N-Alkylphthalimides: structural requirement of thalidomidal action on 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor alpha production by human leukemia HL-60 cells

Chem Pharm Bull (Tokyo). 1995 Jan;43(1):177-9. doi: 10.1248/cpb.43.177.

Abstract

Phthalimide analogs N-substituted with n-butyl, tert-butyl, hexyl and adamantyl groups were designed and prepared as simplified analogs of thalidomide and methylthalidomide. All the compounds prepared except N-n-butylphthalimide showed thalidomidal activity on 12-O-tetradecanoylphorbol-13-acetate-induced tumor necrosis factor (TNF)-alpha production by human leukemia HL-60 cells. Among the investigated compounds, including thalidomide and methylthalidomide, N-adamantylphthalimide showed the most potent TNF-alpha production-enhancing activity.

MeSH terms

  • Humans
  • Leukemia / metabolism
  • Leukemia / pathology
  • Phthalimides / chemistry
  • Phthalimides / pharmacology*
  • Tetradecanoylphorbol Acetate / pharmacology*
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Phthalimides
  • Tumor Necrosis Factor-alpha
  • Tetradecanoylphorbol Acetate