null

SMILES CC(C)C[C@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](N)[C@@H](C)O)C(C)C)[C@@H](C)O)C(O)=O

InChI Key InChIKey=GZCWUHWQDMPLIJ-YSRZENEASA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50185636   

TargetProteasome subunit beta type-5(Saccharomyces cerevisiae)
CNRS-Université Paris VI

Curated by ChEMBL
LigandPNGBDBM50185636(CHEMBL210501 | TVTYKL)copy SMILEScopy InChI
Affinity DataKi:  5.45E+5nMAssay Description:Inhibition of chymotrypsin like activity of yeast 20S proteasomeMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280527ZPubMed