BDBM50278236 CHEMBL4168051

SMILES C[C@H](C(=O)Nc1ccc(nc1)C(=O)Nc1ccc(F)cc1N)c1ccccc1

InChI Key InChIKey=JFVYUMCLAOMZHX-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 = 50278236   

TargetHistone deacetylase 1(Human)
National Taiwan University

Curated by ChEMBL
LigandPNGBDBM50278236(CHEMBL4168051)
Affinity DataIC50: 1.40E+3nMAssay Description:Inhibition of human HDAC1 using p53 (379 to 382 residues) derived fluorogenic peptide RHKKAcMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2020
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
National Taiwan University

Curated by ChEMBL
LigandPNGBDBM50278236(CHEMBL4168051)
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human HDAC2 using p53 (379 to 382 residues) derived fluorogenic peptide RHKKAcMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2020
Entry Details Article
PubMed
TargetHistone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)(Human)
National Taiwan University

Curated by ChEMBL
LigandPNGBDBM50278236(CHEMBL4168051)
Affinity DataIC50: 130nMAssay Description:Inhibition of human HDAC3/NCOR2 using p53 (379 to 382 residues) derived fluorogenic peptide RHKKAcMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2020
Entry Details Article
PubMed