[Stereospecific hydroxylation of (+)-sparteine (pachycarpine) in the rat]

Arch Pharm (Weinheim). 1989 Jul;322(7):399-403. doi: 10.1002/ardp.19893220704.
[Article in German]

Abstract

Pachycarpine (4), the optical antipode of the lupine alkaloid (-)-sparteine (1), has been prepared from (-)-lupanine; its metabolism was studied in rats. After isolation and chromatographic purification, streochemically homogeneous (+)-(4S)-hydroxysparteine (7) was identified as the major urinary metabolite by use of mass spectrometry and high-field NMR-spectroscopy.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Hydroxylation
  • Male
  • Rats
  • Rats, Inbred Strains
  • Sparteine / metabolism*
  • Stereoisomerism

Substances

  • Sparteine