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首页> 外文期刊>Chemical and Pharmaceutical Bulletin >Development and application of a method to investigate drug-metabolizing enzyme inhibitors using sparteine for probe of cytochrome P450 2D6 and tris(2,2′-bipyridine)ruthenium(II)-electrogenerated chemiluminescence detection
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Development and application of a method to investigate drug-metabolizing enzyme inhibitors using sparteine for probe of cytochrome P450 2D6 and tris(2,2′-bipyridine)ruthenium(II)-electrogenerated chemiluminescence detection

机译:用斯巴丁碱研究药物代谢酶抑制剂的方法的开发和应用,用于研究细胞色素P450 2D6和三(2,2'-联吡啶)钌(II)-电化学发光检测

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We studied the detection of drug-metabolizing enzyme inhibitiors using column-switching high performance liquid chromatography with tris(2,2′-bipyridine)ruthenium(II) (Ru(bpy)_3~(2+))-electrogenerated chemiluminescence detection. This can be applied to evaluate the genetic diversity concerning the ability of cytochrome P450 (CYP) 2D6 to metabolize drug in vitro. We demonstrated the ability of CYP2D6 to enable us to examine drugs metabolizing enzyme inhibition with high performance and sensitivity. This method can be applied to investigate metabolite inhibitors of CYP2D6 in vitro and in vivo. Thus, Metixene was found to be a potential CYP2D6 inhibitor.
机译:我们研究了使用三(2,2'-联吡啶)钌(II)(Ru(bpy)_3〜(2 +))-电化学发光检测的柱切换高效液相色谱法检测药物代谢酶抑制剂的方法。这可用于评估有关细胞色素P450(CYP)2D6在体外代谢药物能力的遗传多样性。我们证明了CYP2D6的能力,使我们能够以高性能和高灵敏度检查代谢酶抑制的药物。该方法可用于体外和体内研究CYP2D6的代谢抑制剂。因此,发现Metixene是潜在的CYP2D6抑制剂。

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