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dc.contributor.authorMaillard, Ludovic T.
dc.contributor.authorBertout, Sebastien
dc.contributor.authorQuinÖnero, Ophelie
dc.contributor.authorAkalın Çiftçi, Gülsen
dc.contributor.authorTuran, Gülhanulan
dc.contributor.authorFulcrand, Pierre
dc.contributor.authorMasurier, Nicolas
dc.date.accessioned2019-10-19T14:44:48Z
dc.date.available2019-10-19T14:44:48Z
dc.date.issued2013
dc.identifier.issn0960-894X
dc.identifier.issn1464-3405
dc.identifier.urihttps://dx.doi.org/10.1016/j.bmcl.2013.01.039
dc.identifier.urihttps://hdl.handle.net/11421/13617
dc.descriptionWOS: 000315331500049en_US
dc.descriptionPubMed ID: 23403080en_US
dc.description.abstractEighteen new hydrazino-1,3-thiazole derivatives were evaluated against 8 strains of multi-resistant Candida spp. Introduction of an indolyl moiety linked to the hydrazone function enhanced the in vitro anti-Candida activity, with an activity spectrum towards Candida albicans strains. Introduction of a (S)-2-aminoethyl chain on the thiazole nucleus largely enhanced the in vitro antifungal activity, with a selectivity oriented towards non-C. albicans speciesen_US
dc.language.isoengen_US
dc.publisherPergamon-Elsevier Science LTDen_US
dc.relation.isversionof10.1016/j.bmcl.2013.01.039en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectThiazoleen_US
dc.subjectHydrazoneen_US
dc.subjectCandida Spp.en_US
dc.subjectAntifungal Activityen_US
dc.titleSynthesis and anti-Candida activity of novel 2-hydrazino-1,3-thiazole derivativesen_US
dc.typearticleen_US
dc.relation.journalBioorganic & Medicinal Chemistry Lettersen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume23en_US
dc.identifier.issue6en_US
dc.identifier.startpage1803en_US
dc.identifier.endpage1807en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.institutionauthorAkalın Çiftçi, Gülsen


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