Abstract
Griseochelin, C33H60O7, isolated from an asporogenous strain of Streptomyces griseus represents a novel carboxylic acid antibiotic. The metabolite, which is active against Gram-positive bacteria, forms water-insoluble salts with mono- and divalent cations and binds alkaline-earth metal ions specifically in 2: 1 (X2M) stoichiometry. Detailed spectral (IR, MS and NMR) studies provide full characterization of its constitution featuring a carboxylic acid function, a substituted tetrahydropyran ring, an allylic OH group which are accomodated within a tetrahydroxylated-octamethyl-C25 diene backbone. © 1984, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
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CITATION STYLE
Gräfe, U., Schade, W., Roth, M., Radics, L., Incze, M., & Ujszászy, K. (1984). Griseochelin, a novel carboxylic acid antibiotic from streptomyces griseus. Journal of Antibiotics, 37(8), 836–846. https://doi.org/10.7164/antibiotics.37.836
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