The structures of fortimicins A and B have been determined by PMR, CMR, mass spectra and CD combined with chemical degradations. Both antibiotics are pseudodisaccharides and incorporate a novel aminocyclitol, fortamine. Incontrast to the diaminocyclitol moieties of known aminoglycosides, fortamine is a 1,4-diamine, contains both TV- and O-me-thyl groups and possesses chiro stereochemistry. Both antibiotics are glycosides of 6-epl-pur-purosamine B, but fortimicin A differs from fortimicin B by being a glycyl amide. © 1977, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Egan, R. S., Stanaszek, R. S., Cirovic, M., Mueller, S. L., Tadanier, J., Martin, J. R., … Mitscher, L. A. (1977). Fortimicins A And B, New Aminoglycoside Antibiotics III. Structural Identification. The Journal of Antibiotics, 30(7), 552–563. https://doi.org/10.7164/antibiotics.30.552
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