Departamento de Química, Universidade Federal de Mato Grosso do Sul, Campo Grande, MS, Brazil.
Planta Med. 2011 Mar;77(4):383-7. doi: 10.1055/s-0030-1250401. Epub 2010 Oct 4.
Two new aporphinoid alkaloids, (+)-6 S-ocoteine N-oxide and (+)-norocoxylonine, were isolated from the leaves and trunk bark of OCOTEA ACUTIFOLIA (Lauraceae) along with thirteen aporphine analogues, one morphinan alkaloid, and one flavonoid. The aporphine alkaloids (+)-thalicsimidine and (+)-neolitsine are reported for the first time for the genus OCOTEA. The structures of all compounds were established on the basis of 1D- and 2D-NMR spectroscopic techniques, optical rotation and/or mass spectrometry data. The cytotoxic potential of eight of the aporphine alkaloids against four human cancer cell lines (Hep-2, MCF-7, B16-F10 and 786-0) was also evaluated.
从 OCOTEA ACUTIFOLIA(樟科)的叶和干皮中分离得到两种新的阿朴啡类生物碱(+)-6 S-ocoteine N-氧化物和(+)-norocoxylonine,以及十三种阿朴啡类似物、一种吗啡类生物碱和一种类黄酮。(+)-thalicsimidine 和(+)-neolitsine 这两种阿朴啡生物碱是首次在 OCOTEA 属中发现的。所有化合物的结构均基于 1D 和 2D-NMR 光谱技术、旋光度和/或质谱数据确定。还评估了八种阿朴啡生物碱对四种人癌细胞系(Hep-2、MCF-7、B16-F10 和 786-0)的细胞毒性潜力。