Affinity DataIC50: 64nMAssay Description:In vitro antagonist activity against rat prostatic androgen receptor (AR)More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 2(Homo sapiens (Human))
Chul Research Center
Curated by ChEMBL
Chul Research Center
Curated by ChEMBL
Affinity DataIC50: 84nMAssay Description:In vitro inhibition of human Steroid 5-alpha-reductase type 2 in transfected SW-13 cells using [3H]- delta4-Androstenedione as substrateMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)
Curated by ChEMBL
Chu De Qu£Bec-Research Center (Chul)
Curated by ChEMBL
Affinity DataIC50: 169nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Affinity DataIC50: 489nMAssay Description:Ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity transfected in human embryonic kidney (HEK)-293 cells experiment 3More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Affinity DataIC50: 650nMAssay Description:Ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity transfected in human embryonic kidney (HEK)-293 cells experiment 2More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Affinity DataIC50: 758nMAssay Description:Inhibitory concentration against type-3 17-beta-HSD expressed in HEK293 cellsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Affinity DataIC50: 758nMAssay Description:Ability to inhibit the Type-3 17-beta- hydroxysteroid dehydrogenase activity transfected in human embryonic kidney (HEK)-293 cells experiment 1More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Centre Hospitalier Universitaire De Qu£Bec And Universit£
Curated by ChEMBL
Affinity DataIC50: 758nMAssay Description:Inhibition of type-3 17 beta-hydroxysteroid dehydrogenase expressed in HEK293 cells at 37 degree C pH7.4 More data for this Ligand-Target Pair
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibitory concentration against recombinant rat androgen receptor expressed in Escherichia coli using [3H]methyltrienolone (R 1881)More data for this Ligand-Target Pair
Affinity DataIC50: 1.55E+3nMAssay Description:AChE and BChE inhibiting activities were measured in vitro by a modified spectrophotometric method previously developed by Ellman et. al.More data for this Ligand-Target Pair
Target3-oxo-5-alpha-steroid 4-dehydrogenase 1(Homo sapiens (Human))
Chul Research Center
Curated by ChEMBL
Chul Research Center
Curated by ChEMBL
Affinity DataIC50: 2.70E+3nMAssay Description:In vitro inhibition of human tSteroid 5-alpha-reductase type I in transfected 293 cells using [3H]- delta4-Androstenedione as substrate.More data for this Ligand-Target Pair
Affinity DataIC50: 8.59E+4nMAssay Description:Inhibition of alpha-synuclein aggregation (unknown origin) incubated for 8 days by thioflavin S based fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.30E+5nMpH: 7.0 T: 2°CAssay Description:β-Glucuronidase inhibitory activity was evaluated by a biochemical assay, based on the measurement of the absorbance of p-nitrophenol at 405 nm,...More data for this Ligand-Target Pair
Affinity DataIC50: >6.98E+5nMAssay Description:Inhibition of HIV1 RTMore data for this Ligand-Target Pair