Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Glutamate receptor ionotropic, NMDA 2B' and Ligand = 'BDBM50212690'   

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
Glutamate receptor ionotropic, NMDA 2B (Homo sapiens (Human))	BDBM50212690 (2-(3-chloro-4-(trifluoromethoxy)phenyl)-5-(2-(trif...) Show SMILES FC(F)(F)Oc1ccc(cc1Cl)C1=NC(CN1)c1ccccc1C(F)(F)F |t:13| Show InChI InChI=1S/C17H11ClF6N2O/c18-12-7-9(5-6-14(12)27-17(22,23)24)15-25-8-13(26-15)10-3-1-2-4-11(10)16(19,20)21/h1-7,13H,8H2,(H,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	353	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Binding affinity to NMDA NR2B receptor				Bioorg Med Chem Lett 17: 3997-4000 (2007) Article DOI: 10.1016/j.bmcl.2007.04.084 BindingDB Entry DOI: 10.7270/Q21J99GV
					More data for this Ligand-Target Pair
Glutamate receptor ionotropic, NMDA 2B (Homo sapiens (Human))	BDBM50212690 (2-(3-chloro-4-(trifluoromethoxy)phenyl)-5-(2-(trif...) Show SMILES FC(F)(F)Oc1ccc(cc1Cl)C1=NC(CN1)c1ccccc1C(F)(F)F |t:13| Show InChI InChI=1S/C17H11ClF6N2O/c18-12-7-9(5-6-14(12)27-17(22,23)24)15-25-8-13(26-15)10-3-1-2-4-11(10)16(19,20)21/h1-7,13H,8H2,(H,25,26)	PDB MMDB NCI pathway Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.27E+3	n/a	n/a	n/a	n/a	n/a	n/a
Merck Research Laboratories Curated by ChEMBL					Assay Description Antagonist activity at NMDA NR2B receptor assessed as calcium flux				Bioorg Med Chem Lett 17: 3997-4000 (2007) Article DOI: 10.1016/j.bmcl.2007.04.084 BindingDB Entry DOI: 10.7270/Q21J99GV
					More data for this Ligand-Target Pair