Compile Data Set for Download or QSAR
Found 21 with Last Name = 'hendriks' and Initial = 'cm'
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124574(CHEMBL3623737)copy SMILEScopy InChI
Affinity DataIC50: 35nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124577(CHEMBL3623738)copy SMILEScopy InChI
Affinity DataIC50: 36nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124575(CHEMBL3623735)copy SMILEScopy InChI
Affinity DataIC50: 57nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C3(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124576(CHEMBL3623736)copy SMILEScopy InChI
Affinity DataIC50: 86nMAssay Description:Inhibition of recombinant AKR1C3 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124577(CHEMBL3623738)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124575(CHEMBL3623735)copy SMILEScopy InChI
Affinity DataIC50: 270nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124575(CHEMBL3623735)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of COX1 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124575(CHEMBL3623735)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of COX2 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124576(CHEMBL3623736)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAldo-keto reductase family 1 member C2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124574(CHEMBL3623737)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of recombinant AKR1C2 (unknown origin) using S-tetralol as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124577(CHEMBL3623738)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of COX1 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124574(CHEMBL3623737)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX1 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124574(CHEMBL3623737)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX2 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124577(CHEMBL3623738)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX2 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124576(CHEMBL3623736)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX2 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124576(CHEMBL3623736)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX1 (unknown origin) using arachidonic acid substrate by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAcid-sensing ion channel 5(Rattus norvegicus)
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM17636(2-{[3-(trifluoromethyl)phenyl]amino}benzoic acid |...)copy SMILEScopy InChI
Affinity DataEC50:  2.60E+6nMAssay Description:Binding affinity to rat bile acid-sensitive ion channel expressed in xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAcid-sensing ion channel 5(Rattus norvegicus)
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124575(CHEMBL3623735)copy SMILEScopy InChI
Affinity DataEC50:  1.40E+6nMAssay Description:Binding affinity to rat bile acid-sensitive ion channel expressed in xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAcid-sensing ion channel 5(Rattus norvegicus)
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124576(CHEMBL3623736)copy SMILEScopy InChI
Affinity DataEC50:  2.90E+6nMAssay Description:Binding affinity to rat bile acid-sensitive ion channel expressed in xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAcid-sensing ion channel 5(Rattus norvegicus)
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124574(CHEMBL3623737)copy SMILEScopy InChI
Affinity DataEC50:  2.80E+6nMAssay Description:Binding affinity to rat bile acid-sensitive ion channel expressed in xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed
TargetAcid-sensing ion channel 5(Rattus norvegicus)
RWTH Aachen University

Curated by ChEMBL
LigandPNGBDBM50124577(CHEMBL3623738)copy SMILEScopy InChI
Affinity DataEC50:  2.60E+6nMAssay Description:Binding affinity to rat bile acid-sensitive ion channel expressed in xenopus oocytesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M04786PubMed