Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 1.80nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 4nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 5.70nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 7.30nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 11nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 47nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 48nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 61nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 64nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 83nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: 128nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 398nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 590nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 763nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >1.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.09E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: 1.36E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-8-OH-DPAT binding to 5-hydroxytryptamine 1A receptor in rat cortical membranesMore data for this Ligand-Target Pair
Affinity DataKi: >3.00E+3nMAssay Description:In vitro ability to inhibit [3H]-raclopride binding to cloned human D2A receptors expressed in mouse fibroblast (LtK-) cellsMore data for this Ligand-Target Pair