Compile Data Set for Download or QSAR
Found 231 with Last Name = 'ching' and Initial = 'lm'
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in Selectin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126143(Epacadostat | INCB-024360)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126143(Epacadostat | INCB-024360)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
TargetTryptophan 2,3-dioxygenase(Rattus norvegicus)TBA
LigandPNGBDBM50289137(6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole | ...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of TDO2 in rat liver homogenate assessed as reduction in N-formylkynurenine formation using L-tryptophan as substrate incubated for 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of recombinant human IDO1 assessed as reduction in N-formylkynurenine formation using L-tryptophan as substrate incubated for 45 mins by m...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 51nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 80nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50289137(6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole | ...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 130nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235867(CHEMBL1351007)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of full length recombinant human His-tagged IDO1 expressed in mouse LLTC cells using L-tryptophan as substrate after 24 hrs in presence of...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Mus musculus)
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50444455(CHEBI:27924 | Phenylhydrazine)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of mouse IDO1 expressed in mouse LLTC cells using L-tryptophan as substrate after 24 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2377B6FPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50444455(CHEBI:27924 | Phenylhydrazine)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 using L-tryptophan as substrate after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2377B6FPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50289137(6-Fluoro-3-((E)-2-pyridin-3-yl-vinyl)-1H-indole | ...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM24776(1,4-Naphthoquinone | 1,4-Naphthoquinone (5a) | 1,4...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in Selectin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235856(CHEMBL1976581)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibitory activity against cathepsin DMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50126144(CHEMBL3629569 | US10155972, Compound NewLink 1 | U...)copy SMILEScopy InChI
Affinity DataIC50: 590nMAssay Description:Inhibition of full length recombinant human His-tagged IDO1 expressed in mouse LLTC cells using L-tryptophan as substrate after 24 hrsMore data for this Ligand-Target Pair
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235867(CHEMBL1351007)copy SMILEScopy InChI
Affinity DataIC50: 750nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in presence of GSH and tw...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235877(CHEMBL4105391)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in Selectin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM64800(1-oxidanidyl-2-phenyl-indol-1-ium-3-one | 1-oxido-...)copy SMILEScopy InChI
Affinity DataIC50: 870nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM477131(US10888567, Compound 42)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Recombinant human IDO1 (rhIDO1) was expressed and purified from cultures of EC538 strain of E. coli transformed with pREP4 and pQE9-IDO plasmid. Reac...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25142BBUS Patent
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM477158(US10888567, Compound 67)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Recombinant human IDO1 (rhIDO1) was expressed and purified from cultures of EC538 strain of E. coli transformed with pREP4 and pQE9-IDO plasmid. Reac...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25142BBUS Patent
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM477156(US10888567, Compound 66)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Recombinant human IDO1 (rhIDO1) was expressed and purified from cultures of EC538 strain of E. coli transformed with pREP4 and pQE9-IDO plasmid. Reac...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25142BBUS Patent
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM477136(US10888567, Compound 47)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Recombinant human IDO1 (rhIDO1) was expressed and purified from cultures of EC538 strain of E. coli transformed with pREP4 and pQE9-IDO plasmid. Reac...More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q25142BBUS Patent
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM24663(2-(1H-imidazol-4-yl)phenol | 2-(1H-imidazol-4-yl)p...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50444455(CHEBI:27924 | Phenylhydrazine)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human IDO1 expressed in mouse LLTC cells using L-tryptophan as substrate after 24 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2377B6FPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50013793(CHEMBL3192687)copy SMILEScopy InChI
Affinity DataIC50: 1.39E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235869(CHEMBL1600105)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in presence of GSH and tw...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50444457(CHEMBL3092383)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 using L-tryptophan as substrate after 1 hrMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2377B6FPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235919(CHEMBL577939)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in presence of GSH and tw...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235857(CHEMBL581422 | TCMDC-123940)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:In vitro inhibition of plasmepsin-2 from Plasmodium falciparum.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235857(CHEMBL581422 | TCMDC-123940)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50568051(CHEMBL4092918)copy SMILES
Affinity DataIC50: 1.72E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235883(CHEMBL1702248)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in presence of GSH and tw...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50126143(Epacadostat | INCB-024360)copy SMILEScopy InChI
Affinity DataIC50: 2.12E+3nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM64800(1-oxidanidyl-2-phenyl-indol-1-ium-3-one | 1-oxido-...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in P-selectinMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50568048(CHEMBL1981840)copy SMILES
Affinity DataIC50: 2.79E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM58106(6-(1,3-dihydrophenanthr[9,10-d]imidazol-2-ylidene)...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and pre...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50126143(Epacadostat | INCB-024360)copy SMILEScopy InChI
Affinity DataIC50: 3.43E+3nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 3.47E+3nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetTryptophan 2,3-dioxygenase(Homo sapiens (Human))TBA
LigandPNGBDBM50235921(CHEMBL584991)copy SMILEScopy InChI
Affinity DataIC50: 3.62E+3nMAssay Description:Inhibition of recombinant human TDO2 expressed in Escherichia coli BL21 (DE3) assessed as reduction in N-formylkynurenine formation using L-tryptopha...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50568050(CHEMBL4296947)copy SMILES
Affinity DataIC50: 3.78E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in Escherichia coli EC538 assessed as reduction in N-formylkynurenine formation using L-tryptophan as ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6W0VPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235856(CHEMBL1976581)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in Selectin EMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235919(CHEMBL577939)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Compound was tested in a cell-free SLe-polyacrylamide glycoconjugate binding assay (assay B) in P-selectinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235867(CHEMBL1351007)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of recombinant human IDO1 expressed in bacterial expression system using L-Tryptophan as substrate after 25 mins in absence of GSH and twe...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
TargetIndoleamine 2,3-dioxygenase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50235919(CHEMBL577939)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibition of full length recombinant human His-tagged IDO1 expressed in mouse LLTC cells using L-tryptophan as substrate after 24 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2RX9F9KPubMed
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