Compile Data Set for Download or QSAR
Found 216 of ki data for polymerid = 1996,6108
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347454(MO-OH-TM | US9790158, 5)copy SMILEScopy InChI
Affinity DataKi:  0.0400nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50123957((E)-5-(3-Benzenesulfonylamino-phenyl)-pent-2-en-4-...)copy SMILEScopy InChI
Affinity DataKi:  0.100nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B859V9PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347452(MO-OH-SM | US9790158, 3)copy SMILEScopy InChI
Affinity DataKi:  0.140nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347330(MO-OH-PHE | US9790158, 1)copy SMILEScopy InChI
Affinity DataKi:  0.170nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347453(MO-OH-DM | US9790158, 4)copy SMILEScopy InChI
Affinity DataKi:  0.440nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50105327(JNJ-26481585 | Quisinostat)copy SMILEScopy InChI
Affinity DataKi:  0.5nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347330(MO-OH-PHE | US9790158, 1)copy SMILEScopy InChI
Affinity DataKi:  0.530nMAssay Description:Competitive inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM29589(Faridak | LBH-589 | LBH-589B | Panobinostat | US10...)copy SMILEScopy InChI
Affinity DataKi:  0.700nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347330(MO-OH-PHE | US9790158, 1)copy SMILEScopy InChI
Affinity DataKi:  1.10nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347456(US9790158, 7)copy SMILEScopy InChI
Affinity DataKi:  1.36nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347457(US9790158, 8)copy SMILEScopy InChI
Affinity DataKi:  1.42nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50492541(CHEMBL2408242)copy SMILEScopy InChI
Affinity DataKi:  1.5nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50105327(JNJ-26481585 | Quisinostat)copy SMILEScopy InChI
Affinity DataKi:  2.10nMAssay Description:Inhibition of human HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B859V9PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347460(US9790158, 11)copy SMILEScopy InChI
Affinity DataKi:  2.30nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50492540(CHEMBL2408243)copy SMILEScopy InChI
Affinity DataKi:  2.40nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM348884(US9790158, 10)copy SMILEScopy InChI
Affinity DataKi:  2.69nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353233(CHEMBL1830536)copy SMILEScopy InChI
Affinity DataKi:  3.10nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50105327(JNJ-26481585 | Quisinostat)copy SMILEScopy InChI
Affinity DataKi:  4.30nMAssay Description:Inhibition of human recombinant HDAC5 using fluorogenic HDAC substrate class 2a after 30 mins by fluorimetrc methodMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2M0484TPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50210141(CHEMBL388195 | methyl (3S,6S,9S)-9-acetamido-6-[5-...)copy SMILEScopy InChI
Affinity DataKi:  5.32nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26M36H1PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50602203(CHEMBL5171086)copy SMILES
Affinity DataKi:  5.5nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959NMGPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353234(CHEMBL1830537)copy SMILEScopy InChI
Affinity DataKi:  5.60nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353231(CHEMBL1830422)copy SMILEScopy InChI
Affinity DataKi:  6.60nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353230(CHEMBL1830420)copy SMILEScopy InChI
Affinity DataKi:  6.80nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347451(MO-OH-NAP | US9790158, 2)copy SMILEScopy InChI
Affinity DataKi:  7.63nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50492542(CHEMBL2408248)copy SMILEScopy InChI
Affinity DataKi:  7.90nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353232(CHEMBL1830424)copy SMILEScopy InChI
Affinity DataKi:  9.20nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347460(US9790158, 11)copy SMILEScopy InChI
Affinity DataKi:  10.1nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353229(CHEMBL1830397)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353228(CHEMBL1830396)copy SMILEScopy InChI
Affinity DataKi:  11nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM348884(US9790158, 10)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Inhibition of human recombinant HDAC8 by Michaelis-Menten equation analysisMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q28055HSPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50319209(6-[3-(4-Bromo-benzoyl)-ureido]-hexanoic acid hydro...)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Inhibition of HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GT5NCXPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50263458(CHEMBL4085143)copy SMILEScopy InChI
Affinity DataKi:  13nMAssay Description:Inhibition of recombinant human C-terminal His-tagged HDAC8 (1 to 377 residues) expressed in baculovirus-infected insect cells using RHK(Ac)K(Ac)AMC ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q24B33S0PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50248570(3-(1-(3-(dimethylamino)-2,2-dimethylpropyl)-2-phen...)copy SMILEScopy InChI
Affinity DataKi:  16nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50248476(CHEMBL491316 | N-hydroxy-3-(2-phenethyl-1-(2-(pyrr...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50248476(CHEMBL491316 | N-hydroxy-3-(2-phenethyl-1-(2-(pyrr...)copy SMILEScopy InChI
Affinity DataKi:  17nMAssay Description:Inhibition of recombinant HDAC5 by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2FT8KX3PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50248522(CHEMBL489332 | N-hydroxy-3-(2-phenethyl-1-(2-(pipe...)copy SMILEScopy InChI
Affinity DataKi:  18nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50353227(CHEMBL3215861)copy SMILEScopy InChI
Affinity DataKi:  19nMAssay Description:Competitive inhibition of HDAC8 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM348883(US9790158, 6)copy SMILEScopy InChI
Affinity DataKi:  19.4nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50105330(CHEMBL1851943)copy SMILEScopy InChI
Affinity DataKi:  21nMAssay Description:Inhibition of human HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B859V9PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM50353227(CHEMBL3215861)copy SMILEScopy InChI
Affinity DataKi:  21nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM25150((2E)-N-hydroxy-3-[3-(phenylsulfamoyl)phenyl]prop-2...)copy SMILEScopy InChI
Affinity DataKi:  22nMAssay Description:Competitive inhibition of HDAC8 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM29589(Faridak | LBH-589 | LBH-589B | Panobinostat | US10...)copy SMILEScopy InChI
Affinity DataKi:  22nMAssay Description:Competitive inhibition of HDAC8 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM347461(US9790158, 12)copy SMILEScopy InChI
Affinity DataKi:  23.3nMAssay Description:Key enzyme kinetic parameters for one class I HDAC (HDAC8) and one class Ha HDAC (HDAC4) were determined using commercially available human recombina...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2QZ2D3VUS Patent
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50105327(JNJ-26481585 | Quisinostat)copy SMILEScopy InChI
Affinity DataKi:  24nMAssay Description:Inhibition of human recombinant HDAC8 using fluorogenic HDAC substrate after 15 mins by fluorimetrc methodMore data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM25150((2E)-N-hydroxy-3-[3-(phenylsulfamoyl)phenyl]prop-2...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B859V9PubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM25150((2E)-N-hydroxy-3-[3-(phenylsulfamoyl)phenyl]prop-2...)copy SMILEScopy InChI
Affinity DataKi:  25nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50602192(CHEMBL5174998)copy SMILES
Affinity DataKi:  31nMMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2959NMGPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataKi:  33nMAssay Description:Inhibition of HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2GT5NCXPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
S*BIO Pte Ltd.

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataKi:  36nMAssay Description:Competitive inhibition of HDAC5 using KI-104 as substrate by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q29S1RD6PubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UNIVERSITY OF CONNECTICUT

US Patent
LigandPNGBDBM50105329(CHEMBL1213492)copy SMILEScopy InChI
Affinity DataKi:  39nMAssay Description:Inhibition of human HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2B859V9PubMed
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