BDBM50341851 CHEMBL1767036::N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-methylnonanediamide

SMILES CNC(=O)C(CCCCCCC(=O)Nc1cccc(c1)-c1ccccc1)N=O

InChI Key InChIKey=GZLCDSKYHTVXEH-UHFFFAOYSA-N

Data  11 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 11 hits for monomerid = 50341851   

TargetHistone deacetylase 5(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 6.71E+4nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC2 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
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 Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 4(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC4 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 7(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
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 Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 8(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 9(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
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 Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetPolyamine deacetylase HDAC10(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 7.33E+4nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed
TargetHistone deacetylase 11(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341851(N9-([1,1'-Biphenyl]-3-yl)-2-(hydroxyimino)-N1-meth...)
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/3/2011
Entry Details Article
PubMed