Form of presentation | Articles in international journals and collections |
Year of publication | 2016 |
Язык | английский |
|
Kurbangalieva Almira Rafaelovna, author
Saygitbatalova Elena Shiripovna, author
Tanaka Kacunori , author
|
Bibliographic description in the original language |
Pradipta A. R. Uncatalyzed click reaction between phenyl azides and acrolein: 4-formyl-1,2,3-triazolines as “clicked” markers for visualizations of extracellular acrolein released from oxidatively stressed cells / A. R. Pradipta, M. Taichi, I. Nakase, E. Saigitbatalova, A. Kurbangalieva, S. Kitazume, N. Taniguchi, K. Tanaka // ACS Sens. – 2016. – V. 1. – № 5. – P. 623–632. |
Annotation |
Acrolein, a highly toxic α,β-unsaturated aldehyde, has been a longstanding key biomarker associated with a range of disorders related to oxidative stresses. Currently available analytical methods rely on the indirect protocols, e.g., derivatization/HPLC or mAb detection of the lysine adducts. Consequently, developing new analytical tools for acrolein detection that are straightforward, cost-effective, selective, and
preferably feasible using live cells remains a highly essential pursuit in the diagnosis and therapeutic treatment of oxidative stress-related diseases. We demonstrated that for the first time aryl azides can rapidly and selectively react with acrolein in a “click” manner to provide 4-formyl-1,2,3-triazolines and 4-formyl-1,2,3-triazoles, which represents an unexplored reactivity of aryl azides. |
Keywords |
acrolein, aryl azide, oxidative stress, cell imaging, click chemistry |
The name of the journal |
ACS SENSORS
|
URL |
http://pubs.acs.org/doi/abs/10.1021/acssensors.6b00122 |
Please use this ID to quote from or refer to the card |
https://repository.kpfu.ru/eng/?p_id=145620&p_lang=2 |
Full metadata record |
Field DC |
Value |
Language |
dc.contributor.author |
Kurbangalieva Almira Rafaelovna |
ru_RU |
dc.contributor.author |
Saygitbatalova Elena Shiripovna |
ru_RU |
dc.contributor.author |
Tanaka Kacunori |
ru_RU |
dc.date.accessioned |
2016-01-01T00:00:00Z |
ru_RU |
dc.date.available |
2016-01-01T00:00:00Z |
ru_RU |
dc.date.issued |
2016 |
ru_RU |
dc.identifier.citation |
Pradipta A. R. Uncatalyzed click reaction between phenyl azides and acrolein: 4-formyl-1,2,3-triazolines as “clicked” markers for visualizations of extracellular acrolein released from oxidatively stressed cells / A. R. Pradipta, M. Taichi, I. Nakase, E. Saigitbatalova, A. Kurbangalieva, S. Kitazume, N. Taniguchi, K. Tanaka // ACS Sens. – 2016. – V. 1. – № 5. – P. 623–632. |
ru_RU |
dc.identifier.uri |
https://repository.kpfu.ru/eng/?p_id=145620&p_lang=2 |
ru_RU |
dc.description.abstract |
ACS SENSORS |
ru_RU |
dc.description.abstract |
Acrolein, a highly toxic α,β-unsaturated aldehyde, has been a longstanding key biomarker associated with a range of disorders related to oxidative stresses. Currently available analytical methods rely on the indirect protocols, e.g., derivatization/HPLC or mAb detection of the lysine adducts. Consequently, developing new analytical tools for acrolein detection that are straightforward, cost-effective, selective, and
preferably feasible using live cells remains a highly essential pursuit in the diagnosis and therapeutic treatment of oxidative stress-related diseases. We demonstrated that for the first time aryl azides can rapidly and selectively react with acrolein in a “click” manner to provide 4-formyl-1,2,3-triazolines and 4-formyl-1,2,3-triazoles, which represents an unexplored reactivity of aryl azides. |
ru_RU |
dc.language.iso |
ru |
ru_RU |
dc.subject |
acrolein |
ru_RU |
dc.subject |
aryl azide |
ru_RU |
dc.subject |
oxidative stress |
ru_RU |
dc.subject |
cell imaging |
ru_RU |
dc.subject |
click chemistry |
ru_RU |
dc.title |
Uncatalyzed click reaction between phenyl azides and acrolein: 4-formyl-1,2,3-triazolines as “clicked” markers for visualizations of extracellular acrolein released from oxidatively stressed cells |
ru_RU |
dc.type |
Articles in international journals and collections |
ru_RU |
|