Gross Harald, Kehraus Stefan, Nett Markus, König Gabriele M, Beil Winfried, Wright Anthony D
Institute for Pharmaceutical Biology, University of Bonn, Nussallee 6, D-53115 Bonn, Germany.
Org Biomol Chem. 2003 Mar 21;1(6):944-9. doi: 10.1039/b210039h.
Chemical investigation of the two soft corals Nephthea sp. and Sarcophyton cherbonnieri, collected from the Fiji Islands and the Great Barrier Reef, respectively, led to the isolation of three new furano-cembranoids (1-3), two seco-cembranoid acetates (5, 6), along with the known compounds sarcoglaucol (4) and decaryiol (7). The structures of the new compounds were elucidated by employing spectroscopic techniques (NMR, MS, UV, IR and CD). Seco-cembranoids are extremely rare structures. Compounds 1, 3, and 7 were found to be cytotoxic towards several tumor cell lines (GI50 values ranged from 0.15 to 8.6 micrograms mL-1). Compound 7 arrests the cell cycle in the G2/M phase.
分别从斐济群岛和大堡礁采集的两种软珊瑚——肾形软珊瑚属物种(Nephthea sp.)和谢氏肉芝软珊瑚(Sarcophyton cherbonnieri)进行化学研究,从中分离出三种新的呋喃-西松烷类化合物(1-3)、两种裂环西松烷乙酸酯(5, 6),以及已知化合物肉芝软珊瑚醇(4)和德卡里醇(7)。通过光谱技术(核磁共振、质谱、紫外、红外和圆二色光谱)阐明了新化合物的结构。裂环西松烷类化合物是极为罕见的结构。发现化合物1、3和7对几种肿瘤细胞系具有细胞毒性(半数生长抑制浓度值范围为0.15至8.6微克/毫升)。化合物7使细胞周期停滞于G2/M期。