BDBM50020884 CHEMBL3287021::US9216962, CFH326-4

SMILES ONC(=O)CCCCNC(=O)c1csc(n1)-c1cscn1

InChI Key InChIKey=WZTICOBESMFADK-UHFFFAOYSA-N

Data  6 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 6 hits for monomerid = 50020884   

TargetHistone deacetylase 1(Homo sapiens (Human))
Shanghai Puyi Chemical

US Patent
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  816nMAssay Description:Enzyme activity of HDAC1,3 is determined using the substrate Ac-Lys-Tyr-Lys(Ac)-AMC while the enzyme activity of HDAC6 is assayed using the substrate...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetHistone deacetylase 3(Homo sapiens (Human))
Shanghai Puyi Chemical

US Patent
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  193nMAssay Description:Enzyme activity of HDAC1,3 is determined using the substrate Ac-Lys-Tyr-Lys(Ac)-AMC while the enzyme activity of HDAC6 is assayed using the substrate...More data for this Ligand-Target Pair
In DepthDetails US Patent
TargetHistone deacetylase 6(Homo sapiens (Human))
Chinese National Center For Drug Screening

Curated by ChEMBL
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  2.24E+3nMAssay Description:Inhibition of recombinant human HDAC6 using Boc-Lys(epsilon-acetyl)-AMC as substrate after 3 hrs by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Shanghai Puyi Chemical

US Patent
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  450nMAssay Description:Inhibition of recombinant human HDAC1 using Ac-Lys-Tyr-Lys(epsilon-acetyl)-AMC as substrate after 24 hrs by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Shanghai Puyi Chemical

US Patent
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  270nMAssay Description:Inhibition of recombinant human HDAC3 using Ac-Lys-Tyr-Lys(epsilon-acetyl)-AMC as substrate after 24 hrs by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Chinese National Center For Drug Screening

Curated by ChEMBL
LigandPNGBDBM50020884(CHEMBL3287021 | US9216962, CFH326-4)
Affinity DataIC50:  1.33E+3nMAssay Description:Enzyme activity of HDAC1,3 is determined using the substrate Ac-Lys-Tyr-Lys(Ac)-AMC while the enzyme activity of HDAC6 is assayed using the substrate...More data for this Ligand-Target Pair
In DepthDetails US Patent