Dataset of endo- and xenobiotic inhibition of CYP2B6: Comparison to CYP3A4.

Adverse drug reactions CYP2B6 CYP3A4 Enzyme inhibition Lipids Mixtures

Journal

Data in brief
ISSN: 2352-3409
Titre abrégé: Data Brief
Pays: Netherlands
ID NLM: 101654995

Informations de publication

Date de publication:
Apr 2022
Historique:
received: 07 02 2022
revised: 21 02 2022
accepted: 28 02 2022
entrez: 14 3 2022
pubmed: 15 3 2022
medline: 15 3 2022
Statut: epublish

Résumé

Cytochrome P450 2B6 (CYP2B6) is a human enzyme important in chemical detoxification, steroid and fatty acid metabolism that is primarily hepatic. Therefore, induction or inhibition of CYP2B6 may perturb endo- and xenobiotic metabolism and cause adverse reactions. Recent research indicates that mice lacking Cyp2b enzymes are obese with liver steatosis [1] (Heintz et al.,

Identifiants

pubmed: 35282180
doi: 10.1016/j.dib.2022.108013
pii: S2352-3409(22)00224-4
pmc: PMC8914530
doi:

Types de publication

Journal Article

Langues

eng

Pagination

108013

Subventions

Organisme : NIEHS NIH HHS
ID : R15 ES017321
Pays : United States

Informations de copyright

© 2022 The Author(s). Published by Elsevier Inc.

Déclaration de conflit d'intérêts

The authors declare that they have no known competing financial interests or personal relationships which have or could be perceived to have influenced the work reported in this article.

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Auteurs

Emily M Olack (EM)

Biological Sciences, Clemson University, 132 Long Hall, Clemson, SC 29634, USA.

Melissa M Heintz (MM)

Biological Sciences, Clemson University, 132 Long Hall, Clemson, SC 29634, USA.

William S Baldwin (WS)

Biological Sciences, Clemson University, 132 Long Hall, Clemson, SC 29634, USA.

Classifications MeSH