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Found 24 with Last Name = 'shinji' and Initial = 'c'
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  16nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  20nMAssay Description:Inhibitory concentration against histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  29nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
The University Of Tokyo Yayoi

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  39nMAssay Description:Inhibitory concentrationagainst histone deacetylase 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  53nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216518(3-(2-(4-(pyridin-3-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  56nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM19130((2E,4E,6R)-7-[4-(dimethylamino)phenyl]-N-hydroxy-4...)
Affinity DataIC50:  91nMAssay Description:Inhibitory concentration against histone deacetylase 6More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216518(3-(2-(4-(pyridin-3-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  92nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216517(3-(2-biphenyl-4-ylmethyl-3-oxo-2,3-dihydro-1H-isoi...)
Affinity DataIC50:  98nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216519(3-(2-(4-tert-butylbenzyl)-3-oxoisoindolin-5-yl)-N-...)
Affinity DataIC50:  180nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216515(3-(2-benzyl-3-oxoisoindolin-5-yl)-N-hydroxyacrylam...)
Affinity DataIC50:  220nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216517(3-(2-biphenyl-4-ylmethyl-3-oxo-2,3-dihydro-1H-isoi...)
Affinity DataIC50:  220nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216515(3-(2-benzyl-3-oxoisoindolin-5-yl)-N-hydroxyacrylam...)
Affinity DataIC50:  230nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216519(3-(2-(4-tert-butylbenzyl)-3-oxoisoindolin-5-yl)-N-...)
Affinity DataIC50:  230nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216515(3-(2-benzyl-3-oxoisoindolin-5-yl)-N-hydroxyacrylam...)
Affinity DataIC50:  250nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216518(3-(2-(4-(pyridin-3-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  280nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50172787((E)-3-(2-Benzyl-1,3-dioxo-2,3-dihydro-1H-isoindol-...)
Affinity DataIC50:  358nMAssay Description:Inhibitory concentration against histone deacetylase 4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50172787((E)-3-(2-Benzyl-1,3-dioxo-2,3-dihydro-1H-isoindol-...)
Affinity DataIC50:  572nMAssay Description:Inhibitory concentration against histone deacetylase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50172787((E)-3-(2-Benzyl-1,3-dioxo-2,3-dihydro-1H-isoindol-...)
Affinity DataIC50:  709nMAssay Description:Inhibitory concentration against histone deacetylase 6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216517(3-(2-biphenyl-4-ylmethyl-3-oxo-2,3-dihydro-1H-isoi...)
Affinity DataIC50:  750nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216519(3-(2-(4-tert-butylbenzyl)-3-oxoisoindolin-5-yl)-N-...)
Affinity DataIC50:  990nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216516(3-(2-(4-(pyridin-4-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibition of human HDAC4More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216516(3-(2-(4-(pyridin-4-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  3.30E+3nMAssay Description:Inhibition of human HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50216516(3-(2-(4-(pyridin-4-yl)benzyl)-3-oxoisoindolin-5-yl...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of human HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed