Papulacandins, a new family of antibiotics with antifungal activity. Structures of papulacandins A, B, C and D.
- 1 January 1980
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 33 (9) , 967-978
- https://doi.org/10.7164/antibiotics.33.967
Abstract
The structures of the papulacandins A, B, C and D, new antibiotics of Papularia sphaerosperma were established by spectral analysis and degradation reactions. Base catalyzed hydrolysis of the main product papulacandin B (1) gave 2 new hydroxylated long-chain unsaturated fatty acids 5 and 6 along with a hithero unknown spirocyclic diglycoside 7. The structure of 7 was determined by further degradation reactions. The positions of attachment of the 2 fatty acids to the spirocyclic diglycoside 7 through ester-bonds were established by selective base catalyzed hydrolysis of 1 and spectral analysis of 1 and some derivatives and degradation products thereof. The structures of papulacandin A (2), papulacandin C (3) and papulacandin D (4) were determined in an analogous way.This publication has 4 references indexed in Scilit:
- Papulacandin B: an Inhibitor of Glucan Synthesis in Yeast SpheroplastsEuropean Journal of Biochemistry, 1979
- The Structure of TunicamycinAgricultural and Biological Chemistry, 1977
- Zur Struktur von Papulacandin B, einem neuen antifungischen Antibiotikum. Vorläufige MitteilungHelvetica Chimica Acta, 1977
- Papulacandins, a new family of antibiotics with antifungal activity. I. Fermentation, isolation, chemical and biological characterization of papulacandins A, B, C, D and E.The Journal of Antibiotics, 1977