Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Histamine H3 receptor' and Ligand = 'BDBM50186288'   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kJ/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Histamine H3 receptor (Homo sapiens (Human))	BDBM50186288 (2-(methylsulfonyl)-7-(3-(piperidin-1-yl)propoxy)-1...) Show SMILES CS(=O)(=O)N1CCc2ccc(OCCCN3CCCCC3)cc2C1 Show InChI InChI=1S/C18H28N2O3S/c1-24(21,22)20-12-8-16-6-7-18(14-17(16)15-20)23-13-5-11-19-9-3-2-4-10-19/h6-7,14H,2-5,8-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	23.8	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]N-alpha-methylhistamine from human cloned H3 receptor				Bioorg Med Chem Lett 16: 3415-8 (2006) Article DOI: 10.1016/j.bmcl.2006.04.004 BindingDB Entry DOI: 10.7270/Q2WM1D07
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50186288 (2-(methylsulfonyl)-7-(3-(piperidin-1-yl)propoxy)-1...) Show SMILES CS(=O)(=O)N1CCc2ccc(OCCCN3CCCCC3)cc2C1 Show InChI InChI=1S/C18H28N2O3S/c1-24(21,22)20-12-8-16-6-7-18(14-17(16)15-20)23-13-5-11-19-9-3-2-4-10-19/h6-7,14H,2-5,8-13,15H2,1H3	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	74.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Lilly Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]N-alpha-methylhistamine from rat cloned H3 receptor				Bioorg Med Chem Lett 16: 3415-8 (2006) Article DOI: 10.1016/j.bmcl.2006.04.004 BindingDB Entry DOI: 10.7270/Q2WM1D07
					More data for this Ligand-Target Pair