Compile Data Set for Download or QSAR
Found 98 with Last Name = 'baek' and Initial = 'kh'
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM23866(MDL28170 | Z-Val-Phe-CHO | benzyl N-[(1S)-2-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 3.10nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM16509((2S)-1-[(2S,3S)-3-methyl-2-{[(2S,3S)-3-(propylcarb...)copy SMILEScopy InChI
Affinity DataIC50: 4.40nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110185(Z-FF-FMK | benzyl N-[1-[(4-fluoro-3-oxo-1-phenylbu...)copy SMILEScopy InChI
Affinity DataIC50: 5.70nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110185(Z-FF-FMK | benzyl N-[1-[(4-fluoro-3-oxo-1-phenylbu...)copy SMILEScopy InChI
Affinity DataIC50: 65.6nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491472(CHEMBL2368566)copy SMILEScopy InChI
Affinity DataIC50: 66nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491472(CHEMBL2368566)copy SMILEScopy InChI
Affinity DataIC50: 84nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM23866(MDL28170 | Z-Val-Phe-CHO | benzyl N-[(1S)-2-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 95.8nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM23866(MDL28170 | Z-Val-Phe-CHO | benzyl N-[(1S)-2-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 100nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM23866(MDL28170 | Z-Val-Phe-CHO | benzyl N-[(1S)-2-methyl...)copy SMILEScopy InChI
Affinity DataIC50: 150nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110185(Z-FF-FMK | benzyl N-[1-[(4-fluoro-3-oxo-1-phenylbu...)copy SMILEScopy InChI
Affinity DataIC50: 397nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110185(Z-FF-FMK | benzyl N-[1-[(4-fluoro-3-oxo-1-phenylbu...)copy SMILEScopy InChI
Affinity DataIC50: 418nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491474(CHEMBL2382116)copy SMILEScopy InChI
Affinity DataIC50: 1.81E+3nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110191(3-(2,4-Dihydroxyphenyl)-1-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110192(3-(2,4-Dihydroxyphenyl)-1-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 2.87E+3nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491474(CHEMBL2382116)copy SMILEScopy InChI
Affinity DataIC50: 3.15E+3nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491473(CHEMBL2382117)copy SMILEScopy InChI
Affinity DataIC50: 4.72E+3nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491483(CHEMBL2382119)copy SMILEScopy InChI
Affinity DataIC50: 9.42E+3nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110191(3-(2,4-Dihydroxyphenyl)-1-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110190(1-(2,4-Dihydroxyphenyl)-3-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 2.54E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491473(CHEMBL2382117)copy SMILEScopy InChI
Affinity DataIC50: 2.87E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491483(CHEMBL2382119)copy SMILEScopy InChI
Affinity DataIC50: 2.90E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491477(CHEMBL2382054)copy SMILEScopy InChI
Affinity DataIC50: 2.98E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50068267((E)-3-(4-Hydroxy-2-methoxy-phenyl)-1-(4-hydroxy-ph...)copy SMILEScopy InChI
Affinity DataIC50: 3.03E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491468(CHEMBL2382114)copy SMILEScopy InChI
Affinity DataIC50: 3.29E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491478(CHEMBL2382113)copy SMILEScopy InChI
Affinity DataIC50: 3.93E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110189(1-(2,4-Dihydroxyphenyl)-3-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 3.99E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110186(1-(2,4-Dihydroxyphenyl)-3-(pyridin-4-yl)propenone ...)copy SMILEScopy InChI
Affinity DataIC50: 4.44E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491476(CHEMBL2382056)copy SMILEScopy InChI
Affinity DataIC50: 4.53E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491478(CHEMBL2382113)copy SMILEScopy InChI
Affinity DataIC50: 4.68E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110192(3-(2,4-Dihydroxyphenyl)-1-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 4.95E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110186(1-(2,4-Dihydroxyphenyl)-3-(pyridin-4-yl)propenone ...)copy SMILEScopy InChI
Affinity DataIC50: 5.03E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110189(1-(2,4-Dihydroxyphenyl)-3-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 5.30E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491481(CHEMBL2382118)copy SMILEScopy InChI
Affinity DataIC50: 5.43E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110189(1-(2,4-Dihydroxyphenyl)-3-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 5.62E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491481(CHEMBL2382118)copy SMILEScopy InChI
Affinity DataIC50: 5.65E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50068267((E)-3-(4-Hydroxy-2-methoxy-phenyl)-1-(4-hydroxy-ph...)copy SMILEScopy InChI
Affinity DataIC50: 5.77E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110191(3-(2,4-Dihydroxyphenyl)-1-(thiophen-2-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 6.02E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110190(1-(2,4-Dihydroxyphenyl)-3-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 6.06E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491482(CHEMBL2382055)copy SMILEScopy InChI
Affinity DataIC50: 6.75E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491469(CHEMBL2382112)copy SMILEScopy InChI
Affinity DataIC50: 7.32E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491468(CHEMBL2382114)copy SMILEScopy InChI
Affinity DataIC50: 7.65E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110194(1-(3,5-Dihydroxyphenyl)-3-(furan-2-yl)propenone (2...)copy SMILEScopy InChI
Affinity DataIC50: 8.46E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin B was assayed in reaction buffer (50 mM NaOAc-HCl, 2 mM dithiothreitol, 2 mM EDTA, pH 5.5) containing 20 µM substrate an...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110190(1-(2,4-Dihydroxyphenyl)-3-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 8.67E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110190(1-(2,4-Dihydroxyphenyl)-3-(furan-2-yl)propenone (1...)copy SMILEScopy InChI
Affinity DataIC50: 9.05E+4nMpH: 5.5 T: 2°CAssay Description:Inhibition of cathepsin L was assayed in reaction buffer (0.1M NaOAc-HCl, 1 mM EDTA, 0.1% β-mercaptoethanol, pH 5.5) containing 20 µM subst...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491479(CHEMBL2382115)copy SMILEScopy InChI
Affinity DataIC50: 9.12E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCathepsin B(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491469(CHEMBL2382112)copy SMILEScopy InChI
Affinity DataIC50: 9.51E+4nMAssay Description:Inhibition of cathepsin B (unknown origin) using RR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCalpain-2 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110196(1-(3,5-Dihydroxyphenyl)-3-(thiophen-3-yl)propenone...)copy SMILEScopy InChI
Affinity DataIC50: 9.73E+4nMpH: 7.5 T: 2°CAssay Description:Inhibition of m-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 100 mM NaCl, 5 mM β-mercaptoethanol, and 1 mM EDTA, pH 7.5) with 50 ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetProcathepsin L(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM50491466(CHEMBL2148111)copy SMILEScopy InChI
Affinity DataIC50: 9.87E+4nMAssay Description:Inhibition of cathepsin L (unknown origin) using Z-FR-AMC as substrate after 30 mins by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN98J8PubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM16509((2S)-1-[(2S,3S)-3-methyl-2-{[(2S,3S)-3-(propylcarb...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
TargetCalpain-1 catalytic subunit(Homo sapiens (Human))
Ewha Womans University, Seoul 120-750, Republic of Korea.

LigandPNGBDBM110186(1-(2,4-Dihydroxyphenyl)-3-(pyridin-4-yl)propenone ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMpH: 7.5 T: 2°CAssay Description:Inhibition of µ-calpain was assayed in the reaction buffer (50 mM Tris-HCl, 50 mM NaCl, 1 mM EDTA, 1 mM EGTA and 5 mM β-mercaptoethanol, pH...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NP233RPubMed
Displayed 1 to 50 (of 98 total ) | Next | Last >>
Jump to: