• Media type: E-Article
  • Title: Pyrrolizidine Alkaloids from Echium rauwolfii and Echium horridum (Boraginaceae)
  • Contributor: El-Shazly, Assem; Abdel-All, M.; Tei, Andreas; Wink, Michael
  • imprint: Walter de Gruyter GmbH, 1999
  • Published in: Zeitschrift für Naturforschung C
  • Language: English
  • DOI: 10.1515/znc-1999-5-601
  • ISSN: 1865-7125; 0939-5075
  • Keywords: General Biochemistry, Genetics and Molecular Biology
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title> <jats:p> Echimidine was isolated from Echium rauwolfii and Echium horridum and identified by MS, <jats:sup>1</jats:sup>H-and <jats:sup>13</jats:sup>C NMR as a major alkaloid. In addition, structures of 12 minor alkaloids were inferred from GLC and GLC-MS analyses: 7-angeloylretronecine, 7-tigloylretronecine, lycopsamine, 7-acetyllycopsamine, uplandicine, 7-angeloyllycopsamine, 7-tigloyllycopsamine, tigloyl isomer of echimidine, 7-angeloyl-9-(2-methylbutyryl)retronecine, 7-tigloyl-9-(2-methylbutyryl)retronecine, 7-angeloyl-9-(2,3-dihydroxybutyryl)retronecine, and 7-tigloyl-9-(2,3-dihydroxybutyryl)retronecine. Both species had similar alkaloid profiles. Alkaloid extracts exhibited antibacterial effects with a MIC of 1.7 mg/ml in E. coli. Microscopic examination of E. coli treated with different subtoxic alkaloid concentrations (13-52 μg/ml) revealed extensive filamentation.</jats:p>
  • Access State: Open Access