BDBM50013125 CHEMBL3261989
SMILES O=C(/C=N/O)Nc2ccc[n+](CCCCCCC[n+]1cccc(NC(=O)/C=N/O)c1)c2
InChI Key InChIKey=BZDSVXCHLHSRCC-UHFFFAOYSA-P
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50013125
TargetAcetylcholinesterase(Human)
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Affinity DataKd: 6.58E+4nMAssay Description:Binding affinity to VX-inhibited hemoglobin free human erythrocyte ghost acetylcholinesterase using acetylthiocholineiodide as substrate measured up ...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Human)
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Affinity DataKd: 8.43E+4nMAssay Description:Binding affinity to sarin-inhibited hemoglobin free human erythrocyte ghost acetylcholinesterase using acetylthiocholineiodide as substrate measured ...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Human)
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Affinity DataIC50: 9.30E+5nMAssay Description:Inhibition of hemoglobin free human erythrocyte ghost acetylcholinesterase using acetylthiocholineiodide as substrate measured up to 1 hr by Ellman m...More data for this Ligand-Target Pair
