BDBM50175122 CHEMBL199960::N-(4-methoxyphenyl)oleamide

SMILES CCCCCCCC\C=C/CCCCCCCC(=O)Nc1ccc(OC)cc1

InChI Key InChIKey=GVVBDSXGTXGHEV-UHFFFAOYSA-N

Data  3 KI  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 50175122   

TargetCannabinoid receptor 1(Human)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175122(N-(4-methoxyphenyl)oleamide | CHEMBL199960)
Affinity DataKi:  1.50E+3nMAssay Description:Displacement of [3H]CP-55940 from human recombinant CB1 receptor in presence of hydrolase inhibitor PMSFMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/5/2012
Entry Details Article
PubMed
TargetCannabinoid receptor 1(Human)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175122(N-(4-methoxyphenyl)oleamide | CHEMBL199960)
Affinity DataKi:  1.60E+3nMAssay Description:Displacement of [3H]CP-55940 from human recombinant CB1 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/5/2012
Entry Details Article
PubMed
TargetCannabinoid receptor 2(Human)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175122(N-(4-methoxyphenyl)oleamide | CHEMBL199960)
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]CP-55940 from human recombinant CB2 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/5/2012
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rat)
Institute of Biomolecular Chemistry

Curated by ChEMBL
LigandPNGBDBM50175122(N-(4-methoxyphenyl)oleamide | CHEMBL199960)
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibitory activity against rat brain FAAH by [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/5/2012
Entry Details Article
PubMed