Cancer cell targeting driven by selective polyamine reactivity with glycine propargyl esters

Tanei T.; Kitazume S.; Taniguchi N.; Noguchi S.; Tsubokura K.; Nakao Y.; Tanaka K.; Vong K.

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