Clement B, Kunze T
Pharmazeutisches Institut, Christian Albrechts Universität Kiel, F.R.G.
Arch Pharm (Weinheim). 1993 Jan;326(1):25-7. doi: 10.1002/ardp.19933260106.
During investigations on the N-oxygenation of adenine (1) the enzymatic formation of adenine 1-N-oxide 3 was demonstrated for the first time. The identity of this metabolite was confirmed by its chromatographic behaviour and UV-spectrum recorded after HPLC separation. Adenine 1-N-oxide (3) and similar oxygenated derivatives of adenine were synthesized as reference substances. The enzymatic formation of 3 exhibits the typical characteristics of a reaction catalysed by microsomal mono-oxygenases. In induction experiments, an increase in the rate of formation of 3 after pretreatment with phenobarbital was observed. A participation of those isoenzymes of the cytochrome P-450 enzyme system which can be induced by phenobarbital is assumed.
在对腺嘌呤(1)的N-氧化作用进行研究期间,首次证明了腺嘌呤1-N-氧化物3的酶促形成。通过其色谱行为和高效液相色谱分离后记录的紫外光谱确定了该代谢物的身份。合成了腺嘌呤1-N-氧化物(3)和类似的腺嘌呤氧化衍生物作为参考物质。3的酶促形成表现出微粒体单加氧酶催化反应的典型特征。在诱导实验中,观察到用苯巴比妥预处理后3的形成速率增加。假定细胞色素P-450酶系统中那些可被苯巴比妥诱导的同工酶参与其中。