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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
11
hits in this display
Target
Histone deacetylase 6
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 536nM
Assay Description:
Inhibition of human recombinant HDAC6 using fluorogenic HDAC substrate-3 by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
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Target
Polyamine deacetylase HDAC10
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 1.47E+3nM
Assay Description:
Inhibition of HDAC10 (unknown origin) by fluorescence assay
More data for this Ligand-Target Pair
Target Info
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 3
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 1.97E+3nM
Assay Description:
Inhibition of human recombinant HDAC3 using fluorogenic HDAC substrate-3 by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 1
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 3.07E+3nM
Assay Description:
Inhibition of human recombinant HDAC1 using fluorogenic HDAC substrate-3 by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 5
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 8.59E+3nM
Assay Description:
Inhibition of human recombinant HDAC5 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 2
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
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Affinity Data
IC50: 1.36E+4nM
Assay Description:
Inhibition of HDAC2 (unknown origin) using fluorogenic HDAC substrate-3 by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 4
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
Copy SMILES
Copy InChI
Affinity Data
IC50: 1.62E+4nM
Assay Description:
Inhibition of human recombinant HDAC4 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 8
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Inhibition of human recombinant HDAC8 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 7
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Inhibition of human recombinant HDAC7 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 9
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Inhibition of human recombinant HDAC9 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Histone deacetylase 11
(Homo sapiens (Human))
Keimyung University
Curated by
ChEMBL
Ligand
BDBM50531608
(CHEMBL4556817)
Copy SMILES
Copy InChI
Affinity Data
IC50: >1.00E+5nM
Assay Description:
Inhibition of human recombinant HDAC11 using fluorogenic HDAC substrate class 2A by fluorescence assay
More data for this Ligand-Target Pair
Target Info
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
In Depth
Details
Article
PubMed
Copy BDB DOI