BDBM50233999 1-(5-(6-(1H-tetrazol-5-yl)pyridin-2-yl)oxazol-2-yl)-7-phenylheptan-1-one::CHEMBL270284

SMILES O=C(CCCCCCc1ccccc1)c1ncc(o1)-c1cccc(n1)-c1nnn[nH]1

InChI Key InChIKey=DJSDSCYFHLFABO-UHFFFAOYSA-N

Data  1 KI  3 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 = 50233999   

TargetFatty-acid amide hydrolase 1 [30-579](Rat)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50233999(1-(5-(6-(1H-tetrazol-5-yl)pyridin-2-yl)oxazol-2-yl...)
Affinity DataIC50: 500nMAssay Description:Inhibition of rat recombinant FAAH expressed in Escherichia coliMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetNeutral cholesterol ester hydrolase 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50233999(1-(5-(6-(1H-tetrazol-5-yl)pyridin-2-yl)oxazol-2-yl...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of KIAA1363More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetLiver carboxylesterase 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50233999(1-(5-(6-(1H-tetrazol-5-yl)pyridin-2-yl)oxazol-2-yl...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of TGHMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/15/2012
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1(Human)
The Scripps Research Institute

Curated by ChEMBL
LigandPNGBDBM50233999(1-(5-(6-(1H-tetrazol-5-yl)pyridin-2-yl)oxazol-2-yl...)
Affinity DataKi:  40nMpH: 9.0Assay Description:Inhibition of FAAH at pH 9More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/11/2010
Entry Details Article
PubMed