Compile Data Set for Download or QSAR
Found 242 with Last Name = 'heinrich' and Initial = 'dm'
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446016(CHEMBL3103330)copy SMILEScopy InChI
Affinity DataIC50: 3nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446017(CHEMBL3103349)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446018(CHEMBL3103348)copy SMILEScopy InChI
Affinity DataIC50: 12nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446015(CHEMBL3103331)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446014(CHEMBL3103332)copy SMILEScopy InChI
Affinity DataIC50: 13nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446019(CHEMBL3103347)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
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
LigandPNGBDBM50446020(CHEMBL3103346)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446016(CHEMBL3103330)copy SMILEScopy InChI
Affinity DataIC50: 25nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446013(CHEMBL3103334)copy SMILEScopy InChI
Affinity DataIC50: 31nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50445995(CHEMBL3103323)copy SMILEScopy InChI
Affinity DataIC50: 59nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446017(CHEMBL3103349)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446020(CHEMBL3103346)copy SMILEScopy InChI
Affinity DataIC50: 68nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446013(CHEMBL3103334)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446019(CHEMBL3103347)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446015(CHEMBL3103331)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446018(CHEMBL3103348)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446014(CHEMBL3103332)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50446022(CHEMBL3103335)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50445994(CHEMBL3103324)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446031(CHEMBL3103363)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446032(CHEMBL3103362)copy SMILEScopy InChI
Affinity DataIC50: 360nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50445994(CHEMBL3103324)copy SMILEScopy InChI
Affinity DataIC50: 390nMAssay Description:Inhibition of AKR1C3 (unknown origin) expressed in human HCT116 cells assessed as formation of PR-104H from PR-104A preincubated for 2 hrsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
LigandPNGBDBM50445995(CHEMBL3103323)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446021(CHEMBL3103336)copy SMILEScopy InChI
Affinity DataIC50: 480nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446027(CHEMBL1418164)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446023(CHEMBL3103333)copy SMILEScopy InChI
Affinity DataIC50: 530nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446024(CHEMBL3103356)copy SMILEScopy InChI
Affinity DataIC50: 570nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446028(CHEMBL3103345)copy SMILEScopy InChI
Affinity DataIC50: 660nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446034(CHEMBL3103359)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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 C3(Homo sapiens (Human))
University of Auckland

Curated by ChEMBL
LigandPNGBDBM50446035(CHEMBL3103358)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) after 1 hr by competitive fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q25H7HQMPubMed
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
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