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Found 52 with Last Name = 'creighton' and Initial = 'dj'
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126960(CHEMBL3629116)
Affinity DataKi:  0.300nMAssay Description:Inhibition of 6-His tagged recombinant human glyoxalase 1 transfected in Escherichia coli BL21 (DE3) assessed as S-D-lactoylglutathione formation by ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126961(CHEMBL3629115)
Affinity DataKi:  1nMAssay Description:Inhibition of 6-His tagged recombinant human glyoxalase 1 transfected in Escherichia coli BL21 (DE3) assessed as S-D-lactoylglutathione formation by ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092826((2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydrox...)
Affinity DataKi:  14nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039111(S-(N-Hydroxy-N-(4-bromophenyl)carbamoyl)glutathion...)
Affinity DataKi:  14nMAssay Description:Tested for inhibitory activity against human erythrocyte glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092826((2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydrox...)
Affinity DataKi:  14nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092827(CHEMBL127840 | S-(N-hexyl-N-hydroxycarbamoyl)gluta...)
Affinity DataKi:  16nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092831(CHEMBL128836 | S-(N-heptyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  18nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  46nMAssay Description:Competitive inhibition of GLO1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039108(S-(N-Hydroxy-N-(4-chlorophenyl)carbamoyl)glutathio...)
Affinity DataKi:  46nMAssay Description:Tested for inhibitory activity against human erythrocyte glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  46nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126957(CHEMBL3629119)
Affinity DataKi:  46nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  46nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50241121((S)-5-((R)-3-(4-bromobenzylthio)-1-(carboxymethyla...)
Affinity DataKi:  80nMAssay Description:Inhibition of GLO1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Bos taurus)
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126960(CHEMBL3629116)
Affinity DataKi:  81nMAssay Description:Inhibition of bovine liver glyoxalase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126958(CHEMBL3629118)
Affinity DataKi:  130nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Bos taurus)
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126961(CHEMBL3629115)
Affinity DataKi:  138nMAssay Description:Inhibition of bovine liver glyoxalase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039113(S-(N-Hydroxy-N-phenylcarbamoyl)glutathione)
Affinity DataKi:  160nMAssay Description:Tested for inhibitory activity against human erythrocyte glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092825(CHEMBL128935 | S-(N-phenyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  160nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092830(CHEMBL129965 | S-(N-pentyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  170nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092822(CHEMBL128447 | S-(N-butyl-N-hydroxycarbamoyl)gluta...)
Affinity DataKi:  180nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50126959(CHEMBL3629117)
Affinity DataKi:  330nMAssay Description:Inhibition of human glyoxalase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092829(CHEMBL129597 | S-(N-propyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  800nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092832(CHEMBL128867 | S-(N-ethyl-N-hydroxycarbamoyl)gluta...)
Affinity DataKi:  1.18E+3nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092826((2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydrox...)
Affinity DataKi:  1.20E+3nMAssay Description:Binding affinity of the compound on yeast glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039111(S-(N-Hydroxy-N-(4-bromophenyl)carbamoyl)glutathion...)
Affinity DataKi:  1.20E+3nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50039111(S-(N-Hydroxy-N-(4-bromophenyl)carbamoyl)glutathion...)
Affinity DataKi:  1.20E+3nMAssay Description:Inhibition constants obtained from using the enediol analogs as competitive inhibitors for the inhibition of thehydrolysis of S-D-lactoylglutathione ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Bos taurus)
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  1.70E+3nMAssay Description:Inhibition of bovine liver glyoxalase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039110(S-(N-Methyl-N-hydroxycarbomyl)ethylglutathione)
Affinity DataKi:  1.70E+3nMAssay Description:Tested for inhibitory activity against human erythrocyte glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092823(CHEMBL129435 | S-(N-methyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  1.70E+3nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50039108(S-(N-Hydroxy-N-(4-chlorophenyl)carbamoyl)glutathio...)
Affinity DataKi:  3.40E+3nMAssay Description:Inhibition constants obtained from using the enediol analogs as competitive inhibitors for the inhibition of thehydrolysis of S-D-lactoylglutathione ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  3.60E+3nMAssay Description:Binding affinity of the compound on yeast glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039108(S-(N-Hydroxy-N-(4-chlorophenyl)carbamoyl)glutathio...)
Affinity DataKi:  3.60E+3nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092826((2S)-2-amino-5-{[(1R)-1-[({[(4-bromophenyl)(hydrox...)
Affinity DataKi:  1.00E+4nMAssay Description:Binding affinity of the compound on Pseudomonas putida glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50039113(S-(N-Hydroxy-N-phenylcarbamoyl)glutathione)
Affinity DataKi:  1.10E+4nMAssay Description:Inhibition constant for the inhibition of the hydrolysis of S-D-lactoylglutathione by glyoxalase IIMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039113(S-(N-Hydroxy-N-phenylcarbamoyl)glutathione)
Affinity DataKi:  1.10E+4nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092825(CHEMBL128935 | S-(N-phenyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  1.10E+4nMAssay Description:Binding affinity of the compound on yeast glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092824(CHEMBL131578 | S-(N-4chlorophenyl-N-hydroxycarbamo...)
Affinity DataKi:  1.60E+4nMAssay Description:Binding affinity of the compound on Pseudomonas putida glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092825(CHEMBL128935 | S-(N-phenyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  2.80E+4nMAssay Description:Binding affinity of the compound on Pseudomonas putida glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039110(S-(N-Methyl-N-hydroxycarbomyl)ethylglutathione)
Affinity DataKi:  6.80E+4nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092823(CHEMBL129435 | S-(N-methyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  6.80E+4nMAssay Description:Binding affinity of the compound on yeast glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092823(CHEMBL129435 | S-(N-methyl-N-hydroxycarbamoyl)glut...)
Affinity DataKi:  8.60E+4nMAssay Description:Binding affinity of the compound on Pseudomonas putida glyoxalase I (GlxI) was determinedMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50092828(CHEMBL419969 | S-(N-hydroxycarbamoyl)glutathione)
Affinity DataKi:  1.83E+5nMAssay Description:Binding affinity for Glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHydroxyacylglutathione hydrolase, mitochondrial(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50039110(S-(N-Methyl-N-hydroxycarbomyl)ethylglutathione)
Affinity DataKi:  4.26E+5nMAssay Description:Inhibition constants obtained from using the enediol analogs as competitive inhibitors for the inhibition of thehydrolysis of S-D-lactoylglutathione ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039115(CHEMBL68824 | S-(N-Methyl-N-hydroxycarbomyl)glutat...)
Affinity DataKi:  6.80E+5nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039114(1,2-Dicarboxy-3-propionylsulfanyl-propyl-ammonium)
Affinity DataKi:  1.98E+6nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039109(S-D-Lactoylglutathione)
Affinity DataKi:  2.23E+6nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039116(CHEMBL68031 | S-D-Lactoylethylglutathione)
Affinity DataKi:  3.16E+6nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLactoylglutathione lyase(Homo sapiens (Human))
Chengdu University

Curated by ChEMBL
LigandPNGBDBM50039112(S-(N-Methyl-N-carbomyl)glutathione)
Affinity DataKi:  5.67E+6nMAssay Description:Tested for inhibitory activity against yeast glyoxalase IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50175526((7-Oxo-cyclohept-1-enyl)-acetic acid (E)-propenyl ...)
Affinity DataIC50:  2.60E+3nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF-7piGST cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutathione S-transferase P(Homo sapiens (Human))
University Of Maryland

Curated by ChEMBL
LigandPNGBDBM50175526((7-Oxo-cyclohept-1-enyl)-acetic acid (E)-propenyl ...)
Affinity DataIC50:  1.08E+4nMAssay Description:Inhibitory concentration against GSTP1-1 overexpressed in MCF7wt cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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