Structure, function, regulation and polymorphism and the clinical significance of human cytochrome P450 1A2

SF Zhou, B Wang, LP Yang, JP Liu - Drug metabolism reviews, 2010 - Taylor & Francis
Human CYP1A2 is one of the major CYPs in human liver and metabolizes a number of
clinical drugs (eg, clozapine, tacrine, tizanidine, and theophylline; n> 110), a number of …

Substrates, inducers, inhibitors and structure-activity relationships of human Cytochrome P450 2C9 and implications in drug development

SF Zhou, ZW Zhou, LP Yang… - Current medicinal …, 2009 - ingentaconnect.com
Cytochrome P450 2C9 (CYP2C9) is one of the most abundant CYP enzymes in the human
liver. CYP2C9 metabolizes more than 100 therapeutic drugs, including tolbutamide …

Assessment of orally administered Δ9-tetrahydrocannabinol when coadministered with cannabidiol on Δ9-tetrahydrocannabinol pharmacokinetics and …

CA Zamarripa, TR Spindle, R Surujunarain… - JAMA Network …, 2023 - jamanetwork.com
Importance Controlled clinical laboratory studies have shown that cannabidiol (CBD) can
sometimes attenuate or exacerbate the effects ofΔ9-tetrahydrocannabinol (Δ9-THC). No …

Pharmacokinetics and metabolism of natural methylxanthines in animal and man

BB Fredholm, MJ Arnaud - Methylxanthines, 2011 - Springer
Caffeine, theophylline, theobromine, and paraxanthine administered to animals and humans
distribute in all body fluids and cross all biological membranes. They do not accumulate in …

Evaluation of cytochrome P450‐mediated cannabinoid‐drug interactions in healthy adult participants

S Bansal, CA Zamarripa, TR Spindle… - Clinical …, 2023 - Wiley Online Library
Understanding cannabis‐drug interactions is critical given regulatory changes that have
increased access to and use of cannabis. Cannabidiol (CBD) and Δ‐9 …

Geneva cocktail for cytochrome p450 and P‐glycoprotein activity assessment using dried blood spots

M Bosilkovska, CF Samer, J Déglon… - ClInICAl …, 2014 - Wiley Online Library
The suitability of the capillary dried blood spot (DBS) sampling method was assessed for
simultaneous phenotyping of cytochrome P450 (CYP) enzymes and P‐glycoprotein (P‐gp) …

Pharmacokinetic and pharmacodynamic drug–drug interactions: research methods and applications

L Sun, K Mi, Y Hou, T Hui, L Zhang, Y Tao, Z Liu… - Metabolites, 2023 - mdpi.com
Because of the high research and development cost of new drugs, the long development
process of new drugs, and the high failure rate at later stages, combining past drugs has …

Interactions of ginseng with therapeutic drugs

MK Choi, IS Song - Archives of pharmacal research, 2019 - Springer
Ginseng is the most frequently used herbal medicine for immune system stimulation and as
an adjuvant with prescribed drugs owing to its numerous pharmacologic activities. It is …

Single-cell metabolic profiling reveals subgroups of primary human hepatocytes with heterogeneous responses to drug challenge

E Sanchez-Quant, ML Richter, M Colomé-Tatché… - Genome Biology, 2023 - Springer
Background Xenobiotics are primarily metabolized by hepatocytes in the liver, and primary
human hepatocytes are the gold standard model for the assessment of drug efficacy, safety …

Pharmacokinetic assessment of a five‐probe cocktail for CYPs 1A2, 2C9, 2C19, 2D6 and 3A

S Turpault, W Brian, R Van Horn… - British journal of …, 2009 - Wiley Online Library
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT• Numerous cocktails using concurrent
administration of several cytochrome P450 (CYP) isoform‐selective probe drugs have been …