BDBM50438782 CHEMBL2413162

SMILES CC\C=C/C\C=C/C\C=C/CCCCCCCC(=O)NCc1cccc(OC)c1

InChI Key InChIKey=XKHCEDYSKNATME-UHFFFAOYSA-N

Data  2 KI  7 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 9 hits for monomerid = 50438782   

TargetBifunctional epoxide hydrolase 2(Rat)
University of California Davis

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 9.30nMAssay 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
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 27nMAssay 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
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 76nMAssay 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
TargetCannabinoid receptor 1(Human)
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataKi:  8.67E+3nMAssay Description:Displacement of [3H]CP55,940 from human CB1 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2016
Entry Details Article
PubMed
TargetFatty-acid amide hydrolase 1(Human)
Mcphs University

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 1.37E+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
TargetFatty-acid amide hydrolase 1(Human)
Mcphs University

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 1.37E+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)
Mcphs University

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 1.91E+4nMAssay Description:Inhibition of FAAH-mediated [ethanol-amine-1-3H]AEA hydrolysis in human U937 cells preincubated for 15 mins measured 15 mins post AEA addition by liq...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2016
Entry Details Article
PubMed
TargetCannabinoid receptor 2(Human)
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataKi: >5.00E+4nMAssay Description:Displacement of [3H]CP55,940 from human CB2 expressed in CHO-K1 cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2016
Entry Details Article
PubMed
TargetMonoglyceride lipase(Mouse)
University of Szeged

Curated by ChEMBL
LigandPNGBDBM50438782(CHEMBL2413162)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of mouse brain MAGL-mediated [glycerol-1,2,3-3H]-2-OG hydrolysis preincubated for 15 mins measured 15 mins post 2-OG addition by liquid sc...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2016
Entry Details Article
PubMed