Natural Products Research Institute, College of Pharmacy, Seoul National University, Seoul 151-742, Korea.
Mar Drugs. 2013 Aug 13;11(8):2882-93. doi: 10.3390/md11082882.
Separacenes A-D (1-4), novel polyene polyols, were isolated from Streptomyces sp. collected from the southern area of Jeju Island, Korea. The chemical structures of 1-4 were established by NMR, mass, UV, and IR spectroscopy as well as the modified Mosher's method. Separacenes A-B (1-2), which share an identical planar structure but possess different relative configurations, bear tetraene units flanked by two diol moieties, whereas the stereoisomeric separacenes C-D (3-4) possess a triene moiety between two diol substructures. Separacenes A-D each contain a terminal olefinic methylene. Separacene A displayed inhibitory activity against Candida albicans isocitrate lyase and weak cytotoxicity against both the colon carcinoma cell line HCT-116 and the lung cancer cell line A549.
分离烯 A-D(1-4)是从韩国济州岛南部采集的链霉菌属中分离得到的新型多烯多元醇。通过 NMR、质谱、紫外和红外光谱以及改进的莫歇尔法确定了 1-4 的化学结构。分离烯 A-B(1-2)具有相同的平面结构,但具有不同的相对构型,它们的四烯单元被两个二醇部分包围,而立体异构体分离烯 C-D(3-4)则在两个二醇亚结构之间具有三烯部分。分离烯 A-D 各含有一个末端烯丙基亚甲基。分离烯 A 对白色念珠菌异柠檬酸裂解酶具有抑制活性,对结肠癌细胞系 HCT-116 和肺癌细胞系 A549 也具有较弱的细胞毒性。