Compile Data Set for Download or QSAR
Found 83 with Last Name = 'kwak' and Initial = 'sy'
LigandPNGBDBM50085045(5-((4-((6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-...)copy SMILEScopy InChI
Affinity DataKi:  200nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RSJPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataKi:  4.74E+3nMAssay Description:Competitive inhibition of cathepsin B (unknown origin) using varying level of RR-AMC as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
LigandPNGBDBM50049391(3,5,7-Trihydroxyflavone | 3,5,7-triOH-flavone | 3,...)copy SMILEScopy InChI
Affinity DataKi:  5.60E+3nMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29G5RSJPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataKi:  5.73E+3nMAssay Description:Competitive inhibition of human erythrocytes mu-calpain using varying level of Pep2 as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
LigandPNGBDBM7461(5,7-dihydroxy-2-phenyl-4H-chromen-4-one | 5,7-dihy...)copy SMILEScopy InChI
Affinity DataKi:  7.86E+3nMMore data for this Ligand-Target Pair
In DepthDetails
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataKi:  1.06E+4nMAssay Description:Competitive inhibition of cathepsin B (unknown origin) using varying level of RR-AMC as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50300459(CHEMBL573709 | Kojic acid-phenylalanine amide)copy SMILEScopy InChI
Affinity DataKi:  1.10E+4nMAssay Description:Inhibition of mushroom tyrosinase assessed as oxidation of L-DOPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6R8SPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataKi:  1.93E+4nMAssay Description:Competitive inhibition of human erythrocytes mu-calpain using varying level of Pep2 as substrate by Lineweaver-Burk plot analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50031467(5-HYDROXY-2-(HYDROXYMETHYL)-4H-PYRAN-4-ONE | 5-Hyd...)copy SMILEScopy InChI
Affinity DataKi:  5.83E+5nMAssay Description:Inhibition of mushroom tyrosinase assessed as oxidation of L-DOPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6R8SPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM16509((2S)-1-[(2S,3S)-3-methyl-2-{[(2S,3S)-3-(propylcarb...)copy SMILEScopy InChI
Affinity DataIC50: 2.40nMAssay Description:Inhibition of cathepsin B in human SH-SY5Y cells using RR-AMC as substrate by fluorescence microplate reader assayMore data for this Ligand-Target Pair
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50073850((S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyr...)copy SMILEScopy InChI
Affinity DataIC50: 3.10nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM16509((2S)-1-[(2S,3S)-3-methyl-2-{[(2S,3S)-3-(propylcarb...)copy SMILEScopy InChI
Affinity DataIC50: 3.70nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50491472(CHEMBL2368566)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50084655(CHEMBL92708 | Calpeptin | Z-Leu-Nle-CHO | [(S)-1-(...)copy SMILEScopy InChI
Affinity DataIC50: 72nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50491472(CHEMBL2368566)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50073850((S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyr...)copy SMILEScopy InChI
Affinity DataIC50: 96nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50073850((S)-2-((S)-2-Benzyloxycarbonylamino-3-methyl-butyr...)copy SMILEScopy InChI
Affinity DataIC50: 99nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50084655(CHEMBL92708 | Calpeptin | Z-Leu-Nle-CHO | [(S)-1-(...)copy SMILEScopy InChI
Affinity DataIC50: 297nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50491472(CHEMBL2368566)copy SMILEScopy InChI
Affinity DataIC50: 397nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50052693((2S,3S)-3-[(S)-3-Methyl-1-(3-methyl-butylcarbamoyl...)copy SMILEScopy InChI
Affinity DataIC50: 2.41E+3nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataIC50: 3.81E+3nMAssay Description:Inhibition of cathepsin B in human SH-SY5Y cells using RR-AMC as substrate by fluorescence microplate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50490576(CHEMBL2332235)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA substrate incubated for 10 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29P34KQPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50490575(CHEMBL1825209 | Caffeoylphenylalanyl-Hydroxamic Ac...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of mushroom tyrosinase using L-DOPA substrate incubated for 10 minsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29P34KQPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataIC50: 6.34E+3nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558314(CHEMBL4765091)copy SMILES
Affinity DataIC50: 1.02E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataIC50: 1.11E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of cathepsin B in human SH-SY5Y cells using RR-AMC as substrate by fluorescence microplate reader assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558308(CHEMBL4799634)copy SMILES
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558307(CHEMBL4786246)copy SMILES
Affinity DataIC50: 1.37E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558308(CHEMBL4799634)copy SMILES
Affinity DataIC50: 1.39E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50052693((2S,3S)-3-[(S)-3-Methyl-1-(3-methyl-butylcarbamoyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.44E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558314(CHEMBL4765091)copy SMILES
Affinity DataIC50: 1.46E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetPolyphenol oxidase 2(Agaricus bisporus (Common mushroom))
Seoul National University

Curated by ChEMBL
LigandPNGBDBM50300459(CHEMBL573709 | Kojic acid-phenylalanine amide)copy SMILEScopy InChI
Affinity DataIC50: 1.47E+4nMAssay Description:Inhibition of mushroom tyrosinase assessed as oxidation of L-DOPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2DF6R8SPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558315(CHEMBL4743183)copy SMILES
Affinity DataIC50: 1.48E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataIC50: 1.49E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558316(CHEMBL4741582)copy SMILES
Affinity DataIC50: 1.54E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep2 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50558312(CHEMBL4746320)copy SMILES
Affinity DataIC50: 1.56E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCathepsin B(Homo sapiens (Human))TBA
LigandPNGBDBM50558312(CHEMBL4746320)copy SMILES
Affinity DataIC50: 1.57E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated fo...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetProcathepsin L(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate preincubated for 30 mins followed by substrate addition and further incubated ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558317(CHEMBL4784996)copy SMILES
Affinity DataIC50: 1.67E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep2 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558309(CHEMBL4756611)copy SMILES
Affinity DataIC50: 1.68E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50492024(2''-Methoxy Liquiritigenin | 2''-Methoxyisoliquiri...)copy SMILEScopy InChI
Affinity DataIC50: 1.69E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep2 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))TBA
LigandPNGBDBM50558313(CHEMBL4740912)copy SMILES
Affinity DataIC50: 1.88E+4nMAssay Description:Inhibition of human erythrocytes mu-calpain using Pep1 as substrate incubated for 30 mins under shaking condition in presence of CaCl2 by fluorescenc...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2736VMHPubMed
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