Compile Data Set for Download or QSAR
Report error Found 25 Enz. Inhib. hit(s) with all data for entry = 50008007
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070046((4aR,10bR)-4,10b-Dimethyl-8-((E)-2-quinolin-3-yl-v...)
Affinity DataIC50: 3.40nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070049((4aR,10bR)-4,10b-Dimethyl-8-((Z)-styryl)-1,4,4a,5,...)
Affinity DataIC50: 6nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I enzyme based on the conversion of [3H]-T to [3H]DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070054((4aR,10bR)-4,10b-Dimethyl-8-phenylethynyl-1,4,4a,5...)
Affinity DataIC50: 21nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I enzyme based on the conversion of [3H]-T to [3H]DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070051((4aR,10bR)-4,10b-Dimethyl-8-((E)-styryl)-1,4,4a,5,...)
Affinity DataIC50: 23nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type I enzyme based on the conversion of [3H]-T to [3H]DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070044((4aR,10bR)-4,10b-Dimethyl-8-((E)-2-quinolin-2-yl-v...)
Affinity DataIC50: 32nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070054((4aR,10bR)-4,10b-Dimethyl-8-phenylethynyl-1,4,4a,5...)
Affinity DataIC50: 52nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070047((4aR,10bR)-8-Furan-2-yl-4,10b-dimethyl-1,4,4a,5,6,...)
Affinity DataIC50: 59nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070055((4aR,10bR)-8-((E)-2-Isoquinolin-4-yl-vinyl)-4,10b-...)
Affinity DataIC50: 63nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070051((4aR,10bR)-4,10b-Dimethyl-8-((E)-styryl)-1,4,4a,5,...)
Affinity DataIC50: 180nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070046((4aR,10bR)-4,10b-Dimethyl-8-((E)-2-quinolin-3-yl-v...)
Affinity DataIC50: 320nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070045(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 520nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070044((4aR,10bR)-4,10b-Dimethyl-8-((E)-2-quinolin-2-yl-v...)
Affinity DataIC50: 550nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070053(((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,10...)
Affinity DataIC50: 870nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070055((4aR,10bR)-8-((E)-2-Isoquinolin-4-yl-vinyl)-4,10b-...)
Affinity DataIC50: 1.34E+3nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070049((4aR,10bR)-4,10b-Dimethyl-8-((Z)-styryl)-1,4,4a,5,...)
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070052(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070048((4aR,10bR)-4,10b-Dimethyl-8-thiophen-2-yl-1,4,4a,5...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070050(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070045(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070048((4aR,10bR)-4,10b-Dimethyl-8-thiophen-2-yl-1,4,4a,5...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070052(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070056(N-tert-Butyl-2-((4aR,10bR)-4,10b-dimethyl-3-oxo-1,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070050(2-((4aR,10bR)-4,10b-Dimethyl-3-oxo-1,2,3,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070047((4aR,10bR)-8-Furan-2-yl-4,10b-dimethyl-1,4,4a,5,6,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 2 as [3H]T to [3H]-DHT conversion human prostate nuclear membraneMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Human)
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070056(N-tert-Butyl-2-((4aR,10bR)-4,10b-dimethyl-3-oxo-1,...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibitory activity against Steroid 5-alpha-reductase type 1 enzyme based on the conversion of [3H]T to [3H]-DHT in nuclear membrane preparations fro...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed