Antioxidant, antiepileptic, and anticholinergic properties of 4′,5,7-Trihydroxy-3,6-dimethoxyflavone as natural phenolic compound: a toxicology approach
Özet
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.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Durmaz, Lokman | |
| dc.date.accessioned | 2026-10-18T20:28:13.784888652Z | |
| dc.date.available | 2026-10-18T20:28:13.784888652Z | |
| dc.date.issued | 2021 | |
| dc.description.abstract | 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. | |
| dc.identifier.doi | 10.1080/15569543.2019.1610894 | |
| dc.identifier.eissn | 1556-9551 | |
| dc.identifier.endpage | 299 | |
| dc.identifier.issn | 1556-9543 | |
| dc.identifier.issue | 3 | |
| dc.identifier.scopus | 2-s2.0-85065548939 | |
| dc.identifier.startpage | 292 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/13391 | |
| dc.identifier.volume | 40 | |
| dc.identifier.wos | WOS:000469722000001 | |
| dc.language.iso | en | |
| dc.publisher | Taylor and Francis Ltd. | |
| dc.relation.ispartof | Toxin Reviews | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | 4′,5,7-Trihydroxy-3,6-dimethoxyflavone | |
| dc.subject | acetylcholinesterase | |
| dc.subject | antioxidant activity | |
| dc.subject | enzyme inhibition | |
| dc.subject | metabolic enzymes | |
| dc.subject | 4',5,7 trihydroxy 3,6 dimethoxyflavone | |
| dc.subject | acetazolamide | |
| dc.subject | alpha tocopherol | |
| dc.subject | anticonvulsive agent | |
| dc.subject | antioxidant | |
| dc.subject | butylated hydroxyanisole | |
| dc.subject | butylcresol | |
| dc.subject | carbonate dehydratase I | |
| dc.subject | carbonate dehydratase II | |
| dc.subject | cholinergic receptor blocking agent | |
| dc.subject | cholinesterase | |
| dc.subject | copper | |
| dc.subject | cupric ion | |
| dc.subject | ferric ion | |
| dc.subject | ferrous ion | |
| dc.subject | isoenzyme | |
| dc.subject | natural product | |
| dc.subject | phenol derivative | |
| dc.subject | trolox C | |
| dc.subject | unclassified drug | |
| dc.subject | ABTS radical scavenging assay | |
| dc.subject | analytic method | |
| dc.subject | anticonvulsant activity | |
| dc.subject | antioxidant assay | |
| dc.subject | Article | |
| dc.title | Antioxidant, antiepileptic, and anticholinergic properties of 4′,5,7-Trihydroxy-3,6-dimethoxyflavone as natural phenolic compound: a toxicology approach | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 4 | |
| rdl.citation.wos | 7 | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
