BDBM50100864 (Z)-1-(oxazol-2-yl)octadec-9-en-1-one::(Z)-1-Oxazol-2-yl-octadec-9-en-1-one::1-(oxazol-2-yl)octadec-9-en-1-one::1-Oxazol-2-yl-nonadec-10-en-2-one::CHEMBL39412

SMILES CCCCCCCC\C=C/CCCCCCCC(=O)c1ncco1

InChI Key InChIKey=WWYUNXGFLPTVRR-KTKRTIGZSA-N

Data  9 KI  4 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 13 hits for monomerid = 50100864   

TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  17nMAssay Description:Inhibition of rat FAAHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  45nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from human expressed in COS-7 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibition of rat FAAH assessed as conversion [14]C-oleamide to oleic acidMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Mus musculus (mouse))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibitor affinity of the compound towards enzymes of class serine hydrolase was determined using biotin or fluorescent as radioligand (FP-biotin or ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Competitive inhibition of rat FAAH by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibitory constant determined against recombinant Fatty-acid amide hydrolase from rat expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibition of FAAHMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibition of rat FAAH expressed in Escherichia coliMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataKi:  100nMAssay Description:Inhibitory activity against fatty acid amide hydrolase (FAAH)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration against Fatty-acid amide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLiver carboxylesterase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibitory concentration of triacylgylcerol hydrolase using FP-Rh radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory concentration of fatty acid amide hydrolase using FP-Rh radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetLiver carboxylesterase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50100864((Z)-1-(oxazol-2-yl)octadec-9-en-1-one | (Z)-1-Oxaz...)
Affinity DataIC50:  9.00E+3nMAssay Description:Inhibitory concentration against Triacylglycerol hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed