Compile Data Set for Download or QSAR

Found 29 hits Enz. Inhib. hit(s) with all data for entry = 50034655   

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))	BDBM50365773 (CHEMBL1956552) Show SMILES CCN(CC)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C23H25N3O/c1-3-26(4-2)14-6-12-24-17-9-10-18-20(15-17)22-21-16(11-13-25-22)7-5-8-19(21)23(18)27/h5,7-11,13,15,24H,3-4,6,12,14H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	260	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Non-competitive inhibition of Electrophorus electricus AChE assessed as hydrolysis of acetylthiocholineiodide after 15 mins incubation by spectrophot...				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					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	21	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair				3D Structure (crystal)
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	130	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365773 (CHEMBL1956552) Show SMILES CCN(CC)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C23H25N3O/c1-3-26(4-2)14-6-12-24-17-9-10-18-20(15-17)22-21-16(11-13-25-22)7-5-8-19(21)23(18)27/h5,7-11,13,15,24H,3-4,6,12,14H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	210	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365771 (CHEMBL1956550) Show SMILES CN(C)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C21H21N3O/c1-24(2)12-4-10-22-15-7-8-16-18(13-15)20-19-14(9-11-23-20)5-3-6-17(19)21(16)25/h3,5-9,11,13,22H,4,10,12H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	490	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365781 (CHEMBL1956560) Show SMILES O=C1c2ccc(NCCCN3CCCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C24H25N3O/c28-24-19-9-8-18(25-11-5-15-27-13-2-1-3-14-27)16-21(19)23-22-17(10-12-26-23)6-4-7-20(22)24/h4,6-10,12,16,25H,1-3,5,11,13-15H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	580	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365772 (CHEMBL1956551) Show SMILES CCN(CC)CCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C22H23N3O/c1-3-25(4-2)13-12-23-16-8-9-17-19(14-16)21-20-15(10-11-24-21)6-5-7-18(20)22(17)26/h5-11,14,23H,3-4,12-13H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	720	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365779 (CHEMBL1956558) Show SMILES O=C1c2ccc(NCCCN3CCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O/c27-23-18-8-7-17(24-10-4-14-26-12-1-2-13-26)15-20(18)22-21-16(9-11-25-22)5-3-6-19(21)23/h3,5-9,11,15,24H,1-2,4,10,12-14H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	730	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365780 (CHEMBL1956559) Show SMILES O=C1c2ccc(NCCN3CCCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O/c27-23-18-8-7-17(24-11-14-26-12-2-1-3-13-26)15-20(18)22-21-16(9-10-25-22)5-4-6-19(21)23/h4-10,15,24H,1-3,11-14H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.10E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365772 (CHEMBL1956551) Show SMILES CCN(CC)CCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C22H23N3O/c1-3-25(4-2)13-12-23-16-8-9-17-19(14-16)21-20-15(10-11-24-21)6-5-7-18(20)22(17)26/h5-11,14,23H,3-4,12-13H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.13E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365771 (CHEMBL1956550) Show SMILES CN(C)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C21H21N3O/c1-24(2)12-4-10-22-15-7-8-16-18(13-15)20-19-14(9-11-23-20)5-3-6-17(19)21(16)25/h3,5-9,11,13,22H,4,10,12H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.19E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365780 (CHEMBL1956559) Show SMILES O=C1c2ccc(NCCN3CCCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O/c27-23-18-8-7-17(24-11-14-26-12-2-1-3-13-26)15-20(18)22-21-16(9-10-25-22)5-4-6-19(21)23/h4-10,15,24H,1-3,11-14H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.42E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365781 (CHEMBL1956560) Show SMILES O=C1c2ccc(NCCCN3CCCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C24H25N3O/c28-24-19-9-8-18(25-11-5-15-27-13-2-1-3-14-27)16-21(19)23-22-17(10-12-26-23)6-4-7-20(22)24/h4,6-10,12,16,25H,1-3,5,11,13-15H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.54E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365770 (CHEMBL1956549) Show SMILES CN(C)CCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C20H19N3O/c1-23(2)11-10-21-14-6-7-15-17(12-14)19-18-13(8-9-22-19)4-3-5-16(18)20(15)24/h3-9,12,21H,10-11H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.89E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365778 (CHEMBL1956557) Show SMILES O=C1c2ccc(NCCN3CCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C22H21N3O/c26-22-17-7-6-16(23-10-13-25-11-1-2-12-25)14-19(17)21-20-15(8-9-24-21)4-3-5-18(20)22/h3-9,14,23H,1-2,10-13H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365770 (CHEMBL1956549) Show SMILES CN(C)CCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C20H19N3O/c1-23(2)11-10-21-14-6-7-15-17(12-14)19-18-13(8-9-22-19)4-3-5-16(18)20(15)24/h3-9,12,21H,10-11H2,1-2H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.03E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365775 (CHEMBL1956554) Show SMILES O=C1c2ccc(NCCCN3CCOCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O2/c27-23-18-6-5-17(24-8-2-10-26-11-13-28-14-12-26)15-20(18)22-21-16(7-9-25-22)3-1-4-19(21)23/h1,3-7,9,15,24H,2,8,10-14H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.20E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365778 (CHEMBL1956557) Show SMILES O=C1c2ccc(NCCN3CCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C22H21N3O/c26-22-17-7-6-16(23-10-13-25-11-1-2-12-25)14-19(17)21-20-15(8-9-24-21)4-3-5-18(20)22/h3-9,14,23H,1-2,10-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.78E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365773 (CHEMBL1956552) Show SMILES CCN(CC)CCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C23H25N3O/c1-3-26(4-2)14-6-12-24-17-9-10-18-20(15-17)22-21-16(11-13-25-22)7-5-8-19(21)23(18)27/h5,7-11,13,15,24H,3-4,6,12,14H2,1-2H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.81E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365779 (CHEMBL1956558) Show SMILES O=C1c2ccc(NCCCN3CCCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O/c27-23-18-8-7-17(24-10-4-14-26-12-1-2-13-26)15-20(18)22-21-16(9-11-25-22)5-3-6-19(21)23/h3,5-9,11,15,24H,1-2,4,10,12-14H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.97E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365774 (CHEMBL1956553) Show SMILES O=C1c2ccc(NCCN3CCOCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C22H21N3O2/c26-22-17-5-4-16(23-8-9-25-10-12-27-13-11-25)14-19(17)21-20-15(6-7-24-21)2-1-3-18(20)22/h1-7,14,23H,8-13H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.76E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365775 (CHEMBL1956554) Show SMILES O=C1c2ccc(NCCCN3CCOCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C23H23N3O2/c27-23-18-6-5-17(24-8-2-10-26-11-13-28-14-12-26)15-20(18)22-21-16(7-9-25-22)3-1-4-19(21)23/h1,3-7,9,15,24H,2,8,10-14H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.94E+3	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365776 (CHEMBL1956555) Show SMILES OCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C18H14N2O2/c21-9-8-19-12-4-5-13-15(10-12)17-16-11(6-7-20-17)2-1-3-14(16)18(13)22/h1-7,10,19,21H,8-9H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.17E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365774 (CHEMBL1956553) Show SMILES O=C1c2ccc(NCCN3CCOCC3)cc2-c2nccc3cccc1c23 Show InChI InChI=1S/C22H21N3O2/c26-22-17-5-4-16(23-8-9-25-10-12-27-13-11-25)14-19(17)21-20-15(6-7-24-21)2-1-3-18(20)22/h1-7,14,23H,8-13H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.59E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365777 (CHEMBL1956556) Show SMILES OCCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C19H16N2O2/c22-10-2-8-20-13-5-6-14-16(11-13)18-17-12(7-9-21-18)3-1-4-15(17)19(14)23/h1,3-7,9,11,20,22H,2,8,10H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	5.58E+4	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50365769 (CHEMBL1956548) Show SMILES Clc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C16H8ClNO/c17-10-4-5-11-13(8-10)15-14-9(6-7-18-15)2-1-3-12(14)16(11)19/h1-8H	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of Electrophorus electricus AChE using acetylthiocholine chloride as substrate after 15 mins incubation by Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365769 (CHEMBL1956548) Show SMILES Clc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C16H8ClNO/c17-10-4-5-11-13(8-10)15-14-9(6-7-18-15)2-1-3-12(14)16(11)19/h1-8H	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365776 (CHEMBL1956555) Show SMILES OCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C18H14N2O2/c21-9-8-19-12-4-5-13-15(10-12)17-16-11(6-7-20-17)2-1-3-14(16)18(13)22/h1-7,10,19,21H,8-9H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50365777 (CHEMBL1956556) Show SMILES OCCCNc1ccc2C(=O)c3cccc4ccnc(-c2c1)c34 Show InChI InChI=1S/C19H16N2O2/c22-10-2-8-20-13-5-6-14-16(11-13)18-17-12(7-9-21-18)3-1-4-15(17)19(14)23/h1,3-7,9,11,20,22H,2,8,10H2	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>1.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
School of Chemistry& Chemical Engineering of Guangxi Normal University Curated by ChEMBL					Assay Description Inhibition of equine serum BChE after 15 mins incubation by spectrophotometry based Ellman's method				Bioorg Med Chem Lett 22: 2257-61 (2012) Article DOI: 10.1016/j.bmcl.2012.01.090 BindingDB Entry DOI: 10.7270/Q2HH6KJX
					More data for this Ligand-Target Pair