Compile Data Set for Download or QSAR
Report error Found 21 Enz. Inhib. hit(s) with all data for entry = 50001360
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50271142(6-Chloro-9-[(3-{4-[(5,6-Dimethoxy-1-oxoindan-2-yl)...)
Affinity DataIC50: 0.270nMAssay Description:Inhibition of AChE in human erythrocytes acetylthiocholine iodide as substrate by Ellman's spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 5.70nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277655(CHEMBL4166300)
Affinity DataIC50: 14nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM8961(CHEMBL95 | Cognex | cid_1935 | CHEMBL1337960 | 1,2...)
Affinity DataIC50: 40nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM8961(CHEMBL95 | Cognex | cid_1935 | CHEMBL1337960 | 1,2...)
Affinity DataIC50: 230nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMedPDB3D3D Structure (crystal)
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277652(CHEMBL4174269)
Affinity DataIC50: 710nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277655(CHEMBL4166300)
Affinity DataIC50: 3.69E+3nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277650(CHEMBL4172587)
Affinity DataIC50: 4.88E+3nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277651(CHEMBL4174514)
Affinity DataIC50: 5.99E+3nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277652(CHEMBL4174269)
Affinity DataIC50: 6.54E+3nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM8960(2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimethoxy-2...)
Affinity DataIC50: 9.14E+3nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277656(CHEMBL4164347)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277664(CHEMBL4164010)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277654(CHEMBL4163705)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277656(CHEMBL4164347)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277664(CHEMBL4164010)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277650(CHEMBL4172587)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277654(CHEMBL4163705)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277653(CHEMBL4176598)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetCholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277653(CHEMBL4176598)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human serum BuChE using butyrylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetAcetylcholinesterase(Human)
University of S£O Paulo

Curated by ChEMBL
LigandPNGBDBM50277651(CHEMBL4174514)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human AChE using acetylthiocholine iodide as substrate preincubated for 5 mins followed by substrate addition measured over 5 mins by U...More data for this Ligand-Target Pair
In DepthDetails Article
PubMed