null

SMILES CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OCc1cccs1

InChI Key InChIKey=JVBGBRBEKHETSN-DOFZRALJSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 7 hits for monomerid = 50107599   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Binding affinity to human CB2 cannabinoid receptor using [3H]CP-55940 in HEK293 EBNA transfected cellsMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29G5NJ5PubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+3nMAssay Description:Binding affinity to CB1 cannabinoid receptor using [3H]WIN-55212-2 in rat cerebellum membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29G5NJ5PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity to vanilloid VR1 receptor using [3H]resiniferatoxin ([3H]-RTX) in rat spinal cord membranesMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q29G5NJ5PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity against vanilloid receptor 1 (VR1) using [3H]RTX in rat spinal cord membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GQ6ZHSPubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity against G protein coupled human Cannabinoid receptor 2 using [3H]CP-55940 in HEK293 EBNA transfected cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GQ6ZHSPubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataKi: >5.00E+3nMAssay Description:Binding affinity against G protein coupled Cannabinoid receptor 1 using [3H]WIN-55212-2 in rat cerebellum membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GQ6ZHSPubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50107599((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoic acid th...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of fatty acid amide hydrolase (FAAH) was determined using rat brain homogenates as the enzyme source and [3H]anandamide as substrateMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GQ6ZHSPubMed