Compile Data Set for Download or QSAR

Found 10 hits of ki for UniProtKB: P15104   

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
Glutamine synthetase (Homo sapiens (Human))	BDBM85288 (Phosphinothricin analog, 1 (L Isomer)) Show SMILES CP([O-])(=O)CCC([NH3+])C([O-])=O Show InChI InChI=1S/C5H12NO4P/c1-11(9,10)3-2-4(6)5(7)8/h4H,2-3,6H2,1H3,(H,7,8)(H,9,10)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	Purchase MCE KEGG PC cid PC sid UniChem Similars		0.220	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM85291 (Phosphinothricin analog, 4 (D,L Isomer)) Show SMILES CP(O)([O-])C1=C[C@]([NH3+])(CC1)C([O-])=O |r,t:4| Show InChI InChI=1S/C7H13NO4P/c1-13(11,12)5-2-3-7(8,4-5)6(9)10/h4,11,13H,2-3,8H2,1H3,(H,9,10)/q-1/t7-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars		0.470	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM85293 (Phosphinothricin analog, 6 (D,L Isomer)) Show SMILES CP(O)([O-])C1=C[C@]([NH3+])(CO1)C([O-])=O |r,t:4| Show InChI InChI=1S/C6H11NO5P/c1-13(10,11)4-2-6(7,3-12-4)5(8)9/h2,10,13H,3,7H2,1H3,(H,8,9)/q-1/t6-/m0/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem		5	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM85290 (Phosphinothricin analog, 3 (L Isomer)) Show SMILES CP(O)([O-])C(=O)CC([NH3+])C([O-])=O Show InChI InChI=1S/C5H11NO5P/c1-12(10,11)4(7)2-3(6)5(8)9/h3,10,12H,2,6H2,1H3,(H,8,9)/q-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars		45	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM85289 (Phosphinothricin analog, 2 (D,L mixture)) Show SMILES CC(CC([NH3+])C([O-])=O)P(C)([O-])=O Show InChI InChI=1S/C6H14NO4P/c1-4(12(2,10)11)3-5(7)6(8)9/h4-5H,3,7H2,1-2H3,(H,8,9)(H,10,11)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars		140	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM85292 (Phosphinothricin analog, 5 (D,L Isomer)) Show SMILES CP(O)([O-])C1=C[C@]([NH3+])(CCC1)C(O)=O |r,t:4| Show InChI InChI=1S/C8H15NO4P/c1-14(12,13)6-3-2-4-8(9,5-6)7(10)11/h5,12,14H,2-4,9H2,1H3,(H,10,11)/q-1/p+1/t8-/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem Similars		310	n/a	n/a	n/a	n/a	n/a	n/a	7.0	n/a
Chevron Chemical Company					Assay Description The enzyme was assayed at pH 7.0 using the pyruvate kinase/lactate dehydroenase coupling system.				Bioorg Chem 18: 154-9 (1990) BindingDB Entry DOI: 10.7270/Q24J0CNF
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM50113828 (CHEMBL311322 | {1-[1-(1-Cyclohexylmethyl-2-hydroxy...) Show SMILES CNC(=O)[C@H](CC(C)C)C[C@H](O)[C@H](CC1CCCCC1)NC(=O)C(Cc1cnc[nH]1)NC(=O)C(Cc1ccccc1)NC(=O)OC(C)(C)C Show InChI InChI=1S/C37H58N6O6/c1-24(2)17-27(33(45)38-6)20-32(44)29(18-25-13-9-7-10-14-25)41-35(47)31(21-28-22-39-23-40-28)42-34(46)30(19-26-15-11-8-12-16-26)43-36(48)49-37(3,4)5/h8,11-12,15-16,22-25,27,29-32,44H,7,9-10,13-14,17-21H2,1-6H3,(H,38,45)(H,39,40)(H,41,47)(H,42,46)(H,43,48)/t27-,29+,30?,31?,32+/m1/s1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	CHEMBL PC cid PC sid UniChem Similars	PubMed	850	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
University of Parma Curated by ChEMBL					Assay Description Compound was tested for binding affinity against Glutamine synthetase				J Med Chem 45: 2469-83 (2002) BindingDB Entry DOI: 10.7270/Q28916J7
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM50019955 (2-ammonio-4-[hydroxy(phosphonomethyl)phosphoryl]bu...) Show SMILES [NH3+]C(CCP([O-])(=O)CP(O)(O)=O)C([O-])=O Show InChI InChI=1S/C5H13NO7P2/c6-4(5(7)8)1-2-14(9,10)3-15(11,12)13/h4H,1-3,6H2,(H,7,8)(H,9,10)(H2,11,12,13)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	7.50E+4	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pennsylvania State University Curated by ChEMBL					Assay Description Compound was evaluated for binding affinity by the inhibition of Glutamine synthetase (Escherichia coli) activity using biosynthetic assay [mixed Non...				J Med Chem 30: 2062-7 (1987) BindingDB Entry DOI: 10.7270/Q2125T7K
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM50019955 (2-ammonio-4-[hydroxy(phosphonomethyl)phosphoryl]bu...) Show SMILES [NH3+]C(CCP([O-])(=O)CP(O)(O)=O)C([O-])=O Show InChI InChI=1S/C5H13NO7P2/c6-4(5(7)8)1-2-14(9,10)3-15(11,12)13/h4H,1-3,6H2,(H,7,8)(H,9,10)(H2,11,12,13)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	2.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pennsylvania State University Curated by ChEMBL					Assay Description Compound was evaluated for binding affinity by the inhibition of Glutamine synthetase (Pea seed) activity using biosynthetic assay [noncompetitive in...				J Med Chem 30: 2062-7 (1987) BindingDB Entry DOI: 10.7270/Q2125T7K
					More data for this Ligand-Target Pair
Glutamine synthetase (Homo sapiens (Human))	BDBM50019955 (2-ammonio-4-[hydroxy(phosphonomethyl)phosphoryl]bu...) Show SMILES [NH3+]C(CCP([O-])(=O)CP(O)(O)=O)C([O-])=O Show InChI InChI=1S/C5H13NO7P2/c6-4(5(7)8)1-2-14(9,10)3-15(11,12)13/h4H,1-3,6H2,(H,7,8)(H,9,10)(H2,11,12,13)/p-1	PDB MMDB Reactome pathway KEGG UniProtKB/SwissProt B.MOAD DrugBank antibodypedia GoogleScholar AffyNet	PC cid PC sid UniChem	PubMed	7.50E+5	n/a	n/a	n/a	n/a	n/a	n/a	n/a	n/a
Pennsylvania State University Curated by ChEMBL					Assay Description Compound was evaluated for binding affinity by the inhibition of Glutamine synthetase (Escherichia coli) activity using biosynthetic assay [mixed Non...				J Med Chem 30: 2062-7 (1987) BindingDB Entry DOI: 10.7270/Q2125T7K
					More data for this Ligand-Target Pair