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黄嘌呤氧化酶催化5-硝基-2-呋喃甲酸甲酯还原过程中新型硝基呋喃代谢物的形成。

Formation of novel nitrofuran metabolites in xanthine oxidase-catalyzed reduction of methyl 5-nitro-2-furoate.

作者信息

Yamada H, Tatsumi K, Kawazoe Y, Yoshimura H

出版信息

Arch Biochem Biophys. 1984 Jul;232(1):234-9. doi: 10.1016/0003-9861(84)90539-3.

Abstract

After methyl 5-nitro-2-furoate was incubated with milk xanthine oxidase, three reduction products were isolated from the incubation mixture. Among them, two reduction products were new types of nitrofuran metabolites, i.e., metabolites 1 and 2 were identified as the dihydroxyhydrazine derivative (1,2-dihydroxy-1,2-di(5-methoxycarbonyl-2-furyl)hydrazine) and the hydroxylaminofuran derivative (methyl 5-hydroxylamino-2-furoate), respectively. Metabolite 3 was also identified as the aminofuran derivative (methyl 5-amino-2-furoate) by comparison with a synthetic sample.

摘要

5-硝基-2-呋喃甲酸甲酯与牛奶黄嘌呤氧化酶孵育后,从孵育混合物中分离出三种还原产物。其中,两种还原产物是新型硝基呋喃代谢物,即代谢物1和2分别被鉴定为二羟基肼衍生物(1,2-二羟基-1,2-二(5-甲氧基羰基-2-呋喃基)肼)和羟氨基呋喃衍生物(5-羟氨基-2-呋喃甲酸甲酯)。通过与合成样品比较,代谢物3也被鉴定为氨基呋喃衍生物(5-氨基-2-呋喃甲酸甲酯)。

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