Compile Data Set for Download or QSAR
Found 124 with Last Name = 'singh' and Initial = 'yp'
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))TBA
LigandPNGBDBM50587759(CHEMBL4163108)copy SMILES
Affinity DataKi:  110nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAmine oxidase [flavin-containing] A(Homo sapiens (Human))TBA
LigandPNGBDBM50587759(CHEMBL4163108)copy SMILES
Affinity DataKi:  1.95E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587744(CHEMBL5177936)copy SMILES
Affinity DataIC50: 0.590nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587756(CHEMBL5206601)copy SMILES
Affinity DataIC50: 2.60nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587755(CHEMBL5171929)copy SMILES
Affinity DataIC50: 3.10nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587756(CHEMBL5206601)copy SMILES
Affinity DataIC50: 4.40nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587755(CHEMBL5171929)copy SMILES
Affinity DataIC50: 4.80nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587756(CHEMBL5206601)copy SMILES
Affinity DataIC50: 8.60nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50510839(CHEMBL4536838)copy SMILEScopy InChI
Affinity DataIC50: 10nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587756(CHEMBL5206601)copy SMILES
Affinity DataIC50: 12nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAmine oxidase [flavin-containing] B(Homo sapiens (Human))TBA
LigandPNGBDBM50362851(CHEMBL1940390)copy SMILEScopy InChI
Affinity DataIC50: 13nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587755(CHEMBL5171929)copy SMILES
Affinity DataIC50: 19nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587744(CHEMBL5177936)copy SMILES
Affinity DataIC50: 20nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587755(CHEMBL5171929)copy SMILES
Affinity DataIC50: 21nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50510850(CHEMBL4552675)copy SMILEScopy InChI
Affinity DataIC50: 22nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 30nMAssay Description:Inhibition of recombinant human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition ...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 60nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587743(CHEMBL5199151)copy SMILES
Affinity DataIC50: 62nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50510850(CHEMBL4552675)copy SMILEScopy InChI
Affinity DataIC50: 68nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587753(CHEMBL5190569)copy SMILES
Affinity DataIC50: 68nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587742(CHEMBL5169512)copy SMILES
Affinity DataIC50: 90nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587754(CHEMBL5197518)copy SMILES
Affinity DataIC50: 92nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587743(CHEMBL5199151)copy SMILES
Affinity DataIC50: 107nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587750(CHEMBL4087621)copy SMILES
Affinity DataIC50: 110nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587741(CHEMBL5196661)copy SMILES
Affinity DataIC50: 130nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587751(CHEMBL4096250)copy SMILES
Affinity DataIC50: 150nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587746(CHEMBL5205151)copy SMILES
Affinity DataIC50: 150nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587749(CHEMBL5188267)copy SMILES
Affinity DataIC50: 170nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)copy SMILEScopy InChI
Affinity DataIC50: 190nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetBeta-secretase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50587754(CHEMBL5197518)copy SMILES
Affinity DataIC50: 210nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587754(CHEMBL5197518)copy SMILES
Affinity DataIC50: 210nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587753(CHEMBL5190569)copy SMILES
Affinity DataIC50: 255nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetBeta-secretase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50587753(CHEMBL5190569)copy SMILES
Affinity DataIC50: 255nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587740(CHEMBL3819231)copy SMILES
Affinity DataIC50: 390nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50587748(CHEMBL5194599)copy SMILES
Affinity DataIC50: 430nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50195819(CHEMBL3818089)copy SMILEScopy InChI
Affinity DataIC50: 650nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567300(CHEMBL4866457)copy SMILES
Affinity DataIC50: 840nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567299(CHEMBL4869703)copy SMILES
Affinity DataIC50: 960nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587740(CHEMBL3819231)copy SMILES
Affinity DataIC50: 970nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50587739(CHEMBL3818086)copy SMILES
Affinity DataIC50: 1.06E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50195819(CHEMBL3818089)copy SMILEScopy InChI
Affinity DataIC50: 1.22E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567299(CHEMBL4869703)copy SMILES
Affinity DataIC50: 1.23E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50567300(CHEMBL4866457)copy SMILES
Affinity DataIC50: 1.29E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567298(CHEMBL4854322)copy SMILES
Affinity DataIC50: 1.42E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 1.98E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 2.06E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 2.16E+3nMAssay Description:Inhibition of equine serum BChE using butyrylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addition and ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50567296(CHEMBL4848548)copy SMILES
Affinity DataIC50: 2.41E+3nMAssay Description:Inhibition of AChE in human erythrocytes using acetylthiocholine iodide as substrate preincubated with enzyme for 30 mins followed by substrate addit...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28W3J18PubMed
TargetAcetylcholinesterase(Homo sapiens (Human))TBA
LigandPNGBDBM50564485(CHEMBL4799854)copy SMILES
Affinity DataIC50: 2.42E+3nMAssay Description:Inhibition of recombinant human erythrocyte AChE using acetylthiocholine iodide as substrate preincubated for 30 mins followed by substrate addition ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K35ZCBPubMed
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50587739(CHEMBL3818086)copy SMILES
Affinity DataIC50: 2.47E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PR80XJPubMed
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