null

SMILES C[C@H](NC(=O)[C@@H](CO)NS(=O)(=O)Cc1ccc(cc1)C#N)C(=O)NCc1ccc(cc1)C(N)=N

InChI Key InChIKey=UMTXMVBYSMIVTH-IFXJQAMLSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 4 hits for monomerid = 98585   

TargetUrokinase plasminogen activator surface receptor(Rattus norvegicus)
The Medicines Company

US Patent
LigandPNGBDBM98585((2R)-N-[(1S)-2-[(4-carbamimidoylphenyl)methylamino...)copy SMILEScopy InChI
Affinity DataKi:  89nM ΔG°:  -9.58kcal/moleT: 2°CAssay Description:Inhibition constant of the compound against Plasminogen activator urokinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2154FPHUS Patent
TargetSerine protease 1(Rattus norvegicus)
The Medicines Company

US Patent
LigandPNGBDBM98585((2R)-N-[(1S)-2-[(4-carbamimidoylphenyl)methylamino...)copy SMILEScopy InChI
Affinity DataKi:  340nM ΔG°:  -8.79kcal/moleT: 2°CAssay Description:Inhibition constant of the compound against TrypsinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2154FPHUS Patent
TargetProthrombin(Rattus norvegicus)
The Medicines Company

US Patent
LigandPNGBDBM98585((2R)-N-[(1S)-2-[(4-carbamimidoylphenyl)methylamino...)copy SMILEScopy InChI
Affinity DataKi:  8.50E+3nM ΔG°:  -6.89kcal/moleT: 2°CAssay Description:Inhibition constant of the compound against ThrombinMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2154FPHUS Patent
TargetPlasminogen(Rattus norvegicus)
The Medicines Company

US Patent
LigandPNGBDBM98585((2R)-N-[(1S)-2-[(4-carbamimidoylphenyl)methylamino...)copy SMILEScopy InChI
Affinity DataKi:  2.70E+4nM ΔG°:  -6.21kcal/moleT: 2°CAssay Description:Inhibition constant of the compound against PlasminMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2154FPHUS Patent