Pacific Institute of Bioorganic Chemistry, Far East Branch of the Russian Academy of Sciences, Vladivostok, Russia.
Bioorg Med Chem Lett. 2010 Jun 15;20(12):3826-30. doi: 10.1016/j.bmcl.2010.04.005. Epub 2010 Apr 9.
New asterosaponins archasterosides A (1), B (2), and the known regularoside A (3) were isolated from the Vietnamese starfish Archaster typicus and structurally elucidated by extensive NMR techniques and chemical transformations. Compounds 1-3 showed moderate cytotoxic activities against HeLa and mouse JB6 P(+) Cl41 cell lines. The most active, 2, induced basal AP-1- and p53-, but not NF-kappaB-transcriptional activations in JB6 Cl41 cells.
从越南星盘 Asterias typicus 中分离得到三种新的甾醇皂苷类化合物 asterosaponins archasterosides A (1)、B (2) 和已知的 regularoside A (3),并通过广泛的 NMR 技术和化学转化进行了结构解析。化合物 1-3 对 HeLa 和小鼠 JB6 P(+) Cl41 细胞系表现出中等的细胞毒性活性。其中最具活性的 2 可诱导 JB6 Cl41 细胞中基础 AP-1 和 p53 的转录激活,但不诱导 NF-κB 的转录激活。