Affinity DataIC50: 0.260nMAssay Description:Inhibition of [3H]-mepyramine binding to the histamine receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 1.90nMAssay Description:Inhibition of [3H]-mepyramine binding to the histamine receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 8.80nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 24nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 30nMAssay Description:Inhibition of [3H]-mepyramine binding to the histamine receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 70nMAssay Description:-Log (Ki) value for butyrylcholinesterase by inhibiting DFPMore data for this Ligand-Target Pair
Affinity DataIC50: 200nMAssay Description:-Log (Ki) value for butyrylcholinesterase by inhibiting DFPMore data for this Ligand-Target Pair
Affinity DataIC50: 430nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 870nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:Antiparasitic activity of the compound against thiamine transporter of Eimeria tenellaMore data for this Ligand-Target Pair
Affinity DataIC50: 1.19E+4nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of [3H]-mepyramine binding to the Histamine H1 receptor in guinea pig cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+4nMAssay Description:-Log (Ki) value for butyrylcholinesterase by inhibiting DFPMore data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+5nMAssay Description:Compound was evaluated for the protection of butrylcholinesterase against DFT in mice and expressed as Ki.More data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+6nMAssay Description:Displacement of [3H]5-HT binding to serotonin receptor of rat fundus membranesMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+6nMAssay Description:Displacement of [3H]5-HT binding to serotonin receptor of rat fundus membranesMore data for this Ligand-Target Pair
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