Compile Data Set for Download or QSAR

Found 45 hits with Last Name = 'golshani' and Initial = 'm'   

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 (Electrophorus electricus (Electric eel))	BDBM50457028 (CHEMBL4218303) Show SMILES COc1ccccc1C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O3/c1-32-19-13-7-5-11-17(19)22-20-21(26)16-10-4-6-12-18(16)27-23(20)29-25(31)15-9-3-2-8-14(15)24(30)28(22)29/h2-3,5,7-9,11,13,22H,4,6,10,12H2,1H3,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Mixed-type inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measur...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM8961 (1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...) Show SMILES Nc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	13	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair				3D Structure (crystal)
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457026 (CHEMBL4207023) Show SMILES Nc1c2C(c3cccc(F)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-14-7-5-6-13(12-14)21-19-20(26)17-10-3-4-11-18(17)27-22(19)29-24(31)16-9-2-1-8-15(16)23(30)28(21)29/h1-2,5-9,12,21H,3-4,10-11H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	23	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457028 (CHEMBL4218303) Show SMILES COc1ccccc1C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O3/c1-32-19-13-7-5-11-17(19)22-20-21(26)16-10-4-6-12-18(16)27-23(20)29-25(31)15-9-3-2-8-14(15)24(30)28(22)29/h2-3,5,7-9,11,13,22H,4,6,10,12H2,1H3,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	49	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457015 (CHEMBL4203173) Show SMILES Nc1c2C(c3ccc(Cl)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19ClN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	60	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457024 (CHEMBL4207926) Show SMILES Nc1c2C(c3ccc(F)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	69	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457014 (CHEMBL4203040) Show SMILES Nc1c2C(c3ccc(Br)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457023 (CHEMBL4207397) Show SMILES Cc1ccc(cc1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-10-12-15(13-11-14)22-20-21(26)18-8-4-5-9-19(18)27-23(20)29-25(31)17-7-3-2-6-16(17)24(30)28(22)29/h2-3,6-7,10-13,22H,4-5,8-9H2,1H3,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	100	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457025 (CHEMBL4210751) Show SMILES Nc1c2C(c3cccc(c3)[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-17-10-3-4-11-18(17)26-22-19(20)21(13-6-5-7-14(12-13)29(32)33)27-23(30)15-8-1-2-9-16(15)24(31)28(22)27/h1-2,5-9,12,21H,3-4,10-11H2,(H2,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	140	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457030 (CHEMBL4206121) Show SMILES Nc1c2C(c3cccc(O)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H20N4O3/c25-20-17-10-3-4-11-18(17)26-22-19(20)21(13-6-5-7-14(29)12-13)27-23(30)15-8-1-2-9-16(15)24(31)28(22)27/h1-2,5-9,12,21,29H,3-4,10-11H2,(H2,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	160	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457033 (CHEMBL4204269) Show SMILES Cc1ccccc1C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-8-2-3-9-15(14)22-20-21(26)18-12-6-7-13-19(18)27-23(20)29-25(31)17-11-5-4-10-16(17)24(30)28(22)29/h2-5,8-11,22H,6-7,12-13H2,1H3,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	193	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457027 (CHEMBL4203909) Show SMILES Nc1c2C(c3cccc(Br)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-14-7-5-6-13(12-14)21-19-20(26)17-10-3-4-11-18(17)27-22(19)29-24(31)16-9-2-1-8-15(16)23(30)28(21)29/h1-2,5-9,12,21H,3-4,10-11H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	271	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457029 (CHEMBL4209859) Show SMILES Nc1c2C(c3ccccc3[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-15-9-3-5-11-17(15)26-22-19(20)21(16-10-4-6-12-18(16)29(32)33)27-23(30)13-7-1-2-8-14(13)24(31)28(22)27/h1-2,4,6-8,10,12,21H,3,5,9,11H2,(H2,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	280	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457032 (CHEMBL4212290) Show SMILES Nc1c2C(c3ccc(cc3)[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-17-7-3-4-8-18(17)26-22-19(20)21(13-9-11-14(12-10-13)29(32)33)27-23(30)15-5-1-2-6-16(15)24(31)28(22)27/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	310	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM8961 (1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...) Show SMILES Nc1c2CCCCc2nc2ccccc12 Show InChI InChI=1S/C13H14N2/c14-13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13/h1,3,5,7H,2,4,6,8H2,(H2,14,15)	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	365	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457013 (CHEMBL4213928) Show SMILES Cc1cccc(c1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-7-6-8-15(13-14)22-20-21(26)18-11-4-5-12-19(18)27-23(20)29-25(31)17-10-3-2-9-16(17)24(30)28(22)29/h2-3,6-10,13,22H,4-5,11-12H2,1H3,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	467	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457022 (CHEMBL4208973) Show SMILES Nc1c2C(c3ccccc3Cl)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19ClN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	592	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457016 (CHEMBL4210767) Show SMILES Nc1c2C(c3ccccc3Br)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	599	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457021 (CHEMBL4202878) Show SMILES CCCCCC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C23H26N4O2/c1-2-3-4-13-18-19-20(24)16-11-7-8-12-17(16)25-21(19)27-23(29)15-10-6-5-9-14(15)22(28)26(18)27/h5-6,9-10,18H,2-4,7-8,11-13H2,1H3,(H2,24,25)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	612	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457020 (CHEMBL4216504) Show SMILES Nc1c2C(c3ccccc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H20N4O2/c25-20-17-12-6-7-13-18(17)26-22-19(20)21(14-8-2-1-3-9-14)27-23(29)15-10-4-5-11-16(15)24(30)28(22)27/h1-5,8-11,21H,6-7,12-13H2,(H2,25,26)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	614	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457019 (CHEMBL4207471) Show SMILES Nc1c2C(c3ccccc3F)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	618	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457018 (CHEMBL4211075) Show SMILES CCCC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C21H22N4O2/c1-2-7-16-17-18(22)14-10-5-6-11-15(14)23-19(17)25-21(27)13-9-4-3-8-12(13)20(26)24(16)25/h3-4,8-9,16H,2,5-7,10-11H2,1H3,(H2,22,23)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.63E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457017 (CHEMBL4208227) Show SMILES CC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C19H18N4O2/c1-10-15-16(20)13-8-4-5-9-14(13)21-17(15)23-19(25)12-7-3-2-6-11(12)18(24)22(10)23/h2-3,6-7,10H,4-5,8-9H2,1H3,(H2,20,21)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.15E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50457031 (CHEMBL4216769) Show SMILES COc1cc(OC)cc(c1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C26H24N4O4/c1-33-15-11-14(12-16(13-15)34-2)23-21-22(27)19-9-5-6-10-20(19)28-24(21)30-26(32)18-8-4-3-7-17(18)25(31)29(23)30/h3-4,7-8,11-13,23H,5-6,9-10H2,1-2H3,(H2,27,28)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.37E+3	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 mi...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457026 (CHEMBL4207023) Show SMILES Nc1c2C(c3cccc(F)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-14-7-5-6-13(12-14)21-19-20(26)17-10-3-4-11-18(17)27-22(19)29-24(31)16-9-2-1-8-15(16)23(30)28(21)29/h1-2,5-9,12,21H,3-4,10-11H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.72E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457028 (CHEMBL4218303) Show SMILES COc1ccccc1C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O3/c1-32-19-13-7-5-11-17(19)22-20-21(26)16-10-4-6-12-18(16)27-23(20)29-25(31)15-9-3-2-8-14(15)24(30)28(22)29/h2-3,5,7-9,11,13,22H,4,6,10,12H2,1H3,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.33E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457015 (CHEMBL4203173) Show SMILES Nc1c2C(c3ccc(Cl)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19ClN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	9.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457025 (CHEMBL4210751) Show SMILES Nc1c2C(c3cccc(c3)[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-17-10-3-4-11-18(17)26-22-19(20)21(13-6-5-7-14(12-13)29(32)33)27-23(30)15-8-1-2-9-16(15)24(31)28(22)27/h1-2,5-9,12,21H,3-4,10-11H2,(H2,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457014 (CHEMBL4203040) Show SMILES Nc1c2C(c3ccc(Br)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457023 (CHEMBL4207397) Show SMILES Cc1ccc(cc1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-10-12-15(13-11-14)22-20-21(26)18-8-4-5-9-19(18)27-23(20)29-25(31)17-7-3-2-6-16(17)24(30)28(22)29/h2-3,6-7,10-13,22H,4-5,8-9H2,1H3,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457021 (CHEMBL4202878) Show SMILES CCCCCC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C23H26N4O2/c1-2-3-4-13-18-19-20(24)16-11-7-8-12-17(16)25-21(19)27-23(29)15-10-6-5-9-14(15)22(28)26(18)27/h5-6,9-10,18H,2-4,7-8,11-13H2,1H3,(H2,24,25)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457027 (CHEMBL4203909) Show SMILES Nc1c2C(c3cccc(Br)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-14-7-5-6-13(12-14)21-19-20(26)17-10-3-4-11-18(17)27-22(19)29-24(31)16-9-2-1-8-15(16)23(30)28(21)29/h1-2,5-9,12,21H,3-4,10-11H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457029 (CHEMBL4209859) Show SMILES Nc1c2C(c3ccccc3[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-15-9-3-5-11-17(15)26-22-19(20)21(16-10-4-6-12-18(16)29(32)33)27-23(30)13-7-1-2-8-14(13)24(31)28(22)27/h1-2,4,6-8,10,12,21H,3,5,9,11H2,(H2,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457033 (CHEMBL4204269) Show SMILES Cc1ccccc1C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-8-2-3-9-15(14)22-20-21(26)18-12-6-7-13-19(18)27-23(20)29-25(31)17-11-5-4-10-16(17)24(30)28(22)29/h2-5,8-11,22H,6-7,12-13H2,1H3,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457013 (CHEMBL4213928) Show SMILES Cc1cccc(c1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C25H22N4O2/c1-14-7-6-8-15(13-14)22-20-21(26)18-11-4-5-12-19(18)27-23(20)29-25(31)17-10-3-2-9-16(17)24(30)28(22)29/h2-3,6-10,13,22H,4-5,11-12H2,1H3,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457024 (CHEMBL4207926) Show SMILES Nc1c2C(c3ccc(F)cc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-14-11-9-13(10-12-14)21-19-20(26)17-7-3-4-8-18(17)27-22(19)29-24(31)16-6-2-1-5-15(16)23(30)28(21)29/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457022 (CHEMBL4208973) Show SMILES Nc1c2C(c3ccccc3Cl)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19ClN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457016 (CHEMBL4210767) Show SMILES Nc1c2C(c3ccccc3Br)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19BrN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457031 (CHEMBL4216769) Show SMILES COc1cc(OC)cc(c1)C1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C26H24N4O4/c1-33-15-11-14(12-16(13-15)34-2)23-21-22(27)19-9-5-6-10-20(19)28-24(21)30-26(32)18-8-4-3-7-17(18)25(31)29(23)30/h3-4,7-8,11-13,23H,5-6,9-10H2,1-2H3,(H2,27,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457030 (CHEMBL4206121) Show SMILES Nc1c2C(c3cccc(O)c3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H20N4O3/c25-20-17-10-3-4-11-18(17)26-22-19(20)21(13-6-5-7-14(29)12-13)27-23(30)15-8-1-2-9-16(15)24(31)28(22)27/h1-2,5-9,12,21,29H,3-4,10-11H2,(H2,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457017 (CHEMBL4208227) Show SMILES CC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C19H18N4O2/c1-10-15-16(20)13-8-4-5-9-14(13)21-17(15)23-19(25)12-7-3-2-6-11(12)18(24)22(10)23/h2-3,6-7,10H,4-5,8-9H2,1H3,(H2,20,21)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457018 (CHEMBL4211075) Show SMILES CCCC1c2c(nc3CCCCc3c2N)-n2n1c(=O)c1ccccc1c2=O Show InChI InChI=1S/C21H22N4O2/c1-2-7-16-17-18(22)14-10-5-6-11-15(14)23-19(17)25-21(27)13-9-4-3-8-12(13)20(26)24(16)25/h3-4,8-9,16H,2,5-7,10-11H2,1H3,(H2,22,23)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457019 (CHEMBL4207471) Show SMILES Nc1c2C(c3ccccc3F)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19FN4O2/c25-17-11-5-3-9-15(17)21-19-20(26)16-10-4-6-12-18(16)27-22(19)29-24(31)14-8-2-1-7-13(14)23(30)28(21)29/h1-3,5,7-9,11,21H,4,6,10,12H2,(H2,26,27)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457020 (CHEMBL4216504) Show SMILES Nc1c2C(c3ccccc3)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H20N4O2/c25-20-17-12-6-7-13-18(17)26-22-19(20)21(14-8-2-1-3-9-14)27-23(29)15-10-4-5-11-16(15)24(30)28(22)27/h1-5,8-11,21H,6-7,12-13H2,(H2,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50457032 (CHEMBL4212290) Show SMILES Nc1c2C(c3ccc(cc3)[N+]([O-])=O)n3n(-c2nc2CCCCc12)c(=O)c1ccccc1c3=O Show InChI InChI=1S/C24H19N5O4/c25-20-17-7-3-4-8-18(17)26-22-19(20)21(13-9-11-14(12-10-13)29(32)33)27-23(30)15-5-1-2-6-16(15)24(31)28(22)27/h1-2,5-6,9-12,21H,3-4,7-8H2,(H2,25,26)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Tehran University of Medical Sciences Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 10 mins followed by substrate addition measured for 6 ...				Eur J Med Chem 139: 280-289 (2017) Article DOI: 10.1016/j.ejmech.2017.07.072 BindingDB Entry DOI: 10.7270/Q2SX6GVB
					More data for this Ligand-Target Pair