Chemoselective Wittig and Michael ligations of unprotected peptidyl phosphoranes in water furnish potent inhibitors of caspase-3

Org Lett. 2014 Sep 5;16(17):4428-31. doi: 10.1021/ol501910x. Epub 2014 Aug 20.

Abstract

Unprotected peptidyl phosphoranes 1 with sequence Ac-L-aspartyl-L-glutamyl-L-valinyl-L-aspartyl are released from polymer support and react with aliphatic and aromatic aldehydes in aqueous medium in a Wittig ligation. Obtained vinyl ketones 6-12 are potent inhibitors of caspase-3. Vinyl ketone 6, derived from formaldehyde, undergoes Michael ligations with thiol nucleophiles furnishing products 14-16, also in aqueous medium. The demonstrated ligation reactions enable the modification of complex functionalized peptides in water providing bioactive protein ligands without side-chain protection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caspase 3 / drug effects*
  • Caspase Inhibitors / chemical synthesis
  • Caspase Inhibitors / chemistry*
  • Caspase Inhibitors / pharmacology*
  • Molecular Structure
  • Oligopeptides / chemical synthesis
  • Oligopeptides / chemistry*
  • Oligopeptides / pharmacology*
  • Phosphoranes / chemical synthesis
  • Phosphoranes / chemistry*
  • Phosphoranes / pharmacology*
  • Water / chemistry

Substances

  • Caspase Inhibitors
  • Oligopeptides
  • Phosphoranes
  • Water
  • Caspase 3