Compile Data Set for Download or QSAR
maximum 50k data
Found 17 Enz. Inhib. hit(s) with all data for entry = 50039674
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)
Affinity DataIC50:  20nMAssay Description:Inhibition of recombinant COX2More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50:  80nMAssay Description:Inhibition of recombinant AKR1C3 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337281(3-[N-(4-nitrophenyl)amino]benzoic acid | CHEMBL168...)
Affinity DataIC50:  740nMAssay Description:Inhibition of recombinant COX2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)
Affinity DataIC50:  2.23E+3nMAssay Description:Inhibition of recombinant COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAndrogen receptor(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50:  4.70E+3nMAssay Description:Antagonist activity at androgen receptor expressed in HeLa-AR3A-PSA-(ARE)4-Luc13 cells assessed as rightward shift of DHT-induced response incubated ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337281(3-[N-(4-nitrophenyl)amino]benzoic acid | CHEMBL168...)
Affinity DataIC50:  6.74E+3nMAssay Description:Inhibition of recombinant AKR1C1 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50:  8.17E+3nMAssay Description:Inhibition of recombinant AKR1C2 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C4(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50:  8.17E+3nMAssay Description:Inhibition of recombinant AKR1C4 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50:  1.11E+4nMAssay Description:Inhibition of recombinant AKR1C1 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337283(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Affinity DataIC50:  2.27E+4nMAssay Description:Inhibition of recombinant AKR1C1 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337281(3-[N-(4-nitrophenyl)amino]benzoic acid | CHEMBL168...)
Affinity DataIC50:  3.08E+4nMAssay Description:Inhibition of recombinant COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C4(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337281(3-[N-(4-nitrophenyl)amino]benzoic acid | CHEMBL168...)
Affinity DataIC50:  3.27E+4nMAssay Description:Inhibition of recombinant AKR1C4 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAldo-keto reductase family 1 member C4(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337283(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Affinity DataIC50:  6.27E+4nMAssay Description:Inhibition of recombinant AKR1C4 assessed as enzyme catalyzed oxidation of S-tetralol by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337283(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50337283(3-[N-(4-trifluoromethylphenyl)amino]benzoic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant COX2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant COX2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Perelman School Of Medicine University Of Pennsylvania

Curated by ChEMBL
LigandPNGBDBM50382163(CHEMBL2023820)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed