Report error Found 5446 of ic50 data for polymerid = 2252,2272,49000493,49000496,50003097
Affinity DataIC50: 0.0300nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0430nMAssay Description:Inhibition of [125I]RTI-55 binding to dopamine transport sites in rat striatal membranes.More data for this Ligand-Target Pair
Affinity DataIC50: 0.0770nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.0850nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.115nMAssay Description:Inhibition of [125I]RTI-55 binding to dopamine transport sites in rat striatal membranes.More data for this Ligand-Target Pair
Affinity DataIC50: 0.120nMAssay Description:Displacement of [125I]RTI-55 from dopamine transporter of rat brain membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.130nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.146nMAssay Description:The compound was tested in vitro for high binding affinity for the Dopamine transporter (DAT) using competitive binding assay.More data for this Ligand-Target Pair
Affinity DataIC50: 0.150nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.170nMAssay Description:Inhibition of dopamine uptake in rat synaptosomal fractionMore data for this Ligand-Target Pair
Affinity DataIC50: 0.170nMAssay Description:Inhibition of dopamine uptake in rat synaptosomal fractionMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.227nMAssay Description:The compound was tested in vitro for high binding affinity for the Dopamine transporter (DAT) using competitive binding assay.More data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.230nMAssay Description:Displacement of [3H]WIN-35428 from dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.25nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.260nMAssay Description:Inhibition of [3H]dopamine uptake at the dopamine transporter in rat striatal tissueMore data for this Ligand-Target Pair
Affinity DataIC50: 0.280nMAssay Description:Inhibition of [125I]RTI-55 binding to dopamine transport sites in rat striatal membranes.More data for this Ligand-Target Pair
Affinity DataIC50: 0.300nMAssay Description:Displacement of [3H]WIN-35428 from DAT in rhesus monkey caudate-putamenMore data for this Ligand-Target Pair
Affinity DataIC50: 0.300nMAssay Description:Tested for radioligand [3H]BTCP displacement from dopamine transporter in rat forebrainMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.300nMAssay Description:Inhibition of [3H]WIN-35428 binding to Dopamine transporter in rhesus (Macaca mulatta) or cynomolgus monkey (Macaca fascicularis) caudate-putamenMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.320nMAssay Description:Displacement of [3H]WIN-35428 from dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.350nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.360nMAssay Description:Displacement of [3H]mazindol from dopamine transporterMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.360nMAssay Description:Displacement of [3H]mazindol from dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.370nMAssay Description:Binding affinity at the Dopamine transporter in rat striata by inhibition of 0.5 nM [3H]WIN-35428 bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.370nMAssay Description:Inhibition of [3H]WIN-35428 binding at dopamine transporter was determinedMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.380nMAssay Description:Tested for the ability to displace [125I]- RTI-55 binding in rat striatal membrane against dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.380nMAssay Description:Inhibition of [3H]WIN-35428 binding to dopamine transporter (DAT) of cynomolgus monkey caudate-putamenMore data for this Ligand-Target Pair
Affinity DataIC50: 0.380nMAssay Description:Inhibition of [3H]WIN-35428 binding to dopamine transporter (DAT) of cynomolgus monkey caudate-putamenMore data for this Ligand-Target Pair
Affinity DataIC50: 0.390nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.400nMAssay Description:Displacement of [3H]WIN-35428 from DAT in rhesus monkey caudate-putamenMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.400nMAssay Description:inhibition of [3H]WIN-35428 binding to the dopamine transporter (DAT) in monkey caudate-putamen.More data for this Ligand-Target Pair
Affinity DataIC50: 0.430nMAssay Description:Compound was evaluated for the inhibition of [3H]WIN-35428l binding to dopamine transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.430nMAssay Description:Binding affinity at the Dopamine transporter in rat striata by inhibition of 0.5 nM [3H]WIN-35428 bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.430nMAssay Description:Displacement of [125I]RTI-55 dopamine transporter binding in rat striatal membraneMore data for this Ligand-Target Pair
Affinity DataIC50: 0.430nMAssay Description:Inhibition of [3H]WIN-35428 binding to dopamine (DA) transporterMore data for this Ligand-Target Pair
Affinity DataIC50: 0.450nMAssay Description:Inhibitory activity in displacing [125I]- RTI-55 binding to dopamine transporter in rat striatal membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 0.460nMAssay Description:Binding affinity towards dopamine transporter in rat striatum using [3H]WIN-35 428 as radioligandMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.490nMAssay Description:Inhibition of [3H]WIN-35428 binding to the dopamine transporter in cynomolgus (macaca fascicularis) monkey caudate putamen.More data for this Ligand-Target Pair
Affinity DataIC50: 0.5nMAssay Description:Inhibitory concentration required to inhibit dopamine transporter DAT was determined by using [3H]WIN-35428 radioligandMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.570nMAssay Description:Inhibition of [3H]WIN-35428 binding to Dopamine transporter in rhesus (Macaca mulatta) or cynomolgus monkey (Macaca fascicularis) caudate-putamenMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.570nMAssay Description:Inhibition of [3H]WIN-35428 binding to the dopamine transporter in cynomolgus (macaca fascicularis) monkey caudate putamen.More data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.570nMAssay Description:Inhibition of [3H]WIN-35428 binding to Dopamine transporter in rhesus (Macaca mulatta) or cynomolgus monkey (Macaca fascicularis) caudate-putamenMore data for this Ligand-Target Pair
Affinity DataIC50: 0.590nMAssay Description:Inhibitory concentration required to inhibit dopamine transporter DAT was determined by using [3H]WIN-35428 radioligandMore data for this Ligand-Target Pair
Affinity DataIC50: 0.590nMAssay Description:Binding affinity against Dopamine transporter using [3H]WIN-35 428 in rat striatumMore data for this Ligand-Target Pair
Affinity DataIC50: 0.600nMAssay Description:Inhibition of dopamine DA reuptakeMore data for this Ligand-Target Pair
TargetSodium-dependent dopamine transporter(Human)
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Institut F£R Bioanorganische Und Radiopharmazeutische Chemie
Curated by ChEMBL
Affinity DataIC50: 0.600nMAssay Description:Inhibition of dopamine (DA) reuptake using cloned human dopamine transporter was determinedMore data for this Ligand-Target Pair
Affinity DataIC50: 0.610nMAssay Description:Binding affinity at the Dopamine transporter in rat striata by inhibition of 0.5 nM [3H]WIN-35428 bindingMore data for this Ligand-Target Pair
Affinity DataIC50: 0.620nMAssay Description:In vitro inhibitory activity against radioligand [3H]-WN 35,428 binding to dopamine transporter (DAT) in rat striatal tissueMore data for this Ligand-Target Pair
Affinity DataIC50: 0.620nMAssay Description:Inhibition of [3H]WIN-35428 binding to rat striatal dopamine transporterMore data for this Ligand-Target Pair
