Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Histamine H3 receptor' and Ligand = 'BDBM50364965'   

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))	BDBM50364965 (CHEMBL1950644) Show SMILES O=c1ccc(n[nH]1)-c1ccc(OC2CCN(CC2)C2CCCC2)cc1 Show InChI InChI=1S/C20H25N3O2/c24-20-10-9-19(21-22-20)15-5-7-17(8-6-15)25-18-11-13-23(14-12-18)16-3-1-2-4-16/h5-10,16,18H,1-4,11-14H2,(H,22,24)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	5.10	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cephalon, Inc. Curated by ChEMBL					Assay Description Displacement of [3H]NAMH from human histamine H3 receptor expressed in CHO cells				Bioorg Med Chem Lett 22: 1504-9 (2012) Article DOI: 10.1016/j.bmcl.2012.01.026 BindingDB Entry DOI: 10.7270/Q2W37WSF
					More data for this Ligand-Target Pair
Histamine H3 receptor (Rattus norvegicus (rat))	BDBM50364965 (CHEMBL1950644) Show SMILES O=c1ccc(n[nH]1)-c1ccc(OC2CCN(CC2)C2CCCC2)cc1 Show InChI InChI=1S/C20H25N3O2/c24-20-10-9-19(21-22-20)15-5-7-17(8-6-15)25-18-11-13-23(14-12-18)16-3-1-2-4-16/h5-10,16,18H,1-4,11-14H2,(H,22,24)	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	7	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Cephalon, Inc. Curated by ChEMBL					Assay Description Displacement of [3H]NAMH from rat histamine H3 receptor expressed in CHO cells				Bioorg Med Chem Lett 22: 1504-9 (2012) Article DOI: 10.1016/j.bmcl.2012.01.026 BindingDB Entry DOI: 10.7270/Q2W37WSF
					More data for this Ligand-Target Pair