郭颖, 肖颖歆, 郭宗儒, 程桂芳. 依布硒啉衍生物对白三烯B4生物合成抑制作用及其构效关系J. 药学学报, 1999, 34(9): 652-654.
引用本文: 郭颖, 肖颖歆, 郭宗儒, 程桂芳. 依布硒啉衍生物对白三烯B4生物合成抑制作用及其构效关系J. 药学学报, 1999, 34(9): 652-654.
Guo Ying, Xiao Yingxin, Guo Zongru , Cheng Guifang, . INHIBITORY EFFECT AND STRUCTURE-ACTIVITY RELATIONSHIP OF EBSELEN DERIVATIVES ON LEUKOTRIENE B4 BIOSYNTHESISJ. Acta Pharmaceutica Sinica, 1999, 34(9): 652-654.
Citation: Guo Ying, Xiao Yingxin, Guo Zongru , Cheng Guifang, . INHIBITORY EFFECT AND STRUCTURE-ACTIVITY RELATIONSHIP OF EBSELEN DERIVATIVES ON LEUKOTRIENE B4 BIOSYNTHESISJ. Acta Pharmaceutica Sinica, 1999, 34(9): 652-654.

依布硒啉衍生物对白三烯B4生物合成抑制作用及其构效关系

INHIBITORY EFFECT AND STRUCTURE-ACTIVITY RELATIONSHIP OF EBSELEN DERIVATIVES ON LEUKOTRIENE B4 BIOSYNTHESIS

  • 摘要: 目的:研究一系列依布硒啉衍生物对白三烯B4生物合成的影响,并探讨其构效关系。方法:高效液相色谱法测定白三烯B4。结果:依布硒啉的磺酰胺类似物以及N-芳香环取代的磺酰胺衍生物对白三烯B4生物合成具有抑制作用,其IC50在10-5~10-6 mol.L-1之间,并存在一定的构效关系。结论:磺酰胺基团上的酸性氢原子是关键因素,它的存在可以形成分子内氢键,从而使化合物具有活性。

     

    Abstract: AIM: A series of ebselen derivatives were synthesized for studying their effects on LTB4 biosynthesis. Preliminary analysis of structure-activity relationship(SAR) of these compounds were conducted. METHODS: High performance liquid chromatography(HPLC) was used to determine LTB4. RESULTS: Sulfonamide analogues of ebselen and N-aryl substituted derivatives of ebselen showed significant inhibitory effects on LTB4 biosynthesis with IC50 of 10-5 mol.L-1 to 10-6 mol.L-1.CONCLUSION: According to SAR, the presence of an acidic hydrogen atom on the sulfonamido group seemed to be a critical factor for the activity. In the absence of the hydrogen or loss of the ability to form intermolecular hydrogen bonding compounds would abolish the activity.

     

/

返回文章
返回