Novel antimicrobial antibiotics against Pasteurella piscicida, tetrodecamycin (1) and weakly active dihydrotetrodecamycin (2) were isolated from a culture broth of Streptomyces nashvillensis MJ885-mF8. The planar structure of 1 was determined to be 2-acyl-4-ylidene tetronic acid alkyl ether containing decaline ring by various NMR spectral data of 1 and its acetyl derivative (3). The structure of 2 was elucidated by comparison with the spectral data of 1 and confirmed by catalytic reduction of 1 into 2. The X-ray crystallography of 2 showed the relative stereochemistry. Their absolute configurations were determined by using modified Mosher's method. © 1995, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Nakamura, K. T., Iinuma, H., Sawa, R., Takahashi, Y., Nakamura, H., Sawa, T., … Takeuchi, T. (1995). Tetrodecamycin and Dihydrotetrodecamycin, New Antimicrobial Antibiotics against Pasteurella piscicida Produced by Streptomyces nashvillensis MJ885-mF8: II. Structure Determination. The Journal of Antibiotics, 48(10), 1110–1114. https://doi.org/10.7164/antibiotics.48.1110
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