Compile Data Set for Download or QSAR

Found 4 hits Enz. Inhib. hit(s) with Target = 'Acetylcholinesterase' and Ligand = 'BDBM50467888'   

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 (Aedes aegypti)	BDBM50467888 (CHEMBL4292499) Show SMILES CCN1CCN(CCCNC(=O)COc2ccc(cc2)-c2ccc(OC)cc2)CC1 Show InChI InChI=1S/C24H33N3O3/c1-3-26-15-17-27(18-16-26)14-4-13-25-24(28)19-30-23-11-7-21(8-12-23)20-5-9-22(29-2)10-6-20/h5-12H,3-4,13-19H2,1-2H3,(H,25,28)	PDB UniProtKB/TrEMBL GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	3.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Umea University Curated by ChEMBL					Assay Description Inhibition of recombinant Aedes aegypti AChE1 expressed in sf9 insect cells using acetylthiocholine iodide as substrate measured over 60 secs by Ellm...				J Med Chem 61: 10545-10557 (2018) Article DOI: 10.1021/acs.jmedchem.8b01060 BindingDB Entry DOI: 10.7270/Q2FT8PQN
					More data for this Ligand-Target Pair
Acetylcholinesterase (Anopheles gambiae)	BDBM50467888 (CHEMBL4292499) Show SMILES CCN1CCN(CCCNC(=O)COc2ccc(cc2)-c2ccc(OC)cc2)CC1 Show InChI InChI=1S/C24H33N3O3/c1-3-26-15-17-27(18-16-26)14-4-13-25-24(28)19-30-23-11-7-21(8-12-23)20-5-9-22(29-2)10-6-20/h5-12H,3-4,13-19H2,1-2H3,(H,25,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
Umea University Curated by ChEMBL					Assay Description Inhibition of recombinant Anopheles gambiae AChE1 expressed in sf9 insect cells using acetylthiocholine iodide as substrate measured over 60 secs by ...				J Med Chem 61: 10545-10557 (2018) Article DOI: 10.1021/acs.jmedchem.8b01060 BindingDB Entry DOI: 10.7270/Q2FT8PQN
					More data for this Ligand-Target Pair
Acetylcholinesterase (Anopheles gambiae)	BDBM50467888 (CHEMBL4292499) Show SMILES CCN1CCN(CCCNC(=O)COc2ccc(cc2)-c2ccc(OC)cc2)CC1 Show InChI InChI=1S/C24H33N3O3/c1-3-26-15-17-27(18-16-26)14-4-13-25-24(28)19-30-23-11-7-21(8-12-23)20-5-9-22(29-2)10-6-20/h5-12H,3-4,13-19H2,1-2H3,(H,25,28)	PDB UniProtKB/SwissProt GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
Umea University Curated by ChEMBL					Assay Description Inhibition of recombinant Anopheles gambiae AChE1 G122S mutant expressed in sf9 insect cells using acetylthiocholine iodide as substrate measured ove...				J Med Chem 61: 10545-10557 (2018) Article DOI: 10.1021/acs.jmedchem.8b01060 BindingDB Entry DOI: 10.7270/Q2FT8PQN
					More data for this Ligand-Target Pair
Acetylcholinesterase (Homo sapiens (Human))	BDBM50467888 (CHEMBL4292499) Show SMILES CCN1CCN(CCCNC(=O)COc2ccc(cc2)-c2ccc(OC)cc2)CC1 Show InChI InChI=1S/C24H33N3O3/c1-3-26-15-17-27(18-16-26)14-4-13-25-24(28)19-30-23-11-7-21(8-12-23)20-5-9-22(29-2)10-6-20/h5-12H,3-4,13-19H2,1-2H3,(H,25,28)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.10E+5	n/a	n/a	n/a	n/a	n/a	n/a
Umea University Curated by ChEMBL					Assay Description Inhibition of recombinant human AChE using acetylthiocholine iodide as substrate measured over 60 secs by Ellman assay				J Med Chem 61: 10545-10557 (2018) Article DOI: 10.1021/acs.jmedchem.8b01060 BindingDB Entry DOI: 10.7270/Q2FT8PQN
					More data for this Ligand-Target Pair