BDBM50491132 CHEMBL2377261

SMILES CC(C)N(CCOC(=O)C(O)(c1ccccc1)c1ccccc1)C(C)C

InChI Key InChIKey=NHFIEMNGVIAFJO-UHFFFAOYSA-N

Data  3 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50491132   

TargetMuscarinic acetylcholine receptor M2(Human)
Walter Reed Army Institute of Research

Curated by ChEMBL
LigandPNGBDBM50491132(CHEMBL2377261)
Affinity DataKi:  5.85nMAssay Description:Displacement of [3H] N-methylscopolamine from human muscarinic M2 receptor expressed in CHOK1 cells after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetMuscarinic acetylcholine receptor M3(Human)
Walter Reed Army Institute of Research

Curated by ChEMBL
LigandPNGBDBM50491132(CHEMBL2377261)
Affinity DataKi:  59nMAssay Description:Displacement of [3H] N-methylscopolamine from human muscarinic M3 receptor expressed in CHOK1 cells after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed
TargetMuscarinic acetylcholine receptor M1(Human)
Walter Reed Army Institute of Research

Curated by ChEMBL
LigandPNGBDBM50491132(CHEMBL2377261)
Affinity DataKi:  971nMAssay Description:Displacement of [3H] N-methylscopolamine from human muscarinic M1 receptor expressed in CHOK1 cells after 30 mins by scintillation counting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/31/2020
Entry Details Article
PubMed