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卷柏中的木脂素衍生物及其对脂多糖刺激的RAW 264.7细胞中一氧化氮的抑制作用。

Lignan derivatives from Selaginella tamariscina and their nitric oxide inhibitory effects in LPS-stimulated RAW 264.7 cells.

作者信息

Dat Le Duc, Zhao Bing Tian, Hung Nguyen Duc, Lee Jeong Hyung, Min Byung Sun, Woo Mi Hee

机构信息

College of Pharmacy, Catholic University of Daegu, Gyeongsan 38430, Republic of Korea.

College of Pharmacy, Catholic University of Daegu, Gyeongsan 38430, Republic of Korea; Phutho College of Pharmacy, Viettri City, Phutho Province 290000, Viet Nam.

出版信息

Bioorg Med Chem Lett. 2017 Feb 1;27(3):524-529. doi: 10.1016/j.bmcl.2016.12.028. Epub 2016 Dec 9.

DOI:10.1016/j.bmcl.2016.12.028
PMID:28038832
Abstract

The chemical characterization of Selaginella tamariscina leaves resulted in the isolation of five lignanoside derivatives (1-4 and 6) and one neolignan (5). These compounds include three new lignanosides, tamariscinosides D-F (1-3), and one liriodendrin (4) that were isolated for the first time from this plant, together with two known compounds, (2R,3S)-dihydro-2-(3,5-dimethoxy-4-hydroxyphenyl)-7-methoxy-5-acetyl-benzofuran (5) and moellenoside B (6). The chemical structures of these isolated compounds were determined using 1D and 2D NMR, MS, and CD spectroscopic data, and the results were compared to data previously reported in the literatures. These compounds were also evaluated in terms of their inhibition of NO production in lipopolysaccharide (LPS)-stimulated activity in the macrophage cell line RAW 264.7. Among them, compounds 1, 2, 5, and 6 exhibited a significant inhibition with IC values ranging from 32.3 to 55.8μM.

摘要

对卷柏叶进行化学表征后,分离出了五种木脂素苷衍生物(1 - 4和6)和一种新木脂素(5)。这些化合物包括三种新的木脂素苷,卷柏苷D - F(1 - 3),以及首次从该植物中分离出的一种鹅掌楸苷(4),还有两种已知化合物,(2R,3S)-二氢-2-(3,5-二甲氧基-4-羟基苯基)-7-甲氧基-5-乙酰基苯并呋喃(5)和莫伦诺苷B(6)。利用一维和二维核磁共振、质谱和圆二色光谱数据确定了这些分离化合物的化学结构,并将结果与文献中先前报道的数据进行了比较。还评估了这些化合物对巨噬细胞系RAW 264.7中脂多糖(LPS)刺激活性下一氧化氮产生的抑制作用。其中,化合物1、2、5和6表现出显著的抑制作用,IC值范围为32.3至55.8μM。

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