Publication:
Synthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates

dc.contributor.authorsKucukguzel, SG; Rollas, S; Erdeniz, H; Kiraz, M
dc.date.accessioned2022-03-12T16:59:50Z
dc.date.accessioned2026-01-10T18:57:08Z
dc.date.available2022-03-12T16:59:50Z
dc.date.issued1999
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.identifier.doi10.1016/S0223-5234(99)80048-8
dc.identifier.eissn1768-3254
dc.identifier.issn0223-5234
dc.identifier.urihttps://hdl.handle.net/11424/227244
dc.identifier.wosWOS:000079828800006
dc.language.isoeng
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
dc.relation.ispartofEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,2,4-triazoline-3-ones
dc.subject1,2,4-triazoline-3-thiones
dc.subjectsemicarbazides
dc.subjectcoupling products
dc.subjectmicrodilution method
dc.subjectMETHYL-DERIVATIVES
dc.subjectANTIBACTERIAL
dc.subject1,2,4-TRIAZOLES
dc.titleSynthesis, characterization and antimicrobial evaluation of ethyl 2-arylhydrazono-3-oxobutyrates
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage160
oaire.citation.issue2
oaire.citation.startPage153
oaire.citation.titleEUROPEAN JOURNAL OF MEDICINAL CHEMISTRY
oaire.citation.volume34

Files