Journal of Medicinal Chemistry p. 458 - 460 (1977)
Update date:2022-07-29
Topics:
Bobek
Bloch
Berkowitz
Bardos
1,2-Dihydro-1-(2-deoxy-β-D-erythro-pentofuranosyl)-2-oxo-5-methylpyrazine 4-oxide was synthesized by condensation of the silylated pyrazine base with the blocked chloro sugar, followed by removal of the protecting groups. The compound inhibited the growth of leukemia L1210 cells in vitro by 50% at 9x10-7 M. At 400 mg/kg/dayx6 it increased the life span of leukemia L1210 bearing mice by approximately 55%, without apparent toxicity to the host.
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Doi:10.1021/jo00432a019
(1977)Doi:10.1002/hlca.200390068
(2003)Doi:10.1248/cpb.24.2841
(1976)Doi:10.1016/0957-4166(94)00378-O
(1995)Doi:10.1023/A:1012407826196
(2001)Doi:10.1021/ic049263a
(2004)