BDBM50313079 3-Dimethylcarbamoyloxy-1-methyl-pyridinium; bromide::CHEMBL812::Mestinon::PYRIDOSTIGMINE BROMIDE::Pyridostigmine::Pyridostigmine (1)::Regonol
SMILES CN(C)C(=O)Oc1ccc[n+](C)c1
InChI Key InChIKey=RVOLLAQWKVFTGE-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 15 hits for monomerid = 50313079
Affinity DataIC50: 4.00E+4nMpH: 7.4Assay Description:Human erythrocyte AChE or human plasmatic BChE (Prague, Aldrich; commercially purified by affinity chromatography) were suspended into phosphate buff...More data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+7nMpH: 7.4Assay Description:Human erythrocyte AChE or human plasmatic BChE (Prague, Aldrich; commercially purified by affinity chromatography) were suspended into phosphate buff...More data for this Ligand-Target Pair
Affinity DataIC50: 350nMAssay Description:Inhibition of human AChE assessed as acetylthiocholine hydrolysis preincubated for 10 mins followed by addition of substrate measured after 2 mins by...More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human plasma BChE assessed as butyrylthiocholine hydrolysis preincubated for 10 mins followed by addition of substrate measured after 2...More data for this Ligand-Target Pair
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+7nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
Affinity DataIC50: 50nMAssay Description:Concentration required to inhibit hydrolytic activity of bovine erythrocyte acetylcholinesterase by 50%More data for this Ligand-Target Pair
Affinity DataIC50: 360nMAssay Description:Inhibition of human whole RBC AChE pretreated for 30 mins by Ellman techniqueMore data for this Ligand-Target Pair
Affinity DataIC50: 900nMAssay Description:Inhibition of human plasma BChE pretreated for 30 mins by Ellman techniqueMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human BSEP expressed in baculovirus transfected fall armyworm Sf21 cell membranes vesicles assessed as reduction in ATP-dependent [3H]-...More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human BChE using butyrylthiocholine as substrate preincubated for 5 mins followed by substrate addition and measured after 2 mins by Pe...More data for this Ligand-Target Pair
Affinity DataIC50: 350nMAssay Description:Inhibition of human AChE using acetylthiocholine as substrate preincubated for 5 mins followed by substrate addition and measured after 2 mins by Per...More data for this Ligand-Target Pair
Affinity DataKi: 3.50E+3nMAssay Description:Anticholinesterase activity by their ability to inactivate human serum butyrylcholinesteraseMore data for this Ligand-Target Pair
Affinity DataKi: 1.97E+4nMAssay Description:Inhibitory activity against Acetylcholinesterase (AChE)More data for this Ligand-Target Pair
Affinity DataKi: 1.14E+5nMAssay Description:Inhibitory activity against Butyrylcholinesterase (BChE)More data for this Ligand-Target Pair