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,1) 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. © 1992, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Hensens, O. D., Liesch, J. M., Zink, D. L., Smith, J. L., Wichmann, C. F., & Schwartz, R. E. (1992). Pneumocandins from zalerion arboricola iii. Structure elucidation. The Journal of Antibiotics, 45(12), 1875–1885. https://doi.org/10.7164/antibiotics.45.1875
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