Design of mechanism-based inactivators of human placental aromatase.

Abstract

This article reviews the design and study, in our own laboratory and in other laboratories, of new 10 beta-substituted analogs of estr-4-ene-3,17-dione. These compounds, along with a number of known analogs, have been evaluated as reversible or irreversible inhibitors of human placental microsomal aromatase. The only irreversible inhibitors in the group… (More)

Topics

  • Presentations referencing similar topics