BDBM50414582 CHEMBL564347

SMILES: [H][C@]12CC[C@@](CN(C)CCN3CCN(C3=O)c3ccc4OCOc4c3)(CC1)C2(C)C

InChI Key: InChIKey=ABSKTFYOWZQKEU-QBNMFFNISA-N

Data: 2 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 3 hits for monomerid = 50414582   

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))	BDBM50414582 (CHEMBL564347) Show SMILES [H][C@]12CC[C@@](CN(C)CCN3CCN(C3=O)c3ccc4OCOc4c3)(CC1)C2(C)C |r| Show InChI InChI=1S/C23H33N3O3/c1-22(2)17-6-8-23(22,9-7-17)15-24(3)10-11-25-12-13-26(21(25)27)18-4-5-19-20(14-18)29-16-28-19/h4-5,14,17H,6-13,15-16H2,1-3H3/t17-,23-	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	50.1	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cancer Therapeutics Curated by ChEMBL					Assay Description Antagonist activity at human D3 receptor expressed in CHO cells by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 19: 4799-801 (2009) Article DOI: 10.1016/j.bmcl.2009.06.043 BindingDB Entry DOI: 10.7270/Q2154J9T
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50414582 (CHEMBL564347) Show SMILES [H][C@]12CC[C@@](CN(C)CCN3CCN(C3=O)c3ccc4OCOc4c3)(CC1)C2(C)C |r| Show InChI InChI=1S/C23H33N3O3/c1-22(2)17-6-8-23(22,9-7-17)15-24(3)10-11-25-12-13-26(21(25)27)18-4-5-19-20(14-18)29-16-28-19/h4-5,14,17H,6-13,15-16H2,1-3H3/t17-,23-	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	1.58E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cancer Therapeutics Curated by ChEMBL					Assay Description Antagonist activity at human D2 receptor expressed in CHO cells by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 19: 4799-801 (2009) Article DOI: 10.1016/j.bmcl.2009.06.043 BindingDB Entry DOI: 10.7270/Q2154J9T
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50414582 (CHEMBL564347) Show SMILES [H][C@]12CC[C@@](CN(C)CCN3CCN(C3=O)c3ccc4OCOc4c3)(CC1)C2(C)C |r| Show InChI InChI=1S/C23H33N3O3/c1-22(2)17-6-8-23(22,9-7-17)15-24(3)10-11-25-12-13-26(21(25)27)18-4-5-19-20(14-18)29-16-28-19/h4-5,14,17H,6-13,15-16H2,1-3H3/t17-,23-	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	6.31E+3	n/a	n/a	n/a	n/a	n/a	n/a
Cancer Therapeutics Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human ERG channel by scintillation proximity assay				Bioorg Med Chem Lett 19: 4799-801 (2009) Article DOI: 10.1016/j.bmcl.2009.06.043 BindingDB Entry DOI: 10.7270/Q2154J9T
					More data for this Ligand-Target Pair