Compile Data Set for Download or QSAR

Found 50 hits with Last Name = 'ferain' and Initial = 't'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50013811 (9H-beta-Carboline | 9H-pyrido[3,4-b]indole | CHEMB...) Show SMILES c1ccc2c(c1)[nH]c1cnccc21 Show InChI InChI=1S/C11H8N2/c1-2-4-10-8(3-1)9-5-6-12-7-11(9)13-10/h1-7,13H	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	120	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of IDO				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM21975 ((4S)-16'-(2-aminoethyl)-9'-hydroxy-1,3,6',6'-tetra...) Show SMILES CN1C(=O)N(C)[C@@]2(Oc3c(O)cc4c(CC[N+]4(C)C)c3C3=C2C(=O)c2c(CCN)c[nH]c2C3=O)C1=O |r,c:22| Show InChI InChI=1S/C25H25N5O6/c1-28-23(34)25(29(2)24(28)35)18-17(21(33)19-15(20(18)32)11(5-7-26)10-27-19)16-12-6-8-30(3,4)13(12)9-14(31)22(16)36-25/h9-10H,5-8,26H2,1-4H3,(H-,27,31,32,33)/p+1/t25-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	210	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of IDO1 (unknown origin)				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50241727 ((S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic ac...) Show SMILES Cn1cc(C[C@H](N)C(O)=O)c2ccccc12 |r| Show InChI InChI=1S/C12H14N2O2/c1-14-7-8(6-10(13)12(15)16)9-4-2-3-5-11(9)14/h2-5,7,10H,6,13H2,1H3,(H,15,16)/t10-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Competitive inhibition of histidine-tagged human recombinant IDO expressed in bacterial strain BL21 AI using L-Trptophan as substrate measured at 490...				Eur J Med Chem 46: 3058-65 (2011) Article DOI: 10.1016/j.ejmech.2011.02.049 BindingDB Entry DOI: 10.7270/Q2F19029
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM24813 (Brassinin, 1 | N-(1H-indol-3-ylmethyl)(methylsulfa...) Show SMILES CSC(=S)NCc1c[nH]c2ccccc12 Show InChI InChI=1S/C11H12N2S2/c1-15-11(14)13-7-8-6-12-10-5-3-2-4-9(8)10/h2-6,12H,7H2,1H3,(H,13,14)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of IDO				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428658 (MITOMYCIN | Mitomycin C | Mitosol | Mitozytrex | M...) Show SMILES CO[C@]12[C@H]3N[C@H]3CN1C1=C([C@H]2COC(N)=O)C(=O)C(N)=C(C)C1=O |r,c:10,t:22| Show InChI InChI=1S/C15H18N4O5/c1-5-9(16)12(21)8-6(4-24-14(17)22)15(23-2)13-7(18-13)3-19(15)10(8)11(5)20/h6-7,13,18H,3-4,16H2,1-2H3,(H2,17,22)/t6-,7+,13+,15-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase DrugBank KEGG PC cid PC sid UniChem Similars	Article PubMed	2.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Uncompetitive inhibition of hexahistidyl-tagged human IDO1				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50241727 ((S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic ac...) Show SMILES Cn1cc(C[C@H](N)C(O)=O)c2ccccc12 |r| Show InChI InChI=1S/C12H14N2O2/c1-14-7-8(6-10(13)12(15)16)9-4-2-3-5-11(9)14/h2-5,7,10H,6,13H2,1H3,(H,15,16)/t10-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of IDO				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336434 (1-(1H-Indol-2-yl)-2-pyridin-3-yl-ethanone | CHEMBL...) Show SMILES O=C(Cc1cccnc1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C15H12N2O/c18-15(8-11-4-3-7-16-10-11)14-9-12-5-1-2-6-13(12)17-14/h1-7,9-10,17H,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.90E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Uncompetitive inhibition of histidine-tagged human recombinant IDO expressed in bacterial strain BL21 AI using L-Trptophan as substrate measured at 4...				Eur J Med Chem 46: 3058-65 (2011) Article DOI: 10.1016/j.ejmech.2011.02.049 BindingDB Entry DOI: 10.7270/Q2F19029
