ovarian atrophy and reduced fertility. Following in vivo administration, it is rapidly converted
by the liver to 2, 2-bis-(p-hydroxyphenyl)-1, 1, 1-trichloroethane (HPTE), the reported active
metabolite. Both methoxychlor and HPTE have weak estrogenic and antiandrogenic
activities, and these effects are thought to be mediated through the estrogen and androgen
receptors, respectively. Previous in vivo studies on methoxychlor exposure to female …