Quercetin, resveratrol, and curcumin are indirect activators of the aryl hydrocarbon receptor (AHR)

Chemical Research in Toxicology

Volumn 25, Issue 9, 2012, Pages 1878-1884

  Mohammadi Bardbori, Afshin ^a,b   Bengtsson, Johanna ^c   Rannug, Ulf ^c   Rannug, Agneta ^a   Wincent, Emma ^a,c  

^a KAROLINSKA INSTITUTE   (Sweden)

^b SHIRAZ UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c STOCKHOLM UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

6 FORMYLINDOLO[3,2 B]CARBAZOLE; AROMATIC HYDROCARBON RECEPTOR; CARBAZOLE DERIVATIVE; CURCUMIN; CYTOCHROME P450 1A1; LIGAND; QUERCETIN; RECOMBINANT ENZYME; RESVERATROL; UNCLASSIFIED DRUG;

ARTICLE; CELL STRAIN HEPG2; CLEARANCE; CONTROLLED STUDY; CULTURE MEDIUM; ENZYME ACTIVITY; HUMAN; HUMAN CELL; KERATINOCYTE; PROTEIN DEGRADATION; REPORTER GENE; TURNOVER TIME;

CARBAZOLES; CELL LINE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CURCUMIN; CYTOCHROME P-450 CYP1A1; HEP G2 CELLS; HUMANS; KERATINOCYTES; QUERCETIN; RECEPTORS, ARYL HYDROCARBON; RECOMBINANT PROTEINS; STILBENES;

EID: 84866434831     PISSN: 0893228X     EISSN: 15205010     Source Type: Journal    
DOI: 10.1021/tx300169e     Document Type: Article

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