Banks R M, Blanchflower S E, Everett J R, Manger B R, Reading C
Pfizer Central Research, Sandwich, Kent, England.
J Antibiot (Tokyo). 1997 Oct;50(10):840-6. doi: 10.7164/antibiotics.50.840.
Two members of a novel class of anthelmintics, the aspergillimides, have been isolated from the Aspergillus strain IMI 337664. This novel fungus also produced two known and one structurally novel paraherquamide. This paper describes the fermentation, isolation, structure elucidation and anthelmintic activity of aspergillimide (VM55598, 1), 16-keto aspergillimide (SB202327, 2), and the paraherquamides VM54159 (3), SB203105 (4) and SB200437 (5). The aspergillimides are equivalent to paraherquamides which have lost both the dioxygenated 7-membered ring and the phenyl ring to which this is fused; gaining in their place a C8-keto group. SB203105 is the first example of a 4-substituted paraherquamide.
从曲霉属菌株IMI 337664中分离出了新型抗蠕虫药曲霉酰胺类的两个成员。这种新型真菌还产生了两种已知的以及一种结构新颖的对herquamide。本文描述了曲霉酰胺(VM55598,1)、16-酮曲霉酰胺(SB202327,2)以及对herquamide类化合物VM54159(3)、SB203105(4)和SB200437(5)的发酵、分离、结构解析和抗蠕虫活性。曲霉酰胺类相当于失去了二氧代七元环及其稠合的苯环的对herquamide类;取而代之的是获得了一个C8-酮基。SB203105是4-取代对herquamide的首个实例。