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 |
|