null

SMILES: Clc1ccc(CCCCN2CCC(Cc3cnc[nH]3)CC2)cc1

InChI Key: InChIKey=QVDDYWBQAKTMIO-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50175857   

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 (GUINEA PIG)	BDBM50175857 (4-((1H-imidazol-4-yl)methyl)-1-(4-(4-chlorophenyl)...) Show SMILES Clc1ccc(CCCCN2CCC(Cc3cnc[nH]3)CC2)cc1 Show InChI InChI=1S/C19H26ClN3/c20-18-6-4-16(5-7-18)3-1-2-10-23-11-8-17(9-12-23)13-19-14-21-15-22-19/h4-7,14-15,17H,1-3,8-13H2,(H,21,22)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	6	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
The Schering Plough Research Institute Curated by ChEMBL					Assay Description Displacement of [3H]-N-alpha-methylhistamine from histamine H3 receptor in guinea pig brain				Bioorg Med Chem Lett 16: 395-9 (2005) Article DOI: 10.1016/j.bmcl.2005.09.076 BindingDB Entry DOI: 10.7270/Q29S1QK1
					More data for this Ligand-Target Pair
Histamine H3 receptor (GUINEA PIG)	BDBM50175857 (4-((1H-imidazol-4-yl)methyl)-1-(4-(4-chlorophenyl)...) Show SMILES Clc1ccc(CCCCN2CCC(Cc3cnc[nH]3)CC2)cc1 Show InChI InChI=1S/C19H26ClN3/c20-18-6-4-16(5-7-18)3-1-2-10-23-11-8-17(9-12-23)13-19-14-21-15-22-19/h4-7,14-15,17H,1-3,8-13H2,(H,21,22)	UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	1.58	n/a	n/a	n/a	n/a	n/a
The Schering Plough Research Institute Curated by ChEMBL					Assay Description Antagonist potency against histamine H3 receptor in an electrically stimulated guinea pig ileum				Bioorg Med Chem Lett 16: 395-9 (2005) Article DOI: 10.1016/j.bmcl.2005.09.076 BindingDB Entry DOI: 10.7270/Q29S1QK1
					More data for this Ligand-Target Pair