Suppr超能文献

来自东沙环礁软珊瑚 Sarcophyton crassocaule 的生物活性海松烷二萜类化合物 sarcocrassocolides P-R。

Bioactive cembranoids, sarcocrassocolides P-R, 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.

National Museum of Marine Biology and Aquarium, Pingtung 944, Taiwan.

出版信息

Mar Drugs. 2014 Jan 28;12(2):840-50. doi: 10.3390/md12020840.

Abstract

New cembranoids, sarcocrassocolides P-R (1-3) and four known compounds (4-7) were isolated from the soft coral Sarcophyton crassocaule. The structures of the metabolites were determined by extensive spectroscopic analysis. Compounds 3-5 and 7 were shown to exhibit cytotoxicity toward a limited panel of cancer cell lines and all compounds 1-7 displayed potent in vitro anti-inflammatory activity in lipopolysaccharide (LPS)-stimulated RAW264.7 macrophage cells by inhibiting the expression of inducible nitric oxide synthase (iNOS) protein. Compound 7 also showed significant activity in reducing the accumulation of cyclooxygenase-2 (COX-2) protein in the same macrophage cells.

摘要

从软珊瑚 Sarcophyton crassocaule 中分离得到了新的海鞘烷二萜类化合物 sarcocrassocolides P-R(1-3)和四个已知化合物(4-7)。通过广泛的光谱分析确定了代谢产物的结构。化合物 3-5 和 7 对一组有限的癌细胞系表现出细胞毒性,所有化合物 1-7 均通过抑制诱导型一氧化氮合酶(iNOS)蛋白的表达,在脂多糖(LPS)刺激的 RAW264.7 巨噬细胞中表现出很强的体外抗炎活性。化合物 7 还在减少同一巨噬细胞中环氧合酶-2(COX-2)蛋白积累方面表现出显著的活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e831/3944518/57a2dd5fc226/marinedrugs-12-00840-g004.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验