BDBM50115867 2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5-carboxamidine::CHEMBL62370

SMILES NC(=N)c1ccc2nc([nH]c2c1)-c1cccc(Oc2ccccc2)c1O

InChI Key InChIKey=FKTVUGSKIYLIGS-UHFFFAOYSA-N

Data  5 KI

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 5 hits for monomerid = 50115867   

TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115867(2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5...)
Affinity DataKi:  400nMAssay Description:Inhibition of urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115867(2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5...)
Affinity DataKi:  1.00E+3nMAssay Description:Inhibition of tissue-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115867(2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5...)
Affinity DataKi:  2.10E+3nMAssay Description:Inhibition of Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115867(2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5...)
Affinity DataKi:  5.00E+3nMAssay Description:Inhibition of plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115867(2-(2-Hydroxy-3-phenoxy-phenyl)-1H-benzoimidazole-5...)
Affinity DataKi:  1.50E+4nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed