scriptaid [Ligand Id: 7505] activity data from GtoPdb and ChEMBL

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ChEMBL ligand: CHEMBL96051 (GNF-Pf-2024, SJ000016636)
  • histone deacetylase 1/Histone deacetylase 1 in Human [ChEMBL: CHEMBL325] [GtoPdb: 2658] [UniProtKB: Q13547]
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  • histone deacetylase 10/Histone deacetylase 10 in Human [ChEMBL: CHEMBL5103] [GtoPdb: 2614] [UniProtKB: Q969S8]
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  • histone deacetylase 11/Histone deacetylase 11 in Human [ChEMBL: CHEMBL3310] [GtoPdb: 2615] [UniProtKB: Q96DB2]
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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 4/Histone deacetylase 4 in Human [ChEMBL: CHEMBL3524] [GtoPdb: 2659] [UniProtKB: P56524]
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  • histone deacetylase 5/Histone deacetylase 5 in Human [ChEMBL: CHEMBL2563] [GtoPdb: 2660] [UniProtKB: Q9UQL6]
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  • histone deacetylase 6/Histone deacetylase 6 in Human [ChEMBL: CHEMBL1865] [GtoPdb: 2618] [UniProtKB: Q9UBN7]
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  • histone deacetylase 7/Histone deacetylase 7 in Human [ChEMBL: CHEMBL2716] [GtoPdb: 2661] [UniProtKB: Q8WUI4]
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  • Histone deacetylase 8 in Schistosoma mansoni [ChEMBL: CHEMBL3797017] [UniProtKB: A5H660]
  • histone deacetylase 8/Histone deacetylase 8 in Human [ChEMBL: CHEMBL3192] [GtoPdb: 2619] [UniProtKB: Q9BY41]
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  • histone deacetylase 9/Histone deacetylase 9 in Human [ChEMBL: CHEMBL4145] [GtoPdb: 2620] [UniProtKB: Q9UKV0]
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  • Leukotriene A4 hydrolase/Leukotriene A4 hydrolase in Human [ChEMBL: CHEMBL4618] [GtoPdb: 1395] [UniProtKB: P09960]
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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 - - 8.82 pKi 1.5 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human HDAC1 B 8.82 pKi 1.5 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of recombinant full length C-terminal FLAG/His-tagged human HDAC1 (1 to 482 residues) expressed in sf21 cells using RHK-K(Ac)-AMC as substrate by fluorimetric assay B 5.76 pIC50 1740 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
ChEMBL Inhibition of HADC1 (unknown origin) B 6.22 pIC50 600 nM IC50 J Med Chem (2020) 63: 23-39 [PMID:31415174]
ChEMBL Inhibition of HDAC1 by in vitro deacetylation assay B 6.7 pIC50 200 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 10/Histone deacetylase 10 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL5103] [GtoPdb: 2614] [UniProtKB: Q969S8]
ChEMBL Inhibition of HDAC10 by in vitro deacetylation assay B 6.52 pIC50 300 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 11/Histone deacetylase 11 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3310] [GtoPdb: 2615] [UniProtKB: Q96DB2]
ChEMBL Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assay B 4.66 pIC50 22000 nM IC50 J Med Chem (2018) 61: 6574-6591 [PMID:30004697]
ChEMBL Inhibition of human recombinant HDAC11 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assay B 5.28 pIC50 5200 nM IC50 ACS Med Chem Lett (2019) 10: 863-868 [PMID:31223439]
ChEMBL Inhibition of recombinant C-terminal His-tagged human HDAC11 (1 to 347 residues) expressed in Baculovirus infected insect cells using RHKK-Ac as substrate by fluorimetric assay B 6.44 pIC50 360 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
histone deacetylase 2/Histone deacetylase 2 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1937] [GtoPdb: 2616] [UniProtKB: Q92769]
ChEMBL Inhibition of human HDAC2 B 8.66 pKi 2.2 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 8.66 pKi 2.2 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC2 by in vitro deacetylation assay B 6.15 pIC50 700 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 3/Histone deacetylase 3 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1829] [GtoPdb: 2617] [UniProtKB: O15379]
ChEMBL Inhibition of human HDAC3 B 8.39 pKi 4.1 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 8.39 pKi 4.1 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HADC3 (unknown origin) B 6.22 pIC50 600 nM IC50 J Med Chem (2020) 63: 23-39 [PMID:31415174]
ChEMBL Inhibition of HDAC3 by in vitro deacetylation assay B 7 pIC50 100 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
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 - - 8.39 pKi 4.1 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human recombinant full length C-terminal His-tagged HDAC3 (1 to 428 residues)/N-terminal GST-tagged NCOR2 (395 to 489 residues) expressed in insect cells using RHK-K(Ac)-AMC as substrate by fluorimetric assay B 6.43 pIC50 370 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
