Compile Data Set for Download or QSAR
Found 67 with Last Name = 'panetta' and Initial = 'a'
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255853(4-(((R)-2,3-dihydro-2-oxo-3-phenethylquinoxalin-4(...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255852(4-(((R)-3-(4-hydroxybenzyl)-2,3-dihydro-2-oxoquino...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255096(4-(((R)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255854((R)-tert-butyl 4-(1-(4-(hydroxycarbamoyl)benzyl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255809(4-(((R)-3-(3,4-difluorobenzyl)-2,3-dihydro-2-oxoqu...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255914(4-(((R)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255910(4-(((R)-3-(4-tert-butoxybenzyl)-2,3-dihydro-2-oxoq...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255912(4-(((R)-2-((1H-indol-3-yl)methyl)-3,6-dioxopiperaz...)copy SMILEScopy InChI
Affinity DataIC50: 110nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255097(4-((2,3-dihydro-2-oxoquinoxalin-4(1H)-yl)methyl)-N...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255913(CHEMBL481726 | N-hydroxy-4-(((R)-3,6-dioxo-2-((thi...)copy SMILEScopy InChI
Affinity DataIC50: 160nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255911(4-(((R)-2-benzyl-3,6-dioxopiperazin-1-yl)methyl)-N...)copy SMILEScopy InChI
Affinity DataIC50: 170nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50084636(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-benzyloxy)-p...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255095(4-(((S)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 210nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255095(4-(((S)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255910(4-(((R)-3-(4-tert-butoxybenzyl)-2,3-dihydro-2-oxoq...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255096(4-(((R)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255851(4-(((S)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 310nMAssay Description:Inhibition of human recombinant histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255852(4-(((R)-3-(4-hydroxybenzyl)-2,3-dihydro-2-oxoquino...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50080991(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-phenoxymethy...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255809(4-(((R)-3-(3,4-difluorobenzyl)-2,3-dihydro-2-oxoqu...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255913(CHEMBL481726 | N-hydroxy-4-(((R)-3,6-dioxo-2-((thi...)copy SMILEScopy InChI
Affinity DataIC50: 440nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255095(4-(((S)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255809(4-(((R)-3-(3,4-difluorobenzyl)-2,3-dihydro-2-oxoqu...)copy SMILEScopy InChI
Affinity DataIC50: 460nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255853(4-(((R)-2,3-dihydro-2-oxo-3-phenethylquinoxalin-4(...)copy SMILEScopy InChI
Affinity DataIC50: 520nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255097(4-((2,3-dihydro-2-oxoquinoxalin-4(1H)-yl)methyl)-N...)copy SMILEScopy InChI
Affinity DataIC50: 520nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255096(4-(((R)-3-benzyl-2,3-dihydro-2-oxoquinoxalin-4(1H)...)copy SMILEScopy InChI
Affinity DataIC50: 530nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255097(4-((2,3-dihydro-2-oxoquinoxalin-4(1H)-yl)methyl)-N...)copy SMILEScopy InChI
Affinity DataIC50: 560nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287763(5-[1-{4-[3-Hydroxy-4-(2-hydroxy-benzoyl)-2-propyl-...)copy SMILEScopy InChI
Affinity DataIC50: 620nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287749(5-[1-[4-(4-Acetyl-3-hydroxy-2-propyl-benzyloxy)-ph...)copy SMILEScopy InChI
Affinity DataIC50: 640nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255853(4-(((R)-2,3-dihydro-2-oxo-3-phenethylquinoxalin-4(...)copy SMILEScopy InChI
Affinity DataIC50: 640nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255914(4-(((R)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 690nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287758(5-(2-Hydroxy-4-{4-[4-oxo-2-thioxo-thiazolidin-(5Z)...)copy SMILEScopy InChI
Affinity DataIC50: 690nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255852(4-(((R)-3-(4-hydroxybenzyl)-2,3-dihydro-2-oxoquino...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)copy SMILEScopy InChI
Affinity DataIC50: 770nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287743(5-[1-[4-(4-Benzoyl-phenoxymethyl)-phenyl]-meth-(Z)...)copy SMILEScopy InChI
Affinity DataIC50: 780nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287747(5-[1-[4-(4-Benzoyl-2-benzyl-3-hydroxy-phenoxymethy...)copy SMILEScopy InChI
Affinity DataIC50: 820nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255914(4-(((R)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 870nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255854((R)-tert-butyl 4-(1-(4-(hydroxycarbamoyl)benzyl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.15E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255851(4-(((S)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.19E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255912(4-(((R)-2-((1H-indol-3-yl)methyl)-3,6-dioxopiperaz...)copy SMILEScopy InChI
Affinity DataIC50: 1.21E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50080991(5-[1-[4-(4-Benzoyl-3-hydroxy-2-propyl-phenoxymethy...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Compound was evaluated for the inhibition of cathepsin D at an enzyme level of 50 ng/mLMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287761(5-[1-[4-(4-Benzoyl-benzyloxy)-phenyl]-meth-(Z)-yli...)copy SMILEScopy InChI
Affinity DataIC50: 1.31E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255910(4-(((R)-3-(4-tert-butoxybenzyl)-2,3-dihydro-2-oxoq...)copy SMILEScopy InChI
Affinity DataIC50: 1.44E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287759(5-[1-{4-[3-Hydroxy-2-propyl-4-(pyridine-3-carbonyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.46E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255854((R)-tert-butyl 4-(1-(4-(hydroxycarbamoyl)benzyl)-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.48E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255851(4-(((S)-2,3-dihydro-2-oxo-3-((thiophen-2-yl)methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.48E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
MethylGene Inc

Curated by ChEMBL
LigandPNGBDBM50255912(4-(((R)-2-((1H-indol-3-yl)methyl)-3,6-dioxopiperaz...)copy SMILEScopy InChI
Affinity DataIC50: 1.81E+3nMAssay Description:Inhibition of human recombinant histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2G44Q5SPubMed
TargetCathepsin D(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50287742(5-[1-[4-(4-Acetyl-3-methoxy-2-propyl-benzyloxy)-ph...)copy SMILEScopy InChI
Affinity DataIC50: 1.86E+3nMAssay Description:In vitro inhibition of cathepsin D.More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28G8KPZ
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