Compile Data Set for Download or QSAR

Found 126 hits with Last Name = 'firoozpour' and Initial = 'l'   

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
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50235419 (CHEMBL4077932) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1cccc(Br)c1)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25BrN2O3/c1-2-32-27(31)23-21(17-11-8-12-18(28)15-17)22-24(29)19-13-6-7-14-20(19)30-26(22)33-25(23)16-9-4-3-5-10-16/h3-5,8-12,15,21H,2,6-7,13-14H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	49	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Mixed-type inhibition of electric eel AChE preincubated for 5 mins followed by varying levels acetylthiocholine iodide substrate addition by Lineweav...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073207 (CHEMBL3408398) Show SMILES [Br-].Cc1cc(C)cc(C[n+]2ccc(cc2)-c2cc3ccccc3o2)c1 Show InChI InChI=1S/C22H20NO.BrH/c1-16-11-17(2)13-18(12-16)15-23-9-7-19(8-10-23)22-14-20-5-3-4-6-21(20)24-22;/h3-14H,15H2,1-2H3;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.10	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073217 (CHEMBL3408242) Show SMILES [Br-].[O-][N+](=O)c1ccccc1C[n+]1ccc(cc1)-c1cc2ccccc2o1 Show InChI InChI=1S/C20H15N2O3/c23-22(24)18-7-3-1-6-17(18)14-21-11-9-15(10-12-21)20-13-16-5-2-4-8-19(16)25-20/h1-13H,14H2/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.90	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073208 (CHEMBL3408397) Show SMILES [Br-].[O-][N+](=O)c1ccc(C[n+]2ccc(cc2)-c2cc3ccccc3o2)cc1 Show InChI InChI=1S/C20H15N2O3.BrH/c23-22(24)18-7-5-15(6-8-18)14-21-11-9-16(10-12-21)20-13-17-3-1-2-4-19(17)25-20;/h1-13H,14H2;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.80	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073220 (CHEMBL3408241) Show SMILES [Br-].Cc1ccccc1C[n+]1ccc(cc1)-c1cc2ccccc2o1 Show InChI InChI=1S/C21H18NO/c1-16-6-2-3-8-19(16)15-22-12-10-17(11-13-22)21-14-18-7-4-5-9-20(18)23-21/h2-14H,15H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.80	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073202 (CHEMBL3408403) Show SMILES [Br-].[O-][N+](=O)c1ccc(C[n+]2ccc(cc2)-c2cc3cc(Br)ccc3o2)cc1 Show InChI InChI=1S/C20H14BrN2O3/c21-17-3-6-19-16(11-17)12-20(26-19)15-7-9-22(10-8-15)13-14-1-4-18(5-2-14)23(24)25/h1-12H,13H2/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.10	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073204 (CHEMBL3408401) Show SMILES [Br-].Fc1ccc(C[n+]2ccc(cc2)-c2cc3cc(Br)ccc3o2)cc1 Show InChI InChI=1S/C20H14BrFNO.BrH/c21-17-3-6-19-16(11-17)12-20(24-19)15-7-9-23(10-8-15)13-14-1-4-18(22)5-2-14;/h1-12H,13H2;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.70	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073205 (CHEMBL3408400) Show SMILES [Br-].Fc1cccc(C[n+]2ccc(cc2)-c2cc3cc(Br)ccc3o2)c1 Show InChI InChI=1S/C20H14BrFNO.BrH/c21-17-4-5-19-16(11-17)12-20(24-19)15-6-8-23(9-7-15)13-14-2-1-3-18(22)10-14;/h1-12H,13H2;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	9.60	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073191 (CHEMBL3408408) Show SMILES [Br-].COc1cccc2cc(oc12)-c1cc[n+](Cc2ccc(cc2)[N+]([O-])=O)cc1 Show InChI InChI=1S/C21H17N2O4/c1-26-19-4-2-3-17-13-20(27-21(17)19)16-9-11-22(12-10-16)14-15-5-7-18(8-6-15)23(24)25/h2-13H,14H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					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)
Cholinesterase (Homo sapiens (Human))	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 MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of human BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min by E...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair				3D Structure (crystal)
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073206 (CHEMBL3408399) Show SMILES [Br-].Brc1ccc2oc(cc2c1)-c1cc[n+](Cc2ccccc2)cc1 Show InChI InChI=1S/C20H15BrNO.BrH/c21-18-6-7-19-17(12-18)13-20(23-19)16-8-10-22(11-9-16)14-15-4-2-1-3-5-15;/h1-13H,14H2;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073209 (CHEMBL3408243) Show SMILES [Br-].Brc1ccc(C[n+]2ccc(cc2)-c2cc3ccccc3o2)cc1 Show InChI InChI=1S/C20H15BrNO.BrH/c21-18-7-5-15(6-8-18)14-22-11-9-16(10-12-22)20-13-17-3-1-2-4-19(17)23-20;/h1-13H,14H2;1H/q+1;/p-1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	16	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					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	18	n/a	n/a	n/a	n/a	n/a	n/a
Shahid Bahonar University of Kerman					Assay Description The stock solutions of the target compounds were prepared in a mixture of DMSO (1 ml) and ethanol (9 ml) and diluted with 0.1 MKH2PO4/K2HPO4 buffer (...				Chem Biol Drug Des 89: 783-789 (2017) Article DOI: 10.1111/cbdd.12902 BindingDB Entry DOI: 10.7270/Q24M93CN
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073200 (CHEMBL3408405) Show SMILES [Br-].COc1cccc2cc(oc12)-c1cc[n+](Cc2cccc(F)c2)cc1 Show InChI InChI=1S/C21H17FNO2/c1-24-19-7-3-5-17-13-20(25-21(17)19)16-8-10-23(11-9-16)14-15-4-2-6-18(22)12-15/h2-13H,14H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	19	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073193 (CHEMBL3408406) Show SMILES [Br-].COc1cccc2cc(oc12)-c1cc[n+](Cc2cccc(Br)c2)cc1 Show InChI InChI=1S/C21H17BrNO2/c1-24-19-7-3-5-17-13-20(25-21(17)19)16-8-10-23(11-9-16)14-15-4-2-6-18(22)12-15/h2-13H,14H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	22	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
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))	BDBM50073201 (CHEMBL3408404) Show SMILES [Br-].COc1cccc2cc(oc12)-c1cc[n+](Cc2ccccc2)cc1 Show InChI InChI=1S/C21H18NO2/c1-23-19-9-5-8-18-14-20(24-21(18)19)17-10-12-22(13-11-17)15-16-6-3-2-4-7-16/h2-14H,15H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	27	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073192 (CHEMBL3408407) Show SMILES [Br-].COc1cccc2cc(oc12)-c1cc[n+](Cc2ccc(Br)cc2)cc1 Show InChI InChI=1S/C21H17BrNO2/c1-24-19-4-2-3-17-13-20(25-21(17)19)16-9-11-23(12-10-16)14-15-5-7-18(22)8-6-15/h2-13H,14H2,1H3/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	30	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					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	31	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50073203 (CHEMBL3408402) Show SMILES [Br-].Brc1ccc(C[n+]2ccc(cc2)-c2cc3cc(Br)ccc3o2)cc1 Show InChI InChI=1S/C20H14Br2NO/c21-17-3-1-14(2-4-17)13-23-9-7-15(8-10-23)20-12-16-11-18(22)5-6-19(16)24-20/h1-12H,13H2/q+1	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	32	n/a	n/a	n/a	n/a	n/a	n/a
Islamic Azad University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine substrate by Ellman's reagent based method				Eur J Med Chem 93: 196-201 (2015) Article DOI: 10.1016/j.ejmech.2015.02.009 BindingDB Entry DOI: 10.7270/Q2CF9RTS
					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))	BDBM50235419 (CHEMBL4077932) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1cccc(Br)c1)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25BrN2O3/c1-2-32-27(31)23-21(17-11-8-12-18(28)15-17)22-24(29)19-13-6-7-14-20(19)30-26(22)33-25(23)16-9-4-3-5-10-16/h3-5,8-12,15,21H,2,6-7,13-14H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	69	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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))	BDBM50235422 (CHEMBL4079694) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccccc1Br)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25BrN2O3/c1-2-32-27(31)23-21(17-12-6-8-14-19(17)28)22-24(29)18-13-7-9-15-20(18)30-26(22)33-25(23)16-10-4-3-5-11-16/h3-6,8,10-12,14,21H,2,7,9,13,15H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	118	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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))	