histone deacetylase 4/Histone deacetylase 4 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3524] [GtoPdb: 2659] [UniProtKB: P56524]
GtoPdb - - 5.12 pKi 7500 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human HDAC4 B 5.12 pKi 7500 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC4 by in vitro deacetylation assay B 6.52 pIC50 300 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 5/Histone deacetylase 5 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2563] [GtoPdb: 2660] [UniProtKB: Q9UQL6]
GtoPdb - - 6 pKi 1000 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human HDAC5 B 6 pKi 1000 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC5 by in vitro deacetylation assay B 6.52 pIC50 300 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 6/Histone deacetylase 6 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL1865] [GtoPdb: 2618] [UniProtKB: Q9UBN7]
GtoPdb - - 9.6 pKi 0.25 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of human HDAC6 B 9.6 pKi 0.25 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of recombinant N-terminal GST-tagged human HDAC6 (1 to 1215 residues) expressed in Baculovirus infected insect cells using RHKK-Ac as substrate by fluorimetric assay B 7.92 pIC50 12 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
ChEMBL Inhibition of human HDAC6 using (Z-(Ac)Lys-AMC) as substrate after 90 mins by fluorescence analysis B 7.92 pIC50 12 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
ChEMBL Inhibition of HDAC6 by in vitro deacetylation assay B 8 pIC50 10 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 7/Histone deacetylase 7 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL2716] [GtoPdb: 2661] [UniProtKB: Q8WUI4]
ChEMBL Inhibition of human HDAC7 B 5.65 pKi 2250 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 5.65 pKi 2250 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC7 by in vitro deacetylation assay B 5.68 pIC50 2100 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
Histone deacetylase 8 in Schistosoma mansoni (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3797017] [UniProtKB: A5H660]
ChEMBL Inhibition of Schistosoma mansoni KDAC8 using (FAM)-labeled peptide as substrate after 60 mins by microfluidic assay B 5.75 pIC50 1770 nM IC50 Bioorg Med Chem (2017) 25: 2105-2132 [PMID:28259528]
histone deacetylase 8/Histone deacetylase 8 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL3192] [GtoPdb: 2619] [UniProtKB: Q9BY41]
ChEMBL Activity of human HDAC8 B 6.98 pKi 105 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 6.98 pKi 105 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of recombinant C-terminal His-tagged human HDAC8 (1 to 377 residues) expressed in Baculovirus infected insect cells using RHK-K(Ac)-AMC as substrate by fluorimetric assay B 5.82 pIC50 1520 nM IC50 Eur J Med Chem (2019) 162: 321-333 [PMID:30448419]
ChEMBL Inhibition of HADC8 (unknown origin) B 6 pIC50 1000 nM IC50 J Med Chem (2020) 63: 23-39 [PMID:31415174]
ChEMBL Inhibition of HDAC8 by in vitro deacetylation assay B 6.52 pIC50 300 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
histone deacetylase 9/Histone deacetylase 9 in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4145] [GtoPdb: 2620] [UniProtKB: Q9UKV0]
ChEMBL Inhibition of human HDAC9 B 5.1 pKi 8000 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
GtoPdb - - 5.1 pKi 8000 nM Ki Nat Chem Biol (2010) 6: 238-243 [PMID:20139990]
ChEMBL Inhibition of HDAC9 by in vitro deacetylation assay B 6.15 pIC50 700 nM IC50 Nat Chem Biol (2010) 6: 25-33 [PMID:19966789]
Leukotriene A4 hydrolase/Leukotriene A4 hydrolase in Human (target type: SINGLE PROTEIN) [ChEMBL: CHEMBL4618] [GtoPdb: 1395] [UniProtKB: P09960]
ChEMBL Inhibition of recombinant human LTA4H Epoxide Hydrolase expressed in Escherichia coli BL21 (DE3) pLysS preincubated for 10 mins followed by addition of LTA4 as substrate measured after 15 mins by reverse-phase HPLC analysis B 5 pIC50 >10000 nM IC50 J Med Chem (2017) 60: 1817-1828 [PMID:28218840]
Plasmodium falciparum (target type: ORGANISM) [ChEMBL: CHEMBL364]
ChEMBL ST_JUDE: Plasmodium falciparum 3D7 EC50 (uM) as measured by SYBR green dye F 5.42 pEC50 3782.9 nM EC50 Nature (2010) 465: 311-315 [PMID:20485428]
ChEMBL ST_JUDE: Plasmodium falciparum K1 EC50 (uM) as measured by SYBR green dye F 5.65 pEC50 2222.4 nM EC50 Nature (2010) 465: 311-315 [PMID:20485428]
ChEMBL NOVARTIS: Inhibition of Plasmodium falciparum 3D7 (drug-susceptible) proliferation in erythrocyte-based infection assay F 6.25 pEC50 563 nM EC50 Proc Natl Acad Sci U S A (2008) 105: 9059-9064 [PMID:18579783]
ChEMBL NOVARTIS: Inhibition of Plasmodium falciparum W2 (drug-resistant) proliferation in erythrocyte-based infection assay F 6.79 pEC50 164 nM EC50 Proc Natl Acad Sci U S A (2008) 105: 9059-9064 [PMID:18579783]

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]