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

Found 6 hits in this display   

Target5-hydroxytryptamine receptor 1A(Rat)
Merrell Dow Research Institute

Curated by ChEMBL
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  0.631nMAssay Description:Binding affinity towards 5-hydroxytryptamine 1A receptor in rat frontal cortex using [3H]8-OH-DPAT as a radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rat)
Merrell Dow Research Institute

Curated by ChEMBL
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  10nMAssay Description:Binding affinity against Dopamine receptor D2 in rat brain membrane using [3H]-8-OH-DPAT as a selective ligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetD(2) dopamine receptor(Rat)
Merrell Dow Research Institute

Curated by ChEMBL
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  79nMAssay Description:Binding affinity against Dopamine receptor D2 in rat brain membrane using [3H]-8-OH-DPAT as a selective ligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerotonin 2 (5-HT2) receptor(Rat)
Merrell Dow Research Institute

Curated by ChEMBL
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  200nMAssay Description:Inhibition of human placental cytochrome P450 19A1 with testosteroneMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  501nMAssay Description:Binding affinity against alpha-2 adrenergic receptor in rat brain membrane using [3H]8-OH-DPAT as a selective ligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 1B(Rat)
Merrell Dow Research Institute

Curated by ChEMBL
LigandPNGBDBM50421836(CHEMBL12129)
Affinity DataIC50:  794nMAssay Description:Binding affinity against 5-HT1B receptor in rat brain membrane using [3H]8-OH-DPAT as a selective ligand.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed