BDBM50101870 3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo-4-hydroxy-benzoic acid::CHEMBL417020

SMILES NC(=N)c1ccc2[nH]c(c(Cc3ccccc3)c2c1)-c1cc(cc(Br)c1O)C(O)=O

InChI Key InChIKey=VKFGNQCXLCROIA-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50101870   

TargetCoagulation factor X(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101870(3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo...)
Affinity DataKi:  4nMAssay Description:Inhibitory activity against Coagulation factor X in human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101870(3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo...)
Affinity DataKi:  320nMAssay Description:Inhibitory activity against urokinase-type plasminogen activator (microPa) in human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101870(3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo...)
Affinity DataKi:  330nMAssay Description:Inhibitory activity against thrombin(fIIa) in human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101870(3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo...)
Affinity DataKi:  440nMAssay Description:Inhibitory activity against trypsin in human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Axys Pharmaceuticals

Curated by ChEMBL
LigandPNGBDBM50101870(3-(3-Benzyl-5-carbamimidoyl-1H-indol-2-yl)-5-bromo...)
Affinity DataKi:  1.50E+3nMAssay Description:Inhibitory activity against plasmin in human plasmaMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed