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Found 83 with Last Name = 'hu' and Initial = 'gx'
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364455(CHEMBL1950682)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364455(CHEMBL1950682)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364457(CHEMBL1950684)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364456(CHEMBL1950683)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364453(CHEMBL1950680)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364453(CHEMBL1950680)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364459(CHEMBL1950686)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364461(CHEMBL1950688)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364460(CHEMBL1950687)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364460(CHEMBL1950687)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364462(CHEMBL1950689)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364463(CHEMBL1950690)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364463(CHEMBL1950690)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364454(CHEMBL1950681)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364458(CHEMBL1950685)
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
In DepthDetails ArticlePubMed
TargetAmine oxidase [flavin-containing] B(Mus musculus)
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50364458(CHEMBL1950685)
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
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50315884((3S,8R,9S,10S,13S,14S)-10,13-dimethyl-3-phenethoxy...)
Affinity DataIC50:  57nMAssay Description:Inhibition of 17beta-HSD3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50315879(1,5-bis(4-ethoxyphenyl)penta-1,4-dien-3-one | CHEM...)
Affinity DataIC50:  70nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50315878(2,5-bis(3-bromobenzylidene)cyclopentanone | CHEMBL...)
Affinity DataIC50:  97nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50266759((1E,4E)-1,5-bis(4-fluorophenyl)penta-1,4-dien-3-on...)
Affinity DataIC50:  100nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50241208((2E,6E)-2,6-bis(3,4,5-trimethoxybenzylidene)cycloh...)
Affinity DataIC50:  100nMAssay Description:Inhibition of 17beta-HSD3 in human testis microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437203(CHEMBL504452)
Affinity DataIC50:  115nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437203(CHEMBL504452)
Affinity DataIC50:  129nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437200(CHEMBL476847)
Affinity DataIC50:  144nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437202(CHEMBL478480)
Affinity DataIC50:  148nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50264832(2,6-bis(4-hydroxybenzylidene)cyclohexanone | CHEMB...)
Affinity DataIC50:  195nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437202(CHEMBL478480)
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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50266759((1E,4E)-1,5-bis(4-fluorophenyl)penta-1,4-dien-3-on...)
Affinity DataIC50:  229nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50067028((1E,4E)-1,5-Bis-(4-hydroxy-3-methoxy-phenyl)-penta...)
Affinity DataIC50:  257nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437199(2,6-Bis(4-Fluorobenzylidene)Cyclohexanone | CHEMBL...)
Affinity DataIC50:  263nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437203(CHEMBL504452)
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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50067028((1E,4E)-1,5-Bis-(4-hydroxy-3-methoxy-phenyl)-penta...)
Affinity DataIC50:  292nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437197(2,5-Bis(4-Fluorobenzylidene)Cyclopentanone | CHEMB...)
Affinity DataIC50:  310nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437202(CHEMBL478480)
Affinity DataIC50:  346nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50266759((1E,4E)-1,5-bis(4-fluorophenyl)penta-1,4-dien-3-on...)
Affinity DataIC50:  507nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437203(CHEMBL504452)
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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50315878(2,5-bis(3-bromobenzylidene)cyclopentanone | 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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50264832(2,6-bis(4-hydroxybenzylidene)cyclohexanone | CHEMB...)
Affinity DataIC50:  633nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50315878(2,5-bis(3-bromobenzylidene)cyclopentanone | CHEMBL...)
Affinity DataIC50:  700nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50067044((1E,4E)-1,5-Bis-(4-hydroxy-phenyl)-penta-1,4-dien-...)
Affinity DataIC50:  832nMAssay Description:Inhibition of human 11beta-HSD1 transfected in CHOP cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50067044((1E,4E)-1,5-Bis-(4-hydroxy-phenyl)-penta-1,4-dien-...)
Affinity DataIC50:  986nMAssay Description:Inhibition of 11beta-HSD1 in Sprague-Dawley rat leydig cells at 100 uMMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437199(2,6-Bis(4-Fluorobenzylidene)Cyclohexanone | 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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437202(CHEMBL478480)
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
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50315878(2,5-bis(3-bromobenzylidene)cyclopentanone | 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
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50315880(1,5-bis(4-(tetrahydro-2H-pyran-3-yloxy)phenyl)pent...)
Affinity DataIC50:  1.30E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat laydig cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Rattus norvegicus (rat))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50437200(CHEMBL476847)
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
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50241208((2E,6E)-2,6-bis(3,4,5-trimethoxybenzylidene)cycloh...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Wenzhou Medical College

Curated by ChEMBL
LigandPNGBDBM50264832(2,6-bis(4-hydroxybenzylidene)cyclohexanone | CHEMB...)
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
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50067040(((E,E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-hept...)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of 17beta-HSD3 in Sprague-Dawley rat testis microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
School Of Pharmacy

Curated by ChEMBL
LigandPNGBDBM50315882(1,5-bis(4-(dimethylamino)phenyl)penta-1,4-dien-3-o...)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of 17beta-HSD3 in human testis microsomesMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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