Compile Data Set for Download or QSAR
Found 40 from Military Health Sciences
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119798(1,11-bis(pyridinium)-undecane dibromide | 1,11-di(...)copy SMILEScopy InChI
Affinity DataKi:  20nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by noncompetitive Lineweaver-burk plot analysis for enzyme-inhibitor complexMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119798(1,11-bis(pyridinium)-undecane dibromide | 1,11-di(...)copy SMILEScopy InChI
Affinity DataKi:  30nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by noncompetitive Lineweaver-burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313093(1,1'-bis(pyridinium)-naphtyl-3,6-dimethylene dibro...)copy SMILEScopy InChI
Affinity DataKi:  140nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by noncompetitive Lineweaver-burk plot analysis for enzyme-inhibitor complexMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313093(1,1'-bis(pyridinium)-naphtyl-3,6-dimethylene dibro...)copy SMILEScopy InChI
Affinity DataKi:  140nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by noncompetitive Lineweaver-burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50022775((m-Hydroxyphenyl)trimethylammonium dimethylcarbama...)copy SMILEScopy InChI
Affinity DataIC50: 100nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMedDrugBank
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313093(1,1'-bis(pyridinium)-naphtyl-3,6-dimethylene dibro...)copy SMILEScopy InChI
Affinity DataIC50: 200nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119779(1,1'-(decane-1,10-diyl)dipyridinium iodide | 1,10-...)copy SMILEScopy InChI
Affinity DataIC50: 400nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119798(1,11-bis(pyridinium)-undecane dibromide | 1,11-di(...)copy SMILEScopy InChI
Affinity DataIC50: 700nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313093(1,1'-bis(pyridinium)-naphtyl-3,6-dimethylene dibro...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50022775((m-Hydroxyphenyl)trimethylammonium dimethylcarbama...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMedDrugBank
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119781(1,1'-(nonane-1,9-diyl)dipyridinium bromide | 1,9-b...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119779(1,1'-(decane-1,10-diyl)dipyridinium iodide | 1,10-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119781(1,1'-(nonane-1,9-diyl)dipyridinium bromide | 1,9-b...)copy SMILEScopy InChI
Affinity DataIC50: 6.00E+3nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119798(1,11-bis(pyridinium)-undecane dibromide | 1,11-di(...)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119785(1,1'-(octane-1,8-diyl)dipyridinium iodide | 1-[8-(...)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119785(1,1'-(octane-1,8-diyl)dipyridinium iodide | 1-[8-(...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+4nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313079(3-Dimethylcarbamoyloxy-1-methyl-pyridinium; bromid...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMedDrugBank
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119784(1-[6-(1lambda~5~-pyridin-1-yl)hexyl]-1lambda~5~-py...)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+4nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313083(1,7-bis(pyridinium)-heptane dibromide | CHEMBL1088...)copy SMILEScopy InChI
Affinity DataIC50: 7.80E+4nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119783(1,1''-(pentane-1,5-diyl)dipyridinium iodide | 1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119784(1-[6-(1lambda~5~-pyridin-1-yl)hexyl]-1lambda~5~-py...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313083(1,7-bis(pyridinium)-heptane dibromide | CHEMBL1088...)copy SMILEScopy InChI
Affinity DataIC50: 2.41E+5nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313090(1,1'-bis(pyridinium)-1,2-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 3.45E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313080(1,4-bis(pyridinium)-butane dibromide | CHEMBL10880...)copy SMILEScopy InChI
Affinity DataIC50: 5.05E+5nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313092(1,1'-bis(pyridinium)-1,4-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 5.29E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313088((E)-1,4-bis(pyridinium)-but-2-ene dibromide | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 5.41E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313086(1,3-bis(pyridinium)-2-oxapropane dichloride | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 5.83E+5nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313090(1,1'-bis(pyridinium)-1,2-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 6.36E+5nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50119783(1,1''-(pentane-1,5-diyl)dipyridinium iodide | 1-(5...)copy SMILEScopy InChI
Affinity DataIC50: 1.27E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313089((Z)-1,4-bis(pyridinium)-but-2-ene dichloride | CHE...)copy SMILEScopy InChI
Affinity DataIC50: 1.27E+6nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313091(1,1'-bis(pyridinium)-1,3-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 1.38E+6nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313092(1,1'-bis(pyridinium)-1,4-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 1.54E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313086(1,3-bis(pyridinium)-2-oxapropane dichloride | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 1.77E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313089((Z)-1,4-bis(pyridinium)-but-2-ene dichloride | CHE...)copy SMILEScopy InChI
Affinity DataIC50: 1.99E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313087(1,5-bis(pyridinium)-3-oxapentane dibromide | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2.01E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313088((E)-1,4-bis(pyridinium)-but-2-ene dibromide | CHEM...)copy SMILEScopy InChI
Affinity DataIC50: 2.29E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313091(1,1'-bis(pyridinium)-1,3-phenyldimethylene dibromi...)copy SMILEScopy InChI
Affinity DataIC50: 2.36E+6nMAssay Description:Inhibition of human erythrocyte AChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313087(1,5-bis(pyridinium)-3-oxapentane dibromide | CHEMB...)copy SMILEScopy InChI
Affinity DataIC50: 2.36E+6nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313080(1,4-bis(pyridinium)-butane dibromide | CHEMBL10880...)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+6nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMed
TargetCholinesterase(Homo sapiens (Human))
Military Health Sciences

Curated by ChEMBL
LigandPNGBDBM50313079(3-Dimethylcarbamoyloxy-1-methyl-pyridinium; bromid...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+7nMAssay Description:Inhibition of human plasma BChE after 5 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1CGSPubMedDrugBank