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dc.contributor.authorKiraz, M
dc.contributor.authorKucukguzel, SG
dc.contributor.authorRollas, S
dc.contributor.authorErdeniz, H
dc.date.accessioned2021-03-05T14:06:10Z
dc.date.available2021-03-05T14:06:10Z
dc.date.issued1999
dc.identifier.citationKucukguzel S., Rollas S., Erdeniz H., Kiraz M., "Synthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates", EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, cilt.34, ss.153-160, 1999
dc.identifier.issn0223-5234
dc.identifier.otherav_b57c5e97-d5c5-4673-ba3a-c53dc1383a21
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/120829
dc.identifier.urihttps://doi.org/10.1016/s0223-5234(99)80048-8
dc.description.abstractEthyl 2-arylhydrazono-3-oxobutyrates 6a-f, 5-(4-aminophenyl)-2,4-dihydro-4-phenyl-3H-1,2,4-triazole-3-one 5d and 1-[4-(benzoylamino)benzoyI]-4-phenylsemicarbazide 4d were synthesized in order to determine their antimicrobial properties. Their structures were elucidated using spectral data. The synthesized compounds were tested in vitro against one Gram-positive and 2 Gram-negative bacterial strains, one Mycobacterial strain and a fungus Candida albicans. Compound 6d showed significant activity against Staphylococcus aureus whereas the others had no remarkable activity on this strain. Componnd 6e was found to be more active than the others against Mycobacterium fortuitum at a MIC value of 32 mu g/mL. The antibacterial and antifungal activities of ld, 5d and 6a-f were also compared with various standard drugs. (C) Elsevier, Paris.
dc.language.isoeng
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectKİMYA, TIP
dc.subjectKimya
dc.subjectTemel Bilimler (SCI)
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectYaşam Bilimleri
dc.subjectTemel Eczacılık Bilimleri
dc.subjectEczacılık
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectTemel Bilimler
dc.subjectBiyokimya
dc.titleSynthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates
dc.typeMakale
dc.relation.journalEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
dc.contributor.department, ,
dc.identifier.volume34
dc.identifier.issue2
dc.identifier.startpage153
dc.identifier.endpage160
dc.contributor.firstauthorID122714


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