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428674 (CHEMBL576950) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C1=NCCc3c[nH]c(c13)C2=O |t:15| Show InChI InChI=1S/C19H15N3O2/c1-24-12-4-2-10(3-5-12)13-9-22-18-15(13)16-14-11(6-7-20-16)8-21-17(14)19(18)23/h2-5,8-9,21-22H,6-7H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	900	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428673 (CHEMBL574910) Show SMILES COc1ccc(cc1)C1CN=C2C1C(=O)c1ccn(c1C2=O)S(=O)(=O)c1ccc(C)cc1 |c:11| Show InChI InChI=1S/C24H20N2O5S/c1-14-3-9-17(10-4-14)32(29,30)26-12-11-18-22(26)24(28)21-20(23(18)27)19(13-25-21)15-5-7-16(31-2)8-6-15/h3-12,19-20H,13H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428672 (CHEMBL572914) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C1=NCCc3cn(c(c13)C2=O)S(=O)(=O)c1ccc(C)cc1 |t:15| Show InChI InChI=1S/C26H21N3O4S/c1-15-3-9-19(10-4-15)34(31,32)29-14-17-11-12-27-23-21(17)25(29)26(30)24-22(23)20(13-28-24)16-5-7-18(33-2)8-6-16/h3-10,13-14,28H,11-12H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428671 (CHEMBL574690) Show SMILES COc1ccc(cc1)C(=O)CNc1cc(O)c2ccn(c2c1O)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C24H22N2O6S/c1-15-3-9-18(10-4-15)33(30,31)26-12-11-19-21(27)13-20(24(29)23(19)26)25-14-22(28)16-5-7-17(32-2)8-6-16/h3-13,25,27,29H,14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428670 (CHEMBL576757) Show SMILES COc1ccc(cc1)C1CN=C2C1C(=O)c1c(CCN)cn(c1C2=O)S(=O)(=O)c1ccc(C)cc1 |c:11| Show InChI InChI=1S/C26H25N3O5S/c1-15-3-9-19(10-4-15)35(32,33)29-14-17(11-12-27)21-24(29)26(31)23-22(25(21)30)20(13-28-23)16-5-7-18(34-2)8-6-16/h3-10,14,20,22H,11-13,27H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428669 (CHEMBL575549) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1c3c(CCN=C23)cn1S(=O)(=O)c1ccc(C)cc1 |t:22| Show InChI InChI=1S/C26H21N3O4S/c1-15-3-9-19(10-4-15)34(31,32)29-14-17-11-12-27-23-21(17)25(29)26(30)22-20(13-28-24(22)23)16-5-7-18(33-2)8-6-16/h3-10,13-14,28H,11-12H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428668 (CHEMBL575780) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1c(CCN)cn(c1C2=O)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C26H23N3O5S/c1-15-3-9-19(10-4-15)35(32,33)29-14-17(11-12-27)21-24(29)26(31)23-22(25(21)30)20(13-28-23)16-5-7-18(34-2)8-6-16/h3-10,13-14,28H,11-12,27H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.40E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428667 (CHEMBL575331) Show SMILES COc1ccc(cc1)C1CN=C2C1C(=O)c1c(c(CCN)cn1S(=O)(=O)c1ccc(C)cc1)C2=O |c:11| Show InChI InChI=1S/C26H25N3O5S/c1-15-3-9-19(10-4-15)35(32,33)29-14-17(11-12-27)21-24(29)26(31)22-20(13-28-23(22)25(21)30)16-5-7-18(34-2)8-6-16/h3-10,14,20,22H,11-13,27H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428666 (CHEMBL574691) Show SMILES COc1ccc(cc1)C1CN=C2C1C(=O)c1c(ccn1S(=O)(=O)c1ccc(C)cc1)C2=O |c:11| Show InChI InChI=1S/C24H20N2O5S/c1-14-3-9-17(10-4-14)32(29,30)26-12-11-18-22(26)24(28)20-19(13-25-21(20)23(18)27)15-5-7-16(31-2)8-6-15/h3-12,19-20H,13H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428665 (CHEMBL573179) Show SMILES Oc1ccc(cc1)-c1c[nH]c2c1C(=O)c1[nH]cc3CCN=C2c13 |t:22| Show InChI InChI=1S/C18H13N3O2/c22-11-3-1-9(2-4-11)12-8-21-16-14(12)18(23)17-13-10(7-20-17)5-6-19-15(13)16/h1-4,7-8,20-22H,5-6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428664 (CHEMBL576344) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1[nH]cc3CCN=C2c13 |t:23| Show InChI InChI=1S/C19H15N3O2/c1-24-12-4-2-10(3-5-12)13-9-22-17-15(13)19(23)18-14-11(8-21-18)6-7-20-16(14)17/h2-5,8-9,21-22H,6-7H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428663 (CHEMBL574896) Show SMILES COc1ccc(cc1)C(=O)CNc1cc(O)c2n(ccc2c1O)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C24H22N2O6S/c1-15-3-9-18(10-4-15)33(30,31)26-12-11-19-23(26)21(27)13-20(24(19)29)25-14-22(28)16-5-7-17(32-2)8-6-16/h3-13,25,27,29H,14H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428662 (CHEMBL573014) Show SMILES COc1ccc(cc1)C(=O)CNc1cc(O)c2n(cc(CCNC(=O)OC(C)(C)C)c2c1O)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C31H35N3O8S/c1-19-6-12-23(13-7-19)43(39,40)34-18-21(14-15-32-30(38)42-31(2,3)4)27-28(34)25(35)16-24(29(27)37)33-17-26(36)20-8-10-22(41-5)11-9-20/h6-13,16,18,33,35,37H,14-15,17H2,1-5H3,(H,32,38)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428661 (CHEMBL575568) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1c(c(CCN)cn1S(=O)(=O)c1ccc(C)cc1)C2=O Show InChI InChI=1S/C26H23N3O5S/c1-15-3-9-19(10-4-15)35(32,33)29-14-17(11-12-27)21-24(29)26(31)22-20(13-28-23(22)25(21)30)16-5-7-18(34-2)8-6-16/h3-10,13-14,28H,11-12,27H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.19E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428660 (CHEMBL2332688) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1cc[nH]c1C2=O Show InChI InChI=1S/C17H12N2O3/c1-22-10-4-2-9(3-5-10)12-8-19-15-13(12)16(20)11-6-7-18-14(11)17(15)21/h2-8,18-19H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336444 (2-Pyridin-3-yl-1-(5-trifluoromethoxy-1H-indol-2-yl...) Show SMILES FC(F)(F)Oc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H11F3N2O2/c17-16(18,19)23-12-3-4-13-11(7-12)8-14(21-13)15(22)6-10-2-1-5-20-9-10/h1-5,7-9,21H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.31E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336440 (1-(5-Bromo-1H-indol-2-yl)-2-pyridin-3-yl-ethanone ...) Show SMILES Brc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H11BrN2O/c16-12-3-4-13-11(7-12)8-14(18-13)15(19)6-10-2-1-5-17-9-10/h1-5,7-9,18H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428659 (CHEMBL583951) Show SMILES COc1ccc(cc1)-c1c[nH]c2c1C(=O)c1[nH]ccc1C2=O Show InChI InChI=1S/C17H12N2O3/c1-22-10-4-2-9(3-5-10)12-8-19-15-13(12)17(21)14-11(16(15)20)6-7-18-14/h2-8,18-19H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.24E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336439 (1-(5-Chloro-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Clc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H11ClN2O/c16-12-3-4-13-11(7-12)8-14(18-13)15(19)6-10-2-1-5-17-9-10/h1-5,7-9,18H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.46E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336453 (1-(1H-Indol-2-yl)-2-pyrazin-2-yl-ethanone | CHEMBL...) Show SMILES O=C(Cc1cnccn1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C14H11N3O/c18-14(8-11-9-15-5-6-16-11)13-7-10-3-1-2-4-12(10)17-13/h1-7,9,17H,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50428657 (CHEMBL573203) Show SMILES COc1ccc(cc1)C(=O)CNc1cc(O)c2c(CCNC(=O)OC(C)(C)C)cn(c2c1O)S(=O)(=O)c1ccc(C)cc1 Show InChI InChI=1S/C31H35N3O8S/c1-19-6-12-23(13-7-19)43(39,40)34-18-21(14-15-32-30(38)42-31(2,3)4)27-25(35)16-24(29(37)28(27)34)33-17-26(36)20-8-10-22(41-5)11-9-20/h6-13,16,18,33,35,37H,14-15,17H2,1-5H3,(H,32,38)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.69E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336454 (1-(1H-Indol-2-yl)-2-phenylethanone | CHEMBL1667871) Show SMILES O=C(Cc1ccccc1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C16H13NO/c18-16(10-12-6-2-1-3-7-12)15-11-13-8-4-5-9-14(13)17-15/h1-9,11,17H,10H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336456 (1-(1-Methyl-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Cn1c(cc2ccccc12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O/c1-18-14-7-3-2-6-13(14)10-15(18)16(19)9-12-5-4-8-17-11-12/h2-8,10-11H,9H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336438 (1-(5-Fluoro-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Fc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H11FN2O/c16-12-3-4-13-11(7-12)8-14(18-13)15(19)6-10-2-1-5-17-9-10/h1-5,7-9,18H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336445 (1-(5-Hydroxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanon...) Show SMILES Oc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H12N2O2/c18-12-3-4-13-11(7-12)8-14(17-13)15(19)6-10-2-1-5-16-9-10/h1-5,7-9,17-18H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336452 (1-(1H-Indol-2-yl)-2-pyridin-2-yl-ethanone | CHEMBL...) Show SMILES O=C(Cc1ccccn1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C15H12N2O/c18-15(10-12-6-3-4-8-16-12)14-9-11-5-1-2-7-13(11)17-14/h1-9,17H,10H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336446 (1-(6-Fluoro-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Fc1ccc2cc([nH]c2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H11FN2O/c16-12-4-3-11-7-14(18-13(11)8-12)15(19)6-10-2-1-5-17-9-10/h1-5,7-9,18H,6H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336450 (1-(4,6-Dimethoxy-1H-indol-2-yl)-2-pyridin-3-yl-eth...) Show SMILES COc1cc(OC)c2cc([nH]c2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C17H16N2O3/c1-21-12-7-14-13(17(8-12)22-2)9-15(19-14)16(20)6-11-4-3-5-18-10-11/h3-5,7-10,19H,6H2,1-2H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336442 (1-(5-Methoxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanon...) Show SMILES COc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O2/c1-20-13-4-5-14-12(8-13)9-15(18-14)16(19)7-11-3-2-6-17-10-11/h2-6,8-10,18H,7H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336436 (1-(4-Methoxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanon...) Show SMILES COc1cccc2[nH]c(cc12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O2/c1-20-16-6-2-5-13-12(16)9-14(18-13)15(19)8-11-4-3-7-17-10-11/h2-7,9-10,18H,8H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.80E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336448 (1-(4-Hydroxy-5-methoxy-1H-indol-2-yl)-2-pyridin-3-...) Show SMILES COc1ccc2[nH]c(cc2c1O)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O3/c1-21-15-5-4-12-11(16(15)20)8-13(18-12)14(19)7-10-3-2-6-17-9-10/h2-6,8-9,18,20H,7H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336434 (1-(1H-Indol-2-yl)-2-pyridin-3-yl-ethanone | CHEMBL...) Show SMILES O=C(Cc1cccnc1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C15H12N2O/c18-15(8-11-4-3-7-16-10-11)14-9-12-5-1-2-6-13(12)17-14/h1-7,9-10,17H,8H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.50E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336447 (1-(7-methoxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanon...) Show SMILES COc1cccc2cc([nH]c12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O2/c1-20-15-6-2-5-12-9-13(18-16(12)15)14(19)8-11-4-3-7-17-10-11/h2-7,9-10,18H,8H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336437 (1-(4-Hydroxy-1H-indol-2-yl)-2-pyridin-3-yl-ethanon...) Show SMILES Oc1cccc2[nH]c(cc12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H12N2O2/c18-14-5-1-4-12-11(14)8-13(17-12)15(19)7-10-3-2-6-16-9-10/h1-6,8-9,17-18H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336441 (1-(5-Methyl-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Cc1ccc2[nH]c(cc2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H14N2O/c1-11-4-5-14-13(7-11)9-15(18-14)16(19)8-12-3-2-6-17-10-12/h2-7,9-10,18H,8H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50347507 (CHEMBL1802300) Show SMILES Cn1c(cc2cc(F)ccc12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C16H13FN2O/c1-19-14-5-4-13(17)8-12(14)9-15(19)16(20)7-11-3-2-6-18-10-11/h2-6,8-10H,7H2,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Competitive inhibition of histidine-tagged human recombinant IDO expressed in bacterial strain BL21 AI using L-Trptophan as substrate measured at 490...				Eur J Med Chem 46: 3058-65 (2011) Article DOI: 10.1016/j.ejmech.2011.02.049 BindingDB Entry DOI: 10.7270/Q2F19029
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336455 (1H-Indole-2-carboxylic acid pyridin-3-ylamide | CH...) Show SMILES O=C(Nc1cccnc1)c1cc2ccccc2[nH]1 Show InChI InChI=1S/C14H11N3O/c18-14(16-11-5-3-7-15-9-11)13-8-10-4-1-2-6-12(10)17-13/h1-9,17H,(H,16,18)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336443 (1-(5-Phenyl-1H-indol-2-yl)-2-pyridin-3-ylethanone ...) Show SMILES O=C(Cc1cccnc1)c1cc2cc(ccc2[nH]1)-c1ccccc1 Show InChI InChI=1S/C21H16N2O/c24-21(11-15-5-4-10-22-14-15)20-13-18-12-17(8-9-19(18)23-20)16-6-2-1-3-7-16/h1-10,12-14,23H,11H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.60E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50241727 ((S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic ac...) Show SMILES Cn1cc(C[C@H](N)C(O)=O)c2ccccc12 |r| Show InChI InChI=1S/C12H14N2O2/c1-14-7-8(6-10(13)12(15)16)9-4-2-3-5-11(9)14/h2-5,7,10H,6,13H2,1H3,(H,15,16)/t10-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50241727 ((S)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic ac...) Show SMILES Cn1cc(C[C@H](N)C(O)=O)c2ccccc12 |r| Show InChI InChI=1S/C12H14N2O2/c1-14-7-8(6-10(13)12(15)16)9-4-2-3-5-11(9)14/h2-5,7,10H,6,13H2,1H3,(H,15,16)/t10-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.39E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human recombinant IDO1 using L-Trp as substrate assessed as kynurenine level after 30 mins				Bioorg Med Chem Lett 23: 47-54 (2012) Article DOI: 10.1016/j.bmcl.2012.11.036 BindingDB Entry DOI: 10.7270/Q2JM2C03
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336449 (1-(4,6-Dichloro-1H-indol-2-yl)-2-pyridin-3-yl-etha...) Show SMILES Clc1cc(Cl)c2cc([nH]c2c1)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H10Cl2N2O/c16-10-5-12(17)11-7-14(19-13(11)6-10)15(20)4-9-2-1-3-18-8-9/h1-3,5-8,19H,4H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.39E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336451 (1-(1H-Indol-2-yl)-2-pyridin-3-yl-propan-1-one | CH...) Show SMILES CC(C(=O)c1cc2ccccc2[nH]1)c1cccnc1 Show InChI InChI=1S/C16H14N2O/c1-11(13-6-4-8-17-10-13)16(19)15-9-12-5-2-3-7-14(12)18-15/h2-11,18H,1H3	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.41E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair
Indoleamine 2,3-dioxygenase 1 (Homo sapiens (Human))	BDBM50336435 (1-(4-Fluoro-1H-indol-2-yl)-2-pyridin-3-yl-ethanone...) Show SMILES Fc1cccc2[nH]c(cc12)C(=O)Cc1cccnc1 Show InChI InChI=1S/C15H11FN2O/c16-12-4-1-5-13-11(12)8-14(18-13)15(19)7-10-3-2-6-17-9-10/h1-6,8-9,18H,7H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.53E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Namur Curated by ChEMBL					Assay Description Inhibition of human IDO activity by spectrophotometry				Bioorg Med Chem 19: 1550-61 (2011) Article DOI: 10.1016/j.bmc.2010.12.032 BindingDB Entry DOI: 10.7270/Q27M087F
					More data for this Ligand-Target Pair