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Compile Data Set for Download or QSAR

Found 28 hits Enz. Inhib. hit(s) with all data for entry = 50048563   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222318
PNG
(CHEMBL123626)
Show SMILES COc1ccc(cc1)-c1cnc(CCCCCCC(=O)NO)o1
Show InChI InChI=1S/C17H22N2O4/c1-22-14-10-8-13(9-11-14)15-12-18-17(23-15)7-5-3-2-4-6-16(20)19-21/h8-12,21H,2-7H2,1H3,(H,19,20)
PDB

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n/an/a 2.10n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222327
PNG
(CHEMBL124282)
Show SMILES COc1ccc(cc1)-c1csc(CCCCCCC(=O)NO)n1
Show InChI InChI=1S/C17H22N2O3S/c1-22-14-10-8-13(9-11-14)15-12-23-17(18-15)7-5-3-2-4-6-16(20)19-21/h8-12,21H,2-7H2,1H3,(H,19,20)
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n/an/a 2.5n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222343
PNG
(CHEMBL339720)
Show SMILES ONC(=O)CCCCCCc1ncc(o1)-c1ccc(Br)cc1
Show InChI InChI=1S/C16H19BrN2O3/c17-13-9-7-12(8-10-13)14-11-18-16(22-14)6-4-2-1-3-5-15(20)19-21/h7-11,21H,1-6H2,(H,19,20)
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n/an/a 2.70n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222339
PNG
(CHEMBL340885)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccc2ccccc2c1
Show InChI InChI=1S/C20H22N2O2S/c23-19(22-24)9-3-1-2-4-10-20-21-18(14-25-20)17-12-11-15-7-5-6-8-16(15)13-17/h5-8,11-14,24H,1-4,9-10H2,(H,22,23)
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n/an/a 4.30n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222342
PNG
(CHEMBL435415)
Show SMILES COc1cccc(OC)c1-c1csc(CCCCCCC(=O)NO)n1
Show InChI InChI=1S/C18H24N2O4S/c1-23-14-8-7-9-15(24-2)18(14)13-12-25-17(19-13)11-6-4-3-5-10-16(21)20-22/h7-9,12,22H,3-6,10-11H2,1-2H3,(H,20,21)
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n/an/a 4.30n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222345
PNG
(CHEMBL123905)
Show SMILES ONC(=O)CCCCCCc1cnc(o1)-c1ccc(Br)cc1
Show InChI InChI=1S/C16H19BrN2O3/c17-13-9-7-12(8-10-13)16-18-11-14(22-16)5-3-1-2-4-6-15(20)19-21/h7-11,21H,1-6H2,(H,19,20)
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n/an/a 4.40n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222363
PNG
(CHEMBL125042)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1cccc(Br)c1
Show InChI InChI=1S/C16H19BrN2O2S/c17-13-7-5-6-12(10-13)14-11-22-16(18-14)9-4-2-1-3-8-15(20)19-21/h5-7,10-11,21H,1-4,8-9H2,(H,19,20)
PDB

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n/an/a 5.80n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222341
PNG
(CHEMBL124650)
Show SMILES ONC(=O)CCCCCCc1ncc(o1)-c1ccc(cc1)-c1ccc(Cl)cc1
Show InChI InChI=1S/C22H23ClN2O3/c23-19-13-11-17(12-14-19)16-7-9-18(10-8-16)20-15-24-22(28-20)6-4-2-1-3-5-21(26)25-27/h7-15,27H,1-6H2,(H,25,26)
PDB

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n/an/a 6.80n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222319
PNG
(CHEMBL340835)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccc(Br)cc1
Show InChI InChI=1S/C16H19BrN2O2S/c17-13-9-7-12(8-10-13)14-11-22-16(18-14)6-4-2-1-3-5-15(20)19-21/h7-11,21H,1-6H2,(H,19,20)
PDB

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n/an/a 8.5n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222334
PNG
(CHEMBL127846)
Show SMILES ONC(=O)CCCCCCc1ncc(o1)-c1ccccc1
Show InChI InChI=1S/C16H20N2O3/c19-15(18-20)10-6-1-2-7-11-16-17-12-14(21-16)13-8-4-3-5-9-13/h3-5,8-9,12,20H,1-2,6-7,10-11H2,(H,18,19)
PDB

