null

SMILES: [H][C@]12CCc3cc(O)ccc3[C@]1([H])CCN2CCCCNC(=O)c1ccc(cc1)-c1ccccc1

InChI Key: InChIKey=GFWJJPMDPCQZBK-NSOVKSMOSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50216360   

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))	BDBM50216360 (CHEMBL97856) Show SMILES [H][C@]12CCc3cc(O)ccc3[C@]1([H])CCN2CCCCNC(=O)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C29H32N2O2/c32-25-13-14-26-24(20-25)12-15-28-27(26)16-19-31(28)18-5-4-17-30-29(33)23-10-8-22(9-11-23)21-6-2-1-3-7-21/h1-3,6-11,13-14,20,27-28,32H,4-5,12,15-19H2,(H,30,33)/t27-,28-/m0/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	13	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity at Dopamine receptor D3 expressed in CHO cells by [125I]iodosulpiride displacement.				Bioorg Med Chem Lett 8: 2859-64 (1998) BindingDB Entry DOI: 10.7270/Q2319Z1B
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50216360 (CHEMBL97856) Show SMILES [H][C@]12CCc3cc(O)ccc3[C@]1([H])CCN2CCCCNC(=O)c1ccc(cc1)-c1ccccc1 Show InChI InChI=1S/C29H32N2O2/c32-25-13-14-26-24(20-25)12-15-28-27(26)16-19-31(28)18-5-4-17-30-29(33)23-10-8-22(9-11-23)21-6-2-1-3-7-21/h1-3,6-11,13-14,20,27-28,32H,4-5,12,15-19H2,(H,30,33)/t27-,28-/m0/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	316	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
SmithKline Beecham Pharmaceuticals Curated by ChEMBL					Assay Description Binding affinity at Dopamine receptor D2 expressed in CHO cells by [125I]iodosulpiride displacement.				Bioorg Med Chem Lett 8: 2859-64 (1998) BindingDB Entry DOI: 10.7270/Q2319Z1B
					More data for this Ligand-Target Pair