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抗坏血酸生成呋喃妥因、米索硝唑和甲硝唑的自由基阴离子 。

Generation of radical anions of nitrofurantoin, misonidazole, and metronidazole by ascorbate.

作者信息

Rao D N, Harman L, Motten A, Schreiber J, Mason R P

出版信息

Arch Biochem Biophys. 1987 Jun;255(2):419-27. doi: 10.1016/0003-9861(87)90410-3.

Abstract

Nitrofurantoin, misonidazole, and metronidazole were reduced to their corresponding nitro anion radicals by ascorbate in anaerobic solutions at high pH. The nitrofurantoin anion radical could be detected at neutral pH. In neutral solutions, the nitro anion radicals of misonidazole and metronidazole were too unstable to be observed by electron spin resonance spectroscopy. At neutral pH, solutions containing ascorbate, nitrofurantoin, or misonidazole consumed oxygen. The addition of superoxide dismutase, catalase, or both superoxide dismutase and catalase decreased the rate of oxygen consumption. These results show that nitro anion radicals are formed by reduction with ascorbate, and superoxide anion radical and hydrogen peroxide are produced by reactions of these radicals with oxygen.

摘要

在高pH值的厌氧溶液中,呋喃妥因、米索硝唑和甲硝唑被抗坏血酸还原为相应的硝基阴离子自由基。呋喃妥因阴离子自由基在中性pH值下可以被检测到。在中性溶液中,米索硝唑和甲硝唑的硝基阴离子自由基过于不稳定,无法通过电子自旋共振光谱法观察到。在中性pH值下,含有抗坏血酸、呋喃妥因或米索硝唑的溶液会消耗氧气。添加超氧化物歧化酶、过氧化氢酶或同时添加超氧化物歧化酶和过氧化氢酶会降低氧气消耗速率。这些结果表明,硝基阴离子自由基是由抗坏血酸还原形成的,并且这些自由基与氧气反应会产生超氧阴离子自由基和过氧化氢。

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