BDBM50602361 CHEMBL5206304

SMILES ONC(=O)CCCCCCNC(=O)c1ccc(NC(=O)CCCCCCCNC(=O)COc2cccc3C(=O)N(C4CCC(=O)NC4=O)C(=O)c23)cc1

InChI Key InChIKey=FQLCLMHMOFLVSV-UHFFFAOYSA-N

Data  10 IC50  2 EC50

  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 12 hits for monomerid = 50602361   

TargetHistone deacetylase 6(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 4.90nMAssay Description:Inhibition of recombinant full length N-terminal GST-tagged human HDAC6 (1 to 1215 residues) using Z-Lys(Ac)-AMC as substrate preincubated for 90 min...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/24/2023
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataEC50:  6.5nMAssay Description:Protac activity at HDAC6 in human MM1.S cells assessed as HDAC6 protein degradation incubated for 24 hrs by immunoblotting analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
12/20/2024
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 7nMAssay Description:Inhibition of N-terminal GST-tagged human full length recombinant HDAC6 (1 to 1215 residues) expressed in Sf9 cells using ZMAL (Z-(Ac)Lys-AMC) as sub...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 9nMAssay Description:Inhibition of human HDAC6 using ZMAL (Z-(Ac)Lys-AMC) as substrate incubated for 90 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 100nMAssay Description:Inhibition of recombinant full length C-terminal His/Flag-tagged human HDAC1 (1 to 482 residues) using Z-Lys(Ac)-AMC as substrate preincubated for 90...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/24/2023
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 125nMAssay Description:Inhibition of human recombinant HDAC1 using ZMAL (Z-(Ac)Lys-AMC) as substrate incubated for 90 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 136nMAssay Description:Inhibition of full length C-terminal 6His/FLAG tagged human recombinant HDAC1 (1 to 482 residues) extracted from sf9 cells using Z-Lys(Ac)-AMC as sub...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 164nMAssay Description:Inhibition of C-terminal His tagged human recombinant HDAC3 (1 to 428 end residues)/N-terminal GST-tagged human NcoR2 expressed in Sf9 insect cells u...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
University of Bonn institution

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 274nMAssay Description:Inhibition of human HDAC2 using ZMAL (Z-(Ac)Lys-AMC) as substrate incubated for 90 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
University of Bonn institution

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 276nMAssay Description:Inhibition of full length C-terminal 6His/FLAG tagged human recombinant HDAC2 (1 to 488 end residues) extracted from sf9 cells using Z-Lys(Ac)-AMC as...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/5/2026
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
Leipzig University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataEC50:  460nMAssay Description:Induction of HDAC6 degradation in human HL-60 cells assessed as hyperacetylation of alpha-tubulin after 6 hrs by Western immunoassayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/24/2023
Entry Details
PubMed
TargetHistone deacetylase 4(Human)
University of Bonn institution

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50602361BDBM50602361(CHEMBL5206304)
Affinity DataIC50: 5.26E+3nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(Tfa)-AMC as substrate incubated for 90 mins by fluorescence based assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/4/2026
Entry Details
PubMed