Compile Data Set for Download or QSAR
Found 345 with Last Name = 'mancini' and Initial = 'f'
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50351015(CHEMBL1819176)copy SMILEScopy InChI
Affinity DataKi:  1nMAssay Description:Mixed-type inhibition of human AChE assessed as hydrolysis of acetylthiocholine by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP24TKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271142(6-Chloro-9-[(3-{4-[(5,6-Dimethoxy-1-oxoindan-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.0900nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271142(6-Chloro-9-[(3-{4-[(5,6-Dimethoxy-1-oxoindan-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.270nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271140(9-[(3-{4-[(5,6-Dimethoxy-1-oxoindan-2-yl)methyl]pi...)copy SMILEScopy InChI
Affinity DataIC50: 0.290nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50275723(2,7-bis(6-(ethyl(2-methoxybenzyl)amino)hexyl)benzo...)copy SMILEScopy InChI
Affinity DataIC50: 0.370nMAssay Description:Inhibition of human recombinant AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2J3WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271141(6-Chloro-9-[(2-{4-[(5,6-dimethoxy-1-oxoindan-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.570nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetCholinesterase(Homo sapiens (Human))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM9063(5,6-Dimethoxy-2-{[7-(1,2,3,4-tetrahydro-acridin-9-...)copy SMILEScopy InChI
Affinity DataIC50: 0.600nMAssay Description:Inhibition of human serum BChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271141(6-Chloro-9-[(2-{4-[(5,6-dimethoxy-1-oxoindan-2-yl)...)copy SMILEScopy InChI
Affinity DataIC50: 0.670nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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))
Institut f£r Molekulare Physiologie

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
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM8963(CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)copy SMILEScopy InChI
Affinity DataIC50: 0.810nMAssay Description:Mixed-type inhibition of human AChE assessed as hydrolysis of acetylthiocholine by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP24TKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271190(9-[(3-{4-[(5,6-dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271192(6-Chloro-9-[(3-{4-[(5,6-dimethoxyindan-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 0.820nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271140(9-[(3-{4-[(5,6-Dimethoxy-1-oxoindan-2-yl)methyl]pi...)copy SMILEScopy InChI
Affinity DataIC50: 0.880nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271192(6-Chloro-9-[(3-{4-[(5,6-dimethoxyindan-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.06nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50351015(CHEMBL1819176)copy SMILEScopy InChI
Affinity DataIC50: 1.10nMAssay Description:Mixed-type inhibition of human AChE assessed as hydrolysis of acetylthiocholine by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP24TKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM10589(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{8-[(6-...)copy SMILEScopy InChI
Affinity DataIC50: 1.30nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM10585(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{8-[(1,...)copy SMILEScopy InChI
Affinity DataIC50: 1.40nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50275719(1,4-bis(6-(ethyl(2-methoxybenzyl)amino)hexyl)quino...)copy SMILEScopy InChI
Affinity DataIC50: 1.41nMAssay Description:Inhibition of human recombinant AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2J3WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50231951(2,5-bis(6-((2-methoxybenzyl)(ethyl)amino)hexylamin...)copy SMILEScopy InChI
Affinity DataIC50: 1.60nMAssay Description:Inhibition of human recombinant AChE using acetylthiocholine iodide as substrate after 20 mins preincubation by Ellman methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V40VNMPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50377921(SODIUM NITROPRUSSIDE)copy SMILEScopy InChI
Affinity DataIC50: 1.74nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271191(6-Chloro-9-[(2-{4-[(5,6-dimethoxyindan-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.86nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM10584(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{7-[(1,...)copy SMILEScopy InChI
Affinity DataIC50: 1.90nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271190(9-[(3-{4-[(5,6-dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 2.16nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271189(9-[(2-{4-[(5,6-Dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 2.28nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271191(6-Chloro-9-[(2-{4-[(5,6-dimethoxyindan-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50027470(CHEMBL3216778)copy SMILEScopy InChI
Affinity DataIC50: 3.30nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50157597(6-[ethyl-(2-methoxy-benzyl)-amino]-1-(1'-{6-[ethyl...)copy SMILEScopy InChI
Affinity DataIC50: 3.32nMAssay Description:Inhibition of human recombinant AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2J3WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM10588(3-Chloro-6,7,10,11-tetrahydro-9-methyl-12-{{7-[(6-...)copy SMILEScopy InChI
Affinity DataIC50: 4nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50377921(SODIUM NITROPRUSSIDE)copy SMILEScopy InChI
Affinity DataIC50: 4.04nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50027471(CHEMBL3216554)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay 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))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50275716(1,1'-(benzo[lmn][3,8]phenanthroline-2,7(1H,3H,6H,8...)copy SMILEScopy InChI
Affinity DataIC50: 4.83nMAssay Description:Inhibition of human recombinant AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2J3WPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50271189(9-[(2-{4-[(5,6-Dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 5.13nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetCholinesterase(Homo sapiens (Human))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8963(CHEMBL32823 | Homodimeric Tacrine Analog 3b | N-[7...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of human serum recombinant BChE using butyrylthiocholine iodide as substrate preincubated for 20 mins by Ellman's methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP24TKPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMAssay Description:Inhibition of rat cortex AChEMore data for this Ligand-Target Pair
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 5.73nMpH: 8.0 T: 2°CAssay Description:AChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using AChE from bovine or human erythrocytes and acetylthiocho...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2707ZSBPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 5.73nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Rattus norvegicus (rat))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8979(CHEMBL486901 | N-[2-(1-benzylpiperidin-4-yl)ethyl]...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of rat cortex AChEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM31895(Pyrano[3,2-c]quinoline-6-chlorotacrine hybrid, 20....)copy SMILEScopy InChI
Affinity DataIC50: 7.03nMpH: 8.0 T: 2°CAssay Description:AChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using AChE from bovine or human erythrocytes and acetylthiocho...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2707ZSBPubMed
TargetCholinesterase(Homo sapiens (Human))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271190(9-[(3-{4-[(5,6-dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 7.25nMAssay Description:Inhibition of human serum BChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM50275722(2,6-Bis-{6-[ethyl-(2-methoxybenzyl)amino]hexyl}pyr...)copy SMILEScopy InChI
Affinity DataIC50: 7.70nMAssay Description:Inhibition of human recombinant AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2MW2J3WPubMed
TargetCholinesterase(Homo sapiens (Human))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM50271189(9-[(2-{4-[(5,6-Dimethoxyindan-2-yl)methyl]piperidi...)copy SMILEScopy InChI
Affinity DataIC50: 8.06nMAssay Description:Inhibition of human serum BChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
TargetAcetylcholinesterase(Bos taurus (bovine))
Laboratori de Qu�mica Farmac�utica (Unitat Associada al CSIC)

Curated by ChEMBL
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 8.12nMAssay Description:Inhibition of bovine erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 8.32nMpH: 8.0 T: 2°CAssay Description:AChE inhibitory activity was evaluated spectrophotometrically by the method of Ellman, using AChE from bovine or human erythrocytes and acetylthiocho...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2707ZSBPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))
Institut f£r Molekulare Physiologie

Curated by ChEMBL
LigandPNGBDBM8987(6-chloro-1,2,3,4-tetrahydroacridin-9-amine | 6-chl...)copy SMILEScopy InChI
Affinity DataIC50: 8.32nMAssay Description:Inhibition of human erythrocyte AChE by Ellman's assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2F76DGKPubMed
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