Corlay Nina, Delang Leen, Girard-Valenciennes Emmanuelle, Neyts Johan, Clerc Patricia, Smadja Jacqueline, Guéritte Françoise, Leyssen Pieter, Litaudon Marc
Centre de Recherche de Gif, Institut de Chimie des Substances Naturelles (ICSN), CNRS, 1 Avenue de la Terrasse, 91198 Gif-sur-Yvette cedex, France.
Rega Institute for Medical Research (KU Leuven), Minderbroedersstraat 10, B-3000 Leuven, Belgium.
Fitoterapia. 2014 Sep;97:87-91. doi: 10.1016/j.fitote.2014.05.015. Epub 2014 May 28.
A bioassay-guided purification of an EtOAc extract of the leaves of Croton mauritianus using a chikungunya virus-cell-based assay led to the isolation of 12-O-decanoylphorbol-13-acetate (1) and the new 12-O-decanoyl-7-hydroperoxy-phorbol-5-ene-13-acetate (2), along with loliolide, vomifoliol, dehydrovomifoliol, annuionone D and bluemol C. The planar structure and the relative configuration of compound 2 were elucidated based on spectroscopic analysis, including 1D- and 2D-NMR experiments, mass spectrometry, and comparison with literature data. Compounds 1 and 2 inhibited chikungunya virus-induced cell death in cell culture with EC50s of 2.4±0.3 and 4.0±0.8 μM, respectively.
利用基于基孔肯雅病毒细胞的检测方法,对毛里求斯巴豆叶的乙酸乙酯提取物进行生物测定导向的纯化,从中分离出12 - O - 癸酰佛波醇 - 13 - 乙酸酯(1)和新的12 - O - 癸酰 - 7 - 氢过氧佛波醇 - 5 - 烯 - 13 - 乙酸酯(2),以及洛里内酯、呕吐叶醇、脱氢呕吐叶醇、环氧紫罗酮D和蓝叶醇C。基于光谱分析,包括一维和二维核磁共振实验、质谱分析以及与文献数据的比较,阐明了化合物2的平面结构和相对构型。化合物1和2在细胞培养中抑制基孔肯雅病毒诱导的细胞死亡,其半数有效浓度(EC50)分别为2.4±0.3和4.0±0.8 μM。