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从微叶菊蒿(菊科)中提取的黄酮类化合物对大豆脂氧合酶和前列腺素合成酶的活性

The activity of flavonoids extracted from Tanacetum microphyllum DC. (Compositae) on soybean lipoxygenase and prostaglandin synthetase.

作者信息

Abad M J, Bermejo P, Villar A

机构信息

Department of Pharmacology, Faculty of Pharmacy, University Complutense, Madrid, Spain.

出版信息

Gen Pharmacol. 1995 Jul;26(4):815-9. doi: 10.1016/0306-3623(94)00242-f.

Abstract
  1. The in vitro effects of centaureidin and 5,3'-dihydroxy-4'-methoxy-7-carbomethoxyflavonol (Fig. 1), two anti-inflammatory flavonoids extracted from Tanacetum microphyllum DC., have been examined on both cyclooxygenase and lipoxygenase activity. 2. These flavonoids produced an inhibition of soybean lipoxygenase activity in a dose-dependent manner, with IC50 values (20 and 29 microM respectively) similar to the reference drug. 3. The IC50 values for the in vitro inhibition of cyclooxygenase activity by these flavonoids, were higher than those that produced lipoxygenase activity (318 and 60 microM respectively). 4. These results suggest that the anti-inflammatory activity of our flavonoids may, at least in part, be due to the inhibition of leukotriene synthesis. 5. This is the first report of the biological activity in vitro of these compounds.
摘要
  1. 已经对从小叶菊蒿(Tanacetum microphyllum DC.)中提取的两种抗炎黄酮类化合物矢车菊素和5,3'-二羟基-4'-甲氧基-7-甲氧羰基黄酮醇(图1)对环氧合酶和脂氧合酶活性的体外作用进行了研究。2. 这些黄酮类化合物以剂量依赖性方式抑制大豆脂氧合酶活性,其半数抑制浓度(IC50)值(分别为20和29微摩尔)与参考药物相似。3. 这些黄酮类化合物体外抑制环氧合酶活性的IC50值高于产生脂氧合酶活性的IC50值(分别为318和60微摩尔)。4. 这些结果表明,我们所研究的黄酮类化合物的抗炎活性可能至少部分归因于对白三烯合成的抑制。5. 这是关于这些化合物体外生物活性的首次报道。

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