Compile Data Set for Download or QSAR
Found 112 Enz. Inhib. hit(s) with all data for entry = 50039593
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380548(CHEMBL2019055)copy SMILEScopy InChI
Affinity DataKi:  9.70nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380542(CHEMBL2019037)copy SMILEScopy InChI
Affinity DataKi:  620nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380544(CHEMBL2019043)copy SMILEScopy InChI
Affinity DataKi:  820nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380545(CHEMBL2019046)copy SMILEScopy InChI
Affinity DataKi:  850nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380543(CHEMBL2019040)copy SMILEScopy InChI
Affinity DataKi:  880nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380546(CHEMBL2019047)copy SMILEScopy InChI
Affinity DataKi:  1.06E+3nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380547(CHEMBL2019053)copy SMILEScopy InChI
Affinity DataKi:  3.99E+3nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380552(CHEMBL2019035)copy SMILEScopy InChI
Affinity DataKi:  4.23E+3nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380541(CHEMBL2019032)copy SMILEScopy InChI
Affinity DataKi:  6.58E+3nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetBeta-secretase 1(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM7458(5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one...)copy SMILEScopy InChI
Affinity DataKi:  1.13E+4nMAssay Description:Competitive inhibition of human recombinant BChE using panvera peptide as substrate preincubated for 60 mins before substrate addition by FRET assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380559(CHEMBL2019048)copy SMILEScopy InChI
Affinity DataIC50: 0.0350nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380553(CHEMBL2019034)copy SMILEScopy InChI
Affinity DataIC50: 0.0400nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380558(CHEMBL2019049)copy SMILEScopy InChI
Affinity DataIC50: 0.0700nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380541(CHEMBL2019032)copy SMILEScopy InChI
Affinity DataIC50: 0.0800nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380547(CHEMBL2019053)copy SMILEScopy InChI
Affinity DataIC50: 0.0900nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380551(CHEMBL2019038)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380552(CHEMBL2019035)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380552(CHEMBL2019035)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380542(CHEMBL2019037)copy SMILEScopy InChI
Affinity DataIC50: 0.100nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380537(CHEMBL2019030)copy SMILEScopy InChI
Affinity DataIC50: 0.150nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380541(CHEMBL2019032)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380559(CHEMBL2019048)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380537(CHEMBL2019030)copy SMILEScopy InChI
Affinity DataIC50: 0.180nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380550(CHEMBL2019041)copy SMILEScopy InChI
Affinity DataIC50: 0.200nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380536(CHEMBL2019031)copy SMILEScopy InChI
Affinity DataIC50: 0.25nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380541(CHEMBL2019032)copy SMILEScopy InChI
Affinity DataIC50: 0.300nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380553(CHEMBL2019034)copy SMILEScopy InChI
Affinity DataIC50: 0.320nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380542(CHEMBL2019037)copy SMILEScopy InChI
Affinity DataIC50: 0.330nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380546(CHEMBL2019047)copy SMILEScopy InChI
Affinity DataIC50: 0.350nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380551(CHEMBL2019038)copy SMILEScopy InChI
Affinity DataIC50: 0.350nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380552(CHEMBL2019035)copy SMILEScopy InChI
Affinity DataIC50: 0.430nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380539(CHEMBL2019028)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380543(CHEMBL2019040)copy SMILEScopy InChI
Affinity DataIC50: 0.550nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380538(CHEMBL2019029)copy SMILEScopy InChI
Affinity DataIC50: 0.580nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380562(CHEMBL2019039)copy SMILEScopy InChI
Affinity DataIC50: 0.75nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380553(CHEMBL2019034)copy SMILEScopy InChI
Affinity DataIC50: 0.780nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380546(CHEMBL2019047)copy SMILEScopy InChI
Affinity DataIC50: 0.800nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380550(CHEMBL2019041)copy SMILEScopy InChI
Affinity DataIC50: 0.850nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380545(CHEMBL2019046)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380545(CHEMBL2019046)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380551(CHEMBL2019038)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380544(CHEMBL2019043)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380549(CHEMBL2019044)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380549(CHEMBL2019044)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380544(CHEMBL2019043)copy SMILEScopy InChI
Affinity DataIC50: 1.5nMAssay Description:Inhibition of human serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380543(CHEMBL2019040)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380540(CHEMBL2019027)copy SMILEScopy InChI
Affinity DataIC50: 1.80nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetCholinesterase(Equus caballus (Horse))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380545(CHEMBL2019046)copy SMILEScopy InChI
Affinity DataIC50: 2nMAssay Description:Inhibition of horse serum BChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380542(CHEMBL2019037)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Instituto de Qu£mica M£dica

Curated by ChEMBL
LigandPNGBDBM50380546(CHEMBL2019047)copy SMILEScopy InChI
Affinity DataIC50: 2.30nMAssay Description:Inhibition of human erythrocytes AChE by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M32WS2PubMed
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