Synthesis of 2-(pyridylvinyl)chromen-4-ones and their N-oxide analogs for assessment of their biological activities as anticancer agents

Arch Pharm (Weinheim). 2024 Apr;357(4):e2300445. doi: 10.1002/ardp.202300445. Epub 2024 Jan 16.

Abstract

2-Styrylchromones have been shown to possess a broad spectrum of biological activities. Replacing the carbon atom in 2-styrylchromones with a nitrogen atom in the benzene rings forms 2-(pyridylvinyl)chromen-4-ones (aza-2-styrylchromones). We have synthesized a series of novel 2-(pyridylvinyl)chromen-4-ones and their pyridine N-oxides to evaluate them as potential anticancer agents against human non-small-cell lung cancer cells (A549). Among the 18 synthesized molecules, compounds 18 and 8a exhibited comparable inhibitory effects to 5-fluorouracil and showed no toxicity against normal cells.

Keywords: aza‐2‐styrylchromones; human non‐small‐cell lung cancer cells; pyridine N‐oxides.

MeSH terms

  • Antineoplastic Agents* / pharmacology
  • Carcinoma, Non-Small-Cell Lung*
  • Cell Line, Tumor
  • Drug Screening Assays, Antitumor
  • Fluorouracil
  • Humans
  • Lung Neoplasms*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Fluorouracil