人脾二氢酸脱氢酶:抑制该酶的研究

Annette M. Gero , William J. O'Sullivan , Desmond J. Brown
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引用次数: 14

摘要

已经测试了71种嘧啶类似物作为人脾脏线粒体二氢羟酸脱氢酶的可能抑制剂。其中九种被证明是有效的酶活性抑制剂。两种化合物,二氢-5-偶氮酸酯和6-硫代巴比妥酸酯似乎是DHO-DHase的特异性抑制剂。此外,5-氮草酸酯、5-溴草酸酯和巴比妥酸酯三种化合物对该途径后续的两种酶——羊角酸磷酸核糖基转移酶和羊角酸脱羧酶也有抑制作用,从而可以作用于哺乳动物嘧啶新生生物合成途径的三种酶。
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Human spleen dihydroorotate dehydrogenase: A study of inhibition of the enzyme

Seventy-one pyrimidine analogs have been tested as possible inhibitors of human spleen mitochondrial dihydroorotate dehydrogenase. Of these nine were demonstrated to be effective inhibitors of the enzymic activity. Two compounds, dihydro-5-azaorotate and 6-thiobarbiturate appeared to be specific inhibitors of the DHO-DHase. In addition, three compounds, 5-azaorotate, 5-bromoorotate, and barbiturate were also inhibitory against the two subsequent enzymes of the pathway, orotate phosphoribosyltransferase and orotidylate decarboxylase, so that they could act against three enzymes of the mammalian pyrimidine de novo biosynthetic pathway.

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