BDBM50546485 CHEMBL4793558

SMILES CCC(=O)CCCCCC(NC(=O)c1cncs1)c1[nH]c(nc1C(=O)N1CCOCC1)-c1ccccc1

InChI Key InChIKey=WWUHRAHHBCTRRW-UHFFFAOYSA-N

Data  1 EC50

  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 1 hit for monomerid = 50546485   

TargetHistone deacetylase 1/2/3/8(Human)
Merck

Curated by ChEMBL
LigandPNGBDBM50546485(CHEMBL4793558)
Affinity DataEC50:  3.77E+3nMAssay Description:Inhibition of Class 1 HDAC in VSV-G-pseudotyped HIV infected human 2C4 cell Jurkat model assessed as reactivation of HIV latency in presence of 5% NH...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/21/2022
Entry Details Article
PubMed