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dc.contributor.authorBaltacı, Nurnehir
dc.contributor.authorAydoğdu, Nida
dc.contributor.authorSarıkürkçü, Cengiz
dc.contributor.authorTepe, Bektaş
dc.date.accessioned2021-05-05T22:11:49Z
dc.date.available2021-05-05T22:11:49Z
dc.date.issued2021
dc.identifier.issn0254-6299
dc.identifier.urihttps://doi.org/10.1016/j.sajb.2021.03.022
dc.identifier.urihttps://hdl.handle.net/20.500.12933/150
dc.description2-s2.0-85103958750en_US
dc.description.abstractIn this study, it was aimed to determine the in vitro antioxidant and enzyme inhibitory activities of methanol (MeOH) extracts isolated from Onosma gracilis (Trautv.) and O. oreodoxa (Boiss. & Heldr.). O. oreodoxa was found to be richer in both phenolics and flavonoids than O. gracilis. The amounts of total phenolics and flavonoids in O. oreodoxa were 53.76 mg GAEs/g and 25.29 mg QEs/g, respectively. In addition to spectrophometric analysis, in chromatographic analyzes, twenty-four and twenty-six compounds were identified in O. gracilis and O. oreodoxa, respectively. High amounts of hesperidin (6647.2 and 5260.75 µg/g extract, respectively), hyperoside (7153.26 and 10216.74 µg/g extract, respectively) and rosmarinic acid (21824.33 and 87493.19 µg/g extract, respectively) were found in O. gracilis and O. oreodoxa. While O. oreodoxa showed higher activity in cupric reducing antioxidant power (CUPRAC), ferric reducing antioxidant power (FRAP), phosphomolybdenum, 1, 1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging, and ferrous ion chelating assays (324.22, 175.41, 719.50, 125.60 mg TEs/g extract and 25.11 mg EDTAEs/g extract, respectively), ABTS radical scavenging activity of O. gracilis (164.55 mg TEs/g extract) was higher than that of O. oreodoxa. O. gracilis also exhibited higher inhibitory activity on acetylcholinesterase (AChE), butyrylcholinesterase (BChE) (2.57 mg GALAEs/g extract) and ?-glucosidase (1674.24 mg ACEs/g extract). On the other hand, the sample showing the most effective inhibition on ?-amylase and tyrosinase was O. oreodoxa (417.34 mg ACEs/g extract and 136.18 mg KAEs/g extract, respectively). As a result of the molecular docking analysis performed to determine the contribution of hesperidin, hyperoside and rosmarinic acid to the enzyme inhibitory activity, the binding affinity and inhibition constant of hyperoside to all enzymes were quite high and therefore it was concluded that it may be the compound that contribute to the activity. © 2021 SAABen_US
dc.description.sponsorshipKARIYER.001en_US
dc.description.sponsorshipThis work was carried out with the financial support of Scientific Research Council of Afyonkarahisar Health Sciences University, Afyonkarahisar-Turkey (Project Number: 20.KARIYER.001).en_US
dc.language.isoengen_US
dc.publisherElsevier B.V.en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntioxidant activityen_US
dc.subjectChemical compositionen_US
dc.subjectEnzyme inhibitory activityen_US
dc.subjectMolecular dockingen_US
dc.subjectOnosma gracilisen_US
dc.subjectOnosma oreodoxaen_US
dc.titleOnosma gracilis (Trautv.) and O. oreodoxa (Boiss. & Heldr.): Phytochemistry, in silico docking, antioxidant and enzyme inhibitory activitiesen_US
dc.typearticleen_US
dc.departmentAFSÜ, Eczacılık Fakültesi, Temel Eczacılık Bilimleri Bölümü
dc.contributor.institutionauthorBaltacı, Nurnehir
dc.contributor.institutionauthorAydoğdu, Nida
dc.contributor.institutionauthorSarıkürkçü, Cengiz
dc.identifier.doi10.1016/j.sajb.2021.03.022
dc.relation.journalSouth African Journal of Botanyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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