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腺嘌呤及其9-烷基衍生物的生物N-氧化作用。

Biological N-oxidation of adenine and 9-alkyl derivatives.

作者信息

Lam S P, Devinsky F, Gorrod J W

机构信息

Chelsea Department of Pharmacy, King's College London, University of London, UK.

出版信息

Eur J Drug Metab Pharmacokinet. 1987 Oct-Dec;12(4):239-43. doi: 10.1007/BF03189906.

Abstract

In vitro metabolism of adenine, 9-methyladenine, and 9-benzyladenine using hepatic microsomes of hamster, mouse and rat was investigated. The results indicated that adenine was apparently not susceptible to microsomal N-oxidation. N-oxidation of 9-methyladenine was also not detected, whereas N-demethylation was observed with hepatic microsomes derived from hamster and rat but not from mouse. With 9-benzyladenine, both 1-N-oxide formation and N-debenzylation occurred with microsomes of all species in various amounts. N-Hydroxylation of the 6-amino group was not observed with any substrate in any species. Metabolic results are discussed in relation to chemical structure, electronic, lipophilic and steric factors.

摘要

利用仓鼠、小鼠和大鼠的肝微粒体研究了腺嘌呤、9-甲基腺嘌呤和9-苄基腺嘌呤的体外代谢。结果表明,腺嘌呤显然不易发生微粒体N-氧化。9-甲基腺嘌呤的N-氧化也未检测到,而仓鼠和大鼠来源的肝微粒体可观察到N-去甲基化,小鼠来源的肝微粒体则未观察到。对于9-苄基腺嘌呤,所有物种的微粒体均会不同程度地发生1-N-氧化物形成和N-去苄基化。在任何物种中,任何底物均未观察到6-氨基的N-羟基化。结合化学结构、电子、亲脂性和空间因素对代谢结果进行了讨论。

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