dc.contributor.author |
Vong K. |
|
dc.contributor.author |
Tsubokura K. |
|
dc.contributor.author |
Nakao Y. |
|
dc.contributor.author |
Tanei T. |
|
dc.contributor.author |
Noguchi S. |
|
dc.contributor.author |
Kitazume S. |
|
dc.contributor.author |
Taniguchi N. |
|
dc.contributor.author |
Tanaka K. |
|
dc.date.accessioned |
2018-04-05T07:09:50Z |
|
dc.date.available |
2018-04-05T07:09:50Z |
|
dc.date.issued |
2017 |
|
dc.identifier.issn |
1359-7345 |
|
dc.identifier.uri |
http://dspace.kpfu.ru/xmlui/handle/net/130007 |
|
dc.description.abstract |
© 2017 The Royal Society of Chemistry. Rapidly growing cancer cells have increased levels of intracellular polyamines compared to normal, healthy tissues. Based on the selective reactivity of glycine propargyl esters, probes were synthesized that show evidence for selective polyamine reactivity, which was then applied for selective cancer cell imaging studies. |
|
dc.relation.ispartofseries |
Chemical Communications |
|
dc.title |
Cancer cell targeting driven by selective polyamine reactivity with glycine propargyl esters |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
60 |
|
dc.relation.ispartofseries-volume |
53 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
8403 |
|
dc.source.id |
SCOPUS13597345-2017-53-60-SID85026328584 |
|