Piperlongumine B and analogs are promising and selective inhibitors for acetylcholinesterase

Eur J Med Chem. 2017 Oct 20:139:222-231. doi: 10.1016/j.ejmech.2017.07.081. Epub 2017 Aug 2.

Abstract

Piperlongumine B (19), an alkaloid previously isolated from long pepper (Piper longum) has been synthesized for the first time in a short sequence and in good yield together with 19 analogs. Screening of these compounds in Ellman's assays showed several of them to be good inhibitors of acetylcholinesterase while being less active for butyrylcholinesterase. Activity of the compounds increased with the ring size of the heterocycle, and a maximum of activity was observed for an analog holding 12 methylene groups in the aliphatic side chain. These compounds may be regarded as promising candidates for the development of efficient inhibitors of acetylcholinesterase being useful for the treatment of Alzheimer's disease.

Keywords: Acetylcholinesterase; Butyrylcholinesterase; Natural product; Piper longum; Piperlongumine B.

MeSH terms

  • Acetylcholinesterase / metabolism*
  • Animals
  • Butyrylcholinesterase / metabolism
  • Cholinesterase Inhibitors / chemical synthesis
  • Cholinesterase Inhibitors / chemistry
  • Cholinesterase Inhibitors / pharmacology*
  • Dioxolanes / chemical synthesis
  • Dioxolanes / chemistry
  • Dioxolanes / pharmacology*
  • Dose-Response Relationship, Drug
  • Electrophorus / metabolism
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Cholinesterase Inhibitors
  • Dioxolanes
  • Acetylcholinesterase
  • Butyrylcholinesterase
  • piperlongumine