Compile Data Set for Download or QSAR
maximum 50k data
Found 220 Enz. Inhib. hit(s) with all data for entry = 50033234
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  20nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  61nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 11(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  150nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  150nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  180nMAssay Description:Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  210nMAssay Description:Inhibition of human HDAC4 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  240nMAssay Description:Inhibition of human HDAC2 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  250nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.88E+3nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  1.99E+3nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  2.48E+3nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  2.55E+3nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  4.44E+3nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  5.25E+3nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  6.50E+3nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  8.12E+3nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(CHEMBL1767036 | N9-([1,1'-Biphenyl]-3-yl)-2-(hydro...)
Affinity DataIC50:  9.60E+3nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341842((S)-2-(Hydroxyimino)-8-((4-methoxybenzyl)amino)-N1...)
Affinity DataIC50:  1.06E+4nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.16E+4nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  1.33E+4nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.53E+4nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.54E+4nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.65E+4nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  1.68E+4nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341842((S)-2-(Hydroxyimino)-8-((4-methoxybenzyl)amino)-N1...)
Affinity DataIC50:  1.75E+4nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341853(2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...)
Affinity DataIC50:  1.84E+4nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)
Affinity DataIC50:  1.86E+4nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  1.93E+4nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(CHEMBL1767036 | N9-([1,1'-Biphenyl]-3-yl)-2-(hydro...)
Affinity DataIC50:  1.94E+4nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  2.10E+4nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341852(3'-(8-(Hydroxyimino)-9-(methylamino)-9-oxononanami...)
Affinity DataIC50:  2.11E+4nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  2.18E+4nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)
Affinity DataIC50:  2.26E+4nMAssay Description:Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  2.31E+4nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(CHEMBL1767036 | N9-([1,1'-Biphenyl]-3-yl)-2-(hydro...)
Affinity DataIC50:  2.31E+4nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  2.81E+4nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341842((S)-2-(Hydroxyimino)-8-((4-methoxybenzyl)amino)-N1...)
Affinity DataIC50:  2.87E+4nMAssay Description:Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341852(3'-(8-(Hydroxyimino)-9-(methylamino)-9-oxononanami...)
Affinity DataIC50:  2.94E+4nMAssay Description:Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  2.97E+4nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)
Affinity DataIC50:  3.07E+4nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341853(2-(Hydroxyimino)-N1-methyl-N9-(3-(pyridine-3-yl)ph...)
Affinity DataIC50:  3.21E+4nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  3.30E+4nMAssay Description:Inhibition of human HDAC2 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341854(CHEMBL1767039 | N9-(3-(6-Chloropyridin-3-yl)phenyl...)
Affinity DataIC50:  3.41E+4nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341843((S)-2-(Dibenzylamino)-8-(hydroxyimino)-N9-methyl-N...)
Affinity DataIC50:  3.58E+4nMAssay Description:Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)
Affinity DataIC50:  3.62E+4nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341842((S)-2-(Hydroxyimino)-8-((4-methoxybenzyl)amino)-N1...)
Affinity DataIC50:  3.78E+4nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341839(5-(3-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)
Affinity DataIC50:  3.89E+4nMAssay Description:Inhibition of human HDAC4 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Displayed 1 to 50 (of 220 total ) | Next | Last >>
Jump to: