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来自台湾软珊瑚柱形棘柳珊瑚的多氧化甾醇。

Polyoxygenated sterols from the Formosan soft coral Sinularia gibberosa.

作者信息

Ahmed Atallah F, Hsieh Ya-Ting, Wen Zhi-Hong, Wu Yang-Chang, Sheu Jyh-Horng

机构信息

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

出版信息

J Nat Prod. 2006 Sep;69(9):1275-9. doi: 10.1021/np0601509.

Abstract

Chemical investigation on the dichloromethane-soluble fraction from the EtOH extract of Sinularia gibberosa Tixier-Durivault has led to the isolation of three new polyoxygenated sterols, gibberoketosterols B (1) and C (2) and gibberoepoxysterol (3), along with two known steroids, gibberoketosterol (4) and 24-methylenecholest-5-en-3beta-ol (5). These cholestane-type sterols possessing a 22,24(28)-conjugated diene (1 and 2) in the side chain or a 5alpha,6alpha-epoxide in the B-ring (3) were isolated for the first time from marine sources. Compound 4 showed significant inhibition against the up-regulation of the pro-inflammatory iNOS and COX-2 proteins of LPS-stimulated RAW264.7 macrophage cells, while 1 was found to be inactive. The cytotoxicity of 1-4 toward a limited panel of cancer cell lines is also reported.

摘要

对软珊瑚(Sinularia gibberosa Tixier-Durivault)乙醇提取物的二氯甲烷可溶部分进行化学研究,分离得到了三种新的多氧甾醇,即软珊瑚酮甾醇B(1)、软珊瑚酮甾醇C(2)和软珊瑚环氧甾醇(3),以及两种已知的甾体化合物,软珊瑚酮甾醇(4)和24-亚甲基胆甾-5-烯-3β-醇(5)。这些在侧链上具有22,24(28)-共轭二烯(1和2)或在B环上具有5α,6α-环氧化物(3)的胆甾烷型甾醇首次从海洋来源中分离得到。化合物4对脂多糖刺激的RAW264.7巨噬细胞中促炎iNOS和COX-2蛋白的上调具有显著抑制作用,而1则无活性。还报道了1-4对一组有限的癌细胞系的细胞毒性。

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