Structure-activity studies of trichothecenes: cytotoxicity of analogues and reaction products derived from T-2 toxin and neosolaniol

J Med Chem. 1989 Mar;32(3):555-62. doi: 10.1021/jm00123a008.

Abstract

Forty-two analogues and reaction products derived from T-2 toxin or neosolaniol were assayed for their cytotoxicity to cultured mouse lymphoma cells. Structure-activity relationships confirmed the stereospecific nature of the cytotoxic action of T-2. Cytotoxicity was particularly susceptible to changes at C3, C4, C9, and C10 but was relatively unaffected by changes at C8, which appears to represent a region of steric tolerance in the interaction of T-2 with a cellular constituent. The most potent compounds were T-2, diacetoxyscirpenol, and a series of C8 ester analogues 11 and 31-35.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemical synthesis*
  • Antineoplastic Agents / therapeutic use
  • Chemical Phenomena
  • Chemistry
  • Drug Screening Assays, Antitumor
  • Lymphoma / drug therapy
  • Mice
  • Sesquiterpenes / chemical synthesis*
  • Structure-Activity Relationship
  • T-2 Toxin
  • Trichothecenes / chemical synthesis*
  • Trichothecenes / therapeutic use
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Sesquiterpenes
  • Trichothecenes
  • neosolaniol
  • T-2 Toxin