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来自东沙环礁软珊瑚 Sarcophyton crassocaule 的细胞毒性和抗炎的海鞘萜类化合物。

Cytotoxic and anti-inflammatory cembranoids from the Dongsha Atoll soft coral Sarcophyton crassocaule.

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-sen University, Kaohsiung 804, Taiwan.

出版信息

Bioorg Med Chem. 2010 Mar 1;18(5):1936-41. doi: 10.1016/j.bmc.2010.01.036. Epub 2010 Jan 22.

Abstract

Five new cembranoids, sarcocrassocolides A-E (1-5), along with three known cembranoids 6-8, have been isolated from a Formosan soft coral Sarcophyton crassocaule. The structures of the new metabolites were elucidated by extensive spectroscopic analysis and the absolute configuration of 1 was determined by a modified Mosher's method. Compounds 1-4 exhibited significantly cytotoxic activity against a limited panel of cancer cell lines. Compounds 1-4, 6 and 8 were shown to exert significant in vitro anti-inflammatory activity in LPS-stimulated RAW264.7 macrophage cells. Compound 6 also significantly inhibited the accumulation of pro-inflammatory COX-2 protein.

摘要

从台湾产软珊瑚 Sarcophyton crassocaule 中分离得到了 5 个新的海鞘烷类化合物 sarcocrassocolides A-E(1-5)以及 3 个已知的海鞘烷类化合物 6-8。通过广泛的光谱分析阐明了新代谢产物的结构,并且通过改进的 Mosher 方法确定了 1 的绝对构型。化合物 1-4 对一组有限的癌细胞系表现出显著的细胞毒性活性。化合物 1-4、6 和 8 在 LPS 刺激的 RAW264.7 巨噬细胞中显示出显著的体外抗炎活性。化合物 6 还显著抑制了促炎 COX-2 蛋白的积累。

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