Compile Data Set for Download or QSAR
Report error Found 28 Enz. Inhib. hit(s) with all data for entry = 50043603
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443517BDBM50443517(CHEMBL3087899)
Affinity DataIC50: 0.300nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443513BDBM50443513(CHEMBL3087903)
Affinity DataIC50: 2nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443518BDBM50443518(CHEMBL3087898)
Affinity DataIC50: 2nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443515BDBM50443515(CHEMBL3087901)
Affinity DataIC50: 5nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman 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 acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443519BDBM50443519(CHEMBL3087897)
Affinity DataIC50: 26nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443524BDBM50443524(CHEMBL3087905)
Affinity DataIC50: 30nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443516BDBM50443516(CHEMBL3087900)
Affinity DataIC50: 70nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443514BDBM50443514(CHEMBL3087902)
Affinity DataIC50: 143nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443522BDBM50443522(CHEMBL3087907)
Affinity DataIC50: 183nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443515BDBM50443515(CHEMBL3087901)
Affinity DataIC50: 357nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443519BDBM50443519(CHEMBL3087897)
Affinity DataIC50: 371nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443518BDBM50443518(CHEMBL3087898)
Affinity DataIC50: 420nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443523BDBM50443523(CHEMBL3087906)
Affinity DataIC50: 430nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443521BDBM50443521(CHEMBL3087908)
Affinity DataIC50: 633nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443525BDBM50443525(CHEMBL3087904)
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetAcetylcholinesterase(Electric eel)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443520BDBM50443520(CHEMBL3087896)
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibition of electric eel AChE using acetylcholine as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman 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 preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443517BDBM50443517(CHEMBL3087899)
Affinity DataIC50: 7.90E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443516BDBM50443516(CHEMBL3087900)
Affinity DataIC50: 1.56E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443525BDBM50443525(CHEMBL3087904)
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443513BDBM50443513(CHEMBL3087903)
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443521BDBM50443521(CHEMBL3087908)
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443523BDBM50443523(CHEMBL3087906)
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443522BDBM50443522(CHEMBL3087907)
Affinity DataIC50: 2.70E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443524BDBM50443524(CHEMBL3087905)
Affinity DataIC50: 4.20E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443514BDBM50443514(CHEMBL3087902)
Affinity DataIC50: 4.60E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed
TargetCholinesterase(Horse)
Kerman University of Medical Sciences

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50443520BDBM50443520(CHEMBL3087896)
Affinity DataIC50: 5.50E+4nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated for 15 mins prior to substrate addition by Ellman's methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
7/25/2014
Entry Details Article
PubMed