Home
About
Info
Download
WebServices
Contact
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
3
hits in this display
Target
Serine/threonine-protein kinase pim-2
(Homo sapiens (Human))
Medical University Of South Carolina
Ligand
BDBM26632
((5Z)-5-[(4-methoxyphenyl)methylidene]-1,3-thiazoli...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 300nM
Assay Description:
The primary screen and evaluation of the compounds was conducted using an ATP-depletion assay. Recombinant human Pim kinase was incubated with S6 kin...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Serine/threonine-protein kinase pim-1
(Homo sapiens (Human))
Medical University Of South Carolina
Ligand
BDBM26632
((5Z)-5-[(4-methoxyphenyl)methylidene]-1,3-thiazoli...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 5.10E+3nM
pH: 7.0 T: 2°C
Assay Description:
The primary screen and evaluation of the compounds was conducted using an ATP-depletion assay. Recombinant human Pim kinase was incubated with S6 kin...
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
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Aldo-keto reductase family 1 member B1
(Homo sapiens (Human))
University Of Messina
Curated by
ChEMBL
Ligand
BDBM26632
((5Z)-5-[(4-methoxyphenyl)methylidene]-1,3-thiazoli...)
Copy SMILES
Copy InChI
Affinity Data
IC50: 4.08E+4nM
Assay Description:
Inhibition of aldose reductase
More data for this Ligand-Target Pair
Target Info
PDB
Reactome pathway
UniProtKB/SwissProt
antibodypedia
GoogleScholar
Ligand Info
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI