null
SMILES CN(C)Cc1ccc(CSCCNc2cc(N)c(cc2[N+]([O-])=O)[N+]([O-])=O)o1
InChI Key InChIKey=HAFSYIUXFNUVMN-UHFFFAOYSA-N
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 6 hits for monomerid = 50004664
TargetMuscarinic acetylcholine receptor M2(Mus musculus)
University of South Carolina
Curated by ChEMBL
University of South Carolina
Curated by ChEMBL
Affinity DataKi: 460nMAssay Description:Ability of the compound to displace [3H]-methylscopolamine ([3H]-NMS) from mouse cerebral cortexMore data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M2(Mus musculus)
University of South Carolina
Curated by ChEMBL
University of South Carolina
Curated by ChEMBL
Affinity DataKi: 9.50E+3nMAssay Description:Ability of the compound to displace [3H]-methylscopolamine ([3H]-NMS) from mouse cerebral cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 83nMAssay Description:In vitro inhibition of human acetylcholinesterase.More data for this Ligand-Target Pair
Affinity DataIC50: 2.40E+3nMAssay Description:In vitro inhibition of human butryl cholinesterase.More data for this Ligand-Target Pair
TargetMuscarinic acetylcholine receptor M1(Mus musculus)
University of South Carolina
Curated by ChEMBL
University of South Carolina
Curated by ChEMBL
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of [3H]-pirenzepine binding to mouse muscarinic acetylcholine receptor M1 from cerebral cortexMore data for this Ligand-Target Pair
Affinity DataIC50: 6.80E+3nMAssay Description:Binding affinity of the compound against rat muscarinic acetylcholine receptor M2 using heart tissue and [3H]-N-methylscopolamineMore data for this Ligand-Target Pair