Towards immunoproteasome-specific inhibitors: An improved synthesis of dihydroeponemycin

Abby Ho, Kedra Cyrus, Kyung Bo Kim

Research output: Contribution to journalArticlepeer-review

15 Scopus citations

Abstract

Eponemycin, an antitumor and antiangiogenic epoxy ketone natural product, is previously shown to target proteasome for its activity. Although there have been many synthetic approaches developed, practical and efficient synthetic strategy for eponemycin has yet to be accomplished. Here, we report an efficient new route for the preparation of dihydroeponemycin, an active eponemycin derivative. This will aid the design of proteasome inhibitors with novel activity.

Original languageEnglish
Pages (from-to)4829-4834
Number of pages6
JournalEuropean Journal of Organic Chemistry
Issue number22
DOIs
StatePublished - Nov 11 2005

Keywords

  • Baylis-Hillman reaction
  • Dihydroeponemycin
  • Immunoproteasome
  • Phosphonate
  • Wittig-Horner reaction

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

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