Structures of a series of new antibiotics, agglomerins A, B, C and D, which are active against a variety of anaerobic bacteria, were determined to be 1-acyl-2,3-dihydroxy-1,3-butadiene-I-carboxylic acid, (1→3)-γ-lactones, i.e., 2-acyl-4-ylidenetetronic acids with different hydrocarbon chains in the acyl group. Their common chromophore exhibited tautomerism in solution. The relationship of their structure to the activity against anaerobes is discussed. © 1990, JAPAN ANTIBIOTICS RESEARCH ASSOCIATION. All rights reserved.
CITATION STYLE
Terui, Y., Sakazaki, R., & Shoji, J. (1990). Structures of agglomerins. The Journal of Antibiotics, 43(10), 1245–1253. https://doi.org/10.7164/antibiotics.43.1245
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