Abstract
AMONG the α,ω-substituted sugar-alcohols the dibromo derivatives represent a special group because of their biological properties1. The first dibromo-hexitol introduced into clinical use, the dibromo-mannitol (‘Myelo-bromolR’), has myelotoxic effects2. Its diastereoisomer dibromo-dulcitol (DBD) revealed, in pharmacological experiments, remarkable qualities.
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KELLNER, B., NÉMETH, L., HORVÁTH, P. et al. 1,6-Dibromo-1,6-dideoxy-dulcitol: a New Antitumoral Agent. Nature 213, 402–403 (1967). https://doi.org/10.1038/213402a0
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DOI: https://doi.org/10.1038/213402a0
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