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Synthesis and mutagenicity of 2-aryl-substitute (o-hydroxy-, m-bromo-, o-methoxy-, o-nitro-phenyl or 4-pyridyl) benzothiazole derivatives on Salmonella typhimurium and human lymphocytes exposed in vitro

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dc.contributor.authorTüylü, Berrin Ayaz
dc.contributor.authorZeyti̇noǧlu, Hülya
dc.contributor.authorIşıkdağ, İlhan
dc.date.accessioned2025-11-13T10:18:55Z
dc.date.issued2007-08-25
dc.identifier.doihttps://doi.org/10.2478/s11756-007-0122-4
dc.identifier.endpage632
dc.identifier.issn0006-3088
dc.identifier.issue5
dc.identifier.openalexW2004768695
dc.identifier.startpage626
dc.identifier.urihttps://hdl.handle.net/11421/3776
dc.identifier.urihttps://doi.org/10.2478/s11756-007-0122-4
dc.identifier.volume62
dc.language.isoen
dc.relation.ispartofBiologia
dc.rightsrestrictedAccess
dc.subjectBenzothiazole
dc.subjectSalmonella
dc.subjectNitro
dc.subjectIn vitro
dc.subjectChemistry
dc.subjectAryl
dc.subjectMedicinal chemistry
dc.subjectStereochemistry
dc.subjectBiology
dc.subjectBacteria
dc.subjectOrganic chemistry
dc.subjectBiochemistry
dc.subjectGenetics
dc.subjectAlkyl
dc.titleSynthesis and mutagenicity of 2-aryl-substitute (o-hydroxy-, m-bromo-, o-methoxy-, o-nitro-phenyl or 4-pyridyl) benzothiazole derivatives on Salmonella typhimurium and human lymphocytes exposed in vitro
dc.typeArticle
dspace.entity.typePublication
local.authorid.openalexA5007861747
local.authorid.openalexA5020841384
local.authorid.openalexA5112167696

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