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Binding affinity Karenia brevis TrxR assessed as formation at 7.2 uM by LC-MS/MS analysis
Assay data:1 Active, 1 Tested
SummaryCompounds, ActivePubMed Citation
Inhibition of Karenia brevis TrxR assessed as reduction in substrate reduction using H2O2 as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 15 mins by absorbance based assay
Assay data:1 Tested
SummaryPubMed Citation
Inhibition of Karenia brevis TrxRD3 assessed as reduction in substrate reduction at 40 uM using DTNB as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 5 mins by absorbance based assay relative to control
Inhibition of Karenia brevis TrxR assessed as reduction in substrate reduction at 40 uM using GSSG as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 30 mins by absorbance based assay relative to control
Inhibition of Karenia brevis TrxR assessed as reduction in substrate reduction at 40 uM using human Trx and insulin as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 5 mins by absorbance based assay relative to control
Inhibition of Karenia brevis TrxR assessed as reduction in substrate reduction at 10 to 100 uM using H2O2 as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 15 mins by absorbance based assay relative to control
Inhibition of Karenia brevis TrxR assessed as reduction in substrate reduction at 40 uM using DTNB as a substrate incubated for 60 mins in the presence of NADPH followed by substrate addition measured for 5 mins by absorbance based assay relative to control
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