null

SMILES: C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccccc1

InChI Key: InChIKey=AQDOKZUTZTUMSW-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50303989   

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))	BDBM50303989 (2-Benzyl-5-piperazin-1-yl-1H-benzimidazole | CHEMB...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccccc1 Show InChI InChI=1S/C18H20N4/c1-2-4-14(5-3-1)12-18-20-16-7-6-15(13-17(16)21-18)22-10-8-19-9-11-22/h1-7,13,19H,8-12H2,(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))	BDBM50303989 (2-Benzyl-5-piperazin-1-yl-1H-benzimidazole | CHEMB...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccccc1 Show InChI InChI=1S/C18H20N4/c1-2-4-14(5-3-1)12-18-20-16-7-6-15(13-17(16)21-18)22-10-8-19-9-11-22/h1-7,13,19H,8-12H2,(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