Compile Data Set for Download or QSAR

Found 76 hits Enz. Inhib. hit(s) with all data for entry = 50030740   

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
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM35361 ((5-oxidanidyl-4-thiophen-2-ylcarbonyl-1,2,5-oxadia...) Show SMILES [O-]n1[o+]nc(C(=O)c2cccs2)c1C(=O)c1cccs1 Show InChI InChI=1S/C12H6N2O4S2/c15-11(7-3-1-5-19-7)9-10(14(17)18-13-9)12(16)8-4-2-6-20-8/h1-6H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	40	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300734 (4-thienoyl-3-cyanofuroxan | CHEMBL576265) Show SMILES [O-][n+]1onc(C(=O)c2cccs2)c1C#N Show InChI InChI=1S/C8H3N3O3S/c9-4-5-7(10-14-11(5)13)8(12)6-2-1-3-15-6/h1-3H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	63	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300756 (3-formyl-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEMB...) Show SMILES [O-][n+]1onc(c1C=O)-c1ccccc1 Show InChI InChI=1S/C9H6N2O3/c12-6-8-9(10-14-11(8)13)7-4-2-1-3-5-7/h1-6H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	110	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300760 (4,4'-(thiophene-2,4-diyl)bis(3-cyano-1,2,5-oxadiaz...) Show SMILES [O-]n1[o+]nc(-c2cc(cs2)-c2no[n+]([O-])c2C#N)c1C#N Show InChI InChI=1S/C10H2N6O4S/c11-2-6-9(13-19-15(6)17)5-1-8(21-4-5)10-7(3-12)16(18)20-14-10/h1,4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	350	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300761 (4,4'-(thiophene-2,5-diyl)bis(3-cyano-1,2,5-oxadiaz...) Show SMILES [O-][n+]1onc(-c2ccc(s2)-c2no[n+]([O-])c2C#N)c1C#N Show InChI InChI=1S/C10H2N6O4S/c11-3-5-9(13-19-15(5)17)7-1-2-8(21-7)10-6(4-12)16(18)20-14-10/h1-2H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300762 (4,4'-(5-fluoro-1,3-phenylene)bis(3-cyano-1,2,5-oxa...) Show SMILES [O-][n+]1onc(c1C#N)-c1cc(F)cc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C12H3FN6O4/c13-8-2-6(11-9(4-14)18(20)22-16-11)1-7(3-8)12-10(5-15)19(21)23-17-12/h1-3H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300755 (3-carboxy-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEM...) Show SMILES OC(=O)c1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H6N2O4/c12-9(13)8-7(10-15-11(8)14)6-4-2-1-3-5-6/h1-5H,(H,12,13)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300763 (4,4'-(1,4-phenylene)bis(3-cyano-1,2,5-oxadiazole 2...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(cc1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C12H4N6O4/c13-5-9-11(15-21-17(9)19)7-1-2-8(4-3-7)12-10(6-14)18(20)22-16-12/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300753 (3-cyano-4-(3-nitrophenyl)-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][N+](=O)c1cccc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C9H4N4O4/c10-5-8-9(11-17-13(8)16)6-2-1-3-7(4-6)12(14)15/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300752 (3-cyano-4-(3-(trifluoromethyl)phenyl)-1,2,5-oxadia...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C10H4F3N3O2/c11-10(12,13)7-3-1-2-6(4-7)9-8(5-14)16(17)18-15-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD 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
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300751 (4-(3-bromo-4-fluorophenyl)-3-cyano-1,2,5-oxadiazol...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(F)c(Br)c1 Show InChI InChI=1S/C9H3BrFN3O2/c10-6-3-5(1-2-7(6)11)9-8(4-12)14(15)16-13-9/h1-3H	PDB MMDB UniProtKB/TrEMBL B.MOAD 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
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300750 (4-(3-bromophenyl)-3-cyano-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(Br)c1 Show InChI InChI=1S/C9H4BrN3O2/c10-7-3-1-2-6(4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD 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
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300736 (3-cyano-4-(furan-2-yl)-1,2,5-oxadiazole 2-oxide | ...) Show SMILES [O-][n+]1onc(-c2ccco2)c1C#N Show InChI InChI=1S/C7H3N3O3/c8-4-5-7(9-13-10(5)11)6-2-1-3-12-6/h1-3H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300735 (3-cyano-4-(thiophen-2-yl)-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(-c2cccs2)c1C#N Show InChI InChI=1S/C7H3N3O2S/c8-4-5-7(9-12-10(5)11)6-2-1-3-13-6/h1-3H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300748 (4-(4-bromophenyl)-3-cyano-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(Br)cc1 Show InChI InChI=1S/C9H4BrN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300749 (4-(3-chlorophenyl)-3-cyano-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(Cl)c1 Show InChI InChI=1S/C9H4ClN3O2/c10-7-3-1-2-6(4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300759 (4,4'-(1,3-phenylene)bis(3-cyano-1,2,5-oxadiazole 2...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C12H4N6O4/c13-5-9-11(15-21-17(9)19)7-2-1-3-8(4-7)12-10(6-14)18(20)22-16-12/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300747 (4-(4-chlorophenyl)-3-cyano-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(Cl)cc1 Show InChI InChI=1S/C9H4ClN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50038412 (2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccccc1 Show InChI InChI=1S/C9H5N3O2/c10-6-8-9(11-14-12(8)13)7-4-2-1-3-5-7/h1-5H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300746 (3-cyano-4-(4-(trifluoromethyl)phenyl)-1,2,5-oxadia...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C10H4F3N3O2/c11-10(12,13)7-3-1-6(2-4-7)9-8(5-14)16(17)18-15-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD 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
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300745 (3-cyano-4-(3-hydroxyphenyl)-1,2,5-oxadiazole 2-oxi...) Show SMILES Oc1cccc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C9H5N3O3/c10-5-8-9(11-15-12(8)14)6-2-1-3-7(13)4-6/h1-4,13H	PDB MMDB UniProtKB/TrEMBL B.MOAD 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
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300743 (3-cyano-4-(2-methoxyphenyl)-1,2,5-oxadiazole 2-oxi...) Show SMILES COc1ccccc1-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C10H7N3O3/c1-15-9-5-3-2-4-7(9)10-8(6-11)13(14)16-12-10/h2-5H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300744 (3-cyano-4-(4-fluorophenyl)-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(F)cc1 Show InChI InChI=1S/C9H4FN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300742 (3-cyano-4-(3,4,5-trimethoxyphenyl)-1,2,5-oxadiazol...) Show SMILES COc1cc(cc(OC)c1OC)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C12H11N3O5/c1-17-9-4-7(5-10(18-2)12(9)19-3)11-8(6-13)15(16)20-14-11/h4-5H,1-3H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300741 (3-cyano-4-(3-methoxyphenyl)-1,2,5-oxadiazole 2-oxi...) Show SMILES COc1cccc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C10H7N3O3/c1-15-8-4-2-3-7(5-8)10-9(6-11)13(14)16-12-10/h2-5H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.90E+3	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300740 (3-cyano-4-(4-methoxyphenyl)-1,2,5-oxadiazole 2-oxi...) Show SMILES COc1ccc(cc1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C10H7N3O3/c1-15-8-4-2-7(3-5-8)10-9(6-11)13(14)16-12-10/h2-5H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300739 (3-cyano-4-p-tolyl-1,2,5-oxadiazole 2-oxide | CHEMB...) Show SMILES Cc1ccc(cc1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C10H7N3O2/c1-7-2-4-8(5-3-7)10-9(6-11)13(14)15-12-10/h2-5H,1H3	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300757 (3-(hydroxymethyl)-4-phenyl-1,2,5-oxadiazole 2-oxid...) Show SMILES OCc1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H8N2O3/c12-6-8-9(10-14-11(8)13)7-4-2-1-3-5-7/h1-5,12H,6H2	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin reductase 1, cytoplasmic (Rattus norvegicus)	BDBM50300749 (4-(3-chlorophenyl)-3-cyano-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(Cl)c1 Show InChI InChI=1S/C9H4ClN3O2/c10-7-3-1-2-6(4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of rat recombinant TrxR1 after 10 mins				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin reductase 1, cytoplasmic (Rattus norvegicus)	BDBM50300746 (3-cyano-4-(4-(trifluoromethyl)phenyl)-1,2,5-oxadia...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C10H4F3N3O2/c11-10(12,13)7-3-1-6(2-4-7)9-8(5-14)16(17)18-15-9/h1-4H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of rat recombinant TrxR1 after 10 mins				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin reductase 1, cytoplasmic (Rattus norvegicus)	BDBM50300756 (3-formyl-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEMB...) Show SMILES [O-][n+]1onc(c1C=O)-c1ccccc1 Show InChI InChI=1S/C9H6N2O3/c12-6-8-9(10-14-11(8)13)7-4-2-1-3-5-7/h1-6H	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	<1.25E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of rat recombinant TrxR1 after 10 mins				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300738 (4-(biphenyl-4-yl)-3-cyano-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C15H9N3O2/c16-10-14-15(17-20-18(14)19)13-8-6-12(7-9-13)11-4-2-1-3-5-11/h1-9H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.58E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300754 (2-Oxy-4-phenyl-furazan-3-carboxylic acid amide | 3...) Show SMILES NC(=O)c1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H7N3O3/c10-9(13)8-7(11-15-12(8)14)6-4-2-1-3-5-6/h1-5H,(H2,10,13)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.78E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Thioredoxin glutathione reductase (Schistosoma mansoni)	BDBM50300737 (3-cyano-4-(4-hydroxyphenyl)-1,2,5-oxadiazole 2-oxi...) Show SMILES Oc1ccc(cc1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C9H5N3O3/c10-5-8-9(11-15-12(8)14)6-1-3-7(13)4-2-6/h1-4,13H	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.79E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of Schistosoma mansoni TGR				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300756 (3-formyl-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEMB...) Show SMILES [O-][n+]1onc(c1C=O)-c1ccccc1 Show InChI InChI=1S/C9H6N2O3/c12-6-8-9(10-14-11(8)13)7-4-2-1-3-5-7/h1-6H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.52E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300749 (4-(3-chlorophenyl)-3-cyano-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(Cl)c1 Show InChI InChI=1S/C9H4ClN3O2/c10-7-3-1-2-6(4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.57E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300746 (3-cyano-4-(4-(trifluoromethyl)phenyl)-1,2,5-oxadia...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(cc1)C(F)(F)F Show InChI InChI=1S/C10H4F3N3O2/c11-10(12,13)7-3-1-6(2-4-7)9-8(5-14)16(17)18-15-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300758 (3-methyl-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEMB...) Show SMILES Cc1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H8N2O2/c1-7-9(10-13-11(7)12)8-5-3-2-4-6-8/h2-6H,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50038412 (2-Oxy-4-phenyl-furazan-3-carbonitrile | 3-cyano-4-...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccccc1 Show InChI InChI=1S/C9H5N3O2/c10-6-8-9(11-14-12(8)13)7-4-2-1-3-5-7/h1-5H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300755 (3-carboxy-4-phenyl-1,2,5-oxadiazole 2-oxide | CHEM...) Show SMILES OC(=O)c1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H6N2O4/c12-9(13)8-7(10-15-11(8)14)6-4-2-1-3-5-6/h1-5H,(H,12,13)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300757 (3-(hydroxymethyl)-4-phenyl-1,2,5-oxadiazole 2-oxid...) Show SMILES OCc1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H8N2O3/c12-6-8-9(10-14-11(8)13)7-4-2-1-3-5-7/h1-5,12H,6H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300754 (2-Oxy-4-phenyl-furazan-3-carboxylic acid amide | 3...) Show SMILES NC(=O)c1c(no[n+]1[O-])-c1ccccc1 Show InChI InChI=1S/C9H7N3O3/c10-9(13)8-7(11-15-12(8)14)6-4-2-1-3-5-6/h1-5H,(H2,10,13)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300752 (3-cyano-4-(3-(trifluoromethyl)phenyl)-1,2,5-oxadia...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(c1)C(F)(F)F Show InChI InChI=1S/C10H4F3N3O2/c11-10(12,13)7-3-1-2-6(4-7)9-8(5-14)16(17)18-15-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300753 (3-cyano-4-(3-nitrophenyl)-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][N+](=O)c1cccc(c1)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C9H4N4O4/c10-5-8-9(11-17-13(8)16)6-2-1-3-7(4-6)12(14)15/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300751 (4-(3-bromo-4-fluorophenyl)-3-cyano-1,2,5-oxadiazol...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(F)c(Br)c1 Show InChI InChI=1S/C9H3BrFN3O2/c10-6-3-5(1-2-7(6)11)9-8(4-12)14(15)16-13-9/h1-3H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300750 (4-(3-bromophenyl)-3-cyano-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(c1C#N)-c1cccc(Br)c1 Show InChI InChI=1S/C9H4BrN3O2/c10-7-3-1-2-6(4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300748 (4-(4-bromophenyl)-3-cyano-1,2,5-oxadiazole 2-oxide...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(Br)cc1 Show InChI InChI=1S/C9H4BrN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300747 (4-(4-chlorophenyl)-3-cyano-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(Cl)cc1 Show InChI InChI=1S/C9H4ClN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300744 (3-cyano-4-(4-fluorophenyl)-1,2,5-oxadiazole 2-oxid...) Show SMILES [O-][n+]1onc(c1C#N)-c1ccc(F)cc1 Show InChI InChI=1S/C9H4FN3O2/c10-7-3-1-6(2-4-7)9-8(5-11)13(14)15-12-9/h1-4H	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair
Glutathione reductase, mitochondrial (Homo sapiens (Human))	BDBM50300742 (3-cyano-4-(3,4,5-trimethoxyphenyl)-1,2,5-oxadiazol...) Show SMILES COc1cc(cc(OC)c1OC)-c1no[n+]([O-])c1C#N Show InChI InChI=1S/C12H11N3O5/c1-17-9-4-7(5-10(18-2)12(9)19-3)11-8(6-13)15(16)20-14-11/h4-5H,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
National Human Genome Research Institute Curated by ChEMBL					Assay Description Inhibition of human recombinant GR after 15 mins in presence of NADPH				J Med Chem 52: 6474-83 (2009) Article DOI: 10.1021/jm901021k BindingDB Entry DOI: 10.7270/Q2TH8MS1
					More data for this Ligand-Target Pair

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