Novel 2-phenyl-4H-chromen derivatives: synthesis and anti-inflammatory activity evaluation in vitro and in vivo

J Enzyme Inhib Med Chem. 2022 Dec;37(1):2589-2597. doi: 10.1080/14756366.2022.2124983.

Abstract

It is significant to design, synthesise and optimise flavonoid derivatives with better anti-inflammatory activity. This study aims to design and synthesise a series of novel 2-phenyl-4H-chromen-4-one compounds with anti-inflammatory; among them, compound 8 was discovered as the best one. And then, the effects of compound 8 on the TLR4/MAPK signalling pathway was carried out in vivo, the results indicated that compound 8 could downregulate NO, IL-6, and TNF-α expression, and suppress LPS-induced inflammation by inhibiting the TLR4/MAPK pathways. Furthermore, compound 8 reduced inflammation by a mouse model of LPS-induced inflammatory disease in vivo. The results suggest that compound 8 has the potential against inflammation through regulating TLR4/MAPK pathway and can be assessed further for drug development.

Keywords: 2-Phenyl-4H-chromen-4-one derivatives; TLR4/MAPK pathway; anti-inflammatory.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / pharmacology
  • Anti-Inflammatory Agents / therapeutic use
  • Flavonoids
  • Inflammation / chemically induced
  • Inflammation / drug therapy
  • Interleukin-6
  • Lipopolysaccharides* / pharmacology
  • Mice
  • Toll-Like Receptor 4 / metabolism
  • Toll-Like Receptor 4 / therapeutic use
  • Tumor Necrosis Factor-alpha*

Substances

  • Anti-Inflammatory Agents
  • Flavonoids
  • Interleukin-6
  • Lipopolysaccharides
  • Toll-Like Receptor 4
  • Tumor Necrosis Factor-alpha

Grants and funding

The study was supported by the National Natural Science Foundation of China [21977001].