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Found 74 Enz. Inhib. hit(s) with all data for entry = 50040402
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393668(CHEMBL2158989)
Affinity DataIC50:  155nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393684(CHEMBL2158918)
Affinity DataIC50:  355nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393704(CHEMBL2158988)
Affinity DataIC50:  437nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393702(CHEMBL2158986)
Affinity DataIC50:  813nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393700(CHEMBL2158984)
Affinity DataIC50:  832nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393694(CHEMBL2158928)
Affinity DataIC50:  933nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393701(CHEMBL2158985)
Affinity DataIC50:  977nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393699(CHEMBL2158983)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393704(CHEMBL2158988)
Affinity DataIC50:  1.15E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393668(CHEMBL2158989)
Affinity DataIC50:  1.74E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393703(CHEMBL2158987)
Affinity DataIC50:  1.78E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393685(CHEMBL2158919)
Affinity DataIC50:  1.78E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393700(CHEMBL2158984)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393693(CHEMBL2158927)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393694(CHEMBL2158928)
Affinity DataIC50:  2.19E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393688(CHEMBL2158922)
Affinity DataIC50:  2.40E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393703(CHEMBL2158987)
Affinity DataIC50:  2.57E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393692(CHEMBL2158926)
Affinity DataIC50:  2.63E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393698(CHEMBL2158982)
Affinity DataIC50:  2.75E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393691(CHEMBL2158925)
Affinity DataIC50:  3.02E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393689(CHEMBL2158923)
Affinity DataIC50:  3.72E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393686(CHEMBL2158920)
Affinity DataIC50:  4.27E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393701(CHEMBL2158985)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393697(CHEMBL2158931)
Affinity DataIC50:  5.01E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393687(CHEMBL2158921)
Affinity DataIC50:  5.13E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393695(CHEMBL2158929)
Affinity DataIC50:  5.25E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393695(CHEMBL2158929)
Affinity DataIC50:  5.37E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393690(CHEMBL2158924)
Affinity DataIC50:  6.03E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393697(CHEMBL2158931)
Affinity DataIC50:  6.76E+3nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393696(CHEMBL2158930)
Affinity DataIC50:  7.08E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393683(CHEMBL2158917)
Affinity DataIC50:  7.41E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393698(CHEMBL2158982)
Affinity DataIC50:  7.76E+3nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393702(CHEMBL2158986)
Affinity DataIC50:  1.58E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393699(CHEMBL2158983)
Affinity DataIC50:  1.86E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393689(CHEMBL2158923)
Affinity DataIC50:  1.91E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393672(CHEMBL2158906)
Affinity DataIC50:  2.19E+4nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393691(CHEMBL2158925)
Affinity DataIC50:  2.24E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393685(CHEMBL2158919)
Affinity DataIC50:  2.34E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393670(CHEMBL2158904)
Affinity DataIC50:  2.95E+4nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393690(CHEMBL2158924)
Affinity DataIC50:  4.47E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393688(CHEMBL2158922)
Affinity DataIC50:  4.68E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393696(CHEMBL2158930)
Affinity DataIC50:  5.25E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393686(CHEMBL2158920)
Affinity DataIC50:  5.37E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393680(CHEMBL2158914)
Affinity DataIC50:  6.92E+4nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393677(CHEMBL2158911)
Affinity DataIC50:  9.55E+4nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393687(CHEMBL2158921)
Affinity DataIC50:  9.77E+4nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393669(CHEMBL2158903)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393682(CHEMBL2158916)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of human recombinant MAGL using [3H]-2-OG as substrate after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393671(CHEMBL2158905)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50393672(CHEMBL2158906)
Affinity DataIC50: >1.00E+6nMAssay Description:Inhibition of human recombinant FAAH assessed as conversion of [3H]AEA to [3H]ethanolamine after 10 mins by liquid scintillation counterMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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