BDBM50013122 CHEMBL3261988
SMILES O=C(/C=N/O)Nc2ccc[n+](CCCCCC[n+]1cccc(NC(=O)/C=N/O)c1)c2
InChI Key InChIKey=XZRDJRVQNUXHQW-UHFFFAOYSA-P
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 3 hits for monomerid = 50013122
TargetAcetylcholinesterase(Human)
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Defence Research & Development Establishment (Drde)
Curated by ChEMBL
Affinity DataKd: 1.69E+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: 2.44E+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: 1.43E+6nMAssay 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
