Affinity DataKi: 0.920nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 1.30nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 1.80nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 2.60nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 4.30nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 5.5nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 14nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 20nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 27nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 27nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 65nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 70nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 97nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 152nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 178nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 195nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 208nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 237nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 293nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 324nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 521nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 642nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 674nMAssay Description:Antagonist activity at DP1 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 873nMAssay Description:Antagonist activity at DP1 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataKi: 2.34E+3nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 2.36E+3nMAssay Description:Inhibition of human PDE2More data for this Ligand-Target Pair
Affinity DataKi: 6.90E+3nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 7.81E+3nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 1.01E+4nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 1.17E+4nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 1.50E+4nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKi: 2.24E+4nMAssay Description:Binding affinity to PDE2 (unknown origin) by SPR analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 0.340nMAssay Description:Inhibition of human IDO1 assessed as unbound compound concentration by human whole blood assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.450nMAssay Description:Inhibition of human IDO1 assessed as unbound compound concentration by human whole blood assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.630nMAssay Description:Inhibition of human IDO1 assessed as unbound compound concentration by human whole blood assayMore data for this Ligand-Target Pair
Affinity DataIC50: 0.800nMAssay Description:Inhibition of IDO1 in IFN-gamma-stimulated human HeLa cells assessed as reduction in kynurenine production using L-Tryptophan as substrate incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 0.840nMAssay Description:Inhibition of human IDO1 assessed as unbound compound concentration by human whole blood assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of IDO1 in IFN-gamma-stimulated human HeLa cells assessed as reduction in kynurenine production using L-Tryptophan as substrate incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of human IDO1 in human Hela cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60nMAssay Description:Inhibition of IDO1 in IFN-gamma-stimulated human HeLa cells assessed as reduction in kynurenine production using L-Tryptophan as substrate incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human IDO1 in human Hela cellsMore data for this Ligand-Target Pair
Affinity DataIC50: 1.70nMAssay Description:Inhibition of heme binding to IDO1 in interferon-gamma-induced human HeLa cells assessed as reduction in N-formylkynurenine production using L-trypto...More data for this Ligand-Target Pair
Affinity DataIC50: 1.70nMAssay Description:Inhibition of IDO1 in IFN-gamma-stimulated human HeLa cells assessed as reduction in kynurenine production using L-Tryptophan as substrate incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 1.80nMAssay Description:Inhibition of IDO1 in IFN-gamma-stimulated human HeLa cells assessed as reduction in kynurenine production using L-Tryptophan as substrate incubated ...More data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Antagonist activity at DP1 receptor (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibition of human IDO1 in human Hela cellsMore data for this Ligand-Target Pair