Compile Data Set for Download or QSAR
Found 69 with Last Name = 'minehira' and Initial = 'd'
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50049730(2-(5-(2-methyl-3-phenylallylidene)-4-oxo-2-thioxot...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363064(CHEMBL1944855)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363053(CHEMBL1944862)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363063(CHEMBL1944854)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363066(CHEMBL1944857)copy SMILEScopy InChI
Affinity DataIC50: 190nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363070(CHEMBL1944861)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363065(CHEMBL1944856)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363054(CHEMBL1946959)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363055(CHEMBL1946960)copy SMILEScopy InChI
Affinity DataIC50: 230nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363061(CHEMBL1946966)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363057(CHEMBL1946962)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363060(CHEMBL1946965)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50049730(2-(5-(2-methyl-3-phenylallylidene)-4-oxo-2-thioxot...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363062(CHEMBL1944853)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363069(CHEMBL1944860)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363067(CHEMBL1944858)copy SMILEScopy InChI
Affinity DataIC50: 480nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363072(CHEMBL1944852)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363059(CHEMBL1946964)copy SMILEScopy InChI
Affinity DataIC50: 850nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363067(CHEMBL1944858)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363061(CHEMBL1946966)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363060(CHEMBL1946965)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363062(CHEMBL1944853)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363063(CHEMBL1944854)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363056(CHEMBL1946961)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363057(CHEMBL1946962)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363069(CHEMBL1944860)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363070(CHEMBL1944861)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50049730(2-(5-(2-methyl-3-phenylallylidene)-4-oxo-2-thioxot...)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+3nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363064(CHEMBL1944855)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363055(CHEMBL1946960)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363065(CHEMBL1944856)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363058(CHEMBL1946963)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363072(CHEMBL1944852)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363067(CHEMBL1944858)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363054(CHEMBL1946959)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363059(CHEMBL1946964)copy SMILEScopy InChI
Affinity DataIC50: 5.90E+3nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363066(CHEMBL1944857)copy SMILEScopy InChI
Affinity DataIC50: 6.10E+3nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363054(CHEMBL1946959)copy SMILEScopy InChI
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363056(CHEMBL1946961)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363066(CHEMBL1944857)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363060(CHEMBL1946965)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetBeta-galactosidase(Bos taurus (Bovine))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50204206(CHEMBL3896958)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of bovine liver beta-galactosidase using p-nitrophenyl-glycoside as substrate by spectrophotometric methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4KC4PubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363063(CHEMBL1944854)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363064(CHEMBL1944855)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363058(CHEMBL1946963)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human recombinant AKR1B1 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363059(CHEMBL1946964)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363062(CHEMBL1944853)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363065(CHEMBL1944856)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member A1(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363055(CHEMBL1946960)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+4nMAssay Description:Inhibition of human recombinant AKR1A1 expressed in Escherichia coli BL21 cells using D-glucuronate as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
TargetAldo-keto reductase family 1 member B10(Homo sapiens (Human))
University of Toyama

Curated by ChEMBL
LigandPNGBDBM50363068(CHEMBL1944859)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of recombinant N-His6-tagged AKR1B10 expressed in Escherichia coli BL21 cells using pyridine-3-aldehyde as substrate by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2N58MTGPubMed
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