null

SMILES: C(CCc1ccccc1)CC#CCCc1cnc[nH]1

InChI Key: InChIKey=MSBRTBBFZFRZEJ-UHFFFAOYSA-N

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50070216   

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))	BDBM50070216 (4-(8-Phenyl-oct-3-ynyl)-1H-imidazole | CHEMBL14811) Show SMILES C(CCc1ccccc1)CC#CCCc1cnc[nH]1 Show InChI InChI=1S/C17H20N2/c1(2-4-9-13-17-14-18-15-19-17)3-6-10-16-11-7-5-8-12-16/h5,7-8,11-12,14-15H,1,3,6,9-10,13H2,(H,18,19)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	Article PubMed	3.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Gliatech Inc. Curated by ChEMBL					Assay Description Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.				J Med Chem 42: 903-9 (1999) Article DOI: 10.1021/jm980310g BindingDB Entry DOI: 10.7270/Q2ST7P1D
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50070216 (4-(8-Phenyl-oct-3-ynyl)-1H-imidazole | CHEMBL14811) Show SMILES C(CCc1ccccc1)CC#CCCc1cnc[nH]1 Show InChI InChI=1S/C17H20N2/c1(2-4-9-13-17-14-18-15-19-17)3-6-10-16-11-7-5-8-12-16/h5,7-8,11-12,14-15H,1,3,6,9-10,13H2,(H,18,19)	Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents	PubMed	3.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Gliatech Inc. Curated by ChEMBL					Assay Description Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptor				Bioorg Med Chem Lett 8: 1133-8 (1999) BindingDB Entry DOI: 10.7270/Q2GF0SPX
					More data for this Ligand-Target Pair