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

Authors :
Arthur C. Sinclair
Jerry R. Martin
Momir Cirovic
Richard S. Egan
Lester A. Mitscher
Alma W. Goldstein
Ruth S. Stanaszek
R. Larry De Vault
Paulette Collum
Earl E. Fager
Jack Tadanier
Sandra L. Mueller
Source :
The Journal of Antibiotics. 30:552-563
Publication Year :
1977
Publisher :
Japan Antibiotics Research Association, 1977.

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 pseudodisaccha-rides and incorporate a novel aminocyclitol, fortamine. Incontrast 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-pur-purosamine B, but fort imicin A differs from fortimicin B by being a glycyl amide.

Details

ISSN :
18811469 and 00218820
Volume :
30
Database :
OpenAIRE
Journal :
The Journal of Antibiotics
Accession number :
edsair.doi.dedup.....ef809dd58b4633215009766e92a5aeab
Full Text :
https://doi.org/10.7164/antibiotics.30.552