BDBM50235079 CHEMBL4103112
SMILES [H][C@@]1(CC[C@@H](Cc2ccc(cc2)C(=O)N2CCN(Cc3nnn(CC(F)F)n3)CC2)N1)[C@H](O)c1ccccc1
InChI Key InChIKey=YDJMKEIHCDSIFC-PPJWLVRDSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 7 hits for monomerid = 50235079
Affinity DataEC50: 1.5nMAssay Description:Agonist activity at human beta3 adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataIC50: >2.00E+4nMAssay Description:Activity at human beta1 adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataIC50: >2.00E+4nMAssay Description:Activity at human beta2 adrenergic receptorMore data for this Ligand-Target Pair
Affinity DataEC50: 827nMAssay Description:Inhibition of the EPSP synthase PEP-Pi site by the compound expressed as apparent valueMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of SERT (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: >3.00E+4nMAssay Description:Dissociation constant against EPSP synthaseMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Merck
Curated by ChEMBL
Merck
Curated by ChEMBL
Affinity DataIC50: >6.00E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair