Suppr超能文献

来自流苏虾脊兰的降二萜类化合物及其对小鼠巨噬细胞中一氧化氮和肿瘤坏死因子-α产生的抑制活性。

Norditerpenoids from Flickingeria fimbriata and their inhibitory activities on nitric oxide and tumor necrosis factor-α production in mouse macrophages.

作者信息

Chen Jin-Long, Zhong Wen-Jun, Tang Gui-Hua, Li Jing, Zhao Zhi-Min, Yang De-Po, Jiang Lin

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou 510006, Guangdong, China.

出版信息

Molecules. 2014 May 6;19(5):5863-75. doi: 10.3390/molecules19055863.

Abstract

Bioassay-guided fractionation of the ethanolic extract of the leaves of Flickingeria flimbriata led to the isolation of two new degraded diterpenoids 1 and 2, a new ent-pimarane type diterpenoid 3, and four known steroids 4-7. The structures of 1-3 were elucidated by spectroscopic analysis, and their absolute configurations were determined by chemical methods, TDDFT quantum chemical calculations of ECD spectra, and CD exiton chirality method. Compounds 1 and 2, named flickinflimilins A and B, possess a rare 15,16-dinor-ent-pimarane skeleton. Compounds 1-7 were screened for the inhibitory activity against lipopolysaccharide (LPS)-induced NO and TNF-α production in RAW264.7 cells. Compounds 1-3 exhibited potent inhibitory activities, with IC50 values of less than 10 µM.

摘要

对毛叶白点兰叶片乙醇提取物进行生物活性导向的分离,得到了两个新的降解二萜类化合物1和2、一个新的对映-海松烷型二萜类化合物3以及四个已知的甾体化合物4 - 7。通过光谱分析阐明了1 - 3的结构,并通过化学方法、ECD光谱的TDDFT量子化学计算以及CD激子手性方法确定了它们的绝对构型。化合物1和2分别命名为毛叶白点兰素A和B,具有罕见的15,16-二降-对映-海松烷骨架。对化合物1 - 7进行了针对脂多糖(LPS)诱导的RAW264.7细胞中NO和TNF-α产生的抑制活性筛选。化合物1 - 3表现出强效的抑制活性,IC50值小于10 μM。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/844e/6271523/5fa3d6366e8f/molecules-19-05863-g001.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