Reaction kinetics of alpha-tocopheroxyl radical with biologically and pharmacologically active substances.

K Ondrias, V Misík, V Brezová, A Stasko
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引用次数: 6

Abstract

The alpha-tocopheroxyl radical (alpha TR.)generated in the reaction with 1,1-diphenyl-2-picrylhydrazyl in n-butanol decayed according to second-order kinetics with a rate constant k alpha = 3 x 10(3) M-1s-1 as determined by EPR spectroscopy. Various biologically and pharmacologically active substances like isoprenaline (ISO), epinephrine (EPI), histamine (HIS), stobadine (STO), nafazatrom (NAF) and Kampo C medicine (KMC) accelerated the decay rate of alpha TR(.). The whole process is formally a third-order reaction with the rate constants (in 10(9) M-2s-1): ks(ISO) = 1.28, ks(NAF) = 1.25, ks(EPI) = 0.6, ks(HIS) = 0.4, and ks(STO) = 0.1. In the kinetics of the reaction mechanism, bimolecular intermediates are assumed and the rate constants of their formation were determined.

α -生育酚自由基与生物和药理学活性物质的反应动力学。
在正丁醇中与1,1-二苯基-2- picryhydrazyl反应生成的α -生育酚自由基(α TR.)按照二级动力学衰变,其衰变速率常数为k α = 3 × 10(3) M-1s-1。各种生物和药理学活性物质,如异丙肾上腺素(ISO)、肾上腺素(EPI)、组胺(HIS)、斯托巴定(STO)、纳伐唑仑(NAF)和Kampo C药(KMC),加速了α - TR(.)的衰变速度。整个反应过程是一个三阶反应,速率常数为(10(9)M-2s-1): ks(ISO) = 1.28, ks(NAF) = 1.25, ks(EPI) = 0.6, ks(HIS) = 0.4, ks(STO) = 0.1。在反应机理动力学中,假设了双分子中间体,并确定了它们的形成速率常数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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