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Stolonidiol, a new marine diterpenoid with a strong cytotoxic activity from the Japanese soft coral
β Scribed by Kenichiro Mori; Kazuo Iguchi; Nobuko Yamada; Yasuji Yamada; Yoshinobu Inouye
- Publisher
- Elsevier Science
- Year
- 1987
- Tongue
- French
- Weight
- 289 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
Structures of stolonidiol
(1) and stolonidiol monoacetate (z), new marine diterpenoids with a strong cytotoxic activity from the Japanese soft coral Clavularia sp., were established by -means of spectroscopic analyses, chemical reactions, and X-ray crystallographic analysis.
π SIMILAR VOLUMES
The structure of gersolide (4), a diterpenoid isolated from extracts of the soft coral Gersemia rubiformis, has been solved via single crystal x-ray diffraction analysis. Soft corals are the richest marine source of diterpenoids. Many laboratories are finding functional group variants of well-know
Two new marine carbocyclic oxylipins, clavirin I (1) and II (2), were isolated from the Okinawan soft coral, Clavularia viridis. Their structures containing unique c~-side chains were determined, based on spectroscopic analysis and stereoseleetive total synthesis. Clavirins showed growth-inhibitory