Culinary processing of cruciferous vegetables leads to both enzymatic and n
on-enzymatic degradation of indole glucosinolates to various indole compoun
ds. This paper summarizes the mechanisms of glucobrassicin breakdown under
different conditions and the subsequent transformations of the products tha
t are formed. Some of the indole derivatives that result from glucobrassici
n hydrolysis (ascorbigen, indole-3-carbinol) are of interest because of the
ir ability to block chemically induced carcinogenesis.