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从人参种子中分离得到的一种新的五环三萜化合物及其对 NF-κB 的抑制作用。

A new lupane-type triterpene from the seeds of Panax ginseng with its inhibition of NF-κB.

机构信息

College of Pharmacy, Chungnam National University, Daejeon, 305-764, Korea.

出版信息

Arch Pharm Res. 2012 Mar;35(4):647-51. doi: 10.1007/s12272-012-0408-0. Epub 2012 May 3.

Abstract

A new lupane-triterpene, 3β-cis-feruloyloxy-16β-hydroxylup-20(29)-ene (1) were isolated from the ethyl acetate extract of Panax ginseng seeds along with the known compound, 3β-transferuloyloxy-16β-hydroxylup-20(29)-ene (2). Compound 2 was isolated from this plant for the first time. Their chemical structures were determined by mass spectroscopy and one-dimensional and two-dimensional magnetic resonance spectra. The bioactive effects of these compounds on TNF-α-induced NF-κB transcription were evaluated in transfected HepG2 cells. Effects on the expression of NF-κB target genes were also examined using a reverse transcription-polymerase chain reaction. Both compounds 1 and 2 were inhibited NF-κB activity in HepG2 cells by decreasing the cellular concentrations of inflammatory factors iNOS and COX2.

摘要

从人参种子的乙酸乙酯提取物中分离得到一种新的羽扇豆烷三萜,3β-顺式-阿魏酰氧基-16β-羟基羽扇-20(29)-烯(1),以及已知化合物 3β-转移阿魏酰氧基-16β-羟基羽扇-20(29)-烯(2)。化合物 2 是首次从这种植物中分离得到的。它们的化学结构通过质谱和一维和二维磁共振谱确定。评估了这些化合物对 TNF-α 诱导的 NF-κB 转录的生物活性影响在转染 HepG2 细胞中。还使用逆转录聚合酶链反应检查了它们对 NF-κB 靶基因表达的影响。两种化合物 1 和 2 都通过降低炎症因子 iNOS 和 COX2 的细胞浓度来抑制 HepG2 细胞中的 NF-κB 活性。

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