Literature DB >> 16749118

The metabolism of 2,6-di-tert.-butyl-4-hydroxymethylphenol (Ionox 100) in the dog and rat.

A S Wright1, D A Akintonwa, R S Crowne, D E Hathway.   

Abstract

1. A single oral dose of [(14)C]Ionox 100 to rats is almost entirely eliminated in 11 days: 89.1-107.2% of the (14)C is excreted and 0.29+/-0.02% of the dose is present in the carcass plus viscera after removal of the gut. Rats exhibit an individual variation in the elimination pattern, 15.6-70.8% of (14)C being excreted in the urine and 75.2-27.0% in the faeces during 11 days. 2. After the oral administration of [(14)C]Ionox 100 to dogs, 87.1-90.3% of the (14)C is excreted in the faeces and urine during 4 days. 3. Dogs and rats do not show a species difference in this pattern of elimination. 4. The rate of elimination from dogs and rats given a single dose of Ionox 100 is not affected by the size of the dose and the presence of triglyceride fat in the diet. 5. Ionox 100 is completely metabolized in dogs and rats: unchanged Ionox 100 is absent from the urine and faeces, and from the carcass when elimination is complete. In rats, 3,5-di-tert.-butyl-4-hydroxybenzoic acid accounts for 50-85% of a dose of Ionox 100 and (3,5-di-tert.-butyl-4-hydroxybenzoyl beta-d-glucopyranosid)uronic acid for 47-10%; in dogs, the unconjugated acid accounts for 85% and the ester glucuronide for 10-12%. 3,5-Di-tert.-butyl-4-hydroxyhippuric acid is not formed. Other metabolites, which have been detected in small quantity in the faeces and urine of animals dosed with Ionox 100, have not been identified. 6. 3,5-Di-tert.-butyl-4-hydroxybenzoic acid and (3,5-di-tert.-butyl-4-hydroxybenzoyl beta-d-glucopyranosid)uronic acid are also the major metabolites of Ionol (2,6-di-tert.-butyl-p-cresol) in rats. 7. The elimination of Ionox 100 metabolites from rats is faster than that of Ionol and its metabolites. Unlike Ionol, unchanged Ionox 100 could not be detected in the bodies of these animals.

Entities:  

Year:  1965        PMID: 16749118      PMCID: PMC1264575          DOI: 10.1042/bj0970303

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  12 in total

1.  METABOLISM OF TRANYLEYPROMINE-C14 AND DL AMPHETAMINE-C14 IN THE RAT.

Authors:  J J ALLEVA
Journal:  J Med Chem       Date:  1963-11       Impact factor: 7.446

2.  THE URINARY EXCRETION OF 14C-LABELLED BUTYLATED HYDROXYTOLUENE BY THE RAT.

Authors:  L G LADOMERY; A J RYAN; S E WRIGHT
Journal:  J Pharm Pharmacol       Date:  1963-11       Impact factor: 3.765

3.  The urinary excretion of tritiated butylated hydroxyanisole and butylated hydroxytoluene in the rat.

Authors:  W S GOLDER; A J RYAN; S E WRIGHT
Journal:  J Pharm Pharmacol       Date:  1962-05       Impact factor: 3.765

4.  Studies in detoxication. 79. The metabolism of cyclo [14C] hexane and its derivatives.

Authors:  T H ELLIOTT; D V PARKE; R T WILLIAMS
Journal:  Biochem J       Date:  1959-06       Impact factor: 3.857

5.  The excretion of radioactivity following administration of tri-C14-ethylenimino-s-triazine in normal mice.

Authors:  E I GOLDENTHAL; M V NADKARNI; P K SMITH
Journal:  J Pharmacol Exp Ther       Date:  1958-04       Impact factor: 4.030

6.  [Decomposition of alpha-phenylpropylalcohol in rabbits, dogs & men].

Authors:  J GRUNEBERG; H LANGECKER
Journal:  Naunyn Schmiedebergs Arch Exp Pathol Pharmakol       Date:  1957

7.  Studies in detoxication. 56. The metabolism of alkylbenzenes: stereochemical aspects of the biological hydroxylation of ethylbenzene to methylphenylcarbinol.

Authors:  J N SMITH; R H SMITHIES; R T WILLIAMS
Journal:  Biochem J       Date:  1954-02       Impact factor: 3.857

8.  The quantitative determination of hippuric acid.

Authors:  G W GAFFNEY; K SCHREIER; N DIFERRANTE; K I ALTMAN
Journal:  J Biol Chem       Date:  1954-02       Impact factor: 5.157

9.  Kinetic studies of the metabolism of foreign organic compounds; the formation of benzoic acid from benzamide toluene, benzyl alcohol and benzaldehyde and its conjugation with glycine and glucuronic acid in the rabbit.

Authors:  H G BRAY; W V THORPE; K WHITE
Journal:  Biochem J       Date:  1951-01       Impact factor: 3.857

10.  Studies in detoxication. 60. The metabolism of alkylbenzenes: isopropylbenzene (cumene) and derivatives of hydratropic acid.

Authors:  D ROBINSON; J N SMITH; R T WILLIAMS
Journal:  Biochem J       Date:  1955-01       Impact factor: 3.857

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  8 in total

1.  The metabolism of N-triphenylmethylmorpholine in the dog and rat.

Authors:  M H Griffiths
Journal:  Biochem J       Date:  1968-08       Impact factor: 3.857

2.  Ring hydroxylation of di-t-butylhydroxytoluene by rat liver microsomal preparations.

Authors:  Y S Shaw; C Chen
Journal:  Biochem J       Date:  1972-08       Impact factor: 3.857

3.  The metabolism of 3,5-di-tert.-butyl-4-hydroxytoluene in the rat and in man.

Authors:  J W Daniel; J C Gage; D I Jones
Journal:  Biochem J       Date:  1968-02       Impact factor: 3.857

4.  The metabolism of di-(3,5-di-tert.-butyl-4-hydroxybenzyl) ether (Ionox 201) in the rat.

Authors:  A S Wright; R S Crowne; D E Hathway
Journal:  Biochem J       Date:  1967-01       Impact factor: 3.857

5.  The metabolism of 2-chloro-1-(2',4'-dichlorophenyl)vinyl diethyl phosphate (Chlorfenvinphos) in the dog and rat.

Authors:  D H Hutson; D A Akintonwa; D E Hathway
Journal:  Biochem J       Date:  1967-01       Impact factor: 3.857

6.  The comparative metabolism of 2,6-dichlorothiobenzamide (Prefix) and 2,6-dichlorobenzonitrile in the dog and rat.

Authors:  M H Griffiths; J A Moss; J A Rose; D E Hathway
Journal:  Biochem J       Date:  1966-03       Impact factor: 3.857

7.  The fate of di-(3,5-di-tert.-butyl-4-hydroxyphenyl)methane (Ionox 22) in the rat.

Authors:  A S Wright; R S Crowne; D E Hathway
Journal:  Biochem J       Date:  1966-04       Impact factor: 3.857

8.  Break-down of the molluscicide N-tritylmorpholine in soil and in rice.

Authors:  K I Beynon; A N Wright
Journal:  Bull World Health Organ       Date:  1967       Impact factor: 9.408

  8 in total

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