The structure–activity relationship between oxycoumarin derivatives showing inhibitory effects on iNOS in mouse macrophage RAW264.7 cells

被引:6
作者
Tomonori Nakamura
Naoko Kodama
Manabu Oda
Shizuko Tsuchiya
Yu Arai
Takuya Kumamoto
Tsutomu Ishikawa
Koichi Ueno
Shingo Yano
机构
[1] Chiba University,Department of Molecular Pharmacology and Pharmacotherapeutics, Graduate School of Pharmaceutical Sciences
[2] Chiba University,Department of Geriatric Pharmacology and Therapeutics, Graduate School of Pharmaceutical Sciences
[3] Chiba University,Department of Medicinal Organic Chemistry, Graduate School of Pharmaceutical Sciences
来源
Journal of Natural Medicines | 2009年 / 63卷
关键词
Inducible nitric oxide synthase; Macrophage; Oxycoumarin; RAW264.7; Structure–activity relationship;
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学科分类号
摘要
We have investigated the structure–activity relationship between 63 natural oxycoumarin derivatives and their effects on the expression of inducible-nitric oxide synthase (iNOS) induced by lipopolysaccharide. The protein expression of iNOS was screened by Western blot analysis, and four 5,7-dimethoxycoumarins were selected as potent inhibitors of iNOS expression. In terms of structural specificity, the methoxyl group on C-5 and C-7 and the short alkyl chain (1–5 carbons) on C-6 may be essential for the potent activities. These compounds also showed inhibitory effects on nitric oxide generation and mRNA expression of inflammatory mediators, namely, iNOS and COX-2. Interestingly, the inhibitory effect on mRNA expression was specific for iNOS and was not detected for neuronal NOS. It is expected that these compounds will show anti-inflammatory activities via inhibition of the expressions of iNOS and COX-2.
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页码:15 / 20
页数:5
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