BDBM13556 2-[4-(benzyloxy)-3-methoxyphenyl]-2-[(4-carbamimidoylphenyl)amino]acetic acid::phenylglycine deriv. 4

SMILES COc1cc(ccc1OCc1ccccc1)C(Nc1ccc(cc1)C(N)=N)C(O)=O

InChI Key InChIKey=OBEJFOHWQWJNIL-UHFFFAOYSA-N

Data  4 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 13556   

TargetCoagulation factor VII(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13556(2-[4-(benzyloxy)-3-methoxyphenyl]-2-[(4-carbamimid...)
Affinity DataKi:  61nM ΔG°:  -9.74kcal/molepH: 7.8 T: 2°CAssay 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
In DepthDetails Article
PubMed
TargetProthrombin(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13556(2-[4-(benzyloxy)-3-methoxyphenyl]-2-[(4-carbamimid...)
Affinity DataKi:  74nMAssay 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
In DepthDetails Article
PubMed
TargetSerine protease 1(Bovine)
F. Hoffmann-La Roche

LigandPNGBDBM13556(2-[4-(benzyloxy)-3-methoxyphenyl]-2-[(4-carbamimid...)
Affinity DataKi:  310nMAssay 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
In DepthDetails Article
PubMed
TargetCoagulation factor X(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13556(2-[4-(benzyloxy)-3-methoxyphenyl]-2-[(4-carbamimid...)
Affinity DataKi:  730nMAssay 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
In DepthDetails Article
PubMed