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Dibenzyl trisulfide binds to and competitively inhibits the cytochrome P450 1A1 active site without impacting the expression of the aryl hydrocarbon receptor

  • Shaniece Wauchope
  • , Monika A. Roy
  • , William Irvine
  • , Isaac Morrison
  • , Eileen Brantley
  • , Maxine Gossell-Williams
  • , Alicia R. Timme-Laragy
  • , Rupika Delgoda

Research output: Contribution to journal › Article › peer-review

Original languageEnglish
Article number115502
JournalToxicology and Applied Pharmacology
Volume419
DOIs
StatePublished - May 15 2021

ASJC Scopus Subject Areas

  • Toxicology
  • Pharmacology

Keywords

  • AHR pathway
  • Aryl hydrocarbon receptor
  • CYP1
  • Carcinogenesis
  • Chemoprevention
  • Cytochrome P450 1
  • Dibenzyl trisulfide
  • Ethnomedicine
  • Petiveria alliacea
  • Activation, Metabolic
  • Benzo(a)pyrene/metabolism
  • Humans
  • Benzyl Compounds/metabolism
  • Zebrafish Proteins/genetics
  • Cytochrome P-450 CYP1A1/antagonists & inhibitors
  • Sulfides/metabolism
  • Zebrafish/embryology
  • Binding Sites
  • Binding, Competitive
  • Catalytic Domain
  • Receptors, Aryl Hydrocarbon/genetics
  • Gene Expression Regulation
  • Animals
  • Protein Binding
  • Cytochrome P-450 Enzyme Inhibitors/metabolism
  • Cytochrome P-450 CYP1B1/antagonists & inhibitors
  • Polychlorinated Biphenyls/metabolism

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