ON THE MECHANISM OF TOXICITY OF ILLUDINS - THE ROLE OF GLUTATHIONE

Illudin M and illudin S, antitumor sesquiterpenes from Omphalotus illudens, have been found to react with thiols in a pH-dependent manner. The optimum pH values for reaction of illudin M with methyl thioglycolate, cysteine, and glutathione were 5.8, 5.6, and 6.1, respectively, and pseudo-first-order rate constants at 25 °C (10-fold excess of thiol) were 44 × 10−3, 11.5 × 10−3, and 11.3 × 10−3 min−1. In all cases, thiol added to the α,β-unsaturated ketone giving an unstable intermediate. Subsequent loss of the tertiary hydroxyl and opening of the cyclopropane ring afforded a stable aromatic product. The toxicity of illudin S to HL60 cells was increased by lowering glutathione levels in the cells and vice versa. General toxicity and antitumor activity of illudins are discussed in the light of these results. © 1990, American Chemical Society. All rights reserved.