Compile Data Set for Download or QSAR
Found 92 Enz. Inhib. hit(s) with all data for entry = 50042767
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430719(CHEMBL2333522)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) overexpressed in human HCT116 cells assessed as inhibition of aerobic reduction of dinitrobenzamide...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430718(CHEMBL2333523)copy SMILEScopy InChI
Affinity DataIC50: 15nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) overexpressed in human HCT116 cells assessed as inhibition of aerobic reduction of dinitrobenzamide...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430719(CHEMBL2333522)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) overexpressed in human HCT116 cells assessed as inhibition of aerobic reduction of dinitrobenzamide...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430716(CHEMBL2333525)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) overexpressed in human HCT116 cells assessed as inhibition of aerobic reduction of dinitrobenzamide...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50396700(CHEMBL2172076)copy SMILEScopy InChI
Affinity DataIC50: 24nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) overexpressed in human HCT116 cells assessed as inhibition of aerobic reduction of dinitrobenzamide...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50396700(CHEMBL2172076)copy SMILEScopy InChI
Affinity DataIC50: 52nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430716(CHEMBL2333525)copy SMILEScopy InChI
Affinity DataIC50: 56nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430718(CHEMBL2333523)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430719(CHEMBL2333522)copy SMILEScopy InChI
Affinity DataIC50: 88nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430719(CHEMBL2333522)copy SMILEScopy InChI
Affinity DataIC50: 94nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430722(CHEMBL1726890)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430717(CHEMBL2333524)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM22971(2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of COX1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibition of AKR1C3 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM22971(2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 540nMAssay Description:Inhibition of AKR1C3 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50134036(2-(2,3-Dimethyl-phenylamino)-benzoic acid | 2-(2,3...)copy SMILEScopy InChI
Affinity DataIC50: 560nMAssay Description:Inhibition of AKR1C3 (unknown origin)More data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM22971(2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of COX2 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430714(CHEMBL2333527)copy SMILEScopy InChI
Affinity DataIC50: 1.55E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 2.64E+3nMAssay Description:Inhibition of AKR1C1 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430703(CHEMBL2333919)copy SMILEScopy InChI
Affinity DataIC50: 2.77E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50134036(2-(2,3-Dimethyl-phenylamino)-benzoic acid | 2-(2,3...)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of COX2 (unknown origin)More data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+3nMAssay Description:Inhibition of COX1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 3.14E+3nMAssay Description:Inhibition of AKR1C2 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM22971(2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 3.16E+3nMAssay Description:Inhibition of AKR1C1 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430708(CHEMBL2333533)copy SMILEScopy InChI
Affinity DataIC50: 3.77E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50134036(2-(2,3-Dimethyl-phenylamino)-benzoic acid | 2-(2,3...)copy SMILEScopy InChI
Affinity DataIC50: 3.91E+3nMAssay Description:Inhibition of AKR1C1 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430723(CHEMBL2333924)copy SMILEScopy InChI
Affinity DataIC50: 5.22E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430709(CHEMBL2333532)copy SMILEScopy InChI
Affinity DataIC50: 5.61E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430700(CHEMBL2333922)copy SMILEScopy InChI
Affinity DataIC50: 5.94E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50134036(2-(2,3-Dimethyl-phenylamino)-benzoic acid | 2-(2,3...)copy SMILEScopy InChI
Affinity DataIC50: 6.97E+3nMAssay Description:Inhibition of AKR1C2 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM22971(2-[(2,6-dichloro-3-methylphenyl)amino]benzoic acid...)copy SMILEScopy InChI
Affinity DataIC50: 8.74E+3nMAssay Description:Inhibition of AKR1C2 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430715(CHEMBL2333526)copy SMILEScopy InChI
Affinity DataIC50: 8.98E+3nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+3nMAssay Description:Inhibition of COX2 (unknown origin)More data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430705(CHEMBL2333917)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+4nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430720(CHEMBL2333521)copy SMILEScopy InChI
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430724(CHEMBL2333923)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+4nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430712(CHEMBL2333529)copy SMILEScopy InChI
Affinity DataIC50: 2.12E+4nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50134036(2-(2,3-Dimethyl-phenylamino)-benzoic acid | 2-(2,3...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of COX1 (unknown origin)More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430721(CHEMBL2333519)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C3 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430723(CHEMBL2333924)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430700(CHEMBL2333922)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430703(CHEMBL2333919)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430708(CHEMBL2333533)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430709(CHEMBL2333532)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430714(CHEMBL2333527)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430715(CHEMBL2333526)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430716(CHEMBL2333525)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430717(CHEMBL2333524)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430718(CHEMBL2333523)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50430719(CHEMBL2333522)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of His-tagged human AKR1C2 expressed in Escherichia coli BL21 (DE3) assessed as inhibition of reduction of non-fluorescent ketone probe to...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2H133CXPubMed
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