Fortimicins A and B, new aminoglycoside antibiotics. III. Structural identification.

Richard S. Egan, RUTH S. STANASZEK, MOMIR CIROVIC, SANDRA L. MUELLER, Jack Tadanier, Jerry R. Martin, Paulette Collum, Alma W. Goldstein, R. Larry De Vault, Arthur C. Sinclair,

The Journal of Antibiotics · 1977 · 68 citations · 17 references

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Abstract

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. In contrast to the diaminocyclitol moieties of known aminoglycosides, fortamine is a 1,4-diamine, contains both N- and O-methyl groups and possesses chiro stereochemistry. Both antibiotics are glycosides of 6-epi-purpurosamine B, but fortimicin A differs from fortimicin B by being a glycyl amide.

References

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