null

SMILES CCCCCCc1ccc(O)cc1OCCCCCCCCCCC(=O)NC1CC1

InChI Key InChIKey=BHJRHOCTESKVMJ-UHFFFAOYSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50176954   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Universit£ degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50176954(11-(2-hexyl-5-hydroxyphenoxy)undecanoic acid cyclo...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Displacement of [3H]CP-55940 from human CB2 receptor expressed in COS cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7B7WPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Universit£ degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50176954(11-(2-hexyl-5-hydroxyphenoxy)undecanoic acid cyclo...)copy SMILEScopy InChI
Affinity DataKi:  210nMAssay Description:Displacement of [3H]CP-55940 from human CB1 receptor expressed in COS cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7B7WPubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Universit£ degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50176954(11-(2-hexyl-5-hydroxyphenoxy)undecanoic acid cyclo...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of rat brain FAAH assessed as [14C]anandamide hydrolysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FX7B7WPubMed