Advanced Search

Show simple item record

dc.contributor.authorSarıkürkçü, Cengiz
dc.contributor.authorŞahinler, Saliha Şeyma
dc.contributor.authorHüsunet, Mehmet Tahir
dc.contributor.authorİstifli, Erman Salih
dc.contributor.authorTepe, Bektaş
dc.date.accessioned2021-05-05T22:14:06Z
dc.date.available2021-05-05T22:14:06Z
dc.date.issued2020
dc.identifier.issn0926-6690
dc.identifier.issn1872-633X
dc.identifier.urihttps://doi.org/10.1016/j.indcrop.2020.112656
dc.identifier.urihttps://hdl.handle.net/20.500.12933/284
dc.descriptionIstifli, Erman Salih/0000-0003-2189-0703en_US
dc.descriptionWOS:000554526900043en_US
dc.description.abstractThere are convincing evidences that species belonging to the Onosma genus have been used in the treatment of various diseases for centuries. In this study, antioxidant and tyrosinase and a-amylase inhibitory activities of the methanol (MeOH) extracts of two endemic Onosma species (O. sieheana Hayek and O. stenoloba Hausskn. ex Riedl), which are endemic to the flora of Turkey, were compared. Phosphomolybdenum, reducing power [Cupric reducing antioxidant capacity (CUPRAC) and ferric reducing antioxidant power (FRAP)], radical scavenging [on '2,2-diphenyl-1-picrylhydrazyl' (DPPH) and 2,2'-azino-bis-3-ethylbenzthiazoline-6-sulphonic acid (ABTS)] and ferrous ion chelating assays were used to determine the antioxidant activities of the extracts. All test systems except for the ferrous ion chelating assay resulted in O. sieheana's superiority. The antioxidant activity of O. sieheana in the test systems mentioned above was found to be 2.11, 1.57, 1.01, 3.54 and 3.19 mg/mL, respectively. However, in ferrous ion chelating activity assay, O. stenoloba showed higher activity with an IC50 value of 2.98 mg/mL. In the tyrosinase inhibitor activity test, O. stenoloba extract showed higher activity (1.89 mg/mL), while in the a-amylase inhibitory activity assay, O. sieheana was found to be more effective (3.02 mg/mL). As a result of total phenolic and flavonoid compound analysis, O. sieheana was found to be richer than the other in terms of both groups. LC-ESI-MS/MS analysis revealed that rosmarinic acid, apigenin 7-glucoside, luteolin 7-glucoside, chlorogenic acid, hesperidin, pinoresinol, hyperoside and 4-hydroxybenzoic are the main compounds of the extracts. According to the results of docking analysis performed to reveal the interactions of the main components with tyrosinase, it is thought that pinoresinol, hesperidin, luteolin 7-glucoside, apigenin 7-glucoside, and hyperoside may be phytochemicals responsible for the inhibitory activity. Additionally, the binding energies of pinorecinol, apigenin 7-glucoside, luteolin 7-glucoside, hyperoside, chlorogenic acid, and rosmarinic acid to a-amylase were found to be quite high.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectOnosma sieheanaen_US
dc.subjectOnosma stenoloba antioxidanten_US
dc.subjectEnzyme inhibitionen_US
dc.subjectDockingen_US
dc.titleTwo endemic Onosma species (O. sieheana and O. stenoloba): A comparative study including docking data on biological activity and phenolic compositionen_US
dc.typearticleen_US
dc.departmentAFSÜ, Eczacılık Fakültesi, Temel Eczacılık Bilimleri Bölümüen_US
dc.contributor.institutionauthorSarıkürkçü, Cengiz
dc.contributor.institutionauthorŞahinler, Saliha Şeyma
dc.identifier.doi10.1016/j.indcrop.2020.112656
dc.identifier.volume154en_US
dc.relation.journalIndustrial Crops And Productsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record