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Found 25 Enz. Inhib. hit(s) with all data for entry = 50038902
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296704(3-{4-[2-Amino-6-(4-benzyl-piperazin-1-yl)-pyrimidi...)
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 reductase activity expressed in HEK293 cells by scintillation proximity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50185127((3beta,20beta)-20-carboxy-11-oxo-30-norolean-12-en...)
Affinity DataIC50:  15nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM32530(arylsulfonylpiperazine, 2)
Affinity DataIC50:  45nMAssay Description:Inhibition of human 11betaHSD1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM32530(arylsulfonylpiperazine, 2)
Affinity DataIC50:  122nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296702(3-{4-{2-Amino-6-[4-(4-propyl-benzoyl)-piperazin-1-...)
Affinity DataIC50:  490nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296704(3-{4-[2-Amino-6-(4-benzyl-piperazin-1-yl)-pyrimidi...)
Affinity DataIC50:  710nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296706(3-{4-{2-Amino-6-[4-(4-tert-butyl-benzyl)-piperazin...)
Affinity DataIC50:  850nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296708(3-{4-{2-Amino-6-[4-(3-trifluoromethyl-benzyl)-pipe...)
Affinity DataIC50:  1.04E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296703(3-{4-[2-Amino-6-(4-cyclohexylmethyl-piperazin-1-yl...)
Affinity DataIC50:  1.32E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296711(3-{4-{2-Amino-6-[4-(3-chloro-phenyl)-piperazin-1-y...)
Affinity DataIC50:  1.52E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296710(3-{4-[2-Amino-6-(4-phenyl-piperazin-1-yl)-pyrimidi...)
Affinity DataIC50:  1.92E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296705(3-{4-[2-Amino-6-(4-(naphthalen-1-ylmethyl)-piperaz...)
Affinity DataIC50:  2.34E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296707(3-{4-{2-Amino-6-[4-(3-methyl-benzyl)-piperazin-1-y...)
Affinity DataIC50:  2.37E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target11-beta-hydroxysteroid dehydrogenase 1(Mus musculus (mouse))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296701(3-{4-[2-Amino-6-(4-benzoyl-piperazin-1-yl)-pyrimid...)
Affinity DataIC50:  3.29E+3nMAssay Description:Inhibition of mouse liver microsome 11betaHSD1 expressed in HEK293 cells assessed as conversion of [3H]cortisone into [3H]cortisol by scintillation p...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296710(3-{4-[2-Amino-6-(4-phenyl-piperazin-1-yl)-pyrimidi...)
Affinity DataEC50:  4.94E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296708(3-{4-{2-Amino-6-[4-(3-trifluoromethyl-benzyl)-pipe...)
Affinity DataEC50:  4.79E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296711(3-{4-{2-Amino-6-[4-(3-chloro-phenyl)-piperazin-1-y...)
Affinity DataEC50:  4.47E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296707(3-{4-{2-Amino-6-[4-(3-methyl-benzyl)-piperazin-1-y...)
Affinity DataEC50:  4.46E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296712(3-{4-[2-Amino-6-(4-pyrimidin-2-yl-piperazin-1-yl)-...)
Affinity DataEC50:  6.13E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296709(3-{4-[2-Amino-6-(4-furan-2-ylmethyl-piperazin-1-yl...)
Affinity DataEC50:  5.01E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296706(3-{4-{2-Amino-6-[4-(4-tert-butyl-benzyl)-piperazin...)
Affinity DataEC50:  6.36E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296705(3-{4-[2-Amino-6-(4-(naphthalen-1-ylmethyl)-piperaz...)
Affinity DataEC50:  3.50E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296704(3-{4-[2-Amino-6-(4-benzyl-piperazin-1-yl)-pyrimidi...)
Affinity DataEC50:  6.62E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50296703(3-{4-[2-Amino-6-(4-cyclohexylmethyl-piperazin-1-yl...)
Affinity DataEC50:  5.54E+3nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM28681(5-[(4-{2-[methyl(pyridin-2-yl)amino]ethoxy}phenyl)...)
Affinity DataEC50:  50nMAssay Description:Agonist activity at human PPARgamma expressed in U2OS cells by luciferase transactivation assayMore data for this Ligand-Target Pair