Compile Data Set for Download or QSAR

Found 694 hits with Last Name = 'luo' and Initial = 'w'   

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))	BDBM50140562 (CHEMBL3753044) Show SMILES O=c1cc(oc2cc(OCCCCCCCCN3CCCC3)ccc12)-c1cccc2ccccc12 Show InChI InChI=1S/C31H35NO3/c33-29-23-31(27-15-11-13-24-12-5-6-14-26(24)27)35-30-22-25(16-17-28(29)30)34-21-10-4-2-1-3-7-18-32-19-8-9-20-32/h5-6,11-17,22-23H,1-4,7-10,18-21H2	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	206	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Henan University Curated by ChEMBL					Assay Description Mixed-type inhibition of electric eel AChE using ATC as substrate assessed as hydrolysis of ATC preincubated with protein for 15 mins followed by sub...				Bioorg Med Chem 24: 672-80 (2016) Article DOI: 10.1016/j.bmc.2015.12.031 BindingDB Entry DOI: 10.7270/Q2ZP4801
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50443692 (CHEMBL3093837) Show SMILES CCN(CC)CCCCCCCCOc1ccc2c(c1)oc(cc2=O)-c1ccc(cc1)N(C)C Show InChI InChI=1S/C29H40N2O3/c1-5-31(6-2)19-11-9-7-8-10-12-20-33-25-17-18-26-27(32)22-28(34-29(26)21-25)23-13-15-24(16-14-23)30(3)4/h13-18,21-22H,5-12,19-20H2,1-4H3	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	386	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Henan University Curated by ChEMBL					Assay Description Mixed-type inhibition of electric eel AChE using acetylthiocholine chloride as substrate incubated for 15 mins prior to substrate addition by Linewea...				Bioorg Med Chem 21: 7275-82 (2013) Article DOI: 10.1016/j.bmc.2013.09.061 BindingDB Entry DOI: 10.7270/Q25B03ZD
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571672 (CHEMBL4865480) Show SMILES COc1cccc(c1)S(=O)(=O)NC(=O)C(C)(C)Oc1cccc(c1)N1CCC[C@@H](C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.30E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571674 (CHEMBL4867597) Show SMILES CC(C)(Oc1cccc(c1)N1CCC[C@@H](C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1ccc(cc1)C#N |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571673 (CHEMBL4871518) Show SMILES CC(C)(Oc1cccc(c1)N1CCC[C@H](C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1ccc(cc1)C#N |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571670 (CHEMBL4863831) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1ccc(cc1)C#N Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571666 (CHEMBL4876302) Show SMILES COc1cccc(c1)S(=O)(=O)NC(=O)C(C)(C)Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571671 (CHEMBL4873369) Show SMILES COc1cccc(c1)S(=O)(=O)NC(=O)C(C)(C)Oc1cccc(c1)N1CCC[C@H](C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.60E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571667 (CHEMBL4859967) Show SMILES COc1ccc(cc1)S(=O)(=O)NC(=O)C(C)(C)Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.90E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571669 (CHEMBL4870345) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1cccc(c1)C#N Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.10E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571668 (CHEMBL4855648) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1cccc(O)c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.80E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571665 (CHEMBL4853758) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)c1ccccc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.40E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571664 (CHEMBL4866328) Show SMILES CC(C)S(=O)(=O)NC(=O)C(C)(C)Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571645 (CHEMBL4861591) Show SMILES CC(C)c1ccc(COC(=O)N2CCC[C@H](C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 |r| Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem	Article PubMed	1.