E. Caspi et al., ESTROGEN BIOSYNTHESIS - 2-BETA-HYDROXY-19-OXOANDROST-4-ENE-3,17-DIONEREVISITED, Journal of the Chemical Society. Perkin transactions. I, (10), 1993, pp. 1191-1195
Current evidence is consistent with the view that biosynthesis of estr
ogens by human microsomal placental aromatase proceeds through several
different pathways. One of the proposed mechanisms of aromatization o
f androgens involves the intermediacy of 2beta-hydroxy-19-oxoandrost-4
-ene-3,17-dione 1a. It is shown that incubation of 2beta[(OH)-O-18]-1b
with placental aromatase gave (HCOOH)-O-18 which differs from previou
s observations. The incorporation of isotopic oxygen in the formic aci
d is consistent with the view that one of the alternative routes of es
trogen elaboration may involve a 2beta,19-dioxygenated androgen.