Coptisine modulates the pharmacokinetics of florfenicol by targeting CYP1A2, CYP2C11 and CYP3A1 in the liver and P-gp in the jejunum of rats: a pilot study.
Rats
Male
Animals
Cytochrome P-450 CYP1A2
/ metabolism
Pilot Projects
ATP Binding Cassette Transporter, Subfamily B, Member 1
/ metabolism
Jejunum
/ metabolism
Rats, Sprague-Dawley
Cytochrome P-450 Enzyme System
/ metabolism
Liver
/ metabolism
Cytochrome P-450 CYP3A
/ metabolism
Cytochrome P450 Family 2
/ metabolism
Aryl Hydrocarbon Hydroxylases
/ metabolism
Steroid 16-alpha-Hydroxylase
/ metabolism
Coptisine
Florfenicol
P-glycoprotein
cytochrome P450
pharmacokinetics
Journal
Xenobiotica; the fate of foreign compounds in biological systems
ISSN: 1366-5928
Titre abrégé: Xenobiotica
Pays: England
ID NLM: 1306665
Informations de publication
Date de publication:
Mar 2023
Mar 2023
Historique:
medline:
7
6
2023
pubmed:
5
5
2023
entrez:
5
5
2023
Statut:
ppublish
Résumé
Coptisine (COP) is the main active ingredient of
Identifiants
pubmed: 37144948
doi: 10.1080/00498254.2023.2211135
doi:
Substances chimiques
Cytochrome P-450 CYP1A2
EC 1.14.14.1
ATP Binding Cassette Transporter, Subfamily B, Member 1
0
coptisine
0GCL71VN14
florfenicol
9J97307Y1H
Cytochrome P-450 Enzyme System
9035-51-2
Cytochrome P-450 CYP3A
EC 1.14.14.1
CYP2C11 protein, rat
EC 1.14.14.1
Cytochrome P450 Family 2
EC 1.14.14.1
Aryl Hydrocarbon Hydroxylases
EC 1.14.14.1
Steroid 16-alpha-Hydroxylase
EC 1.14.14.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM