null

SMILES: O=C(c1nc2c(cccc2[nH]1)N1CCNCC1)c1ccccc1

InChI Key: InChIKey=FZBMMXWYKQENCZ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50303996   

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))	BDBM50303996 (CHEMBL568329 | Phenyl(4-piperazin-1-yl-1H-benzimid...) Show SMILES O=C(c1nc2c(cccc2[nH]1)N1CCNCC1)c1ccccc1 Show InChI InChI=1S/C18H18N4O/c23-17(13-5-2-1-3-6-13)18-20-14-7-4-8-15(16(14)21-18)22-11-9-19-10-12-22/h1-8,19H,9-12H2,(H,20,21)	PDB 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))	BDBM50303996 (CHEMBL568329 | Phenyl(4-piperazin-1-yl-1H-benzimid...) Show SMILES O=C(c1nc2c(cccc2[nH]1)N1CCNCC1)c1ccccc1 Show InChI InChI=1S/C18H18N4O/c23-17(13-5-2-1-3-6-13)18-20-14-7-4-8-15(16(14)21-18)22-11-9-19-10-12-22/h1-8,19H,9-12H2,(H,20,21)	PDB 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