BDBM50626973 CHEMBL5421943

SMILES CCOP(=O)(OCC)C(Nc1ccc(cc1)[N+]([O-])=O)c1ccc(OCc2nc3ccccc3c(=O)n2-c2ccc(F)cc2)c(OC)c1

InChI Key InChIKey=IGFAIZMGHCSJKW-UHFFFAOYSA-N

Data  3 IC50

  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 = 50626973   

TargetAcetylcholinesterase(Electric eel)
Yogi Vemana University

Curated by ChEMBL
LigandPNGBDBM50626973(CHEMBL5421943)
Affinity DataIC50: 315nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition by DTNB based Ellm...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/18/2024
Entry Details
PubMed
TargetAcetylcholinesterase(Human)
Yogi Vemana University

Curated by ChEMBL
LigandPNGBDBM50626973(CHEMBL5421943)
Affinity DataIC50: 1.78E+3nMAssay Description:Inhibition of human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition by DTNB based...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/18/2024
Entry Details
PubMed
TargetCholinesterase(Horse)
Yogi Vemana University

Curated by ChEMBL
LigandPNGBDBM50626973(CHEMBL5421943)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of equine serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition by DTNB based El...More data for this Ligand-Target Pair
In Depth
Date in BDB:
12/18/2024
Entry Details
PubMed