Compile Data Set for Download or QSAR
maximum 50k data
Found 40 Enz. Inhib. hit(s) with all data for entry = 50002866
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463913(CHEMBL4242226)
Affinity DataIC50:  7nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463922(CHEMBL4245134)
Affinity DataIC50:  23nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463905(CHEMBL4238895)
Affinity DataIC50:  39nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463914(CHEMBL4241365)
Affinity DataIC50:  50nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463913(CHEMBL4242226)
Affinity DataIC50:  73nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463910(CHEMBL4238561)
Affinity DataIC50:  87nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463902(CHEMBL4248543)
Affinity DataIC50:  117nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463903(CHEMBL4248088)
Affinity DataIC50:  119nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463906(CHEMBL3612772)
Affinity DataIC50:  127nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463907(CHEMBL4237632)
Affinity DataIC50:  134nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463916(CHEMBL4243692)
Affinity DataIC50:  148nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463923(CHEMBL4243788)
Affinity DataIC50:  156nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463909(CHEMBL4245579)
Affinity DataIC50:  188nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463919(CHEMBL4240957)
Affinity DataIC50:  288nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463904(CHEMBL4250699)
Affinity DataIC50:  299nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463924(CHEMBL458765 | NSC-119236)
Affinity DataIC50:  332nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463912(CHEMBL4242333)
Affinity DataIC50:  361nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463905(CHEMBL4238895)
Affinity DataIC50:  372nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463908(CHEMBL4239450)
Affinity DataIC50:  390nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463921(CHEMBL4238071)
Affinity DataIC50:  394nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463925(CHEMBL4240537)
Affinity DataIC50:  420nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463915(CHEMBL4250771)
Affinity DataIC50:  427nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463918(CHEMBL4248497)
Affinity DataIC50:  438nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463911(CHEMBL4248954)
Affinity DataIC50:  448nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463917(CHEMBL4237476)
Affinity DataIC50:  714nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463906(CHEMBL3612772)
Affinity DataIC50:  738nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463901(CHEMBL465913)
Affinity DataIC50:  977nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463914(CHEMBL4241365)
Affinity DataIC50:  1.08E+3nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463920(CHEMBL4248240)
Affinity DataIC50:  1.19E+3nMAssay Description:Inhibition of IDO1 (unknown origin) assessed as reduction in N'-formlylkynurenine formation using D-Tryptophan as substrate in presence of aspartate ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463922(CHEMBL4245134)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463909(CHEMBL4245579)
Affinity DataIC50:  1.24E+3nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463907(CHEMBL4237632)
Affinity DataIC50:  2.66E+3nMAssay Description:Inhibition of IFN-gamma-stimulated IDO1 in human HeLa cells after 24 hrs by Ehrlich's reagent based assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463906(CHEMBL3612772)
Affinity DataIC50:  3.35E+3nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463909(CHEMBL4245579)
Affinity DataIC50:  7.15E+3nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463912(CHEMBL4242333)
Affinity DataIC50:  7.30E+3nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463916(CHEMBL4243692)
Affinity DataIC50:  4.16E+4nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463903(CHEMBL4248088)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463908(CHEMBL4239450)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463915(CHEMBL4250771)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50463907(CHEMBL4237632)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant TDO (unknown origin) assessed as reduction in N-formylkynurenine formation using L-Tryptophan as substrate after 75 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed