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New insights into quetiapine metabolism using molecular networking
by
Ferron, Pierre-Jean
, Morel, Isabelle
, Gicquel, Thomas
, Allard, Pierre-Marie
, Clément, Bruno
, Le Daré, Brendan
in
631/1647
/ 631/80
/ 692/308
/ 692/53
/ Antifungal agents
/ Antipsychotic Agents - pharmacology
/ Antipsychotics
/ Bioinformatics
/ Carcinoma, Hepatocellular - drug therapy
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Cell culture
/ CYP2D6 protein
/ Cytochrome P450
/ Drug metabolism
/ Female
/ Hepatocytes
/ High-performance liquid chromatography
/ Humanities and Social Sciences
/ Humans
/ Ketoconazole
/ Life Sciences
/ Liquid chromatography
/ Liver Neoplasms - drug therapy
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Mass spectrometry
/ Mass spectroscopy
/ Metabolic Networks and Pathways - drug effects
/ Metabolic pathways
/ Metabolism
/ Metabolites
/ Metabolome - drug effects
/ multidisciplinary
/ Networking
/ Pharmacology
/ Prognosis
/ Quetiapine
/ Quetiapine Fumarate - pharmacology
/ Quinidine
/ Science
/ Science (multidisciplinary)
/ Toxicology
/ Tumor Cells, Cultured
/ Xenobiotics
2020
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New insights into quetiapine metabolism using molecular networking
by
Ferron, Pierre-Jean
, Morel, Isabelle
, Gicquel, Thomas
, Allard, Pierre-Marie
, Clément, Bruno
, Le Daré, Brendan
in
631/1647
/ 631/80
/ 692/308
/ 692/53
/ Antifungal agents
/ Antipsychotic Agents - pharmacology
/ Antipsychotics
/ Bioinformatics
/ Carcinoma, Hepatocellular - drug therapy
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Cell culture
/ CYP2D6 protein
/ Cytochrome P450
/ Drug metabolism
/ Female
/ Hepatocytes
/ High-performance liquid chromatography
/ Humanities and Social Sciences
/ Humans
/ Ketoconazole
/ Life Sciences
/ Liquid chromatography
/ Liver Neoplasms - drug therapy
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Mass spectrometry
/ Mass spectroscopy
/ Metabolic Networks and Pathways - drug effects
/ Metabolic pathways
/ Metabolism
/ Metabolites
/ Metabolome - drug effects
/ multidisciplinary
/ Networking
/ Pharmacology
/ Prognosis
/ Quetiapine
/ Quetiapine Fumarate - pharmacology
/ Quinidine
/ Science
/ Science (multidisciplinary)
/ Toxicology
/ Tumor Cells, Cultured
/ Xenobiotics
2020
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New insights into quetiapine metabolism using molecular networking
by
Ferron, Pierre-Jean
, Morel, Isabelle
, Gicquel, Thomas
, Allard, Pierre-Marie
, Clément, Bruno
, Le Daré, Brendan
in
631/1647
/ 631/80
/ 692/308
/ 692/53
/ Antifungal agents
/ Antipsychotic Agents - pharmacology
/ Antipsychotics
/ Bioinformatics
/ Carcinoma, Hepatocellular - drug therapy
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Cell culture
/ CYP2D6 protein
/ Cytochrome P450
/ Drug metabolism
/ Female
/ Hepatocytes
/ High-performance liquid chromatography
/ Humanities and Social Sciences
/ Humans
/ Ketoconazole
/ Life Sciences
/ Liquid chromatography
/ Liver Neoplasms - drug therapy
/ Liver Neoplasms - metabolism
/ Liver Neoplasms - pathology
/ Mass spectrometry
/ Mass spectroscopy
/ Metabolic Networks and Pathways - drug effects
/ Metabolic pathways
/ Metabolism
/ Metabolites
/ Metabolome - drug effects
/ multidisciplinary
/ Networking
/ Pharmacology
/ Prognosis
/ Quetiapine
/ Quetiapine Fumarate - pharmacology
/ Quinidine
/ Science
/ Science (multidisciplinary)
/ Toxicology
/ Tumor Cells, Cultured
/ Xenobiotics
2020
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New insights into quetiapine metabolism using molecular networking
Journal Article
New insights into quetiapine metabolism using molecular networking
2020
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Overview
Metabolism is involved in both pharmacology and toxicology of most xenobiotics including drugs. Yet, visualization tools facilitating metabolism exploration are still underused, despite the availibility of pertinent bioinformatics solutions. Since molecular networking appears as a suitable tool to explore structurally related molecules, we aimed to investigate its interest in in vitro metabolism exploration. Quetiapine, a widely prescribed antipsychotic drug, undergoes well-described extensive metabolism, and is therefore an ideal candidate for such a proof of concept. Quetiapine was incubated in metabolically competent human liver cell models (HepaRG) for different times (0 h, 3 h, 8 h, 24 h) with or without cytochrom P450 (CYP) inhibitor (ketoconazole as CYP3A4/5 inhibitor and quinidine as CYP2D6 inhibitor), in order to study its metabolism kinetic and pathways. HepaRG culture supernatants were analyzed on an ultra-high performance liquid chromatography coupled with tandem mass spectrometry (LC-HRMS/MS). Molecular networking approach on LC-HRMS/MS data allowed to quickly visualize the quetiapine metabolism kinetics and determine the major metabolic pathways (CYP3A4/5 and/or CYP2D6) involved in metabolite formation. In addition, two unknown putative metabolites have been detected. In vitro metabolite findings were confirmed in blood sample from a patient treated with quetiapine. This is the first report using LC-HRMS/MS untargeted screening and molecular networking to explore in vitro drug metabolism. Our data provide new evidences of the interest of molecular networking in drug metabolism exploration and allow our in vitro model consistency assessment.
Publisher
Nature Publishing Group UK,Nature Publishing Group
Subject
/ 631/80
/ 692/308
/ 692/53
/ Antipsychotic Agents - pharmacology
/ Carcinoma, Hepatocellular - drug therapy
/ Carcinoma, Hepatocellular - metabolism
/ Carcinoma, Hepatocellular - pathology
/ Female
/ High-performance liquid chromatography
/ Humanities and Social Sciences
/ Humans
/ Liver Neoplasms - drug therapy
/ Liver Neoplasms - metabolism
/ Metabolic Networks and Pathways - drug effects
/ Quetiapine Fumarate - pharmacology
/ Science
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