• A.G. Shavva
  • S.N. Morozkina
  • I.V. Ishchenko
  • I.I. Eliseev
  • S.I. Selivanov
  • Sh.N. Abusalimov
  • S.S. Selivanov
  • I.Yu. Kameneva
  • N.D. Eshchenko
Modifications of D-homo-6-oxa-8α-analogues of steroid estrogens were found to lead to a complete loss of the uterotropic and hypertriglyceridemic activities. These compounds may be promising for the design on their basis of inhibitors of the steroid hormone metabolism and transporters of other compounds to the estrogen target organs. © Nauka/Interperiodica 2007.
Original languageEnglish
Pages (from-to)288-292
JournalRussian Journal of Bioorganic Chemistry
Issue number3
StatePublished - 2007

ID: 5025338