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Pneumocandins from Zalerion arboricola. III. Structure elucidation.

Authors :
Hensens OD
Liesch JM
Zink DL
Smith JL
Wichmann CF
Schwartz RE
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.

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