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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
7
hits in this display
Target
Aurora kinase A
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
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Affinity Data
Ki: 9.20nM
Assay Description:
Inhibition of human recombinant Aurora A after 30 mins
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
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
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Target
Aurora kinase B
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
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Affinity Data
Ki: 18nM
Assay Description:
Inhibition of human recombinant Aurora B after 60 mins
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 9
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
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Affinity Data
Ki: 1.47E+3nM
Assay Description:
Inhibition of CDK9
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 2
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
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Affinity Data
Ki: 3.97E+3nM
Assay Description:
Inhibition of CDK2
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
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 7
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Inhibition of CDK7
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 4
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Inhibition of CDK4
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
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Cyclin-dependent kinase 1
(Homo sapiens (Human))
Cyclacel
Curated by
ChEMBL
Ligand
BDBM50319626
(4-(2,4-Dimethylthiazol-5-yl)-N-(4-(4-(methylsulfon...)
Copy SMILES
Copy InChI
Affinity Data
Ki: >1.00E+4nM
Assay Description:
Inhibition of CDK1
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
KEGG
UniProtKB/SwissProt
DrugBank
antibodypedia
GoogleScholar
Ligand Info
CHEMBL
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI