Skeleton Synthesis of a Plant-Derived Radioprotective Alkaloid Born to Produce a Novel Fused Heterocycle

Molecules. 2023 Apr 30;28(9):3829. doi: 10.3390/molecules28093829.

Abstract

Alkaloids are a material treasure bestowed on humans by nature owing to their numerous biological activities. Orychophragine D, an alkaloid isolated from the seeds of Orychophragmus violaceus was identified as bearing a novel skeleton and proved to have an excellent radioprotective effect. Different from the common alkaloid structure, the main block of orychophragine D is constructed of an oxotriazine and an oxopiperazine, which are connected in parallel by a C-N bond. In this paper, a preparation method for the novel heterocycle skeleton of orychophragine D is proposed for the first time. N-Boc-L-serine was utilized as the original material to complete the preparation with 11 steps in a 13% overall yield. A hydroxyl group was established on the side chain of the skeleton as the reaction site for researchers to conduct further structural modification or derivatization.

Keywords: alkaloid; chemical synthesis; novel molecular skeleton; orychophragine D.

MeSH terms

  • Alkaloids* / chemistry
  • Alkaloids* / pharmacology
  • Antineoplastic Agents*
  • Binding Sites
  • Humans
  • Molecular Structure
  • Skeleton

Substances

  • Alkaloids
  • Antineoplastic Agents