• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Characterization of mephenytoin metabolites in human urine by gas chromatography and mass spectrometry.

作者信息

Lynn R K, Bauer J E, Gordon W P, Smith R G, Griffin D, Thompson R M, Jenkins R, Gerber N

出版信息

Drug Metab Dispos. 1979 May-Jun;7(3):138-44.

PMID:38083
Abstract

Metabolites of mephenytoin (5-ethyl-3-methyl-5-phenylhydantoin) were characterized in human urine following chromatography on XAD-2 resin, permethylation, and combined gas chromatography and mass spectrometry. Four glucuronide metabolites previously unidentified in man were characterized as their permethylated derivatives by chemical-ionization and electron-impact mass spectrometry. These metabolites included 5-ethyl-5-(hydroxyphenyl)-3-methylhydantoin O-glucuronide; 5-hydroxyethyl-3-methyl-5-phenyl-hydantoin O-glucuronide; 5-ethyl-5-(hydroxymethoxyphenyl)-3-methylhydantoin O-glucuronide; and a metabolite tentatively identified as 5-ethyl-5-phenylhydantoin N3-glucuronide in which both N-demethylation and glucuronide conjugation of the hydantoin ring have occurred. Mephenytoin, N-demethylmephenytoin, 5-ethyl-5-(hydroxyphenyl)-3-methylhydantoin, and 5-ethyl-5-(hydroxymethoxyphenyl)-3-methylhydantoin were characterized in extracts of enzymatically hydrolyzed urine.

摘要

相似文献

1
Characterization of mephenytoin metabolites in human urine by gas chromatography and mass spectrometry.
Drug Metab Dispos. 1979 May-Jun;7(3):138-44.
2
Characterization of glucuronide metabolites of carbamazepine in human urine by gas chromatography and mass spectrometry.气相色谱-质谱联用法定性分析人尿液中卡马西平的葡萄糖醛酸代谢物
Drug Metab Dispos. 1978 Jul-Aug;6(4):494-501.
3
A major pathway of mephenytoin metabolism in man. Aromatic hydroxylation to p-hydroxymephenytoin.
Drug Metab Dispos. 1980 Jan-Feb;8(1):1-4.
4
5-ethyl-5-phenylhydantoin N-glucuronide, the major urinary metabolite of 5-ethyl-5-phenylhydantoin (Nirvanol) in the dog.
Drug Metab Dispos. 1982 Nov-Dec;10(6):595-8.
5
Identification of mephenytoin metabolites in the dog.
Drug Metab Dispos. 1980 May-Jun;8(3):173-7.
6
Evidence for the epoxide-diol pathway in the biotransformation of mephenytoin.
Epilepsia. 1979 Jun;20(3):287-94. doi: 10.1111/j.1528-1157.1979.tb04806.x.
7
Gas chromatographic-mass spectrometric studies on the metabolic fate of ethotoin in man.
Drug Metab Dispos. 1980 Jul-Aug;8(4):223-9.
8
Determination of n-hexane metabolites by liquid chromatography/mass spectrometry. 2. Glucuronide-conjugated metabolites in untreated urine samples by electrospray ionization.用液相色谱/质谱法测定正己烷代谢物。2. 采用电喷雾电离法测定未处理尿液样本中的葡萄糖醛酸结合代谢物。
Rapid Commun Mass Spectrom. 1998;12(21):1615-24. doi: 10.1002/(SICI)1097-0231(19981115)12:21<1615::AID-RCM372>3.0.CO;2-M.
9
Stereochemical aspects of the metabolism of 5-ethyl-5-phenylhydantoin (Nirvanol) in the dog.
Drug Metab Dispos. 1981 Sep-Oct;9(5):393-401.
10
Biotransformation of 12C- and 2-13C-labeled methyl tert-butyl ether, ethyl tert-butyl ether, and tert-butyl alcohol in rats: identification of metabolites in urine by 13C nuclear magnetic resonance and gas chromatography/mass spectrometry.大鼠体内12C和2-13C标记的甲基叔丁基醚、乙基叔丁基醚及叔丁醇的生物转化:通过13C核磁共振和气相色谱/质谱法鉴定尿液中的代谢产物
Chem Res Toxicol. 1998 Jun;11(6):651-8. doi: 10.1021/tx970215v.

引用本文的文献

1
Stereochemical characterization of the diastereomers of the phenobarbital N-beta-D-glucose conjugate excreted in human urine.人尿中排泄的苯巴比妥N-β-D-葡萄糖共轭物非对映异构体的立体化学特征
Pharm Res. 1990 Apr;7(4):402-6. doi: 10.1023/a:1015831725205.
2
Formation of active metabolites of anticonvulsant drugs. A review of their pharmacokinetic and therapeutic significance.抗惊厥药物活性代谢物的形成。其药代动力学及治疗意义综述。
Clin Pharmacokinet. 1991 Jul;21(1):27-41. doi: 10.2165/00003088-199121010-00003.