null
SMILES CN(C)c1ccc2c(-c3ccc(cc3C([O-])=O)C(=O)NCCOCCOCCOCCNC(=O)C3CCN(Cc4ccc(OCCCN5CCCCC5)cc4)CC3)c3ccc(cc3oc2c1)=[N+](C)C
InChI Key
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50586476
Affinity DataKi: 0.158nMAssay Description:Binding affinity in Nluc-hH3R assessed in HEK293 cells by NanoBRET binding assayMore data for this Ligand-Target Pair
Affinity DataKi: 0.302nMAssay Description:Displacement of [3H]UR-P1294 from human H3R receptor expressed in HEK293 cells by radioligand competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: <1.00E+5nMAssay Description:Displacement of [3H]UR-DE25 from human H2R receptor expressed in HEK293 cells by radioligand competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: <1.00E+5nMAssay Description:Displacement of [3H]histamine from human H4R receptor expressed in HEK293 cells by radioligand competition binding assayMore data for this Ligand-Target Pair
Affinity DataKi: <1.00E+5nMAssay Description:Displacement of [3H]mepyramine from human H1R receptor expressed in HEK293 cells by radioligand competition binding assayMore data for this Ligand-Target Pair
Affinity DataKd: 0.676nMAssay Description:Binding affinity to human H3R expressed in HEK293 cells by flow cytometric analysisMore data for this Ligand-Target Pair