BDBM50171392 CHEMBL3805559
SMILES CNC(=O)c1cccc(OCCCCN2CCC(CC2)c2noc3cc(F)ccc23)c1
InChI Key InChIKey=SHFBSNNAMYYULF-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50171392
Affinity DataIC50: 46nMAssay Description:Antagonistic activity at human 5-HT2A receptor assessed as calcium flux after 10 mins by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataEC50: 13nMAssay Description:Agonistic activity at human 5-HT1A receptor measured after 60 mins by Ultra Lance cAMP assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.5nMAssay Description:Antagonistic activity at human dopamine D2 receptor measured after 60 mins by Ultra Lance cAMP assayMore data for this Ligand-Target Pair
Affinity DataIC50: 35nMAssay Description:Antagonistic activity at alpha-1A adrenergic receptor (unknown origin) after 10 mins by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 190nMAssay Description:Antagonistic activity at 5-HT2c receptor (unknown origin) after 10 mins by FLIPR assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.56E+3nMAssay Description:Antagonistic activity at histamine1 receptor (unknown origin) after 10 mins by FLIPR assayMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Shanghai Institute of Materia Medica
Curated by ChEMBL
Shanghai Institute of Materia Medica
Curated by ChEMBL
Affinity DataIC50: 1.03E+3nMAssay Description:Inhibition of human ERG after 10 minsMore data for this Ligand-Target Pair