BDBM50533195 CHEMBL3747904
SMILES CC1CCCN(CCCCCCCOc2cccc(Cl)c2)C1
InChI Key InChIKey=QVTJBLMDJBZOAB-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50533195
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Affinity DataIC50: 5.15E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...More data for this Ligand-Target Pair
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured after 5 m...More data for this Ligand-Target Pair
Affinity DataIC50: 5.15E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine chloride as substrate preincubated for 5 mins followed by substrate addition measured after ...More data for this Ligand-Target Pair
Affinity DataKi: 446nMAssay Description:Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...More data for this Ligand-Target Pair
Affinity DataKi: 446nMAssay Description:Displacement of [3H]Nalpha-methylhistamine from human full length recombinant histamine H3 receptor expressed in HEK293 cell membranes after 90 mins ...More data for this Ligand-Target Pair