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dc.contributor.authorSTASEVYCH, Maryna V.
dc.contributor.authorTuyun, AMAÇ FATİH
dc.contributor.authorMUSYANOVYCH, Rostyslav Ya
dc.contributor.authorKomarovska-Porokhnyavets, Olena
dc.contributor.authorNOVIKOV, Volodymyr
dc.contributor.authorIbis, Cemil
dc.contributor.authorOzsoy-Gunes, Zeliha
dc.contributor.authorAyla, Sibel Sahinler
dc.contributor.authorBahar, Hakan
dc.date.accessioned2021-03-04T14:39:43Z
dc.date.available2021-03-04T14:39:43Z
dc.date.issued2016
dc.identifier.citationIbis C., Ozsoy-Gunes Z., Tuyun A. F. , Ayla S. S. , Bahar H., STASEVYCH M. V. , MUSYANOVYCH R. Y. , Komarovska-Porokhnyavets O., NOVIKOV V., "Synthesis, antibacterial and antifungal evaluation of thio- or piperazinyl-substituted 1,4-naphthoquinone derivatives", Journal of Sulfur Chemistry, cilt.37, sa.5, ss.477-487, 2016
dc.identifier.issn1741-5993
dc.identifier.othervv_1032021
dc.identifier.otherav_82b79a66-5afb-49ef-9d01-1c3b1b7f00df
dc.identifier.urihttp://hdl.handle.net/20.500.12627/89021
dc.identifier.urihttps://doi.org/10.1080/17415993.2016.1187734
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84971434675&origin=inward
dc.description.abstractA series of S-, S,S-, S,O-, N- and N,S-derivatives from 2,3-dichloro-1,4-naphthoquinone compound 1 were synthesized in different reaction media and evaluated for their antibacterial and antifungal activities. The structures of the novel products were characterized by spectroscopic methods, such as microanalysis, H-1 NMR, C-13 NMR and MS. Among the tested compounds 9, 12 and 18 are the most effective compounds against Candida tenuis as potent antifungal compounds. Compound 9 is also the most effective compound against Staphylococcus aureus as a potent antifungal compound.
dc.language.isoeng
dc.subjectKimya
dc.subjectTemel Bilimler (SCI)
dc.subjectBiyokimya
dc.subjectAlkoloidler
dc.subjectTemel Bilimler
dc.subjectKİMYA, MULTİDİSİPLİNER
dc.titleSynthesis, antibacterial and antifungal evaluation of thio- or piperazinyl-substituted 1,4-naphthoquinone derivatives
dc.typeMakale
dc.relation.journalJournal of Sulfur Chemistry
dc.contributor.departmentLviv Polytech National University , ,
dc.identifier.volume37
dc.identifier.issue5
dc.identifier.startpage477
dc.identifier.endpage487
dc.contributor.firstauthorID102590


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