BDBM50426668 CHEMBL2326492

SMILES: CN(C)C(=O)CN1CCc2cc3nc(N)sc3cc2CC1

InChI Key: InChIKey=RQPDIRHNVASJQG-UHFFFAOYSA-N

Data: 1 KI  2 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 = 50426668   

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(2) dopamine receptor (Homo sapiens (Human))	BDBM50426668 (CHEMBL2326492) Show SMILES CN(C)C(=O)CN1CCc2cc3nc(N)sc3cc2CC1 Show InChI InChI=1S/C15H20N4OS/c1-18(2)14(20)9-19-5-3-10-7-12-13(21-15(16)17-12)8-11(10)4-6-19/h7-8H,3-6,9H2,1-2H3,(H2,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	5.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Displacement of [3H]raclopride from human D2 dopamine receptor expressed in CHO cell membranes				Bioorg Med Chem Lett 23: 543-7 (2012) Article DOI: 10.1016/j.bmcl.2012.11.023 BindingDB Entry DOI: 10.7270/Q2639R2X
					More data for this Ligand-Target Pair
D(2) dopamine receptor (Homo sapiens (Human))	BDBM50426668 (CHEMBL2326492) Show SMILES CN(C)C(=O)CN1CCc2cc3nc(N)sc3cc2CC1 Show InChI InChI=1S/C15H20N4OS/c1-18(2)14(20)9-19-5-3-10-7-12-13(21-15(16)17-12)8-11(10)4-6-19/h7-8H,3-6,9H2,1-2H3,(H2,16,17)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	7.80E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Antagonist activity at human D2 dopamine receptor expressed in CHO cell membrane by GTPgammaS-binding assay				Bioorg Med Chem Lett 23: 543-7 (2012) Article DOI: 10.1016/j.bmcl.2012.11.023 BindingDB Entry DOI: 10.7270/Q2639R2X
					More data for this Ligand-Target Pair
Potassium voltage-gated channel subfamily H member 2 (Homo sapiens (Human))	BDBM50426668 (CHEMBL2326492) Show SMILES CN(C)C(=O)CN1CCc2cc3nc(N)sc3cc2CC1 Show InChI InChI=1S/C15H20N4OS/c1-18(2)14(20)9-19-5-3-10-7-12-13(21-15(16)17-12)8-11(10)4-6-19/h7-8H,3-6,9H2,1-2H3,(H2,16,17)	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	>3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of human ERG				Bioorg Med Chem Lett 23: 543-7 (2012) Article DOI: 10.1016/j.bmcl.2012.11.023 BindingDB Entry DOI: 10.7270/Q2639R2X
					More data for this Ligand-Target Pair