The chemical structure of a unique polyenic antibiotic enacyloxin IIa (former name: fr. 2) produced by Frateuria (formerly Gluconobacter) sp. W-315 has been determined by extensive spectroscopic studies, in particular by NMR spectral analysis. It has a novel non-lactonic structure involving 3,4-dihydroxycyclohexanecarboxylic acid with a chlorine-containing polyenic and polyhydroxy acyl side chain attached as an ester to the 3-hydroxyI substituent of the acid. © 1992, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Watanabe, T., Sugiyama, T., Takahashi, M., Shima, J., Yamashita, K., Izaki, K., … Seto, H. (1992). New polyenic antibiotics active against gram-positive and gram-negative bacteria: IV. structural elucidation of enacyloxin ha. The Journal of Antibiotics, 45(4), 470–475. https://doi.org/10.7164/antibiotics.45.470
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