Compile Data Set for Download or QSAR
Report error Found 32 Enz. Inhib. hit(s) with all data for entry = 50043395
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 8960BDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 14nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440434BDBM50440434(CHEMBL2425838)
Affinity DataIC50: 38nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440433BDBM50440433(CHEMBL2425839)
Affinity DataIC50: 44nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440435BDBM50440435(CHEMBL2425837)
Affinity DataIC50: 480nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440432BDBM50440432(CHEMBL2425840)
Affinity DataIC50: 566nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440427BDBM50440427(CHEMBL2425830)
Affinity DataIC50: 790nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440432BDBM50440432(CHEMBL2425840)
Affinity DataIC50: 831nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440430BDBM50440430(CHEMBL2425827)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440433BDBM50440433(CHEMBL2425839)
Affinity DataIC50: 1.27E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440439BDBM50440439(CHEMBL2425833)
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440431BDBM50440431(CHEMBL2425841)
Affinity DataIC50: 1.80E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440434BDBM50440434(CHEMBL2425838)
Affinity DataIC50: 1.84E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440436BDBM50440436(CHEMBL2425836)
Affinity DataIC50: 1.90E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440429BDBM50440429(CHEMBL2425828)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440426BDBM50440426(CHEMBL2425831)
Affinity DataIC50: 2.17E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440426BDBM50440426(CHEMBL2425831)
Affinity DataIC50: 2.17E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440437BDBM50440437(CHEMBL2425835)
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440440BDBM50440440(CHEMBL2425832)
Affinity DataIC50: 2.90E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440438BDBM50440438(CHEMBL2425834)
Affinity DataIC50: 3.70E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440439BDBM50440439(CHEMBL2425833)
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 8960BDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 5.38E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440436BDBM50440436(CHEMBL2425836)
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440428BDBM50440428(CHEMBL2425829)
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of electric eel AChE using acetylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440430BDBM50440430(CHEMBL2425827)
Affinity DataIC50: 1.12E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440427BDBM50440427(CHEMBL2425830)
Affinity DataIC50: 1.43E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440438BDBM50440438(CHEMBL2425834)
Affinity DataIC50: 1.78E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440435BDBM50440435(CHEMBL2425837)
Affinity DataIC50: 2.18E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440440BDBM50440440(CHEMBL2425832)
Affinity DataIC50: 3.60E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440428BDBM50440428(CHEMBL2425829)
Affinity DataIC50: 3.84E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440431BDBM50440431(CHEMBL2425841)
Affinity DataIC50: 4.10E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440429BDBM50440429(CHEMBL2425828)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Tehran University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50440437BDBM50440437(CHEMBL2425835)
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate after 2 mins by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
4/13/2014
Entry Details Article
PubMed