BDBM14863 ({3-[3-(5-carbamimidoyl-1H-1,3-benzodiazol-2-yl)-2-hydroxyphenyl]-4-hydroxyphenyl}methyl)urea::5-amidinobenzimidazole analog 1::CHEMBL378916
SMILES NC(=O)NCc1ccc(O)c(c1)-c1cccc(-c2nc3ccc(cc3[nH]2)C(N)=N)c1O
InChI Key InChIKey=AEOYTBFWYXDAMX-UHFFFAOYSA-N
Data 8 KI
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 8 hits for monomerid = 14863
Affinity DataKi: 13nM ΔG°: -10.6kcal/molepH: 7.4 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
Affinity DataKi: 13nMAssay Description:Binding affinity to f7a/TF complexMore data for this Ligand-Target Pair
Affinity DataKi: 2.70E+3nM ΔG°: -7.52kcal/molepH: 7.4 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
Affinity DataKi: 2.70E+3nMAssay Description:Binding affinity to f10aMore data for this Ligand-Target Pair
Affinity DataKi: 3.60E+3nM ΔG°: -7.35kcal/molepH: 7.4 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
Affinity DataKi: 9.00E+4nM ΔG°: -5.46kcal/molepH: 7.4 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
Affinity DataKi: 9.00E+4nMAssay Description:Binding affinity to thrombinMore data for this Ligand-Target Pair