Compile Data Set for Download or QSAR

Found 37 hits with Last Name = 'farao' and Initial = 'm'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019010 (CHEMBL3288082) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(C)C |r| Show InChI InChI=1S/C30H52O8S2.2Na/c1-18(2)19-11-14-28(6)24(38-40(34,35)36)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(37-39(31,32)33)26(3,4)21(27)12-16-29(22,30)7;;/h18-25H,9-17H2,1-8H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.44E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Uncompetitive inhibition of Pacific electric ray AChE using acetylthiocholine as substrate by Lineweaver-Burk plot analysis				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					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	4	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair				3D Structure (crystal)
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50004000 ((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...) Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	11	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50004000 ((3aS,8aR)-1,3a,8-trimethyl-1,2,3,3a,8,8a-hexahydro...) Show SMILES CNC(=O)Oc1ccc2N(C)[C@H]3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H21N3O2/c1-15-7-8-17(3)13(15)18(4)12-6-5-10(9-11(12)15)20-14(19)16-2/h5-6,9,13H,7-8H2,1-4H3,(H,16,19)/t13-,15+/m1/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	14	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	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 UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	29	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288994 (CHEMBL545578 | N'-((S)-4-Ethyl-4-hydroxy-3,13-diox...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(\N=C\N(C)c5ccccc5)c4cc3Cn1c2=O |r| Show InChI InChI=1S/C28H24N4O4/c1-3-28(35)21-13-24-25-17(14-32(24)26(33)20(21)15-36-27(28)34)12-19-22(10-7-11-23(19)30-25)29-16-31(2)18-8-5-4-6-9-18/h4-13,16,35H,3,14-15H2,1-2H3/b29-16+/t28-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288991 (CHEMBL555409 | N'-((S)-4-Ethyl-4-hydroxy-3,13-diox...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(N=C(C)N(C)C)c4cc3Cn1c2=O |r,w:19.19| Show InChI InChI=1S/C24H24N4O4/c1-5-24(31)17-10-20-21-14(11-28(20)22(29)16(17)12-32-23(24)30)9-15-18(25-13(2)27(3)4)7-6-8-19(15)26-21/h6-10,31H,5,11-12H2,1-4H3/t24-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288989 (CHEMBL540086 | N'-((S)-4,11-Diethyl-4-hydroxy-3,13...) Show SMILES CCc1c2Cn3c(cc4c(COC(=O)[C@]4(O)CC)c3=O)-c2nc2cccc(\N=C\N(C)C)c12 |r| Show InChI InChI=1S/C25H26N4O4/c1-5-14-15-11-29-20(10-17-16(23(29)30)12-33-24(31)25(17,32)6-2)22(15)27-19-9-7-8-18(21(14)19)26-13-28(3)4/h7-10,13,32H,5-6,11-12H2,1-4H3/b26-13+/t25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	3.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50008936 ((S)-10-Amino-4-ethyl-4-hydroxy-1,12-dihydro-4H-2-o...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(N)c4cc3Cn1c2=O |r| Show InChI InChI=1S/C20H17N3O4/c1-2-20(26)13-7-16-17-10(6-11-14(21)4-3-5-15(11)22-17)8-23(16)18(24)12(13)9-27-19(20)25/h3-7,26H,2,8-9,21H2,1H3/t20-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article	n/a	n/a	4.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288988 (CHEMBL542775 | N-((S)-4-Ethyl-4-hydroxy-3,13-dioxo...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(N=CNC)c4cc3Cn1c2=O |r,w:19.19| Show InChI InChI=1S/C22H20N4O4/c1-3-22(29)15-8-18-19-12(9-26(18)20(27)14(15)10-30-21(22)28)7-13-16(24-11-23-2)5-4-6-17(13)25-19/h4-8,11,29H,3,9-10H2,1-2H3,(H,23,24)/t22-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288993 (CHEMBL543237 | N'-((S)-4-Ethyl-4-hydroxy-3,13-diox...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(\N=C\N(C)C)c4cc3Cn1c2=O |r| Show InChI InChI=1S/C23H22N4O4/c1-4-23(30)16-9-19-20-13(10-27(19)21(28)15(16)11-31-22(23)29)8-14-17(24-12-26(2)3)6-5-7-18(14)25-20/h5-9,12,30H,4,10-11H2,1-3H3/b24-12+/t23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	1.92E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288992 (CHEMBL543000 | N-((S)-4-Ethyl-4-hydroxy-3,13-dioxo...