BDBM50341838 CHEMBL1767042::tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-oxooctylcarbamoyl)isoxazol-5-yl)phenylcarbamate

SMILES CNC(=O)C(CCCCCCNC(=O)c1cc(on1)-c1ccc(NC(=O)OC(C)(C)C)cc1)N=O

InChI Key InChIKey=ZHSZISXSXFCTGV-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 = 50341838   

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

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
Affinity DataIC50: 5.18E+4nMAssay 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 5(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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 9(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
Affinity DataIC50: 1.00E+5nMAssay 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
TargetHistone deacetylase 2(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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 4(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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 8(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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 1(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
Affinity DataIC50: 1.00E+5nMAssay 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 7(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
Affinity DataIC50: 1.00E+5nMAssay 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 11(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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
TargetHistone deacetylase 6(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
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
TargetPolyamine deacetylase HDAC10(Human)
Universita` Degli Studi Di Siena

Curated by ChEMBL
LigandPNGBDBM50341838(tert-Butyl 4-(3-(7-Hydroxyimino-8-(methylamino)-8-...)
Affinity DataIC50: 1.00E+5nMAssay 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