Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Ephrin type-B receptor 4' and Ligand = 'BDBM50293240'   

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
Ephrin type-B receptor 4 (Homo sapiens (Human))	BDBM50293240 (CHEMBL523088 | N-(3-(4-(5-chlorobenzo[d][1,3]dioxo...) Show SMILES CS(=O)(=O)Nc1cc(Nc2nccc(Nc3c4OCOc4ccc3Cl)n2)cc(c1)S(C)(=O)=O Show InChI InChI=1S/C19H18ClN5O6S2/c1-32(26,27)13-8-11(7-12(9-13)25-33(2,28)29)22-19-21-6-5-16(24-19)23-17-14(20)3-4-15-18(17)31-10-30-15/h3-9,25H,10H2,1-2H3,(H2,21,22,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	12	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of EphB4				Bioorg Med Chem Lett 18: 5717-21 (2009) Article DOI: 10.1016/j.bmcl.2008.09.087 BindingDB Entry DOI: 10.7270/Q2N016JJ
					More data for this Ligand-Target Pair
Ephrin type-B receptor 4 (Homo sapiens (Human))	BDBM50293240 (CHEMBL523088 | N-(3-(4-(5-chlorobenzo[d][1,3]dioxo...) Show SMILES CS(=O)(=O)Nc1cc(Nc2nccc(Nc3c4OCOc4ccc3Cl)n2)cc(c1)S(C)(=O)=O Show InChI InChI=1S/C19H18ClN5O6S2/c1-32(26,27)13-8-11(7-12(9-13)25-33(2,28)29)22-19-21-6-5-16(24-19)23-17-14(20)3-4-15-18(17)31-10-30-15/h3-9,25H,10H2,1-2H3,(H2,21,22,23,24)	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.05E+3	n/a	n/a	n/a	n/a	n/a	n/a
AstraZeneca Curated by ChEMBL					Assay Description Inhibition of Myc-His-tagged EphB4 expressed in CHOK1 cells assessed as phosphorylation by ELISA				Bioorg Med Chem Lett 18: 5717-21 (2009) Article DOI: 10.1016/j.bmcl.2008.09.087 BindingDB Entry DOI: 10.7270/Q2N016JJ
					More data for this Ligand-Target Pair