Compile Data Set for Download or QSAR
Found 33 Enz. Inhib. hit(s) with all data for entry = 50037974
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 2.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371165(CHEMBL236237)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 1.06E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)copy SMILEScopy InChI
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371167(CHEMBL236030)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371164(CHEMBL413980)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371173(CHEMBL397792)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetProstaglandin G/H synthase 2(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371166(CHEMBL236444)copy SMILEScopy InChI
Affinity DataIC50: 1.29E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371171(CHEMBL235586)copy SMILEScopy InChI
Affinity DataIC50: 2.09E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371162(CHEMBL394393)copy SMILEScopy InChI
Affinity DataIC50: 2.09E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)copy SMILEScopy InChI
Affinity DataIC50: 2.18E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371163(CHEMBL236239)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371161(CHEMBL236235)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371170(CHEMBL236029)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+5nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371174(CHEMBL236236)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371169(CHEMBL235588)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371172(CHEMBL236434)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed
TargetDehydrogenase/reductase SDR family member 9(Rattus norvegicus)
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50371168(CHEMBL236445)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of rat liver 3-alpha-HSD assessed as 5-beta-dihydrocortisone reductionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VH5PN7PubMed