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- W2081053586 abstract "The role of progesterone in women's cancers as well as the knowledge of the progesterone receptor (PR) structure has prompted the design of different therapies. The aim of this review is to describe the basic structure of PR agonists and antagonists as well as the recent treatments for illness associated with the progesterone receptor. The rational design for potent and effective drugs for the treatment of female cancer must consider the structural changes of the androgen and progestogen skeleton which are an indicator of their activity as progestins or antiprogestins. The presence of a hydroxyl group at C-17 in the progesterone skeleton brings about a loss of progestational activity whereas acetylation induces a progestational effect. The incorporation of an ethynyl functional group to the testosterone framework results in a loss of androgenic activity with a concomitant enhancement of the progestational effect. On the other hand, an ester function at C-3 of dehydroepiandrosterone skeleton induces partial antagonism to the PR." @default.
- W2081053586 created "2016-06-24" @default.
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- W2081053586 date "2014-03-25" @default.
- W2081053586 modified "2023-09-30" @default.
- W2081053586 title "Recent advances in structure of progestins and their binding to progesterone receptors" @default.
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- W2081053586 doi "https://doi.org/10.3109/14756366.2014.895719" @default.
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