BDBM50146141 4-(3-Butoxy-propyl)-1H-imidazole; compound with (Z)-but-2-enedioic acid::CHEMBL314526

SMILES: CCCCOCCCc1cnc[nH]1

InChI Key: InChIKey=OVWICVLHNAZEKN-UHFFFAOYSA-N

Data: 1 KI  1 EC50

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 2 hits for monomerid = 50146141   

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 (Rattus norvegicus (rat))	BDBM50146141 (4-(3-Butoxy-propyl)-1H-imidazole; compound with (Z...) Show SMILES CCCCOCCCc1cnc[nH]1 Show InChI InChI=1S/C10H18N2O/c1-2-3-6-13-7-4-5-10-8-11-9-12-10/h8-9H,2-7H2,1H3,(H,11,12)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	56	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Freie Universität Berlin Curated by ChEMBL					Assay Description In vitro binding affinity against rat histamine H3 receptor				J Med Chem 47: 2678-87 (2004) Article DOI: 10.1021/jm031065q BindingDB Entry DOI: 10.7270/Q2SQ8ZTC
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50146141 (4-(3-Butoxy-propyl)-1H-imidazole; compound with (Z...) Show SMILES CCCCOCCCc1cnc[nH]1 Show InChI InChI=1S/C10H18N2O/c1-2-3-6-13-7-4-5-10-8-11-9-12-10/h8-9H,2-7H2,1H3,(H,11,12)	Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	n/a	n/a	311	n/a	n/a	n/a	n/a
Freie Universität Berlin Curated by ChEMBL					Assay Description Effect on specific [35S]-GTP-gammaS, Binding to HEK293 cell membranes expressing the human Histamine H3 receptor				J Med Chem 47: 2678-87 (2004) Article DOI: 10.1021/jm031065q BindingDB Entry DOI: 10.7270/Q2SQ8ZTC
					More data for this Ligand-Target Pair