van Boxtel C J, Rane A, Wilson J T
Res Commun Chem Pathol Pharmacol. 1977 Nov;18(3):573-6.
The formation of the stable 10,11-epoxide from carbamazepine by rat liver microsomes was studied. A biphasic activity-substrate profile was consistently found with microsomes from both control and phenobarbital pretreated rats. These data could either indicate epoxide formation by multiple catalytic sites with differential substrate affinity or a solvent effect on the enzyme or its environment.
研究了大鼠肝微粒体将卡马西平转化为稳定的10,11-环氧化物的过程。在来自对照大鼠和苯巴比妥预处理大鼠的微粒体中,均始终发现双相活性-底物曲线。这些数据要么表明由具有不同底物亲和力的多个催化位点形成环氧化物,要么表明溶剂对酶或其环境的影响。