Compile Data Set for Download or QSAR
maximum 50k data
Found 36 Enz. Inhib. hit(s) with all data for entry = 50030672
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299922(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(4-phenylbutanoyloxy...)
Affinity DataIC50:  5nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299926(1-(Hexa-5-enoyl)-(3S)-3-[1(R)-(4-phenylbutanoyloxy...)
Affinity DataIC50:  10nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299923(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(biphenylacetyloxy)-...)
Affinity DataIC50:  12nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299927(1-(Hexa-5-enoyl)-(3S)-3-[1(R)-(biphenylacetyloxy)-...)
Affinity DataIC50:  14nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299917(1-(4-Phenylbutanoyl)-(3S)-3-[1(R)-(4-phenylbutanoy...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299919(1-(4-Phenylbutanoyl)-(3S)-3-[1(R)-(biphenylacetylo...)
Affinity DataIC50:  32nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299925(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(hexa-5-enoyloxy)-et...)
Affinity DataIC50:  32nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299918(1-(4-Phenylbutanoyl)-(3S)-3-[1(R)-(5-phenylpentano...)
Affinity DataIC50:  45nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299913(1-(3-Phenylpropanoyl)-(3S)-3-[1(R)-(4-phenylbutano...)
Affinity DataIC50:  49nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299915(1-(3-Phenylpropanoyl)-(3S)-3-[1(R)-(biphenylacetyl...)
Affinity DataIC50:  50nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299916(1-(4-Phenylbutanoyl)-(3S)-3-[1(R)-(3-phenylpropano...)
Affinity DataIC50:  57nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299914(1-(3-Phenylpropanoyl)-(3S)-3-[1(R)-(5-phenylpentan...)
Affinity DataIC50:  91nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299924(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(pent-4-enoyloxy)-et...)
Affinity DataIC50:  98nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299912(1-(3-Phenylpropanoyl)-(3S)-3-[1(R)-(3-phenylpropan...)
Affinity DataIC50:  157nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299921(1-(5-Phenylpentanoyl)-(3S)-3-[1(R)-(biphenylacetyl...)
Affinity DataIC50:  236nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299920(1-(5-Phenylpentanoyl)-(3S)-3-[1(R)-(4-phenylbutano...)
Affinity DataIC50:  449nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299938(1-(4-Phenylbutanoyl)-(3R,4R)-3-[1(R)-(biphenylacet...)
Affinity DataIC50:  708nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299935(1-(3-Phenylpropanoyl)-(3R,4R)-3-[1(R)-(biphenylace...)
Affinity DataIC50:  826nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299934(1-(3-Phenylpropanoyl)-(3R,4R)-3-[1(R)-(4-phenylbut...)
Affinity DataIC50:  960nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299923(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(biphenylacetyloxy)-...)
Affinity DataIC50:  1.84E+3nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299929(1-(Pent-4-enoyl)-(3R,4R)-3-[1(R)-(pent-4-enoyloxy)...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299933(1-(3-Phenylpropanoyl)-(3R,4R)-3-[1(R)-(3-phenylpro...)
Affinity DataIC50:  2.19E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299937(1-(4-Phenylbutanoyl)-(3R,4R)-3-[1(R)-(4-phenylbuta...)
Affinity DataIC50:  3.12E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299922(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(4-phenylbutanoyloxy...)
Affinity DataIC50:  4.06E+3nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299925(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(hexa-5-enoyloxy)-et...)
Affinity DataIC50:  4.72E+3nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299936(1-(4-Phenylbutanoyl)-(3R,4R)-3-[1(R)-(3-phenylprop...)
Affinity DataIC50:  4.90E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299928((3S)-3-[1(R)-(Biphenylacetyloxy)-ethyl]-azetidin-2...)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299911(1-(Pent-4-enoyl)-(3S)-3-[1(R)-hydroxyethyl]-azetid...)
Affinity DataIC50:  7.90E+3nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299926(1-(Hexa-5-enoyl)-(3S)-3-[1(R)-(4-phenylbutanoyloxy...)
Affinity DataIC50:  8.51E+3nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299927(1-(Hexa-5-enoyl)-(3S)-3-[1(R)-(biphenylacetyloxy)-...)
Affinity DataIC50:  1.46E+4nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299924(1-(Pent-4-enoyl)-(3S)-3-[1(R)-(pent-4-enoyloxy)-et...)
Affinity DataIC50:  2.33E+4nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMonoglyceride lipase(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299929(1-(Pent-4-enoyl)-(3R,4R)-3-[1(R)-(pent-4-enoyloxy)...)
Affinity DataIC50:  1.33E+5nMAssay Description:Inhibition of human recombinant MGL using 2-oleoylglycerol by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299931(1-(4-Phenylbutanoyl)-(3R,4R)-3-[1(R)-hydroxyethyl]...)
Affinity DataIC50:  1.83E+5nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299930(1-(3-Phenylpropanoyl)-(3R,4R)-3-[1(R)-hydroxyethyl...)
Affinity DataIC50:  2.24E+5nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299939(1-(3-Phenylpropanoyl)-(3S)-3-[1(R)-hydroxyethyl]-a...)
Affinity DataIC50:  4.09E+5nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
Universite Catholique De Louvain

Curated by ChEMBL
LigandPNGBDBM50299932(1-(Pent-4-enoyl)-(3R,4R)-3-[1(R)-(hydroxyethyl]-4-...)
Affinity DataIC50:  5.37E+5nMAssay Description:Inhibition of human recombinant FAAH using [3H]anandamide by competitive hydrolysis assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed