Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Duncan Allardyce"'
Publikováno v:
RSC Medicinal Chemistry. 14:573-582
A new class of competitive proteasome inhibitors was identified from screening of the ZINC library of natural products. Structure–activity studies highlighted the importance of hydrophobic interactions in enhanced binding affinity.
Publikováno v:
Chemical Biology & Drug Design.
Inhibitors of the proteasome have found broad therapeutic applications; however, they show severe toxicity due to the abundance of proteasomes in healthy cells. In contrast, inhibitors of the immunoproteasome, which is upregulated during disease stat