Challenges in exploring the cytochrome P450 system as a source of variation in canine drug pharmacokinetics

MN Martinez, L Antonovic, M Court… - Drug metabolism …, 2013 - Taylor & Francis
The cytochrome P450 (CYP) superfamily constitutes a collection of enzymes responsible for
the metabolism of a wide array of endo-and xenobiotic compounds. Much of the knowledge …

Cytochrome P450 and its role in veterinary drug interactions

LA Trepanier - Veterinary Clinics: Small Animal Practice, 2006 - vetsmall.theclinics.com
976 TREPANIER into inactive metabolites (eg, warfarin, phenytoin), bioactivate prodrugs
into active drugs (eg, codeine, tramadol, enalapril), or generate reactive toxic metabolites …

Evidence for polymorphism in the canine metabolism of the cyclooxygenase 2 inhibitor, celecoxib

SK Paulson, L Engel, B Reitz, S Bolten… - Drug metabolism and …, 2018 - Elsevier
The pharmacokinetics of celecoxib, a cyclooxygenase-2 inhibitor, was characterized in
beagle dogs. Celecoxib is extensively metabolized by dogs to a hydroxymethyl metabolite …

Expression and characterization of canine cytochrome P450 2D15

F Roussel, DB Duignan, MP Lawton, RS Obach… - Archives of Biochemistry …, 1998 - Elsevier
CYP2D15 is the canine ortholog of human CYP2D6, the human CYP2D isoform involved in
the metabolism of drugs such as antiarhythmics, adrenoceptor antagonists, and tricyclic …

Association of cytochrome P450 2D15 (CYP2D15) nonsynonymous polymorphisms and exon 3 deleted RNA splice variant with CYP2D15 protein content and …

TP Jimenez, Z Zhu, MH Court - Journal of Veterinary …, 2023 - Wiley Online Library
CYP2D15 is a major drug metabolizing P450 in canine liver. Like the human orthologue
(CYP2D6), this enzyme is highly polymorphic with at least five common nonsynonymous …

[图书][B] Cytochrome P450 2D6: structure, function, regulation and polymorphism

S Zhou - 2018 - taylorfrancis.com
Cytochromes are proteins that catalyze electron transfer reactions of well-known metabolic
pathways and are classified in various superfamilies. The CYP, or P450, superfamily …

A variety of cytochrome P450 enzymes and flavin-containing monooxygenases in dogs and pigs commonly used as preclinical animal models

Y Uno, M Shimizu, H Yamazaki - Biochemical Pharmacology, 2024 - Elsevier
Drug oxygenation is mainly mediated by cytochromes P450 (P450s, CYPs) and flavin-
containing monooxygenases (FMOs). Polymorphic variants of P450s and FMOs are known …

Genetic polymorphism of cytochrome P450s in beagles: possible influence of CYP1A2 deficiency on toxicological evaluations

H Kamimura - Archives of toxicology, 2006 - Springer
A number of human cytochrome P450 (CYP) isozymes have been shown to be genetically
polymorphic, and extensive pharmaceutical studies have been conducted to characterize …

The CYP3 family

DJ Greenblatt, P He, LL von Moltke - 2008 - books.rsc.org
The CYP3 Family | Cytochromes P450: Role in the Metabolism and Toxicity of Drugs and other
Xenobiotics | Books Gateway | Royal Society of Chemistry Skip to Main Content Umbrella Alt …

Molecular cloning and expression of cytochrome P450 2D6 in the livers of domestic cats

T Komatsu, K Honda, A Kubota, T Kitazawa… - Journal of Veterinary …, 2010 - jstage.jst.go.jp
Cytochrome P450 2D (CYP2D) is one of the major metabolizing enzymes for drugs in
humans and other mammals. Although domestic cats (Felis catus) are the most common …