null

SMILES: Fc1ccc(cc1C#N)N1CCN(CCN2Cc3ccccc3C2)C1=O

InChI Key: InChIKey=DGTBKKBZRIVWMP-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50414407   

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))	BDBM50414407 (CHEMBL562176) Show SMILES Fc1ccc(cc1C#N)N1CCN(CCN2Cc3ccccc3C2)C1=O Show InChI InChI=1S/C20H19FN4O/c21-19-6-5-18(11-17(19)12-22)25-10-9-24(20(25)26)8-7-23-13-15-3-1-2-4-16(15)14-23/h1-6,11H,7-10,13-14H2	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	15.8	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))	BDBM50414407 (CHEMBL562176) Show SMILES Fc1ccc(cc1C#N)N1CCN(CCN2Cc3ccccc3C2)C1=O Show InChI InChI=1S/C20H19FN4O/c21-19-6-5-18(11-17(19)12-22)25-10-9-24(20(25)26)8-7-23-13-15-3-1-2-4-16(15)14-23/h1-6,11H,7-10,13-14H2	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	794	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))	BDBM50414407 (CHEMBL562176) Show SMILES Fc1ccc(cc1C#N)N1CCN(CCN2Cc3ccccc3C2)C1=O Show InChI InChI=1S/C20H19FN4O/c21-19-6-5-18(11-17(19)12-22)25-10-9-24(20(25)26)8-7-23-13-15-3-1-2-4-16(15)14-23/h1-6,11H,7-10,13-14H2	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	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