dc.contributor.author |
Tsutsui A. |
|
dc.contributor.author |
Imamaki R. |
|
dc.contributor.author |
Kitazume S. |
|
dc.contributor.author |
Hanashima S. |
|
dc.contributor.author |
Yamaguchi Y. |
|
dc.contributor.author |
Kaneda M. |
|
dc.contributor.author |
Oishi S. |
|
dc.contributor.author |
Fujii N. |
|
dc.contributor.author |
Kurbangalieva A. |
|
dc.contributor.author |
Taniguchi N. |
|
dc.contributor.author |
Tanaka K. |
|
dc.date.accessioned |
2018-09-18T20:22:53Z |
|
dc.date.available |
2018-09-18T20:22:53Z |
|
dc.date.issued |
2014 |
|
dc.identifier.issn |
1477-0520 |
|
dc.identifier.uri |
https://dspace.kpfu.ru/xmlui/handle/net/139286 |
|
dc.description.abstract |
Acrolein, a toxic unsaturated aldehyde generated as a result of oxidative stress, readily reacts with a variety of nucleophilic biomolecules. Polyamines, which produced acrolein in the presence of amine oxidase, were then found to react with acrolein to produce 1,5-diazacyclooctane, a previously unrecognized but significant downstream product of oxidative stress. Although diazacyclooctane formation effectively neutralized acrolein toxicity, the diazacyclooctane hydrogel produced through a sequential diazacyclooctane polymerization reaction was highly cytotoxic. This study suggests that diazacyclooctane formation is involved in the mechanism underlying acrolein-mediated oxidative stress. © 2014 the Partner Organisations. |
|
dc.relation.ispartofseries |
Organic and Biomolecular Chemistry |
|
dc.title |
Polyamine modification by acrolein exclusively produces 1,5-diazacyclooctanes: A previously unrecognized mechanism for acrolein-mediated oxidative stress |
|
dc.type |
Article |
|
dc.relation.ispartofseries-issue |
28 |
|
dc.relation.ispartofseries-volume |
12 |
|
dc.collection |
Публикации сотрудников КФУ |
|
dc.relation.startpage |
5151 |
|
dc.source.id |
SCOPUS14770520-2014-12-28-SID84903118251 |
|