Grupo de Investigación Productos Naturales Marinos, Facultad de Química Farmacéutica, Universidad de Antioquia, A.A 1226, Medellín, Colombia.
Molecules. 2013 Feb 27;18(3):2598-610. doi: 10.3390/molecules18032598.
Three new triterpene glycosides, named ulososide F (1), urabosides A (2) and B (3), together with the previously reported ulososide A (4), were isolated from the Caribbean marine sponge Ectyoplasia ferox. Their structures were elucidated using extensive interpretation of 1D and 2D-NMR data, as well as HRESIMS. The aglycon of all compounds is a rare 30-norlonastane and the sugar residues were identified after acid hydrolysis and GC analyses. Cytotoxicities of the isolated compounds were evaluated against Jurkat and CHO cell lines by a MTT in vitro assay as well as a hemolysis assay. Unexpectedly, all these saponin derivatives showed very low activity in our bioassays.
从加勒比海海绵 Ectyoplasia ferox 中分离得到三种新的三萜糖苷,分别命名为 ulososide F(1)、urabosides A(2)和 B(3),以及先前报道的 ulososide A(4)。通过对 1D 和 2D-NMR 数据以及 HRESIMS 的广泛解析,确定了它们的结构。所有化合物的糖苷配基均为罕见的 30-降洛烷,糖残基经酸水解和 GC 分析鉴定。采用 MTT 体外法和溶血法测定了分离化合物对 Jurkat 和 CHO 细胞系的细胞毒性。出乎意料的是,在我们的生物测定中,所有这些皂苷衍生物的活性都非常低。