Compile Data Set for Download or QSAR

Found 296 hits with Last Name = 'mishra' and Initial = 'n'   

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
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341160 (3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1cccc(c1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-9-5-8-17(13-18)21-14-22(25-24-21)23-19-10-3-1-6-15(19)12-16-7-2-4-11-20(16)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.310	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341160 (3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1cccc(c1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-9-5-8-17(13-18)21-14-22(25-24-21)23-19-10-3-1-6-15(19)12-16-7-2-4-11-20(16)23/h1-13,21-22H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.450	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341161 (3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...) Show SMILES COc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:12| Show InChI InChI=1S/C24H20N2O/c1-27-19-12-10-16(11-13-19)22-15-23(26-25-22)24-20-8-4-2-6-17(20)14-18-7-3-5-9-21(18)24/h2-14,22-23H,15H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.600	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341152 (3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.15	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341161 (3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...) Show SMILES COc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:12| Show InChI InChI=1S/C24H20N2O/c1-27-19-12-10-16(11-13-19)22-15-23(26-25-22)24-20-8-4-2-6-17(20)14-18-7-3-5-9-21(18)24/h2-14,22-23H,15H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.70	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341154 (3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...) Show SMILES Clc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H17ClN2/c24-18-11-9-15(10-12-18)21-14-22(26-25-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341154 (3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...) Show SMILES Clc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H17ClN2/c24-18-11-9-15(10-12-18)21-14-22(26-25-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341152 (3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	2.30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341156 (3-(anthracen-9-yl)-5-phenyl-4,5-dihydro-1H-pyrazol...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccc1 |c:2| Show InChI InChI=1S/C23H18N2/c1-2-8-16(9-3-1)21-15-22(25-24-21)23-19-12-6-4-10-17(19)14-18-11-5-7-13-20(18)23/h1-14,21-22H,15H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.43	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341155 (3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...) Show SMILES Cc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C24H20N2/c1-16-10-12-17(13-11-16)22-15-23(26-25-22)24-20-8-4-2-6-18(20)14-19-7-3-5-9-21(19)24/h2-14,22-23H,15H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341155 (3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...) Show SMILES Cc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C24H20N2/c1-16-10-12-17(13-11-16)22-15-23(26-25-22)24-20-8-4-2-6-18(20)14-19-7-3-5-9-21(19)24/h2-14,22-23H,15H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	3.80	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341156 (3-(anthracen-9-yl)-5-phenyl-4,5-dihydro-1H-pyrazol...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccc1 |c:2| Show InChI InChI=1S/C23H18N2/c1-2-8-16(9-3-1)21-15-22(25-24-21)23-19-12-6-4-10-17(19)14-18-11-5-7-13-20(18)23/h1-14,21-22H,15H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.21	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341158 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(C2CC(N=N2)c2c3ccccc3cc3ccccc23)c(O)c1 |c:8| Show InChI InChI=1S/C23H18N2O2/c26-16-9-10-19(22(27)12-16)20-13-21(25-24-20)23-17-7-3-1-5-14(17)11-15-6-2-4-8-18(15)23/h1-12,20-21,26-27H,13H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	4.77	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341158 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(C2CC(N=N2)c2c3ccccc3cc3ccccc23)c(O)c1 |c:8| Show InChI InChI=1S/C23H18N2O2/c26-16-9-10-19(22(27)12-16)20-13-21(25-24-20)23-17-7-3-1-5-14(17)11-15-6-2-4-8-18(15)23/h1-12,20-21,26-27H,13H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.54	