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571656 (CHEMBL4864865) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571663 (CHEMBL4855866) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(=O)(=O)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	1.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571662 (CHEMBL4875573) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1)C(=O)NS(C)(=O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	2.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571657 (CHEMBL4863201) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1ccsc1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571651 (CHEMBL4855222) Show SMILES CC(C)c1ccc(CN(C2CC2)C(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	3.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571658 (CHEMBL4860163) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1ccco1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571650 (CHEMBL4868062) Show SMILES CC(C)N(Cc1ccc(cc1)C(C)C)C(=O)C1CCCN(C1)c1cccc(OC(C)(C)C(O)=O)c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	4.60E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571649 (CHEMBL4853547) Show SMILES CCN(Cc1ccc(cc1)C(C)C)C(=O)C1CCCN(C1)c1cccc(OC(C)(C)C(O)=O)c1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571648 (CHEMBL4856471) Show SMILES CC(C)c1ccc(CN(C)C(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	5.90E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571654 (CHEMBL4869581) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1ccn[nH]1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	6.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571646 (CHEMBL4859575) Show SMILES CC(C)c1ccc(CNC(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	7.10E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571647 (CHEMBL4873220) Show SMILES CC(C)c1ccc(CCNC(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	8.20E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571661 (CHEMBL4861802) Show SMILES CC(C)(C)OC(=O)C(C)(C)Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571652 (CHEMBL4857876) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cn[nH]c1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571655 (CHEMBL4868027) Show SMILES Cn1nccc1-c1ccc(CN(C2CC2)C(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571659 (CHEMBL4855718) Show SMILES CC(C)(Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1ccoc1)C1CC1)C(O)=O Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571660 (CHEMBL4863752) Show SMILES COC(=O)C(C)(C)Oc1cccc(c1)N1CCCC(C1)C(=O)N(Cc1ccc(cc1)-c1cccs1)C1CC1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
B-cell CLL/lymphoma 9 protein (Homo sapiens)	BDBM50571653 (CHEMBL4859974) Show SMILES Cn1cc(cn1)-c1ccc(CN(C2CC2)C(=O)C2CCCN(C2)c2cccc(OC(C)(C)C(O)=O)c2)cc1 Show InChI	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	>9.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
TBA					Assay Description Inhibition of full length C-terminal 6-His-tagged beta-catenin (1 to 781 residues) (unknown origin) expressed in Escherichia coli BL21 (DE3)-N-termin...				Citation and Details Article DOI: 10.1021/acs.jmedchem.1c00046 BindingDB Entry DOI: 10.7270/Q28G8QHC
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10616 ((3aS)-3a,8-dimethyl-2H,3H,3aH,8H,8aH-furo[2,3-b]in...) Show SMILES CCNC(=O)Oc1ccc2N(C)C3OCC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H20N2O3/c1-4-16-14(18)20-10-5-6-12-11(9-10)15(2)7-8-19-13(15)17(12)3/h5-6,9,13H,4,7-8H2,1-3H3,(H,16,18)/t13?,15-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
National Institutes of Health					Assay Description The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...				J Med Chem 49: 2174-85 (2006) Article DOI: 10.1021/jm050578p BindingDB Entry DOI: 10.7270/Q2S75DJ6
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10616 ((3aS)-3a,8-dimethyl-2H,3H,3aH,8H,8aH-furo[2,3-b]in...) Show SMILES CCNC(=O)Oc1ccc2N(C)C3OCC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C15H20N2O3/c1-4-16-14(18)20-10-5-6-12-11(9-10)15(2)7-8-19-13(15)17(12)3/h5-6,9,13H,4,7-8H2,1-3H3,(H,16,18)/t13?,15-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Aging Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma Butyrylcholinesterase				J Med Chem 48: 986-94 (2005) Article DOI: 10.1021/jm049309+ BindingDB Entry DOI: 10.7270/Q2TM7BWQ
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Equus caballus (Horse))	BDBM50333767 (CHEMBL1644288 | N1-(1,2,3,4-Tetrahydroacridin-9-yl...) Show SMILES COc1cc(CNCCCCCCNc2c3CCCCc3nc3ccccc23)cc(OC)c1OC Show InChI InChI=1S/C29H39N3O3/c1-33-26-18-21(19-27(34-2)29(26)35-3)20-30-16-10-4-5-11-17-31-28-22-12-6-8-14-24(22)32-25-15-9-7-13-23(25)28/h6,8,12,14,18-19,30H,4-5,7,9-11,13,15-17,20H2,1-3H3,(H,31,32)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.59	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine BChE by Ellman's method				Bioorg Med Chem 19: 763-70 (2011) Article DOI: 10.1016/j.bmc.2010.12.022 BindingDB Entry DOI: 10.7270/Q2T43TB0
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Equus caballus (Horse))	BDBM50333763 (CHEMBL1644292 | N1-(3,4-Dimethoxybenzyl)-N6-(1,2,3...) Show SMILES COc1ccc(CNCCCCCCNc2c3CCCCc3nc3ccccc23)cc1OC Show InChI InChI=1S/C28H37N3O2/c1-32-26-16-15-21(19-27(26)33-2)20-29-17-9-3-4-10-18-30-28-22-11-5-7-13-24(22)31-25-14-8-6-12-23(25)28/h5,7,11,13,15-16,19,29H,3-4,6,8-10,12,14,17-18,20H2,1-2H3,(H,30,31)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.68	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine BChE by Ellman's method				Bioorg Med Chem 19: 763-70 (2011) Article DOI: 10.1016/j.bmc.2010.12.022 BindingDB Entry DOI: 10.7270/Q2T43TB0
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10598 ((2S)-2-methyl-5,7-dioxatricyclo[6.4.0.0^{2,6}]dode...) Show SMILES CCNC(=O)Oc1ccc2OC3OCC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C14H17NO4/c1-3-15-13(16)18-9-4-5-11-10(8-9)14(2)6-7-17-12(14)19-11/h4-5,8,12H,3,6-7H2,1-2H3,(H,15,16)/t12?,14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3	n/a	n/a	n/a	n/a	n/a	n/a
National Institutes of Health					Assay Description The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...				J Med Chem 49: 2174-85 (2006) Article DOI: 10.1021/jm050578p BindingDB Entry DOI: 10.7270/Q2S75DJ6
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Equus caballus (Horse))	BDBM50333765 (CHEMBL1644290 | N1-(1,2,3,4-Tetrahydroacridin-9-yl...) Show SMILES COc1cc(CNCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc(OC)c1OC Show InChI InChI=1S/C31H43N3O3/c1-35-28-20-23(21-29(36-2)31(28)37-3)22-32-18-12-6-4-5-7-13-19-33-30-24-14-8-10-16-26(24)34-27-17-11-9-15-25(27)30/h8,10,14,16,20-21,32H,4-7,9,11-13,15,17-19,22H2,1-3H3,(H,33,34)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.38	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine BChE by Ellman's method				Bioorg Med Chem 19: 763-70 (2011) Article DOI: 10.1016/j.bmc.2010.12.022 BindingDB Entry DOI: 10.7270/Q2T43TB0
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50345200 (2-Methoxy-4-((8-(1,2,3,4-tetrahydroacridin-9-ylami...) Show SMILES COc1cc(CNCCCCCCCCNc2c3CCCCc3nc3ccccc23)ccc1O Show InChI InChI=1S/C29H39N3O2/c1-34-28-20-22(16-17-27(28)33)21-30-18-10-4-2-3-5-11-19-31-29-23-12-6-8-14-25(23)32-26-15-9-7-13-24(26)29/h6,8,12,14,16-17,20,30,33H,2-5,7,9-11,13,15,18-19,21H2,1H3,(H,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.41	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE assessed as inhibition of butylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50345205 (CHEMBL1783241 | N1-(Benzo[d][1,3]dioxol-5-ylmethyl...) Show SMILES C(CCCCNc1c2CCCCc2nc2ccccc12)CCCNCc1ccc2OCOc2c1 Show InChI InChI=1S/C29H37N3O2/c1(3-9-17-30-20-22-15-16-27-28(19-22)34-21-33-27)2-4-10-18-31-29-23-11-5-7-13-25(23)32-26-14-8-6-12-24(26)29/h5,7,11,13,15-16,19,30H,1-4,6,8-10,12,14,17-18,20-21H2,(H,31,32)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.44	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE assessed as inhibition of butylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair
Carboxylic ester hydrolase (Equus caballus (Horse))	BDBM50333766 (CHEMBL1644289 | N1-(1,2,3,4-Tetrahydroacridin-9-yl...) Show SMILES COc1cc(CNCCCCCCCNc2c3CCCCc3nc3ccccc23)cc(OC)c1OC Show InChI InChI=1S/C30H41N3O3/c1-34-27-19-22(20-28(35-2)30(27)36-3)21-31-17-11-5-4-6-12-18-32-29-23-13-7-9-15-25(23)33-26-16-10-8-14-24(26)29/h7,9,13,15,19-20,31H,4-6,8,10-12,14,16-18,21H2,1-3H3,(H,32,33)	PDB MMDB UniProtKB/TrEMBL B.MOAD GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	3.55	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine BChE by Ellman's method				Bioorg Med Chem 19: 763-70 (2011) Article DOI: 10.1016/j.bmc.2010.12.022 BindingDB Entry DOI: 10.7270/Q2T43TB0
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10610 ((3aS)-1,3a,8-trimethyl-1H,2H,3H,3aH,8H,8aH-pyrrolo...) Show SMILES CCNC(=O)Oc1ccc2N(C)C3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C16H23N3O2/c1-5-17-15(20)21-11-6-7-13-12(10-11)16(2)8-9-18(3)14(16)19(13)4/h6-7,10,14H,5,8-9H2,1-4H3,(H,17,20)/t14?,16-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
National Institutes of Health					Assay Description The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...				J Med Chem 49: 2174-85 (2006) Article DOI: 10.1021/jm050578p BindingDB Entry DOI: 10.7270/Q2S75DJ6
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10614 ((3aS)-3a,8-dimethyl-2H,3H,3aH,8H,8aH-furo[2,3-b]in...) Show SMILES CNC(=O)Oc1ccc2N(C)C3OCC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C14H18N2O3/c1-14-6-7-18-12(14)16(3)11-5-4-9(8-10(11)14)19-13(17)15-2/h4-5,8,12H,6-7H2,1-3H3,(H,15,17)/t12?,14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
National Institutes of Health					Assay Description The cholinesterase assays were performed using colorimetric method reported by Ellman. The absorbance changes at 412 nm were recorded for 5 min with ...				J Med Chem 49: 2174-85 (2006) Article DOI: 10.1021/jm050578p BindingDB Entry DOI: 10.7270/Q2S75DJ6
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10610 ((3aS)-1,3a,8-trimethyl-1H,2H,3H,3aH,8H,8aH-pyrrolo...) Show SMILES CCNC(=O)Oc1ccc2N(C)C3N(C)CC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C16H23N3O2/c1-5-17-15(20)21-11-6-7-13-12(10-11)16(2)8-9-18(3)14(16)19(13)4/h6-7,10,14H,5,8-9H2,1-4H3,(H,17,20)/t14?,16-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Aging Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma Butyrylcholinesterase				J Med Chem 48: 986-94 (2005) Article DOI: 10.1021/jm049309+ BindingDB Entry DOI: 10.7270/Q2TM7BWQ
					More data for this Ligand-Target Pair
Cholinesterase (Homo sapiens (Human))	BDBM10614 ((3aS)-3a,8-dimethyl-2H,3H,3aH,8H,8aH-furo[2,3-b]in...) Show SMILES CNC(=O)Oc1ccc2N(C)C3OCC[C@@]3(C)c2c1 |r| Show InChI InChI=1S/C14H18N2O3/c1-14-6-7-18-12(14)16(3)11-5-4-9(8-10(11)14)19-13(17)15-2/h4-5,8,12H,6-7H2,1-3H3,(H,15,17)/t12?,14-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Aging Curated by ChEMBL					Assay Description Inhibitory concentration against human plasma Butyrylcholinesterase				J Med Chem 48: 986-94 (2005) Article DOI: 10.1021/jm049309+ BindingDB Entry DOI: 10.7270/Q2TM7BWQ
