Publication:
Novel Aldehyde and Thiosemicarbazone Derivatives: Synthesis, Spectroscopic Characterization, Structural Studies and Molecular Docking Studies

dc.authorscopusid8399085400
dc.authorscopusid24463062800
dc.authorscopusid57190185902
dc.authorscopusid8354984000
dc.authorscopusid7003281189
dc.contributor.authorKarakurt, T.
dc.contributor.authorTahtaci, H.
dc.contributor.authorSubasi, N.T.
dc.contributor.authorEr, M.
dc.contributor.authorAģar, E.
dc.date.accessioned2020-06-21T13:28:26Z
dc.date.available2020-06-21T13:28:26Z
dc.date.issued2016
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Karakurt] Tuncay, Department of Chemical Engineering, Kırşehir Ahi Evran Üniversitesi, Kirsehir, Kirsehir, Turkey; [Tahtaci] Hakan, Department of Polymer Engineering, Karabük Üniversitesi, Karabuk, Turkey; [Subasi] Tuna Tuna, Department of Food Engineering, Kırşehir Ahi Evran Üniversitesi, Kirsehir, Kirsehir, Turkey; [Er] Mustafa, Department of Chemical Engineering, Karabük Üniversitesi, Karabuk, Turkey; [Aģar] Erbil, Ondokuz Mayis University Faculty of Science and Arts, Samsun, Turkeyen_US
dc.description.abstractIn this study our purpose is that, synthesis and characterization of compounds containing the aldehyde and thiosemicarbazone groups and comparison of the theoretical results with the experimental results. The structures of all synthesized compounds were elucidated by IR, 1H NMR, 13C NMR, elemental analyses techniques. The structure of compound (4) (C<inf>9</inf>H<inf>8</inf>N<inf>4</inf>O<inf>2</inf>S) was also elucidated by X-ray diffraction analysis. In addition, the theoretical IR spectrum, 1H NMR and 13C NMR chemical shift values, frontier molecular orbital values (FMO) of these molecules were analyzed by using Becke-3- Lee-Yang-Parr (B3LYP) method with LanL2DZ basis set. Finally, molecular docking studies were performed on synthesized compounds using the 4DKI beta-lactam protein structure to determine the potential binding mode of inhibitors. © 2016 Elsevier B.V.en_US
dc.identifier.doi10.1016/j.molstruc.2016.07.013
dc.identifier.endpage480en_US
dc.identifier.issn0022-2860
dc.identifier.scopus2-s2.0-84978286071
dc.identifier.scopusqualityQ1
dc.identifier.startpage470en_US
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2016.07.013
dc.identifier.volume1125en_US
dc.identifier.wosWOS:000384785100052
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofJournal of Molecular Structureen_US
dc.relation.journalJournal of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAldehydeen_US
dc.subjectB3LYPen_US
dc.subjectBeta-Lactamen_US
dc.subjectNMRen_US
dc.subjectThiosemicarbazoneen_US
dc.titleNovel Aldehyde and Thiosemicarbazone Derivatives: Synthesis, Spectroscopic Characterization, Structural Studies and Molecular Docking Studiesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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