null

SMILES C[C@H](NC(=O)[C@@H](CO)NC(=O)OCc1ccccc1)C(=O)NC(CCCNC(N)=N)P(=O)(Oc1ccccc1)Oc1ccccc1

InChI Key InChIKey=NVXNLVNWFQMECM-FYFZKTLJSA-N

  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 8 hits for monomerid = 50145688   

TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibitory activity of the compound was tested against Urokinase-type plasminogen activatorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348JTBPubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 1.08E+4nMAssay Description:Inhibitory activity of the compound was tested against plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348JTBPubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibitory activity of the compound was tested against thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348JTBPubMed
TargetCoagulation factor X(Bos taurus)
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibition of bovine F10aMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetProthrombin(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetPlasminogen(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 1.08E+4nMAssay Description:Inhibition of human plasminMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 61nMAssay Description:Inhibition of human uPAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VT3PubMed
TargetCoagulation factor X(Homo sapiens (Human))
University of Antwerp

Curated by ChEMBL
LigandPNGBDBM50145688(CHEMBL311067 | benzyl (R)-1-((S)-1-(1-(diphenoxyph...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibitory activity of the compound was tested against Coagulation factor XaMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2348JTBPubMed