Inhibition of Aspartate Transcarbamylase by a Phenobarbital Derivative

M. Balbaa, G. Yacout, Taysseer Ghonaim, Doaa Othman
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引用次数: 5

Abstract

Mammalian and hepatic aspartate transcarbamylase is inhibited by phenobarbital p-nitrophenylhydra-zone in a reversible and non-competitive type with Ki values 8.45 × 10−5 and 9.64×10−5 M in the reactions toward carbamyl phosphate and aspartate, respectively. In vivo inhibition occurred in a dose-dependent manner in which less than 50% of the activity was retained. These observations suggest that this inhibitor may interfere with the in vivo regulation of this enzyme and lead to an additional biological effect of phenobarbitals.
苯巴比妥衍生物对天冬氨酸转氨基甲酰基酶的抑制作用
哺乳动物和肝脏的天冬氨酸转氨基酰基酶被苯巴比妥对硝基苯肼区以可逆和非竞争性的方式抑制,Ki值分别为8.45 ×10−5和9.64×10−5 M。体内抑制以剂量依赖的方式发生,其中不到50%的活性被保留。这些观察结果表明,这种抑制剂可能干扰这种酶的体内调节,并导致苯巴比妥的额外生物学效应。
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