Compile Data Set for Download or QSAR
Report error Found 84 Enz. Inhib. hit(s) with all data for entry = 50023691
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 23nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 29nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50509450BDBM50509450(CHEMBL4474656)
Affinity DataIC50: 69nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 71nMAssay Description:Inhibition of HDAC in human CAL-27 cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured afte...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 88nMAssay Description:Inhibition of HDAC in human Cal27CisR cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50509450BDBM50509450(CHEMBL4474656)
Affinity DataIC50: 128nMAssay Description:Inhibition of HDAC2 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 147nMAssay Description:Inhibition of HDAC in human A2780 cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 160nMAssay Description:Inhibition of HDAC in human Cal27CisR cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured af...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 170nMAssay Description:Inhibition of HDAC in human A2780 cisR cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 220nMAssay Description:Inhibition of HDAC in human CAL-27 cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 277nMAssay Description:Inhibition of HDAC in human A2780 cisR cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured a...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50509450BDBM50509450(CHEMBL4474656)
Affinity DataIC50: 310nMAssay Description:Inhibition of HDAC3 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 19410BDBM19410(benzamide-type inhibitor, 3 | CHEMBL27759 | pyridi...)
Affinity DataIC50: 312nMAssay Description:Inhibition of HDAC3 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 19410BDBM19410(benzamide-type inhibitor, 3 | CHEMBL27759 | pyridi...)
Affinity DataIC50: 354nMAssay Description:Inhibition of HDAC2 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 367nMAssay Description:Inhibition of human HDAC6 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 15 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 401nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 402nMAssay Description:Inhibition of HDAC in human A2780 cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 19410BDBM19410(benzamide-type inhibitor, 3 | CHEMBL27759 | pyridi...)
Affinity DataIC50: 426nMAssay Description:Inhibition of HDAC1 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 575nMAssay Description:Inhibition of HDAC in human CAL-27 cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured afte...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 607nMAssay Description:Inhibition of HDAC in human Cal27CisR cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured a...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 2.91E+3nMAssay Description:Inhibition of HDAC in human A2780 cisR cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured ...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666811BDBM50666811(CHEMBL6162062)
Affinity DataIC50: 2.97E+3nMAssay Description:Inhibition of HDAC in human A2780 cells using Boc-Lys(TFA)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sidPDB
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 2(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 3.01E+3nMAssay Description:Inhibition of human HDAC2 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666807BDBM50666807(CHEMBL6175996)
Affinity DataIC50: 3.31E+3nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 3.98E+3nMAssay Description:Inhibition of HDAC in human CAL-27 cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 4.15E+3nMAssay Description:Inhibition of HDAC in human Cal27CisR cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured af...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666810BDBM50666810(CHEMBL6170723)
Affinity DataIC50: 4.54E+3nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 6.80E+3nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666815BDBM50666815(CHEMBL6162607)
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 162864BDBM162864(US9056843, 155)
Affinity DataIC50: 7.47E+3nMAssay Description:Inhibition of HDAC in human A2780 cisR cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured a...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 8.24E+3nMAssay Description:Inhibition of HDAC in human A2780 cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after ...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 8.76E+3nMAssay Description:Inhibition of HDAC in human CAL-27 cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured after...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 9.29E+3nMAssay Description:Inhibition of HDAC in human Cal27CisR cells using Boc-Lys(Ac)-AMC as substrate preincubated for 18 hrs followed by substrate addition and measured af...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666813BDBM50666813(CHEMBL6175022)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666814BDBM50666814(CHEMBL6171506)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666816BDBM50666816(CHEMBL6170726)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666812BDBM50666812(CHEMBL5433064)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666806BDBM50666806(CHEMBL6175270)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666808BDBM50666808(CHEMBL6172510)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666817BDBM50666817(CHEMBL6175463)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666804BDBM50666804(CHEMBL6176185)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 3(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666805BDBM50666805(CHEMBL6172069)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC3 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666805BDBM50666805(CHEMBL6172069)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666806BDBM50666806(CHEMBL6175270)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666807BDBM50666807(CHEMBL6175996)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666808BDBM50666808(CHEMBL6172510)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 1(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50666804BDBM50666804(CHEMBL6176185)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC1 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 60 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 4(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50509450BDBM50509450(CHEMBL4474656)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC4 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 6(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50254780BDBM50254780(CHEMBL4078477 | US10301323, Compound D2 | US990889...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human HDAC6 using ZMAL(Z-Lys(Ac)-AMC as substrate preincubated for 15 mins followed by substrate addition and measured after 90 mins by...More data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
TargetHistone deacetylase 8(Human)
University of Bonn

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 19410BDBM19410(benzamide-type inhibitor, 3 | CHEMBL27759 | pyridi...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC8 (unknown origin) preincubated for 15 minsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
6/6/2026
Entry Details
PubMed
Displayed 1 to 50 (of 84 total ) | Next | Last >>
Jump to: