Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan.
J Nat Prod. 2010 Aug 27;73(8):1438-40. doi: 10.1021/np1002498.
Notoamides O-R were isolated from a marine-derived Aspergillus sp. Notoamide O possesses a novel hemiacetal/hemiaminal ether functionality hitherto unknown among this family of prenylated indole alkaloids. The structure represents an unusual branch point for the oxidative modification of other members in the family of prenylated indole alkaloids in the biogenetic pathway.
从海洋来源的曲霉属(Aspergillus sp.)中分离到 Notoamides O-R。Notoamide O 具有新颖的半缩醛/半亚胺醚官能团,这在该家族的类异戊二烯吲哚生物碱中是前所未知的。该结构代表了生物合成途径中其他类异戊二烯吲哚生物碱家族成员氧化修饰的一个不寻常的分支点。