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341159 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccn1 |c:2| Show InChI InChI=1S/C22H17N3/c1-3-9-17-15(7-1)13-16-8-2-4-10-18(16)22(17)21-14-20(24-25-21)19-11-5-6-12-23-19/h1-13,20-21H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.75	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341157 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccccc1C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-22-12-6-5-11-19(22)20-14-21(25-24-20)23-17-9-3-1-7-15(17)13-16-8-2-4-10-18(16)23/h1-13,20-21,26H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.91	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.75	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM8960 ((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...) Show SMILES COc1cc2CC(CC3CCN(Cc4ccccc4)CC3)C(=O)c2cc1OC Show InChI InChI=1S/C24H29NO3/c1-27-22-14-19-13-20(24(26)21(19)15-23(22)28-2)12-17-8-10-25(11-9-17)16-18-6-4-3-5-7-18/h3-7,14-15,17,20H,8-13,16H2,1-2H3	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	DrugBank PDB Article PubMed	7.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair				3D Structure (crystal)
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425411 (CHEMBL2312573) Show SMILES Oc1ccc([C@@H]2CC(N=N2)c2c3ccccc3cc3ccccc23)c(O)c1 |r,c:8| Show InChI InChI=1S/C23H18N2O2/c26-16-9-10-19(22(27)12-16)20-13-21(25-24-20)23-17-7-3-1-5-14(17)11-15-6-2-4-8-18(15)23/h1-12,20-21,26-27H,13H2/t20-,21?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341157 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccccc1C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-22-12-6-5-11-19(22)20-14-21(25-24-20)23-17-9-3-1-7-15(17)13-16-8-2-4-10-18(16)23/h1-13,20-21,26H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.35	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	7.51	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Rattus norvegicus (rat))	BDBM50341159 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccn1 |c:2| Show InChI InChI=1S/C22H17N3/c1-3-9-17-15(7-1)13-16-8-2-4-10-18(16)22(17)21-14-20(24-25-21)19-11-5-6-12-23-19/h1-13,20-21H,14H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	9.91	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-B after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341152 (3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	17.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341152 (3-(anthracen-9-yl)-5-(4-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	20.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425409 (CHEMBL2312575) Show SMILES [O-][N+](=O)c1cccc(c1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-9-5-8-17(13-18)21-14-22(25-24-21)23-19-10-3-1-6-15(19)12-16-7-2-4-11-20(16)23/h1-13,21-22H,14H2/t21-,22?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	21	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425412 (CHEMBL2312285) Show SMILES Oc1ccccc1[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:11| Show InChI InChI=1S/C23H18N2O/c26-22-12-6-5-11-19(22)20-14-21(25-24-20)23-17-9-3-1-7-15(17)13-16-8-2-4-10-18(16)23/h1-13,20-21,26H,14H2/t20-,21?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	24	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425408 (CHEMBL2312576) Show SMILES COc1ccc(cc1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:12| Show InChI InChI=1S/C24H20N2O/c1-27-19-12-10-16(11-13-19)22-15-23(26-25-22)24-20-8-4-2-6-17(20)14-18-7-3-5-9-21(18)24/h2-14,22-23H,15H2,1H3/t22-,23?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	25	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425413 (CHEMBL2312284) Show SMILES C1[C@H](N=NC1c1c2ccccc2cc2ccccc12)c1ccccc1 |r,c:2| Show InChI InChI=1S/C23H18N2/c1-2-8-16(9-3-1)21-15-22(25-24-21)23-19-12-6-4-10-17(19)14-18-11-5-7-13-20(18)23/h1-14,21-22H,15H2/t21-,22?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425417 (CHEMBL2312282) Show SMILES Clc1ccc(cc1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:11| Show InChI InChI=1S/C23H17ClN2/c24-18-11-9-15(10-12-18)21-14-22(26-25-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2/t21-,22?