Isolation and Structure Elucidation of Additional Alkaloids from the Tropical Rainforest Tree Galbulimima baccata

J Nat Prod. 2021 Sep 24;84(9):2525-2535. doi: 10.1021/acs.jnatprod.1c00537. Epub 2021 Sep 7.

Abstract

The structures of five new natural products (GB 27-GB 31, 1-5), isolated as minor components from the bark of Galbulimima baccata, have been determined by 2D NMR spectroscopy in combination with DFT calculations. Among the alkaloids, GB 31 (5) belongs to Class I, GB 27 (1) and 28 (2) belong to Class II, and GB 30 (4) belongs to Class III GB alkaloids. GB 31 is the first non-nitrogen-containing GB "alkaloid", being a biosynthetic oxidation product of himbacine, himandravine, or himbeline. GB 29 (3) has an entirely new natural product scaffold but belongs to Class IV (miscellaneous alkaloids). The isolation of a new Galbulimima scaffold has revealed a new pathway in the biosynthesis of the GB alkaloids. The new molecules isolated have shed further light on the biogenetic relationship among these structurally unique and complex groups of alkaloids. We present, for the first time, a unified biogenesis for the GB alkaloids that were first isolated in the 1950s and now number over 40 examples. This work also brings full circle the story of Galbulimima alkaloids. A life-long project of Wal Taylor involving one of his first students (Lew Mander) and one of his last students (Peter Karuso), a story stretching over six decades, has come to a final conclusion.

MeSH terms

  • Alkaloids / chemistry*
  • Alkaloids / isolation & purification
  • Furans
  • Magnoliopsida / chemistry*
  • Molecular Structure
  • Naphthalenes
  • Papua New Guinea
  • Phytochemicals / chemistry
  • Phytochemicals / isolation & purification
  • Piperidines
  • Rainforest
  • Trees / chemistry

Substances

  • Alkaloids
  • Furans
  • Naphthalenes
  • Phytochemicals
  • Piperidines
  • himandravine
  • himbacine