EIMS Laboratory UMR 241 EIO, University of French Polynesia, 98702 Faa'a, Tahiti, French Polynesia.
Molecules. 2012 Oct 12;17(10):12015-22. doi: 10.3390/molecules171012015.
The first phytochemical inspection of the Marquesan endemic plant Rauvolfia nukuhivensis led to the isolation and structure characterization of two new indolo[2,3-a]quinolizinium derivatives named nukuhivensium and N₁₂-methyl-nukuhivensium. They feature an aromatic indolo[2,3-a]quinolizinium core, substituted at C-2 by a n-propyl group, which is unusual in this family of alkaloid derivatives. The structure elucidation was performed on the basis of NMR spectroscopy and especially by interpretation of 2D HMBC correlations. A biosynthetic pathway is proposed on the basis of known enzymatic transformations for this family of natural products. These compounds exhibited low antimicrobial activities.
对马克萨斯群岛特有植物 Rauvolfia nukuhivensis 的首次植物化学研究导致了两种新的吲哚并[2,3-a]喹啉鎓衍生物的分离和结构特征的确定,分别命名为 nukuhivensium 和 N₁₂-甲基-nukuhivensium。它们具有芳香性的吲哚并[2,3-a]喹啉鎓核心,在 C-2 位被一个正丙基取代,这在该生物碱衍生物家族中是不常见的。结构阐明是基于 NMR 光谱学完成的,特别是通过对 2D HMBC 相关的解释。根据该类天然产物已知的酶转化,提出了一种生物合成途径。这些化合物表现出低的抗菌活性。