Literature DB >> 7870667

Identification of the diastereomers of pentobarbital N-glucosides excreted in human urine.

W H Soine1, P J Soine, T M England, R M Graham, G Capps.   

Abstract

A study was undertaken to determine if humans excreted pentobarbital N-glucosides as urinary metabolites following oral administration of pentobarbital. (1'RS,5RS)-1-(beta-D-Glucopyranosyl)pentobarbital ((1'RS,5RS)-PTBG) was isolated from the urine of one subject. The two diastereomers, (1'RS,5R)-PTBG and (1'RS,5S)-PTBG were separated and found to be identical to synthetic standards when compared using HPLC retention times coupled with UV (with and without post-column ionization) and mass spectrometry (HPLC/MS). A HPLC method was developed for detecting and quantifying (1'RS,5R)-PTBG, (1'RS,5S)-PTBG and pentobarbital in urine. Following a single oral dose of sodium pentobarbital to male subjects (n = 6), 1.6-6.2% of the pentobarbital dose was excreted as (1'RS,5S)-PTBG over 60 hours. (1'RS,5R)-PTBG was also detected in one subject and accounted for 0.3% of the pentobarbital dose. Using a modified HPLC system, the four pentobarbital N-glucosides were resolved and analysis of a partially purified pentobarbital N-glucoside extract from one subject indicated that only (1'R,5R)-PTBG and (1'S,5S)-PTBG could be detected as urinary excretion products. These results indicate that the side chain chirality of pentobarbital may influence the observed enantioselectivity for the formation and/or urinary excretion of the pentobarbital N-glucosides.

Entities:  

Mesh:

Substances:

Year:  1994        PMID: 7870667     DOI: 10.1023/a:1018989116505

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  19 in total

1.  Stereochemical characterization of the diastereomers of the amobarbital N-glucosides excreted in human urine.

Authors:  W H Soine; P J Soine; F C Wireko; D J Abraham
Journal:  Pharm Res       Date:  1990-08       Impact factor: 4.200

2.  Identification of phenobarbital N-glucosides as urinary metabolites of phenobarbital in mice.

Authors:  W H Soine; P J Soine; T M England; J W Ferkany; B E Agriesti
Journal:  J Pharm Sci       Date:  1991-02       Impact factor: 3.534

Review 3.  Metabolism of certain commonly used barbiturates.

Authors:  R I Freudenthal; F I Carroll
Journal:  Drug Metab Rev       Date:  1973       Impact factor: 4.518

4.  The alcoholic metabolites of pentobarbital and amobarbital in man.

Authors:  E W Maynert
Journal:  J Pharmacol Exp Ther       Date:  1965-10       Impact factor: 4.030

5.  Product enantioselectivity in the N-glucosylation of amobarbital.

Authors:  W H Soine; P J Soine; B W Overton; L K Garrettson
Journal:  Drug Metab Dispos       Date:  1986 Sep-Oct       Impact factor: 3.922

6.  Multidose studies in the human metabolism of pentobarbitone.

Authors:  W C Baldeo; J N Gilbert; J W Powell
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1980       Impact factor: 2.441

Review 7.  Drug glucosidation.

Authors:  B K Tang
Journal:  Pharmacol Ther       Date:  1990       Impact factor: 12.310

8.  Effect of barbiturate therapy on phenytoin pharmacokinetics.

Authors:  N Yoshida; Y Oda; S Nishi; J Abe; A Kaji; A Asada; M Fujimori
Journal:  Crit Care Med       Date:  1993-10       Impact factor: 7.598

9.  Stereochemical characterization of the diastereomers of the phenobarbital N-beta-D-glucose conjugate excreted in human urine.

Authors:  W H Soine; P J Soine; S E Mongrain; T M England
Journal:  Pharm Res       Date:  1990-04       Impact factor: 4.200

10.  4'-Hydroxylated derivatives as urinary metabolites of two barbiturates.

Authors:  M A Al Sharifi; J N Gilbert; J W Powell
Journal:  Xenobiotica       Date:  1983-03       Impact factor: 1.908

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.