Publication:
New Carbazol Derivatives Containing 1,2,4-Triazole: Synthesis, Characterization, DFT Study, Acetylcholinesterase Activity and Docking Study

dc.authorscopusid8354984100
dc.authorscopusid26644545800
dc.authorscopusid8361744500
dc.authorscopusid56803453100
dc.authorscopusid55337455800
dc.authorscopusid57257231600
dc.authorscopusid57257231600
dc.authorwosidÜnver, Yasemin/Aak-2181-2021
dc.authorwosidGuler, Halil/E-4888-2017
dc.authorwosidBektaş, Kadriye/Aak-2012-2021
dc.authorwosidÇelik, Fatih/Aak-8325-2021
dc.contributor.authorUnver, Yasemin
dc.contributor.authorSuleymanoglu, Nevin
dc.contributor.authorUstabas, Resat
dc.contributor.authorGuler, Halil Ibrahim
dc.contributor.authorBektas, Ersan
dc.contributor.authorBektas, Kadriye Inan
dc.contributor.authorCelik, Fatih
dc.contributor.authorIDBektaş, Ersan/0000-0001-9030-6908
dc.date.accessioned2025-12-11T00:53:06Z
dc.date.issued2022
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Unver, Yasemin; Celik, Fatih] Karadeniz Tech Univ, Fac Sci, Dept Chem, TR-61080 Trabzon, Turkey; [Suleymanoglu, Nevin] Gazi Univ, Grad Sch Nat & Appl Sci Adv Technol, TR-06500 Ankara, Turkey; [Ustabas, Resat] Ondokuz Mayis Univ, Educ Fac, Dept Math & Sci Educ, TR-55139 Kurupelit, Turkey; [Guler, Halil Ibrahim; Bektas, Kadriye Inan] Karadeniz Tech Univ, Dept Mol Biol & Genet, Fac Sci, TR-61080 Trabzon, Turkey; [Bektas, Ersan] Giresun Univ, Espiye Vocat Sch, TR-26800 Giresun, Turkeyen_US
dc.descriptionBektaş, Ersan/0000-0001-9030-6908;en_US
dc.description.abstractCarbazol derivatives, 4-(((9-ethyl-9H-carbazol-3-yl)methylene)amino)-5-methyl-2,4-dihydro-3H-1,2,4-triazole-3-one (3) and 5-benzyl-4-(((9-ethyl-9H-carbazol-3-yl) methylene) amino)-2,4-dihydro-3H-1,2,4-triazole-3-one (4), were synthesized. Compounds 3 and 4 were characterized by The Fourier transform infrared (FTIR), pro-ton and carbon-13 nuclear magnetic resonance (1H-and 13C-NMR) spectroscopic methods. Density Functional Theory (DFT) calculations for compounds 3 and 4 were performed at B3LYP/6-311++G(d,p) level. Optimized geometry, IR and NMR parameters of compounds 3 and 4 were obtained. The in vitro anti-acetylcholinesterase activity of the compounds were examinated. In addition, Compounds 3 and 4 were tested to determine possible interactions against human acetylcholinesterase by in silico analysis.en_US
dc.description.woscitationindexScience Citation Index Expanded - Index Chemicus
dc.identifier.doi10.1016/j.jics.2022.100690
dc.identifier.issn0019-4522
dc.identifier.issue10en_US
dc.identifier.scopus2-s2.0-85137634778
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://doi.org/10.1016/j.jics.2022.100690
dc.identifier.urihttps://hdl.handle.net/20.500.12712/39949
dc.identifier.volume99en_US
dc.identifier.wosWOS:000862297200009
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.relation.ispartofJournal of the Indian Chemical Societyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCarbazolen_US
dc.subjectTriazoleen_US
dc.subjectSynthesisen_US
dc.subjectDFTen_US
dc.subjectAcetylcholinesterase Activityen_US
dc.subjectMolecular Docking Studyen_US
dc.titleNew Carbazol Derivatives Containing 1,2,4-Triazole: Synthesis, Characterization, DFT Study, Acetylcholinesterase Activity and Docking Studyen_US
dc.typeArticleen_US
dspace.entity.typePublication

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