Compile Data Set for Download or QSAR
maximum 50k data
Found 45 Enz. Inhib. hit(s) with all data for entry = 50003287
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50469087(CHEMBL4293263)
Affinity DataIC50:  18nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469058(CHEMBL4291792)
Affinity DataIC50:  18nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469077(CHEMBL4281167)
Affinity DataIC50:  22nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469075(CHEMBL4285752)
Affinity DataIC50:  26nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469082(CHEMBL4278127)
Affinity DataIC50:  29nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469064(CHEMBL4292949)
Affinity DataIC50:  48nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469079(CHEMBL4285003)
Affinity DataIC50:  61nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50126143(Epacadostat | INCB-024360)
Affinity DataIC50:  65nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore data for this Ligand-Target Pair
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50469060(CHEMBL4293312)
Affinity DataIC50:  73nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469060(CHEMBL4293312)
Affinity DataIC50:  120nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469059(CHEMBL4286913)
Affinity DataIC50:  134nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469062(CHEMBL4282064)
Affinity DataIC50:  152nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469069(CHEMBL4281581)
Affinity DataIC50:  208nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469058(CHEMBL4291792)
Affinity DataIC50:  215nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469081(CHEMBL4282661)
Affinity DataIC50:  234nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469074(CHEMBL4289462)
Affinity DataIC50:  290nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469077(CHEMBL4281167)
Affinity DataIC50:  322nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469078(CHEMBL4292858)
Affinity DataIC50:  338nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50289137(6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole | ...)
Affinity DataIC50:  377nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
Peking University

Curated by ChEMBL
LigandPNGBDBM50469066(CHEMBL4286335)
Affinity DataIC50:  577nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469065(CHEMBL4294501)
Affinity DataIC50:  590nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469068(CHEMBL4277474)
Affinity DataIC50:  598nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469084(CHEMBL4287177)
Affinity DataIC50:  684nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469069(CHEMBL4281581)
Affinity DataIC50:  684nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469063(CHEMBL4291095)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469074(CHEMBL4289462)
Affinity DataIC50:  1.20E+3nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469080(CHEMBL4293615)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469075(CHEMBL4285752)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469085(CHEMBL4280882)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469061(CHEMBL4285486)
Affinity DataIC50:  2.70E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469070(CHEMBL4285062)
Affinity DataIC50:  3.30E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469083(CHEMBL4288859)
Affinity DataIC50:  7.80E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469067(CHEMBL4280409)
Affinity DataIC50:  9.50E+3nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469086(CHEMBL4285421)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469071(CHEMBL4291850)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469072(CHEMBL4288429)
Affinity DataIC50:  4.22E+4nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469057(CHEMBL4292907)
Affinity DataIC50:  5.03E+4nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469057(CHEMBL4292907)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469070(CHEMBL4285062)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469076(CHEMBL4281233)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469073(CHEMBL4277781)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469076(CHEMBL4281233)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of human IDO1 using D-Trp as substrateMore 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
LigandPNGBDBM50469072(CHEMBL4288429)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469073(CHEMBL4277781)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore 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
LigandPNGBDBM50469071(CHEMBL4291850)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human TDO using L-Trp as substrate after 75 mins by UV absorption analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed