The suggested physiologic aryl hydrocarbon receptor activator and cytochrome P4501 substrate 6-formylindolo[3,2-b]carbazole is present in humans

Journal of Biological Chemistry

Volumn 284, Issue 5, 2009, Pages 2690-2696

  Wincent, Emma ^a   Amini, Nahid ^a   Luecke, Sandra ^b   Glatt, Hansruedi ^c   Bergman, Jan ^b   Crescenzi, Carlo ^a   Rannug, Agneta ^b   Rannug, Ulf ^a,d  

^a STOCKHOLM UNIVERSITY   (Sweden)

^b KAROLINSKA INSTITUTE   (Sweden)

^c GERMAN INSTITUTE OF HUMAN NUTRITION   (Germany)

^d STOCKHOLM UNIVERSITY   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

AMINES; AMINO ACIDS; ANIMAL CELL CULTURE; ANIMALS; AROMATIC COMPOUNDS; BIOCHEMISTRY; BIOMOLECULES; CARBOXYLIC ACIDS; CHEMICAL ACTIVATION; FOSSIL FUELS; HEALTH RISKS; HYDROCARBONS; INCINERATION; LIGANDS; METABOLISM; METABOLITES; ORGANIC ACIDS; ORGANIC COMPOUNDS; PHENOLS; PHOTOLYSIS; ULTRAVIOLET RADIATION; WASTE INCINERATION;

6-CARBOXYLIC ACIDS; ARYL HYDROCARBON RECEPTORS; EXPERIMENTAL ANIMALS; HIGH-AFFINITY LIGANDS; HUMAN URINES; HYDROXYLATED METABOLITES; MECHANISM OF ACTIONS; NEW CLASS; PHENOLIC METABOLITES; POLYCYCLIC AROMATIC COMPOUNDS; RISK TO HUMAN HEALTHS; SIGNALING PATHWAYS; VISIBLE LIGHTS; WELL BEINGS; XENOBIOTIC COMPOUNDS;

SUBSTRATES;

6 FORMYLINDOLO[3,2 B]CARBAZOLE; AROMATIC HYDROCARBON RECEPTOR; CARBOXYLIC ACID DERIVATIVE; CYTOCHROME; CYTOCHROME P450 1A1; CYTOCHROME P450 1A2; CYTOCHROME P450 1B1; INDOLO[3,2-B]CARBAZOLE-6-CARBOXYLIC ACID; SULFOTRANSFERASE; SULFOTRANSFERASE 1A1; SULFOTRANSFERASE 1A2; SULFOTRANSFERASE 1B1; SULFOTRANSFERASE 1E1; UNCLASSIFIED DRUG;

ARTICLE; CONJUGATION; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME KINETICS; ENZYME METABOLISM; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; PHOTOLYSIS; PRIORITY JOURNAL; PROTEIN EXPRESSION;

CARBAZOLES; CELL LINE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; CYTOCHROME P-450 ENZYME SYSTEM; ENZYME INHIBITORS; HUMANS; KINETICS; RECEPTORS, ARYL HYDROCARBON; SUBSTRATE SPECIFICITY; TANDEM MASS SPECTROMETRY;

ANIMALIA;

EID: 59149105791     PISSN: 00219258     EISSN: 1083351X     Source Type: Journal    
DOI: 10.1074/jbc.M808321200     Document Type: Article

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