tacedinaline [Ligand Id: 8367] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL235191 (CI-994, GOE 5549, GOE-5549, PD 123654, PD-123654, Tacedinaline)
  • histone deacetylase 1/Histone deacetylase 1 in Human [ChEMBL: CHEMBL325] [GtoPdb: 2658] [UniProtKB: Q13547]
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  • histone deacetylase 2/Histone deacetylase 2 in Human [ChEMBL: CHEMBL1937] [GtoPdb: 2616] [UniProtKB: Q92769]
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  • histone deacetylase 3/Histone deacetylase 3 in Human [ChEMBL: CHEMBL1829] [GtoPdb: 2617] [UniProtKB: O15379]
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  • histone deacetylase 3/Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2) in Human [ChEMBL: CHEMBL2111363] [GtoPdb: 2617] [UniProtKB: O15379Q9Y618]
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  • histone deacetylase 6/Histone deacetylase 6 in Human [ChEMBL: CHEMBL1865] [GtoPdb: 2618] [UniProtKB: Q9UBN7]
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  • histone deacetylase 8/Histone deacetylase 8 in Human [ChEMBL: CHEMBL3192] [GtoPdb: 2619] [UniProtKB: Q9BY41]
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DB Assay description Assay Type Standard value Standard parameter Original value Original units Original parameter Reference
histone deacetylase 1/Histone deacetylase 1 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL325] [GtoPdb: 2658] [UniProtKB: Q13547]
GtoPdb - - 7.3 pKi 50 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human HDAC1 B 7.3 pKi 50 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC1 (unknown origin) by fluorimetric assay B 4.74 pIC50 18220 nM IC50 Bioorg Med Chem Lett (2016) 26: 154-159 [PMID:26611919]
ChEMBL Inhibition of recombinant human His tagged HDAC1 expressed in baculovirus infected insect cells assessed as decrease in deacetylation of FLUOR DE LYS Green substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence based assay B 5.78 pIC50 1670 nM IC50 Eur J Med Chem (2019) 176: 195-207 [PMID:31103900]
ChEMBL Inhibition of human recombinant His-tagged HDAC1 (482 residues) expressed in baculovirus infected insect cells using FLUOR DE LYS SIRT1 as substrate incubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence method B 5.78 pIC50 1670 nM IC50 Eur J Med Chem (2019) 173: 185-202 [PMID:31003060]
ChEMBL Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorometric assay B 5.79 pIC50 1620 nM IC50 Eur J Med Chem (2017) 134: 1-12 [PMID:28391133]
ChEMBL Inhibition of human recombinant HDAC1 using Fluor de Lys-Green as substrate preincubated for 5 mins followed by substrate addition and measured after 1 hr by fluorescence assay B 5.79 pIC50 1620 nM IC50 Eur J Med Chem (2018) 143: 320-333 [PMID:29202397]
ChEMBL Inhibition of human recombinant HDAC1 (1 to 482 residues) expressed in Baculovirus using Ac-Leu-Gly-Lys(Ac)-AMC as substrate preincubated for 5 mins followed by substrate addition measured after 30 mins by fluorescence assay B 5.92 pIC50 1200 nM IC50 J Med Chem (2017) 60: 7965-7983 [PMID:28885834]
ChEMBL Inhibition of human recombinant full length HDAC1 using fluorogenic substrate 3 after 30 mins by fluorescence assay B 5.96 pIC50 1090 nM IC50 J Med Chem (2018) 61: 7245-7260 [PMID:30045621]
ChEMBL Inhibition of human recombinant HDAC1 B 6.05 pIC50 900 nM IC50 J Med Chem (2007) 50: 5543-5546 [PMID:17941625]
GtoPdb - - 6.24 pIC50 570 nM IC50 Bioorg Med Chem Lett (2008) 18: 973-8 [PMID:18182289]
ChEMBL Inhibition of HDAC1 B 6.24 pIC50 570 nM IC50 Bioorg Med Chem Lett (2008) 18: 973-978 [PMID:18182289]
ChEMBL Inhibition of recombinant human C-terminal His/FLAG-tagged HDAC1 (1 to 482 residues) expressed in Sf9 insect cells using Boc-Lys(epsilon-Ac)-AMC as substrate measured after 90 mins by fluorescence assay B 6.89 pIC50 130 nM IC50 Eur J Med Chem (2020) 208: 112800-112800 [PMID:32971411]
