The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine. - Wikidata - awgldk - TriplyDB

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

http://www.wikidata.org/entity/Q37422747

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Interactions between CYP3A4 and Dietary Polyphenols Use of In Vitro and Predictive In Silico Models to Study the Inhibition of Cytochrome P4503A by Stilbenes Reductive metabolism of oxymatrine is catalyzed by microsomal CYP3A4.Inhibition of cytochrome P450 3A by acetoxylated analogues of resveratrol in in vitro and in silico models.Functioning of drug-metabolizing microsomal cytochrome P450s: In silico probing of proteins suggests that the distal heme 'active site' pocket plays a relatively 'passive role' in some enzyme-substrate interactions Editor's Highlight: Neonatal Activation of the Xenobiotic-Sensors PXR and CAR Results in Acute and Persistent Down-regulation of PPARα-Signaling in Mouse Liver.Identification of human papillomavirus status specific biomarker in head and neck cancer.

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The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

http://www.wikidata.org/entity/Q37422747

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 18 June 2013

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@en

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@nl

type

label

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@en

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@nl

prefLabel

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@en

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@nl

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Drug Metabolism and Disposition

P1476

The relative contributions of CYP3A4 and CYP3A5 to the metabolism of vinorelbine.

@en

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Ariel R Topletz

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Chad E Hadden

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Jamie L Renbarger

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Jennifer B Dennison

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Robert J Barbuch

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Stephen D Hall

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Genetic contribution to variable human CYP3A-mediated metabolism

Twenty years of MOPP therapy for Hodgkin's disease

Genetic variability in CYP3A5 and its possible consequences.

Application of higher throughput screening (HTS) inhibition assays to evaluate the interaction of antiparasitic drugs with cytochrome P450s.

Selective metabolism of vincristine in vitro by CYP3A5.

Blood and plasma pharmacokinetics of vinorelbine in elderly patients with advanced metastatic cancer.

Role of itraconazole metabolites in CYP3A4 inhibition.

Increased risk of vincristine neurotoxicity associated with low CYP3A5 expression genotype in children with acute lymphoblastic leukemia.

Clinical pharmacokinetics of vinorelbine.

New sensitive liquid chromatography method coupled with tandem mass spectrometric detection for the clinical analysis of vinorelbine and its metabolites in blood, plasma, urine and faeces.

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1651-1661

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scholarly article

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10.1124/DMD.113.051094

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9

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41

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23780963

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