null

SMILES: C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccc2ccccc2c1

InChI Key: InChIKey=LVIVSXZSQFOYOT-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50304005   

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))	BDBM50304005 (2-(2-Naphthylmethyl)-5-piperazin-1-yl-1H-benzimida...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccc2ccccc2c1 Show InChI InChI=1S/C22H22N4/c1-2-4-18-13-16(5-6-17(18)3-1)14-22-24-20-8-7-19(15-21(20)25-22)26-11-9-23-10-12-26/h1-8,13,15,23H,9-12,14H2,(H,24,25)	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))	BDBM50304005 (2-(2-Naphthylmethyl)-5-piperazin-1-yl-1H-benzimida...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1ccc2ccccc2c1 Show InChI InChI=1S/C22H22N4/c1-2-4-18-13-16(5-6-17(18)3-1)14-22-24-20-8-7-19(15-21(20)25-22)26-11-9-23-10-12-26/h1-8,13,15,23H,9-12,14H2,(H,24,25)	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