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Found 7 with Last Name = 'baston' and Initial = 'e'
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50043604((8S,9S,10R,13S,14S,17S)-17-(tert-butylcarbamoyl)-1...)
Affinity DataIC50:  3nMAssay Description:Inhibitory activity against human Steroid 5-alpha-reductase type 2 using 18213 3H testosterone 210 nM as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Rattus norvegicus)
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50043604((8S,9S,10R,13S,14S,17S)-17-(tert-butylcarbamoyl)-1...)
Affinity DataIC50:  45nMAssay Description:Inhibitory activity against rat Steroid 5-alpha-reductase type I using 18213 3H testosterone 210 nM as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50043604((8S,9S,10R,13S,14S,17S)-17-(tert-butylcarbamoyl)-1...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibitory concentration of the compound against human Steroid 5-alpha-reductase type I in DU 145 cell culture using 3H androstenedione 5 nM as subs...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50078264(4-(1-Cyclohexylmethyl-1H-indol-5-yl)-benzoic acid ...)
Affinity DataIC50:  2.10E+6nMAssay Description:Inhibitory concentration of the compound against human Steroid 5-alpha-reductase type I in DU 145 cell culture using 3H androstenedione 5 nM as subs...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50078265(4-(1-Benzhydryl-1H-indol-5-yl)-benzoic acid | CHEM...)
Affinity DataIC50:  2.78E+6nMAssay Description:Inhibitory concentration of the compound against human Steroid 5-alpha-reductase type I in DU 145 cell culture using 3H androstenedione 5 nM as subs...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50078266(4-[1-(1-Propyl-butyl)-1H-indol-5-yl]-benzoic acid ...)
Affinity DataIC50:  3.20E+6nMAssay Description:Inhibitory concentration of the compound against human Steroid 5-alpha-reductase type I in DU 145 cell culture using 3H androstenedione 5 nM as subs...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
UniversitäT Des Saarlandes

Curated by ChEMBL
LigandPNGBDBM50078267(4-(1-Benzyl-1H-indol-5-yl)-benzoic acid | CHEMBL40...)
Affinity DataIC50:  6.20E+6nMAssay Description:Inhibitory activity of the compound against human 5-alpha-reductase type 2 using 18213 3H testosterone 210 nM as substrateMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed