Compile Data Set for Download or QSAR
maximum 50k data
Found 12 Enz. Inhib. hit(s) with all data for entry = 50044413
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)
Affinity DataIC50:  10nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016492(CHEMBL3265401)
Affinity DataIC50:  700nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016491(CHEMBL3265400)
Affinity DataIC50:  900nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016485(CHEMBL3265396)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016486(CHEMBL3265397)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016488(CHEMBL3265399)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016493(CHEMBL3259875)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016494(CHEMBL3265402)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016484(CHEMBL3265395)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016483(CHEMBL3265394)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016482(CHEMBL3265393)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto De Qu£Mica M£Dica

Curated by ChEMBL
LigandPNGBDBM50016487(CHEMBL3265398)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of horse serum BuChE using butyrylthiocholine as substrate by UV spectroscopic analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed