Diflubenzuron, a benzoyl-urea insecticide, is a potent inhibitor of TCDD-induced CYP1A1 expression in HepG2 cells

Toxicology and Applied Pharmacology

Volumn 164, Issue 3, 2000, Pages 273-279

  Ledirac, N ^a   Delescluse, C ^a   Lesca, P ^a   Piechocki, M P ^a,b   Hines, R N ^a,b   De Sousa, G ^a   Pralavorio, M ^a   Rahmani, R ^a  

^a CEMAGREF   (France)

^b MEDICAL COLLEGE OF WISCONSIN   (United States)

Author keywords

2,3,7,8 tetrachlorodibenzo p dioxin; 3 methylcholanthrene; Ah receptor; CYP1A1; Diflubenzuron; TCDD

Indexed keywords

2,3,7,8 TETRACHLORODIBENZOFURAN; 3 METHYLCHOLANTHRENE; AROMATIC HYDROCARBON RECEPTOR; CHITIN; CHLORAMPHENICOL ACETYLTRANSFERASE; CYTOCHROME P450 1A1; CYTOCHROME P450 ISOENZYME; DIFLUBENZURON; ETHOXYRESORUFIN DEETHYLASE; INSECTICIDE; RIBONUCLEASE; UNCLASSIFIED DRUG; UREA DERIVATIVE;

ARTICLE; BINDING KINETICS; CELL STRAIN HEPG2; CONCENTRATION RESPONSE; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME INDUCTION; HUMAN; HUMAN CELL; PROTEIN EXPRESSION; RECEPTOR BINDING; TOXICOKINETICS; TRANSCRIPTION REGULATION;

FELIS CATUS; MURINAE;

EID: 0034192570     PISSN: 0041008X     EISSN: None     Source Type: Journal    
DOI: 10.1006/taap.2000.8920     Document Type: Article

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