BDBM50157122 (Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-one::(Z)-1-(5-Pyridin-2-yl-oxazol-2-yl)-octadec-9-en-1-one::1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-one::1-(5-Pyridin-2-yl-oxazol-2-yl)-nonadec-10-en-2-one::CHEMBL426230

SMILES CCCCCCCC\C=C/CCCCCCCC(=O)c1ncc(o1)-c1ccccn1

InChI Key InChIKey=MTEOAQVTLKPFRA-KTKRTIGZSA-N

Data  8 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 12 hits for monomerid = 50157122   

TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  3nMAssay Description:Inhibition of 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  10nMAssay 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(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  10nMAssay Description:Inhibition of human recombinant 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  18nMAssay Description:Inhibition of rat 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  18nMAssay 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  18nMAssay Description:Binding affinity against purified rat Fatty-acid amide hydrolase (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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  18nMAssay 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(Mus musculus (mouse))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataKi:  18nMAssay 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
TargetLiver carboxylesterase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataIC50:  5.00E+4nMAssay Description:Inhibitory concentration of triacylgylcerol 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory concentration against Triacylglycerol hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetFatty-acid amide hydrolase 1(Homo sapiens (Human))
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataIC50:  200nMAssay Description:Inhibitory concentration of fatty acid amide 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
LigandPNGBDBM50157122((Z)-1-(5-(pyridin-2-yl)oxazol-2-yl)octadec-9-en-1-...)
Affinity DataIC50:  150nMAssay Description:Inhibitory concentration against Fatty-acid amide hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed