Compile Data Set for Download or QSAR
Found 33 of ic50 data for polymerid = 50001366
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50111440(4-(1-carbamoyl-4-methylpentanamide-2-yl-cyclopropy...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Inhibition of p53 binding to Glutathione S-transferase 2 (hdm2-GST)More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CN74NDPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088969(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(1-ethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088974(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(3-oxo-1-...)copy SMILEScopy InChI
Affinity DataIC50: 8.40E+3nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088966(2-[2-(4-Amino-4-carboxy-butyrylamino)-2-(carboxyme...)copy SMILEScopy InChI
Affinity DataIC50: 1.91E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088967(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(4-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 3.19E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361799(CHEMBL1938640)copy SMILEScopy InChI
Affinity DataIC50: 3.31E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361800(CHEMBL1938641)copy SMILEScopy InChI
Affinity DataIC50: 3.78E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088971(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(3-oxo-1-...)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088976(2-[2-(4-Amino-4-carboxy-butyrylamino)-2-(carboxyme...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088975(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(1-isopro...)copy SMILEScopy InChI
Affinity DataIC50: 6.60E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361798(CHEMBL1938639)copy SMILEScopy InChI
Affinity DataIC50: 6.63E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361793(CHEMBL1938634)copy SMILEScopy InChI
Affinity DataIC50: 7.76E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088968(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(1-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+4nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361795(CHEMBL1938636)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361797(CHEMBL1938638)copy SMILEScopy InChI
Affinity DataIC50: 9.42E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361794(CHEMBL1938635)copy SMILEScopy InChI
Affinity DataIC50: 9.63E+4nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361792(CHEMBL1938633)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361812(CHEMBL1938630)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361811(CHEMBL1938629)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361809(CHEMBL1938627)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361801(CHEMBL1938618)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361802(CHEMBL1938619)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361803(CHEMBL1938620)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361804(CHEMBL1938621)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361815(CHEMBL1938622)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361805(CHEMBL1938623)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361806(CHEMBL1938624)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361807(CHEMBL1938625)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361808(CHEMBL1938626)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088970(2-[2-(4-Amino-4-carboxy-butyrylamino)-2-(carboxyme...)copy SMILEScopy InChI
Affinity DataIC50: 1.43E+5nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50361796(CHEMBL1938637)copy SMILEScopy InChI
Affinity DataIC50: 1.79E+5nMAssay Description:Inhibition of human GSTA2 using GSH as substrate after 3 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26D5TDTPubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088973(2-Amino-4-[1-(carboxymethyl-carbamoyl)-2-(3-oxo-cy...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+5nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed
TargetGlutathione S-transferase A2(Homo sapiens (Human))
Pfizer Global Research and Development

Curated by ChEMBL
LigandPNGBDBM50088972(2-[2-(4-Amino-4-carboxy-butyrylamino)-2-(carboxyme...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:The compound was tested for it's inhibitory activity against Onchocerca volvulus Glutathione S-transferase 2More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2BZ6589PubMed