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Found 93 with Last Name = 'neubauer' and Initial = 'bl'
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50057479(7-Bromo-9,10-dihydro-phenanthrene-2-carboxylic aci...)
Affinity DataKi:  26nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50031890((10R,13S)-17-tert-Butylcarbamoyl-10,13-dimethyl-2,...)
Affinity DataIC50:  8nMAssay Description:Compound was tested for inhibition of Type II 5-alpha-reductase in Human Prostate Homogenates (HPH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50368782(Bexlosteride | CHEMBL24955 | LY-191704)
Affinity DataIC50:  8nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)
Affinity DataIC50:  10nMAssay Description:Compound was tested for inhibition of Type II 5-alpha-reductase in Human Prostate Homogenates (HPH).More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044878(4,8-Dimethyl-1,4,4a,5,6,10b-hexahydro-2H-benzo[f]q...)
Affinity DataIC50:  11nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044879((4aR,10bR)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-...)
Affinity DataIC50:  17nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044879((4aR,10bR)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-...)
Affinity DataIC50:  17nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50070051((4aR,10bR)-4,10b-Dimethyl-8-((E)-styryl)-1,4,4a,5,...)
Affinity DataIC50:  23nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044881(8-Chloro-4-methyl-1,4,5,6-tetrahydro-2H-benzo[f]qu...)
Affinity DataIC50:  30nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044891(8-Fluoro-4-methyl-1,4,4a,5,6,10b-hexahydro-2H-benz...)
Affinity DataIC50:  35nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044885((4aS,10bR)-8-Chloro-4-methyl-1,4,4a,5,6,10b-hexahy...)
Affinity DataIC50:  41nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044886(8-Chloro-1,4,4a,5,6,10b-hexahydro-2H-benzo[f]quino...)
Affinity DataIC50:  60nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50334788((17beta-(N-tert-butylcarbamoyl)-4-aza-5alpha-andro...)
Affinity DataIC50:  62nMAssay Description:Compound was tested for inhibition of Type I 5-alpha-reductase in Human genital skin (Hs68) foreskin fibroblast cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

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 fr...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091707(1-Methyl-5-[4-((E)-styryl)-phenyl]-piperidin-2-one...)
Affinity DataIC50:  107nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044892(8-Methoxy-4-methyl-1,4,4a,5,6,10b-hexahydro-2H-ben...)
Affinity DataIC50:  120nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091704((R)-8-Chloro-4,10b-dimethyl-1,4,6,10b-tetrahydro-2...)
Affinity DataIC50:  120nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044893(8-Chloro-4,10b-dimethyl-1,4,6,10b-tetrahydro-2H-be...)
Affinity DataIC50:  120nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091706(7-((E)-Styryl)-9,10-dihydro-phenanthrene-2-carboxy...)
Affinity DataIC50:  152nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50070051((4aR,10bR)-4,10b-Dimethyl-8-((E)-styryl)-1,4,4a,5,...)
Affinity DataIC50:  180nMAssay Description:Compound was evaluated in vitro for its inhibitory activity against Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091708((4aR,10bR)-8-Chloro-4,10b-dimethyl-1,4,4a,5,6,10b-...)
Affinity DataIC50:  183nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50099216((2S,3S)-1-[2-(3-Benzyloxycarbonyl-phenyl)-acetyl]-...)
Affinity DataIC50:  226nMAssay Description:Concentration required for inhibition of 50% of the cleavage of para-nitroanilide from MeO-Suc-Arg-Pro-Tyr-pNA.HCl by Prostate specific antigen PSAMore data for this Ligand-Target Pair
In DepthDetails Article
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50099216((2S,3S)-1-[2-(3-Benzyloxycarbonyl-phenyl)-acetyl]-...)
Affinity DataIC50:  226nMAssay Description:Concentration required for inhibition of 50% of the cleavage of para-nitroanilide from MeO-Suc-Arg-Pro-Tyr-pNA.HCl by Prostate specific antigen PSAMore data for this Ligand-Target Pair
In DepthDetails Article
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091710(1-Methyl-5-(4-phenylazo-phenyl)-piperidin-2-one | ...)
Affinity DataIC50:  302nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044877(8-Fluoro-4-methyl-1,4,4a,5,6,10b-hexahydro-2H-benz...)
Affinity DataIC50:  320nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091706(7-((E)-Styryl)-9,10-dihydro-phenanthrene-2-carboxy...)
Affinity DataIC50:  340nMAssay Description:Compound was evaluated in vitro for its inhibitory activity against Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50099216((2S,3S)-1-[2-(3-Benzyloxycarbonyl-phenyl)-acetyl]-...)
Affinity DataIC50:  348nMAssay Description:Inhibition of Prostate specific antigen PSA (Serine Protease)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50099216((2S,3S)-1-[2-(3-Benzyloxycarbonyl-phenyl)-acetyl]-...)
Affinity DataIC50:  348nMAssay Description:Inhibition of Prostate specific antigen PSA (Serine Protease)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50091705((R)-8-Chloro-4,10b-dimethyl-1,4,6,10b-tetrahydro-2...)
Affinity DataIC50:  377nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044890(8-Chloro-1,4,5,6-tetrahydro-2H-benzo[f]quinolin-3-...)
Affinity DataIC50:  460nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044876((4aR,10bR)-4-Methyl-1,4,4a,5,6,10b-hexahydro-2H-be...)
Affinity DataIC50:  560nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044876((4aR,10bR)-4-Methyl-1,4,4a,5,6,10b-hexahydro-2H-be...)
Affinity DataIC50:  560nMAssay Description:In vitro inhibitory activity against Steroid 5-alpha-reductase type IMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091710(1-Methyl-5-(4-phenylazo-phenyl)-piperidin-2-one | ...)
Affinity DataIC50:  579nMAssay Description:Compound was evaluated in vitro for its inhibitory activity against Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
University Of Canterbury

Curated by ChEMBL
LigandPNGBDBM50044880(8-Fluoro-1,4,5,6-tetrahydro-2H-benzo[f]quinolin-3-...)
Affinity DataIC50:  600nMAssay Description:In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Eli Lilly

Curated by ChEMBL
LigandPNGBDBM50091707(1-Methyl-5-[4-((E)-styryl)-phenyl]-piperidin-2-one...)
Affinity DataIC50:  617nMAssay Description:Compound was evaluated in vitro for its inhibitory activity against Steroid 5-alpha-reductase type 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50289630((2S,3S)-3-Benzyl-1-[2-(3-carboxy-phenyl)-acetyl]-4...)
Affinity DataIC50:  1.34E+3nMAssay Description:Concentration required for inhibition of 50% of the cleavage of para-nitroanilide from MeO-Suc-Arg-Pro-Tyr-pNA.HCl by Prostate specific antigen PSAMore data for this Ligand-Target Pair
In DepthDetails Article
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (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 ArticlePubMed
TargetGlutamate carboxypeptidase 2(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50099212(3-Benzyl-1-[2-(3-benzyloxycarbonyl-phenyl)-acetyl]...)
Affinity DataIC50:  1.34E+3nMAssay Description:Inhibition of Prostate specific antigen PSA (Serine Protease)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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