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(N=CN)c4cc3Cn1c2=O |r,w:20.21| Show InChI InChI=1S/C21H18N4O4/c1-2-21(28)14-7-17-18-11(8-25(17)19(26)13(14)9-29-20(21)27)6-12-15(23-10-22)4-3-5-16(12)24-18/h3-7,10,28H,2,8-9H2,1H3,(H2,22,23)/t21-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	2.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019013 (CHEMBL3288094) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)C(=O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CCC(=O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=C)C=O |r| Show InChI InChI=1S/C30H44O3/c1-18(17-31)19-10-13-28(5)24(33)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(32)26(2,3)21(27)11-15-29(22,30)6/h17,19-22,25H,1,8-16H2,2-7H3/t19-,20+,21-,22+,25+,27-,28+,29+,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.15E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288995 (CHEMBL554038 | N'-((S)-4-Ethyl-4-hydroxy-3,13-diox...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4ccc(cc4cc3Cn1c2=O)\N=C\N(C)C |r| Show InChI InChI=1S/C23H22N4O4/c1-4-23(30)17-9-19-20-14(10-27(19)21(28)16(17)11-31-22(23)29)7-13-8-15(24-12-26(2)3)5-6-18(13)25-20/h5-9,12,30H,4,10-11H2,1-3H3/b24-12+/t23-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	4.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019010 (CHEMBL3288082) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(C)C |r| Show InChI InChI=1S/C30H52O8S2.2Na/c1-18(2)19-11-14-28(6)24(38-40(34,35)36)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(37-39(31,32)33)26(3,4)21(27)12-16-29(22,30)7;;/h18-25H,9-17H2,1-8H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.88E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019003 (CHEMBL3288074) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(C)=C |r| Show InChI InChI=1S/C30H50O8S2.2Na/c1-18(2)19-11-14-28(6)24(38-40(34,35)36)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(37-39(31,32)33)26(3,4)21(27)12-16-29(22,30)7;;/h19-25H,1,9-17H2,2-8H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	6.43E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
DNA topoisomerase 1 (Homo sapiens (Human))	BDBM50288990 ((S)-4-Ethyl-4-hydroxy-10-{[1-morpholin-4-yl-meth-(...) Show SMILES CC[C@@]1(O)C(=O)OCc2c1cc1-c3nc4cccc(\N=C\N5CCOCC5)c4cc3Cn1c2=O |r| Show InChI InChI=1S/C25H24N4O5/c1-2-25(32)18-11-21-22-15(12-29(21)23(30)17(18)13-34-24(25)31)10-16-19(4-3-5-20(16)27-22)26-14-28-6-8-33-9-7-28/h3-5,10-11,14,32H,2,6-9,12-13H2,1H3/b26-14+/t25-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article	n/a	n/a	6.90E+4	n/a	n/a	n/a	n/a	n/a	n/a
TBA Curated by ChEMBL					Assay Description Compound was tested in vitro for inhibition of topoisomerase I.				Bioorg Med Chem Lett 6: 671-674 (1996) Article DOI: 10.1016/0960-894X(96)00083-2 BindingDB Entry DOI: 10.7270/Q2T153MM
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019012 (CHEMBL3288092) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OC(=O)CCCCC(O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OC(=O)CCCCC(O)=O)C(C)=C |r| Show InChI InChI=1S/C42H66O8/c1-26(2)27-19-22-40(6)32(50-36(48)16-12-10-14-34(45)46)25-42(8)28(37(27)40)17-18-30-39(5)23-21-31(49-35(47)15-11-9-13-33(43)44)38(3,4)29(39)20-24-41(30,42)7/h27-32,37H,1,9-25H2,2-8H3,(H,43,44)(H,45,46)/t27-,28+,29-,30+,31-,32-,37+,39-,40+,41+,42+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	8.06E+4	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019010 (CHEMBL3288082) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(C)C |r| Show InChI InChI=1S/C30H52O8S2.2Na/c1-18(2)19-11-14-28(6)24(38-40(34,35)36)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(37-39(31,32)33)26(3,4)21(27)12-16-29(22,30)7;;/h18-25H,9-17H2,1-8H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.04E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019009 (CHEMBL3288081) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(=C)CO |r| Show InChI