null

SMILES: Oc1ccccc1C(=O)NC\C=C\CN1CCN(CC1)c1cccc(Cl)c1Cl

InChI Key: InChIKey=GXAWEOGMNHTNSL-ONEGZZNKSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50161230   

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(3) dopamine receptor (Homo sapiens (Human))	BDBM50161230 (CHEMBL372022 | N-{4-[4-(2,3-Dichloro-phenyl)-piper...) Show SMILES Oc1ccccc1C(=O)NC\C=C\CN1CCN(CC1)c1cccc(Cl)c1Cl Show InChI InChI=1S/C21H23Cl2N3O2/c22-17-7-5-8-18(20(17)23)26-14-12-25(13-15-26)11-4-3-10-24-21(28)16-6-1-2-9-19(16)27/h1-9,27H,10-15H2,(H,24,28)/b4-3+	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	0.800	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse-Intramural Research Program Curated by ChEMBL					Assay Description Binding affinity for human dopamine D3 receptor				J Med Chem 48: 839-48 (2005) Article DOI: 10.1021/jm049465g BindingDB Entry DOI: 10.7270/Q27H1J4R
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50161230 (CHEMBL372022 | N-{4-[4-(2,3-Dichloro-phenyl)-piper...) Show SMILES Oc1ccccc1C(=O)NC\C=C\CN1CCN(CC1)c1cccc(Cl)c1Cl Show InChI InChI=1S/C21H23Cl2N3O2/c22-17-7-5-8-18(20(17)23)26-14-12-25(13-15-26)11-4-3-10-24-21(28)16-6-1-2-9-19(16)27/h1-9,27H,10-15H2,(H,24,28)/b4-3+	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6.60	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
National Institute on Drug Abuse-Intramural Research Program Curated by ChEMBL					Assay Description Binding affinity for human dopamine D2 receptor				J Med Chem 48: 839-48 (2005) Article DOI: 10.1021/jm049465g BindingDB Entry DOI: 10.7270/Q27H1J4R
					More data for this Ligand-Target Pair