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来自山楂的具有抑制细胞间黏附分子-1表达活性的呋喃并[1,2]萘醌

Furo-1,2-naphthoquinones from Crataegus pinnatifida with ICAM-1 expression inhibition activity.

作者信息

Min Byung-Sun, Huong Ha-Thi-Thanh, Kim Jung-Hee, Jun Hyun-Ju, Na Min-Kyun, Nam Nguyen-Hai, Lee Hyeong-Kyu, Bae KiHwan, Kang Sam-Sik

机构信息

Laboratory of Immunomodulator, Korea Research Institute of Bioscience and Biotechnology, Daejeon, Korea.

出版信息

Planta Med. 2004 Dec;70(12):1166-9. doi: 10.1055/s-2004-835846.

DOI:10.1055/s-2004-835846
PMID:15643552
Abstract

Two new furo-1,2-naphthoquinones, crataequinones A (1) and B (2), were isolated from the fruits of Crataegus pinnatifida. The structures of two new compounds were determined as 11,12-dimethoxy-3,4-furo-1,2-naphthoquinone (1) and 11,12-dimethoxy-5-hydroxy-3,4-furo-1,2-naphthoquinone (2) by spectroscopic analysis. The two compounds 1 and 2 showed significant inhibitory activity with IC50 values of 33 and 90 microM, respectively, against the expression of intercellular adhesion molecule-1 (ICAM-1).

摘要

从山楂果实中分离出两种新的呋喃并[1,2]萘醌,即山楂醌A(1)和山楂醌B(2)。通过光谱分析确定这两种新化合物的结构分别为11,12-二甲氧基-3,4-呋喃并[1,2]萘醌(1)和11,12-二甲氧基-5-羟基-3,4-呋喃并[1,2]萘醌(2)。化合物1和2对细胞间黏附分子-1(ICAM-1)的表达显示出显著的抑制活性,IC50值分别为33和90微摩尔。

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