BDBM50110009 3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcarbamoyl]-methyl}-2-phenylmethanesulfonylamino-propionamide::CHEMBL157479

SMILES OC[C@@H](NS(=O)(=O)Cc1ccccc1)C(=O)NCC(=O)NCc1ccc(cc1)C(=N)NO

InChI Key InChIKey=YVPCSDBGVOOVDK-QGZVFWFLSA-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 = 50110009   

TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110009(3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcar...)
Affinity DataKi:  6.10E+4nMAssay Description:In vitro inhibition of plasminogen activator urokinase.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110009(3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcar...)
Affinity DataKi: >1.00E+6nMAssay Description:In vitro inhibition of Plasmin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetSerine protease 1(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110009(3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcar...)
Affinity DataKi: >1.00E+6nMAssay Description:In vitro inhibition of trypsin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCoagulation factor X(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110009(3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcar...)
Affinity DataKi: >1.00E+6nMAssay Description:In vitro inhibition of Coagulation factor Xa.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProthrombin(Homo sapiens (Human))
Universitat Jena

Curated by ChEMBL
LigandPNGBDBM50110009(3-Hydroxy-N-{[4-(N-hydroxycarbamimidoyl)-benzylcar...)
Affinity DataKi: >1.00E+6nMAssay Description:In vitro inhibition of thrombin.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed