null

SMILES: CN1CCN(CC1)c1ccc2nc([nH]c2c1)C(=O)c1ccccc1

InChI Key: InChIKey=ROBSAPBLDQSRBH-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50303993   

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
5-hydroxytryptamine receptor 7 (Homo sapiens (Human))	BDBM50303993 (CHEMBL577994 | [5-(4-Methylpiperazin-1-yl)-1H-benz...) Show SMILES CN1CCN(CC1)c1ccc2nc([nH]c2c1)C(=O)c1ccccc1 Show InChI InChI=1S/C19H20N4O/c1-22-9-11-23(12-10-22)15-7-8-16-17(13-15)21-19(20-16)18(24)14-5-3-2-4-6-14/h2-8,13H,9-12H2,1H3,(H,20,21)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>500	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Complutense de Madrid Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5HT7 receptor expressed in HEK293 cells by liquid scintillation counting				J Med Chem 53: 1357-69 (2010) Article DOI: 10.1021/jm901672k BindingDB Entry DOI: 10.7270/Q2Z320KQ
					More data for this Ligand-Target Pair
5-hydroxytryptamine receptor 6 (Homo sapiens (Human))	BDBM50303993 (CHEMBL577994 | [5-(4-Methylpiperazin-1-yl)-1H-benz...) Show SMILES CN1CCN(CC1)c1ccc2nc([nH]c2c1)C(=O)c1ccccc1 Show InChI InChI=1S/C19H20N4O/c1-22-9-11-23(12-10-22)15-7-8-16-17(13-15)21-19(20-16)18(24)14-5-3-2-4-6-14/h2-8,13H,9-12H2,1H3,(H,20,21)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	>1.00E+3	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Universidad Complutense de Madrid Curated by ChEMBL					Assay Description Displacement of [3H]LSD from human 5HT6 receptor expressed in HEK293 cells by liquid scintillation counting				J Med Chem 53: 1357-69 (2010) Article DOI: 10.1021/jm901672k BindingDB Entry DOI: 10.7270/Q2Z320KQ
					More data for this Ligand-Target Pair