dc.contributor.author |
Puplampu J. |
|
dc.contributor.author |
Yakimova L. |
|
dc.contributor.author |
Vavilova A. |
|
dc.contributor.author |
Rizvanov I. |
|
dc.contributor.author |
Stoikov I. |
|
dc.date.accessioned |
2018-09-18T20:35:07Z |
|
dc.date.available |
2018-09-18T20:35:07Z |
|
dc.date.issued |
2015 |
|
dc.identifier.issn |
1998-9539 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/141388 |
|
dc.description.abstract |
© ISUCT Publishing. New tetrasubstituted derivatives of thiacalix[4]arene functionalized with bis(3-aminopropyl)amide fragments at the lower rim in the cone and 1,3-alternate conformations have been synthesized. It was demonstrated that the synthesized thiacalix[4]arenes derivatives interact with DNA resulting in a shift in absorption maxima to 257 nm with clear isosbestic point at 300 nm. |
|
dc.relation.ispartofseries |
Macroheterocycles |
|
dc.subject |
DNA |
|
dc.subject |
Macrocycles |
|
dc.subject |
Molecular recognition |
|
dc.subject |
Synthesis |
|
dc.subject |
Thiacalix[4]arene |
|
dc.title |
p-tert-butyl thiacalix[4]arene derivatives functionalized in the lower rim with bis(3-aminopropyl)amine: Synthesis and interaction with DNA |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
1 |
|
dc.relation.ispartofseries-volume |
8 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
75 |
|
dc.source.id |
SCOPUS19989539-2015-8-1-SID84932633348 |
|