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Pneumocandins from Zalerion arboricola. III. Structure elucidation.
- Source :
-
The Journal of antibiotics [J Antibiot (Tokyo)] 1992 Dec; Vol. 45 (12), pp. 1875-85. - Publication Year :
- 1992
-
Abstract
- Pneumocandin B0 (6) and six related lipopeptides are antifungal and anti-Pneumocystis carinii agents from mutants of Zalerion arboricola, whose structures were determined mainly on the basis of spectroscopic analysis. They belong, along with pneumocandin A0 (L-671,329) previously isolated from these laboratories, to the echinocandin class of antifungal agents. The product from base-catalyzed ring opening involving the hemiaminal position of the dihydroxyornithine residue of B0, has been clearly defined as 6b. Modifications were limited to the 3-hydroxy-4-methylproline, 3,4-dihydroxyhomotyrosine and 4,5-dihydroxyornithine residues of pneumocandin A0.
- Subjects :
- Antifungal Agents pharmacology
Antiviral Agents chemistry
Candida albicans drug effects
Crystallography
Echinocandins
Magnetic Resonance Spectroscopy
Peptides, Cyclic chemistry
Peptides, Cyclic pharmacology
Pneumocystis drug effects
Stereoisomerism
Structure-Activity Relationship
Anti-Bacterial Agents
Antifungal Agents chemistry
Mitosporic Fungi chemistry
Peptides
Subjects
Details
- Language :
- English
- ISSN :
- 0021-8820
- Volume :
- 45
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- The Journal of antibiotics
- Publication Type :
- Academic Journal
- Accession number :
- 1490878
- Full Text :
- https://doi.org/10.7164/antibiotics.45.1875