Alkaloids with acetylcholinesterase inhibitory activity from Corydalis racemosa (Thunb.) Pers

Nat Prod Res. 2021 Nov;35(22):4272-4278. doi: 10.1080/14786419.2019.1696796. Epub 2019 Dec 7.

Abstract

Two new isoquinoline alkaloids (1 and 2) along with fourteen known alkaloids (3-16) were isolated from Corydalis racemosa (Thunb.) Pers. Their structures were elucidated by analyzing spectroscopic and spectrometric data (NMR, UV, IR, and MS) and comparing their spectroscopic, spectrometric and physicochemical data with the values archived in the literature. The absolute configurations of new compounds were determined via X-ray crystallographic assay and electronic circular dichroism calculations. Acetylcholinesterase (AChE) inhibitory activity of all compounds was evaluated. Compounds 5, 6, 9, 11, and 12 exhibited inhibitory activity against AChE with IC50 values ranged from 10.2 to 63.4 μM.

Keywords: Corydalis racemosa; acetylcholinesterase inhibitory activity; isoquinoline alkaloids.

MeSH terms

  • Acetylcholinesterase
  • Alkaloids* / pharmacology
  • Cholinesterase Inhibitors / pharmacology
  • Circular Dichroism
  • Corydalis*
  • Molecular Structure

Substances

  • Alkaloids
  • Cholinesterase Inhibitors
  • Acetylcholinesterase