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硝基咪唑类作为黄嘌呤氧化酶的厌氧电子受体。

Nitroimidazoles as anaerobic electron acceptors for xanthine oxidase.

作者信息

Clarke E D, Goulding K H, Wardman P

出版信息

Biochem Pharmacol. 1982 Oct 15;31(20):3237-42. doi: 10.1016/0006-2952(82)90556-1.

Abstract

The rates of anaerobic nitroreduction of 15 nitroimidazoles by xanthine-xanthine oxidase were measured. The compounds studied were mainly 2-nitroimidazoles, including misonidazole and analogues of potential value in cancer therapy; most 5-nitroimidazoles such as metronidazole and nimorazole reacted too slowly for measurement under the conditions used. Using 0.1 mM nitroimidazole, reduction rates varied between ca. 4 and 680 nmole min-1 U-1 xanthine oxidase at 37 degrees and pH 7.4. These rates were correlated with the reduction potential characterizing one-electron reduction to the nitro radical-anion, and compared with those for other nitroaryl compounds and with reduction by free flavin mononucleotide.

摘要

测定了黄嘌呤 - 黄嘌呤氧化酶对15种硝基咪唑的厌氧硝基还原速率。所研究的化合物主要是2 - 硝基咪唑,包括米索硝唑和在癌症治疗中具有潜在价值的类似物;大多数5 - 硝基咪唑,如甲硝唑和尼莫唑,在所用条件下反应太慢,无法进行测定。使用0.1 mM硝基咪唑时,在37℃和pH 7.4条件下,还原速率在约4至680 nmole min⁻¹ U⁻¹黄嘌呤氧化酶之间变化。这些速率与表征单电子还原为硝基自由基阴离子的还原电位相关,并与其他硝基芳基化合物的速率以及游离黄素单核苷酸的还原速率进行了比较。

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