Biosynthetic studies on the tropane ring system of the tropane alkaloids from Datura stramonium

R Duran-Patron, David O'Hagan, JG Hamilton, CW Wong

Research output: Other contribution

Abstract

Isotopic labelling experiments have been carried out in Dautura stramonium root cultures with the Following isotopically labelled precursors; [H-2(3)]-, [2-C-13, H-2(3)], [1-C-13, O-18(2)]-acetates, 2H(2)O, [H-2(3)-methyl]-methionine, [2-C-13]-phenyllacetate, [3-H-3]-tropine and [2'-C-13, 3-H-2]-littorine. The study explored the incorporation of isotope into the tropane ring system of littorine 1 and hyoscyamine 2 and revealed that deuterium from acetate is incorporated only into C-6 and C-7, and not into C-2 and C-4 as previously reported. Oxygen-18 was not retained at a detectable level into the C(3)-O bond from [1-C-13, O-18(2)]-acetate. The intramolecular nature of the rearrangement of littorine 1 to hyoscyamine 2 is revealed again by a labelling study using [2'-C-13, 3-H-2]-littorine, [2-C-13]-phenyllactate and [3-H-2]-tropine. (C) 2000 Elsevier Science Ltd. All rights reserved.

Original languageEnglish
Volume53
Publication statusPublished - Apr 2000

Keywords

  • Datura stramonium
  • biosynthesis
  • tropane alkaloids
  • hyoscyamine
  • littorine
  • TROPIC ACID
  • HYOSCYAMUS-ALBUS
  • ROOT CULTURES
  • OXYGEN-ATOMS
  • REARRANGEMENT
  • INTERMEDIATE
  • ORIGIN

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