BDBM50056471 (9Z,12Z)-Octadeca-9,12-dienoic acid (2-hydroxy-ethyl)-amide::CHEMBL149859::N-(2-hydroxyethyl)linoleoylamide
SMILES CCCCC\C=C/C\C=C/CCCCCCCC(=O)NCCO
InChI Key InChIKey=KQXDGUVSAAQARU-HZJYTTRNSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 12 hits for monomerid = 50056471
Affinity DataKi: 4.60E+3nMAssay Description:In vitro binding affinity was determined against rat brain Cannabinoid receptor 1More data for this Ligand-Target Pair
Affinity DataKi: >1.00E+4nMAssay Description:Tested for binding affinity to Cannabinoid receptor 1More data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Binding affinity towards cannabinoid receptor 1 from rat forebrain membranes in the presence of phenylmethanesulfonylfluoride (PMSF) using 0.8 nM [3H...More data for this Ligand-Target Pair
Affinity DataKi: 2.50E+4nMAssay Description:Binding affinity towards Cannabinoid receptor 2 from mouse spleen membranes using 0.8 nM [3H]-CP-55,940 as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: >2.50E+4nMAssay Description:In vitro binding affinity was determined against rat brain Cannabinoid receptor 1More data for this Ligand-Target Pair
Affinity DataKi: 4.00E+4nMAssay Description:Binding affinity towards cannabinoid receptor 1 from rat forebrain membranes in the absence of phenylmethanesulfonylfluoride (PMSF) using 0.8 nM [3H]...More data for this Ligand-Target Pair
Affinity DataKi: >4.14E+4nMAssay Description:Binding affinity against the cloned human Cannabinoid receptor 1More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 2(Rattus norvegicus)
National Research Council (Cnr)
Curated by ChEMBL
National Research Council (Cnr)
Curated by ChEMBL
Affinity DataIC50: 1.40E+3nMAssay Description:Antagonist activity at recombinant rat TRPV2 expressed in HEK293 cells assessed as inhibition of LPC-induced Ca2+ levels preincubated for 5 mins foll...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Ghent University
Curated by ChEMBL
Ghent University
Curated by ChEMBL
Affinity DataIC50: 7.59E+3nMAssay Description:Inhibition of rat recombinant FAAH-mediated hydrolysis of [3H]AEAMore data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Hebrew University of Jerusalem
Curated by ChEMBL
Hebrew University of Jerusalem
Curated by ChEMBL
Affinity DataEC50: 630nMAssay Description:Agonist activity at TRPV1 receptor (unknown origin)More data for this Ligand-Target Pair
TargetTransient receptor potential cation channel subfamily V member 2(Rattus norvegicus)
National Research Council (Cnr)
Curated by ChEMBL
National Research Council (Cnr)
Curated by ChEMBL
Affinity DataIC50: 650nMAssay Description:Antagonist activity at recombinant rat TRPV2 expressed in HEK293 cells assessed as inhibition of CBD-induced Ca2+ levels preincubated for 5 mins foll...More data for this Ligand-Target Pair
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Ghent University
Curated by ChEMBL
Ghent University
Curated by ChEMBL
Affinity DataIC50: 7.58E+3nMAssay Description:Inhibition of rat recombinant FAAH assessed as [3H]AEA hydrolysisMore data for this Ligand-Target Pair