The effect and mechanism of novel methoxy curcumin analogs based on network pharmacology

Medicine (Baltimore). 2024 Feb 16;103(7):e36483. doi: 10.1097/MD.0000000000036483.

Abstract

In this study, a series of novel compounds were synthesized by introducing the 3,4,5-trimethoxyphenyl and isatin groups into the monocarbonyl skeleton of curcumin. The possible biological activities and potential targets for these compounds were explored through network pharmacology. The results revealed that these compounds could significantly inhibit production of the inflammatory factors IL-6 and TNF-α, and suppress phosphorylation of the extracellular signal-regulated kinase (ERK) protein. Moreover, molecular docking experiments showed that the ERK protein was the potential target for these compounds. In summary, this study, through network pharmacology, presents a novel series of methoxy curcumin analogs as potent anti-inflammatory drugs.

MeSH terms

  • Anti-Inflammatory Agents / pharmacology
  • Curcumin* / pharmacology
  • Drugs, Chinese Herbal*
  • Humans
  • Molecular Docking Simulation
  • Network Pharmacology
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Curcumin
  • Anti-Inflammatory Agents
  • Tumor Necrosis Factor-alpha
  • Drugs, Chinese Herbal