Enantioselective synthesis of adamantylalanine and carboranylalanine and their incorporation into the proteasome inhibitor bortezomib

Chem Commun (Camb). 2016 Mar 14;52(21):4064-7. doi: 10.1039/c6cc01156j.

Abstract

The incorporation of adamantylalanine and carboranylalanine at the P2 site of bortezomib is well tolerated and provided potent cell permeable proteasome inhibitors with increased off-rates compared to bortezomib. Adamantylalanine and carboranylalanine were synthesized enantioselectively by an asymmetric Strecker reaction on Ellmans tert-butyl sulfinimines.

MeSH terms

  • Adamantane / chemical synthesis*
  • Adamantane / chemistry
  • Boron Compounds / chemical synthesis*
  • Boron Compounds / chemistry
  • Bortezomib / chemistry*
  • Bortezomib / pharmacology*
  • Cell Line, Tumor
  • Humans
  • Phenylalanine / analogs & derivatives*
  • Phenylalanine / chemical synthesis
  • Phenylalanine / chemistry
  • Proteasome Endopeptidase Complex / chemistry*
  • Proteasome Endopeptidase Complex / metabolism
  • Proteasome Inhibitors / chemistry*
  • Proteasome Inhibitors / pharmacology*
  • Stereoisomerism
  • Sulfonium Compounds / chemistry

Substances

  • Boron Compounds
  • Proteasome Inhibitors
  • Sulfonium Compounds
  • Phenylalanine
  • carboranylalanine
  • Bortezomib
  • Proteasome Endopeptidase Complex
  • Adamantane