BDBM50411690 CHEMBL271844

SMILES: Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4ncoc4cc3CC2)n1C

InChI Key: InChIKey=HRBGKICNPOCYPZ-UHFFFAOYSA-N

Data: 3 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 4 hits for monomerid = 50411690   

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))	BDBM50411690 (CHEMBL271844) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4ncoc4cc3CC2)n1C Show InChI InChI=1S/C27H28N6OS/c1-18-7-8-21-22(5-3-6-23(21)29-18)26-30-31-27(32(26)2)35-14-4-11-33-12-9-19-15-24-25(34-17-28-24)16-20(19)10-13-33/h3,5-8,15-17H,4,9-14H2,1-2H3	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
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))	BDBM50411690 (CHEMBL271844) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4ncoc4cc3CC2)n1C Show InChI InChI=1S/C27H28N6OS/c1-18-7-8-21-22(5-3-6-23(21)29-18)26-30-31-27(32(26)2)35-14-4-11-33-12-9-19-15-24-25(34-17-28-24)16-20(19)10-13-33/h3,5-8,15-17H,4,9-14H2,1-2H3	PDB Reactome pathway KEGG UniProtKB/SwissProt UniProtKB/TrEMBL 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
Histamine H1 receptor (Homo sapiens (Human))	BDBM50411690 (CHEMBL271844) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4ncoc4cc3CC2)n1C Show InChI InChI=1S/C27H28N6OS/c1-18-7-8-21-22(5-3-6-23(21)29-18)26-30-31-27(32(26)2)35-14-4-11-33-12-9-19-15-24-25(34-17-28-24)16-20(19)10-13-33/h3,5-8,15-17H,4,9-14H2,1-2H3	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 histamine H1 receptor by FLIPR 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))	BDBM50411690 (CHEMBL271844) Show SMILES Cc1ccc2c(cccc2n1)-c1nnc(SCCCN2CCc3cc4ncoc4cc3CC2)n1C Show InChI InChI=1S/C27H28N6OS/c1-18-7-8-21-22(5-3-6-23(21)29-18)26-30-31-27(32(26)2)35-14-4-11-33-12-9-19-15-24-25(34-17-28-24)16-20(19)10-13-33/h3,5-8,15-17H,4,9-14H2,1-2H3	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	3.98E+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