BDBM50235417 (CHEMBL4103948) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccccc1Cl)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25ClN2O3/c1-2-32-27(31)23-21(17-12-6-8-14-19(17)28)22-24(29)18-13-7-9-15-20(18)30-26(22)33-25(23)16-10-4-3-5-11-16/h3-6,8,10-12,14,21H,2,7,9,13,15H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	153	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of human Protein kinase C beta 2				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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))	BDBM50235414 (CHEMBL4095975) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1cccc(Cl)c1)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25ClN2O3/c1-2-32-27(31)23-21(17-11-8-12-18(28)15-17)22-24(29)19-13-6-7-14-20(19)30-26(22)33-25(23)16-9-4-3-5-10-16/h3-5,8-12,15,21H,2,6-7,13-14H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	228	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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	356	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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))	BDBM50235418 (CHEMBL4103021) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccccc1F)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25FN2O3/c1-2-32-27(31)23-21(17-12-6-8-14-19(17)28)22-24(29)18-13-7-9-15-20(18)30-26(22)33-25(23)16-10-4-3-5-11-16/h3-6,8,10-12,14,21H,2,7,9,13,15H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	370	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50235408 (CHEMBL4080395) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccc(F)cc1)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25FN2O3/c1-2-32-27(31)23-21(16-12-14-18(28)15-13-16)22-24(29)19-10-6-7-11-20(19)30-26(22)33-25(23)17-8-4-3-5-9-17/h3-5,8-9,12-15,21H,2,6-7,10-11H2,1H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	404	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50235410 (CHEMBL4089184) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccccc1)c1ccccc1 |t:5| Show InChI InChI=1S/C27H26N2O3/c1-2-31-27(30)23-21(17-11-5-3-6-12-17)22-24(28)19-15-9-10-16-20(19)29-26(22)32-25(23)18-13-7-4-8-14-18/h3-8,11-14,21H,2,9-10,15-16H2,1H3,(H2,28,29)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	423	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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))	BDBM50235420 (CHEMBL4096891) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccc(OC)cc1)c1ccccc1 |t:5| Show InChI InChI=1S/C28H28N2O4/c1-3-33-28(31)24-22(17-13-15-19(32-2)16-14-17)23-25(29)20-11-7-8-12-21(20)30-27(23)34-26(24)18-9-5-4-6-10-18/h4-6,9-10,13-16,22H,3,7-8,11-12H2,1-2H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	480	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50235416 (CHEMBL4088245) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1cccc(OC)c1)c1ccccc1 |t:5| Show InChI InChI=1S/C28H28N2O4/c1-3-33-28(31)24-22(18-12-9-13-19(16-18)32-2)23-25(29)20-14-7-8-15-21(20)30-27(23)34-26(24)17-10-5-4-6-11-17/h4-6,9-13,16,22H,3,7-8,14-15H2,1-2H3,(H2,29,30)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50235412 (CHEMBL4066967) Show SMILES CCOC(=O)C1=C(Oc2nc3CCCCc3c(N)c2C1c1ccc(cc1)[N+]([O-])=O)c1ccccc1 |t:5| Show InChI InChI=1S/C27H25N3O5/c1-2-34-27(31)23-21(16-12-14-18(15-13-16)30(32)33)22-24(28)19-10-6-7-11-20(19)29-26(22)35-25(23)17-8-4-3-5-9-17/h3-5,8-9,12-15,21H,2,6-7,10-11H2,1H3,(H2,28,29)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	583	n/a	n/a	n/a	n/a	n/a	n/a
University of Mazandaran Curated by ChEMBL					Assay Description Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured for 1 min...				Eur J Med Chem 128: 237-246 (2017) Article DOI: 10.1016/j.ejmech.2017.01.042 BindingDB Entry DOI: 10.7270/Q2GM89J3
					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

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