Suppr超能文献

来自岗松的抗炎杂萜类化合物。

Anti-inflammatory Meroterpenoids from Baeckea frutescens.

作者信息

Hou Ji-Qin, Guo Cui, Zhao Jian-Juan, Dong Yang-Yang, Hu Xiao-Long, He Qi-Wei, Zhang Bao-Bao, Yan Ming, Wang Hao

机构信息

State Key Laboratory of Natural Medicines, Department of Natural Medicinal Chemistry, and ‡Jiangsu Key Laboratory of Drug Screening, China Pharmaceutical University , Nanjing 210009, People's Republic of China.

出版信息

J Nat Prod. 2017 Aug 25;80(8):2204-2214. doi: 10.1021/acs.jnatprod.7b00042. Epub 2017 Jul 28.

Abstract

Frutescones H-R (1-11), new sesqui- or monoterpene-based meroterpenoids, were isolated from the aerial parts of Baeckea frutescens. Their structures and absolute configurations were established by means of spectroscopic analyses (HRESIMS, 1D and 2D NMR, and ECD), as well as single-crystal X-ray crystallography of 1, (-)-7, and 9. The anti-inflammatory activities of all isolates were evaluated by measuring their inhibitory effects on NO production in LPS-stimulated RAW 264.7 macrophages, and the structure-activity relationships of 1-11 are also discussed. Compound 8 exhibited anti-inflammatory activity with an IC value of 0.36 μM, which might be related to the regulation of the NF-κB signaling pathway via the suppression of p65 nuclear translocation and the consequent decrease of IL-6 and TNF-α.

摘要

从岗松(Baeckea frutescens)地上部分分离得到了新的基于倍半萜或单萜的半萜类化合物弗鲁特松H-R(1-11)。通过光谱分析(高分辨电喷雾电离质谱、一维和二维核磁共振以及电子圆二色谱)以及1、(-)-7和9的单晶X射线晶体学确定了它们的结构和绝对构型。通过测量所有分离物对脂多糖刺激的RAW 264.7巨噬细胞中一氧化氮产生的抑制作用来评估其抗炎活性,并讨论了1-11的构效关系。化合物8表现出抗炎活性,IC值为0.36 μM,这可能与通过抑制p65核转位以及随后白细胞介素-6和肿瘤坏死因子-α的减少来调节核因子κB信号通路有关。

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