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Brasiliquinones A–C, new cytotoxic benz[a]anthraquinones with an ethyl group at C-3 from actinomycete Nocardia brasiliensis
52
Citations
8
References
1996
Year
Bioorganic ChemistryMedicinal FungiAntimicrobial ChemotherapyPharmaceutical ChemistryMedicinal ChemistryBrasiliquinones B 2Natural Product BiosynthesisAntimicrobial Drug DiscoveryBiochemistryBrasiliquinones A–cFirst BenzAntimicrobial CompoundNew Cytotoxic BenzPharmacologyNatural SciencesActinomycete Nocardia BrasiliensisMicrobiologyMedicineDrug Discovery
Three new cytotoxic benz[a]anthraquinones with an ethyl group at C-3, brasiliquinones A–C 1–3, have been isolated from the actinomycete Nocardia brasiliensis IFM 0089, and their structures elucidated on the basis of spectroscopic data and by chemical means. Brasiliquinone A 1 is the first benz[a]anthraquinone possessing ristosamine as an O-glycoside moiety, while brasiliquinones B 2 and C 3 correspond to the aglycone of 1 and the 8-O-methyl derivative of 2, respectively.
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