期刊
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
卷 82, 期 11, 页码 1426-1432出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/bcsj.82.1426
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资金
- NMMBA [981001101]
- NDHU
- APORC
- NSYSU
- NSTPBP
- National Science Council [NSC 97-2323-B-291-001, 98-2320-B-291-001-MY3, 98-2323-B-291-001]
Four briarane-type diterpenoids, including two new chlorinated metabolites, fragilides F (1) and G (2), along with two known compounds, junceellonoid D (3) and juncin Z (4), were isolated from the gorgonian coral Junceella fragilis. The structures of new briaranes 1 and 2 were elucidated by spectral data analysis and the absolute configuration of 1 was directly determined by a single-crystal X-ray diffraction analysis. The relationships between proton chemical shifts and conformations of the methylenecyclohexane ring in briaranes possessing a C-11/20 carbon-carbon double bond are described. Briarane 4 was found to exhibit significant cytotoxicity toward the CCRF-CEM tumor cells.
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