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去甲丹皮酚衍生物的合成及其抗炎活性
Synthesis and Anti-inflammatory Activity of Resacetophenone Derivatives
【摘要】 去甲丹皮酚或丹皮酚分别与非甾体抗炎药(NSAIDs)阿司匹林、布洛芬和双氯芬酸偶联,合成了5个新的去甲丹皮酚衍生物(3a~3c,4b)和丹皮酚衍生物(5b),其结构经1H NMR,IR和HR-MS表征。二甲苯致小鼠耳肿胀试验结果表明,3和5均有较强的抗炎活性,与阴性对照对CMC-Na相比,表现出显著性差异(P<0.01)。
【Abstract】 Five novel resacetophenone derivatives(3a~3c,4b) and paeonol derivatives(5b) were synthesized by coupling NSAIDs with resacetophenone and paeonol,respectively.The structures were characterized by 1H NMR,IR and HR-MS.In xylene-induced mice ear swelling model,3 and 5 exhibited potent anti-inflammatory activities comparable with CMC-Na(P<0.01).
【关键词】 非甾体抗炎药(NSAIDs);
去甲丹皮酚;
丹皮酚;
合成;
抗炎活性;
【Key words】 NSAIDs; resacetophenone; paeonol; synthesis; anti-inflammatory activity;
【Key words】 NSAIDs; resacetophenone; paeonol; synthesis; anti-inflammatory activity;
- 【文献出处】 合成化学 ,Chinese Journal of Synthetic Chemistry , 编辑部邮箱 ,2011年01期
- 【分类号】R914;TQ460.1
- 【被引频次】18
- 【下载频次】434