Compile Data Set for Download or QSAR

Found 52 hits Enz. Inhib. hit(s) with all data for entry = 50036362   

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 (Rattus norvegicus (rat))	BDBM50342601 (CHEMBL1255901 | Huperzine A) Show SMILES C\C=C1/[C@@H]2Cc3[nH]c(=O)ccc3[C@]1(N)CC(C)=C2 |r,c:18,TLB:1:2:11.5.4:17.14.15| Show InChI InChI=1S/C15H18N2O/c1-3-11-10-6-9(2)8-15(11,16)12-4-5-14(18)17-13(12)7-10/h3-6,10H,7-8,16H2,1-2H3,(H,17,18)/b11-3+/t10-,15-/m0/s1	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	80	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033519 (5-[2-(4-Hydroxy-phenyl)-ethylamino]-1-(3-methyl-bu...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(-[#8])cc3)-c2ccc1=O Show InChI InChI=1S/C22H28N2O2/c1-16(2)13-15-24-21-5-3-4-20(19(21)10-11-22(24)26)23-14-12-17-6-8-18(25)9-7-17/h6-11,13,20,23,25H,3-5,12,14-15H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	400	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033527 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)c(Cl)c3)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(17(21)7-9-22(26)27)25-12-10-16-6-8-18(23)19(24)14-16/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	510	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033521 (5-[2-(3-Chloro-phenyl)-ethylamino]-1-(3-methyl-but...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3cccc(Cl)c3)-c2ccc1=O Show InChI InChI=1S/C22H27ClN2O/c1-16(2)12-14-25-21-8-4-7-20(19(21)9-10-22(25)26)24-13-11-17-5-3-6-18(23)15-17/h3,5-6,9-10,12,15,20,24H,4,7-8,11,13-14H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033491 (5-[2-(2-Chloro-phenyl)-ethylamino]-1-(3-methyl-but...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccccc3Cl)-c2ccc1=O Show InChI InChI=1S/C22H27ClN2O/c1-16(2)13-15-25-21-9-5-8-20(18(21)10-11-22(25)26)24-14-12-17-6-3-4-7-19(17)23/h3-4,6-7,10-11,13,20,24H,5,8-9,12,14-15H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	520	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	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 MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase CHEMBL DrugBank MCE KEGG MMDB PC cid PC sid PDB UniChem Patents Similars	PDB PubMed	n/a	n/a	630	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair				3D Structure (crystal)
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033495 (5-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamin...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)c(c3)C(F)(F)F)-c2ccc1=O Show InChI InChI=1S/C23H26ClF3N2O/c1-15(2)11-13-29-21-5-3-4-20(17(21)7-9-22(29)30)28-12-10-16-6-8-19(24)18(14-16)23(25,26)27/h6-9,11,14,20,28H,3-5,10,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	790	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033496 (5-[2-(2,4-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)cc3Cl)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(18(21)8-9-22(26)27)25-12-10-16-6-7-17(23)14-19(16)24/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	790	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033512 (5-[2-(3,5-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3cc(Cl)cc(Cl)c3)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)9-11-26-21-5-3-4-20(19(21)6-7-22(26)27)25-10-8-16-12-17(23)14-18(24)13-16/h6-7,9,12-14,20,25H,3-5,8,10-11H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033510 (5-[2-(3,4-Difluoro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(F)c(F)c3)-c2ccc1=O Show InChI InChI=1S/C22H26F2N2O/c1-15(2)11-13-26-21-5-3-4-20(17(21)7-9-22(26)27)25-12-10-16-6-8-18(23)19(24)14-16/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	