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dc.contributor.authorYurttaş, Leyla
dc.contributor.authorErtaş, Merve
dc.contributor.authorCankılıç, Meral Yılmaz
dc.contributor.authorDemirayak, Şeref
dc.date.accessioned2019-10-19T16:02:34Z
dc.date.available2019-10-19T16:02:34Z
dc.date.issued2017
dc.identifier.issn1307-2080
dc.identifier.urihttps://dx.doi.org/10.23893/1307-2080.APS.0554
dc.identifier.urihttps://hdl.handle.net/11421/13804
dc.description.abstractA series of 3-[(4-aryl-2-thiazolyl)hydrazone]-1H-indol-2,3-dione derivatives (2a-f) were designed and synthesized using isatin as starting material. The obtained thiazole compounds were screened to investigate their antituberculosis activity against Mycobacterum tuberculosis H37RV (ATCC 27294). Among them, two compounds 2c and 2d were displayed antitubercular potential two-fold greater than standard drugsen_US
dc.language.isoengen_US
dc.publisherUniversity of Istanbulen_US
dc.relation.isversionof10.23893/1307-2080.APS.0554en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAntimycobacterial Activityen_US
dc.subjectIndoleen_US
dc.subjectIsatinen_US
dc.subjectThiazoleen_US
dc.titleSynthesis and antimycobacterial activity evaluation of isatin-derived 3- [(4-aryl-2-thiazolyl])hydrazone]-1H-indol-2,3-dionesen_US
dc.typearticleen_US
dc.relation.journalActa Pharmaceutica Scienciaen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume55en_US
dc.identifier.issue1en_US
dc.identifier.startpage51en_US
dc.identifier.endpage58en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorYurttaş, Leyla
dc.contributor.institutionauthorDemirayak, Şeref


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