Pneumocandins from zalerion arboricola iii. Structure elucidation

55Citations
Citations of this article
17Readers
Mendeley users who have this article in their library.

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.

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free