null

SMILES: CCN(CC)CC1Cc2c(C(=O)C1)c1ccccc1n2C

InChI Key: InChIKey=QFCOCPQCMWDBNO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50215389   

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 (Rattus norvegicus (rat))	BDBM50215389 (CHEMBL118477) Show SMILES CCN(CC)CC1Cc2c(C(=O)C1)c1ccccc1n2C Show InChI InChI=1S/C18H24N2O/c1-4-20(5-2)12-13-10-16-18(17(21)11-13)14-8-6-7-9-15(14)19(16)3/h6-9,13H,4-5,10-12H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Santiago de Compostela Curated by ChEMBL					Assay Description Compound was measured for the inhibition of [3H]spiperone binding to striatal membrane Dopamine receptor D2				Bioorg Med Chem Lett 8: 3571-6 (1999) BindingDB Entry DOI: 10.7270/Q26H4JKD
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 2A (Rattus norvegicus (rat))	BDBM50215389 (CHEMBL118477) Show SMILES CCN(CC)CC1Cc2c(C(=O)C1)c1ccccc1n2C Show InChI InChI=1S/C18H24N2O/c1-4-20(5-2)12-13-10-16-18(17(21)11-13)14-8-6-7-9-15(14)19(16)3/h6-9,13H,4-5,10-12H2,1-3H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	<1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad de Santiago de Compostela Curated by ChEMBL					Assay Description Compound was measured for the inhibition of [3H]ketanserin binding to rat frontal cortex membrane (5-HT2A receptor)				Bioorg Med Chem Lett 8: 3571-6 (1999) BindingDB Entry DOI: 10.7270/Q26H4JKD
					More data for this Ligand-Target Pair