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Compile Data Set for Download or QSAR

Found 293 hits with Last Name = 'nepali' and Initial = 'k'   
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
ADAM17


(Homo sapiens (Human))
BDBM50245492
PNG
(CHEMBL4082554)
PDB
MMDB

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n/an/a 0.100n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 60: 527-553 (2017)


Article DOI: 10.1021/acs.jmedchem.6b00935
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247556
PNG
(CHEMBL4104117)
PDB
MMDB

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n/an/a 0.291n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
ADAM17


(Homo sapiens (Human))
BDBM50236621
PNG
(CHEMBL4078142)
Show SMILES Cc1cc(COc2ccc(cc2)S(=O)(=O)N[C@@H]2CCC[C@@H]2C(=O)NO)c2ccccc2n1 |r|
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n/an/a 0.600n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 60: 527-553 (2017)


Article DOI: 10.1021/acs.jmedchem.6b00935
More data for this
Ligand-Target Pair
Mitogen-activated protein kinase kinase kinase 5


(Homo sapiens (Human))
BDBM50245498
PNG
(CHEMBL4083562)
PDB

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n/an/a 0.700n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 60: 527-553 (2017)


Article DOI: 10.1021/acs.jmedchem.6b00935
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Sus scrofa)
BDBM50235214
PNG
(CHEMBL4084903)
Show SMILES Fc1cc(F)cc(c1)-c1cc(=O)c2ccc3ccccc3c2o1
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n/an/a 0.780n/an/an/an/an/an/a



Guru Nanak Dev University

Curated by ChEMBL




Bioorg Med Chem Lett 27: 850-854 (2017)


Article DOI: 10.1016/j.bmcl.2017.01.020
BindingDB Entry DOI: 10.7270/Q2PC34PC
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247553
PNG
(CHEMBL4095667)
PDB
MMDB

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n/an/a 0.795n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232359
PNG
(CHEMBL4078822)
Show SMILES CN(C)C(=O)c1cn(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232364
PNG
(CHEMBL4086671)
Show SMILES CN(C)C(=O)c1cn(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50380399
PNG
(CHEMBL2018302 | Tubastatin A | US10227295, Compoun...)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(cc1)C(=O)NO
Show InChI InChI=1S/C20H21N3O2/c1-22-11-10-19-17(13-22)16-4-2-3-5-18(16)23(19)12-14-6-8-15(9-7-14)20(24)21-25/h2-9,25H,10-13H2,1H3,(H,21,24)
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50380399
PNG
(CHEMBL2018302 | Tubastatin A | US10227295, Compoun...)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(cc1)C(=O)NO
Show InChI InChI=1S/C20H21N3O2/c1-22-11-10-19-17(13-22)16-4-2-3-5-18(16)23(19)12-14-6-8-15(9-7-14)20(24)21-25/h2-9,25H,10-13H2,1H3,(H,21,24)
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232358
PNG
(CHEMBL4096845)
Show SMILES CN(C)C(=O)c1cn(Cc2ccc(cc2)C(=O)NO)c2ccccc12
PDB
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n/an/a>1n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232351
PNG
(CHEMBL4100664)
Show SMILES CN(C)Cc1c(C)n(Cc2ccc(cc2)C(=O)NO)c2ccccc12
PDB
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n/an/a>1n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232360
PNG
(CHEMBL4104572)
Show SMILES CN(C)C(=O)c1cn(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 1.10n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232363
PNG
(CHEMBL4102147)
Show SMILES CN(C)Cc1cn(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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n/an/a 1.10n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232354
PNG
(CHEMBL4066920)
Show SMILES CN(C)Cc1cn(Cc2ccc(cc2)C(=O)NO)c2ccccc12
PDB
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n/an/a 1.20n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232352
PNG
(CHEMBL4073888)
Show SMILES CN(C)Cc1c(C)n(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 1.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232353
PNG
(CHEMBL4104052)
Show SMILES CN(C)Cc1c(C)n(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Sus scrofa)
BDBM50235213
PNG
(CHEMBL4102852)
Show SMILES Fc1ccc(c(F)c1)-c1cc(=O)c2ccc3ccccc3c2o1
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n/an/a 1.40n/an/an/an/an/an/a



Guru Nanak Dev University

Curated by ChEMBL




Bioorg Med Chem Lett 27: 850-854 (2017)


Article DOI: 10.1016/j.bmcl.2017.01.020
BindingDB Entry DOI: 10.7270/Q2PC34PC
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50380399
PNG
(CHEMBL2018302 | Tubastatin A | US10227295, Compoun...)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(cc1)C(=O)NO
Show InChI InChI=1S/C20H21N3O2/c1-22-11-10-19-17(13-22)16-4-2-3-5-18(16)23(19)12-14-6-8-15(9-7-14)20(24)21-25/h2-9,25H,10-13H2,1H3,(H,21,24)
PDB
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n/an/a 1.40n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232360
PNG
(CHEMBL4104572)
Show SMILES CN(C)C(=O)c1cn(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 1.5n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232356
PNG
(CHEMBL4094410)
Show SMILES CN(C)Cc1cn(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232356
PNG
(CHEMBL4094410)
Show SMILES CN(C)Cc1cn(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 1.60n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232361
PNG
(CHEMBL4084222)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 1.60n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232361
PNG
(CHEMBL4084222)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 1.70n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232357
PNG
(CHEMBL4077893)
Show SMILES CN(C)Cc1cn(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 1.70n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232350
PNG
(CHEMBL4062520)
Show SMILES CN1CCc2c(C1)c1ccccc1n2S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 1.90n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232357
PNG
(CHEMBL4077893)
Show SMILES CN(C)Cc1cn(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232352
PNG
(CHEMBL4073888)
Show SMILES CN(C)Cc1c(C)n(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 1.90n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232360
PNG
(CHEMBL4104572)
Show SMILES CN(C)C(=O)c1cn(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 2n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Sus scrofa)
BDBM50235212
PNG
(CHEMBL4092661)
Show SMILES Fc1cccc(F)c1-c1cc(=O)c2ccc3ccccc3c2o1
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Guru Nanak Dev University

