Synthesis, structure, cytotoxic and antioxidant properties of 6-ethoxy-4-methylcoumarin

dc.contributor.authorCelikezen, F. C.
dc.contributor.authorOrek, C.
dc.contributor.authorParlak, A. E.
dc.contributor.authorSarac, K.
dc.contributor.authorTurkez, H.
dc.contributor.authorTozlu, Ozlem Ozdemir
dc.date.accessioned2026-08-12T17:35:07Z
dc.date.issued2020
dc.departmentFırat Üniversitesi
dc.description.abstractCoumarins have a wide usage area in medicinal applications. It is known that the design and synthesis of new coumarin derivatives are performed to prepare new drugs in many laboratories. The aim of the study was to synthesize 6-ethoxy-4-methylcoumarin and detect its chemical and biological properties for the first time. 6-ethoxy-4-methylcoumarin was synthesized using Pechmann method. Atomic orbital (GIAO) H-1 and C-13 NMR chemical shift values in the ground state were calculated and Density Functional Method (DFT) was applied with the 6-311++G (d, p) basis set to determine chemical properties. 6-ethoxy-4-methylcoumarin was applied to cultured blood samples at various concentrations (10-400 mg/L) for determining biological activity. 3-(4,5-dimethylthiazol-2-yl)-2,5 diphenyltetrazolium bromide (MTT) and lactate dehydrogenase (LDH) release assays were used to evaluate cytotoxic effect. In addition, total antioxidant capacity (TAC) and total oxidative status (TOS) were examined to determine antioxidant properties. The results showed that theoretical vibrational frequencies and chemical shift values were close to experimental values. Moreover, 6-ethoxy-4-methylcoumarin showed a slight cytotoxic effect at dose of 200 mg/L and exhibited an antioxidant activity at 25 mg/L concentration without changing oxidative status at all of doses. (c) 2019 Elsevier B.V. All rights reserved.
dc.description.sponsorshipKastamonu University Scientific Research Projects Coordination Department [KU-BAP01/2019-63]
dc.description.sponsorshipThis research was supported by Kastamonu University Scientific Research Projects Coordination Department under the Grant no. KU-BAP01/2019-63. Computational resources were provided by the FeynmanGrid HPC Cluster at the CompecTA The HPC Company.
dc.identifier.doi10.1016/j.molstruc.2019.127577
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.orcid0000-0002-3854-1537
dc.identifier.orcid0000-0002-2579-9985
dc.identifier.scopus2-s2.0-85076882336
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2019.127577
dc.identifier.urihttps://hdl.handle.net/11508/57425
dc.identifier.volume1205
dc.identifier.wosWOS:000511287400079
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Molecular Structure
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260511
dc.subjectCoumarins
dc.subjectDFT
dc.subjectNMR
dc.subjectVibrational spectra
dc.subjectCytotoxic
dc.subjectAntioxidant
dc.titleSynthesis, structure, cytotoxic and antioxidant properties of 6-ethoxy-4-methylcoumarin
dc.typeArticle

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