BDBM50326028 CHEMBL1240611

SMILES CC[C@H](C)[C@@H]1NC(=O)[C@H](CSCc2cc3CSC[C@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](Cc4c[nH]c5ccccc45)NC(=O)[C@H](Cc4c[nH]c5ccccc45)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc4cnc[nH]4)NC(=O)[C@H](CSCc(c3)c2)NC(=O)[C@H](Cc2ccccc2)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](Cc2ccccc2)NC1=O)C(=O)NCC(N)=O)NC(=O)[C@H](C)N

InChI Key InChIKey=YIARGVACRGPTFL-UHFFFAOYSA-N

Data  1 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50326028   

TargetCathepsin G(Human)
Laboratory of Molecular Biology, Medical Research Council

Curated by ChEMBL
LigandPNGBDBM50326028(CHEMBL1240611)
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
In Depth
Date in BDB:
6/10/2011
Entry Details Article
PubMed