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Fortimicins A and B, new aminoglycoside antibiotics. III. Structural identification
- 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.
- Subjects :
- Pharmacology
chemistry.chemical_classification
Magnetic Resonance Spectroscopy
Chemical Phenomena
medicine.drug_class
Stereochemistry
Hydrolysis
Aminoglycoside
Antibiotics
Molecular Conformation
Glycoside
Mass Spectrometry
Fortimicin B
Anti-Bacterial Agents
Aminocyclitol
Chemistry
chemistry.chemical_compound
Aminoglycosides
chemistry
Fortimicins
Amide
Drug Discovery
medicine
Mass spectrum
Organic chemistry
Subjects
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