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SMILES: [H][C@]12CN(Cc3ccccc3)C[C@]1([H])c1cc(ccc1OC2)C#N

InChI Key: InChIKey=JLHYDFVXCXCPKN-AEFFLSMTSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50216893   

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))	BDBM50216893 (CHEMBL293159) Show SMILES [H][C@]12CN(Cc3ccccc3)C[C@]1([H])c1cc(ccc1OC2)C#N Show InChI InChI=1S/C19H18N2O/c20-9-15-6-7-19-17(8-15)18-12-21(11-16(18)13-22-19)10-14-4-2-1-3-5-14/h1-8,16,18H,10-13H2/t16-,18+/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	2.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre de Recherches de Croissy Curated by ChEMBL					Assay Description Ability to displace [125I]iodosulpiride from human dopamine D3 (hD3) receptor transfected into CHO cells.				Bioorg Med Chem Lett 9: 2059-64 (1999) BindingDB Entry DOI: 10.7270/Q2WD42R1
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50216893 (CHEMBL293159) Show SMILES [H][C@]12CN(Cc3ccccc3)C[C@]1([H])c1cc(ccc1OC2)C#N Show InChI InChI=1S/C19H18N2O/c20-9-15-6-7-19-17(8-15)18-12-21(11-16(18)13-22-19)10-14-4-2-1-3-5-14/h1-8,16,18H,10-13H2/t16-,18+/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	20	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Centre de Recherches de Croissy Curated by ChEMBL					Assay Description Ability to displace [125I]iodosulpiride from human dopamine D2 (hD2) receptor transfected into CHO cells.				Bioorg Med Chem Lett 9: 2059-64 (1999) BindingDB Entry DOI: 10.7270/Q2WD42R1
					More data for this Ligand-Target Pair