| Форма представления | Статьи в зарубежных журналах и сборниках |
| Год публикации | 2016 |
| Язык | английский |
|
Курбангалиева Альмира Рафаэловна, автор
|
|
Прадипта Абмара Рахмат, автор
|
| Библиографическое описание на языке оригинала |
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. |
| Аннотация |
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. |
| Ключевые слова |
acrolein, aryl azide, oxidative stress, cell imaging, click chemistry |
| Название журнала |
ACS SENSORS
|
| URL |
http://pubs.acs.org/doi/abs/10.1021/acssensors.6b00122 |
| Пожалуйста, используйте этот идентификатор, чтобы цитировать или ссылаться на эту карточку |
https://repository.kpfu.ru/?p_id=174364 |
Полная запись метаданных  |
| Поле DC |
Значение |
Язык |
| dc.contributor.author |
Курбангалиева Альмира Рафаэловна |
ru_RU |
| dc.contributor.author |
Прадипта Абмара Рахмат |
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/?p_id=174364 |
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 |
Статьи в зарубежных журналах и сборниках |
ru_RU |
|
EN 
中文 
ES 
Карта сайта
