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Inhibition of SE-Rh binding to human recombinant GSTO1 in human MDA-MB-435 cells incubated for 1 hrs by SDS-PAGE based fluorescence analysis
Assay data:1 Active, 1 Activity ≤ 1 µM, 1 Tested
SummaryCompounds, ActiveCompounds, activity ≤ 1 µMPubMed CitationRelated BioAssays by Target
Inhibition of SE-Rh binding to human recombinant GSTO1 preincubated with compound for 30 mins followed by SE-Rh addition and measured after 1 hrs by SDS-PAGE based fluorescence analysis
Binding affinity to GSTO1 in human DOHH-2 cells by MS analysis
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed CitationRelated BioAssays by Target
Binding affinity to GSTO1 in human MDA-MB-453 cells at 10 uM measured after 6 hrs in presence of 100 uM PES by pull-down assay
Assay data:1 Tested
SummaryPubMed CitationRelated BioAssays by Target
Binding affinity to GSTO1 in human DOHH-2 cells at 10 uM measured after 6 hrs in presence of 100 uM PES by pull-down assay
Binding affinity to GSTO1 in human MDA-MB-453 cells measured after 6 hrs by pull-down assay
Binding affinity to GSTO1 in human DOHH-2 cells measured after 6 hrs by pull-down assay
Binding affinity to GSTO1 in human NCI-H522 cells at 10 uM incubated for 1 hr by Biotin-TAMRA pull down based western blot analysis
Binding affinity to GSTO1 in human NCI-H522 cells at 10 uM incubated for 1 hr by Biotin-TAMRA pull down based mass spectrometry
Inhibition of GSTO1-1 (unknown origin) at 100 uM using reduced GSH and CDNB as substrate incubated for 10 mins followed by substrate addition by microplate reader analysis
Inhibition of GSTO1-1 in mouse bone marrow derived macrophage cells assessed as reduction in LPS-induced IL-1beta release by measuring IL1 beta level at 5 uM pretreated with LPS for 3 hrs followed by compound addition and measured after 1 hr by ELISA relative to control
Assay data:11 Tested
Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as Kinact/Ki ratio using S-(4-nitrophenacyl)glutathione as substrate preincubated for 1 to 6 mins followed by substrate addition by spectrophotmetric analysis
Assay data:10 Tested
Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as inhibitor constant using S-(4-nitrophenacyl)glutathione as substrate preincubated for 1 to 6 mins followed by substrate addition by spectrophotmetric analysis
Assay data:10 Active, 2 Activity ≤ 1 µM, 10 Tested
Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli using S-(4-nitrophenacyl)glutathione as substrate preincubated for 2 mins followed by substrate addition by 4-NPG assay
Assay data:21 Active, 19 Activity ≤ 1 µM, 33 Tested
Inhibition of recombinant GSTO1-1 (unknown origin) expressed in Escherichia coli assessed as Kinact using S-(4-nitrophenacyl)glutathione as substrate preincubated for 1 to 6 mins followed by substrate addition by spectrophotmetric analysis
Inhibition of CMFDA binding to human N-terminal 6x-His-tagged GSTO1-1 assessed as reduction in reduction of 4-NPG to 4-nitroacetophenone at 0.00001 to 1 uM incubated for 30 mins by 4NPG reductase assay
Inhibition of CMFDA binding to human N-terminal 6x-His-tagged GSTO1-1 at 10 uM preincubated for 30 mins followed by CMFDA addition and measured after 30 mins in presence of 10 uM ZnCl2 by in-gel fluorescence binding assay
Inhibition of CMFDA binding to human N-terminal 6x-His-tagged GSTO1-1 at 10 uM preincubated for 30 mins followed by CMFDA addition and measured after 30 mins in presence of 10 uM MnCl2 by in-gel fluorescence binding assay
Inhibition of CMFDA binding to human N-terminal 6x-His-tagged GSTO1-1 at 10 uM preincubated for 30 mins followed by CMFDA addition and measured after 30 mins in presence of 1 to 10 uM KCl by in-gel fluorescence binding assay
Inhibition of CMFDA binding to human N-terminal 6x-His-tagged GSTO1-1 at 10 uM preincubated for 30 mins followed by CMFDA addition and measured after 30 mins in presence of 1 to 10 uM FeCl3 by in-gel fluorescence binding assay
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