BDBM17280 1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluoro-6-[3-(1-methyl-4,5-dihydro-1H-imidazol-2-yl)phenoxy]pyridin-4-yl]piperidine-3-carboxylic acid::Pyridine template, V

SMILES CN1CCN=C1c1cccc(Oc2nc(Oc3cc(ccc3O)C(N)=N)c(F)c(N3CCCC(C3)C(O)=O)c2F)c1

InChI Key InChIKey=NRCRZGGGYMSXER-UHFFFAOYSA-N

Data  4 KI

PDB links: 1 PDB ID matches this monomer.

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 17280   

TargetCoagulation factor X(Human)
Berlex

LigandPNGBDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  0.110nM ΔG°:  -13.4kcal/molepH: 7.5 T: 22°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Human)
Berlex

LigandPNGBDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  0.110nM ΔG°:  -13.4kcal/molepH: 7.5 T: 22°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Bovine)
Berlex

LigandPNGBDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  170nM ΔG°:  -9.14kcal/molepH: 7.5 T: 22°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair
TargetSerine protease 1(Bovine)
Berlex

LigandPNGBDBM17280(1-[2-(5-carbamimidoyl-2-hydroxyphenoxy)-3,5-difluo...)
Affinity DataKi:  170nM ΔG°:  -9.14kcal/molepH: 7.5 T: 22°CAssay Description:The enzyme activities were determined kinetically as the initial rate of cleavage of a peptide p-nitroanilide. Km for enzyme and substrate was determ...More data for this Ligand-Target Pair