BDBM50151653 CHEMBL3774884

SMILES [#6]-[#6](-[#6])\[#6]=[#6]\[#6@@H](-[#6][C@@]12[#6]-[#6@@H](\[#6]=[#6]/[#6](-[#6])-[#6])C([#6])([#6])[C@@]([#6]\[#6]=[#6](\[#6])-[#6])([#6](=O)-[#6](-[#6](=O)-c3ccc(-[#8])c(-[#8])c3)=[#6]1-[#8])[#6]2=O)-[#6](-[#6])=[#6]

InChI Key

Data  2 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 2 hits for monomerid = 50151653   

TargetHistone acetyltransferase KAT2B(Human)
University of Freiburg

Curated by ChEMBL
LigandPNGBDBM50151653(CHEMBL3774884)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of full length recombinant human FLAG-tagged PCAF expressed in baculovirus infected Sf21 cells using N-terminal H3 peptide substrate after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/1/2017
Entry Details Article
PubMed
TargetHistone acetyltransferase p300(Human)
University of Freiburg

Curated by ChEMBL
LigandPNGBDBM50151653(CHEMBL3774884)
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of full length recombinant human His6-tagged p300 expressed in baculovirus infected Sf21 cells using N-terminal H3 peptide substrate after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
7/1/2017
Entry Details Article
PubMed