Design, synthesis, and cytotoxic activity of pyridine-based stilbenes

Nat Prod Res. 2024 Jun;38(11):1961-1966. doi: 10.1080/14786419.2023.2227991. Epub 2023 Jun 29.

Abstract

In the present study, three series of 35 pyridine-based stilbenes include 10 new compounds prepared by Horner-Wadsworth-Emmons (HWE) reaction were assayed for cytotoxic activities toward two tumoral cell lines (K562 and MDA-MB-231) and one non-tumoral cell line (L-02). The bioassay results indicated that hybrid stilbenes formed at the C-3 position of pyridine displayed stronger antiproliferative activities against K562 cells and C-4 pyridine-based stilbenes showed broad-spectrum cytotoxic effects. Among them, C-3 pyridine-based stilbene PS2g bearing 2,6-dimethoxy possessed extremely potent antiproliferative activity with IC50 values 1.46 µM against K562 cells, along with excellent selectivity towards normal L-02 cells. In summary, the present study contributes to the development of natural stilbene-based derivatives as antitumor agents and PS2g may serve as a promising lead for the treatment of chronic myeloid leukemia (CML) worthy further investigation.

Keywords: CML; Pyridine-based stilbene; cytotoxicity.

MeSH terms

  • Antineoplastic Agents* / chemical synthesis
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Cell Line, Tumor
  • Cell Proliferation* / drug effects
  • Drug Design
  • Drug Screening Assays, Antitumor
  • Humans
  • K562 Cells
  • Molecular Structure
  • Pyridines* / chemistry
  • Pyridines* / pharmacology
  • Stilbenes* / chemical synthesis
  • Stilbenes* / chemistry
  • Stilbenes* / pharmacology
  • Structure-Activity Relationship

Substances

  • Stilbenes
  • Pyridines
  • Antineoplastic Agents