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dc.contributor.advisorŞahin, M. Fethi
dc.contributor.authorA. Gök, Seyhan
dc.date.accessioned2020-12-29T08:21:15Z
dc.date.available2020-12-29T08:21:15Z
dc.date.submitted1994
dc.date.issued2018-08-06
dc.identifier.urihttps://acikbilim.yok.gov.tr/handle/20.500.12812/361337
dc.description.abstract- 57 - VII. SUMMARY Two compounds which bear 3-pyrazoline-5-one moiety at the position 2 have been found v&ry active against some yeast-like fungi in our previous study. In this study, synthesis of the two compounds (compounds 1,3) in addition to that of rabenzazole have been carried out and two new additional compounds which had similar chemical structure have been synthesized (compounds 2,4). The chemical structure of the compounds have been elucidated by their IR, NMR spectral and elemental analysis. All the compounds synthesized have been tested against yeast-like fungi Candida parapsilosis. Candida albicans. Candida stellatoidea. Candida pseudptropicalis.- 58 - Candida guilliermondii for antifungal activity purpose, and they have been found more active than rabenzazole against the fungi employed. Compounds 1,2 and 3 have been, found almost equally potent, to the standard, miconazole.
dc.description.abstract- 57 - VII. SUMMARY Two compounds which bear 3-pyrazoline-5-one moiety at the position 2 have been found v&ry active against some yeast-like fungi in our previous study. In this study, synthesis of the two compounds (compounds 1,3) in addition to that of rabenzazole have been carried out and two new additional compounds which had similar chemical structure have been synthesized (compounds 2,4). The chemical structure of the compounds have been elucidated by their IR, NMR spectral and elemental analysis. All the compounds synthesized have been tested against yeast-like fungi Candida parapsilosis. Candida albicans. Candida stellatoidea. Candida pseudptropicalis.- 58 - Candida guilliermondii for antifungal activity purpose, and they have been found more active than rabenzazole against the fungi employed. Compounds 1,2 and 3 have been, found almost equally potent, to the standard, miconazole.en_US
dc.languageTurkish
dc.language.isotr
dc.rightsinfo:eu-repo/semantics/embargoedAccess
dc.rightsAttribution 4.0 United Statestr_TR
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectEczacılık ve Farmakolojitr_TR
dc.subjectPharmacy and Pharmacologyen_US
dc.titleBazı 2-(1-pirazolil) benzimidazol türevleri üzerinde çalışmalar
dc.typemasterThesis
dc.date.updated2018-08-06
dc.contributor.departmentDiğer
dc.subject.ytmBenzimidazoles
dc.subject.ytmAntifungal agents
dc.identifier.yokid37938
dc.publisher.instituteSağlık Bilimleri Enstitüsü
dc.publisher.universityGAZİ ÜNİVERSİTESİ
dc.identifier.thesisid37938
dc.description.pages66
dc.publisher.disciplineDiğer


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