BDBM50020913 CHEMBL3287006

SMILES CC(C)[C@@H]1NC(=O)c2csc(n2)-c2csc(CNC(=O)C[C@H](OC1=O)\C=C\CCS)n2

InChI Key InChIKey=RJAMNODUHLUDOA-UHFFFAOYSA-N

Data  3 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 3 hits for monomerid = 50020913   

TargetHistone deacetylase 3(Human)
Chinese National Center For Drug Screening

Curated by ChEMBL
LigandPNGBDBM50020913(CHEMBL3287006)
Affinity DataIC50: 85nMAssay Description:Inhibition of recombinant human HDAC3 using Ac-Lys-Tyr-Lys(epsilon-acetyl)-AMC as substrate after 24 hrs by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/12/2015
Entry Details Article
PubMed
TargetHistone deacetylase 6(Human)
Chinese National Center For Drug Screening

Curated by ChEMBL
LigandPNGBDBM50020913(CHEMBL3287006)
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of recombinant human HDAC6 using Boc-Lys(epsilon-acetyl)-AMC as substrate after 3 hrs by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/12/2015
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Chinese National Center For Drug Screening

Curated by ChEMBL
LigandPNGBDBM50020913(CHEMBL3287006)
Affinity DataIC50: 77nMAssay Description:Inhibition of recombinant human HDAC1 using Ac-Lys-Tyr-Lys(epsilon-acetyl)-AMC as substrate after 24 hrs by fluorescence assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/12/2015
Entry Details Article
PubMed