Antioxidant, antiepileptic, and anticholinergic properties of 4′,5,7-Trihydroxy-3,6-dimethoxyflavone as natural phenolic compound: a toxicology approach

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In this work, the antioxidant properties of 4′,5,7-trihydroxy-3,6-dimethoxyflavone using several bioanalytical assays is investigated in vitro. These methods are Cu2+-Cu+ reducing, Fe3+-Fe2+reducing, DPPH• scavenging, and ABTS•+ scavenging. The IC50 values of the 4′,5,7-trihydroxy-3,6-dimethoxyflavone for DPPH• and ABTS•+ scavenging assays were 9.36 and 3.55 μg m–1, respectively. Additionally, 4′,5,7-trihydroxy-3,6-dimethoxyflavone compound recorded best inhibitory effects against human carbonic anhydrase (hCA) I and II isoenzymes, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE) enzymes. 4′,5,7-Trihydroxy-3,6-dimethoxyflavone had K i value of 389.56 ± 29 nM against hCA I and 306.90 ± 41 nM toward hCA II, respectively. Also, the K i values of AChE and BChE were found as 1005.37 ± 117 nM and 814.22 ± 87 nM, respectively. © 2019 Informa UK Limited, trading as Taylor & Francis Group.

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AlanDeğerDil
dc.contributor.authorDurmaz, Lokman
dc.date.accessioned2026-10-18T20:28:13.784888652Z
dc.date.available2026-10-18T20:28:13.784888652Z
dc.date.issued2021
dc.description.abstractIn this work, the antioxidant properties of 4′,5,7-trihydroxy-3,6-dimethoxyflavone using several bioanalytical assays is investigated in vitro. These methods are Cu2+-Cu+ reducing, Fe3+-Fe2+reducing, DPPH• scavenging, and ABTS•+ scavenging. The IC50 values of the 4′,5,7-trihydroxy-3,6-dimethoxyflavone for DPPH• and ABTS•+ scavenging assays were 9.36 and 3.55 μg m–1, respectively. Additionally, 4′,5,7-trihydroxy-3,6-dimethoxyflavone compound recorded best inhibitory effects against human carbonic anhydrase (hCA) I and II isoenzymes, acetylcholinesterase (AChE), and butyrylcholinesterase (BChE) enzymes. 4′,5,7-Trihydroxy-3,6-dimethoxyflavone had K i value of 389.56 ± 29 nM against hCA I and 306.90 ± 41 nM toward hCA II, respectively. Also, the K i values of AChE and BChE were found as 1005.37 ± 117 nM and 814.22 ± 87 nM, respectively. © 2019 Informa UK Limited, trading as Taylor & Francis Group.
dc.identifier.doi10.1080/15569543.2019.1610894
dc.identifier.eissn1556-9551
dc.identifier.endpage299
dc.identifier.issn1556-9543
dc.identifier.issue3
dc.identifier.scopus2-s2.0-85065548939
dc.identifier.startpage292
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13391
dc.identifier.volume40
dc.identifier.wosWOS:000469722000001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofToxin Reviews
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subject4′,5,7-Trihydroxy-3,6-dimethoxyflavone
dc.subjectacetylcholinesterase
dc.subjectantioxidant activity
dc.subjectenzyme inhibition
dc.subjectmetabolic enzymes
dc.subject4',5,7 trihydroxy 3,6 dimethoxyflavone
dc.subjectacetazolamide
dc.subjectalpha tocopherol
dc.subjectanticonvulsive agent
dc.subjectantioxidant
dc.subjectbutylated hydroxyanisole
dc.subjectbutylcresol
dc.subjectcarbonate dehydratase I
dc.subjectcarbonate dehydratase II
dc.subjectcholinergic receptor blocking agent
dc.subjectcholinesterase
dc.subjectcopper
dc.subjectcupric ion
dc.subjectferric ion
dc.subjectferrous ion
dc.subjectisoenzyme
dc.subjectnatural product
dc.subjectphenol derivative
dc.subjecttrolox C
dc.subjectunclassified drug
dc.subjectABTS radical scavenging assay
dc.subjectanalytic method
dc.subjectanticonvulsant activity
dc.subjectantioxidant assay
dc.subjectArticle
dc.titleAntioxidant, antiepileptic, and anticholinergic properties of 4′,5,7-Trihydroxy-3,6-dimethoxyflavone as natural phenolic compound: a toxicology approach
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus4
rdl.citation.wos7
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)