Affinity DataKi: 0.0676nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.110nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.130nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.130nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.140nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.178nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.180nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.180nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.190nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.200nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.220nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.230nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.25nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.25nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.280nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.300nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.320nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.340nMAssay Description:Binding affinity to human 5-hydroxytryptamine 1A receptor was measured using [3H]-8-hydroxy-2-(di-n-propylamine) tetraline [3H]-8-OH-DPAT) as radioli...More data for this Ligand-Target Pair
Affinity DataKi: 0.370nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.370nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.389nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.410nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.410nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.420nMAssay Description:Binding affinity towards human cloned alpha1B-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.427nMAssay Description:Displacement of [3H]prazosin from human adrenergic alpha1A expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.430nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.440nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.468nMAssay Description:Displacement of [3H]prazosin from human adrenergic alpha1A expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.490nMAssay Description:Binding affinity towards human cloned alpha1d-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.501nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1B expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.513nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.513nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.530nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.537nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1B expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.540nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.540nMAssay Description:Binding affinity to human 5-hydroxytryptamine 1A receptor was measured using [3H]-8-hydroxy-2-(di-n-propylamine) tetraline [3H]-8-OH-DPAT) as radioli...More data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.610nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.630nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.640nMAssay Description:Binding affinity towards human cloned alpha1B-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.670nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.741nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.75nMAssay Description:Binding affinity towards human cloned alpha1B-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
TargetAlpha-1B adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.794nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1B expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:Binding affinity to human 5-hydroxytryptamine 1A receptor was measured using [3H]-8-hydroxy-2-(di-n-propylamine) tetraline [3H]-8-OH-DPAT) as radioli...More data for this Ligand-Target Pair
Affinity DataKi: 0.830nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.840nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
TargetAlpha-1A adrenergic receptor(Homo sapiens (Human))
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Istituto Chimico Farmaceutico E Tossicologico
Curated by ChEMBL
Affinity DataKi: 0.890nMAssay Description:Binding affinity towards human cloned alpha1A-adrenoceptor using [3H]-prazosin as radioligandMore data for this Ligand-Target Pair
Affinity DataKi: 0.910nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair
Affinity DataKi: 0.912nMAssay Description:Displacement of [3H]prazosin from human adrenergic Alpha-1D expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 0.930nMAssay Description:Binding affinity to the adrenergic receptor alpha-1D of rat aortaMore data for this Ligand-Target Pair