Synthesis, Hydrolytic Stability, and Antileukemic Activity of Azacytidine Nucleoside Analogs


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Abstract

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.

About the authors

T. S. Bozhok

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus

Email: kalinichenko@iboch.bas-net.by
Belarus, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141

E. N. Kalinichenko

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus

Author for correspondence.
Email: kalinichenko@iboch.bas-net.by
Belarus, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141

B. B. Kuz’mitskii

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus

Email: kalinichenko@iboch.bas-net.by
Belarus, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141

M. B. Golubeva

Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus

Email: kalinichenko@iboch.bas-net.by
Belarus, 5/2 Akad. V. F. Kuprevicha St., Minsk, 220141


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