BDBM26057 4-(2,3-dihydro-1,4-benzodioxin-6-yl)-5-[(5-nitro-1,3-thiazol-2-yl)sulfanyl]-4H-1,2,4-triazol-3-ol::BI-78D3
SMILES [O-][N+](=O)c1cnc(Sc2n[nH]c(=O)n2-c2ccc3OCCOc3c2)s1
InChI Key InChIKey=QFRLDZGQEZCCJZ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 26057
Affinity DataIC50: 500nMpH: 7.8 T: 0°CAssay Description:Compound was evaluated for its ability to disrupt the interaction of pepJIP1 with JNK1 by using DELFIA assay. DELFIA is a heterogeneous assay whereby...More data for this Ligand-Target Pair
Affinity DataIC50: 280nMpH: 7.5 T: 22°CAssay Description:Compounds were tested for their ability to inhibit JNK1 phosphorylation of ATF2 in the Time-Resolved Fluorescence Resonance Energy Transfer (TR-FRET)...More data for this Ligand-Target Pair
Affinity DataKd: 8.10E+3nMAssay Description:Inhibition of wild-type JNK2 by isothermal calorimetryMore data for this Ligand-Target Pair
Affinity DataIC50: 280nMAssay Description:Inhibition of JNK1 by TR-FRET assayMore data for this Ligand-Target Pair
Affinity DataIC50: 500nMAssay Description:Displacement of biotin-labeled pep-JIP1from JNK2 by DELFIA assayMore data for this Ligand-Target Pair
Activity Spreadsheet -- ITC Data from BindingDB
Found 3 hits for monomerid = 26057
ITC Datalogk: 1.23E+5
pH: 7.4 T: 25.00°C
pH: 7.4 T: 25.00°C
CellMitogen-Activated Protein Kinase 9 (JNK2) Mutant (R127A)(Human)
Burnham Institute For Medical Research
Burnham Institute For Medical Research
ITC Datalogk: 6.80E+4
pH: 7.4 T: 25.00°C
pH: 7.4 T: 25.00°C
CellMitogen-Activated Protein Kinase 9 (JNK2) Mutant (C162S)(Human)
Burnham Institute For Medical Research
Burnham Institute For Medical Research
ITC Datalogk: 1.96E+4
pH: 7.4 T: 25.00°C
pH: 7.4 T: 25.00°C