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	30	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341160 (3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1cccc(c1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-9-5-8-17(13-18)21-14-22(25-24-21)23-19-10-3-1-6-15(19)12-16-7-2-4-11-20(16)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	32.2	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425410 (CHEMBL2312574) Show SMILES C1[C@H](N=NC1c1c2ccccc2cc2ccccc12)c1ccccn1 |r,c:2| Show InChI InChI=1S/C22H17N3/c1-3-9-17-15(7-1)13-16-8-2-4-10-18(16)22(17)21-14-20(24-25-21)19-11-5-6-12-23-19/h1-13,20-21H,14H2/t20-,21?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	41	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341160 (3-(anthracen-9-yl)-5-(3-nitrophenyl)-4,5-dihydro-1...) Show SMILES [O-][N+](=O)c1cccc(c1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-9-5-8-17(13-18)21-14-22(25-24-21)23-19-10-3-1-6-15(19)12-16-7-2-4-11-20(16)23/h1-13,21-22H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	43.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341157 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccccc1C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-22-12-6-5-11-19(22)20-14-21(25-24-20)23-17-9-3-1-7-15(17)13-16-8-2-4-10-18(16)23/h1-13,20-21,26H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	69.9	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341157 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccccc1C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-22-12-6-5-11-19(22)20-14-21(25-24-20)23-17-9-3-1-7-15(17)13-16-8-2-4-10-18(16)23/h1-13,20-21,26H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	77.6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341158 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(C2CC(N=N2)c2c3ccccc3cc3ccccc23)c(O)c1 |c:8| Show InChI InChI=1S/C23H18N2O2/c26-16-9-10-19(22(27)12-16)20-13-21(25-24-20)23-17-7-3-1-5-14(17)11-15-6-2-4-8-18(15)23/h1-12,20-21,26-27H,13H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	81.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Bromodomain-containing protein 4 (Homo sapiens (Human))	BDBM50443232 (CHEMBL3086883) Show SMILES Cc1cc(N=Nc2ccc(cc2)S(=O)(=O)Nc2ccccn2)c(N)cc1O |w:4.3| Show InChI InChI=1S/C18H17N5O3S/c1-12-10-16(15(19)11-17(12)24)22-21-13-5-7-14(8-6-13)27(25,26)23-18-4-2-3-9-20-18/h2-11,24H,19H2,1H3,(H,20,23)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	PDB Article PubMed	<85	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Minnesota Curated by ChEMBL					Assay Description Inhibition of human 6x-His-tagged BRD4 bromodomain 1 expressed in Escherichia coli				J Med Chem 61: 9316-9334 (2018) Article DOI: 10.1021/acs.jmedchem.8b01248 BindingDB Entry DOI: 10.7270/Q25T3PRQ
					More data for this Ligand-Target Pair				3D Structure (crystal)
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341158 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(C2CC(N=N2)c2c3ccccc3cc3ccccc23)c(O)c1 |c:8| Show InChI InChI=1S/C23H18N2O2/c26-16-9-10-19(22(27)12-16)20-13-21(25-24-20)23-17-7-3-1-5-14(17)11-15-6-2-4-8-18(15)23/h1-12,20-21,26-27H,13H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	95.7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425415 (CHEMBL2312577) Show SMILES [O-][N+](=O)c1ccc(cc1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:13| Show InChI InChI=1S/C23H17N3O2/c27-26(28)18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2/t21-,22?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425416 (CHEMBL2312578) Show SMILES Oc1ccc(cc1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2/t21-,22?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Bromodomain-containing protein 3 (Homo sapiens (Human))	BDBM50443232 (CHEMBL3086883) Show SMILES Cc1cc(N=Nc2ccc(cc2)S(=O)(=O)Nc2ccccn2)c(N)cc1O |w:4.3| Show InChI InChI=1S/C18H17N5O3S/c1-12-10-16(15(19)11-17(12)24)22-21-13-5-7-14(8-6-13)27(25,26)23-18-4-2-3-9-20-18/h2-11,24H,19H2,1H3,(H,20,23)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Minnesota Curated by ChEMBL					Assay Description Inhibition of human 6x-His-tagged BRD3 bromodomain 1 expressed in Escherichia coli				J Med Chem 61: 9316-9334 (2018) Article DOI: 10.1021/acs.jmedchem.8b01248 BindingDB Entry DOI: 10.7270/Q25T3PRQ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50425414 (CHEMBL2312283) Show SMILES Cc1ccc(cc1)[C@@H]1CC(N=N1)c1c2ccccc2cc2ccccc12 |r,c:11| Show InChI InChI=1S/C24H20N2/c1-16-10-12-17(13-11-16)22-15-23(26-25-22)24-20-8-4-2-6-18(20)14-19-7-3-5-9-21(19)24/h2-14,22-23H,15H2,1H3/t22-,23?/m0/s1	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>100	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem Lett 23: 702-5 (2013) Article DOI: 10.1016/j.bmcl.2012.11.100 BindingDB Entry DOI: 10.7270/Q2F19118
					More data for this Ligand-Target Pair
Bromodomain-containing protein 3 (Homo sapiens (Human))	BDBM50443232 (CHEMBL3086883) Show SMILES Cc1cc(N=Nc2ccc(cc2)S(=O)(=O)Nc2ccccn2)c(N)cc1O |w:4.3| Show InChI InChI=1S/C18H17N5O3S/c1-12-10-16(15(19)11-17(12)24)22-21-13-5-7-14(8-6-13)27(25,26)23-18-4-2-3-9-20-18/h2-11,24H,19H2,1H3,(H,20,23)	PDB KEGG UniProtKB/SwissProt B.MOAD antibodypedia GoogleScholar AffyNet	Purchase CHEMBL PC cid PC sid PDB UniChem Similars	Article PubMed	140	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Minnesota Curated by ChEMBL					Assay Description Inhibition of human 6x-His-tagged BRD3 bromodomain 2 expressed in Escherichia coli				J Med Chem 61: 9316-9334 (2018) Article DOI: 10.1021/acs.jmedchem.8b01248 BindingDB Entry DOI: 10.7270/Q25T3PRQ
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341159 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccn1 |c:2| Show InChI InChI=1S/C22H17N3/c1-3-9-17-15(7-1)13-16-8-2-4-10-18(16)22(17)21-14-20(24-25-21)19-11-5-6-12-23-19/h1-13,20-21H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	205	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341153 (4-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES Oc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H18N2O/c26-18-11-9-15(10-12-18)21-14-22(25-24-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22,26H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	225	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341161 (3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...) Show SMILES COc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:12| Show InChI InChI=1S/C24H20N2O/c1-27-19-12-10-16(11-13-19)22-15-23(26-25-22)24-20-8-4-2-6-17(20)14-18-7-3-5-9-21(18)24/h2-14,22-23H,15H2,1H3	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	230	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341159 (2-(3-(anthracen-9-yl)-4,5-dihydro-1H-pyrazol-5-yl)...) Show SMILES C1C(N=NC1c1c2ccccc2cc2ccccc12)c1ccccn1 |c:2| Show InChI InChI=1S/C22H17N3/c1-3-9-17-15(7-1)13-16-8-2-4-10-18(16)22(17)21-14-20(24-25-21)19-11-5-6-12-23-19/h1-13,20-21H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	242	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341155 (3-(anthracen-9-yl)-5-p-tolyl-4,5-dihydro-1H-pyrazo...) Show SMILES Cc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C24H20N2/c1-16-10-12-17(13-11-16)22-15-23(26-25-22)24-20-8-4-2-6-18(20)14-19-7-3-5-9-21(19)24/h2-14,22-23H,15H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	250	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341154 (3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...) Show SMILES Clc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H17ClN2/c24-18-11-9-15(10-12-18)21-14-22(26-25-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	281	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50341161 (3-(anthracen-9-yl)-5-(4-methoxyphenyl)-4,5-dihydro...) Show SMILES COc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:12| Show InChI InChI=1S/C24H20N2O/c1-27-19-12-10-16(11-13-19)22-15-23(26-25-22)24-20-8-4-2-6-17(20)14-18-7-3-5-9-21(18)24/h2-14,22-23H,15H2,1H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	301	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of human recombinant MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Rattus norvegicus (rat))	BDBM50341154 (3-(anthracen-9-yl)-5-(4-chlorophenyl)-4,5-dihydro-...) Show SMILES Clc1ccc(cc1)C1CC(N=N1)c1c2ccccc2cc2ccccc12 |c:11| Show InChI InChI=1S/C23H17ClN2/c24-18-11-9-15(10-12-18)21-14-22(26-25-21)23-19-7-3-1-5-16(19)13-17-6-2-4-8-20(17)23/h1-13,21-22H,14H2	PDB MMDB UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	320	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Birla Institute of Technology Curated by ChEMBL					Assay Description Competitive inhibition of rat liver MAO-A after 60 mins using p-tyramine as substrate by spectrophotometry				Bioorg Med Chem Lett 21: 1969-73 (2011) Article DOI: 10.1016/j.bmcl.2011.02.030 BindingDB Entry DOI: 10.7270/Q2JM29XC
					More data for this Ligand-Target Pair

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