• Media type: E-Article
  • Title: Isolation, Structure, Synthesis and Cytotoxicity of an Unprecedented Flupirtine Dimer
  • Contributor: Csuk, René; Sommerwerk, Sven; Wiese, Jana; Wagner, Christoph; Siewert, Bianka; Kluge, Ralph; Ströhl, Dieter
  • imprint: Walter de Gruyter GmbH, 2012
  • Published in: Zeitschrift für Naturforschung B
  • Language: English
  • DOI: 10.5560/znb.2012-0258
  • ISSN: 1865-7117; 0932-0776
  • Keywords: General Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:p>A previously unknown dimer of the well-established analgesic flupirtine has been found, and its structure was revealed by ESI-MS, NMR spectroscopy and an independent synthesis. Thus, starting from 2-amino-6-chloro-3-nitro-pyridine the target compound was obtained in a four-step synthesis. Key-step of this synthesis is a nickel-mediated aryl-aryl coupling. The dimer 4 did not show any cytotoxicity, and its IC<jats:sub>50</jats:sub> values were &gt; 30 μm for all six human cancer cell lines and mouse fibroblasts used in this study</jats:p>
  • Access State: Open Access