Compile Data Set for Download or QSAR
Found 375 with Last Name = 'rodríguez-franco' and Initial = 'mi'
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50379268(CHEMBL3216556)copy SMILEScopy InChI
Affinity DataKi:  1.5nMAssay Description:Competitive inhibition of human recombinant AChE by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
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
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
Universit£ de Sfax

Curated by ChEMBL
LigandPNGBDBM50401238(CHEMBL2206895)copy SMILEScopy InChI
Affinity DataKi:  81nMAssay Description:Mixed-type inhibition of electric eel AChE using acetylthiocholine iodide as substrate by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2R78GCMPubMed
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))
Universitat de Barcelona

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))
Universitat de Barcelona

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))
Universitat de Barcelona

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
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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

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
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
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
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
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
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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

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))
Universitat de Barcelona

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM10590(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{3-{N-{...)copy SMILEScopy InChI
Affinity DataIC50: 0.310nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
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))
Universitat de Barcelona

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM10586(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{3-{N-{...)copy SMILEScopy InChI
Affinity DataIC50: 0.420nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50379273(CHEMBL1994202 | US9238626, (-)-Huprine Y HCl)copy SMILEScopy InChI
Affinity DataIC50: 0.430nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50322767(2-Methyl-7-{[8-(1,2,3,4-tetrahydroacridin-9-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 0.5nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z15QRPubMed
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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50200340((+/-)-huprine Y-HCl | (+/-)-huprineY hydrochloride...)copy SMILEScopy InChI
Affinity DataIC50: 0.690nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM10587(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{6-[(6-...)copy SMILEScopy InChI
Affinity DataIC50: 0.740nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
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))
Universitat de Barcelona

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))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM10583(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{6-[(1,...)copy SMILEScopy InChI
Affinity DataIC50: 0.890nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate preincubated for 20 mins prior substrate addition measured after 5 m...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26974KHPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

Curated by ChEMBL
LigandPNGBDBM50322768(5-Chloro-7-{[9-(1,2,3,4-tetrahydroacridin-9-ylamin...)copy SMILEScopy InChI
Affinity DataIC50: 1nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's reactionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q22Z15QRPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Universitat de Barcelona

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
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