Compile Data Set for Download or QSAR

Found 16 hits with Last Name = 'clifton' and Initial = 'ij'   

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
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM26106 (CHEMBL90852 | N-oxalyl glycine, 1a | NOG | Oxalylg...) Show SMILES OC(=O)CNC(=O)C(O)=O Show InChI InChI=1S/C4H5NO5/c6-2(7)1-5-3(8)4(9)10/h1H2,(H,5,8)(H,6,7)(H,9,10)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents Similars	Article PubMed	n/a	n/a	842	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306579 ((R)-2-(carboxyformamido)-3-(4-(2-fluorobenzyloxy)p...) Show SMILES OC(=O)[C@@H](Cc1ccc(OCc2ccccc2F)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C18H16FNO6/c19-14-4-2-1-3-12(14)10-26-13-7-5-11(6-8-13)9-15(17(22)23)20-16(21)18(24)25/h1-8,15H,9-10H2,(H,20,21)(H,22,23)(H,24,25)/t15-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306580 ((R)-3-(4-(4-bromophenylsulfonyloxy)phenyl)-2-(carb...) Show SMILES OC(=O)[C@@H](Cc1ccc(OS(=O)(=O)c2ccc(Br)cc2)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C17H14BrNO8S/c18-11-3-7-13(8-4-11)28(25,26)27-12-5-1-10(2-6-12)9-14(16(21)22)19-15(20)17(23)24/h1-8,14H,9H2,(H,19,20)(H,21,22)(H,23,24)/t14-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.20E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306581 ((R)-3-(4-(4-tert-butylphenylsulfonyloxy)phenyl)-2-...) Show SMILES CC(C)(C)c1ccc(cc1)S(=O)(=O)Oc1ccc(C[C@@H](NC(=O)C(O)=O)C(O)=O)cc1 |r| Show InChI InChI=1S/C21H23NO8S/c1-21(2,3)14-6-10-16(11-7-14)31(28,29)30-15-8-4-13(5-9-15)12-17(19(24)25)22-18(23)20(26)27/h4-11,17H,12H2,1-3H3,(H,22,23)(H,24,25)(H,26,27)/t17-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306582 ((R)-2-(carboxyformamido)-3-(4-(2-oxo-2-(4-(pyrroli...) Show SMILES OC(=O)[C@@H](Cc1ccc(OCC(=O)c2ccc(cc2)N2CCCC2)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C23H24N2O7/c26-20(16-5-7-17(8-6-16)25-11-1-2-12-25)14-32-18-9-3-15(4-10-18)13-19(22(28)29)24-21(27)23(30)31/h3-10,19H,1-2,11-14H2,(H,24,27)(H,28,29)(H,30,31)/t19-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306583 ((R)-2-(carboxyformamido)-3-(4-(phenylsulfonyloxy)p...) Show SMILES OC(=O)[C@@H](Cc1ccc(OS(=O)(=O)c2ccccc2)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C17H15NO8S/c19-15(17(22)23)18-14(16(20)21)10-11-6-8-12(9-7-11)26-27(24,25)13-4-2-1-3-5-13/h1-9,14H,10H2,(H,18,19)(H,20,21)(H,22,23)/t14-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	1.40E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306584 ((R)-2-(carboxyformamido)-3-(4-(2-nitrobenzyloxy)ph...) Show SMILES OC(=O)[C@@H](Cc1ccc(OCc2ccccc2[N+]([O-])=O)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C18H16N2O8/c21-16(18(24)25)19-14(17(22)23)9-11-5-7-13(8-6-11)28-10-12-3-1-2-4-15(12)20(26)27/h1-8,14H,9-10H2,(H,19,21)(H,22,23)(H,24,25)/t14-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem	Article PubMed	n/a	n/a	1.70E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM26110 (N,3-dihydroxybenzamide | aromatic hydroxamic acid,...) Show SMILES ONC(=O)c1cccc(O)c1 Show InChI InChI=1S/C7H7NO3/c9-6-3-1-2-5(4-6)7(10)8-11/h1-4,9,11H,(H,8,10)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE MMDB PC cid PC sid PDB UniChem Similars	Article PubMed	n/a	n/a	1.84E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306585 ((R)-2-(carboxyformamido)-3-(4-(4-fluorophenylsulfo...) Show SMILES OC(=O)[C@@H](Cc1ccc(OS(=O)(=O)c2ccc(F)cc2)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C17H14FNO8S/c18-11-3-7-13(8-4-11)28(25,26)27-12-5-1-10(2-6-12)9-14(16(21)22)19-15(20)17(23)24/h1-8,14H,9H2,(H,19,20)(H,21,22)(H,23,24)/t14-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	Article PubMed	n/a	n/a	2.00E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair
Lysine-specific demethylase 4A (Homo sapiens (Human))	BDBM50306586 ((R)-3-(4-(benzyloxy)phenyl)-2-(carboxyformamido)pr...) Show SMILES OC(=O)[C@@H](Cc1ccc(OCc2ccccc2)cc1)NC(=O)C(O)=O |r| Show InChI InChI=1S/C18H17NO6/c20-16(18(23)24)19-15(17(21)22)10-12-6-8-14(9-7-12)25-11-13-4-2-1-3-5-13/h1-9,15H,10-11H2,(H,19,20)(H,21,22)(H,23,24)/t15-/m1/s1	PDB UniProtKB/SwissProt antibodypedia GoogleScholar AffyNet	CHEMBL MMDB PC cid PC sid PDB UniChem Similars	PDB Article PubMed	n/a	n/a	3.30E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of JMJD2A by MALDI-TOF assay				J Med Chem 53: 1810-8 (2010) Article DOI: 10.1021/jm901680b BindingDB Entry DOI: 10.7270/Q2959HPQ
					More data for this Ligand-Target Pair				3D Structure (crystal)
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM50328019 (2-(3-hydroxypicolinamido)acetic acid | CHEMBL12565...) Show SMILES OC(=O)CNC(=O)c1ncccc1O Show InChI InChI=1S/C8H8N2O4/c11-5-2-1-3-9-7(5)8(14)10-4-6(12)13/h1-3,11H,4H2,(H,10,14)(H,12,13)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	9.11E+4	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM50328018 (2-(3-hydroxyphenyl)-2-mercaptoacetic acid | CHEMBL...) Show SMILES OC(=O)C(S)c1cccc(O)c1 Show InChI InChI=1S/C8H8O3S/c9-6-3-1-2-5(4-6)7(12)8(10)11/h1-4,7,9,12H,(H,10,11)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL KEGG PC cid PC sid UniChem	Article PubMed	n/a	n/a	5.00E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM26113 (2,4 PDCA | cid_10365 | pyridine carboxylate, 6a | ...) Show SMILES OC(=O)c1ccnc(c1)C(O)=O Show InChI InChI=1S/C7H5NO4/c9-6(10)4-1-2-8-5(3-4)7(11)12/h1-3H,(H,9,10)(H,11,12)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	6.25E+5	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM50328021 ((2-Hydroxy-benzoylamino)-acetic acid | 2-(2-hydrox...) Show SMILES OC(=O)CNC(=O)c1ccccc1O Show InChI InChI=1S/C9H9NO4/c11-7-4-2-1-3-6(7)9(14)10-5-8(12)13/h1-4,11H,5H2,(H,10,14)(H,12,13)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE KEGG PC cid PC sid UniChem Patents Similars	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM50328020 (2-(picolinamido)acetic acid | CHEMBL221255) Show SMILES OC(=O)CNC(=O)c1ccccn1 Show InChI InChI=1S/C8H8N2O3/c11-7(12)5-10-8(13)6-3-1-2-4-9-6/h1-4H,5H2,(H,10,13)(H,11,12)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MCE PC cid PC sid UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair
Prolyl hydroxylase EGLN2 (Homo sapiens (Human))	BDBM50328017 (2-(3-HYDROXYPHENYL)-2-OXO-ETHANOIC ACID | 2-(3-hyd...) Show SMILES OC(=O)C(=O)c1cccc(O)c1 Show InChI InChI=1S/C8H6O4/c9-6-3-1-2-5(4-6)7(10)8(11)12/h1-4,9H,(H,11,12)	PDB Reactome pathway KEGG UniProtKB/SwissProt DrugBank antibodypedia GoogleScholar AffyNet	Purchase CHEMBL MMDB PC cid PC sid PDB UniChem Patents	Article PubMed	n/a	n/a	>1.00E+6	n/a	n/a	n/a	n/a	n/a	n/a
University of Oxford Curated by ChEMBL					Assay Description Inhibition of PHD1 by HTRF assay				Bioorg Med Chem Lett 20: 6125-8 (2010) Article DOI: 10.1016/j.bmcl.2010.08.032 BindingDB Entry DOI: 10.7270/Q22B8Z7F
					More data for this Ligand-Target Pair