BDBM13558 2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyphenyl)acetic acid::phenylglycine deriv. 6::phenylglycine derivative 1

SMILES CCOc1cc(OCC)cc(c1)C(Nc1ccc(cc1)C(N)=N)C(O)=O

InChI Key InChIKey=UXQFXLBBPPHNHB-UHFFFAOYSA-N

Data  9 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 9 hits for monomerid = 13558   

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

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  190nM ΔG°:  -9.07kcal/molepH: 7.8 T: 22°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 ArticlePubMed
TargetCoagulation factor VII(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  190nM ΔG°:  -9.07kcal/molepH: 7.8 T: 22°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 ArticlePubMed
TargetCoagulation factor VII(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  190nMAssay Description:Inhibition of human factor 7aMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  5.60E+3nMAssay 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 ArticlePubMed
TargetCoagulation factor X(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  5.60E+3nMAssay 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 ArticlePubMed
TargetSerine protease 1(Bovine)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  1.69E+4nMAssay 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 ArticlePubMed
TargetSerine protease 1(Bovine)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi:  1.69E+4nMAssay 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 ArticlePubMed
TargetProthrombin(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi: >3.50E+4nM ΔG°: >-6.01kcal/molepH: 7.8 T: 22°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 ArticlePubMed
TargetProthrombin(Human)
F. Hoffmann-La Roche

LigandPNGBDBM13558(2-[(4-carbamimidoylphenyl)amino]-2-(3,5-diethoxyph...)
Affinity DataKi: >3.50E+4nMAssay 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 ArticlePubMed