null

SMILES ONC(=O)CCCCC[C@@H]1NC(=O)[C@H]2CCCN2C(=O)[C@@H]2CCCCCCCCC[C@@H](NC1=O)C(=O)N2

InChI Key InChIKey=QGARLIKKHCLNGY-IVAOSVALSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50309929   

TargetHistone deacetylase 1(Homo sapiens (Human))
Graduate School of Life Science and Systems Engineering

Curated by ChEMBL
LigandPNGBDBM50309929(6-((1S,7R,10S,13R)-2,8,11,24-Tetraoxo-3,9,12,23-te...)copy SMILEScopy InChI
Affinity DataIC50: 9.10nMAssay Description:Inhibition of HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZNRPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Graduate School of Life Science and Systems Engineering

Curated by ChEMBL
LigandPNGBDBM50309929(6-((1S,7R,10S,13R)-2,8,11,24-Tetraoxo-3,9,12,23-te...)copy SMILEScopy InChI
Affinity DataIC50: 330nMAssay Description:Inhibition of HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZNRPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Graduate School of Life Science and Systems Engineering

Curated by ChEMBL
LigandPNGBDBM50309929(6-((1S,7R,10S,13R)-2,8,11,24-Tetraoxo-3,9,12,23-te...)copy SMILEScopy InChI
Affinity DataIC50: 5.40nMAssay Description:Inhibition of HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BC3ZNRPubMed