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n/an/a 9.80n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222365
PNG
(CHEMBL340113)
Show SMILES CNC(=O)C(=O)CCCCCCc1ncc(o1)-c1ccc(OC)cc1
Show InChI InChI=1S/C19H24N2O4/c1-20-19(23)16(22)7-5-3-4-6-8-18-21-13-17(25-18)14-9-11-15(24-2)12-10-14/h9-13H,3-8H2,1-2H3,(H,20,23)
PDB

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n/an/a 11n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222323
PNG
(CHEMBL126274)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C22H24N2O2S/c25-21(24-26)10-6-1-2-7-11-22-23-20(16-27-22)19-14-12-18(13-15-19)17-8-4-3-5-9-17/h3-5,8-9,12-16,26H,1-2,6-7,10-11H2,(H,24,25)
PDB

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n/an/a 11n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222344
PNG
(CHEMBL339796)
Show SMILES ONC(=O)CCCCCCc1cnc(o1)-c1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C22H24N2O3/c25-21(24-26)11-7-2-1-6-10-20-16-23-22(27-20)19-14-12-18(13-15-19)17-8-4-3-5-9-17/h3-5,8-9,12-16,26H,1-2,6-7,10-11H2,(H,24,25)
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n/an/a 12n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222338
PNG
(CHEMBL127184)
Show SMILES ONC(=O)CCCCCCc1cnc(o1)-c1ccccc1
Show InChI InChI=1S/C16H20N2O3/c19-15(18-20)11-7-2-1-6-10-14-12-17-16(21-14)13-8-4-3-5-9-13/h3-5,8-9,12,20H,1-2,6-7,10-11H2,(H,18,19)
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n/an/a 13n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222316
PNG
(CHEMBL124909)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccccc1
Show InChI InChI=1S/C16H20N2O2S/c19-15(18-20)10-6-1-2-7-11-16-17-14(12-21-16)13-8-4-3-5-9-13/h3-5,8-9,12,20H,1-2,6-7,10-11H2,(H,18,19)
PDB

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n/an/a 19n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222366
PNG
(CHEMBL339534)
Show SMILES CNC(=O)C(=O)CCCCCCc1cnc(o1)-c1ccccc1
Show InChI InChI=1S/C18H22N2O3/c1-19-17(22)16(21)12-8-3-2-7-11-15-13-20-18(23-15)14-9-5-4-6-10-14/h4-6,9-10,13H,2-3,7-8,11-12H2,1H3,(H,19,22)
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n/an/a 21n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222362
PNG
(CHEMBL338776)
Show SMILES ONC(=O)CCCCCCc1cnc(o1)-c1ccc(F)cc1
Show InChI InChI=1S/C16H19FN2O3/c17-13-9-7-12(8-10-13)16-18-11-14(22-16)5-3-1-2-4-6-15(20)19-21/h7-11,21H,1-6H2,(H,19,20)
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n/an/a 23n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222364
PNG
(CHEMBL127269)
Show SMILES CNC(=O)C(=O)CCCCCCc1cnc(o1)-c1ccc(Br)cc1
Show InChI InChI=1S/C18H21BrN2O3/c1-20-17(23)16(22)7-5-3-2-4-6-15-12-21-18(24-15)13-8-10-14(19)11-9-13/h8-12H,2-7H2,1H3,(H,20,23)
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n/an/a 30n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222328
PNG
(CHEMBL126273)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccc(cc1)C(F)(F)F
Show InChI InChI=1S/C17H19F3N2O2S/c18-17(19,20)13-9-7-12(8-10-13)14-11-25-16(21-14)6-4-2-1-3-5-15(23)22-24/h7-11,24H,1-6H2,(H,22,23)
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n/an/a 42n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222321
PNG
(CHEMBL127360)
Show SMILES CNC(=O)C(=O)CCCCCCc1cnc(s1)-c1ccccc1
Show InChI InChI=1S/C18H22N2O2S/c1-19-17(22)16(21)12-8-3-2-7-11-15-13-20-18(23-15)14-9-5-4-6-10-14/h4-6,9-10,13H,2-3,7-8,11-12H2,1H3,(H,19,22)
PDB

