BDBM50132713 Arachidonic acid derivative::CHEMBL113262::Methyl arachidonoyl fluorophophonate::methyl ((5Z,8Z,11Z,14Z)-2-Icosa-5,8,11,14-tetraenyl)phosphonofluoridoate::methyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenylphosphonofluoridate::methyl -icosa-5,8,11,14-tetraenylphosphonofluoridate::methyl(5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenylphosphonofluoridate::methylarachidonyl fluorophosphonate
SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCCP(F)(=O)OC
InChI Key InChIKey=KWKZCGMJGHHOKJ-ZKWNWVNESA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 18 hits for monomerid = 50132713
Affinity DataIC50: 2.5nMAssay Description:Inhibitory potency of Fatty-acid amide hydrolase with rat brain memebraneMore data for this Ligand-Target Pair
Affinity DataIC50: 17nMAssay Description:Inhibition of ABHD6 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 20nMAssay Description:Binding affinity towards Cannabinoid receptor 1 was determined using [3H]-CP- cannabinoid as radioligand with rat brain memebraneMore data for this Ligand-Target Pair
Affinity DataIC50: 0.100nMAssay Description:Inhibitory potency of Fatty-acid amide hydrolase with Mouse brain memebraneMore data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Reversible inhibition of human recombinant MAGL using 2-arachidonoylglycerol substrate assessed as arachidonic acid after 10 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 25nMAssay Description:Reversible inhibition of human recombinant MAGL using 2-arachidonoylglycerol substrate assessed as arachidonic acid after 30 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 28nMAssay Description:Reversible inhibition of human recombinant MAGL using 2-arachidonoylglycerol substrate assessed as arachidonic acid after 90 mins by HPLC analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 26nMAssay Description:Reversible inhibition of human recombinant MAGL using 2-arachidonoylglycerol substrate assessed as arachidonic acid after 60 mins by HPLC analysisMore data for this Ligand-Target Pair
TargetPlatelet-activating factor acetylhydrolase IB subunit alpha2(Human)
Shiv Nadar University
Curated by ChEMBL
Shiv Nadar University
Curated by ChEMBL
Affinity DataIC50: 72nMAssay Description:Inhibition of PAFAH1B2 (unknown origin) using 2-thiol-PAF as substrate by Ellman's assayMore data for this Ligand-Target Pair
Affinity DataIC50: 26.3nMAssay Description:Inhibition of human MGLMore data for this Ligand-Target Pair
Affinity DataIC50: 0.330nMAssay Description:Inhibition of human FAAHMore data for this Ligand-Target Pair
Affinity DataIC50: 23nMAssay Description:Inhibition of FAAH from rat brain microsomes by RP-HPLCMore data for this Ligand-Target Pair
Affinity DataIC50: 640nMAssay Description:Inhibition of cPLA2 from human platelets by RP-HPLCMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Irreversible inhibition of fatty acid amide hydrolase; range=1-3 nMMore data for this Ligand-Target Pair
Affinity DataIC50: 0.331nMAssay Description:Inhibition of human recombinant FAAH-maltose binding proteinMore data for this Ligand-Target Pair
Affinity DataIC50: 26.3nMAssay Description:Inhibition of human MGL activity using [3H]2-oleoylglycerol substrate by liquid scintillation countingMore data for this Ligand-Target Pair
Affinity DataIC50: 530nMAssay Description:Binding affinity towards Cannabinoid receptor 1 was determined using [3H]-CP- cannabinoid as radioligand with mouse brain memebraneMore data for this Ligand-Target Pair