BDBM50422268 GLUTATHIONE::GSH
SMILES N[C@@H](CCC(=O)N[C@@H](CS)C(=O)NCC(O)=O)C(O)=O
InChI Key InChIKey=RWSXRVCMGQZWBV-WDSKDSINSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50422268
Affinity DataKi: 9.55E+5nMAssay Description:Inhibition constant of compound against binding of Yeast Glyoxalase IMore data for this Ligand-Target Pair
Affinity DataKd: 1.90E+3nMpH: 7.4 T: 2°CAssay Description:Experiments were carried out using a VP-ITC MicroCalorimeter (MicroCal) at 37°C, and data were analyzed using the Origen ITC analysis software packag...More data for this Ligand-Target Pair
Affinity DataKd: 260nMpH: 7.4 T: 2°CAssay Description:Experiments were carried out using a VP-ITC MicroCalorimeter (MicroCal) at 37°C, and data were analyzed using the Origen ITC analysis software packag...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EHMT2(Homo sapiens (Human))
Radboud University
Curated by ChEMBL
Radboud University
Curated by ChEMBL
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of wild type recombinant human histone lysine methyltransferase G9a (913 to 1193 residues) expressed in Escherichia coli Rosetta BL21 DE3 ...More data for this Ligand-Target Pair
TargetHistone-lysine N-methyltransferase EHMT1(Homo sapiens (Human))
Radboud University
Curated by ChEMBL
Radboud University
Curated by ChEMBL
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of wild type recombinant human histone lysine methyltransferase GLP (951 to 1235 residues) expressed in Escherichia coli Rosetta BL21 DE3 ...More data for this Ligand-Target Pair
Affinity DataKd: 1.58E+3nMpH: 7.4 T: 2°CAssay Description:Experiments were carried out using a VP-ITC MicroCalorimeter (MicroCal) at 37°C, and data were analyzed using the Origen ITC analysis software packag...More data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Affinity towards recombinant Glutathione S-transferase (GST) Enzyme.More data for this Ligand-Target Pair