Compile Data Set for Download or QSAR
maximum 50k data
Found 58 Enz. Inhib. hit(s) with all data for entry = 50028742
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258646(CHEMBL468935 | N1-(4-(3-aminophenyl)thiazol-2-yl)-...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258645(CHEMBL511212 | N1-hydroxy-N8-(4-phenylthiazol-2-yl...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258645(CHEMBL511212 | N1-hydroxy-N8-(4-phenylthiazol-2-yl...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258646(CHEMBL468935 | N1-(4-(3-aminophenyl)thiazol-2-yl)-...)
Affinity DataIC50:  4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258647(CHEMBL512644 | N1-(biphenyl-4-yl)-N8-hydroxyoctane...)
Affinity DataIC50:  5nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258647(CHEMBL512644 | N1-(biphenyl-4-yl)-N8-hydroxyoctane...)
Affinity DataIC50:  7nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  14nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  17nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258649(5-(5-(4-(3-aminophenyl)thiazol-2-ylamino)-5-oxopen...)
Affinity DataIC50:  25nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258648(CHEMBL469134 | N-hydroxy-5-(5-oxo-5-(4-phenylthiaz...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258647(CHEMBL512644 | N1-(biphenyl-4-yl)-N8-hydroxyoctane...)
Affinity DataIC50:  33nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258685(CHEMBL511715 | N-hydroxy-5-(5-oxo-5-(quinolin-3-yl...)
Affinity DataIC50:  51nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258648(CHEMBL469134 | N-hydroxy-5-(5-oxo-5-(4-phenylthiaz...)
Affinity DataIC50:  68nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  72nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258649(5-(5-(4-(3-aminophenyl)thiazol-2-ylamino)-5-oxopen...)
Affinity DataIC50:  82nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  96nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258685(CHEMBL511715 | N-hydroxy-5-(5-oxo-5-(quinolin-3-yl...)
Affinity DataIC50:  102nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258649(5-(5-(4-(3-aminophenyl)thiazol-2-ylamino)-5-oxopen...)
Affinity DataIC50:  139nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258649(5-(5-(4-(3-aminophenyl)thiazol-2-ylamino)-5-oxopen...)
Affinity DataIC50:  164nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258649(5-(5-(4-(3-aminophenyl)thiazol-2-ylamino)-5-oxopen...)
Affinity DataIC50:  250nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258648(CHEMBL469134 | N-hydroxy-5-(5-oxo-5-(4-phenylthiaz...)
Affinity DataIC50:  254nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  282nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258648(CHEMBL469134 | N-hydroxy-5-(5-oxo-5-(4-phenylthiaz...)
Affinity DataIC50:  303nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258685(CHEMBL511715 | N-hydroxy-5-(5-oxo-5-(quinolin-3-yl...)
Affinity DataIC50:  328nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258648(CHEMBL469134 | N-hydroxy-5-(5-oxo-5-(4-phenylthiaz...)
Affinity DataIC50:  430nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258685(CHEMBL511715 | N-hydroxy-5-(5-oxo-5-(quinolin-3-yl...)
Affinity DataIC50:  469nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258685(CHEMBL511715 | N-hydroxy-5-(5-oxo-5-(quinolin-3-yl...)
Affinity DataIC50:  471nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258686(5-(5-(biphenyl-4-ylamino)-5-oxopentyl)-N-hydroxyis...)
Affinity DataIC50:  885nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258686(5-(5-(biphenyl-4-ylamino)-5-oxopentyl)-N-hydroxyis...)
Affinity DataIC50:  885nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258720(CHEMBL466459 | tert-butyl 4-(3-(2-(4-(3-(hydroxyca...)
Affinity DataIC50:  920nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258720(CHEMBL466459 | tert-butyl 4-(3-(2-(4-(3-(hydroxyca...)
Affinity DataIC50:  1.71E+3nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258720(CHEMBL466459 | tert-butyl 4-(3-(2-(4-(3-(hydroxyca...)
Affinity DataIC50:  1.92E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258686(5-(5-(biphenyl-4-ylamino)-5-oxopentyl)-N-hydroxyis...)
Affinity DataIC50:  3.75E+3nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258686(5-(5-(biphenyl-4-ylamino)-5-oxopentyl)-N-hydroxyis...)
Affinity DataIC50:  7.41E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258683(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50:  1.06E+4nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258719(5-(5-(cyclohexylamino)-5-oxopentyl)-N-hydroxyisoxa...)
Affinity DataIC50:  1.23E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258719(5-(5-(cyclohexylamino)-5-oxopentyl)-N-hydroxyisoxa...)
Affinity DataIC50:  1.23E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258720(CHEMBL466459 | tert-butyl 4-(3-(2-(4-(3-(hydroxyca...)
Affinity DataIC50:  1.33E+4nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258718(5-(5-(cyclopentylamino)-5-oxopentyl)-N-hydroxyisox...)
Affinity DataIC50:  1.71E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258718(5-(5-(cyclopentylamino)-5-oxopentyl)-N-hydroxyisox...)
Affinity DataIC50:  1.71E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258682(5-(3-(hydroxymethyl)isoxazol-5-yl)-N-(4-phenylthia...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258683(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258684(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258683(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258684(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258683(5-(5-oxo-5-(4-phenylthiazol-2-ylamino)pentyl)isoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258682(5-(3-(hydroxymethyl)isoxazol-5-yl)-N-(4-phenylthia...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC10More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258720(CHEMBL466459 | tert-butyl 4-(3-(2-(4-(3-(hydroxyca...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258719(5-(5-(cyclohexylamino)-5-oxopentyl)-N-hydroxyisoxa...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50258682(5-(3-(hydroxymethyl)isoxazol-5-yl)-N-(4-phenylthia...)
Affinity DataIC50: >3.00E+4nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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