BDBM50348378 CHEMBL1800377

SMILES Cc1cc(=O)[nH]c(SCC(=O)c2ccc3OCCOc3c2)n1

InChI Key InChIKey=YOCPSWNLBPSEPL-UHFFFAOYSA-N

Data  9 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 9 hits for monomerid = 50348378   

TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC5 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC4 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC6 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC7 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC3 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC9 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC1 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC2 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute Of Harvard And Mit

Curated by ChEMBL
LigandPNGBDBM50348378(CHEMBL1800377)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant HDAC8 assessed as inhibition of fluorogenic aminocoumarin release from substrate by trypsin-coupled biochemical assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed