BDBM50005686 2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamino-ethyl ester::CHEMBL443780

SMILES: CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1

InChI Key: InChIKey=KFFUMWAFMBSHHP-UHFFFAOYSA-N

Data: 4 KI  1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50005686   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Muscarinic acetylcholine receptor M1 (Homo sapiens (Human))	BDBM50005686 (2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamin...) Show SMILES CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1 Show InChI InChI=1S/C21H33NO2/c1-4-22(5-2)16-17-24-20(23)21(3,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6,8-9,12-13,19H,4-5,7,10-11,14-17H2,1-3H3	UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Research Curated by ChEMBL					Assay Description Antimuscurinic potency and subset specificity of the compound was characterised by its inhibition of the [3H]-NMS Binding to Muscarinic acetylcholine...				J Med Chem 35: 1290-5 (1992) BindingDB Entry DOI: 10.7270/Q28914T0
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M3 (Homo sapiens (Human))	BDBM50005686 (2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamin...) Show SMILES CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1 Show InChI InChI=1S/C21H33NO2/c1-4-22(5-2)16-17-24-20(23)21(3,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6,8-9,12-13,19H,4-5,7,10-11,14-17H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	9.90	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Research Curated by ChEMBL					Assay Description Antimuscurinic potency and subset specificity of the compound was characterised by its inhibition of the [3H]-NMS Muscarinic acetylcholine receptor M...				J Med Chem 35: 1290-5 (1992) BindingDB Entry DOI: 10.7270/Q28914T0
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M4 (Homo sapiens (Human))	BDBM50005686 (2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamin...) Show SMILES CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1 Show InChI InChI=1S/C21H33NO2/c1-4-22(5-2)16-17-24-20(23)21(3,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6,8-9,12-13,19H,4-5,7,10-11,14-17H2,1-3H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	19	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Research Curated by ChEMBL					Assay Description Antimuscurinic potency and subset specificity of the compound was characterised by its inhibition of the [3H]-NMS Binding to Muscarinic acetylcholine...				J Med Chem 35: 1290-5 (1992) BindingDB Entry DOI: 10.7270/Q28914T0
					More data for this Ligand-Target Pair
Muscarinic acetylcholine receptor M2 (Homo sapiens (Human))	BDBM50005686 (2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamin...) Show SMILES CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1 Show InChI InChI=1S/C21H33NO2/c1-4-22(5-2)16-17-24-20(23)21(3,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6,8-9,12-13,19H,4-5,7,10-11,14-17H2,1-3H3	PDB UniProtKB/SwissProt UniProtKB/TrEMBL antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	23	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Research Curated by ChEMBL					Assay Description Antimuscurinic potency and subset specificity of the compound was characterised by its inhibition of the [3H]-NMS Binding to Muscarinic acetylcholine...				J Med Chem 35: 1290-5 (1992) BindingDB Entry DOI: 10.7270/Q28914T0
					More data for this Ligand-Target Pair
Pancreatic alpha-amylase (Rattus norvegicus)	BDBM50005686 (2-Cyclohexyl-2-phenyl-propionic acid 2-diethylamin...) Show SMILES CCN(CC)CCOC(=O)C(C)(C1CCCCC1)c1ccccc1 Show InChI InChI=1S/C21H33NO2/c1-4-22(5-2)16-17-24-20(23)21(3,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6,8-9,12-13,19H,4-5,7,10-11,14-17H2,1-3H3	PDB KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	n/a	n/a	52	n/a	n/a	n/a	n/a	n/a	n/a
Institute of Research Curated by ChEMBL					Assay Description Inhibition of the release of Alpha-amylase from rat pancreatic acinar cells.				J Med Chem 35: 1290-5 (1992) BindingDB Entry DOI: 10.7270/Q28914T0
					More data for this Ligand-Target Pair