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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 9 hits in this display   

TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50370314(CHEMBL1907956)
Affinity DataKi: >1.00E+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 ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50126859(CHEMBL39351 | Icosa-5,8,11,14-tetraenoic acid 1-fu...)
Affinity DataKi: >1.00E+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 ArticlePubMed
TargetCannabinoid receptor 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50126859(CHEMBL39351 | Icosa-5,8,11,14-tetraenoic acid 1-fu...)
Affinity DataKi: >1.00E+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 ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50370314(CHEMBL1907956)
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 ArticlePubMed
TargetCannabinoid receptor 2(Homo sapiens (Human))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50370314(CHEMBL1907956)
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 ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50126859(CHEMBL39351 | Icosa-5,8,11,14-tetraenoic acid 1-fu...)
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 ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50126859(CHEMBL39351 | Icosa-5,8,11,14-tetraenoic acid 1-fu...)
Affinity DataIC50: >1.20E+5nMAssay 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 ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50370314(CHEMBL1907956)
Affinity DataIC50: >1.20E+5nMAssay 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 ArticlePubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Universidad Complutense

Curated by ChEMBL
LigandPNGBDBM50409815(CHEMBL2093099)
Affinity DataIC50: >1.20E+5nMAssay 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 ArticlePubMed