| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 5848453 | Chemico-Biological Interactions | 2011 | 10 Pages | 
Abstract
												⺠Sunlight has an important role in generating bioactive molecules that can activate the AHR. ⺠Identification of 1-(1H-indol-3-yl)-9H-pyrido[3,4-b]indole (IPI) as a new AHR-inducing tryptophan (TRP) photoproduct. ⺠IPI induces AHR-mediated P450 activity (EROD) and suppresses glucose output. ⺠IPI, a prominent component of photoactivated TRP, induces EROD additively with FICZ or TCDD. ⺠IPI was detected in tissue culture medium in ordinary ambient light conditions.
											Keywords
												EROD6-formylindolo[3,2-b]carbazoleESIMSCEHFICZIPITCDDTOFMRMRP-HPLCCyPATRPAHRCIDTrp2,3,7,8-Tetrachlorodibenzo-p-dioxinLC/MSMS/MSAbbreviationsCollision-induced dissociationElectrospray Ionization Mass SpectrometryTryptophanTime-of-Flight Cytochrome P4501ACytochrome P450Mass spectrometryTandem mass spectrometrymultiple reaction monitoringLiquid chromatography/mass spectrometryreverse phase high pressure liquid chromatographyglucose outputaryl hydrocarbon receptor
												Related Topics
												
													Life Sciences
													Environmental Science
													Health, Toxicology and Mutagenesis
												
											Authors
												Silvia Diani-Moore, Yuliang Ma, Erin Labitzke, Hui Tao, J. David Warren, Jared Anderson, Qiuying Chen, Steven S. Gross, Arleen B. Rifkind, 
											![First Page Preview: Discovery and biological characterization of 1-(1H-indol-3-yl)-9H-pyrido[3,4-b]indole as an aryl hydrocarbon receptor activator generated by photoactivation of tryptophan by sunlight Discovery and biological characterization of 1-(1H-indol-3-yl)-9H-pyrido[3,4-b]indole as an aryl hydrocarbon receptor activator generated by photoactivation of tryptophan by sunlight](/preview/png/5848453.png)