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SMILES: CN1CCN(CC1)c1ccc2nc(Cc3ccccc3)[nH]c2c1

InChI Key: InChIKey=QSRZOCWYBAMMSP-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50303988   

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))	BDBM50303988 (2-Benzyl-5-(4-methylpiperazin-1-yl)-1H-benzimidazo...) Show SMILES CN1CCN(CC1)c1ccc2nc(Cc3ccccc3)[nH]c2c1 Show InChI InChI=1S/C19H22N4/c1-22-9-11-23(12-10-22)16-7-8-17-18(14-16)21-19(20-17)13-15-5-3-2-4-6-15/h2-8,14H,9-13H2,1H3,(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))	BDBM50303988 (2-Benzyl-5-(4-methylpiperazin-1-yl)-1H-benzimidazo...) Show SMILES CN1CCN(CC1)c1ccc2nc(Cc3ccccc3)[nH]c2c1 Show InChI InChI=1S/C19H22N4/c1-22-9-11-23(12-10-22)16-7-8-17-18(14-16)21-19(20-17)13-15-5-3-2-4-6-15/h2-8,14H,9-13H2,1H3,(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