Compile Data Set for Download or QSAR
Report error Found 70 Enz. Inhib. hit(s) with all data for entry = 50011712
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476626BDBM476626(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 0.950nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476611BDBM476611(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)benzami...)
Affinity DataIC50: 3.5nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476627BDBM476627(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 3.70nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476606BDBM476606(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 8.60nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476626BDBM476626(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 12nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC1 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476613BDBM476613(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)benzami...)
Affinity DataIC50: 19nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476625BDBM476625(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 20nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476625BDBM476625(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 29nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC1 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476629BDBM476629(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 33nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476615BDBM476615(N-(4-(2- (cyclopropylmethyl)hydrazine- 1-carbonyl)...)
Affinity DataIC50: 40nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476629BDBM476629(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 47nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC1 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476627BDBM476627(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 60nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC1 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476614BDBM476614(N-(4-(2-(3,3,3- trifluoropropyl)hydrazine-1- carbo...)
Affinity DataIC50: 69nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 468609BDBM468609(US10807944, Compound RLS3-43 | US10870618, Compoun...)
Affinity DataIC50: 69nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476627BDBM476627(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 70nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC2 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476625BDBM476625(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 77nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC2 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 1(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476630BDBM476630(N-(4-(2-hexylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 81nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC1 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476623BDBM476623(N-(4-(2- (cyclobutylmethyl)hydrazine- 1-carbonyl)b...)
Affinity DataIC50: 84nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476626BDBM476626(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 95nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC2 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476629BDBM476629(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 100nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC2 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476626BDBM476626(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 124nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 2(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476630BDBM476630(N-(4-(2-hexylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 139nMAssay Description:Inhibition of C-terminal His-tagged recombinant human HDAC2 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminomethyl couma...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476630BDBM476630(N-(4-(2-hexylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 150nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476611BDBM476611(N-(4-(2-propylhydrazine-1- carbonyl)benzyl)benzami...)
Affinity DataIC50: 155nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 163623BDBM163623(SR-3206 | US10807944, Compound RLS2-126 | US108706...)
Affinity DataIC50: 157nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476625BDBM476625(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 171nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476619BDBM476619(N-(4-(2-hexylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 184nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476622BDBM476622(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 187nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476606BDBM476606(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 261nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476613BDBM476613(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)benzami...)
Affinity DataIC50: 264nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476602BDBM476602(N'-butylcinnamohydrazide | US10870618, Compound 1i)
Affinity DataIC50: 295nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476565BDBM476565(N'-butyl-4- phenoxybenzohydrazide | US10870618, Co...)
Affinity DataIC50: 312nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476622BDBM476622(N-(4-(2-ethylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 427nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476627BDBM476627(N-(4-(2-butylhydrazine-1- carbonyl)benzyl)cinnamam...)
Affinity DataIC50: 494nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476619BDBM476619(N-(4-(2-hexylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 550nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476617BDBM476617(N-(4-(2-heptylhydrazine-1- carbonyl)benzyl)benzami...)
Affinity DataIC50: 569nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476629BDBM476629(N-(4-(2-pentylhydrazine-1- carbonyl)benzyl)cinnama...)
Affinity DataIC50: 691nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 163623BDBM163623(SR-3206 | US10807944, Compound RLS2-126 | US108706...)
Affinity DataIC50: 727nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 468586BDBM468586(US10807944, Compound RLS2-238 | US10870618, Compou...)
Affinity DataIC50: 892nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476598BDBM476598(N'-butylthiophene-2- carbohydrazide | US10870618, ...)
Affinity DataIC50: 904nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476618BDBM476618(N-(4-(2-octylhydrazine-1- carbonyl)benzyl)benzamid...)
Affinity DataIC50: 1.09E+3nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476614BDBM476614(N-(4-(2-(3,3,3- trifluoropropyl)hydrazine-1- carbo...)
Affinity DataIC50: 1.23E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 468609BDBM468609(US10807944, Compound RLS3-43 | US10870618, Compoun...)
Affinity DataIC50: 1.31E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476564BDBM476564(N'-butylbenzofuran-2- carbohydrazide | US10870618,...)
Affinity DataIC50: 1.36E+3nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476602BDBM476602(N'-butylcinnamohydrazide | US10870618, Compound 1i)
Affinity DataIC50: 1.44E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 468597BDBM468597(US10807944, Compound RLS2-289 | US10870618, Compou...)
Affinity DataIC50: 1.55E+3nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476607BDBM476607((E)-N-(4-(2-(but-2-en-1- yl)hydrazine-1- carbonyl)...)
Affinity DataIC50: 1.55E+3nMAssay Description:Allosteric inhibition of C-terminal His-tagged recombinant human HDAC3 expressed in Sf9 cells pre-incubated for 2 hrs before acetylated lysine-aminom...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476615BDBM476615(N-(4-(2- (cyclopropylmethyl)hydrazine- 1-carbonyl)...)
Affinity DataIC50: 1.62E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476564BDBM476564(N'-butylbenzofuran-2- carbohydrazide | US10870618,...)
Affinity DataIC50: 1.69E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
TargetHistone deacetylase 3(Human)
Medical University of South Carolina

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 476565BDBM476565(N'-butyl-4- phenoxybenzohydrazide | US10870618, Co...)
Affinity DataIC50: 1.69E+3nMAssay Description:Allosteric inhibition of HDAC3 in HEK293 cell lysates pre-incubated for 2 hrs before acetylated lysine-aminomethyl coumarin-BOC addition and measured...More data for this Ligand-Target Pair
In Depth
Date in BDB:
3/23/2022
Entry Details Article
PubMed
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