Compile Data Set for Download or QSAR

Found 58 hits with Last Name = 'longo' and Initial = 'jp'   

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))	BDBM10404 ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...) Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1	UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	3.56E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536287 (CHEMBL4581664) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc3ccccc3c2)nn1 Show InChI InChI=1S/C27H29N5O2/c1-20-6-8-24(17-25(20)27(33)28-10-11-31-12-14-34-15-13-31)26-19-32(30-29-26)18-21-7-9-22-4-2-3-5-23(22)16-21/h2-9,16-17,19H,10-15,18H2,1H3,(H,28,33)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.23E+3	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536290 (CHEMBL4525497) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2Cl)nn1 Show InChI InChI=1S/C23H25ClFN5O2/c1-16-2-3-17(12-20(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-18-4-5-19(25)13-21(18)24/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536298 (CHEMBL4551175) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)C#N)nn1 Show InChI InChI=1S/C24H26N6O2/c1-18-2-7-21(14-22(18)24(31)26-8-9-29-10-12-32-13-11-29)23-17-30(28-27-23)16-20-5-3-19(15-25)4-6-20/h2-7,14,17H,8-13,16H2,1H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.22E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536299 (CHEMBL4525580) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)c(F)c2)nn1 Show InChI InChI=1S/C23H25F2N5O2/c1-16-2-4-18(13-19(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-17-3-5-20(24)21(25)12-17/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.54E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM10404 ((1S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetrac...) Show SMILES COc1ccc2CN(C)CC[C@@]34C=C[C@H](O)C[C@@H]3Oc1c24 |r,c:12| Show InChI InChI=1S/C17H21NO3/c1-18-8-7-17-6-5-12(19)9-14(17)21-16-13(20-2)4-3-11(10-18)15(16)17/h3-6,12,14,19H,7-10H2,1-2H3/t12-,14-,17-/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	1.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536288 (CHEMBL4561751) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)[N+]([O-])=O)nn1 Show InChI InChI=1S/C23H26N6O4/c1-17-2-5-19(14-21(17)23(30)24-8-9-27-10-12-33-13-11-27)22-16-28(26-25-22)15-18-3-6-20(7-4-18)29(31)32/h2-7,14,16H,8-13,15H2,1H3,(H,24,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536294 (CHEMBL4581887) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(Br)cc2)nn1 Show InChI InChI=1S/C23H26BrN5O2/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-18-3-6-20(24)7-4-18/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536296 (CHEMBL4578074) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-18-3-6-20(24)7-4-18/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.12E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536291 (CHEMBL4513605) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2F)nn1 Show InChI InChI=1S/C23H25F2N5O2/c1-16-2-3-17(12-20(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-18-4-5-19(24)13-21(18)25/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.44E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536306 (CHEMBL4513836) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)C(F)(F)F)nn1 Show InChI InChI=1S/C24H26F3N5O2/c1-17-2-5-19(14-21(17)23(33)28-8-9-31-10-12-34-13-11-31)22-16-32(30-29-22)15-18-3-6-20(7-4-18)24(25,26)27/h2-7,14,16H,8-13,15H2,1H3,(H,28,33)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.74E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536293 (CHEMBL4524162) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(Br)c2)nn1 Show InChI InChI=1S/C23H26BrN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536295 (CHEMBL4516485) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(F)c2)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536292 (CHEMBL4536296) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)c(c2)[N+]([O-])=O)nn1 Show InChI InChI=1S/C23H25FN6O4/c1-16-2-4-18(13-19(16)23(31)25-6-7-28-8-10-34-11-9-28)21-15-29(27-26-21)14-17-3-5-20(24)22(12-17)30(32)33/h2-5,12-13,15H,6-11,14H2,1H3,(H,25,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536285 (CHEMBL4521556) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(OC(F)(F)F)cc2)nn1 Show InChI InChI=1S/C24H26F3N5O3/c1-17-2-5-19(14-21(17)23(33)28-8-9-31-10-12-34-13-11-31)22-16-32(30-29-22)15-18-3-6-20(7-4-18)35-24(25,26)27/h2-7,14,16H,8-13,15H2,1H3,(H,28,33)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536286 (CHEMBL4522818) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)S(N)(=O)=O)nn1 Show InChI InChI=1S/C23H28N6O4S/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-33-13-11-28)22-16-29(27-26-22)15-18-3-6-20(7-4-18)34(24,31)32/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)(H2,24,31,32)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.03E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536307 (CHEMBL4541730) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2Cl)nn1 Show InChI InChI=1S/C23H26ClN5O2/c1-17-6-7-18(14-20(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-19-4-2-3-5-21(19)24/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.13E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536309 (CHEMBL4576458) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2Br)nn1 Show InChI InChI=1S/C23H25BrFN5O2/c1-16-2-3-17(12-20(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-18-4-5-19(25)13-21(18)24/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.14E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536303 (CHEMBL4531267) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(Cl)c2)nn1 Show InChI InChI=1S/C23H26ClN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.26E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536305 (CHEMBL4584351) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2C(F)(F)F)nn1 Show InChI InChI=1S/C24H26F3N5O2/c1-17-6-7-18(14-20(17)23(33)28-8-9-31-10-12-34-13-11-31)22-16-32(30-29-22)15-19-4-2-3-5-21(19)24(25,26)27/h2-7,14,16H,8-13,15H2,1H3,(H,28,33)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536307 (CHEMBL4541730) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2Cl)nn1 Show InChI InChI=1S/C23H26ClN5O2/c1-17-6-7-18(14-20(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-19-4-2-3-5-21(19)24/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.45E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536292 (CHEMBL4536296) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)c(c2)[N+]([O-])=O)nn1 Show InChI InChI=1S/C23H25FN6O4/c1-16-2-4-18(13-19(16)23(31)25-6-7-28-8-10-34-11-9-28)21-15-29(27-26-21)14-17-3-5-20(24)22(12-17)30(32)33/h2-5,12-13,15H,6-11,14H2,1H3,(H,25,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.48E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536304 (CHEMBL4530986) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2Br)nn1 Show InChI InChI=1S/C23H26BrN5O2/c1-17-6-7-18(14-20(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-19-4-2-3-5-21(19)24/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.52E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536303 (CHEMBL4531267) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(Cl)c2)nn1 Show InChI InChI=1S/C23H26ClN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.63E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536282 (CHEMBL4572737) Show SMILES Cc1cc(F)ccc1Cn1cc(nn1)-c1ccc(C)c(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C24H28FN5O2/c1-17-3-4-19(14-22(17)24(31)26-7-8-29-9-11-32-12-10-29)23-16-30(28-27-23)15-20-5-6-21(25)13-18(20)2/h3-6,13-14,16H,7-12,15H2,1-2H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.76E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536289 (CHEMBL4539017) Show SMILES COC(=O)c1ccc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)cc1 Show InChI InChI=1S/C25H29N5O4/c1-18-3-6-21(15-22(18)24(31)26-9-10-29-11-13-34-14-12-29)23-17-30(28-27-23)16-19-4-7-20(8-5-19)25(32)33-2/h3-8,15,17H,9-14,16H2,1-2H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536308 (CHEMBL4571408) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2F)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-6-7-18(14-20(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-19-4-2-3-5-21(19)24/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.93E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536293 (CHEMBL4524162) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(Br)c2)nn1 Show InChI InChI=1S/C23H26BrN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.03E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536300 (CHEMBL4545234) Show SMILES COc1ccc(Br)c(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1 Show InChI InChI=1S/C24H28BrN5O3/c1-17-3-4-18(14-21(17)24(31)26-7-8-29-9-11-33-12-10-29)23-16-30(28-27-23)15-19-13-20(32-2)5-6-22(19)25/h3-6,13-14,16H,7-12,15H2,1-2H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536296 (CHEMBL4578074) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-18-3-6-20(24)7-4-18/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536283 (CHEMBL4589486) Show SMILES COC(=O)\C=C\c1ccc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)cc1 Show InChI InChI=1S/C27H31N5O4/c1-20-3-9-23(17-24(20)27(34)28-11-12-31-13-15-36-16-14-31)25-19-32(30-29-25)18-22-6-4-21(5-7-22)8-10-26(33)35-2/h3-10,17,19H,11-16,18H2,1-2H3,(H,28,34)/b10-8+	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.47E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536305 (CHEMBL4584351) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2C(F)(F)F)nn1 Show InChI InChI=1S/C24H26F3N5O2/c1-17-6-7-18(14-20(17)23(33)28-8-9-31-10-12-34-13-11-31)22-16-32(30-29-22)15-19-4-2-3-5-21(19)24(25,26)27/h2-7,14,16H,8-13,15H2,1H3,(H,28,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.52E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536302 (CHEMBL4534953) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(C)nn1 Show InChI InChI=1S/C17H23N5O2/c1-13-3-4-14(16-12-21(2)20-19-16)11-15(13)17(23)18-5-6-22-7-9-24-10-8-22/h3-4,11-12H,5-10H2,1-2H3,(H,18,23)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.52E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536286 (CHEMBL4522818) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)S(N)(=O)=O)nn1 Show InChI InChI=1S/C23H28N6O4S/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-33-13-11-28)22-16-29(27-26-22)15-18-3-6-20(7-4-18)34(24,31)32/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)(H2,24,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.55E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536294 (CHEMBL4581887) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(Br)cc2)nn1 Show InChI InChI=1S/C23H26BrN5O2/c1-17-2-5-19(14-21(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-18-3-6-20(24)7-4-18/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.56E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536297 (CHEMBL4549496) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc3ccccc23)nn1 Show InChI InChI=1S/C27H29N5O2/c1-20-9-10-22(17-25(20)27(33)28-11-12-31-13-15-34-16-14-31)26-19-32(30-29-26)18-23-7-4-6-21-5-2-3-8-24(21)23/h2-10,17,19H,11-16,18H2,1H3,(H,28,33)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536308 (CHEMBL4571408) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccccc2F)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-6-7-18(14-20(17)23(30)25-8-9-28-10-12-31-13-11-28)22-16-29(27-26-22)15-19-4-2-3-5-21(19)24/h2-7,14,16H,8-13,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	4.72E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536300 (CHEMBL4545234) Show SMILES COc1ccc(Br)c(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1 Show InChI InChI=1S/C24H28BrN5O3/c1-17-3-4-18(14-21(17)24(31)26-7-8-29-9-11-33-12-10-29)23-16-30(28-27-23)15-19-13-20(32-2)5-6-22(19)25/h3-6,13-14,16H,7-12,15H2,1-2H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536301 (CHEMBL4547644) Show SMILES Cc1cc(C)cc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1 Show InChI InChI=1S/C25H31N5O2/c1-18-12-19(2)14-21(13-18)16-30-17-24(27-28-30)22-5-4-20(3)23(15-22)25(31)26-6-7-29-8-10-32-11-9-29/h4-5,12-15,17H,6-11,16H2,1-3H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.62E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536284 (CHEMBL4515828) Show SMILES Cc1ccc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)cc1 Show InChI InChI=1S/C24H29N5O2/c1-18-3-6-20(7-4-18)16-29-17-23(26-27-29)21-8-5-19(2)22(15-21)24(30)25-9-10-28-11-13-31-14-12-28/h3-8,15,17H,9-14,16H2,1-2H3,(H,25,30)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.01E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536285 (CHEMBL4521556) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(OC(F)(F)F)cc2)nn1 Show InChI InChI=1S/C24H26F3N5O3/c1-17-2-5-19(14-21(17)23(33)28-8-9-31-10-12-34-13-11-31)22-16-32(30-29-22)15-18-3-6-20(7-4-18)35-24(25,26)27/h2-7,14,16H,8-13,15H2,1H3,(H,28,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.02E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536288 (CHEMBL4561751) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(cc2)[N+]([O-])=O)nn1 Show InChI InChI=1S/C23H26N6O4/c1-17-2-5-19(14-21(17)23(30)24-8-9-27-10-12-33-13-11-27)22-16-28(26-25-22)15-18-3-6-20(7-4-18)29(31)32/h2-7,14,16H,8-13,15H2,1H3,(H,24,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.05E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536295 (CHEMBL4516485) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc(F)c2)nn1 Show InChI InChI=1S/C23H26FN5O2/c1-17-5-6-19(14-21(17)23(30)25-7-8-28-9-11-31-12-10-28)22-16-29(27-26-22)15-18-3-2-4-20(24)13-18/h2-6,13-14,16H,7-12,15H2,1H3,(H,25,30)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536282 (CHEMBL4572737) Show SMILES Cc1cc(F)ccc1Cn1cc(nn1)-c1ccc(C)c(c1)C(=O)NCCN1CCOCC1 Show InChI InChI=1S/C24H28FN5O2/c1-17-3-4-19(14-22(17)24(31)26-7-8-29-9-11-32-12-10-29)23-16-30(28-27-23)15-20-5-6-21(25)13-18(20)2/h3-6,13-14,16H,7-12,15H2,1-2H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50536301 (CHEMBL4547644) Show SMILES Cc1cc(C)cc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)c1 Show InChI InChI=1S/C25H31N5O2/c1-18-12-19(2)14-21(13-18)16-30-17-24(27-28-30)22-5-4-20(3)23(15-22)25(31)26-6-7-29-8-10-32-11-9-29/h4-5,12-15,17H,6-11,16H2,1-3H3,(H,26,31)	UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.42E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of electric eel AChE preincubated for 6 mins followed by addition of acetylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536289 (CHEMBL4539017) Show SMILES COC(=O)c1ccc(Cn2cc(nn2)-c2ccc(C)c(c2)C(=O)NCCN2CCOCC2)cc1 Show InChI InChI=1S/C25H29N5O4/c1-18-3-6-21(15-22(18)24(31)26-9-10-29-11-13-34-14-12-29)23-17-30(28-27-23)16-19-4-7-20(8-5-19)25(32)33-2/h3-8,15,17H,9-14,16H2,1-2H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.78E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536302 (CHEMBL4534953) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(C)nn1 Show InChI InChI=1S/C17H23N5O2/c1-13-3-4-14(16-12-21(2)20-19-16)11-15(13)17(23)18-5-6-22-7-9-24-10-8-22/h3-4,11-12H,5-10H2,1-2H3,(H,18,23)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.81E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536290 (CHEMBL4525497) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2Cl)nn1 Show InChI InChI=1S/C23H25ClFN5O2/c1-16-2-3-17(12-20(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-18-4-5-19(25)13-21(18)24/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	6.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536309 (CHEMBL4576458) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2ccc(F)cc2Br)nn1 Show InChI InChI=1S/C23H25BrFN5O2/c1-16-2-3-17(12-20(16)23(31)26-6-7-29-8-10-32-11-9-29)22-15-30(28-27-22)14-18-4-5-19(25)13-21(18)24/h2-5,12-13,15H,6-11,14H2,1H3,(H,26,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.08E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50536297 (CHEMBL4549496) Show SMILES Cc1ccc(cc1C(=O)NCCN1CCOCC1)-c1cn(Cc2cccc3ccccc23)nn1 Show InChI InChI=1S/C27H29N5O2/c1-20-9-10-22(17-25(20)27(33)28-11-12-31-13-15-34-16-14-31)26-19-32(30-29-26)18-23-7-4-6-21-5-2-3-8-24(21)23/h2-10,17,19H,11-16,18H2,1H3,(H,28,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.29E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Jinan Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE preincubated for 6 mins followed by addition of S-butyrylthiocholine iodide by Ellman's method				Bioorg Med Chem Lett 26: 3881-5 (2016) Article DOI: 10.1016/j.bmcl.2016.07.017 BindingDB Entry DOI: 10.7270/Q2KW5KJZ
					More data for this Ligand-Target Pair

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