Curated by ChEMBL




Bioorg Med Chem Lett 27: 850-854 (2017)


Article DOI: 10.1016/j.bmcl.2017.01.020
BindingDB Entry DOI: 10.7270/Q2PC34PC
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232359
PNG
(CHEMBL4078822)
Show SMILES CN(C)C(=O)c1cn(c2ccccc12)S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232362
PNG
(CHEMBL4079799)
Show SMILES CN(C)Cc1c(C)n(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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n/an/a 2.10n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232354
PNG
(CHEMBL4066920)
Show SMILES CN(C)Cc1cn(Cc2ccc(cc2)C(=O)NO)c2ccccc12
PDB
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n/an/a 2.20n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247560
PNG
(CHEMBL4063376)
PDB
MMDB

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n/an/a 2.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247580
PNG
(CHEMBL4091237)
PDB
MMDB

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n/an/a 2.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232363
PNG
(CHEMBL4102147)
Show SMILES CN(C)Cc1cn(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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n/an/a 2.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232362
PNG
(CHEMBL4079799)
Show SMILES CN(C)Cc1c(C)n(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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n/an/a 2.40n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232350
PNG
(CHEMBL4062520)
Show SMILES CN1CCc2c(C1)c1ccccc1n2S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 2.70n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247582
PNG
(CHEMBL4098833)
PDB
MMDB

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n/an/a 2.80n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 2


(Homo sapiens (Human))
BDBM50232350
PNG
(CHEMBL4062520)
Show SMILES CN1CCc2c(C1)c1ccccc1n2S(=O)(=O)c1cccc(\C=C\C(=O)NO)c1
PDB
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n/an/a 3.10n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Carboxylic ester hydrolase


(Sus scrofa)
BDBM50159614
PNG
(2-(2-Fluoro-phenyl)-benzo[h]chromen-4-one | CHEMBL...)
Show SMILES Fc1ccccc1-c1cc(=O)c2ccc3ccccc3c2o1
Show InChI InChI=1S/C19H11FO2/c20-16-8-4-3-7-14(16)18-11-17(21)15-10-9-12-5-1-2-6-13(12)19(15)22-18/h1-11H
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n/an/a 3.20n/an/an/an/an/an/a



Guru Nanak Dev University

Curated by ChEMBL




Bioorg Med Chem Lett 27: 850-854 (2017)


Article DOI: 10.1016/j.bmcl.2017.01.020
BindingDB Entry DOI: 10.7270/Q2PC34PC
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247570
PNG
(CHEMBL4079874)
PDB
MMDB

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n/an/a 3.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247561
PNG
(CHEMBL4085971)
PDB
MMDB

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n/an/a 3.40n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247592
PNG
(CHEMBL4101436)
PDB
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n/an/a 3.60n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50005711
PNG
(CHEBI:46024 | GNF-Pf-1011 | TRICHOSTATIN | Trichos...)
Show SMILES C[C@H](\C=C(/C)\C=C\C(=O)NO)C(=O)c1ccc(cc1)N(C)C |r|
Show InChI InChI=1S/C17H22N2O3/c1-12(5-10-16(20)18-22)11-13(2)17(21)14-6-8-15(9-7-14)19(3)4/h5-11,13,22H,1-4H3,(H,18,20)/b10-5+,12-11+/t13-/m1/s1
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n/an/a 3.60n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
3D
3D Structure (crystal)
Histone deacetylase 1


(Homo sapiens (Human))
BDBM50232353
PNG
(CHEMBL4104052)
Show SMILES CN(C)Cc1c(C)n(c2ccccc12)S(=O)(=O)c1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 4n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50247579
PNG
(CHEMBL4073165)
PDB
MMDB

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n/an/a 4.20n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232361
PNG
(CHEMBL4084222)
Show SMILES CN1CCc2c(C1)c1ccccc1n2Cc1ccc(\C=C\C(=O)NO)cc1
PDB
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n/an/a 4.20n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 6


(Homo sapiens (Human))
BDBM50232363
PNG
(CHEMBL4102147)
Show SMILES CN(C)Cc1cn(Cc2ccc(\C=C\C(=O)NO)cc2)c2ccccc12
PDB
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n/an/a 4.30n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




Eur J Med Chem 127: 115-127 (2017)


BindingDB Entry DOI: 10.7270/Q20K2BT4
More data for this
Ligand-Target Pair
Histone deacetylase 1/6


(Homo sapiens (Human))
BDBM50439674
PNG
(RICOLINOSTAT | US8609678, 2-(diphenylamino)-N-(7-(...)
Show SMILES ONC(=O)CCCCCCNC(=O)c1cnc(nc1)N(c1ccccc1)c1ccccc1
Show InChI InChI=1S/C24H27N5O3/c30-22(28-32)15-9-1-2-10-16-25-23(31)19-17-26-24(27-18-19)29(20-11-5-3-6-12-20)21-13-7-4-8-14-21/h3-8,11-14,17-18,32H,1-2,9-10,15-16H2,(H,25,31)(H,28,30)
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n/an/a 4.70n/an/an/an/an/an/a



Taipei Medical University

Curated by ChEMBL




J Med Chem 61: 905-917 (2018)

More data for this
Ligand-Target Pair
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