Compile Data Set for Download or QSAR
Report error Found 20 Enz. Inhib. hit(s) with all data for entry = 50003022
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465901BDBM50465901(CHEMBL4285826)
Affinity DataKi:  1.20E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465900BDBM50465900(CHEMBL4281350)
Affinity DataKi:  2.10E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465902BDBM50465902(CHEMBL4277895)
Affinity DataKi:  2.20E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465903BDBM50465903(CHEMBL4289221)
Affinity DataKi:  2.40E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50020522BDBM50020522(1-(((4-carbamoylpyridinium-1-yl)methoxy)methyl)-2-...)
Affinity DataKi:  2.50E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465904BDBM50465904(CHEMBL4284764)
Affinity DataKi:  3.60E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465899BDBM50465899(CHEMBL4292643)
Affinity DataKi:  4.20E+4nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50333782BDBM50333782(4-(aminocarbonyl)-1-(3-{4-[(E)-(hydroxyimino)methy...)
Affinity DataKi:  7.30E+4nMAssay Description:Reversible inhibition of human erythrocytic AChE using acetylthiocholine iodide as substrate measured up to 2 mins by spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50333783BDBM50333783((E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomet...)
Affinity DataKi:  9.00E+4nMAssay Description:Reversible inhibition of human erythrocytic AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50025010BDBM50025010(CHEMBL116379)
Affinity DataKi:  1.10E+5nMAssay Description:Reversible inhibition of human erythrocytic AChE using acetylthiocholine iodide as substrate measured up to 2 mins by spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465901BDBM50465901(CHEMBL4285826)
Affinity DataKi:  1.40E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetAcetylcholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 234367BDBM234367(Pralidoxime (3))
Affinity DataKi:  1.80E+5nMAssay Description:Reversible inhibition of recombinant human recombinant AChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465902BDBM50465902(CHEMBL4277895)
Affinity DataKi:  1.87E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465900BDBM50465900(CHEMBL4281350)
Affinity DataKi:  1.95E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50020522BDBM50020522(1-(((4-carbamoylpyridinium-1-yl)methoxy)methyl)-2-...)
Affinity DataKi:  2.15E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465904BDBM50465904(CHEMBL4284764)
Affinity DataKi:  2.65E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465899BDBM50465899(CHEMBL4292643)
Affinity DataKi:  2.73E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50465903BDBM50465903(CHEMBL4289221)
Affinity DataKi:  2.94E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 234367BDBM234367(Pralidoxime (3))
Affinity DataKi:  3.90E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed
TargetCholinesterase(Human)
Institute For Medical Research and Occupational Health

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50333783BDBM50333783((E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomet...)
Affinity DataKi:  9.10E+5nMAssay Description:Reversible inhibition of human plasma BChE using acetylthiocholine iodide as substrate by Ellman spectrophotometric methodMore data for this Ligand-Target Pair
In Depth
Date in BDB:
8/18/2020
Entry Details Article
PubMed