BDBM50187683 CHEMBL1186488

SMILES: COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC

InChI Key: InChIKey=UZZFAUDNCIFFPM-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 = 50187683   

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
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50187683 (CHEMBL1186488) Show SMILES COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC Show InChI InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	321	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Displacement of [3H]-raclopride from D2 receptor of Wistar rat striatal membranes after 1 hr by liquid scintillation counting				Bioorg Med Chem Lett 23: 4824-7 (2013) Article DOI: 10.1016/j.bmcl.2013.06.078 BindingDB Entry DOI: 10.7270/Q2BK1G9S
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Rattus norvegicus (rat))	BDBM50187683 (CHEMBL1186488) Show SMILES COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC Show InChI InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	323	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Displacement of [3H]-raclopride from D2 receptor of Wistar rat striatal membranes after 1 hr by liquid scintillation counting				Bioorg Med Chem Lett 23: 4824-7 (2013) Article DOI: 10.1016/j.bmcl.2013.06.078 BindingDB Entry DOI: 10.7270/Q2BK1G9S
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50187683 (CHEMBL1186488) Show SMILES COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC Show InChI InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	2.92E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Displacement of [3H]-SCH23390 from D1 receptor of Wistar rat striatal membranes after 1 hr by liquid scintillation counting				Bioorg Med Chem Lett 23: 4824-7 (2013) Article DOI: 10.1016/j.bmcl.2013.06.078 BindingDB Entry DOI: 10.7270/Q2BK1G9S
					More data for this Ligand-Target Pair
D(1A) dopamine receptor (RAT)	BDBM50187683 (CHEMBL1186488) Show SMILES COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC Show InChI InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	Article PubMed	2.94E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Valencia Curated by ChEMBL					Assay Description Displacement of [3H]-SCH23390 from D1 receptor of Wistar rat striatal membranes after 1 hr by liquid scintillation counting				Bioorg Med Chem Lett 23: 4824-7 (2013) Article DOI: 10.1016/j.bmcl.2013.06.078 BindingDB Entry DOI: 10.7270/Q2BK1G9S
					More data for this Ligand-Target Pair
Butyrylcholinesterase (BuChE) (Equus caballus (Horse))	BDBM50187683 (CHEMBL1186488) Show SMILES COc1cc(CCN(C)C)c2ccc3ccccc3c2c1OC Show InChI InChI=1S/C20H23NO2/c1-21(2)12-11-15-13-18(22-3)20(23-4)19-16-8-6-5-7-14(16)9-10-17(15)19/h5-10,13H,11-12H2,1-4H3	PDB UniProtKB/SwissProt GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Similars	PubMed	n/a	n/a	1.93E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Malaya Curated by ChEMBL					Assay Description Inhibition of equine serum BChE preincubated for 15 mins followed by addition of S-butyrylthiocholine chloride as substrate measured after 30 mins by...				Bioorg Med Chem 24: 4464-4469 (2016) BindingDB Entry DOI: 10.7270/Q2MG7RFM
					More data for this Ligand-Target Pair