Abstract
Under conditions which give total conversion of C14-androstenedione to estrogen by placental microsomes, 19-hydroxyandrostenedione was also introduced to act as a trapping agent for radioactivity. The results obtained in these experiments show that the 19-hydroxyandrostenedione had a much lower specific activity than the estrogen at any time and therefore that free 19-hydroxyandrostenedione could not be an obligatory intermediate in aromatization.