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
4
hits in this display
Target
Coagulation factor VII
(Homo sapiens (Human))
F. Hoffmann-La Roche
Ligand
BDBM13563
(2-[(4-carbamimidoylphenyl)amino]-2-{3-ethoxy-5-[(4...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 110nM ΔG°: -39.3kJ/mole
pH: 7.8 T: 2°C
Assay Description:
The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...
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
Serine protease 1
(Bos taurus (bovine))
F. Hoffmann-La Roche
Ligand
BDBM13563
(2-[(4-carbamimidoylphenyl)amino]-2-{3-ethoxy-5-[(4...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 4.00E+3nM
Assay Description:
The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...
More data for this Ligand-Target Pair
Target Info
PDB
MMDB
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
GoogleScholar
Ligand Info
PC cid
PC sid
Patents
Similars
In Depth
Details
Article
PubMed
Copy BDB DOI
Target
Prothrombin
(Homo sapiens (Human))
F. Hoffmann-La Roche
Ligand
BDBM13563
(2-[(4-carbamimidoylphenyl)amino]-2-{3-ethoxy-5-[(4...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 5.50E+3nM
Assay Description:
The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...
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
Target
Coagulation factor X
(Homo sapiens (Human))
F. Hoffmann-La Roche
Ligand
BDBM13563
(2-[(4-carbamimidoylphenyl)amino]-2-{3-ethoxy-5-[(4...)
Copy SMILES
Copy InChI
Affinity Data
Ki: 1.22E+4nM
Assay Description:
The enzyme reactions were initiated by the addition of substrate, and the color developed from the release of p-nitroanilide from each chromogenic su...
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