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Induction of CYP1A1 in rat hepatocytes at 0.1 to 10 uM incubated for 48 hrs
Assay data:1 Tested
SummaryPubMed CitationRelated BioAssays by Target
Drug metabolism assessed as rat recombinant CYP1A1-mediated sulindac sulfone formation measured per pmol of protein at 200 uM after 90 mins by HPLC analysis
Drug metabolism assessed as rat recombinant CYP1A1-mediated sulindac sulfone formation measured per pmol of protein at 500 uM after 90 mins by HPLC analysis
Activity of rat recombinant CYP1A1 expressed in baculovirus-infected insect cells assessed as enzyme-mediated N-((4-(4-fluorophenyl)-2-oxochroman-7-yl)methyl)-2-((S)-2-hydroxy-2-(trifluoromethyl)butanoyl)hydrazinecarboxamide formation preincubated for 3 mins by Michaelis-Menten equation in presence of NADPH for 10 mins
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Activity of rat recombinant CYP1A1 expressed in baculovirus-infected insect cells assessed as enzyme-mediated compound formation treated with setileuton at 10 uM preincubated for 3 mins measured after 30 mins in presence of 1 mM NADPH
Activity of rat recombinant CYP1A1 expressed in baculovirus-infected insect cells assessed as enzyme-mediated N-((4-(4-fluorophenyl)-2-oxochroman-7-yl)methyl)-2-((S)-2-hydroxy-2-(trifluoromethyl)butanoyl)hydrazinecarboxamide formation at 10 uM preincubated for 3 mins measured after 30 mins in presence of 1 mM NADPH
Inhibition of CYP1A1 activity in rat liver microsomes using benzo[alpha]pyrene as substrate after 10 mins by fluorescence analysis
Assay data:12 Active, 12 Activity ≤ 1 µM, 13 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of CYP1A1 activity in rat liver microsomes using benzo[alpha]pyrene as substrate at 100 nmol after 10 mins by fluorescence analysis
Assay data:13 Tested
Mechanism based inhibition of rat cytochrome P450 CYP1A1 measured by ethoxyresorufin O-deethylation warfarin R-6 and R-8 hydroxylation
Mechanism based inhibition of rat cytochrome P450 CYP1A1 measured by 7-ethoxyresorufin O-deethylation (EROD)
Assay data:9 Active, 8 Activity ≤ 1 µM, 10 Tested
Mechanism based inhibition of rat cytochrome P450 CYP1A1
Interaction (Ks) with cytochrome P450 in 3-methylcholanthrene-induced rat hepatic microsomes
Assay data:2 Tested
Interaction with cytochrome P450 in 3-methylcholanthrene-induced rat hepatic microsomes
Assay data:1 Active, 5 Tested
Spectral dissociation constant for rat liver Cytochrome P450 1A1
Inhibition of Aryl hydrocarbon hydroxylase in phenobarbitone-treated rats
Assay data:8 Tested
Effect on Aryl hydrocarbon hydroxylase activity in 3-methylcolanthrene-induced rat liver microsomes at 2.6x10E-4M
Effect on Aryl hydrocarbon hydroxylase activity in 3-methylcolanthrene-induced rat liver microsomes at 8x10E-4M
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