Highly enantioselective catalytic synthesis of neurite growth-promoting secoyohimbanes

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Andrey P. Antonchick - , Max Planck Institute of Molecular Physiology (Author)
  • Sara López-Tosco - , Max Planck Institute of Molecular Physiology (Author)
  • Juan Parga - , Max Planck Institute for Molecular Biomedicine (Author)
  • Sonja Sievers - , Max Planck Institute of Molecular Physiology (Author)
  • Markus Schürmann - , Dortmund University of Technology (Author)
  • Hans Preut - , Dortmund University of Technology (Author)
  • Susanne Höing - , Max Planck Institute for Molecular Biomedicine (Author)
  • Hans R. Schöler - , Max Planck Institute for Molecular Biomedicine, University of Münster (Author)
  • Jared Sterneckert - , Max Planck Institute for Molecular Biomedicine (Author)
  • Daniel Rauh - , Dortmund University of Technology (Author)
  • Herbert Waldmann - , Max Planck Institute of Molecular Physiology, Dortmund University of Technology (Author)

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

Original languageEnglish
Pages (from-to)500-509
Number of pages10
JournalChemistry and Biology
Volume20
Issue number4
Publication statusPublished - 18 Apr 2013
Peer-reviewedYes
Externally publishedYes

External IDs

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