Abstract
The synthesis and structural determination of a number of new rhodomycin derivatives, modified in the sugar part are described. The cytotoxicity against leukemic L1210 cells of these compounds is reported, along with beta-rhodomycinone and two regioisomers of the above compounds, which were isolated during the synthetic procedure.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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Animals
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Anthracyclines / pharmacology*
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Antibiotics, Antineoplastic / chemical synthesis*
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Antibiotics, Antineoplastic / pharmacology
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Leukemia L1210 / drug therapy*
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Molecular Structure
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Structure-Activity Relationship
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Tumor Cells, Cultured / drug effects
Substances
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Anthracyclines
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Antibiotics, Antineoplastic
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rhodomycin