Nucleophilic substitution reactions of 1,4-naphthoquinone and biologic properties of novel S-, S,S-, N-, and N,S-substituted 1,4-naphthoquinone derivatives
dc.contributor.author | Ibis, Cemil | |
dc.contributor.author | Tuyun, Amac Fatih | |
dc.contributor.author | Bahar, Hakan | |
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 | 2024-03-13T10:30:41Z | |
dc.date.available | 2024-03-13T10:30:41Z | |
dc.date.issued | 2014 | |
dc.department | İstanbul Beykent Üniversitesi | en_US |
dc.description.abstract | A novel series of S-, S,S-, N- and N,S-substituted 1,4-naphthoquinone derivatives were synthesized and evaluated for their antibacterial and antifungal activity. Among the synthesized compounds especially 10a and 11b have been discovered as an antibacterial or antifungal agents, and 15f is the most effective compound against M. luteum as potent antifungal. The structures of the novel products were characterized by micro analysis, UV/Vis, H-1 NMR, C-13 NMR, and MS. The electrochemical properties of some of the novel 1,4-naphthoquinone derivatives were also investigated by cyclic voltammetry. | en_US |
dc.description.sponsorship | TUBITAK [109T617]; State Agency on Science, Innovations and Informatization of Ukraine [M/309-2011] | en_US |
dc.description.sponsorship | The financial support from TUBITAK for Ukraine-Turkey agreement gratefully acknowledged (Project No. 109T617) and from State Agency on Science, Innovations and Informatization of Ukraine (Project No. M/309-2011). | en_US |
dc.identifier.doi | 10.1007/s00044-013-0806-y | |
dc.identifier.endpage | 2149 | en_US |
dc.identifier.issn | 1054-2523 | |
dc.identifier.issn | 1554-8120 | |
dc.identifier.issue | 4 | en_US |
dc.identifier.scopus | 2-s2.0-84898952740 | en_US |
dc.identifier.scopusquality | Q2 | en_US |
dc.identifier.startpage | 2140 | en_US |
dc.identifier.uri | https://doi.org/10.1007/s00044-013-0806-y | |
dc.identifier.uri | https://hdl.handle.net/20.500.12662/3496 | |
dc.identifier.volume | 23 | en_US |
dc.identifier.wos | WOS:000331003400049 | en_US |
dc.identifier.wosquality | Q3 | en_US |
dc.indekslendigikaynak | Web of Science | en_US |
dc.indekslendigikaynak | Scopus | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer Birkhauser | en_US |
dc.relation.ispartof | Medicinal Chemistry Research | 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 | 1,4-Naphthoquinone | en_US |
dc.subject | Amines | en_US |
dc.subject | Thiols | en_US |
dc.subject | Antibacterial activity | en_US |
dc.subject | Antifungal activity | en_US |
dc.title | Nucleophilic substitution reactions of 1,4-naphthoquinone and biologic properties of novel S-, S,S-, N-, and N,S-substituted 1,4-naphthoquinone derivatives | en_US |
dc.type | Article | en_US |