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Report error Found 33 Enz. Inhib. hit(s) with all data for entry = 50037974
TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
Affinity DataIC50:  2.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213558(2-[N-(2,3-dihydro-1,4-benzodioxin-6-yl)-pyrrol-2-y...)
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 ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
Affinity DataIC50:  6.20E+3nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank
PDB3D3D Structure (crystal)

TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedPDB3D3D Structure (crystal)

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371165(CHEMBL236237)
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 ArticlePubMed

TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
Affinity DataIC50:  1.06E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
Affinity DataIC50:  1.65E+4nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
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 ArticlePubMed

TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213563(2-(N-(2-fluorophenyl)pyrrol-2-yl) acetic acid | CH...)
Affinity DataIC50:  1.98E+4nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213559(2-(N-(2-Ffuorophenyl)pyrrol-3-yl) acetic acid | CH...)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371167(CHEMBL236030)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371164(CHEMBL413980)
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 ArticlePubMed

TargetProstaglandin G/H synthase 1(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of COX1 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371173(CHEMBL397792)
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 ArticlePubMed

TargetProstaglandin G/H synthase 2(Human)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of COX2 in human whole blood after 15 minsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50009859((+-)-2-(p-isobutylphenyl)propionic acid | (+-)-alp...)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371166(CHEMBL236444)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371171(CHEMBL235586)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371162(CHEMBL394393)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213566(2-(2,3-dihydro-1,4-benzodioxin-6-yl) acetic acid |...)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371163(CHEMBL236239)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371161(CHEMBL236235)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371170(CHEMBL236029)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371174(CHEMBL236236)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371169(CHEMBL235588)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371172(CHEMBL236434)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50213553((S)-2-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)propano...)
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 ArticlePubMed

TargetDehydrogenase/reductase SDR family member 9(Rat)
Universitat De Barcelona

Curated by ChEMBL
LigandPNGBDBM50371168(CHEMBL236445)
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 ArticlePubMed