BDBM50336884 2-Propyl-pentanoic acid hydroxyamide::CHEMBL186311::Valpropylhydroxamic acid

SMILES CCCC(CCC)C(=O)NO

InChI Key InChIKey=ROJGIRXXBBBMPL-UHFFFAOYSA-N

Data  9 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 50336884   

TargetHistone deacetylase 1(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 5.60E+5nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 6.80E+5nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 3.40E+5nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 3.90E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 1.70E+5nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 5(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 7(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 9.90E+4nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 9.10E+4nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Broad Institute of Harvard and Mit

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | Valpropylhy...)
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In Depth
Date in BDB:
1/5/2013
Entry Details Article
PubMed