BDBM50326042 CHEMBL1240595
SMILES [H][C@@]12CCCN1C(=O)[C@]1([H])CSCC3=CC(CSC[C@]([H])(NC(=O)[C@H](C)N)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC4=CC=CC=C4)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CC(N)=O)C(=O)N1)=CC(CSC[C@H](NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CCSC)NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CNC4=C1C=CC=C4)NC2=O)C(=O)NCC(N)=O)=C3
InChI Key InChIKey=KNJXXDLWQHWAJJ-UHFFFAOYSA-N
Data 1 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50326042
TargetPlasma kallikrein(Human)
Laboratory of Molecular Biology, Medical Research Council
Curated by ChEMBL
Laboratory of Molecular Biology, Medical Research Council
Curated by ChEMBL
Affinity DataIC50: 1.50E+3nMAssay Description:Inhibition of human plasma kallikrein using Z-Phe-Arg-AMC substrate after 30 mins by spectrophotometric assayMore data for this Ligand-Target Pair
