JPET xPharm- The Comprehensive Pharmacology Reference

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


This Article
Right arrow Full Text (PDF)
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by BUTLER, T. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by BUTLER, T. C.
Journal of Pharmacology And Experimental Therapeutics, Vol. 116, Issue 3, 326-336, 1956
Copyright © 1956 by American Society for Pharmacology and Experimental Therapeutics


THE METABOLIC HYDROXYLATION OF PHENOBARBITAL

THOMAS C. BUTLER 1

1 Department of Pharmacology, University of North Carolina School of Medicine, Chapel Hill, North Carolina

The p-hydroxy derivative of phenobarbital has been found in the urine of dogs and of men after the administration of phenobarbital.

p-Hydroxy phenobarbital has been synthesized and the identity of the synthetic compound with the metabolic product demonstrated.

In dog urine p-hydroxy phenobarbital is almost completely conjugated. The conjugated material consists for the most part of the glucuronide.

In human urine p-hydroxy phenobarbital is only partially conjugated. Little if any of the conjugated material is the glucuronide. It is presumably the sulfate.

p-Hydroxy phenobarbital is not anesthetic in doses as high as 1 gm. per kgm.

The hydroxylation reaction is a mechanism of major importance in the pharmacological inactivation of phenobarbital.

Submitted on October 17, 1955




This article has been cited by other articles:


Home page
Drug Metab. Dispos.Home page
P. J. Murphy
The Development of Drug Metabolism Research as Expressed in the Publications of ASPET: Part 1, 1909-1958
Drug Metab. Dispos., January 1, 2008; 36(1): 1 - 5.
[Abstract] [Full Text] [PDF]


Home page
The Annals of PharmacotherapyHome page
M. D Liedtke, S. M Lockhart, and R C. Rathbun
Anticonvulsant and Antiretroviral Interactions
Ann. Pharmacother., March 1, 2004; 38(3): 482 - 489.
[Abstract] [Full Text] [PDF]


Home page
Drug Metab. Dispos.Home page
T. Shinohara, K.-i. Taura, T. Imamura, H. Yamada, and K. Oguri
Induction of Rat Hepatic Cytochrome P450 2B Subfamily by Azidophenobarbital, as a Possible Photoaffinity Probe for the Putative Phenobarbital Receptor. Comparative Study with Modified Phenobarbitals with Different Functional Groups
Drug Metab. Dispos., December 1, 1997; 25(12): 1442 - 1446.
[Abstract] [Full Text]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
All ASPET Journals Molecular Pharmacology Pharmacological Reviews
 Molecular Interventions Drug Metabolism and Disposition

Copyright © 1956 by the American Society for Pharmacology and Experimental Therapeutics.