BDBM50545224 CHEMBL4633911

SMILES COc1ccc(NC(=O)N2CCCC3(CCC(=O)N(C3)C3CC3)C2)cc1

InChI Key InChIKey=IPXGBJBXPNSNFW-UHFFFAOYSA-N

Data  4 IC50

  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 4 hits for monomerid = 50545224   

LigandPNGBDBM50545224(CHEMBL4633911)
Affinity DataIC50: 1.00E+5nMAssay Description:Reversible inhibition of recombinant human KAT2 assessed as reduction in kynurenic acid formation using L-kynurenine as substrate by fluorescence ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/14/2021
Entry Details Article
PubMed
LigandPNGBDBM50545224(CHEMBL4633911)
Affinity DataIC50: 1.55E+4nMAssay Description:Reversible inhibition of recombinant human KAT2 assessed as reduction in kynurenic acid formation using L-kynurenine as substrate by fluorescence ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/14/2021
Entry Details Article
PubMed
LigandPNGBDBM50545224(CHEMBL4633911)
Affinity DataIC50: 1.00E+5nMAssay Description:Reversible inhibition of recombinant human KAT2 assessed as reduction in kynurenic acid formation using L-kynurenine as substrate by fluorescence ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/14/2021
Entry Details Article
PubMed
LigandPNGBDBM50545224(CHEMBL4633911)
Affinity DataIC50: 1.55E+4nMAssay Description:Reversible inhibition of recombinant human KAT2 assessed as reduction in kynurenic acid formation using L-kynurenine as substrate by fluorescence ass...More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/14/2021
Entry Details Article
PubMed