null
SMILES OC(CCCN1CCN(CC1)c1ncc(F)cn1)c1ccc(F)cc1
InChI Key InChIKey=ZXUYYZPJUGQHLQ-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 37 hits for monomerid = 50002238
Affinity DataKi: 71nMAssay Description:Binding affinity against the sigma receptor from guinea pig brain using the radioligand [3H]SKF-10047More data for this Ligand-Target Pair
Affinity DataKi: 164nMAssay Description:Binding affinity for Sigma opioid receptor type 2 in guinea pig brain homogenate with 4 nM [3H]-(+)-DTGMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Mus musculus (Mouse))
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Affinity DataKi: 174nMAssay Description:In vitro binding affinity for the mouse sigma opioid receptorMore data for this Ligand-Target Pair
Affinity DataKi: 265nMAssay Description:Ability to displace [3H](+)-pentazocine from Sigma opioid receptor type 1 of guinea pig brainMore data for this Ligand-Target Pair
Affinity DataKi: 265nMAssay Description:Sigma opioid receptor type 1 affinity in guinea pig brain by employing [3H](+)-pentazocine as radioligand.More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(Cavia porcellus (Guinea pig))
Institut für Pharmazeutische und Medizinische Chemie
Curated by ChEMBL
Institut für Pharmazeutische und Medizinische Chemie
Curated by ChEMBL
Affinity DataKi: 265nMAssay Description:Displacement of [3H](+)-pentazocine from sigma 1 receptor in guinea pig brain membrane by liquid scintillation analyzerMore data for this Ligand-Target Pair
Affinity DataKi: 265nMAssay Description:Binding affinity for Sigma opioid receptor type 1 in guinea pig brain homogenate with 0.5 nM [3H]-(+)-PENTMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataKi: 391nMAssay Description:Ability to displace [3H]ditolylguanidine in the presence of 100 nM (+)-pentazocine from Sigma opioid receptor type 2 of rat liverMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataKi: 391nMAssay Description:Sigma opioid receptor type 2 affinity in rat liver by employing [3H]ditolylguanidine as radioligandMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 2A/2B/2C(Mus musculus (Mouse))
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Affinity DataKi: 410nMAssay Description:In vitro binding affinity for serotonin 5-hydroxytryptamine (5-HT) 2 receptorsMore data for this Ligand-Target Pair
Affinity DataIC50: 8.40E+3nMAssay Description:Binding affinity towards Dopamine receptor D2 binding site using [3H]spiroperidol.More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataIC50: 60nMAssay Description:Binding affinity towards sigma receptor binding site 1 using [3H](+)-pentazocineMore data for this Ligand-Target Pair
Affinity DataIC50: 830nMAssay Description:Binding affinity towards 5-hydroxytryptamine 2A receptor binding site using [3H]ketanserin .More data for this Ligand-Target Pair
Affinity DataIC50: 320nMAssay Description:Binding affinity towards 5-hydroxytryptamine 1A receptor binding site using [3H]8-OH-DPAT .More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataIC50: 60nMAssay Description:Compound was evaluated for the binding affinity towards Sigma receptor type 1 using radioligand ([3H]-(+)- Pentazocine) binding assay.More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataIC50: 158nMAssay Description:Inhibitory concentration against radioligand [3H]3-PPP binding to Sigma opioid receptor type 1 in rat brain membraneMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against radioligand [3H](-)-sulpiride binding to Dopamine receptor D2 in ratMore data for this Ligand-Target Pair
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
Bristol-Myers Squibb Co.
Curated by ChEMBL
Bristol-Myers Squibb Co.
Curated by ChEMBL
Affinity DataIC50: 460nMAssay Description:Inhibitory concentration against radioligand [3H](+)-NAN binding to haloperidol-sensitive sigma binding site in whole guinea pig brainMore data for this Ligand-Target Pair
TargetBeta-1/Beta-2/Beta-3 adrenergic receptor(Rattus norvegicus (Rat))
Bristol-Myers Squibb Co.
Curated by ChEMBL
Bristol-Myers Squibb Co.
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against radioligand [3H]dihydroalprenolol binding to Beta adrenergic receptor in rat cortexMore data for this Ligand-Target Pair
TargetAlpha-1A/Alpha-1B/Alpha-1D adrenergic receptor(Rattus norvegicus (rat))
Bristol-Myers Squibb Co.
Curated by ChEMBL
Bristol-Myers Squibb Co.
Curated by ChEMBL
Affinity DataIC50: 520nMAssay Description:Inhibition of [3H]WB-4101 binding to rat cortical Alpha-1 adrenergic receptor in vitroMore data for this Ligand-Target Pair
TargetGamma-aminobutyric acid receptor subunit gamma-1(Rattus norvegicus)
Bristol-Myers Squibb Co.
Curated by ChEMBL
Bristol-Myers Squibb Co.
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of [3H]muscimol binding to GABA-A of rat cerebellumMore data for this Ligand-Target Pair
TargetAlpha-2A adrenergic receptor [16-465]/Alpha-2B adrenergic receptor/Alpha-2C adrenergic receptor(RAT)
Bristol-Myers Squibb Co.
Curated by ChEMBL
Bristol-Myers Squibb Co.
Curated by ChEMBL
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against radioligand [3H]clonidine binding to Alpha-2 adrenergic receptor in rat cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibitory concentration against radioligand [3H]spiperone binding to 5-hydroxytryptamine 2 receptor in rat cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against radioligand [3H]-SCH- 23390 binding to Dopamine receptor D1 receptors in rat striatumMore data for this Ligand-Target Pair
Affinity DataIC50: 83nMAssay Description:Inhibitory concentration against radioligand [3H](+)-NAN binding to haloperidol-sensitive sigma binding site in whole guinea pig brainMore data for this Ligand-Target Pair
Affinity DataIC50: 120nMAssay Description:Inhibition of specific binding of [3H]3-PPP to sigma receptor in Guinea pig brain membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 6.43E+3nMAssay Description:In vitro inhibitory against radioligand [3H]spiperone binding to rat striatal Dopamine receptor D2More data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataIC50: 112nMAssay Description:Displacement of (+)-[3H]-3-PPP from rat cortical sigma siteMore data for this Ligand-Target Pair
Affinity DataIC50: 320nMAssay Description:Inhibitory concentration against radioligand [3H]8-OH-DPAT binding to rat hippocampal 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
TargetD(2) dopamine receptor(Mus musculus (Mouse))
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Du Pont Merck Pharmaceutical Company
Curated by ChEMBL
Affinity DataIC50: 2.43E+3nMAssay Description:In vitro binding affinity towards dopamine receptor D2More data for this Ligand-Target Pair
Affinity DataIC50: 4.90E+3nMAssay Description:Binding affinity against the Dopamine receptor D2 in rat striatum by using [3H]spiperone radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 320nMAssay Description:In vitro binding affinity towards serotonin 5-HT1A receptor by the displacement of [3H]-8-OH-DPAT from rat hippocampusMore data for this Ligand-Target Pair
Affinity DataIC50: 1.70E+3nMAssay Description:In vitro binding affinity towards serotonin 5-HT2A receptor by the displacement of [3H]-spiperone from rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 112nMAssay Description:In vitro binding affinity of the compound towards sigma receptor by the displacement of [3H]-PPP from guinea pig brainMore data for this Ligand-Target Pair
Affinity DataIC50: 71nMAssay Description:Inhibition of specific binding of [125I]PIPAG to sigma receptor in Guinea pig brain membranesMore data for this Ligand-Target Pair
TargetSigma non-opioid intracellular receptor 1(RAT)
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Pharmazeutisches Institut der Universit£t Freiburg
Curated by ChEMBL
Affinity DataIC50: 230nMAssay Description:Binding affinity towards Sigma receptor site 2 in rat brain using [3H]DTG as radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 112nMAssay Description:Inhibitory concentration against radioligand [3H]3-PPP binding to haloperidol-sensitive sigma binding site in whole guinea pig brainMore data for this Ligand-Target Pair