BDBM50115870 2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-carboxamidine::CHEMBL64838

SMILES CCOc1cccc(-c2nc3ccc(cc3[nH]2)C(N)=N)c1O

InChI Key InChIKey=LNZOGIFQFBYRHJ-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 = 50115870   

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

Curated by ChEMBL
LigandPNGBDBM50115870(2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-...)
Affinity DataKi:  700nMAssay Description:Inhibition of urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115870(2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-...)
Affinity DataKi:  1.60E+3nMAssay Description:Inhibition of plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTissue-type plasminogen activator(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115870(2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-...)
Affinity DataKi:  3.20E+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
LigandPNGBDBM50115870(2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-...)
Affinity DataKi:  6.80E+3nMAssay Description:Inhibition of Coagulation factor XMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Celera

Curated by ChEMBL
LigandPNGBDBM50115870(2-(3-Ethoxy-2-hydroxy-phenyl)-1H-benzoimidazole-5-...)
Affinity DataKi:  3.10E+4nMAssay Description:Inhibition of thrombinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed