Compile Data Set for Download or QSAR

Found 51 hits Enz. Inhib. hit(s) with all data for entry = 50045568   

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
Cholinesterase (Equus caballus (Horse))	BDBM50068350 (CHEMBL3402303) Show SMILES C(CNC1CCN(Cc2ccccc2)CC1)Cn1ccc2ccccc12 Show InChI InChI=1S/C23H29N3/c1-2-7-20(8-3-1)19-25-16-12-22(13-17-25)24-14-6-15-26-18-11-21-9-4-5-10-23(21)26/h1-5,7-11,18,22,24H,6,12-17,19H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068302 (CHEMBL3402305) Show SMILES C(CCCn1ccc2ccccc12)CCNC1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C26H35N3/c1(2-9-18-29-21-14-24-12-6-7-13-26(24)29)8-17-27-25-15-19-28(20-16-25)22-23-10-4-3-5-11-23/h3-7,10-14,21,25,27H,1-2,8-9,15-20,22H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	10	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068306 (CHEMBL3402304) Show SMILES C(CCNC1CCN(Cc2ccccc2)CC1)CCn1ccc2ccccc12 Show InChI InChI=1S/C25H33N3/c1-3-9-22(10-4-1)21-27-18-14-24(15-19-27)26-16-7-2-8-17-28-20-13-23-11-5-6-12-25(23)28/h1,3-6,9-13,20,24,26H,2,7-8,14-19,21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	20	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068345 (CHEMBL3402314) Show SMILES COc1ccc(CN2CCC(CC2)NCCCCCCCCn2ccc3ccccc23)cc1 Show InChI InChI=1S/C29H41N3O/c1-33-28-14-12-25(13-15-28)24-31-21-17-27(18-22-31)30-19-8-4-2-3-5-9-20-32-23-16-26-10-6-7-11-29(26)32/h6-7,10-16,23,27,30H,2-5,8-9,17-22,24H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	340	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068344 (CHEMBL3402313) Show SMILES COc1ccc(CN2CCC(CC2)NCCCCCCn2ccc3ccccc23)cc1 Show InChI InChI=1S/C27H37N3O/c1-31-26-12-10-23(11-13-26)22-29-19-15-25(16-20-29)28-17-6-2-3-7-18-30-21-14-24-8-4-5-9-27(24)30/h4-5,8-14,21,25,28H,2-3,6-7,15-20,22H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068348 (CHEMBL3402296) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCCCN2C(=O)c3ccccc3C2=O)c1 Show InChI InChI=1S/C28H36ClN3O2/c29-23-11-9-10-22(20-23)21-31-18-14-24(15-19-31)30-16-7-3-1-2-4-8-17-32-27(33)25-12-5-6-13-26(25)28(32)34/h5-6,9-13,20,24,30H,1-4,7-8,14-19,21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	720	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068296 (CHEMBL3402310) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCCCn2ccc3ccccc23)c1 Show InChI InChI=1S/C28H38ClN3/c29-26-12-9-10-24(22-26)23-31-19-15-27(16-20-31)30-17-7-3-1-2-4-8-18-32-21-14-25-11-5-6-13-28(25)32/h5-6,9-14,21-22,27,30H,1-4,7-8,15-20,23H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL 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
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068334 (CHEMBL3402299) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C28H37N3O3/c32-24-13-11-22(12-14-24)21-30-19-15-23(16-20-30)29-17-7-3-1-2-4-8-18-31-27(33)25-9-5-6-10-26(25)28(31)34/h5-6,9-14,23,29,32H,1-4,7-8,15-21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	810	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068297 (CHEMBL3402309) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCn2ccc3ccccc23)c1 Show InChI InChI=1S/C26H34ClN3/c27-24-10-7-8-22(20-24)21-29-17-13-25(14-18-29)28-15-5-1-2-6-16-30-19-12-23-9-3-4-11-26(23)30/h3-4,7-12,19-20,25,28H,1-2,5-6,13-18,21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	830	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068299 (CHEMBL3402308) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCCCn1ccc2ccccc12 Show InChI InChI=1S/C28H38FN3/c29-27-13-7-5-12-25(27)23-31-20-16-26(17-21-31)30-18-9-3-1-2-4-10-19-32-22-15-24-11-6-8-14-28(24)32/h5-8,11-15,22,26,30H,1-4,9-10,16-21,23H2	PDB UniProtKB/SwissProt 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
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068301 (CHEMBL3402306) Show SMILES C(CCCCn1ccc2ccccc12)CCCNC1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C28H39N3/c1(2-4-11-20-31-23-16-26-14-8-9-15-28(26)31)3-10-19-29-27-17-21-30(22-18-27)24-25-12-6-5-7-13-25/h5-9,12-16,23,27,29H,1-4,10-11,17-22,24H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.08E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068342 (CHEMBL3402312) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCCCn2ccc3ccccc23)cc1 Show InChI InChI=1S/C28H39N3O/c32-27-13-11-24(12-14-27)23-30-20-16-26(17-21-30)29-18-7-3-1-2-4-8-19-31-22-15-25-9-5-6-10-28(25)31/h5-6,9-15,22,26,29,32H,1-4,7-8,16-21,23H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.33E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068349 (CHEMBL3402311) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCn2ccc3ccccc23)cc1 Show InChI InChI=1S/C26H35N3O/c30-25-11-9-22(10-12-25)21-28-18-14-24(15-19-28)27-16-5-1-2-6-17-29-20-13-23-7-3-4-8-26(23)29/h3-4,7-13,20,24,27,30H,1-2,5-6,14-19,21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068306 (CHEMBL3402304) Show SMILES C(CCNC1CCN(Cc2ccccc2)CC1)CCn1ccc2ccccc12 Show InChI InChI=1S/C25H33N3/c1-3-9-22(10-4-1)21-27-18-14-24(15-19-27)26-16-7-2-8-17-28-20-13-23-11-5-6-12-25(23)28/h1,3-6,9-13,20,24,26H,2,7-8,14-19,21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.83E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068290 (CHEMBL3402293) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCCCN1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C28H36FN3O2/c29-26-14-8-5-11-22(26)21-31-19-15-23(16-20-31)30-17-9-3-1-2-4-10-18-32-27(33)24-12-6-7-13-25(24)28(32)34/h5-8,11-14,23,30H,1-4,9-10,15-21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.87E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068293 (CHEMBL3400171) Show SMILES O=C1N(CCCCCCCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C28H37N3O2/c32-27-25-14-8-9-15-26(25)28(33)31(27)19-11-4-2-1-3-10-18-29-24-16-20-30(21-17-24)22-23-12-6-5-7-13-23/h5-9,12-15,24,29H,1-4,10-11,16-22H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.98E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068338 (CHEMBL3402298) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C26H33N3O3/c30-22-11-9-20(10-12-22)19-28-17-13-21(14-18-28)27-15-5-1-2-6-16-29-25(31)23-7-3-4-8-24(23)26(29)32/h3-4,7-12,21,27,30H,1-2,5-6,13-19H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.32E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068288 (CHEMBL3402295) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCN2C(=O)c3ccccc3C2=O)c1 Show InChI InChI=1S/C26H32ClN3O2/c27-21-9-7-8-20(18-21)19-29-16-12-22(13-17-29)28-14-5-1-2-6-15-30-25(31)23-10-3-4-11-24(23)26(30)32/h3-4,7-11,18,22,28H,1-2,5-6,12-17,19H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.73E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068300 (CHEMBL3402307) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCn1ccc2ccccc12 Show InChI InChI=1S/C26H34FN3/c27-25-11-5-3-10-23(25)21-29-18-14-24(15-19-29)28-16-7-1-2-8-17-30-20-13-22-9-4-6-12-26(22)30/h3-6,9-13,20,24,28H,1-2,7-8,14-19,21H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.41E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068291 (CHEMBL3402292) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCN1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C26H32FN3O2/c27-24-12-6-3-9-20(24)19-29-17-13-21(14-18-29)28-15-7-1-2-8-16-30-25(31)22-10-4-5-11-23(22)26(30)32/h3-6,9-12,21,28H,1-2,7-8,13-19H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	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 UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	4.46E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068339 (CHEMBL3402297) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C23H27N3O3/c27-19-8-6-17(7-9-19)16-25-14-10-18(11-15-25)24-12-3-13-26-22(28)20-4-1-2-5-21(20)23(26)29/h1-2,4-9,18,24,27H,3,10-16H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	4.52E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068289 (CHEMBL3402294) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCN2C(=O)c3ccccc3C2=O)c1 Show InChI InChI=1S/C23H26ClN3O2/c24-18-6-3-5-17(15-18)16-26-13-9-19(10-14-26)25-11-4-12-27-22(28)20-7-1-2-8-21(20)23(27)29/h1-3,5-8,15,19,25H,4,9-14,16H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.53E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068319 (CHEMBL3402302) Show SMILES COc1ccc(CN2CCC(CC2)NCCCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C29H39N3O3/c1-35-25-14-12-23(13-15-25)22-31-20-16-24(17-21-31)30-18-8-4-2-3-5-9-19-32-28(33)26-10-6-7-11-27(26)29(32)34/h6-7,10-15,24,30H,2-5,8-9,16-22H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.65E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068346 (CHEMBL3402301) Show SMILES COc1ccc(CN2CCC(CC2)NCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C27H35N3O3/c1-33-23-12-10-21(11-13-23)20-29-18-14-22(15-19-29)28-16-6-2-3-7-17-30-26(31)24-8-4-5-9-25(24)27(30)32/h4-5,8-13,22,28H,2-3,6-7,14-20H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.39E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068295 (CHEMBL3402288) Show SMILES O=C1N(CCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C23H27N3O2/c27-22-20-9-4-5-10-21(20)23(28)26(22)14-6-13-24-19-11-15-25(16-12-19)17-18-7-2-1-3-8-18/h1-5,7-10,19,24H,6,11-17H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.11E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					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	8.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair				3D Structure (crystal)
Cholinesterase (Equus caballus (Horse))	BDBM50068339 (CHEMBL3402297) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C23H27N3O3/c27-19-8-6-17(7-9-19)16-25-14-10-18(11-15-25)24-12-3-13-26-22(28)20-4-1-2-5-21(20)23(26)29/h1-2,4-9,18,24,27H,3,10-16H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	9.37E+3	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068292 (CHEMBL3402291) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCN1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C23H26FN3O2/c24-21-9-4-1-6-17(21)16-26-14-10-18(11-15-26)25-12-5-13-27-22(28)19-7-2-3-8-20(19)23(27)29/h1-4,6-9,18,25H,5,10-16H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068294 (CHEMBL3402290) Show SMILES O=C1N(CCCCCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C26H33N3O2/c30-25-23-12-6-7-13-24(23)26(31)29(25)17-9-2-1-8-16-27-22-14-18-28(19-15-22)20-21-10-4-3-5-11-21/h3-7,10-13,22,27H,1-2,8-9,14-20H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.29E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068302 (CHEMBL3402305) Show SMILES C(CCCn1ccc2ccccc12)CCNC1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C26H35N3/c1(2-9-18-29-21-14-24-12-6-7-13-26(24)29)8-17-27-25-15-19-28(20-16-25)22-23-10-4-3-5-11-23/h3-7,10-14,21,25,27H,1-2,8-9,15-20,22H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.53E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068293 (CHEMBL3400171) Show SMILES O=C1N(CCCCCCCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C28H37N3O2/c32-27-25-14-8-9-15-26(25)28(33)31(27)19-11-4-2-1-3-10-18-29-24-16-20-30(21-17-24)22-23-12-6-5-7-13-23/h5-9,12-15,24,29H,1-4,10-11,16-22H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.77E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068296 (CHEMBL3402310) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCCCn2ccc3ccccc23)c1 Show InChI InChI=1S/C28H38ClN3/c29-26-12-9-10-24(22-26)23-31-19-15-27(16-20-31)30-17-7-3-1-2-4-8-18-32-21-14-25-11-5-6-13-28(25)32/h5-6,9-14,21-22,27,30H,1-4,7-8,15-20,23H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068292 (CHEMBL3402291) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCN1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C23H26FN3O2/c24-21-9-4-1-6-17(21)16-26-14-10-18(11-15-26)25-12-5-13-27-22(28)19-7-2-3-8-20(19)23(27)29/h1-4,6-9,18,25H,5,10-16H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.31E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068334 (CHEMBL3402299) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C28H37N3O3/c32-24-13-11-22(12-14-24)21-30-19-15-23(16-20-30)29-17-7-3-1-2-4-8-18-31-27(33)25-9-5-6-10-26(25)28(31)34/h5-6,9-14,23,29,32H,1-4,7-8,15-21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	2.35E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	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	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	2.61E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068347 (CHEMBL3402300) Show SMILES COc1ccc(CN2CCC(CC2)NCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C24H29N3O3/c1-30-20-9-7-18(8-10-20)17-26-15-11-19(12-16-26)25-13-4-14-27-23(28)21-5-2-3-6-22(21)24(27)29/h2-3,5-10,19,25H,4,11-17H2,1H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.68E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068299 (CHEMBL3402308) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCCCn1ccc2ccccc12 Show InChI InChI=1S/C28H38FN3/c29-27-13-7-5-12-25(27)23-31-20-16-26(17-21-31)30-18-9-3-1-2-4-10-19-32-22-15-24-11-6-8-14-28(24)32/h5-8,11-15,22,26,30H,1-4,9-10,16-21,23H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.96E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068338 (CHEMBL3402298) Show SMILES Oc1ccc(CN2CCC(CC2)NCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C26H33N3O3/c30-22-11-9-20(10-12-22)19-28-17-13-21(14-18-28)27-15-5-1-2-6-16-29-25(31)23-7-3-4-8-24(23)26(29)32/h3-4,7-12,21,27,30H,1-2,5-6,13-19H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.98E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068300 (CHEMBL3402307) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCn1ccc2ccccc12 Show InChI InChI=1S/C26H34FN3/c27-25-11-5-3-10-23(25)21-29-18-14-24(15-19-29)28-16-7-1-2-8-17-30-20-13-22-9-4-6-12-26(22)30/h3-6,9-13,20,24,28H,1-2,7-8,14-19,21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068319 (CHEMBL3402302) Show SMILES COc1ccc(CN2CCC(CC2)NCCCCCCCCN2C(=O)c3ccccc3C2=O)cc1 Show InChI InChI=1S/C29H39N3O3/c1-35-25-14-12-23(13-15-25)22-31-20-16-24(17-21-31)30-18-8-4-2-3-5-9-19-32-28(33)26-10-6-7-11-27(26)29(32)34/h6-7,10-15,24,30H,2-5,8-9,16-22H2,1H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.33E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068290 (CHEMBL3402293) Show SMILES Fc1ccccc1CN1CCC(CC1)NCCCCCCCCN1C(=O)c2ccccc2C1=O Show InChI InChI=1S/C28H36FN3O2/c29-26-14-8-5-11-22(26)21-31-19-15-23(16-20-31)30-17-9-3-1-2-4-10-18-32-27(33)24-12-6-7-13-25(24)28(32)34/h5-8,11-14,23,30H,1-4,9-10,15-21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068294 (CHEMBL3402290) Show SMILES O=C1N(CCCCCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C26H33N3O2/c30-25-23-12-6-7-13-24(23)26(31)29(25)17-9-2-1-8-16-27-22-14-18-28(19-15-22)20-21-10-4-3-5-11-21/h3-7,10-13,22,27H,1-2,8-9,14-20H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					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	4.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50068295 (CHEMBL3402288) Show SMILES O=C1N(CCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C23H27N3O2/c27-22-20-9-4-5-10-21(20)23(28)26(22)14-6-13-24-19-11-15-25(16-12-19)17-18-7-2-1-3-8-18/h1-5,7-10,19,24H,6,11-17H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.18E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of horse serum BChE using butyrylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068297 (CHEMBL3402309) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCn2ccc3ccccc23)c1 Show InChI InChI=1S/C26H34ClN3/c27-24-10-7-8-22(20-24)21-29-17-13-25(14-18-29)28-15-5-1-2-6-16-30-19-12-23-9-3-4-11-26(23)30/h3-4,7-12,19-20,25,28H,1-2,5-6,13-18,21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.32E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068288 (CHEMBL3402295) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCCCCN2C(=O)c3ccccc3C2=O)c1 Show InChI InChI=1S/C26H32ClN3O2/c27-21-9-7-8-20(18-21)19-29-16-12-22(13-17-29)28-14-5-1-2-6-15-30-25(31)23-10-3-4-11-24(23)26(30)32/h3-4,7-11,18,22,28H,1-2,5-6,12-17,19H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068289 (CHEMBL3402294) Show SMILES Clc1cccc(CN2CCC(CC2)NCCCN2C(=O)c3ccccc3C2=O)c1 Show InChI InChI=1S/C23H26ClN3O2/c24-18-6-3-5-17(15-18)16-26-13-9-19(10-14-26)25-11-4-12-27-22(28)20-7-1-2-8-21(20)23(27)29/h1-3,5-8,15,19,25H,4,9-14,16H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.83E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068341 (CHEMBL3402289) Show SMILES O=C1N(CCCCCNC2CCN(Cc3ccccc3)CC2)C(=O)c2ccccc12 Show InChI InChI=1S/C25H31N3O2/c29-24-22-11-5-6-12-23(22)25(30)28(24)16-8-2-7-15-26-21-13-17-27(18-14-21)19-20-9-3-1-4-10-20/h1,3-6,9-12,21,26H,2,7-8,13-19H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50068301 (CHEMBL3402306) Show SMILES C(CCCCn1ccc2ccccc12)CCCNC1CCN(Cc2ccccc2)CC1 Show InChI InChI=1S/C28H39N3/c1(2-4-11-20-31-23-16-26-14-8-9-15-28(26)31)3-10-19-29-27-17-21-30(22-18-27)24-25-12-6-5-7-13-25/h5-9,12-16,23,27,29H,1-4,10-11,17-22,24H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
Jagiellonian University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins by Ellman method				Bioorg Med Chem 23: 2445-57 (2015) Article DOI: 10.1016/j.bmc.2015.03.051 BindingDB Entry DOI: 10.7270/Q2CZ38VB
					More data for this Ligand-Target Pair

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