980	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033492 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-propyl-5,...) Show SMILES CCCn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C20H24Cl2N2O/c1-2-12-24-19-5-3-4-18(15(19)7-9-20(24)25)23-11-10-14-6-8-16(21)17(22)13-14/h6-9,13,18,23H,2-5,10-12H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033511 (5-[2-(3-Methoxy-phenyl)-ethylamino]-1-(3-methyl-bu...) Show SMILES [#6]-[#8]-c1cccc(-[#6]-[#6]-[#7]-[#6]-2-[#6]-[#6]-[#6]-c3c-2ccc(=O)n3-[#6]\[#6]=[#6](/[#6])-[#6])c1 Show InChI InChI=1S/C23H30N2O2/c1-17(2)13-15-25-22-9-5-8-21(20(22)10-11-23(25)26)24-14-12-18-6-4-7-19(16-18)27-3/h4,6-7,10-11,13,16,21,24H,5,8-9,12,14-15H2,1-3H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033507 (5-[2-(2,5-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3cc(Cl)ccc3Cl)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(18(21)7-9-22(26)27)25-12-10-16-14-17(23)6-8-19(16)24/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.36E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033523 (5-[2-(3,4-Dimethoxy-phenyl)-ethylamino]-1-(3-methy...) Show SMILES [#6]-[#8]-c1ccc(-[#6]-[#6]-[#7]-[#6]-2-[#6]-[#6]-[#6]-c3c-2ccc(=O)n3-[#6]\[#6]=[#6](\[#6])-[#6])cc1-[#8]-[#6] Show InChI InChI=1S/C24H32N2O3/c1-17(2)13-15-26-21-7-5-6-20(19(21)9-11-24(26)27)25-14-12-18-8-10-22(28-3)23(16-18)29-4/h8-11,13,16,20,25H,5-7,12,14-15H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.64E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033494 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES CC(C)CCn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C22H28Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(17(21)7-9-22(26)27)25-12-10-16-6-8-18(23)19(24)14-16/h6-9,14-15,20,25H,3-5,10-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033527 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)c(Cl)c3)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(17(21)7-9-22(26)27)25-12-10-16-6-8-18(23)19(24)14-16/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.50E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033508 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-methyl-5,...) Show SMILES Cn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C18H20Cl2N2O/c1-22-17-4-2-3-16(13(17)6-8-18(22)23)21-10-9-12-5-7-14(19)15(20)11-12/h5-8,11,16,21H,2-4,9-10H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	2.93E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033509 (5-Phenethylamino-1-propyl-5,6,7,8-tetrahydro-1H-qu...) Show SMILES CCCn1c2CCCC(NCCc3ccccc3)c2ccc1=O Show InChI InChI=1S/C20H26N2O/c1-2-15-22-19-10-6-9-18(17(19)11-12-20(22)23)21-14-13-16-7-4-3-5-8-16/h3-5,7-8,11-12,18,21H,2,6,9-10,13-15H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033522 (5-[2-(1H-Indol-3-yl)-ethylamino]-1-propyl-5,6,7,8-...) Show SMILES CCCn1c2CCCC(NCCc3c[nH]c4ccccc34)c2ccc1=O Show InChI InChI=1S/C22H27N3O/c1-2-14-25-21-9-5-8-20(18(21)10-11-22(25)26)23-13-12-16-15-24-19-7-4-3-6-17(16)19/h3-4,6-7,10-11,15,20,23-24H,2,5,8-9,12-14H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.16E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033500 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-hexyl-5,6...) Show SMILES CCCCCCn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C23H30Cl2N2O/c1-2-3-4-5-15-27-22-8-6-7-21(18(22)10-12-23(27)28)26-14-13-17-9-11-19(24)20(25)16-17/h9-12,16,21,26H,2-8,13-15H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	3.71E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033505 (5-(Indan-2-ylamino)-1-propyl-5,6,7,8-tetrahydro-1H...) Show SMILES CCCn1c2CCCC(NC3Cc4ccccc4C3)c2ccc1=O Show InChI InChI=1S/C21H26N2O/c1-2-12-23-20-9-5-8-19(18(20)10-11-21(23)24)22-17-13-15-6-3-4-7-16(15)14-17/h3-4,6-7,10-11,17,19,22H,2,5,8-9,12-14H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.91E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033517 (1-Propyl-5-(2-pyridin-2-yl-ethylamino)-5,6,7,8-tet...) Show SMILES CCCn1c2CCCC(NCCc3ccccn3)c2ccc1=O Show InChI InChI=1S/C19H25N3O/c1-2-14-22-18-8-5-7-17(16(18)9-10-19(22)23)21-13-11-15-6-3-4-12-20-15/h3-4,6,9-10,12,17,21H,2,5,7-8,11,13-14H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	4.34E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033516 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-(2-methyl...) Show SMILES CC(=C)Cn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C21H24Cl2N2O/c1-14(2)13-25-20-5-3-4-19(16(20)7-9-21(25)26)24-11-10-15-6-8-17(22)18(23)12-15/h6-9,12,19,24H,1,3-5,10-11,13H2,2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.32E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50369050 (CHEMBL1743676) Show SMILES CCCn1c2CCCC(NCCc3cccs3)c2ccc1=O Show InChI InChI=1S/C18H24N2OS/c1-2-12-20-17-7-3-6-16(15(17)8-9-18(20)21)19-11-10-14-5-4-13-22-14/h4-5,8-9,13,16,19H,2-3,6-7,10-12H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	5.97E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033489 (5-[2-(4-Chloro-phenyl)-ethylamino]-1-methyl-5,6,7,...) Show SMILES Cn1c2CCCC(NCCc3ccc(Cl)cc3)c2ccc1=O Show InChI InChI=1S/C18H21ClN2O/c1-21-17-4-2-3-16(15(17)9-10-18(21)22)20-12-11-13-5-7-14(19)8-6-13/h5-10,16,20H,2-4,11-12H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	6.60E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033520 (1-Allyl-5-[2-(3,4-dichloro-phenyl)-ethylamino]-5,6...) Show SMILES Clc1ccc(CCNC2CCCc3c2ccc(=O)n3CC=C)cc1Cl Show InChI InChI=1S/C20H22Cl2N2O/c1-2-12-24-19-5-3-4-18(15(19)7-9-20(24)25)23-11-10-14-6-8-16(21)17(22)13-14/h2,6-9,13,18,23H,1,3-5,10-12H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	9.21E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033513 (5-[2-(4-Methoxy-phenyl)-ethylamino]-1-methyl-5,6,7...) Show SMILES COc1ccc(CCNC2CCCc3c2ccc(=O)n3C)cc1 Show InChI InChI=1S/C19H24N2O2/c1-21-18-5-3-4-17(16(18)10-11-19(21)22)20-13-12-14-6-8-15(23-2)9-7-14/h6-11,17,20H,3-5,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	9.61E+3	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033501 (1-Methyl-5-[2-(4-trifluoromethyl-phenyl)-ethylamin...) Show SMILES Cn1c2CCCC(NCCc3ccc(cc3)C(F)(F)F)c2ccc1=O Show InChI InChI=1S/C19H21F3N2O/c1-24-17-4-2-3-16(15(17)9-10-18(24)25)23-12-11-13-5-7-14(8-6-13)19(20,21)22/h5-10,16,23H,2-4,11-12H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.29E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033525 (5-(3,3-Dimethyl-butylamino)-1-propyl-5,6,7,8-tetra...) Show SMILES CCCn1c2CCCC(NCCC(C)(C)C)c2ccc1=O Show InChI InChI=1S/C18H30N2O/c1-5-13-20-16-8-6-7-15(14(16)9-10-17(20)21)19-12-11-18(2,3)4/h9-10,15,19H,5-8,11-13H2,1-4H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.56E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033499 (1-Benzyl-5-[2-(3,4-dichloro-phenyl)-ethylamino]-5,...) Show SMILES Clc1ccc(CCNC2CCCc3c2ccc(=O)n3Cc2ccccc2)cc1Cl Show InChI InChI=1S/C24H24Cl2N2O/c25-20-11-9-17(15-21(20)26)13-14-27-22-7-4-8-23-19(22)10-12-24(29)28(23)16-18-5-2-1-3-6-18/h1-3,5-6,9-12,15,22,27H,4,7-8,13-14,16H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.73E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033504 (1-Methyl-5-(2-p-tolyl-ethylamino)-5,6,7,8-tetrahyd...) Show SMILES Cc1ccc(CCNC2CCCc3c2ccc(=O)n3C)cc1 