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羟基自由基介导的吗啡向吗啡酮的转化。

Hydroxyl radical-mediated conversion of morphine to morphinone.

作者信息

Kumagai Y, Ikeda Y, Toki S

机构信息

Faculty of Pharmaceutical Sciences, Fukuoka University, Japan.

出版信息

Xenobiotica. 1992 May;22(5):507-13. doi: 10.3109/00498259209053113.

Abstract
  1. The hydroxyl radical-mediated conversion of morphine to morphinone (MO) was examined as an alternative to the enzymic reaction. 2. Hydroxyl radicals were generated by autoxidation of ascorbate in the presence of iron and EDTA. This system oxidized morphine to MO which was identified by h.p.l.c. and t.l.c. The reaction was dependent on the concentration of added Fe2+ and required the addition of ascorbate when Fe3+ was used. 3. Catalase inhibited production of MO whereas superoxide dismutase (SOD) had no effect. Addition of a large amount of H2O2 to the system resulted in a significant decrease in production of MO. No MO production was initiated by H2O2 itself. The oxidation of morphine was inhibited by typical hydroxyl radical-scavenging agents. These results indicate that morphine undergoes oxidation to MO by hydroxyl radical.
摘要
  1. 研究了羟基自由基介导的吗啡向吗啡酮(MO)的转化,以此作为酶促反应的替代方法。2. 在铁和乙二胺四乙酸(EDTA)存在的情况下,抗坏血酸自动氧化产生羟基自由基。该体系将吗啡氧化为MO,通过高效液相色谱(h.p.l.c.)和薄层层析(t.l.c.)对其进行鉴定。该反应依赖于添加的Fe2+浓度,当使用Fe3+时需要添加抗坏血酸。3. 过氧化氢酶抑制MO的产生,而超氧化物歧化酶(SOD)没有作用。向体系中添加大量过氧化氢导致MO的产生显著减少。过氧化氢本身不会引发MO的产生。典型的羟基自由基清除剂可抑制吗啡的氧化。这些结果表明吗啡通过羟基自由基氧化为MO。

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