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n/an/a 47n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222335
PNG
(CHEMBL125098)
Show SMILES ONC(=O)CCCCCCc1ccc(cc1)-c1ccccc1
Show InChI InChI=1S/C19H23NO2/c21-19(20-22)11-7-2-1-4-8-16-12-14-18(15-13-16)17-9-5-3-6-10-17/h3,5-6,9-10,12-15,22H,1-2,4,7-8,11H2,(H,20,21)
PDB

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n/an/a 58n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222322
PNG
(CHEMBL123506)
Show SMILES ONC(=O)CCCCCCc1nc(cs1)-c1ccc(OC(F)(F)F)cc1
Show InChI InChI=1S/C17H19F3N2O3S/c18-17(19,20)25-13-9-7-12(8-10-13)14-11-26-16(21-14)6-4-2-1-3-5-15(23)22-24/h7-11,24H,1-6H2,(H,22,23)
PDB

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n/an/a 74n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222332
PNG
(CHEMBL124593)
Show SMILES ONC(=O)CCCCCCc1cnc(o1)-c1ccc(OC(F)(F)F)cc1
Show InChI InChI=1S/C17H19F3N2O4/c18-17(19,20)26-13-9-7-12(8-10-13)16-21-11-14(25-16)5-3-1-2-4-6-15(23)22-24/h7-11,24H,1-6H2,(H,22,23)
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n/an/a 89n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM19149
PNG
(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Show SMILES ONC(=O)CCCCCCC(=O)Nc1ccccc1
Show InChI InChI=1S/C14H20N2O3/c17-13(15-12-8-4-3-5-9-12)10-6-1-2-7-11-14(18)16-19/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,17)(H,16,18)
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n/an/a 140n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222331
PNG
(7-Phenoxy-Heptanoic Acid Hydroxyamide | CHEMBL1243...)
Show SMILES ONC(=O)CCCCCCOc1ccccc1
Show InChI InChI=1S/C13H19NO3/c15-13(14-16)10-6-1-2-7-11-17-12-8-4-3-5-9-12/h3-5,8-9,16H,1-2,6-7,10-11H2,(H,14,15)
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n/an/a 330n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50221784
PNG
(CHEMBL112211)
Show SMILES CNC(=O)C(=O)CCCCCCC(=O)Nc1ccccc1
Show InChI InChI=1S/C16H22N2O3/c1-17-16(21)14(19)11-7-2-3-8-12-15(20)18-13-9-5-4-6-10-13/h4-6,9-10H,2-3,7-8,11-12H2,1H3,(H,17,21)(H,18,20)
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n/an/a 340n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50222340
PNG
(8-Phenyl-Octanoic Acid Hydroxyamide | CHEMBL123624)
Show SMILES ONC(=O)CCCCCCCc1ccccc1
Show InChI InChI=1S/C14H21NO2/c16-14(15-17)12-8-3-1-2-5-9-13-10-6-4-7-11-13/h4,6-7,10-11,17H,1-3,5,8-9,12H2,(H,15,16)
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n/an/a 560n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair
Histone deacetylase (HDAC1 and HDAC2)


(Homo sapiens (Human))
BDBM50220823
PNG
(CHEMBL57107)
Show SMILES ONC(=O)CCCCCCNC(=O)c1ccccc1
Show InChI InChI=1S/C14H20N2O3/c17-13(16-19)10-6-1-2-7-11-15-14(18)12-8-4-3-5-9-12/h3-5,8-9,19H,1-2,6-7,10-11H2,(H,15,18)(H,16,17)
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n/an/a 1.01E+3n/an/an/an/an/an/a



Abbott Laboratories

Curated by ChEMBL


Assay Description
Inhibitory activity against histone deacetylase (HDAC1 and HDAC2) isolated from K562 erythroleukemia cells


Bioorg Med Chem Lett 13: 3817-20 (2003)


BindingDB Entry DOI: 10.7270/Q23F4RVV
More data for this
Ligand-Target Pair