TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 11nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 14nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 15nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 17nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 18nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 19nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 19nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 21nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 21nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 23nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 24nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 24nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 25nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 26nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 35nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 36nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 37nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 44nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 72nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 78nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 94nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 99nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 101nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 102nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 104nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 104nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 109nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 114nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 115nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 119nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 120nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 121nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 121nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 126nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 130nMAssay Description:Inhibition of recombinant N-terminal His-tagged human IDO1 expressed in Escherichia coli assessed as reduction in N-formylkynurenine formation using ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 132nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 143nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 148nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: >200nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: >200nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: >200nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 2(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 280nMAssay Description:Inhibition of N-terminal His-tagged human IDO2 expressed in Escherichia coli expression systemMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 2(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 490nMAssay Description:Inhibition of N-terminal His-tagged human IDO2 expressed in Escherichia coli expression systemMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 2(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 590nMAssay Description:Inhibition of N-terminal His-tagged human IDO2 expressed in Escherichia coli expression systemMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 2(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 710nMAssay Description:Inhibition of N-terminal His-tagged human IDO2 expressed in Escherichia coli expression systemMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: 850nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Nanjing Medical University
Curated by ChEMBL
Nanjing Medical University
Curated by ChEMBL
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of IDO1 in human HeLa cells using L-tryptophan as substrate incubated for 48 hrsMore data for this Ligand-Target Pair