BDBM50019443 1-(1H-Indol-4-yloxy)-3-isopropylamino-propan-2-ol::1-(1H-Indol-4-yloxy)-3-isopropylamino-propan-2-ol((-)-Pindolol)::1-(1H-Indol-4-yloxy)-3-isopropylamino-propan-2-ol(pindolol)::1-(1H-indol-4-yloxy)-3-(isopropylamino)propan-2-ol::LB-46::PINDOLOL::PINDOLOL,(-)::PRINODOLOL::VISKAZIDE::VISKEN
SMILES CC(C)NCC(O)COc1cccc2[nH]ccc12
InChI Key InChIKey=JZQKKSLKJUAGIC-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 85 hits for monomerid = 50019443
Affinity DataKi: 0.400nMAssay Description:Binding affinity at human adrenergic beta2 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.520nMAssay Description:Binding affinity at human adrenergic beta1 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 20nMAssay Description:Evaluated for the binding affinity to hippocampus striatal membranes at 5-hydroxytryptamine 1A receptor binding site by using [3H]-8-OH- DPAT as a ra...More data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Displacement of [3H]DPAT from human 5HT1A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Binding affinity of a compound to rat brain 5-hydroxytryptamine 1A (serotonin) receptor assayed by radiolabeled [3H]-8-OH-DPAT ligand displacementMore data for this Ligand-Target Pair
Affinity DataKi: 24nMAssay Description:Displacement of specific [3H]- 5-HT binding to cloned human 5-hydroxytryptamine 1A receptor stably expressed in HeLa cellsMore data for this Ligand-Target Pair
Affinity DataKi: 80nMAssay Description:Binding affinity (Ki) to rat cortical membranes at 5-HT1B binding site by using [125 I] ICYP as a radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 81nMAssay Description:Antagonist activity at human 5HT1A expressed in mouse LM(tK-) cells assessed as inhibition of 5HT-stimulated [35S]GTPgammaS bindingMore data for this Ligand-Target Pair
Affinity DataKi: 100nMAssay Description:Evaluated for binding affinity towards rat cortical membranes at 5-hydroxytryptamine 1 receptor binding site by using [3H]-5-HT as a radioligand.More data for this Ligand-Target Pair
Affinity DataKi: 110nMAssay Description:Inhibition constant against 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Human)
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL
Affinity DataKi: 2.60E+3nMAssay Description:Agonist activity to the human recombinant 5-hydroxytryptamine 1B receptorMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Human)
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL
Affinity DataKi: 2.60E+3nMAssay Description:Agonist activity to the human recombinant 5-hydroxytryptamine 1B receptorMore data for this Ligand-Target Pair
Target5-hydroxytryptamine receptor 1B(Human)
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL
Medical College of Virginia/Virginia Commonwealth University
Curated by ChEMBL