The formation of 5,11-dihydroindolo[3,2-b]carbazole, a polyaromatic hy
drocarbon responsiveness-receptor agonist as well as an anti-initiator
and promoter of carcinogenesis, from ascorbigen under conditions of c
hemical synthesis and during incubation with gastric juice at physiolo
gical conditions, is demonstrated. Ascorbigen, rather than indole-3-ca
rbinol, is the most important indole derivative for the enzyme-inducin
g effects of dietary cruciferous vegetables. The concentration of asco
rbigen in these vegetables is at least five times (in molar ratio) hig
her than that of indole-3-carbinol.