Ahmadi Peni, Higashi Masahiro, Voogd Nicole J de, Tanaka Junichi
Department of Chemistry, Biology and Marine Science, University of the Ryukyus, Nishihara, Okinawa 903-0213, Japan.
Naturalis Biodiversity Center, P.O. Box 9517, 2300 RA Leiden, The Netherlands.
Mar Drugs. 2017 Aug 10;15(8):249. doi: 10.3390/md15080249.
Two new sesterterpenoids, and 2, were isolated from the sponge . Their planar structures were characterized with spectroscopic analyses. The sole chiral center of compound was elucidated as 12 by comparing observed and calculated optical rotation values. The configurations of compound 2 were determined by NMR and electronic circular dichroism (ECD) studies. Furthermore, compound 2 showed cytotoxicity at IC 1.0 µM against NBT-T2 cells.
从海绵中分离出两种新的倍半萜化合物,即化合物1和化合物2。通过光谱分析对它们的平面结构进行了表征。通过比较观察到的和计算得到的旋光值,确定化合物1的唯一手性中心为12。通过核磁共振(NMR)和电子圆二色光谱(ECD)研究确定了化合物2的构型。此外,化合物2对NBT-T2细胞显示出细胞毒性,其半数抑制浓度(IC)为1.0 μM。