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dc.contributor.authorKocabalkanli, A
dc.contributor.authorOtuk, G
dc.contributor.authorCesur, N
dc.contributor.authorAtes, O
dc.date.accessioned2021-03-06T20:27:32Z
dc.date.available2021-03-06T20:27:32Z
dc.identifier.citationAtes O., Kocabalkanli A., Cesur N., Otuk G., "Synthesis and antimicrobial activity of some 5-aryl-2-[(N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazoles", FARMACO, cilt.53, ss.541-544, 1998
dc.identifier.issn0014-827X
dc.identifier.othervv_1032021
dc.identifier.otherav_fa4a88d0-028a-4019-ba64-5c90824583d5
dc.identifier.urihttp://hdl.handle.net/20.500.12627/163888
dc.identifier.urihttps://doi.org/10.1016/s0014-827x(98)00063-9
dc.description.abstractIn this study, a number of novel 5-aryl-2-[(N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazole derivatives were synthesized by the reaction of potassium salts of N,N-disubstituted dithiocarbamoic acids with 2-[(alpha-chloro-alpha-phenylacetyl/alpha-bromopropionyl)-amino]-5-aryl-1,3,4-oxadiazoles. Structures of the compounds were confirmed by the spectral data (IR, H-1 NMR, EIMS) and elemental analyses. Most of the compounds were tested against various microorganisms and four of them were found to be weakly active against Staphylococcus aureus and Staphylococcus epidermidis. (C) 1998 Elsevier Science S.A. All rights reserved.
dc.language.isoeng
dc.subjectTemel Bilimler
dc.subjectEczacılık
dc.subjectYaşam Bilimleri
dc.subjectTemel Eczacılık Bilimleri
dc.subjectSağlık Bilimleri
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.titleSynthesis and antimicrobial activity of some 5-aryl-2-[(N,N-disubstituted thiocarbamoylthio)acylamino]-1,3,4-oxadiazoles
dc.typeMakale
dc.relation.journalFARMACO
dc.contributor.department, ,
dc.identifier.volume53
dc.identifier.startpage541
dc.identifier.endpage544
dc.contributor.firstauthorID121134


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