Metabolism, pharmacokinetics and excretion of a potent tachykinin NK1 receptor antagonist (CP-122,721) in rat: Characterization of a novel oxidative pathway
ANIMAL EXPERIMENT;
ARTICLE;
BIOTRANSFORMATION;
CONTROLLED STUDY;
DEMETHYLATION;
DRUG ABSORPTION;
DRUG DISPOSITION;
DRUG EFFECT;
DRUG EFFICACY;
DRUG ELIMINATION;
DRUG EXCRETION;
DRUG METABOLISM;
DRUG POTENCY;
FECES ANALYSIS;
FEMALE;
GLUCURONIDATION;
HYDROXYLATION;
MALE;
NONHUMAN;
RAT;
Benzene and benzene metabolites as embryotoxic agents: Effects on cultured rat embryos
Chapman DE, Namkung MJ, Juchau MR. 1994. Benzene and benzene metabolites as embryotoxic agents: Effects on cultured rat embryos. Toxicology and Applied Pharmacology 128:129-137.
Enzymatic pathways for the formation of cotinine, a major metabolite of nicotine in rabbit liver
Hucker HB, Gillette JR, Brodie BB. 1960. Enzymatic pathways for the formation of cotinine, a major metabolite of nicotine in rabbit liver. Journal of Pharmacology and Experimental Therapy 129:94-100.
Structural characterization of urinary metabolites of the antiarrhythmic drug encainide in human subjects
Jajoo HK, Mayol RF, LaBudde JA, Blair IA. 1990. Structural characterization of urinary metabolites of the antiarrhythmic drug encainide in human subjects. Drug Metabolism and Disposition 18:28-35.
Determination of the substance P receptor antagonist CP-122,721 in plasma by narrow-bore high-performance liquid chromatography-ionspray tandem mass spectrometry
Kamel A, Prakash C. 1997. Determination of the substance P receptor antagonist CP-122,721 in plasma by narrow-bore high-performance liquid chromatography-ionspray tandem mass spectrometry. Journal of Chromatography B: Biomedical Science Applications 700:139-146.
Rate and capacity of hepatic microsomal ring-hydroxylation of phenol to hydroquinone and catechol in rainbow trout (Oncorhynchus mykiss)
Kolanczyk RC, Schmieder PK. 2002. Rate and capacity of hepatic microsomal ring-hydroxylation of phenol to hydroquinone and catechol in rainbow trout (Oncorhynchus mykiss). Toxicology 176:77-90.
Novel metabolic pathway of aryl ethers by cytochrome P450: Cleavage of the oxygen-aromatic ring bond accompanying ipso-substitution by the oxygen atom of the active species in cytochrome P450 models and cytochrome P450
Ohe T, Mashino T, Hirobe M. 1994. Novel metabolic pathway of aryl ethers by cytochrome P450: Cleavage of the oxygen-aromatic ring bond accompanying ipso-substitution by the oxygen atom of the active species in cytochrome P450 models and cytochrome P450. Archives in Biochemistry and Biophysics 19:402-409.
Substituent elimination from p-substituted phenols by cytochrome P450: Ipso-substitution by the oxygen atom of the active species
Ohe T, Mashino T, Hirobe M. 1997. Substituent elimination from p-substituted phenols by cytochrome P450: Ipso-substitution by the oxygen atom of the active species. Drug Metabolism and Disposition 25:116-122.
Metabolism of benzene in rat hepatocytes. Influence of inducers on phenol glucuronidation
Schrenk D, Bock KW. 1990. Metabolism of benzene in rat hepatocytes. Influence of inducers on phenol glucuronidation. Drug Metabolism and Disposition 18:720-725.
Influence of P-4502E1 induction on benzene metabolism in rat hepatocytes and on biliary metabolite excretion
Schrenk D, Ingelman-Sundberg M, Bock KW. 1992. Influence of P-4502E1 induction on benzene metabolism in rat hepatocytes and on biliary metabolite excretion. Drug Metabolism and Disposition 20:137-141.