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Found 108 with Last Name = 'luan' and Initial = 'x'
TargetHistone deacetylase 3(Homo sapiens (Human))TBA
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 3.10nMMore data for this Ligand-Target Pair
In DepthDetails DrugBank
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Tsinghua University

Curated by ChEMBL
LigandPNGBDBM5447(CHEMBL939 | GEFITINIB | Iressa | N-(3-Chloro-4-flu...)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMAssay Description:Inhibition of EGFR after 1 hrs by luminescence assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 4.20nMMore data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 7.10nMMore data for this Ligand-Target Pair
In DepthDetails DrugBank
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50380399(CHEMBL2018302 | Tubastatin A | US10227295, Compoun...)copy SMILEScopy InChI
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610449(CHEMBL5281081)copy SMILES
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610443(CHEMBL5276052)copy SMILES
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610445(CHEMBL5283177)copy SMILES
Affinity DataIC50: 14nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM25150((2E)-N-hydroxy-3-[3-(phenylsulfamoyl)phenyl]prop-2...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406038(CHEMBL5280065)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610446(CHEMBL5272622)copy SMILES
Affinity DataIC50: 23nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610444(CHEMBL5286805)copy SMILES
Affinity DataIC50: 26nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM8960((+/-)-2-[(1-benzylpiperidin-4-yl)methyl]-5,6-dimet...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:The ability of compound to inhibit calpain in a preparation of lysed platelets was measured with a caseinolytic assay(assay 1)More data for this Ligand-Target Pair
In DepthDetails
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:In vitro inhibitory activity against histamine H2-receptor in isolated Guinea pig right atria.More data for this Ligand-Target Pair
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610447(CHEMBL5273721)copy SMILES
Affinity DataIC50: 55nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406037(CHEMBL5268446)copy SMILEScopy InChI
Affinity DataIC50: 67nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM8961(1,2,3,4-tetrahydro-9-acridinamine | 1,2,3,4-tetrah...)copy SMILEScopy InChI
Affinity DataIC50: 70nMAssay Description:The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610448(CHEMBL5278328)copy SMILES
Affinity DataIC50: 79nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetHistone deacetylase 6(Homo sapiens (Human))TBA
LigandPNGBDBM50610450(CHEMBL5285262)copy SMILES
Affinity DataIC50: 89nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406044(CHEMBL5284034)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406021(CHEMBL5288040)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:The compound was tested in vitro for inhibition of rat hepatic HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406051(CHEMBL5283204)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406032(CHEMBL5269960)copy SMILEScopy InChI
Affinity DataIC50: 280nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406043(CHEMBL5289255)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406039(CHEMBL5282067)copy SMILEScopy InChI
Affinity DataIC50: 450nMAssay Description:The compound was tested in vitro for inhibition of rat hepatic HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406047(CHEMBL5275640)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406020(CHEMBL5270654)copy SMILEScopy InChI
Affinity DataIC50: 470nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))TBA
LigandPNGBDBM50406054(CHEMBL5271132)copy SMILEScopy InChI
Affinity DataIC50: 490nMAssay Description:The calpain inhibitory activity(I 50) was measured as ability to enter the platelet to inhibit calpain after cell lysis(assay 2)More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406042(CHEMBL5280795)copy SMILEScopy InChI
Affinity DataIC50: 590nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406017(CHEMBL5274269)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406019(CHEMBL5288873)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 8(Homo sapiens (Human))TBA
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+3nMMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50610446(CHEMBL5272622)copy SMILES
Affinity DataIC50: 1.06E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406060(CHEMBL5278887)copy SMILEScopy InChI
Affinity DataIC50: 1.14E+3nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50610449(CHEMBL5281081)copy SMILES
Affinity DataIC50: 1.19E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetRAF proto-oncogene serine/threonine-protein kinase(Homo sapiens (Human))
Tsinghua University

Curated by ChEMBL
LigandPNGBDBM31088(1-methyl-5-[2-[5-(trifluoromethyl)-1H-imidazol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of RAFMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P60WXPubMed
LigandPNGBDBM50406048(CHEMBL5265953)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+3nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
LigandPNGBDBM50406053(CHEMBL5281121)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+3nMAssay Description:The compound was tested in vitro for inhibition of rat hepatic HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50610443(CHEMBL5276052)copy SMILES
Affinity DataIC50: 1.26E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406055(CHEMBL5270330)copy SMILEScopy InChI
Affinity DataIC50: 1.28E+3nMAssay Description:The compound was tested in vitro for inhibition of rat hepatic HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Tsinghua University

Curated by ChEMBL
LigandPNGBDBM31088(1-methyl-5-[2-[5-(trifluoromethyl)-1H-imidazol-2-y...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of VEGFR2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28P60WXPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50610445(CHEMBL5283177)copy SMILES
Affinity DataIC50: 1.39E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406061(CHEMBL5283091)copy SMILEScopy InChI
Affinity DataIC50: 1.42E+3nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 1(Homo sapiens (Human))TBA
LigandPNGBDBM50610444(CHEMBL5286805)copy SMILES
Affinity DataIC50: 1.43E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
LigandPNGBDBM50406052(CHEMBL5279307)copy SMILEScopy InChI
Affinity DataIC50: 1.62E+3nMAssay Description:In vitro for inhibition of rat HMG-CoA reductase.More data for this Ligand-Target Pair
In DepthDetails
TargetCholinesterase(Equus caballus (Horse))TBA
LigandPNGBDBM50406042(CHEMBL5280795)copy SMILEScopy InChI
Affinity DataIC50: 1.62E+3nMAssay Description:Inhibitory activity against rat liver dihydrofolate reductaseMore data for this Ligand-Target Pair
In DepthDetails
TargetHistone deacetylase 3(Homo sapiens (Human))TBA
LigandPNGBDBM50610445(CHEMBL5283177)copy SMILES
Affinity DataIC50: 1.85E+3nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Tsinghua University

Curated by ChEMBL
LigandPNGBDBM50350237(CHEMBL1812374)copy SMILEScopy InChI
Affinity DataIC50: 1.93E+3nMAssay Description:Inhibition of EGFR after 1 hrs by luminescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2Z89CSBPubMed
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