Compile Data Set for Download or QSAR

Found 58 hits Enz. Inhib. hit(s) with all data for entry = 50047891   

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
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	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair				3D Structure (crystal)
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM15579 (CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...) Show SMILES C[C@H](Cc1ccccc1)N(C)CC#C |r| Show InChI InChI=1S/C13H17N/c1-4-10-14(3)12(2)11-13-8-6-5-7-9-13/h1,5-9,12H,10-11H2,2-3H3/t12-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	17	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195819 (CHEMBL3818089) Show SMILES COc1cc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C24H30N2O3/c1-29-23-17-20(7-9-22(23)27)8-10-24(28)25-14-11-19-12-15-26(16-13-19)18-21-5-3-2-4-6-21/h2-10,17,19,27H,11-16,18H2,1H3,(H,25,28)/b10-8+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	76	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195812 (CHEMBL3818689) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1OC Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-21(18-24(23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-22-6-4-3-5-7-22/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195799 (CHEMBL3965783) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(O)c1 Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-20(22(27)16-21)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-19-4-2-1-3-5-19/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	260	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195819 (CHEMBL3818089) Show SMILES COc1cc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C24H30N2O3/c1-29-23-17-20(7-9-22(23)27)8-10-24(28)25-14-11-19-12-15-26(16-13-19)18-21-5-3-2-4-6-21/h2-10,17,19,27H,11-16,18H2,1H3,(H,25,28)/b10-8+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	390	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195813 (CHEMBL3905695) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1 Show InChI InChI=1S/C24H30N2O2/c1-28-23-10-7-20(8-11-23)9-12-24(27)25-16-13-21-14-17-26(18-15-21)19-22-5-3-2-4-6-22/h2-12,21H,13-19H2,1H3,(H,25,27)/b12-9+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195818 (CHEMBL3916769) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(OC)c1 Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-22(24(18-23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-21-6-4-3-5-7-21/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia 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
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195814 (CHEMBL3818992) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1O Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-19(16-22(21)27)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-20-4-2-1-3-5-20/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	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	690	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195812 (CHEMBL3818689) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1OC Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-21(18-24(23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-22-6-4-3-5-7-22/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	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	690	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195855 (CHEMBL3818512) Show SMILES COc1cccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C24H30N2O2/c1-28-23-9-5-8-21(18-23)10-11-24(27)25-15-12-20-13-16-26(17-14-20)19-22-6-3-2-4-7-22/h2-11,18,20H,12-17,19H2,1H3,(H,25,27)/b11-10+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	750	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195813 (CHEMBL3905695) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1 Show InChI InChI=1S/C24H30N2O2/c1-28-23-10-7-20(8-11-23)9-12-24(27)25-16-13-21-14-17-26(18-15-21)19-22-5-3-2-4-6-22/h2-12,21H,13-19H2,1H3,(H,25,27)/b12-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	760	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195836 (CHEMBL3819320) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1 Show InChI InChI=1S/C23H28N2O2/c26-22-9-6-19(7-10-22)8-11-23(27)24-15-12-20-13-16-25(17-14-20)18-21-4-2-1-3-5-21/h1-11,20,26H,12-18H2,(H,24,27)/b11-8+	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	930	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195855 (CHEMBL3818512) Show SMILES COc1cccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C24H30N2O2/c1-28-23-9-5-8-21(18-23)10-11-24(27)25-15-12-20-13-16-26(17-14-20)19-22-6-3-2-4-7-22/h2-11,18,20H,12-17,19H2,1H3,(H,25,27)/b11-10+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	980	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195799 (CHEMBL3965783) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(O)c1 Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-20(22(27)16-21)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-19-4-2-1-3-5-19/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	990	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195836 (CHEMBL3819320) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1 Show InChI InChI=1S/C23H28N2O2/c26-22-9-6-19(7-10-22)8-11-23(27)24-15-12-20-13-16-25(17-14-20)18-21-4-2-1-3-5-21/h1-11,20,26H,12-18H2,(H,24,27)/b11-8+	PDB MMDB NCI pathway 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+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195820 (CHEMBL3892044) Show SMILES Oc1cccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C23H28N2O2/c26-22-8-4-7-20(17-22)9-10-23(27)24-14-11-19-12-15-25(16-13-19)18-21-5-2-1-3-6-21/h1-10,17,19,26H,11-16,18H2,(H,24,27)/b10-9+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.02E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195820 (CHEMBL3892044) Show SMILES Oc1cccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C23H28N2O2/c26-22-8-4-7-20(17-22)9-10-23(27)24-14-11-19-12-15-25(16-13-19)18-21-5-2-1-3-6-21/h1-10,17,19,26H,11-16,18H2,(H,24,27)/b10-9+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.12E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195814 (CHEMBL3818992) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1O Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-19(16-22(21)27)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-20-4-2-1-3-5-20/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.75E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (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 Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195817 (CHEMBL3949439) Show SMILES CN(Cc1ccccc1)Cc1ccc(NC(=O)\C=C\c2cccc(O)c2)cc1 Show InChI InChI=1S/C24H24N2O2/c1-26(17-20-6-3-2-4-7-20)18-21-10-13-22(14-11-21)25-24(28)15-12-19-8-5-9-23(27)16-19/h2-16,27H,17-18H2,1H3,(H,25,28)/b15-12+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.49E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195814 (CHEMBL3818992) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1O Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-19(16-22(21)27)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-20-4-2-1-3-5-20/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB UniProtKB/SwissProt antibodypedia 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
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195815 (CHEMBL3917990) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)cc1OC Show InChI InChI=1S/C26H28N2O3/c1-28(18-21-7-5-4-6-8-21)19-22-9-13-23(14-10-22)27-26(29)16-12-20-11-15-24(30-2)25(17-20)31-3/h4-17H,18-19H2,1-3H3,(H,27,29)/b16-12+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	3.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195818 (CHEMBL3916769) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(OC)c1 Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-22(24(18-23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-21-6-4-3-5-7-21/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	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	4.39E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195811 (CHEMBL3945872) Show SMILES COc1cc(\C=C\C(=O)Nc2cccc(CN(C)Cc3ccccc3)c2)ccc1O Show InChI InChI=1S/C25H26N2O3/c1-27(17-20-7-4-3-5-8-20)18-21-9-6-10-22(15-21)26-25(29)14-12-19-11-13-23(28)24(16-19)30-2/h3-16,28H,17-18H2,1-2H3,(H,26,29)/b14-12+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195821 (CHEMBL3919086) Show SMILES COc1cccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)c1 Show InChI InChI=1S/C25H26N2O2/c1-27(18-21-7-4-3-5-8-21)19-22-11-14-23(15-12-22)26-25(28)16-13-20-9-6-10-24(17-20)29-2/h3-17H,18-19H2,1-2H3,(H,26,28)/b16-13+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.67E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195799 (CHEMBL3965783) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(O)c1 Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-20(22(27)16-21)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-19-4-2-1-3-5-19/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195870 (CHEMBL3978533) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)cc1 Show InChI InChI=1S/C25H26N2O2/c1-27(18-21-6-4-3-5-7-21)19-22-8-13-23(14-9-22)26-25(28)17-12-20-10-15-24(29-2)16-11-20/h3-17H,18-19H2,1-2H3,(H,26,28)/b17-12+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.76E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195811 (CHEMBL3945872) Show SMILES COc1cc(\C=C\C(=O)Nc2cccc(CN(C)Cc3ccccc3)c2)ccc1O Show InChI InChI=1S/C25H26N2O3/c1-27(17-20-7-4-3-5-8-20)18-21-9-6-10-22(15-21)26-25(29)14-12-19-11-13-23(28)24(16-19)30-2/h3-16,28H,17-18H2,1-2H3,(H,26,29)/b14-12+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.89E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195811 (CHEMBL3945872) Show SMILES COc1cc(\C=C\C(=O)Nc2cccc(CN(C)Cc3ccccc3)c2)ccc1O Show InChI InChI=1S/C25H26N2O3/c1-27(17-20-7-4-3-5-8-20)18-21-9-6-10-22(15-21)26-25(29)14-12-19-11-13-23(28)24(16-19)30-2/h3-16,28H,17-18H2,1-2H3,(H,26,29)/b14-12+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	5.99E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195814 (CHEMBL3818992) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1O Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-19(16-22(21)27)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-20-4-2-1-3-5-20/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM29136 (CHEMBL92401 | Euphozid | Iprazid | Iproniazid) Show SMILES CC(C)NNC(=O)c1ccncc1 Show InChI InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM29136 (CHEMBL92401 | Euphozid | Iprazid | Iproniazid) Show SMILES CC(C)NNC(=O)c1ccncc1 Show InChI InChI=1S/C9H13N3O/c1-7(2)11-12-9(13)8-3-5-10-6-4-8/h3-7,11H,1-2H3,(H,12,13)	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195811 (CHEMBL3945872) Show SMILES COc1cc(\C=C\C(=O)Nc2cccc(CN(C)Cc3ccccc3)c2)ccc1O Show InChI InChI=1S/C25H26N2O3/c1-27(17-20-7-4-3-5-8-20)18-21-9-6-10-22(15-21)26-25(29)14-12-19-11-13-23(28)24(16-19)30-2/h3-16,28H,17-18H2,1-2H3,(H,26,29)/b14-12+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	7.70E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195799 (CHEMBL3965783) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(O)c1 Show InChI InChI=1S/C23H28N2O3/c26-21-8-6-20(22(27)16-21)7-9-23(28)24-13-10-18-11-14-25(15-12-18)17-19-4-2-1-3-5-19/h1-9,16,18,26-27H,10-15,17H2,(H,24,28)/b9-7+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	8.30E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50195810 (CHEMBL3936989) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)c(OC)c1 Show InChI InChI=1S/C26H28N2O3/c1-28(18-20-7-5-4-6-8-20)19-21-9-13-23(14-10-21)27-26(29)16-12-22-11-15-24(30-2)17-25(22)31-3/h4-17H,18-19H2,1-3H3,(H,27,29)/b16-12+	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.73E+3	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for ...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195810 (CHEMBL3936989) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)c(OC)c1 Show InChI InChI=1S/C26H28N2O3/c1-28(18-20-7-5-4-6-8-20)19-21-9-13-23(14-10-21)27-26(29)16-12-22-11-15-24(30-2)17-25(22)31-3/h4-17H,18-19H2,1-3H3,(H,27,29)/b16-12+	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	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM50195815 (CHEMBL3917990) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)cc1OC Show InChI InChI=1S/C26H28N2O3/c1-28(18-21-7-5-4-6-8-21)19-22-9-13-23(14-10-22)27-26(29)16-12-20-11-15-24(30-2)25(17-20)31-3/h4-17H,18-19H2,1-3H3,(H,27,29)/b16-12+	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human serum BuChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition measured for 5 mins by E...				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195819 (CHEMBL3818089) Show SMILES COc1cc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C24H30N2O3/c1-29-23-17-20(7-9-22(23)27)8-10-24(28)25-14-11-19-12-15-26(16-13-19)18-21-5-3-2-4-6-21/h2-10,17,19,27H,11-16,18H2,1H3,(H,25,28)/b10-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195819 (CHEMBL3818089) Show SMILES COc1cc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)ccc1O Show InChI InChI=1S/C24H30N2O3/c1-29-23-17-20(7-9-22(23)27)8-10-24(28)25-14-11-19-12-15-26(16-13-19)18-21-5-3-2-4-6-21/h2-10,17,19,27H,11-16,18H2,1H3,(H,25,28)/b10-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.31E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195816 (CHEMBL3970226) Show SMILES CN(Cc1ccccc1)Cc1ccc(NC(=O)\C=C\c2ccc(O)cc2)cc1 Show InChI InChI=1S/C24H24N2O2/c1-26(17-20-5-3-2-4-6-20)18-21-7-12-22(13-8-21)25-24(28)16-11-19-9-14-23(27)15-10-19/h2-16,27H,17-18H2,1H3,(H,25,28)/b16-11+	PDB UniProtKB/SwissProt 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
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195816 (CHEMBL3970226) Show SMILES CN(Cc1ccccc1)Cc1ccc(NC(=O)\C=C\c2ccc(O)cc2)cc1 Show InChI InChI=1S/C24H24N2O2/c1-26(17-20-5-3-2-4-6-20)18-21-7-12-22(13-8-21)25-24(28)16-11-19-9-14-23(27)15-10-19/h2-16,27H,17-18H2,1H3,(H,25,28)/b16-11+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.97E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195836 (CHEMBL3819320) Show SMILES Oc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1 Show InChI InChI=1S/C23H28N2O2/c26-22-9-6-19(7-10-22)8-11-23(27)24-15-12-20-13-16-25(17-14-20)18-21-4-2-1-3-5-21/h1-11,20,26H,12-18H2,(H,24,27)/b11-8+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.75E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM15579 (CHEMBL972 | DEPRENYL | L-Deprenyl | N-methyl-N-[(2...) Show SMILES C[C@H](Cc1ccccc1)N(C)CC#C |r| Show InChI InChI=1S/C13H17N/c1-4-10-14(3)12(2)11-13-8-6-5-7-9-13/h1,5-9,12H,10-11H2,2-3H3/t12-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.87E+4	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195810 (CHEMBL3936989) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)c(OC)c1 Show InChI InChI=1S/C26H28N2O3/c1-28(18-20-7-5-4-6-8-20)19-21-9-13-23(14-10-21)27-26(29)16-12-22-11-15-24(30-2)17-25(22)31-3/h4-17H,18-19H2,1-3H3,(H,27,29)/b16-12+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] B (Homo sapiens (Human))	BDBM50195855 (CHEMBL3818512) Show SMILES COc1cccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c1 Show InChI InChI=1S/C24H30N2O2/c1-28-23-9-5-8-21(18-23)10-11-24(27)25-15-12-20-13-16-26(17-14-20)19-22-6-3-2-4-7-22/h2-11,18,20H,12-17,19H2,1H3,(H,25,27)/b11-10+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOB using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195818 (CHEMBL3916769) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)c(OC)c1 Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-22(24(18-23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-21-6-4-3-5-7-21/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195870 (CHEMBL3978533) Show SMILES COc1ccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)cc1 Show InChI InChI=1S/C25H26N2O2/c1-27(18-21-6-4-3-5-7-21)19-22-8-13-23(14-9-22)26-25(28)17-12-20-10-15-24(29-2)16-11-20/h3-17H,18-19H2,1-2H3,(H,26,28)/b17-12+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195821 (CHEMBL3919086) Show SMILES COc1cccc(\C=C\C(=O)Nc2ccc(CN(C)Cc3ccccc3)cc2)c1 Show InChI InChI=1S/C25H26N2O2/c1-27(18-21-7-4-3-5-8-21)19-22-11-14-23(15-12-22)26-25(28)16-13-20-9-6-10-24(17-20)29-2/h3-17H,18-19H2,1-2H3,(H,26,28)/b16-13+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair
Amine oxidase [flavin-containing] A (Homo sapiens (Human))	BDBM50195812 (CHEMBL3818689) Show SMILES COc1ccc(\C=C\C(=O)NCCC2CCN(Cc3ccccc3)CC2)cc1OC Show InChI InChI=1S/C25H32N2O3/c1-29-23-10-8-21(18-24(23)30-2)9-11-25(28)26-15-12-20-13-16-27(17-14-20)19-22-6-4-3-5-7-22/h3-11,18,20H,12-17,19H2,1-2H3,(H,26,28)/b11-9+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Instituto de Qu£mica M£dica Curated by ChEMBL					Assay Description Inhibition of human recombinant MAOA using p-tyramine as substrate incubated for 15 mins by fluorimetric method				Eur J Med Chem 121: 376-386 (2016) Article DOI: 10.1016/j.ejmech.2016.05.055 BindingDB Entry DOI: 10.7270/Q2HX1FNV
					More data for this Ligand-Target Pair

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