BDBM50326029 CHEMBL1240609
SMILES CC(C)[C@@H]1NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc2ccc(O)cc2)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CSCc2cc3CSC[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](Cc4ccccc4)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc4c[nH]c5ccccc45)NC(=O)[C@H](CSCc(c3)c2)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC1=O)C(=O)NCC(N)=O)NC(=O)[C@H](C)N
InChI Key InChIKey=IRHKZLUEFHIQGW-MBJFVKNHSA-N
Data 1 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 1 hit for monomerid = 50326029
TargetCathepsin G(Homo sapiens (Human))
Laboratory Of Molecular Biology, Medical Research Council
Curated by ChEMBL
Laboratory Of Molecular Biology, Medical Research Council
Curated by ChEMBL
Affinity DataIC50: 100nMAssay Description:Inhibition of human cathepsin G using N-Suc-Ala-Ala-Phe-Pro-pNA substrate by calorimetric assayMore data for this Ligand-Target Pair