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50289517 (CHEMBL4163312) Show SMILES COC(=O)c1cc(OC)c2OCOc2c1-c1c2OCOc2c(OC)cc1C(=O)NCCCCCCNc1c2CCCCc2nc2ccccc12 |(14.16,-34.73,;15.68,-35.03,;16.7,-33.87,;16.2,-32.41,;18.21,-34.17,;18.21,-32.62,;19.54,-31.85,;19.54,-30.31,;20.87,-29.53,;20.88,-32.61,;22.35,-32.14,;23.26,-33.38,;22.35,-34.63,;20.88,-34.16,;19.55,-34.94,;19.55,-36.48,;20.88,-37.24,;22.33,-36.76,;23.24,-37.98,;22.35,-39.23,;20.9,-38.77,;19.55,-39.56,;19.55,-41.1,;18.22,-41.87,;18.21,-38.78,;18.21,-37.24,;16.75,-37.69,;16.41,-39.18,;15.64,-36.65,;14.17,-37.1,;13.04,-36.05,;11.56,-36.51,;10.43,-35.46,;8.96,-35.91,;7.83,-34.86,;6.36,-35.31,;5.23,-34.26,;5.58,-32.76,;7.04,-32.3,;7.38,-30.8,;6.25,-29.76,;4.78,-30.22,;4.45,-31.71,;2.97,-32.17,;2.63,-33.68,;1.18,-34.14,;.85,-35.64,;1.98,-36.68,;3.43,-36.21,;3.76,-34.72,)| Show InChI InChI=1S/C38H41N3O9/c1-44-28-18-24(30(35-33(28)47-20-49-35)31-25(38(43)46-3)19-29(45-2)34-36(31)50-21-48-34)37(42)40-17-11-5-4-10-16-39-32-22-12-6-8-14-26(22)41-27-15-9-7-13-23(27)32/h6,8,12,14,18-19H,4-5,7,9-11,13,15-17,20-21H2,1-3H3,(H,39,41)(H,40,42)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4	n/a	n/a	n/a	n/a	n/a	n/a
Henan University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE using butyrylthiocholine chloride as substrate preincubated for 15 mins followed by substrate addition measured ever...				Eur J Med Chem 144: 128-136 (2018) Article DOI: 10.1016/j.ejmech.2017.12.005 BindingDB Entry DOI: 10.7270/Q24B33WB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50345201 (2,6-Dimethoxy-4-((8-(1,2,3,4-tetrahydroacridin-9-y...) Show SMILES COc1cc(CNCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc(OC)c1O Show InChI InChI=1S/C30H41N3O3/c1-35-27-19-22(20-28(36-2)30(27)34)21-31-17-11-5-3-4-6-12-18-32-29-23-13-7-9-15-25(23)33-26-16-10-8-14-24(26)29/h7,9,13,15,19-20,31,34H,3-6,8,10-12,14,16-18,21H2,1-2H3,(H,32,33)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.08	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE assessed as inhibition of butylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50345200 (2-Methoxy-4-((8-(1,2,3,4-tetrahydroacridin-9-ylami...) Show SMILES COc1cc(CNCCCCCCCCNc2c3CCCCc3nc3ccccc23)ccc1O Show InChI InChI=1S/C29H39N3O2/c1-34-28-20-22(16-17-27(28)33)21-30-18-10-4-2-3-5-11-19-31-29-23-12-6-8-14-25(23)32-26-15-9-7-13-24(26)29/h6,8,12,14,16-17,20,30,33H,2-5,7,9-11,13,15,18-19,21H2,1H3,(H,31,32)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.55	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE assessed as inhibition of acetylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair
Acetylcholinesterase (Electrophorus electricus (Electric eel))	BDBM50345201 (2,6-Dimethoxy-4-((8-(1,2,3,4-tetrahydroacridin-9-y...) Show SMILES COc1cc(CNCCCCCCCCNc2c3CCCCc3nc3ccccc23)cc(OC)c1O Show InChI InChI=1S/C30H41N3O3/c1-35-27-19-22(20-28(36-2)30(27)34)21-31-17-11-5-3-4-6-12-18-32-29-23-13-7-9-15-25(23)33-26-16-10-8-14-24(26)29/h7,9,13,15,19-20,31,34H,3-6,8,10-12,14,16-18,21H2,1-2H3,(H,32,33)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.61	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of electric eel AChE assessed as inhibition of acetylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair
Cholinesterase (Equus caballus (Horse))	BDBM50345206 (CHEMBL1783242 | N1-(Pyridin-4-ylmethyl)-N8-(1,2,3,...) Show SMILES C(CCCCNc1c2CCCCc2nc2ccccc12)CCCNCc1ccncc1 Show InChI InChI=1S/C27H36N4/c1(3-9-17-29-21-22-15-19-28-20-16-22)2-4-10-18-30-27-23-11-5-7-13-25(23)31-26-14-8-6-12-24(26)27/h5,7,11,13,15-16,19-20,29H,1-4,6,8-10,12,14,17-18,21H2,(H,30,31)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	4.66	n/a	n/a	n/a	n/a	n/a	n/a
Sun Yat-sen University Curated by ChEMBL					Assay Description Inhibition of equine serum BuChE assessed as inhibition of butylthiocholine chloride substrate hydrolysis incubated for 15 mins before substrate addi...				Eur J Med Chem 46: 2609-16 (2011) Article DOI: 10.1016/j.ejmech.2011.03.058 BindingDB Entry DOI: 10.7270/Q2BV7GZB
					More data for this Ligand-Target Pair

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