Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Histamine H3 receptor' and Ligand = 'BDBM50139289'   

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 (Rattus norvegicus (rat))	BDBM50139289 (CHEMBL443817 | Furan-2-carboxylic acid [(R)-2-(4-{...) Show SMILES C[C@@H](NC(=O)c1ccco1)C(=O)N1CCCN(CCCOc2ccc(-c3noc(CCc4ccccc4)n3)c(F)c2)CC1 Show InChI InChI=1S/C32H36FN5O5/c1-23(34-31(39)28-10-5-20-42-28)32(40)38-17-6-15-37(18-19-38)16-7-21-41-25-12-13-26(27(33)22-25)30-35-29(43-36-30)14-11-24-8-3-2-4-9-24/h2-5,8-10,12-13,20,22-23H,6-7,11,14-19,21H2,1H3,(H,34,39)/t23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	0.940	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity for rat histamine H3 receptor on rat cortical cells				Bioorg Med Chem Lett 14: 673-6 (2004) BindingDB Entry DOI: 10.7270/Q2H994MH
					More data for this Ligand-Target Pair
Histamine H3 receptor (Homo sapiens (Human))	BDBM50139289 (CHEMBL443817 | Furan-2-carboxylic acid [(R)-2-(4-{...) Show SMILES C[C@@H](NC(=O)c1ccco1)C(=O)N1CCCN(CCCOc2ccc(-c3noc(CCc4ccccc4)n3)c(F)c2)CC1 Show InChI InChI=1S/C32H36FN5O5/c1-23(34-31(39)28-10-5-20-42-28)32(40)38-17-6-15-37(18-19-38)16-7-21-41-25-12-13-26(27(33)22-25)30-35-29(43-36-30)14-11-24-8-3-2-4-9-24/h2-5,8-10,12-13,20,22-23H,6-7,11,14-19,21H2,1H3,(H,34,39)/t23-/m1/s1	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	7.5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Abbott Laboratories Curated by ChEMBL					Assay Description Binding affinity for human histamine H3 receptor on human colon cells				Bioorg Med Chem Lett 14: 673-6 (2004) BindingDB Entry DOI: 10.7270/Q2H994MH
					More data for this Ligand-Target Pair