ChEMBL Inhibition of human recombinant HDAC1 (1 to 482 residues) expressed in Baculovirus using Ac-Leu-Gly-Lys(Ac)-AMC as substrate after 3 hrs by fluorescence assay B 7.22 pIC50 60 nM IC50 J Med Chem (2017) 60: 7965-7983 [PMID:28885834]
ChEMBL Inhibition of recombinant human full length C-terminal His/FALG-tagged HDAC1 expressed in Sf9 insect cells using FAM-labeled acetylated peptide A as substrate preincubated for 3 hrs followed by substrate addition and measured after 60 mins by fluorescence assay B 7.39 pIC50 41 nM IC50 Eur J Med Chem (2019) 166: 369-380 [PMID:30735902]
histone deacetylase 2/Histone deacetylase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1937] [GtoPdb: 2616] [UniProtKB: Q92769]
ChEMBL Inhibition of human HDAC2 B 6.72 pKi 190 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 6.82 pKi 150 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC2 (unknown origin) by fluorimetric assay B 5.41 pIC50 3850 nM IC50 Bioorg Med Chem Lett (2016) 26: 154-159 [PMID:26611919]
ChEMBL Inhibition of recombinant human HDAC2 assessed as decrease in deacetylation of FLUOR DE LYS Green substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence based assay B 5.72 pIC50 1920 nM IC50 Eur J Med Chem (2019) 176: 195-207 [PMID:31103900]
ChEMBL Inhibition of human recombinant His-tagged HDAC2 (1 to 582 residues) expressed in baculovirus infected insect cells using FLUOR DE LYS Green as substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence method B 5.72 pIC50 1920 nM IC50 Eur J Med Chem (2019) 173: 185-202 [PMID:31003060]
ChEMBL Inhibition of human recombinant HDAC2 using Fluor de Lys green as substrate by fluorometric assay B 5.92 pIC50 1200 nM IC50 Eur J Med Chem (2017) 134: 1-12 [PMID:28391133]
ChEMBL Inhibition of human recombinant HDAC2 using Fluor de Lys-Green as substrate preincubated for 5 mins followed by substrate addition and measured after 1 hr by fluorescence assay B 5.92 pIC50 1200 nM IC50 Eur J Med Chem (2018) 143: 320-333 [PMID:29202397]
ChEMBL Inhibition of human recombinant HDAC2 B 6.05 pIC50 900 nM IC50 J Med Chem (2007) 50: 5543-5546 [PMID:17941625]
ChEMBL Inhibition of recombinant human full-length C-terminal FLAG-tagged HDAC2 expressed in baculovirus infected Sf9 insect cells using Boc-Lys(epsilon-Ac)-AMC as substrate measured after 90 mins by fluorescence assay B 6.08 pIC50 830 nM IC50 Eur J Med Chem (2020) 208: 112800-112800 [PMID:32971411]
ChEMBL Inhibition of recombinant human full length C-terminal FLAG-tagged HDAC2 expressed in Sf9 insect cells using FAM-labeled acetylated peptide A as substrate preincubated for 3 hrs followed by substrate addition and measured after 60 mins by fluorescence assay B 6.83 pIC50 147 nM IC50 Eur J Med Chem (2019) 166: 369-380 [PMID:30735902]
histone deacetylase 3/Histone deacetylase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1829] [GtoPdb: 2617] [UniProtKB: O15379]
ChEMBL Inhibition of human HDAC3 B 6.26 pKi 550 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 6.26 pKi 550 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC3 (unknown origin) by fluorimetric assay B 4 pIC50 >100000 nM IC50 Bioorg Med Chem Lett (2016) 26: 154-159 [PMID:26611919]
ChEMBL Inhibition of human recombinant HDAC3 B 5.92 pIC50 1200 nM IC50 J Med Chem (2007) 50: 5543-5546 [PMID:17941625]
ChEMBL Inhibition of recombinant human full length HDAC3 using FAM-labeled acetylated peptide A as substrate preincubated for 3 hrs followed by substrate addition and measured after 60 mins by fluorescence assay B 7.34 pIC50 46 nM IC50 Eur J Med Chem (2019) 166: 369-380 [PMID:30735902]
histone deacetylase 3/Histone deacetylase 3/NCoR1 in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL3038484] [GtoPdb: 2617] [UniProtKB: O15379O75376]
GtoPdb - - 6.26 pKi 550 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of recombinant human HDAC3/NCOR1 assessed as decrease in deacetylation of FLUOR DE LYS SIRT1 substrate preincubated for 10 mins followed by substrate addition and and measured after 30 mins by fluorescence based assay B 4.49 pIC50 >32000 nM IC50 Eur J Med Chem (2019) 176: 195-207 [PMID:31103900]
histone deacetylase 3/Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2) in Human (target type: PROTEIN COMPLEX) [ChEMBL: CHEMBL2111363] [GtoPdb: 2617] [UniProtKB: O15379Q9Y618]
GtoPdb - - 6.26 pKi 550 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human recombinant C-terminal His-tagged HDAC3 (1 to 428 residues)/N-terminal GST-tagged NCOR2 (395 to 489 residues) expressed in baculovirus infected Sf9 insect cells using Boc-Lys(epsilon-Ac)-AMC as substrate measured after 90 mins by fluorescence assay B 6.72 pIC50 190 nM IC50 Eur J Med Chem (2020) 208: 112800-112800 [PMID:32971411]
histone deacetylase 6/Histone deacetylase 6 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1865] [GtoPdb: 2618] [UniProtKB: Q9UBN7]
ChEMBL Inhibition of HDAC6 (unknown origin) by fluorimetric assay B 4 pIC50 >100000 nM IC50 Bioorg Med Chem Lett (2016) 26: 154-159 [PMID:26611919]
ChEMBL Inhibition of human recombinant HDAC6 using Fluor de Lys as substrate after 60 mins by fluorometric assay B 4.4 pIC50 >40000 nM IC50 Eur J Med Chem (2017) 134: 1-12 [PMID:28391133]
ChEMBL Inhibition of human recombinant HDAC6 using Fluor de Lys-Green as substrate preincubated for 5 mins followed by substrate addition and measured after 1 hr by fluorescence assay B 4.4 pIC50 >40000 nM IC50 Eur J Med Chem (2018) 143: 320-333 [PMID:29202397]
ChEMBL Inhibition of human recombinant His-tagged HDAC6 expressed in baculovirus infected insect cells using FLUOR DE LYS SIRT1 as substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence method B 4.4 pIC50 >40000 nM IC50 Eur J Med Chem (2019) 173: 185-202 [PMID:31003060]
ChEMBL Inhibition of recombinant human His tagged HDAC6 expressed in baculovirus infected insect cells assessed as decrease in deacetylation of FLUOR DE LYS SIRT1 substrate by measuring decrease in fluorescence preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence based assay B 4.49 pIC50 >32000 nM IC50 Eur J Med Chem (2019) 176: 195-207 [PMID:31103900]
histone deacetylase 8/Histone deacetylase 8 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3192] [GtoPdb: 2619] [UniProtKB: Q9BY41]
ChEMBL Inhibition of recombinant human HDAC8 assessed as decrease in deacetylation of FLUOR DE LYS substrate preincubated for 10 mins followed by substrate addition and measured after 30 mins by fluorescence based assay B 4.49 pIC50 >32000 nM IC50 Eur J Med Chem (2019) 176: 195-207 [PMID:31103900]
ChEMBL Inhibition of human recombinant HDAC8 B 4.7 pIC50 >20000 nM IC50 J Med Chem (2007) 50: 5543-5546 [PMID:17941625]
Nicotinamide phosphoribosyltransferase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1744525] [UniProtKB: P43490]
ChEMBL Inhibition of human recombinant NAMPT using NAM as substrate preincubated for 5 mins followed by substrate addition measured after 15 mins by fluorescence assay B 5.7 pIC50 >2000 nM IC50 J Med Chem (2017) 60: 7965-7983 [PMID:28885834]

ChEMBL data shown on this page come from version 33:

Mendez D, Gaulton A, Bento AP, Chambers J, De Veij M, Félix E, Magariños MP, Mosquera JF, Mutowo P, Nowotka M, Gordillo-Marañón M, Hunter F, Junco L, Mugumbate G, Rodriguez-Lopez M, Atkinson F, Bosc N, Radoux CJ, Segura-Cabrera A, Hersey A, Leach AR. (2019) 'ChEMBL: towards direct deposition of bioassay data' Nucleic Acids Res., 47(D1). DOI: 10.1093/nar/gky1075. [EPMCID:30398643]
Davies M, Nowotka M, Papadatos G, Dedman N, Gaulton A, Atkinson F, Bellis L, Overington JP. (2015) 'ChEMBL web services: streamlining access to drug discovery data and utilities.' Nucleic Acids Res., 43(W1). DOI: 10.1093/nar/gkv352. [EPMCID:25883136]