Compile Data Set for Download or QSAR
Found 62 with Last Name = 'liu' and Initial = 'mc'
TargetCytidine deaminase(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50087289(1-beta-D-Arabinofuranosylcytosine | 4-Amino-1-beta...)copy SMILEScopy InChI
Affinity DataKi:  1.90E+5nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23F4Q8TPubMedDrugBank
TargetCytidine deaminase(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50007155(4-Amino-1-(3-hydroxy-5-hydroxymethyl-4-methylene-t...)copy SMILEScopy InChI
Affinity DataKi:  1.60E+6nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23F4Q8TPubMed
TargetCytidine deaminase(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50421893(CHEMBL10128)copy SMILEScopy InChI
Affinity DataKi:  7.69E+6nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23F4Q8TPubMed
TargetCytidine deaminase(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50007156(4-Amino-5-fluoro-1-(4-hydroxy-5-hydroxymethyl-3-me...)copy SMILEScopy InChI
Affinity DataKi:  2.51E+7nMAssay Description:Inhibitory constant was measured on cytidine/deoxycytidine deaminaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q23F4Q8TPubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051772((Z)-N'-(5-amino-6-formylpyridin-2-yl)carbamohydraz...)copy SMILEScopy InChI
Affinity DataIC50: 820nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051776((1Z,N'E)-N'-((5-(ethylamino)pyridin-2-yl)methylene...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051768((1Z,N'E)-N'-((3-(methylamino)pyridin-2-yl)methylen...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051769((1Z,N'E)-N'-((5-(methylamino)pyridin-2-yl)methylen...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051775((1Z,N'E)-N'-((5-(allylamino)pyridin-2-yl)methylene...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051767((1Z,N'E)-N'-((5-(propylamino)pyridin-2-yl)methylen...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051774((1Z,N'E)-N'-((3-(allylamino)pyridin-2-yl)methylene...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051777((1Z,N'E)-N'-((5-(aminomethyl)pyridin-2-yl)methylen...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051766((1Z,N'E)-N'-((5-(butylamino)pyridin-2-yl)methylene...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051773((Z)-N'-(3-amino-6-formylpyridin-2-yl)carbamohydraz...)copy SMILEScopy InChI
Affinity DataIC50: 2.70E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051771((1Z,N'E)-N'-((3,5-diaminopyridin-2-yl)methylene)ca...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50181441(BCX-1812 | CHEBI:85202 | Peramivir)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetRibonucleoside-diphosphate reductase subunit M2(Homo sapiens (Human))
Yale University

Curated by ChEMBL
LigandPNGBDBM50051770((1Z,N'E)-N'-((5-amino-4-(morpholinomethyl)pyridin-...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibitory activity against CDP reductase.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2KS6QN9PubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50078329(1-[4-CARBOXY-2-(3-PENTYLAMINO)PHENYL]-5,5'-DI(HYDR...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+4nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478617(CHEMBL460452)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+5nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50028503(CHEMBL81717 | Guanidino-Oseltamivir Carboxylicacid)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478616(CHEMBL311059)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+5nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM5025(Oseltamivir | US10919856, POSITIVE CONTROL | ethyl...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+5nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478634(CHEMBL513444)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478623(CHEMBL98262)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4994((3R,4R,5S)-5-amino-4-acetamido-3-(pentan-3-yloxy)c...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478622(CHEMBL433269)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4937((2R,3R,4S)-4-amino-2-(diethylcarbamoyl)-3-acetamid...)copy SMILEScopy InChI
Affinity DataIC50: 3.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478627(CHEMBL300461)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50078330(1-(4-CARBOXY-2-GUANIDINOPENTYL)-5,5'-DI(HYDROXYMET...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50330326((4S,5R,6R)-5-Acetylamino-4-guanidino-6-((1R,3R)-1,...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+6nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478624(CHEMBL309192)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4929((2R,3R,4S)-4-amino-2-(dipropylcarbamoyl)-3-acetami...)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+7nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478630(CHEMBL100991)copy SMILEScopy InChI
Affinity DataIC50: 2.39E+7nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478614(CHEMBL118070)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4928((2R,3R,4S)-4-amino-3-acetamido-2-[methyl(propyl)ca...)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478611(CHEMBL459839)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50063303((2R,3R,4S)-3-acetamido-4-amino-2-((1R,2R)-1,2,3-tr...)copy SMILEScopy InChI
Affinity DataIC50: 3.20E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4936((2R,3R,4S)-4-amino-2-(dibutylcarbamoyl)-3-acetamid...)copy SMILEScopy InChI
Affinity DataIC50: 4.50E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478628(CHEMBL54149)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478628(CHEMBL54149)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+8nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478629(CHEMBL459837)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478612(CHEMBL459838)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478613(CHEMBL511178)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478631(CHEMBL460871)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4927((2R,3R,4S)-4-amino-2-(dimethylcarbamoyl)-3-acetami...)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478626(CHEMBL55440)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478635(CHEMBL336080)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4980((3R,4R,5S)-5-amino-4-acetamido-3-hydroxycyclohex-1...)copy SMILEScopy InChI
Affinity DataIC50: 6.30E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM4706((2R,3R,4S)-3-acetamido-4-hydroxy-2-[(1R,2R)-1,2,3-...)copy SMILEScopy InChI
Affinity DataIC50: 8.60E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
TargetNeuraminidase(Influenza A virus)
Lanzhou University

Curated by ChEMBL
LigandPNGBDBM50478633(CHEMBL461287)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+9nMAssay Description:Inhibition of influenza virus neuraminidaseMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2C53PNPPubMed
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