Watanabe Kinzo, Sekine Miyuki, Iguchi Kazuo
School of Life Science, Tokyo University of Pharmacy and Life Science, Horinouchi, Hachioji, Tokyo 192-0392, Japan.
Chem Pharm Bull (Tokyo). 2003 Aug;51(8):909-13. doi: 10.1248/cpb.51.909.
Three marine prostanoids, 1, 2, and 3, were isolated from the extract of the Okinawan soft coral Clavularia viridis. The structures of these compounds were assigned based on the results of spectroscopic analysis. Compound 1 was shown to be preclavulone-A methyl ester, and this is the first isolation of the ester of preclavulone-A as a natural product. Preclavulone-A is proposed to be the key intermediate in the biosynthesis of marine prostanoids exemplified by clavulones in C. viridis. The new prostanoid 3 was suggested to be a biosynthetic intermediate from preclavulone-A to clavulones, and a possible biogenetic pathway via 3 is proposed.
从冲绳软珊瑚绿指形软珊瑚(Clavularia viridis)的提取物中分离出三种海洋前列腺素,即1、2和3。基于光谱分析结果确定了这些化合物的结构。化合物1被证明是前棒曲霉素-A甲酯,这是前棒曲霉素-A的酯作为天然产物的首次分离。有人提出前棒曲霉素-A是绿指形软珊瑚中以棒曲霉素为代表的海洋前列腺素生物合成的关键中间体。新的前列腺素3被认为是从前棒曲霉素-A到棒曲霉素的生物合成中间体,并提出了一条经由3的可能生物合成途径。