Terui Y, Sakazaki R, Shoji J
Shionogi Research Laboratories, Shionogi & Co., Ltd., Osaka, Japan.
J Antibiot (Tokyo). 1990 Oct;43(10):1245-53. doi: 10.7164/antibiotics.43.1245.
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-1-carboxylic acid, (1----3)-gamma-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.
一系列对多种厌氧菌具有活性的新型抗生素——团聚菌素A、B、C和D的结构被确定为1-酰基-2,3-二羟基-1,3-丁二烯-1-羧酸(1→3)-γ-内酯,即酰基中具有不同烃链的2-酰基-4-亚甲基四酮酸。它们的共同发色团在溶液中呈现互变异构现象。文中讨论了它们的结构与对厌氧菌活性之间的关系。