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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 |