Compile Data Set for Download or QSAR

Found 5 hits of ic50 for UniProtKB: P54764   

Target/Host (Institution)	Ligand	Target/Host Links	Ligand Links	Trg + Lig Links	Ki nM	ΔG° kcal/mole	IC50 nM	Kd nM	EC50/IC50 nM	koff s-1	kon M-1s-1	pH	Temp °C
Ephrin type-A receptor 4 [1-949,A922V] (Homo sapiens (Human))	BDBM11985 (4-(2,5-dimethyl-1H-pyrrol-1-yl)-2-hydroxybenzoic a...) Show SMILES Cc1ccc(C)n1-c1ccc(C(O)=O)c(O)c1 Show InChI InChI=1S/C13H13NO3/c1-8-3-4-9(2)14(8)10-5-6-11(13(16)17)12(15)7-10/h3-7,15H,1-2H3,(H,16,17)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.30E+3	n/a	n/a	n/a	n/a	7.5	n/a
Sanford-Burnham Medical Research Institute					Assay Description Protein A-coasted wells (from Pierce Biotechnology) were used to immobilize Eph receptor Fc fusion proteins (from R&D systems)incubated at 1 ug/ml in...				Chem Biol Drug Des 78: 667-78 (2011) Article DOI: 10.1111/j.1747-0285.2011.01199.x BindingDB Entry DOI: 10.7270/Q2FN14QN
					More data for this Ligand-Target Pair
Ephrin type-A receptor 4 [1-949,A922V] (Homo sapiens (Human))	BDBM82187 (Salicylic acid derivative, 76D10) Show SMILES OC(=O)c1cc(ccc1O)-c1ccc(\C=C\C(=O)\C=C\c2ccc(o2)-c2ccc(O)c(c2)C(O)=O)o1 Show InChI InChI=1S/C27H18O9/c28-17(3-5-18-7-11-24(35-18)15-1-9-22(29)20(13-15)26(31)32)4-6-19-8-12-25(36-19)16-2-10-23(30)21(14-16)27(33)34/h1-14,29-30H,(H,31,32)(H,33,34)/b5-3+,6-4+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.60E+3	n/a	n/a	n/a	n/a	7.5	n/a
Sanford-Burnham Medical Research Institute					Assay Description Protein A-coasted wells (from Pierce Biotechnology) were used to immobilize Eph receptor Fc fusion proteins (from R&D systems)incubated at 1 ug/ml in...				Chem Biol Drug Des 78: 667-78 (2011) Article DOI: 10.1111/j.1747-0285.2011.01199.x BindingDB Entry DOI: 10.7270/Q2FN14QN
					More data for this Ligand-Target Pair
Ephrin type-A receptor 4 [1-949,A922V] (Homo sapiens (Human))	BDBM82190 (Salicylic acid derivative, compound 2) Show SMILES Cc1ccc(C)n1-c1ccc(O)c(c1)C(O)=O Show InChI InChI=1S/C13H13NO3/c1-8-3-4-9(2)14(8)10-5-6-12(15)11(7-10)13(16)17/h3-7,15H,1-2H3,(H,16,17)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	Purchase MCE PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	7.5	n/a
Sanford-Burnham Medical Research Institute					Assay Description Protein A-coasted wells (from Pierce Biotechnology) were used to immobilize Eph receptor Fc fusion proteins (from R&D systems)incubated at 1 ug/ml in...				Chem Biol Drug Des 78: 667-78 (2011) Article DOI: 10.1111/j.1747-0285.2011.01199.x BindingDB Entry DOI: 10.7270/Q2FN14QN
					More data for this Ligand-Target Pair
Ephrin type-A receptor 4 [1-949,A922V] (Homo sapiens (Human))	BDBM82188 (Salicylic acid derivative, 76A5) Show SMILES OC(=O)\C=C\c1ccc(o1)-c1ccc(O)c(c1)C(O)=O Show InChI InChI=1S/C14H10O6/c15-11-4-1-8(7-10(11)14(18)19)12-5-2-9(20-12)3-6-13(16)17/h1-7,15H,(H,16,17)(H,18,19)/b6-3+	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	7.5	n/a
Sanford-Burnham Medical Research Institute					Assay Description Protein A-coasted wells (from Pierce Biotechnology) were used to immobilize Eph receptor Fc fusion proteins (from R&D systems)incubated at 1 ug/ml in...				Chem Biol Drug Des 78: 667-78 (2011) Article DOI: 10.1111/j.1747-0285.2011.01199.x BindingDB Entry DOI: 10.7270/Q2FN14QN
					More data for this Ligand-Target Pair
Ephrin type-A receptor 4 [1-949,A922V] (Homo sapiens (Human))	BDBM82189 (Salicylic acid derivative, 76B8) Show SMILES OC(=O)c1ccc(o1)-c1ccc(O)c(c1)C(O)=O Show InChI InChI=1S/C12H8O6/c13-8-2-1-6(5-7(8)11(14)15)9-3-4-10(18-9)12(16)17/h1-5,13H,(H,14,15)(H,16,17)	PDB MMDB UniProtKB/SwissProt B.MOAD GoogleScholar AffyNet	PC cid PC sid UniChem	Article PubMed	n/a	n/a	>5.00E+5	n/a	n/a	n/a	n/a	7.5	n/a
Sanford-Burnham Medical Research Institute					Assay Description Protein A-coasted wells (from Pierce Biotechnology) were used to immobilize Eph receptor Fc fusion proteins (from R&D systems)incubated at 1 ug/ml in...				Chem Biol Drug Des 78: 667-78 (2011) Article DOI: 10.1111/j.1747-0285.2011.01199.x BindingDB Entry DOI: 10.7270/Q2FN14QN
					More data for this Ligand-Target Pair