BDBM50127605 (1S,2S)-2-(1H-Imidazol-4-yl)-cyclopropylamine::(1S,2S)-2-(3H-Imidazol-4-yl)-cyclopropylamine::2-(1H-Imidazol-4-yl)-cyclopropylamine::CHEMBL13795::VUF-5297
SMILES N[C@H]1C[C@@H]1c1cnc[nH]1
InChI Key InChIKey=OWWNABDDYQLERE-WHFBIAKZSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 11 hits for monomerid = 50127605
Affinity DataKi: 1.70nMAssay Description:In vitro binding affinity was measured against Histamine H3 receptor on rat cerebral cortex.More data for this Ligand-Target Pair
Affinity DataKi: 4.30nMAssay Description:Affinity against rat Histamine H3 receptor using [3H]-N-alpha-methyl histamineMore data for this Ligand-Target Pair
Affinity DataKi: 9.30nMAssay Description:Inhibitory activity measured by [3H]- N alpha- methyl-histamine binding to membranes of SK-N-MC cells expressing the human Histamine H3 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 25nMAssay Description:Binding affinity of compound against Histamine H3 receptorMore data for this Ligand-Target Pair
Affinity DataKi: 1.09E+3nMAssay Description:Inhibitory activity measured by [3H]- N alpha- methyl-histamine binding to membranes of SK-N-MC cells expressing the human Histamine H4 receptorMore data for this Ligand-Target Pair
Affinity DataEC50: 7.08E+3nMAssay Description:Inhibitory activity determined by the inhibition of cAMP- stimulated beta-galactosidase transcription in SK-N-MC cells expressing the human Histamine...More data for this Ligand-Target Pair
Affinity DataEC50: 696nMAssay Description:Inhibition of human Histamine H2 receptor using [3H]-tiotidineMore data for this Ligand-Target Pair
Affinity DataEC50: 864nMAssay Description:Inhibition of human Histamine H1 receptor using [3H]-pyrilamineMore data for this Ligand-Target Pair
Affinity DataEC50: 42nMAssay Description:Inhibition of human Histamine H3 receptor using [3H]-N-alpha-methyl histamineMore data for this Ligand-Target Pair
Affinity DataEC50: >0.000100nMAssay Description:Inhibition of human Histamine H4 receptorMore data for this Ligand-Target Pair
Affinity DataEC50: 5.90nMAssay Description:Inhibitory activity determined by the inhibition of cAMP- stimulated beta-galactosidase transcription in SK-N-MC cells expressing the human Histamine...More data for this Ligand-Target Pair