BDBM50263899 CHEMBL492030::N-methyl-N-[2-(piperidin-1-yl)ethyl]-1,3-dihydrospiro[indene-2,4'-piperidine]-1'-carboxamide

SMILES: CN(CCN1CCCCC1)C(=O)N1CCC2(Cc3ccccc3C2)CC1

InChI Key: InChIKey=RURNSGIUVDPHQI-UHFFFAOYSA-N

Data: 1 IC50

Find this compound or compounds like it in BindingDB or PDB:

Substructure Similarity at least:  must be >=0.5 Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50263899   

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
Histamine H3 receptor (Homo sapiens (Human))	BDBM50263899 (CHEMBL492030 | N-methyl-N-[2-(piperidin-1-yl)ethyl...) Show SMILES CN(CCN1CCCCC1)C(=O)N1CCC2(Cc3ccccc3C2)CC1 Show InChI InChI=1S/C22H33N3O/c1-23(15-16-24-11-5-2-6-12-24)21(26)25-13-9-22(10-14-25)17-19-7-3-4-8-20(19)18-22/h3-4,7-8H,2,5-6,9-18H2,1H3	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	530	n/a	n/a	n/a	n/a	n/a	n/a
Tsukuba Research Institute Curated by ChEMBL					Assay Description Inverse agonist activity at human cloned histamine H3 receptor assessed as inhibition of (R)-alpha-methylhistamine-induced [35S]GTPgammaS binding				Bioorg Med Chem Lett 18: 5101-6 (2008) Article DOI: 10.1016/j.bmcl.2008.07.125 BindingDB Entry DOI: 10.7270/Q2PC3268
					More data for this Ligand-Target Pair