BDBM50525820 CHEMBL4457100
SMILES [H][C@@]12[C@H](CC(=O)[C@@]1(C)CC[C@]1([H])c3ccc(OCCCN4CCC[C@H]4C)cc3CC[C@@]21[H])C(=O)NCC
InChI Key InChIKey=HHUDQJYTXZNZNP-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 4 hits for monomerid = 50525820
Affinity DataKi: 3nMAssay Description:Displacement of [3H]methyl- N-alpha methylhistamine dihydrochloride from human recombinant H3 receptor expressed in CHOK1 cells measured after 30 min...More data for this Ligand-Target Pair
Affinity DataKi: 9nMAssay Description:Displacement of [3H]methyl- N-alpha methylhistamine dihydrochloride from Sprague-Dawley rat cerebral cortex H3 receptor measured after 30 mins by sci...More data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1/M2/M3/M4/M5(Rat)
Chemical Works of Gedeon Richter
Curated by ChEMBL
Chemical Works of Gedeon Richter
Curated by ChEMBL
Affinity DataKi: 4.70E+3nMAssay Description:Displacement of [3H]quinuclidinyl benzilate from Wistar rat cortex muscarinic acetylcholine receptor by liquid scintillation counter methodMore data for this Ligand-Target Pair
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Chemical Works of Gedeon Richter
Curated by ChEMBL
Chemical Works of Gedeon Richter
Curated by ChEMBL
Affinity DataIC50: 1.75E+4nMAssay Description:Inhibition of human ERGMore data for this Ligand-Target Pair
