Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.11851/10518
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dc.contributor.authorGür, Maz, T.-
dc.contributor.authorTuranlı, S.-
dc.contributor.authorÇalışkan, H.B.-
dc.date.accessioned2023-07-14T20:18:46Z-
dc.date.available2023-07-14T20:18:46Z-
dc.date.issued2023-
dc.identifier.issn2564-6524-
dc.identifier.urihttps://doi.org/10.33483/jfpau.1181948-
dc.identifier.urihttps://hdl.handle.net/20.500.11851/10518-
dc.description.abstractObjective: The aim was to design, synthesis and investigation of possible interactions in the enzyme active site of a series of arylhydrazone derivatives for the inhibition of the FAAH enzyme.” Material and Method: Arylhydrazone derivatives were obtained through the reaction of nicotinic hydrazide or benzohydrazide with appropriate aldehyde derivatives, and the obtained crude product was recrystallized from ethanol. After elucidating chemical structures of the compounds via spectroscopic methods, the inhibitory activities against hFAAH were screened. The results were further supported with molecular modeling studies. Result and Discussion: In this study, a new series of seven arylhydrazone derivatives were screened against hFAAH. 4-phenoxyphenyl bearing derivative 5 was found to inhibit hFAAH 40 % at 10 µM which indicates that newly developed inhibitor could serve as a starting point for improving inhibitory effect of the new series. © 2023 University of Ankara. All rights reserved.en_US
dc.description.sponsorshipGazi Üniversitesi: 02/2020-24en_US
dc.description.sponsorshipThe authors would like to thank Prof. Dr. Burcu Caliskan for providing her expertise in this research. This research is financially supported by Gazi University Research Project Unit (BAP: 02/2020-24).en_US
dc.language.isoenen_US
dc.publisherUniversity of Ankaraen_US
dc.relation.ispartofAnkara Universitesi Eczacilik Fakultesi Dergisien_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectArylhydrazonesen_US
dc.subjectFAAHen_US
dc.subjectheterocyclesen_US
dc.subjectinflammationen_US
dc.subjectarylhydrazone derivativeen_US
dc.subjectfatty acid amidase inhibitoren_US
dc.subjectn (3 pyridazinyl) 4 [3 (5 trifluoromethyl 2 pyridinyloxy)benzylidene] 1 piperidinecarboxamideen_US
dc.subjectn' [(4 phenoxyphenyl)methylidene]pyridine 3 carbohydrazideen_US
dc.subjectn' [[ 4 (pyridin 2 yloxy)phenyl]methylidene]pyridine 3 carbohydrazideen_US
dc.subjectn' [[4 (benzyloxy)phenyl]methylidene]pyridine 3 carbohydrazideen_US
dc.subjectn' [[4 [(4 cyanophenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazideen_US
dc.subjectn' [[4 [(4 fluorophenyl)methoxy]phenyl]methylidene]benzohydrazideen_US
dc.subjectn' [[4 [(4 fluorophenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazideen_US
dc.subjectn' [[4 [(4 methoxyphenyl)methoxy]phenyl]methylidene]pyridine 3 carbohydrazideen_US
dc.subjectunclassified drugen_US
dc.subjectArticleen_US
dc.subjectcarbon nuclear magnetic resonanceen_US
dc.subjectchemical structureen_US
dc.subjectchemotypeen_US
dc.subjectcontrolled studyen_US
dc.subjectdrug designen_US
dc.subjectdrug synthesisen_US
dc.subjectenzyme active siteen_US
dc.subjectenzyme inhibitionen_US
dc.subjecthumanen_US
dc.subjecthydrogen bonden_US
dc.subjectliquid chromatography-mass spectrometryen_US
dc.subjectmelting pointen_US
dc.subjectmolecular dockingen_US
dc.subjectmolecular modelen_US
dc.subjectproton nuclear magnetic resonanceen_US
dc.subjectX ray crystallographyen_US
dc.titleDesign and Synthesis of Some Arylhydrazone Derivatives as Potential Faah Inhibitorsen_US
dc.title.alternativePotansiyel Faah İnhibitörü Olarak Bazı Arilhidrazon Türevi Bileşiklerin Tasarımı ve Sentezien_US
dc.typeArticleen_US
dc.departmentTOBB ETÜen_US
dc.identifier.volume47en_US
dc.identifier.issue1en_US
dc.identifier.startpage111en_US
dc.identifier.endpage119en_US
dc.identifier.scopus2-s2.0-85147170628en_US
dc.institutionauthor-
dc.identifier.doi10.33483/jfpau.1181948-
dc.authorscopusid57209802146-
dc.authorscopusid57215411277-
dc.authorscopusid57681421200-
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.identifier.scopusqualityQ4-
item.cerifentitytypePublications-
item.languageiso639-1en-
item.openairetypeArticle-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
Appears in Collections:Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
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