Bringmann G, Günther C, Saeb W, Mies J, Brun R, Assi L A
Institut für Organische Chemie, Universität Würzburg, Germany.
Phytochemistry. 2000 Jun;54(3):337-46. doi: 10.1016/s0031-9422(00)00107-2.
The isolation and structural elucidation of a new naphthylisoquinoline alkaloid, 8-O-methyldioncophyllinol B, from Triphyophyllum peltatum (Hutch. et Dalz.) Airy Shaw (Dioncophyllaceae) is described, together with the revised structures of other 'B-type' compounds previously misidentified as dioncophylline D, dioncophyllinol D, and 8-O-methyldioncophylline D. All of the presently described structures are 7,6'-coupled and thus have to be addressed as 'B-type' naphthylisoquinoline alkaloids. This is in contrast to the initially defined 'D-type' structures, which are 7,8'-coupled as confirmed by a total synthesis of dioncophylline D. Some of these natural and synthetic naphthylisoquinolines were found to display good in vitro antiplasmodial activities.
描述了从盾籽穗叶藤(Triphyophyllum peltatum (Hutch. et Dalz.) Airy Shaw,露叶茅膏菜科)中分离出一种新的萘基异喹啉生物碱8-O-甲基二酮叶菲灵醇B及其结构解析,同时还给出了其他先前被错误鉴定为二酮叶菲灵D、二酮叶菲灵醇D和8-O-甲基二酮叶菲灵D的“B型”化合物的修正结构。目前所描述的所有结构都是7,6'-偶联的,因此必须归类为“B型”萘基异喹啉生物碱。这与最初定义的“D型”结构形成对比,后者经二酮叶菲灵D的全合成证实是7,8'-偶联的。发现其中一些天然和合成的萘基异喹啉具有良好的体外抗疟活性。