Found 39 of ki for monomerid = 50366618 
Affinity DataKi: 0.200nMAssay Description:Binding affinity against Alpha-1A adrenergic receptor (recombinant human receptor) using [3H]prazosin.More data for this Ligand-Target Pair
Affinity DataKi: 0.347nMAssay Description:Binding affinity determined by displacement of [3H]prazosin from alpha-1A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.347nMAssay Description:Binding affinity to Homo sapiens (human) alpha1A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:Binding affinity against human Alpha-1a adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.400nMAssay Description:In vitro binding affinity against Alpha-1A adrenergic receptor of human liver microsomes.More data for this Ligand-Target Pair
Affinity DataKi: 1.30nMAssay Description:Inhibition of [3H]prazosin binding to human Alpha-1A adrenergic receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 37nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 74nMAssay Description:In vitro binding affinity against Alpha-1B adrenergic receptor of human liver microsomes.More data for this Ligand-Target Pair
Affinity DataKi: 160nMAssay Description:In vitro binding affinity against Alpha-1D adrenergic receptor of human liver microsomes.More data for this Ligand-Target Pair
Affinity DataKi: 180nMAssay Description:Binding affinity against Alpha-1B adrenergic receptor (recombinant human receptor) using [3H]prazosin.More data for this Ligand-Target Pair
Affinity DataKi: 219nMAssay Description:Binding affinity determined by displacement of [3H]prazosin from alpha-1B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 220nMAssay Description:Binding affinity against human Alpha-1b adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 220nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 269nMAssay Description:Inhibition of [3H]prazosin binding to human Alpha-1B adrenergic receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 370nMAssay Description:Ability to displace [3H]rauwolscine from cloned human Alpha-2C adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 372nMAssay Description:Binding affinity assayed by displacement of [3H]rauwolscine from human alpha-2C adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 410nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 460nMAssay Description:Ability to displace [3H]rauwolscine from cloned human Alpha-2C adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 537nMAssay Description:Binding affinity determined by displacement of [3H]prazosin from alpha-1D adrenergic receptorMore data for this Ligand-Target Pair
TargetVoltage-dependent L-type calcium channel subunit alpha-1S(Rattus norvegicus)
New York University Medical Center
Curated by ChEMBL
New York University Medical Center
Curated by ChEMBL
Affinity DataKi: 537nMAssay Description:Binding affinity at the L-type [Ca2+] channel from rat brain homogenate by [3H]nitrendipine displacement.More data for this Ligand-Target Pair
Affinity DataKi: 540nMAssay Description:Binding affinity against human Alpha-1d adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 630nMAssay Description:Binding affinity against Alpha-1D adrenergic receptor (recombinant human receptor) using [3H]-prazosin.More data for this Ligand-Target Pair
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Synaptic Pharmaceutical
Curated by ChEMBL
Synaptic Pharmaceutical
Curated by ChEMBL
Affinity DataKi: 670nMAssay Description:Binding affinity against rat L-type calcium channelMore data for this Ligand-Target Pair
TargetVoltage-dependent L-type calcium channel subunit alpha-1C(RAT)
Synaptic Pharmaceutical
Curated by ChEMBL
Synaptic Pharmaceutical
Curated by ChEMBL
Affinity DataKi: 741nMAssay Description:Inhibition of [3H]nitrendipine binding to membrane homogenates of of rat cardiac muscle.More data for this Ligand-Target Pair
Affinity DataKi: 780nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1D adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 780nMAssay Description:Ability to displace [3H]prazosin from cloned human Alpha-1D adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 780nMAssay Description:Ability to displace [3H]rauwolscine from cloned human Alpha-2B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 794nMAssay Description:Binding affinity determined by displacement of [3H]rauwolscine from alpha-2B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 912nMAssay Description:Binding affinity against human Alpha-2c adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.05E+3nMAssay Description:Inhibition of [3H]prazosin binding to human Alpha-1D adrenergic receptor expressed in CHO cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.09E+3nMAssay Description:Binding affinity against human Alpha-2b adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.10E+3nMAssay Description:Ability to displace [3H]rauwolscine from cloned human Alpha-2A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.17E+3nMAssay Description:Inhibition of [3H]rauwolscine binding to CHO cells expressing the human Alpha-2B adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.20E+3nMAssay Description:Ability to displace [3H]rauwolscine from cloned human Alpha-2A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.20E+3nMAssay Description:Binding affinity determined by displacement of [3H]rauwolscine from alpha-2A adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.32E+3nMAssay Description:Inhibition of [3H]rauwolscine to CHO cells expressing the human Alpha-2C adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 2.42E+3nMAssay Description:Binding affinity against human Alpha-2a adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataKi: 3.30E+3nMAssay Description:Inhibition of [3H]rauwolscine binding to CHO cells expressing the human Alpha-2A adrenergic receptorMore data for this Ligand-Target Pair