InChI=1S/C30H50O9S2.2Na/c1-18(17-31)19-10-13-28(5)24(39-41(35,36)37)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(38-40(32,33)34)26(2,3)21(27)11-15-29(22,30)6;;/h19-25,31H,1,8-17H2,2-7H3,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.88E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019003 (CHEMBL3288074) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(C)=C |r| Show InChI InChI=1S/C30H50O8S2.2Na/c1-18(2)19-11-14-28(6)24(38-40(34,35)36)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(37-39(31,32)33)26(3,4)21(27)12-16-29(22,30)7;;/h19-25H,1,9-17H2,2-8H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.90E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019016 (CHEMBL3288087) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OC(C)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OC(C)=O)C(=C)C=O |r| Show InChI InChI=1S/C34H52O5/c1-20(19-35)23-12-15-32(7)28(39-22(3)37)18-34(9)24(29(23)32)10-11-26-31(6)16-14-27(38-21(2)36)30(4,5)25(31)13-17-33(26,34)8/h19,23-29H,1,10-18H2,2-9H3/t23-,24+,25-,26+,27-,28-,29+,31-,32+,33+,34+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019008 (CHEMBL3288080) Show SMILES [Na+].[Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(=C)COS([O-])(=O)=O |r| Show InChI InChI=1S/C30H50O12S3.3Na/c1-18(17-40-43(31,32)33)19-10-13-28(5)24(42-45(37,38)39)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(41-44(34,35)36)26(2,3)21(27)11-15-29(22,30)6;;;/h19-25H,1,8-17H2,2-7H3,(H,31,32,33)(H,34,35,36)(H,37,38,39);;;/q;3*+1/p-3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;;/m0.../s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019002 (Calenduladiol) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(C)=C |r| Show InChI InChI=1S/C30H50O2/c1-18(2)19-11-14-28(6)24(32)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019013 (CHEMBL3288094) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)C(=O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CCC(=O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=C)C=O |r| Show InChI InChI=1S/C30H44O3/c1-18(17-31)19-10-13-28(5)24(33)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(32)26(2,3)21(27)11-15-29(22,30)6/h17,19-22,25H,1,8-16H2,2-7H3/t19-,20+,21-,22+,25+,27-,28+,29+,30+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019012 (CHEMBL3288092) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OC(=O)CCCCC(O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OC(=O)CCCCC(O)=O)C(C)=C |r| Show InChI InChI=1S/C42H66O8/c1-26(2)27-19-22-40(6)32(50-36(48)16-12-10-14-34(45)46)25-42(8)28(37(27)40)17-18-30-39(5)23-21-31(49-35(47)15-11-9-13-33(43)44)38(3,4)29(39)20-24-41(30,42)7/h27-32,37H,1,9-25H2,2-8H3,(H,43,44)(H,45,46)/t27-,28+,29-,30+,31-,32-,37+,39-,40+,41+,42+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019011 (CHEMBL3288083) Show SMILES [Na+].[Na+].[H][C@]1(CC[C@]2(C)[C@H](C[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]12[H])OS([O-])(=O)=O)[C@@]1(C)CO1 |r| Show InChI InChI=1S/C30H50O9S2.2Na/c1-25(2)20-11-15-28(5)21(26(20,3)14-12-22(25)38-40(31,32)33)9-8-18-24-19(30(7)17-37-30)10-13-27(24,4)23(16-29(18,28)6)39-41(34,35)36;;/h18-24H,8-17H2,1-7H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t18-,19-,20+,21-,22+,23+,24+,26+,27-,28-,29-,30-;;/m1../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019009 (CHEMBL3288081) Show SMILES [Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(=C)CO |r| Show InChI InChI=1S/C30H50O9S2.2Na/c1-18(17-31)19-10-13-28(5)24(39-41(35,36)37)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(38-40(32,33)34)26(2,3)21(27)11-15-29(22,30)6;;/h19-25,31H,1,8-17H2,2-7H3,(H,32,33,34)(H,35,36,37);;/q;2*+1/p-2/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;/m0../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019008 (CHEMBL3288080) Show SMILES [Na+].[Na+].[Na+].