Показать сокращенную информацию
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 |