BDBM50600298 CHEMBL5187549

SMILES COc1ccc(cc1)C1(CCCCC1)C(=O)N(C)CC(=O)Nc1cccc2[nH]ncc12

InChI Key InChIKey=QEJJXNXKQNDITO-UHFFFAOYSA-N

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 = 50600298   

TargetHistone acetyltransferase p300(Homo sapiens (Human))
Daiichi Sankyo

Curated by ChEMBL
LigandPNGBDBM50600298(CHEMBL5187549)
Affinity DataIC50:  1.01E+3nMAssay Description:Inhibition of EP300 in human LK2 cells assessed as reduction in intracellular histone H3 acetylation at lysine 27 residue incubated for 3 hrs by chem...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetHistone acetyltransferase p300(Homo sapiens (Human))
Daiichi Sankyo

Curated by ChEMBL
LigandPNGBDBM50600298(CHEMBL5187549)
Affinity DataIC50:  190nMAssay Description:Inhibition of N-terminal His tagged human EP300 (1159-1666 residues) expressed in Escherichia coli BL21 (DE3) using biotinylated H4 (1 to 25)-GSGSK p...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed