null

SMILES: Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4OCCN(c4cc3CC2)S(C)(=O)=O)n1C

InChI Key: InChIKey=UTIUIZHJMLEUQC-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50411684   

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))	BDBM50411684 (CHEMBL272379) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4OCCN(c4cc3CC2)S(C)(=O)=O)n1C Show InChI InChI=1S/C29H34N6O3S2/c1-20-8-9-23-24(6-4-7-25(23)30-20)28-31-32-29(33(28)2)39-17-5-12-34-13-10-21-18-26-27(19-22(21)11-14-34)38-16-15-35(26)40(3,36)37/h4,6-9,18-19H,5,10-17H2,1-3H3	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	12.6	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 by cell based GTPgammaS binding assay				Bioorg Med Chem Lett 18: 901-7 (2008) Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50411684 (CHEMBL272379) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4OCCN(c4cc3CC2)S(C)(=O)=O)n1C Show InChI InChI=1S/C29H34N6O3S2/c1-20-8-9-23-24(6-4-7-25(23)30-20)28-31-32-29(33(28)2)39-17-5-12-34-13-10-21-18-26-27(19-22(21)11-14-34)38-16-15-35(26)40(3,36)37/h4,6-9,18-19H,5,10-17H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>2.51E+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 dopamine D2 receptor by GTPgammaS binding assay				Bioorg Med Chem Lett 18: 901-7 (2008) Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50411684 (CHEMBL272379) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4OCCN(c4cc3CC2)S(C)(=O)=O)n1C Show InChI InChI=1S/C29H34N6O3S2/c1-20-8-9-23-24(6-4-7-25(23)30-20)28-31-32-29(33(28)2)39-17-5-12-34-13-10-21-18-26-27(19-22(21)11-14-34)38-16-15-35(26)40(3,36)37/h4,6-9,18-19H,5,10-17H2,1-3H3	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	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				Bioorg Med Chem Lett 18: 901-7 (2008) Article DOI: 10.1016/j.bmcl.2007.12.066 BindingDB Entry DOI: 10.7270/Q2MK6F32
					More data for this Ligand-Target Pair