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dc.contributor.authorSarikurkcu, Cengiz
dc.contributor.authorErdogmus, Sevim Feyza
dc.contributor.authorTepe, Bektas
dc.date.accessioned2025-12-28T16:39:56Z
dc.date.available2025-12-28T16:39:56Z
dc.date.issued2025
dc.identifier.issn0366-6352
dc.identifier.issn2585-7290
dc.identifier.urihttps://doi.org/10.1007/s11696-025-04054-z
dc.identifier.urihttps://hdl.handle.net/20.500.12933/2247
dc.description.abstractUnderstanding the bioactive potential of Clinopodium vulgare subsp. arundanum extracts holds promise for natural antioxidant and enzyme inhibitory applications. This study aimed to evaluate the chemical composition, antioxidant, and enzyme inhibitory capacities of water, methanol, and ethyl acetate extracts of C. vulgare subsp. arundanum. Using liquid chromatography-electrospray ionization-mass spectrometry/mass spectrometry (LC-ESI-MS/MS), each extract's phytochemical profile was characterized, revealing the methanol extract as particularly rich in total phenolic (110.9 mg GAEs/g) and flavonoid content (38.49 mg REs/g), while the water and ethyl acetate extracts contained moderate-to-low phenolic levels. Antioxidant activities, assessed through 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), cupric reducing antioxidant capacity (CUPRAC), and ferric reducing antioxidant power (FRAP) assays, consistently ranked methanol extract as the most effective (DPPH: 340.17 mg TEs/g; CUPRAC: 533.57 mg TEs/g), attributable to phenolics like rosmarinic acid (48,370 mu g/g) and hesperidin (832 mu g/g). In metal chelation, the water extract demonstrated superior activity (11.83 mg EDTAEs/g). Enzyme inhibition assays revealed notable acetylcholinesterase and butyrylcholinesterase inhibitory activities in the ethyl acetate extract, with values of 3.33 mg and 2.32 mg GALAEs/g, respectively, possibly linked to specific solvent-extracted bioactives. The observed variations in bioactivity among the extracts can be attributed to the differing polarity and solvent properties, which influence the solubility and extraction efficiency of phenolic and flavonoid compounds. Future research should prioritize compound isolation to identify specific inhibitors and test these extracts' in vivo effects, extending the therapeutic insights into C. vulgare subsp. arundanum's pharmacological applications.
dc.description.sponsorshipSagbreve;limath;k Bilimleri niversitesi
dc.description.sponsorshipThe authors extend their gratitude to Dr. Olcay CEYLAN for his invaluable assistance in the identification of the plant material utilized in this study. The primary responsibility for designing and executing the experiments, as well as conducting the statistical analyses, lay with the authors. Artificial intelligence was utilized as a supplementary tool to aid in the interpretation of data and to enhance the manuscript's clarity and scientific precision. All outputs generated by AI were thoroughly evaluated by the authors to confirm their validity and relevance to the research objectives.
dc.language.isoen
dc.publisherSpringer Int Publ Ag
dc.relation.ispartofChemical Papers
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectClinopodium vulgare subsp. arundanum
dc.subjectAntioxidant activity
dc.subjectEnzyme inhibition
dc.subjectSolvent extraction
dc.subjectPhenolic compounds
dc.subjectLC-ESI-MS/MS
dc.titleDelving into the enzyme inhibitory and antioxidant potential of Clinopodium vulgare subsp. arundanum: an untapped botanical resource
dc.typeArticle
dc.identifier.orcid0000-0002-4319-7558
dc.identifier.orcid0000-0001-5094-2520
dc.identifier.orcid0000-0001-8982-5188
dc.departmentAfyonkarahisar Sağlık Bilimleri Üniversitesi
dc.identifier.doi10.1007/s11696-025-04054-z
dc.identifier.volume79
dc.identifier.issue7
dc.identifier.startpage4247
dc.identifier.endpage4259
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.department-temp[Sarikurkcu, Cengiz; Erdogmus, Sevim Feyza] Afyonkarahisar Hlth Sci Univ, Fac Pharm, TR-03100 Afyonkarahisar, Turkiye; [Tepe, Bektas] Kilis 7 Aralik Univ, Fac Sci, Dept Mol Biol & Genet, TR-79000 Kilis, Turkiye; [Tepe, Bektas] Necmettin Erbakan Univ, Fac Sci, Dept Mol Biol & Genet, TR-42090 Konya, Turkiye
dc.identifier.scopus2-s2.0-105004363785
dc.identifier.scopusqualityQ2
dc.identifier.wosWOS:001482033200001
dc.identifier.wosqualityN/A
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.snmzKA_WoS_20251227


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