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dc.contributor.authorKaplancıklı, Zafer Asım
dc.contributor.authorTuran, Gülhan
dc.contributor.authorÖzdemir, Ahmet
dc.date.accessioned2019-10-19T16:02:33Z
dc.date.available2019-10-19T16:02:33Z
dc.date.issued2009
dc.identifier.issn1300-4182
dc.identifier.urihttps://hdl.handle.net/11421/13786
dc.description.abstractIn this study, eight new ethyl {2-[3,4-diaryl-3H-thiazol-2-ylidenamino] thiazol-4-yl}acetate were synthesized by reacting ethyl [2-(3-aryl(thiouredio) thiazol-4-yl]acetate and phenacyl bromides in ethanol. The solid was filtered and recrystallized from ethanol. The chemical structures of the synthesized compounds were proven by elemental analysis, IR, 1H-NMR and MS spectral data. The compounds were evaluated for in vitro antituberculosis activity against Mycobacterium tuberculosis H37Rv using the BACTEC 460 radiometric system and BACTEC 12B medium. The preliminary results showed that all of the tested compounds were inactive against the test organism.en_US
dc.language.isoengen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAcetic Acid Ethyl Estersen_US
dc.subjectAntitubercular Activityen_US
dc.subjectThiazoleen_US
dc.titleStudies on thiazolyliminothiazoline derivatives as potential antitubercular agentsen_US
dc.typearticleen_US
dc.relation.journalFabad Journal of Pharmaceutical Sciencesen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume34en_US
dc.identifier.issue1en_US
dc.identifier.startpage25en_US
dc.identifier.endpage31en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorKaplancıklı, Zafer Asım
dc.contributor.institutionauthorTuran, Gülhan
dc.contributor.institutionauthorÖzdemir, Ahmet


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