concentration (MIC) method. Carbon clearance method in albino mice was used for the phagocytic activity at concentrations 50, 70 and 100mg/kg body weight. Spectroscopic techniques were used to elucidate the compounds. Results: Ethyl acetate extract afforded a flavonoid (1) while the n-butanol extract gave four flavonoids (2-5), a cyclitol (6) and a cycloartane-type saponin (7). The ethyl acetate extract exhibited highest antioxidant activity in DPPH (IC50: 67.90 +/- 0.57 mu g/mL), ABTS (IC50: 11.30 +/- 0.09 mu g/mL) and CUPRAC (A(0.50): 50.60 +/- 0.9 mu g/mL) assays. The chloroform extract exhibited the best antibacterial activity against Staphylococcus aureus, Escherichia coli and Pseudomonas aeruginosa, each with 80 mu g/mL MIC values. The n-butanol extract enhanced phagocytic activity. Discussion and conclusion: Isorhamnetin (1), isorhamnetin-3-O-alpha-L-rhamnopyranosyl-(1 -> 6)-beta-D-galactopyranoside (2), isorhamnetin-3-O-beta-D-apiofuranosyl-(1 -> 2)-[alpha-L-rhamnopyranosyl-(1 -> 6)]-beta-D-galactopyranoside (3), kaempferol-3-O-(2,6-di-O-alpha-L-rhamnopyranosyl)-beta-D-galactopyranoside (4), kaempferol-3-O-(2,6-di-O-alpha-L-rhamnopyranosyl)- beta-D-glucopyranoside (5), pinitol (6) and cyclomacroside D (7) were isolated whereas 1, 2, 6 and 7 are reported for the first time from A. armatus.en_US
dc.description.sponsorshipATRSS-DGRSDT (MESRS, Algeria); Mugla Sitki Kocman University, Department of Chemistry; Groupe Isolement et Structure of the Institut de Chimie Moleculaire de Reims (ICMR), Franceen_US
dc.description.sponsorshipThe authors are grateful to ATRSS-DGRSDT (MESRS, Algeria), Mugla Sitki Kocman University, Department of Chemistry and Groupe Isolement et Structure of the Institut de Chimie Moleculaire de Reims (ICMR), France for providing their financial support and facilities during the study.en_US
dc.item-language.isoengen_US
dc.publisherTaylor & Francis Ltden_US
dc.item-rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectBiological Activityen_US
dc.subjectFlavonoidsen_US
dc.subjectSaponinsen_US
dc.subjectStructure Elucidationen_US
dc.titleCompounds from the pods of Astragalus armatus with antioxidant, anticholinesterase, antibacterial and phagocytic activitiesen_US
dc.item-typearticleen_US
dc.contributor.departmentMÜ, Fen Fakültesi, Kimya Fakültesien_US
dc.contributor.authorID0000-0001-8932-4535
dc.contributor.authorID0000-0002-4001-8841
dc.contributor.institutionauthorFerhat, Maria
dc.contributor.institutionauthorKaplaner, Erhan
dc.contributor.institutionauthorÖztürk, Mehmet
dc.identifier.doi10.1080/13880209.2016.1200632
dc.identifier.volume54en_US
dc.identifier.issue12en_US
dc.identifier.startpage3026en_US
dc.identifier.endpage3032en_US
dc.relation.journalPharmaceutical Biologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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