Compile Data Set for Download or QSAR
Report error Found 4 Enz. Inhib. hit(s) with all data for entry = 50014508
TargetLegumain(Human)
School of Chemistry and Biochemistry and The Parker H. Petit Institute For Bioengineering and Bioscience

Curated by ChEMBL
LigandPNGBDBM50143613((E)-3-{(S)-N'-[(S)-2-((S)-2-Benzyloxycarbonylamino...)
Affinity DataIC50: 31nMAssay Description:Inhibitory concentration was evaluated for Irreversible Inhibition of Schistosoma mansoni LegumainMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetLegumain(Human)
School of Chemistry and Biochemistry and The Parker H. Petit Institute For Bioengineering and Bioscience

Curated by ChEMBL
LigandPNGBDBM50143614((E)-3-{(S)-N'-[(S)-2-((S)-2-Benzyloxycarbonylamino...)
Affinity DataIC50: 38nMAssay Description:Inhibitory concentration was evaluated for Irreversible Inhibition of Schistosoma mansoni LegumainMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetLegumain(Human)
School of Chemistry and Biochemistry and The Parker H. Petit Institute For Bioengineering and Bioscience

Curated by ChEMBL
LigandPNGBDBM50143612((S)-N'-[(S)-2-((S)-2-Benzyloxycarbonylamino-propio...)
Affinity DataIC50: 55nMAssay Description:Inhibitory concentration was evaluated for Irreversible Inhibition of Schistosoma mansoni LegumainMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetLegumain(Human)
School of Chemistry and Biochemistry and The Parker H. Petit Institute For Bioengineering and Bioscience

Curated by ChEMBL
LigandPNGBDBM50292159((S)-N'-[(S)-2-((S)-2-Benzyloxycarbonylamino-propio...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration was evaluated for irreversible inhibition of Schistosoma mansoni LegumainMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed