期刊
PHYTOCHEMISTRY LETTERS
卷 33, 期 -, 页码 31-35出版社
ELSEVIER
DOI: 10.1016/j.phytol.2019.07.002
关键词
Cladiella; Cladieunicellin; Sclerophytin; Elastase; Superoxide anion; Cytotoxicity
资金
- National Museum of Marine Biology and Aquarium
- Ministry of Science and Technology, Taiwan [MOST 104-2320-B-291-001-MY3, 107-2320-B-291-001-MY3]
A new eunicellin diterpenoid, cladieunicellin U (1), along with a new natural eunicellin, cladieunicellin V (2), and two known analogues, sclerophytins A (3) and B (4), were obtained from an octocoral identified as Cladiella sp. The structures, including the absolute configurations, of eunicellins 1-4 were elucidated by using spectroscopic methods and compared with the spectroscopic and physical data reported in the literature. Eunicellins 1, 3 and 4 decreased the release of elastase, while eunicellins 2 and 4 showed inhibitory effects in terms of the generation of superoxide anions by human neutrophils. Eunicellins 1 and 4 were found to show moderate cytotoxicity toward the leukemia K562 cells (IC50 = 12.8, 11.4 mu g/mL, respectively) and 2 exhibited moderate cytotoxicity toward the leukemia MOLT-4 cells (IC50 = 18.8 mu g/mL).
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