USE OF TETRAACETYLATED 5-AMINO-4-CARBAMOYL IMIDAZOLYL-1-β-D-RIBOFURANOSIDE AS A PROTEIN KINASE Cδ INHIBITOR
FIELD: chemistry.SUBSTANCE: invention refers to organic chemistry and medicine. Disclosed is use of a tetraacetyled derivative of 5-amino-4-carbamoylimidazolyl-1-β-D-ribofuranoside - ((AcO)AICAR) as a selective inhibitor of protein kinase Cδ. (AcO)AICAR effectively inhibits protein kinase Cδ (PKCδ)...
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24.01.2020
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Abstract | FIELD: chemistry.SUBSTANCE: invention refers to organic chemistry and medicine. Disclosed is use of a tetraacetyled derivative of 5-amino-4-carbamoylimidazolyl-1-β-D-ribofuranoside - ((AcO)AICAR) as a selective inhibitor of protein kinase Cδ. (AcO)AICAR effectively inhibits protein kinase Cδ (PKCδ) due to specific inhibition of PKCδ/NF-κB signaling pathway.EFFECT: because (AcO)AICAR does not possess high toxicity with respect to healthy cells, it allows using it in disturbances prevention of PKCδ/NF-κB signaling pathway, for example to prevent apoptosis or increased thrombosis.4 cl, 4 dwg, 6 ex
Изобретение относится к области органической химии и к медицине. Предложено применение тетраацетилированного производного 5-амино-4-карбамоилимидазолил-1-β-D-рибофуранозида - ((АсО)АИКАР) в качестве селективного ингибитора протеинкиназы Сδ. (АсО)АИКАР эффективно ингибирует протеинкиназу Сδ (ПКСδ) за счёт специфичного ингибирования ПКСδ/NF-κB сигнального пути. Поскольку (АсО)АИКАР не обладает высокой токсичностью в отношении здоровых клеток, это позволяет использовать его в предотвращении нарушений ПКСδ/NF-κB сигнального пути, например для предотвращения апоптоза или повышенного тромбообразования. 3 з.п. ф-лы, 4 ил., 6 пр. |
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AbstractList | FIELD: chemistry.SUBSTANCE: invention refers to organic chemistry and medicine. Disclosed is use of a tetraacetyled derivative of 5-amino-4-carbamoylimidazolyl-1-β-D-ribofuranoside - ((AcO)AICAR) as a selective inhibitor of protein kinase Cδ. (AcO)AICAR effectively inhibits protein kinase Cδ (PKCδ) due to specific inhibition of PKCδ/NF-κB signaling pathway.EFFECT: because (AcO)AICAR does not possess high toxicity with respect to healthy cells, it allows using it in disturbances prevention of PKCδ/NF-κB signaling pathway, for example to prevent apoptosis or increased thrombosis.4 cl, 4 dwg, 6 ex
Изобретение относится к области органической химии и к медицине. Предложено применение тетраацетилированного производного 5-амино-4-карбамоилимидазолил-1-β-D-рибофуранозида - ((АсО)АИКАР) в качестве селективного ингибитора протеинкиназы Сδ. (АсО)АИКАР эффективно ингибирует протеинкиназу Сδ (ПКСδ) за счёт специфичного ингибирования ПКСδ/NF-κB сигнального пути. Поскольку (АсО)АИКАР не обладает высокой токсичностью в отношении здоровых клеток, это позволяет использовать его в предотвращении нарушений ПКСδ/NF-κB сигнального пути, например для предотвращения апоптоза или повышенного тромбообразования. 3 з.п. ф-лы, 4 ил., 6 пр. |
Author | Brovkin Aleksej Nikolaevich Shcherbakov Aleksandr Mikhajlovich Kaluzhskij Vasilij Evgenevich Beburov Mikhail Yurevich Lukyanets Evgenij Antonovich Makarova Elena Aleksandrovna Moshentseva Vera Nikolaevna Tsvetkov Vladimir Borisovich |
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DocumentTitleAlternate | ПРИМЕНЕНИЕ ТЕТРААЦЕТИЛИРОВАННОГО 5-АМИНО-4-КАРБАМОИЛИМИДАЗОЛИЛ-1-β-D-РИБОФУРАНОЗИДА В КАЧЕСТВЕ ИНГИБИТОРА ПРОТЕИНКИНАЗЫ Cδ |
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Title | USE OF TETRAACETYLATED 5-AMINO-4-CARBAMOYL IMIDAZOLYL-1-β-D-RIBOFURANOSIDE AS A PROTEIN KINASE Cδ INHIBITOR |
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