Publication:
Theoretical and Antimicrobial Activity Study for Ethyl{4-[3-(1 H -imidazole-1-yl)propyl]-3-methyl-5-oxo-4,5-dihydro-1 H -1,2,4-triazol-1-yl}acetate

dc.authorscopusid26644545800
dc.authorscopusid8354984100
dc.authorscopusid8361744500
dc.authorscopusid6506730197
dc.authorscopusid28067476100
dc.authorwosidDirekel, Sahin/Abg-1575-2020
dc.contributor.authorSuleymanoglu, Nevin
dc.contributor.authorUnver, Yasemin
dc.contributor.authorUstabas, Resat
dc.contributor.authorDirekel, Sahin
dc.contributor.authorAlpaslan, Yelda Bingol
dc.date.accessioned2020-06-21T09:04:46Z
dc.date.available2020-06-21T09:04:46Z
dc.date.issued2017
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Suleymanoglu, Nevin] Gazi Univ, Tech Sci Vocat High Sch, TR-06374 Ankara, Turkey; [Unver, Yasemin] Karadeniz Tech Univ, Dept Chem, Fac Sci, Trabzon, Turkey; [Ustabas, Resat] Ondokuz Mays Univ, Fac Educ, Dept Middle Educ, Kurupelit, Samsun, Turkey; [Direkel, Sahin] Giresun Univ, Dept Med Microbiol, Fac Med, Giresun, Turkey; [Alpaslan, Yelda Bingol] Giresun Univ, Dept Biophys, Fac Med, Giresun, Turkeyen_US
dc.description.abstractEthyl{4-[3-(1H-imidazole-1-yl)propyl]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-acetate (I) was synthesized as described in the literature and studied by proton and carbon-13 nuclear magnetic resonance, Fourier transform infrared spectroscopic techniques. Theoretical calculations were performed by the density functional method with 6-311G(d,p) and 6-311++G(d,p) basis sets. Structural parameters of compound I, vibrational frequencies, and chemical shift values were determined. The antimicrobial activity of compound I was tested for seven standard bacteria; Staphylococcus aureus, Escherichia coli, Salmonella typhimurium, Yersinia enterocolitica, Listeria monocytogenes, Shigella flexneri, Pseudomonas aeruginosa, and one standard fungi isolate by microdilution broth assay with Alamar Blue Dye. The in vitro results show that compound I has antimicrobial activity against to two standard bacteria, Shigella flexneri and Listeria monocytogenes. And also, the antifungal activity was not detected against selected fungi isolate, Candida tropicalis.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1080/00387010.2017.1287098
dc.identifier.endpage101en_US
dc.identifier.issn0038-7010
dc.identifier.issn1532-2289
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-85016968157
dc.identifier.scopusqualityQ3
dc.identifier.startpage96en_US
dc.identifier.urihttps://doi.org/10.1080/00387010.2017.1287098
dc.identifier.volume50en_US
dc.identifier.wosWOS:000399656200005
dc.identifier.wosqualityQ3
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofSpectroscopy Lettersen_US
dc.relation.journalSpectroscopy Lettersen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1,2,4-Triazolen_US
dc.subjectAntibacterial and Antifungal Activityen_US
dc.subjectDFT Calculationsen_US
dc.subjectHOMO-LUMOen_US
dc.subjectNMR and FTIR Spectroscopiesen_US
dc.titleTheoretical and Antimicrobial Activity Study for Ethyl{4-[3-(1 H -imidazole-1-yl)propyl]-3-methyl-5-oxo-4,5-dihydro-1 H -1,2,4-triazol-1-yl}acetateen_US
dc.typeArticleen_US
dspace.entity.typePublication

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