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dc.contributor.author | Burilov V. | |
dc.contributor.author | Mironova D. | |
dc.contributor.author | Ibragimova R. | |
dc.contributor.author | Solovieva S. | |
dc.contributor.author | Antipin I. | |
dc.date.accessioned | 2018-09-19T23:11:43Z | |
dc.date.available | 2018-09-19T23:11:43Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 2191-1630 | |
dc.identifier.uri | https://dspace.kpfu.ru/xmlui/handle/net/146042 | |
dc.description.abstract | © 2016, Springer Science+Business Media New York.New bis-ammonium thiacalix[4]arene derivatives with different lipophilicity were synthesized using copper(I)-catalyzed azide-alkyne cycloaddition in good yields. Binding of a new thiacalix[4]arene derivatives with bovine serum albumin (BSA) was investigated in detail using fluorescence spectroscopy method. Quenching mechanism, the binding constants, and number of binding sites were determined. | |
dc.relation.ispartofseries | BioNanoScience | |
dc.subject | Ammonium compounds | |
dc.subject | BSA | |
dc.subject | Luminescence | |
dc.subject | Quenching of luminescence | |
dc.subject | Thiacalix[4]arene | |
dc.subject | Triazoles | |
dc.title | Interactions of New bis-Ammonium Thiacalix[4]arene Derivatives in 1,3-Alternate Stereoisomeric Form with Bovine Serum Albumin | |
dc.type | Article | |
dc.relation.ispartofseries-issue | 4 | |
dc.relation.ispartofseries-volume | 6 | |
dc.collection | Публикации сотрудников КФУ | |
dc.relation.startpage | 427 | |
dc.source.id | SCOPUS21911630-2016-6-4-SID84999792333 |