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SMILES: O=C1N(CCN2Cc3ccccc3C2)CCN1c1ccc2occc2c1

InChI Key: InChIKey=HHTPKGOFGTYZBP-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50414420   

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))	BDBM50414420 (CHEMBL559004) Show SMILES O=C1N(CCN2Cc3ccccc3C2)CCN1c1ccc2occc2c1 Show InChI InChI=1S/C21H21N3O2/c25-21-23(9-8-22-14-17-3-1-2-4-18(17)15-22)10-11-24(21)19-5-6-20-16(13-19)7-12-26-20/h1-7,12-13H,8-11,14-15H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	126	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Antagonist activity at human dopamine D3 receptor expressed in CHO cells by [35S]GTP-gamma-S-based scintillation spectrometry				Bioorg Med Chem Lett 19: 4011-3 (2009) Article DOI: 10.1016/j.bmcl.2009.06.028 BindingDB Entry DOI: 10.7270/Q2J67J55
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50414420 (CHEMBL559004) Show SMILES O=C1N(CCN2Cc3ccccc3C2)CCN1c1ccc2occc2c1 Show InChI InChI=1S/C21H21N3O2/c25-21-23(9-8-22-14-17-3-1-2-4-18(17)15-22)10-11-24(21)19-5-6-20-16(13-19)7-12-26-20/h1-7,12-13H,8-11,14-15H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Antagonist activity at human dopamine D2 receptor expressed in CHO cells by [35S]GTP-gamma-S-based scintillation spectrometry				Bioorg Med Chem Lett 19: 4011-3 (2009) Article DOI: 10.1016/j.bmcl.2009.06.028 BindingDB Entry DOI: 10.7270/Q2J67J55
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50414420 (CHEMBL559004) Show SMILES O=C1N(CCN2Cc3ccccc3C2)CCN1c1ccc2occc2c1 Show InChI InChI=1S/C21H21N3O2/c25-21-23(9-8-22-14-17-3-1-2-4-18(17)15-22)10-11-24(21)19-5-6-20-16(13-19)7-12-26-20/h1-7,12-13H,8-11,14-15H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	7.94E+3	n/a	n/a	n/a	n/a	n/a	n/a
GlaxoSmithKline Curated by ChEMBL					Assay Description Displacement of [3H]dofetilide from human ERG channel by scintillation proximity assay				Bioorg Med Chem Lett 19: 4011-3 (2009) Article DOI: 10.1016/j.bmcl.2009.06.028 BindingDB Entry DOI: 10.7270/Q2J67J55
					More data for this Ligand-Target Pair