Affinity DataKi: 0.0880nMAssay Description:Inhibition constant of 50 microM forskolin-stimulated cAMP accumulation against 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 0.100nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.158nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.158nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.200nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.251nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.251nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.316nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.316nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.400nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
Affinity DataKi: 0.400nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.400nMAssay Description:Binding affinity towards dopamine receptor D1 using [3H]-SCH-23,390 was determined in rat striatal membranesChecked by AuthorMore data for this Ligand-Target Pair
Affinity DataKi: 0.450nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.450nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Displacement of [3H]SCH-23390 from dopamine D1-like receptor in porcine striata homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 0.501nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.600nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.700nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.700nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.75nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.794nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.800nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 0.940nMAssay Description:Displacement of [3H]-SCH-23390 from human dopamine D1 receptor expressed in HEK293 cells after 30 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 1nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1.10nMAssay Description:Displacement of [3H]-N-methylspiperone from human dopamine D3 receptor expressed in HEK293 cells after 30 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 1.20nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1.20nMAssay Description:Displacement of [3H]-N-methylspiperone from human dopamine D2long receptor expressed in HEK293 cells after 30 mins by scintillation countingMore data for this Ligand-Target Pair
Affinity DataKi: 1.26nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 1.5nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1.5nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1.58nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 1.58nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:Evaluated for the binding constant at [3H]-8-OH-DPAT-labeled human 5-hydroxytryptamine 1A receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
Affinity DataKi: 2nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 2nMAssay Description:Binding affinity to human cloned adrenergic alpha 2C receptor receptorMore data for this Ligand-Target Pair
Affinity DataKi: 2.20nMAssay Description:In vitro inhibition assay using cathepsin.More data for this Ligand-Target Pair
Affinity DataKi: 2.5nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair
Affinity DataKi: 2.51nMAssay Description:Antagonist activity at human recombinant histamine H1 receptor expressed in intact CHO cells assessed as inhibition of histamine-induced cellular cal...More data for this Ligand-Target Pair
Affinity DataKi: 3.20nMAssay Description:In vitro cathepsin inhibition assay.More data for this Ligand-Target Pair