null

SMILES CC[C@H](C)[C@H](NC(=O)[C@@H](N)[C@@H](C)O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccccc1)C(O)=O

InChI Key InChIKey=OCUSUKPNXDAERP-NCQKMRCOSA-N

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

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50185629   

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

Curated by ChEMBL
LigandPNGBDBM50185629(CHEMBL277277 | TITYKF)copy SMILEScopy InChI
Affinity DataKi:  1.51E+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
TargetProteasome subunit beta type-6(Saccharomyces cerevisiae)
CNRS-Université Paris VI

Curated by ChEMBL
LigandPNGBDBM50185629(CHEMBL277277 | TITYKF)copy SMILEScopy InChI
Affinity DataKi:  2.60E+5nMAssay Description:Inhibition of post acid activity of yeast 20S proteasome at 625 uMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q280527ZPubMed