Show InChI InChI=1S/C19H24N2O/c1-14-6-8-15(9-7-14)12-13-20-17-4-3-5-18-16(17)10-11-19(22)21(18)2/h6-11,17,20H,3-5,12-13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.82E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033529 (1-Methyl-5-phenethylamino-5,6,7,8-tetrahydro-1H-qu...) Show SMILES Cn1c2CCCC(NCCc3ccccc3)c2ccc1=O Show InChI InChI=1S/C18H22N2O/c1-20-17-9-5-8-16(15(17)10-11-18(20)21)19-13-12-14-6-3-2-4-7-14/h2-4,6-7,10-11,16,19H,5,8-9,12-13H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	1.86E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033526 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-isobutyl-...) Show SMILES CC(C)Cn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C21H26Cl2N2O/c1-14(2)13-25-20-5-3-4-19(16(20)7-9-21(25)26)24-11-10-15-6-8-17(22)18(23)12-15/h6-9,12,14,19,24H,3-5,10-11,13H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.34E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033521 (5-[2-(3-Chloro-phenyl)-ethylamino]-1-(3-methyl-but...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3cccc(Cl)c3)-c2ccc1=O Show InChI InChI=1S/C22H27ClN2O/c1-16(2)12-14-25-21-8-4-7-20(19(21)9-10-22(25)26)24-13-11-17-5-3-6-18(23)15-17/h3,5-6,9-10,12,15,20,24H,4,7-8,11,13-14H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	2.38E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033515 (1-Decyl-5-[2-(3,4-dichloro-phenyl)-ethylamino]-5,6...) Show SMILES CCCCCCCCCCn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C27H38Cl2N2O/c1-2-3-4-5-6-7-8-9-19-31-26-12-10-11-25(22(26)14-16-27(31)32)30-18-17-21-13-15-23(28)24(29)20-21/h13-16,20,25,30H,2-12,17-19H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.37E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033524 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-isopropyl...) Show SMILES CC(C)n1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C20H24Cl2N2O/c1-13(2)24-19-5-3-4-18(15(19)7-9-20(24)25)23-11-10-14-6-8-16(21)17(22)12-14/h6-9,12-13,18,23H,3-5,10-11H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	3.45E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033518 (1-Methyl-5-(3-phenyl-propylamino)-5,6,7,8-tetrahyd...) Show SMILES Cn1c2CCCC(NCCCc3ccccc3)c2ccc1=O Show InChI InChI=1S/C19H24N2O/c1-21-18-11-5-10-17(16(18)12-13-19(21)22)20-14-6-9-15-7-3-2-4-8-15/h2-4,7-8,12-13,17,20H,5-6,9-11,14H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	4.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033514 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-phenethyl...) Show SMILES Clc1ccc(CCNC2CCCc3c2ccc(=O)n3CCc2ccccc2)cc1Cl Show InChI InChI=1S/C25H26Cl2N2O/c26-21-11-9-19(17-22(21)27)13-15-28-23-7-4-8-24-20(23)10-12-25(30)29(24)16-14-18-5-2-1-3-6-18/h1-3,5-6,9-12,17,23,28H,4,7-8,13-16H2	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	5.04E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033496 (5-[2-(2,4-Dichloro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)cc3Cl)-c2ccc1=O Show InChI InChI=1S/C22H26Cl2N2O/c1-15(2)11-13-26-21-5-3-4-20(18(21)8-9-22(26)27)25-12-10-16-6-7-17(23)14-19(16)24/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	8.95E+4	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033528 (5-Amino-5-benzyl-5,6,7,8-tetrahydro-1H-quinolin-2-...) Show SMILES NC1(Cc2ccccc2)CCCc2[nH]c(=O)ccc12 Show InChI InChI=1S/C16H18N2O/c17-16(11-12-5-2-1-3-6-12)10-4-7-14-13(16)8-9-15(19)18-14/h1-3,5-6,8-9H,4,7,10-11,17H2,(H,18,19)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033519 (5-[2-(4-Hydroxy-phenyl)-ethylamino]-1-(3-methyl-bu...