Synthesis and Antibacterial and Antifungal Properties of Novel S-, N-, N,S-, and S,O-Substituted 1,4-Naphthoquinone Derivatives
dc.contributor.author | Ibis, Cemil | |
dc.contributor.author | Tuyun, Amac Fatih | |
dc.contributor.author | Ozsoy-Gunes, Zeliha | |
dc.contributor.author | Ayla, Sibel Sahinler | |
dc.contributor.author | Stasevych, Maryna V. | |
dc.contributor.author | Musyanovych, Rostyslav Ya | |
dc.contributor.author | Komarovska-Porokhnyavets, Olena | |
dc.date.accessioned | 2024-03-13T10:35:25Z | |
dc.date.available | 2024-03-13T10:35:25Z | |
dc.date.issued | 2013 | |
dc.department | İstanbul Beykent Üniversitesi | en_US |
dc.description.abstract | A novel series of substituted 1,4-naphthoquinone derivatives were synthesized and evaluated for their antibacterial and antifungal activity. The structures of the novel products were characterized by spectroscopic methods. Among the tested compounds, 2,2,3,3-alkoxy substituted naphthoquinones, S,O-substituted naphthoquinone, and N,S-substituted naphthoquinone derivatives are the most potent antifungals against C. tenuis. 2,3-Thio-2,3-alkoxy substituted naphthoquinones are the most effective antifungal compounds against A. niger. Supplemental materials are available for this article. Go to the publisher's online edition ofPhosphorus, Sulfur, and Silicon and the Related Elementsto view the free supplemental file. | en_US |
dc.description.sponsorship | TUBITAK [109T617]; State Agency on Science, Innovations and Informatization of the Ukraine [M/309-2011] | en_US |
dc.description.sponsorship | Financial support from TUBITAK for the Ukraine-Turkey agreement (Project No. 109T617) and from the State Agency on Science, Innovations and Informatization of the Ukraine (Project No. M/309-2011) is gratefully acknowledged. | en_US |
dc.identifier.doi | 10.1080/10426507.2012.727515 | |
dc.identifier.endpage | 966 | en_US |
dc.identifier.issn | 1042-6507 | |
dc.identifier.issn | 1563-5325 | |
dc.identifier.issue | 7 | en_US |
dc.identifier.scopus | 2-s2.0-84880274112 | en_US |
dc.identifier.scopusquality | Q4 | en_US |
dc.identifier.startpage | 955 | en_US |
dc.identifier.uri | https://doi.org/10.1080/10426507.2012.727515 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12662/4417 | |
dc.identifier.volume | 188 | en_US |
dc.identifier.wos | WOS:000321691300017 | en_US |
dc.identifier.wosquality | Q4 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Taylor & Francis Ltd | en_US |
dc.relation.ispartof | Phosphorus Sulfur And Silicon And The Related Elements | en_US |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
dc.rights | info:eu-repo/semantics/closedAccess | en_US |
dc.subject | N,S-substituted 1 | en_US |
dc.subject | 4-naphthoquinones | en_US |
dc.subject | heterocyclic ethers with quinone group | en_US |
dc.subject | antibacterial activity | en_US |
dc.subject | antifungal activity | en_US |
dc.title | Synthesis and Antibacterial and Antifungal Properties of Novel S-, N-, N,S-, and S,O-Substituted 1,4-Naphthoquinone Derivatives | en_US |
dc.type | Article | en_US |