null

SMILES: C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1cccc2ccccc12

InChI Key: InChIKey=ZAPRICXOFXFLFL-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50304007   

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))	BDBM50304007 (2-(1-Naphthylmethyl)-5-piperazin-1-yl-1H-benzimida...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1cccc2ccccc12 Show InChI InChI=1S/C22H22N4/c1-2-7-19-16(4-1)5-3-6-17(19)14-22-24-20-9-8-18(15-21(20)25-22)26-12-10-23-11-13-26/h1-9,15,23H,10-14H2,(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))	BDBM50304007 (2-(1-Naphthylmethyl)-5-piperazin-1-yl-1H-benzimida...) Show SMILES C(c1nc2ccc(cc2[nH]1)N1CCNCC1)c1cccc2ccccc12 Show InChI InChI=1S/C22H22N4/c1-2-7-19-16(4-1)5-3-6-17(19)14-22-24-20-9-8-18(15-21(20)25-22)26-12-10-23-11-13-26/h1-9,15,23H,10-14H2,(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