Highly enantioselective catalytic synthesis of neurite growth-promoting secoyohimbanes

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Andrey P. Antonchick - , Max Planck Institute of Molecular Physiology (Autor:in)
  • Sara López-Tosco - , Max Planck Institute of Molecular Physiology (Autor:in)
  • Juan Parga - , Max Planck Institute for Molecular Biomedicine (Autor:in)
  • Sonja Sievers - , Max Planck Institute of Molecular Physiology (Autor:in)
  • Markus Schürmann - , Technische Universität (TU) Dortmund (Autor:in)
  • Hans Preut - , Technische Universität (TU) Dortmund (Autor:in)
  • Susanne Höing - , Max Planck Institute for Molecular Biomedicine (Autor:in)
  • Hans R. Schöler - , Max Planck Institute for Molecular Biomedicine, Westfälische Wilhelms-Universität Münster (Autor:in)
  • Jared Sterneckert - , Max Planck Institute for Molecular Biomedicine (Autor:in)
  • Daniel Rauh - , Technische Universität (TU) Dortmund (Autor:in)
  • Herbert Waldmann - , Max Planck Institute of Molecular Physiology, Technische Universität (TU) Dortmund (Autor:in)

Abstract

Natural products endowed with neuromodulatory activity and their underlying structural scaffolds may inspire the synthesis of novel neurotrophic compound classes. The spirocyclic secoyohimbane alkaloid rhynchophylline is the major component of the extracts of Uncaria species used in Chinese traditional medicine for treatment of disorders of the central nervous system. Based on the structure of rhynchophylline, a highly enantioselective and efficient organocatalyzed synthesis method was developed that gives access to the tetracyclic secoyohimbane scaffold, embodying a quaternary and three tertiary stereogenic centers in a one-pot multistep reaction sequence. Investigation of a collection of the secoyohimbanes in primary rat hippocampal neurons and embryonal stem cell-derived motor neurons led to discovery of compounds that promote neurite outgrowth and influence the complexity of neuronal network formation.

Details

OriginalspracheEnglisch
Seiten (von - bis)500-509
Seitenumfang10
FachzeitschriftChemistry and Biology
Jahrgang20
Ausgabenummer4
PublikationsstatusVeröffentlicht - 18 Apr. 2013
Peer-Review-StatusJa
Extern publiziertJa

Externe IDs

PubMed 23601639
ORCID /0000-0002-7688-3124/work/158767647