BDBM50438778 CHEMBL1223510

SMILES CCCCCCCC\C=C/CCCCCCCC(=O)NCc1ccccc1

InChI Key InChIKey=QHXGFOCPQQADIF-UHFFFAOYSA-N

Data  5 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 5 hits for monomerid = 50438778   

TargetBifunctional epoxide hydrolase 2(Rat)
University of California Davis

Curated by ChEMBL
LigandPNGBDBM50438778(CHEMBL1223510)
Affinity DataIC50: 198nMAssay Description:Inhibition of recombinant rat sEH expressed in baculovirus expression system using MNPC as substrate by fluorescence-based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Mouse)
University of California Davis

Curated by ChEMBL
LigandPNGBDBM50438778(CHEMBL1223510)
Affinity DataIC50: 265nMAssay Description:Inhibition of recombinant mouse sEH expressed in baculovirus expression system using MNPC as substrate by fluorescence-based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetBifunctional epoxide hydrolase 2(Human)
University of California Davis

Curated by ChEMBL
LigandPNGBDBM50438778(CHEMBL1223510)
Affinity DataIC50: 893nMAssay Description:Inhibition of recombinant human sEH expressed in baculovirus expression system using MNPC as substrate by fluorescence-based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1(Human)
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50438778(CHEMBL1223510)
Affinity DataIC50: 1.67E+4nMAssay Description:Inhibition of recombinant human FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins followed by substrate additio...More data for this Ligand-Target Pair
In Depth
Date in BDB:
2/27/2021
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1(Human)
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50438778(CHEMBL1223510)
Affinity DataIC50: 1.67E+4nMAssay Description:Inhibition of human recombinant FAAH using N-arachidonyl-7-amino-4-methylcoumarin as substrate preincubated for 20 mins before substrate addition by ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed