BDBM50339878 (S)-3-(1-(4-(benzofuran-2-yl)pyrimidin-2-yl)piperidin-3-yl)-1-ethyl-1H-imidazo[4,5-b]pyridin-2(3H)-one::CHEMBL1761285

SMILES CCn1c2cccnc2n([C@H]2CCCN(C2)c2nccc(n2)-c2cc3ccccc3o2)c1=O

InChI Key InChIKey=IDXXQXPYKNNTDF-UHFFFAOYSA-N

Data  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 4 hits for monomerid = 50339878   

TargetFatty-acid amide hydrolase 1(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50339878((S)-3-(1-(4-(benzofuran-2-yl)pyrimidin-2-yl)piperi...)
Affinity DataIC50: 6nMAssay Description:Inhibition of human FAAH assessed as hydrolysis of anandamido-amino-methyl-cumarinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2011
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1(Human)
Amgen

Curated by ChEMBL
LigandPNGBDBM50339878((S)-3-(1-(4-(benzofuran-2-yl)pyrimidin-2-yl)piperi...)
Affinity DataIC50: 20nMAssay Description:Inhibition of human FAAH assessed as hydrolysis of anandamido-amino-methyl-cumarinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2011
Entry Details Article
PubMed
LigandPNGBDBM50339878((S)-3-(1-(4-(benzofuran-2-yl)pyrimidin-2-yl)piperi...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat FAAH assessed as hydrolysis of anandamido-amino-methyl-cumarinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2011
Entry Details Article
PubMed
LigandPNGBDBM50339878((S)-3-(1-(4-(benzofuran-2-yl)pyrimidin-2-yl)piperi...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat FAAH assessed as hydrolysis of anandamido-amino-methyl-cumarinMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/2/2011
Entry Details Article
PubMed