Affinity DataKi: 260nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 260nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 1.18E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 1.63E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 2.77E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 2.77E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 2.87E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 2.95E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.49E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.49E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.56E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.92E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.92E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 3.97E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 4.21E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Affinity DataKi: 4.21E+3nMAssay Description:Inhibition of MAO-B in mouse cerebral homogenate using kynuramine as substrate after 30 mins by fluorimetry in the presence of MOA-A inhibitor clorgy...More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 57nMAssay Description:Inhibition of 17beta-HSD3More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 70nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 97nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of 17beta-HSD3 in human testis microsomesMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 115nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 129nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 144nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 148nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 195nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 218nMAssay Description:Inhibition of 11beta-HSD1 in rat testis microsomes using [3H]-11-DHC as substrate assessed as formation of CORT after 60 to 90 mins by radiometric an...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 229nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 257nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 263nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 288nMAssay Description:Inhibition of 11beta-HSD1 in rat testis microsomes using [3H]-11-DHC as substrate assessed as formation of CORT after 60 to 90 mins by radiometric an...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 292nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 310nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 346nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 507nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 529nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using [3H]-cortisone as substrate assessed as formation of cortisol after 60 to 90 mins by radiom...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 599nMAssay Description:Inhibition of 11beta-HSD1 in rat testis microsomes using [3H]-11-DHC as substrate assessed as formation of CORT after 60 to 90 mins by radiometric an...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 633nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 700nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 832nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 986nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 1.11E+3nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 1.11E+3nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using [3H]-cortisone as substrate assessed as formation of cortisol after 60 to 90 mins by radiom...More data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 1.45E+3nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College
Curated by ChEMBL
Wenzhou Medical College
Curated by ChEMBL
Affinity DataIC50: 1.94E+3nMAssay Description:Inhibition of 11beta-HSD1 in human liver microsomes using [3H]-cortisone as substrate assessed as formation of cortisol after 60 to 90 mins by radiom...More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 2.30E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy
Curated by ChEMBL
School Of Pharmacy
Curated by ChEMBL
Affinity DataIC50: 2.40E+3nMAssay Description:Inhibition of 17beta-HSD3 in human testis microsomesMore data for this Ligand-Target Pair