[H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]3([H])CC[C@@]12C)OS([O-])(=O)=O)C(=C)COS([O-])(=O)=O |r| Show InChI InChI=1S/C30H50O12S3.3Na/c1-18(17-40-43(31,32)33)19-10-13-28(5)24(42-45(37,38)39)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(41-44(34,35)36)26(2,3)21(27)11-15-29(22,30)6;;;/h19-25H,1,8-17H2,2-7H3,(H,31,32,33)(H,34,35,36)(H,37,38,39);;;/q;3*+1/p-3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+;;;/m0.../s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019007 (CHEMBL3288078) Show SMILES [H][C@]1(CC[C@]2(C)[C@@H](O)C[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)CC[C@H](O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]12[H])[C@@]1(C)CO1 |r| Show InChI InChI=1S/C30H50O3/c1-25(2)20-11-15-28(5)21(26(20,3)14-12-22(25)31)9-8-18-24-19(30(7)17-33-30)10-13-27(24,4)23(32)16-29(18,28)6/h18-24,31-32H,8-17H2,1-7H3/t18-,19-,20+,21-,22+,23+,24+,26+,27-,28-,29-,30-/m1/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019006 (CHEMBL3288077) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(C)C |r| Show InChI InChI=1S/C30H52O2/c1-18(2)19-11-14-28(6)24(32)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h18-25,31-32H,9-17H2,1-8H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019005 (CHEMBL3288076) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=C)CO |r| Show InChI InChI=1S/C30H50O3/c1-18(17-31)19-10-13-28(5)24(33)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(32)26(2,3)21(27)11-15-29(22,30)6/h19-25,31-33H,1,8-17H2,2-7H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019004 (CHEMBL3288075) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(=C)C=O |r| Show InChI InChI=1S/C30H48O3/c1-18(17-31)19-10-13-28(5)24(33)16-30(7)20(25(19)28)8-9-22-27(4)14-12-23(32)26(2,3)21(27)11-15-29(22,30)6/h17,19-25,32-33H,1,8-16H2,2-7H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Acetylcholinesterase (Tetronarce californica (Pacific electric ray) (Tor...)	BDBM50019002 (Calenduladiol) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)C(C)=C |r| Show InChI InChI=1S/C30H50O2/c1-18(2)19-11-14-28(6)24(32)17-30(8)20(25(19)28)9-10-22-27(5)15-13-23(31)26(3,4)21(27)12-16-29(22,30)7/h19-25,31-32H,1,9-17H2,2-8H3/t19-,20+,21-,22+,23-,24-,25+,27-,28+,29+,30+/m0/s1	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of Pacific electric ray AChE using acetylthiocholine iodide as substrate after 60 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019015 (CHEMBL3288086) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@H](C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](O)C(C)(C)[C@]3([H])CC[C@@]12C)OC(C)=O)C(C)=C |r| Show InChI InChI=1S/C32H52O3/c1-19(2)21-12-15-30(7)26(35-20(3)33)18-32(9)22(27(21)30)10-11-24-29(6)16-14-25(34)28(4,5)23(29)13-17-31(24,32)8/h21-27,34H,1,10-18H2,2-9H3/t21-,22+,23-,24+,25-,26-,27+,29-,30+,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019011 (CHEMBL3288083) Show SMILES [Na+].[Na+].[H][C@]1(CC[C@]2(C)[C@H](C[C@]3(C)[C@]([H])(CC[C@]4([H])[C@@]5(C)CC[C@H](OS([O-])(=O)=O)C(C)(C)[C@]5([H])CC[C@@]34C)[C@@]12[H])OS([O-])(=O)=O)[C@@]1(C)CO1 |r| Show InChI InChI=1S/C30H50O9S2.2Na/c1-25(2)20-11-15-28(5)21(26(20,3)14-12-22(25)38-40(31,32)33)9-8-18-24-19(30(7)17-37-30)10-13-27(24,4)23(16-29(18,28)6)39-41(34,35)36;;/h18-24H,8-17H2,1-7H3,(H,31,32,33)(H,34,35,36);;/q;2*+1/p-2/t18-,19-,20+,21-,22+,23+,24+,26+,27-,28-,29-,30-;;/m1../s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50019014 (CHEMBL3288085) Show SMILES [H][C@]12[C@@H](CC[C@]1(C)[C@@H](O)C[C@]1(C)[C@]2([H])CC[C@]2([H])[C@@]3(C)CC[C@H](OC(C)=O)C(C)(C)[C@]3([H])CC[C@@]12C)C(C)=C |r| Show InChI InChI=1S/C32H52O3/c1-19(2)21-12-15-30(7)25(34)18-32(9)22(27(21)30)10-11-24-29(6)16-14-26(35-20(3)33)28(4,5)23(29)13-17-31(24,32)8/h21-27,34H,1,10-18H2,2-9H3/t21-,22+,23-,24+,25-,26-,27+,29-,30+,31+,32+/m0/s1	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>2.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Nacional del Sur Curated by ChEMBL					Assay Description Inhibition of BChE in horse serum using butyrylthiocholine iodide as substrate after 120 mins by Ellman's method				Bioorg Med Chem 22: 3341-50 (2014) Article DOI: 10.1016/j.bmc.2014.04.050 BindingDB Entry DOI: 10.7270/Q28P6220
					More data for this Ligand-Target Pair