Discovery of Novel 2-(piperidin-4-yl)-1H-benzo[d]imidazole Derivatives as Potential Anti-Inflammatory Agents

Chem Biol Drug Des. 2015 Oct;86(4):509-16. doi: 10.1111/cbdd.12513. Epub 2015 Mar 16.

Abstract

A novel 2-(piperidin-4-yl)-1H-benzo[d]imidazole derivative 5 with good anti-inflammatory activity was identified from our in-house library. Based on hit compound 5, two series of 2-(piperidin-4-yl)-1H-benzo[d]imidazole derivative 6a-g and 7a-h were designed and synthesized as novel anti-inflammatory agents. Most of synthesized compounds exhibited good inhibitory activity on NO and TNF-α production in LPS-stimulated RAW 264.7 macrophages, in which the compound 6e showed most potent inhibitory activity on NO (IC50 = 0.86 μm) and TNF-α (IC50 = 1.87 μm) production. Further evaluation revealed that compound 6e displayed more potent in vivo anti-inflammatory activity than ibuprofen did on xylene-induced ear oedema in mice. Additionally, Western blot analysis revealed that compound 6e could restore phosphorylation level of IκBα and protein expression of p65 NF-κB in LPS-stimulated RAW 264.7 macrophages.

Keywords: 2-(piperidin-4-yl)-1H-benzo[d]imidazole derivatives; anti-inflammatory activity; benzimidazole; inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal* / chemistry
  • Anti-Inflammatory Agents, Non-Steroidal* / pharmacology
  • Cell Line
  • Drug Discovery*
  • Edema / chemically induced
  • Edema / drug therapy*
  • Edema / metabolism
  • Edema / pathology
  • Imidazoles* / chemistry
  • Imidazoles* / pharmacology
  • Lipopolysaccharides / toxicity
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Mice
  • Transcription Factor RelA / metabolism
  • Tumor Necrosis Factor-alpha / metabolism
  • Xylenes / toxicity

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Imidazoles
  • Lipopolysaccharides
  • Rela protein, mouse
  • Transcription Factor RelA
  • Tumor Necrosis Factor-alpha
  • Xylenes