Pharmacologic properties of CDB(VA)-2914

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Abstract

CDB(VA)-2914 (17alpha-acetoxy-11beta-(4-N,N-dimethylaminophenyl)-19-norpregna-4,9-diene-3,20-dione) is a synthetic steroid that demonstrates potent progesterone antagonist activity in vitro and in vivo. Its binding and antagonist potency with respect to the glucocorticoid receptor is significantly reduced compared to that of mifepristone, indicating that CDB(VA)-2914 belongs to a new class of dissociated progesterone receptor modulators that have reduced antiglucorticoid activity. The pharmacological effects of CDB(VA)-2914 have been examined in a variety of animal models, the results of which are reviewed in this paper. CDB(VA)-2914 inhibits ovulation in rats in a dose-dependent manner upon single-dose oral administration and exhibits antifertility activity during continuous low-dose administration. CDB(VA)-2914 is also effective in animal models of postcoital contraception. This paper also presents the results of metabolism studies undertaken to link the results of the animal models to potential human applications. Because of its unique pharmacological profile, CDB(VA)-2914 is a promising candidate for use in contraception as well as treatment of uterine fibroids and endometriosis.

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Condition tags

endometriosis

MeSH descriptors

Norpregnadienes Administration, Oral Animals Contraceptives, Postcoital, Synthetic Contraceptives, Postcoital, Synthetic Dose-Response Relationship, Drug Endometriosis Female Glucocorticoids Glucocorticoids Hormone Antagonists Hormone Antagonists Humans Mifepristone Mifepristone Models, Chemical Norpregnadienes Protein Binding Receptors, Progesterone Receptors, Progesterone

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SciLite annotations

chemicals 5
phenyl acetimidate pandamarilactone 31 steroid progesterone mifepristone
organisms 5
rodents rattus sp. rodents rodents human

Source provenance

europepmc
last seen: 2026-06-11T06:19:48.454388+00:00
pubmed
last seen: 2026-05-13T22:12:44.121522+00:00
scilite
last seen: 2026-05-18T04:25:29.313245+00:00
unpaywall
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License: public-domain-us · commercial use OK · attribution required
Courtesy of the U.S. National Library of Medicine