Tumor necrosis factor-alpha production-inhibiting activity of phthalimide analogues on human leukemia THP-1 cells and a structure-activity relationship study

Bioorg Med Chem. 1997 Nov;5(11):2095-102. doi: 10.1016/s0968-0896(97)00148-x.

Abstract

N-Substituted phthalimides (2-substituted 1H-isoindole-1,3-diones) were prepared and their inhibitory effects on tumor necrosis factor-alpha (TNF-alpha) production by human leukemia cell line THP-1 stimulated with 12-O-tetradecanoylphorbol 13-acetate (TPA) or okadaic acid (OA) were examined. A structure-activity relationship study of these phthalimide analogues revealed that their inhibitory effects on TPA- and OA-induced TNF-alpha production by THP-1 cells are well correlated to each other, i.e. they may involve the same target molecule(s). An analysis by the use of phthalimide analogue-immobilized affinity gels indicated the existence of several phthalimide-binding proteins in THP-1 cell extract.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Drug Screening Assays, Antitumor
  • Humans
  • Leukemia, Monocytic, Acute / metabolism*
  • Okadaic Acid / pharmacology
  • Phthalimides / chemical synthesis
  • Phthalimides / pharmacology*
  • Structure-Activity Relationship
  • Tetradecanoylphorbol Acetate / pharmacology
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors*
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Phthalimides
  • Tumor Necrosis Factor-alpha
  • Okadaic Acid
  • Tetradecanoylphorbol Acetate