(±)-Yanhusuomide A, a pair of ornithine-fused benzylisoquinoline enantiomers from Corydalis yanhusuo

Bioorg Chem. 2023 Apr:133:106407. doi: 10.1016/j.bioorg.2023.106407. Epub 2023 Feb 4.

Abstract

(±)-Yanhusuomide A (1), a novel enantiomeric pair of ornithine-fused benzylisoquinoline, were characterized from the dried tubers of Corydalis yanhusuo, along with a biogenetically related intermediate oblongine (2). Yanhusuomide A features an unprecedented skeleton based on a benzylisoquinoline coupled with an ornithine derivative to form a rare 5,6-dihydro-4H-pyrido[3,4,5-de]quinazoline motif. Plausible biosynthetic pathway of 1 was proposed, and (±)-yanhusuomide A (1) presented potential inhibitory bioactivity against acetylcholinesterase (AChE) with IC50 = 14.07 ± 2.38 μM. The simulation of molecular docking displayed that 1 generated strong interaction with Asp-74 and Trp-86 residues of AChE through attractive charge of the quaternary nitrogen.

Keywords: (±)-Yanhusuomide A; Acetylcholinesterase inhibitor; Corydalis yanhusuo; Ornithine-fused benzylisoquinoline.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase
  • Benzylisoquinolines* / chemistry
  • Corydalis* / chemistry
  • Molecular Docking Simulation
  • Plant Tubers / chemistry

Substances

  • Acetylcholinesterase
  • Benzylisoquinolines