Li Shi-Fei, He Hong-Ping, Hao Xiao-Jiang
a Institute of Molecular Science, Shanxi University , Taiyuan 030006 , People's Republic of China.
Nat Prod Res. 2015;29(19):1845-9. doi: 10.1080/14786419.2015.1009066. Epub 2015 Feb 20.
Three new phenanthrenone constituents, trigoxyphins U-W (1, 7 and 9), together with eight known ones, trigoxyphin M (2), 6,9-O-dimethyltrigonostemone (3), trigonstemone (4), thrigonosomone B (5), trigonochinene E (6), actephiiol A (8), epiactephilol A (10) and neoboutomannin (11), were obtained from the methanol extract of the leaves and stems of Trigonostemonlii. The structures of the new metabolites were elucidated by analysing the spectroscopic data (1D NMR, 2D NMR, HR-ESI-MS and IR). Compounds 1-6 were evaluated for their cytotoxic activities on five human tumour cell lines by using the MTT method, and compound 1 exhibited inhibitory activity against HL-60, SMMC-7721, A-549, MCF-7 and SW480 with IC50 values ranging from 3.77 to 14.51 μM.
从三宝木属植物Trigonostemonlii的叶和茎的甲醇提取物中获得了三种新的菲醌类成分,即三宝木素U-W(1、7和9),以及八种已知成分,三宝木素M(2)、6,9-O-二甲基三宝木酮(3)、三宝木酮(4)、三宝木酮B(5)、三宝木烯E(6)、阿克替菲醇A(8)、表阿克替菲醇A(10)和新布托曼宁(11)。通过分析光谱数据(一维核磁共振、二维核磁共振、高分辨电喷雾电离质谱和红外光谱)阐明了新代谢产物的结构。采用MTT法评估了化合物1-6对五种人类肿瘤细胞系的细胞毒性活性,化合物1对HL-60、SMMC-7721、A-549、MCF-7和SW480表现出抑制活性,IC50值在3.77至14.51μM之间。