Division of Pharmacognosy and Natural Products Chemistry, School of Pharmacy, University of Athens, Panepistimioupoli Zografou, Athens, Greece.
Org Lett. 2010 May 7;12(9):1908-11. doi: 10.1021/ol100584w.
A novel class of bisindole alkaloids is established by the isolation and structural determination of raputindoles A-D (1-4) from the Amazonian plant Raputia simulans Kallunki (Rutaceae). Complete spectroscopic characterization was accomplished by means of NMR spectroscopy and APCI (+) HRMS. Raputindoles A-D possess a cyclopentyl moiety fused on the benzene part of the indole ring, originating from the combination of prenylated indole monomers.
从亚马逊植物 Raputia simulans Kallunki(Rutaceae)中分离和结构鉴定出的拉普丁烷 A-D(1-4)建立了一类新型的双吲哚生物碱。通过 NMR 光谱和 APCI(+)HRMS 完成了完整的光谱特征描述。拉普丁烷 A-D 具有一个环戊基部分,与吲哚环的苯部分融合,来源于被prenylated 的吲哚单体的组合。