null

SMILES CC(C)c1cc(C(C)C)c(c(c1)C(C)C)S(=O)(=O)N[C@@H](Cc1cccc(c1)C(N)=N)C(=O)N1CCN(CC1)C(=O)C1CCNCC1

InChI Key InChIKey=XKXAXFJNQDWDNX-HKBQPEDESA-N

PDB links: 1 PDB ID contains this monomer as substructures. 1 PDB ID contains inhibitors having a similarity of 90% to this monomer.

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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 8 hits for monomerid = 23886   

TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  100nM ΔG°:  -9.54kcal/molepH: 8.0 T: 2°CAssay Description:The measurements were carried out on a microplate reader. Two concentrations of the substrate and five concentrations of the inhibitor were used. Af...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1V64PubMed
TargetSuppressor of tumorigenicity 14 protein(Homo sapiens (Human))
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  120nMAssay Description:Inhibition of matripase (unknown origin) using Boc-QAR-AMC as substrate incubated for 30 mins prior to substrate addition by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23F4RB4PubMed
TargetUrokinase-type plasminogen activator(Homo sapiens (Human))
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  1.20E+3nMAssay Description:The measurements were carried out on a microplate reader. Two concentrations of the substrate and five concentrations of the inhibitor were used. Af...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1V64PubMed
TargetPlasminogen(Homo sapiens (Human))
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  1.30E+3nMAssay Description:The measurements were carried out on a microplate reader. Two concentrations of the substrate and five concentrations of the inhibitor were used. Af...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1V64PubMed
TargetProthrombin(Bos taurus (Bovine))
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  5.40E+3nMAssay Description:The measurements were carried out on a microplate reader. Two concentrations of the substrate and five concentrations of the inhibitor were used. Af...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1V64PubMed
TargetHepatocyte growth factor activator(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  5.50E+3nMAssay Description:Inhibition of recombinant N-terminal His-tagged HGFA (unknown origin) expressed in baculovirus-infected Sf9 cells using Boc-QLR-AMC as substrate incu...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23F4RB4PubMed
TargetSerine protease hepsin(Homo sapiens (Human))
Washington University School of Medicine

Curated by ChEMBL
LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  7.40E+3nMAssay Description:Inhibition of hepsin (unknown origin) using Boc-QAR-AMC as substrate after 30 mins prior to substrate addition by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23F4RB4PubMed
TargetCoagulation factor X(Bos taurus)
Curacyte Chemistry GmbH

LigandPNGBDBM23886(3-[(2S)-3-oxo-3-[4-(piperidin-4-ylcarbonyl)piperaz...)copy SMILEScopy InChI
Affinity DataKi:  1.70E+4nMAssay Description:The measurements were carried out on a microplate reader. Two concentrations of the substrate and five concentrations of the inhibitor were used. Af...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q21C1V64PubMed