Synthesis and Anti-Inflammatory Activities of Phloroglucinol-Based Derivatives

Molecules. 2018 Dec 7;23(12):3232. doi: 10.3390/molecules23123232.

Abstract

The natural product phloroglucinol-based derivatives representing monoacyl-, diacyl-, dimeric acyl-, alkylated monoacyl-, and the nitrogen-containing alkylated monoacylphloro- glucinols were synthesized and evaluated for inhibitory activities against the inflammatory mediators such as inducible nitric oxide synthase (iNOS) and nuclear factor kappaB (NF-κB). The diacylphloroglucinol compound 2 and the alkylated acylphloroglucinol compound 4 inhibited iNOS with IC50 values of 19.0 and 19.5 µM, respectively, and NF-κB with IC50 values of 34.0 and 37.5 µM, respectively. These compounds may serve as leads for the synthesis of more potent anti-inflammatory compounds for future drug discovery.

Keywords: NF-κB; acylphloroglucinol; anti-inflammatory; iNOS; phlorogluciniol.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / chemical synthesis*
  • Anti-Inflammatory Agents / chemistry
  • Anti-Inflammatory Agents / pharmacology*
  • Carbon-13 Magnetic Resonance Spectroscopy
  • Cell Line, Tumor
  • Chlorocebus aethiops
  • Humans
  • Phloroglucinol / chemical synthesis*
  • Phloroglucinol / chemistry
  • Phloroglucinol / pharmacology*
  • Proton Magnetic Resonance Spectroscopy
  • Vero Cells

Substances

  • Anti-Inflammatory Agents
  • Phloroglucinol