Synthesis, Hydrolytic Stability, and Antileukemic Activity of Azacytidine Nucleoside Analogs
- Авторы: Bozhok T.S.1, Kalinichenko E.N.1, Kuz’mitskii B.B.1, Golubeva M.B.1
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Учреждения:
- Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus
- Выпуск: Том 49, № 12 (2016)
- Страницы: 804-809
- Раздел: Search for New Drugs
- URL: https://ogarev-online.ru/0091-150X/article/view/244296
- DOI: https://doi.org/10.1007/s11094-016-1375-4
- ID: 244296
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Аннотация
New azacytidine nucleoside analogs with modified carbohydrate moieties were synthesized. Screening identified a highly active 2′-fluoro-containing azacytidine analog that could potentially be of interest as an agent for treating acute myelogenous leukemia and myelodysplastic syndrome.
Об авторах
T. Bozhok
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus
Email: kalinichenko@iboch.bas-net.by
Белоруссия, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141
E. Kalinichenko
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus
Автор, ответственный за переписку.
Email: kalinichenko@iboch.bas-net.by
Белоруссия, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141
B. Kuz’mitskii
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus
Email: kalinichenko@iboch.bas-net.by
Белоруссия, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141
M. Golubeva
Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus
Email: kalinichenko@iboch.bas-net.by
Белоруссия, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141
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