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(-[#8])cc3)-c2ccc1=O Show InChI InChI=1S/C22H28N2O2/c1-16(2)13-15-24-21-5-3-4-20(19(21)10-11-22(24)26)23-14-12-17-6-8-18(25)9-7-17/h6-11,13,20,23,25H,3-5,12,14-15H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033511 (5-[2-(3-Methoxy-phenyl)-ethylamino]-1-(3-methyl-bu...) Show SMILES [#6]-[#8]-c1cccc(-[#6]-[#6]-[#7]-[#6]-2-[#6]-[#6]-[#6]-c3c-2ccc(=O)n3-[#6]\[#6]=[#6](/[#6])-[#6])c1 Show InChI InChI=1S/C23H30N2O2/c1-17(2)13-15-25-22-9-5-8-21(20(22)10-11-23(25)26)24-14-12-18-6-4-7-19(16-18)27-3/h4,6-7,10-11,13,16,21,24H,5,8-9,12,14-15H2,1-3H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033495 (5-[2-(4-Chloro-3-trifluoromethyl-phenyl)-ethylamin...) Show SMILES [#6]\[#6](-[#6])=[#6]/[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(Cl)c(c3)C(F)(F)F)-c2ccc1=O Show InChI InChI=1S/C23H26ClF3N2O/c1-15(2)11-13-29-21-5-3-4-20(17(21)7-9-22(29)30)28-12-10-16-6-8-19(24)18(14-16)23(25,26)27/h6-9,11,14,20,28H,3-5,10,12-13H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033510 (5-[2-(3,4-Difluoro-phenyl)-ethylamino]-1-(3-methyl...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7]-[#6]-[#6]-c3ccc(F)c(F)c3)-c2ccc1=O Show InChI InChI=1S/C22H26F2N2O/c1-15(2)11-13-26-21-5-3-4-20(17(21)7-9-22(26)27)25-12-10-16-6-8-18(23)19(24)14-16/h6-9,11,14,20,25H,3-5,10,12-13H2,1-2H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033506 (5-Amino-1-(3-methyl-but-2-enyl)-5,6,7,8-tetrahydro...) Show SMILES [#6]\[#6](-[#6])=[#6]\[#6]-n1c2-[#6]-[#6]-[#6]-[#6](-[#7])-c2ccc1=O Show InChI InChI=1S/C14H20N2O/c1-10(2)8-9-16-13-5-3-4-12(15)11(13)6-7-14(16)17/h6-8,12H,3-5,9,15H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033503 (5-Phenethylamino-5,6,7,8-tetrahydro-1H-quinolin-2-...) Show SMILES O=c1ccc2C(CCCc2[nH]1)NCCc1ccccc1 Show InChI InChI=1S/C17H20N2O/c20-17-10-9-14-15(7-4-8-16(14)19-17)18-12-11-13-5-2-1-3-6-13/h1-3,5-6,9-10,15,18H,4,7-8,11-12H2,(H,19,20)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033498 (5-Benzylamino-1-methyl-5,6,7,8-tetrahydro-1H-quino...) Show SMILES Cn1c2CCCC(NCc3ccccc3)c2ccc1=O Show InChI InChI=1S/C17H20N2O/c1-19-16-9-5-8-15(14(16)10-11-17(19)20)18-12-13-6-3-2-4-7-13/h2-4,6-7,10-11,15,18H,5,8-9,12H2,1H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Rattus norvegicus (rat))	BDBM50033492 (5-[2-(3,4-Dichloro-phenyl)-ethylamino]-1-propyl-5,...) Show SMILES CCCn1c2CCCC(NCCc3ccc(Cl)c(Cl)c3)c2ccc1=O Show InChI InChI=1S/C20H24Cl2N2O/c1-2-12-24-19-5-3-4-18(15(19)7-9-20(24)25)23-11-10-14-6-8-16(21)17(22)13-14/h6-9,13,18,23H,2-5,10-12H2,1H3	Reactome pathway KEGG UniProtKB/TrEMBL GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description The compound was tested for Butyrylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033493 (5-Amino-1,5-dimethyl-5,6,7,8-tetrahydro-1H-quinoli...) Show SMILES Cn1c2CCCC(C)(N)c2ccc1=O Show InChI InChI=1S/C11H16N2O/c1-11(12)7-3-4-9-8(11)5-6-10(14)13(9)2/h5-6H,3-4,7,12H2,1-2H3	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair
Acetylcholinesterase (Rattus norvegicus (rat))	BDBM50033490 (5-Amino-5-methyl-5,6,7,8-tetrahydro-1H-quinolin-2-...) Show SMILES CC1(N)CCCc2[nH]c(=O)ccc12 Show InChI InChI=1S/C10H14N2O/c1-10(11)6-2-3-8-7(10)4-5-9(13)12-8/h4-5H,2-3,6,11H2,1H3,(H,12,13)	PDB MMDB KEGG UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
Hoechst-Roussel Pharmaceuticals, Inc Curated by ChEMBL					Assay Description Acetylcholinesterase inhibitory activity in rat striatal homogenates				J Med Chem 38: 3645-51 (1995) BindingDB Entry DOI: 10.7270/Q2X34Z3G
					More data for this Ligand-Target Pair

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