Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Hydroxycarboxylic acid receptor 2' and Ligand = 'BDBM50227779'   

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
Hydroxycarboxylic acid receptor 2 (Homo sapiens (Human))	BDBM50227779 (2-(1-(quinoxalin-2-yl)-1,4-diazepane-4-carboxamido...) Show SMILES OC(=O)c1ccccc1NC(=O)N1CCCN(CC1)c1cnc2ccccc2n1 Show InChI InChI=1S/C21H21N5O3/c27-20(28)15-6-1-2-7-16(15)24-21(29)26-11-5-10-25(12-13-26)19-14-22-17-8-3-4-9-18(17)23-19/h1-4,6-9,14H,5,10-13H2,(H,24,29)(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	800	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Displacement of [3H]niacin from human GPR109A				Bioorg Med Chem Lett 17: 6723-8 (2008) Article DOI: 10.1016/j.bmcl.2007.10.055 BindingDB Entry DOI: 10.7270/Q2R2114Q
					More data for this Ligand-Target Pair
Hydroxycarboxylic acid receptor 2 (Homo sapiens (Human))	BDBM50227779 (2-(1-(quinoxalin-2-yl)-1,4-diazepane-4-carboxamido...) Show SMILES OC(=O)c1ccccc1NC(=O)N1CCCN(CC1)c1cnc2ccccc2n1 Show InChI InChI=1S/C21H21N5O3/c27-20(28)15-6-1-2-7-16(15)24-21(29)26-11-5-10-25(12-13-26)19-14-22-17-8-3-4-9-18(17)23-19/h1-4,6-9,14H,5,10-13H2,(H,24,29)(H,27,28)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	n/a	n/a	4.60E+3	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Agonist activity at human GPR106A by [35S]GTPgammaS binding assay				Bioorg Med Chem Lett 17: 6723-8 (2008) Article DOI: 10.1016/j.bmcl.2007.10.055 BindingDB Entry DOI: 10.7270/Q2R2114Q
					More data for this Ligand-Target Pair