Anagestone acetate
![]() a steroidal progestin | |
Systematic (IUPAC) name | |
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(17-Acetyl-6,10,13-trimethyl-1,2,3,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-yl) acetate | |
Clinical data | |
Routes of administration | Oral |
Identifiers | |
CAS Number | 3137-73-3 |
PubChem | CID 18443 |
ChemSpider | 221058 |
Synonyms | Anapregnone acetate; 17α-hydroxy-6α-methylpregn-4-en-20-one acetate |
Chemical data | |
Formula | C24H36O3 |
Molar mass | 372.54084 g/mol |
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Anagestone acetate (USAN) (brand name Anatropin; former developmental code name ORF-1658), also known as 17α-hydroxy-6α-methylpregn-4-en-20-one acetate, is a steroidal progestin that was formerly marketed by Ortho Pharmaceutical.[1][2] Under the brand name Neo-Novum and in combination with the estrogen mestranol, it was introduced in 1968 as an oral contraceptive in the United States.[3][4] Anagestone acetate is the acetate ester of anagestone, which, in contrast to anagestone acetate, was never marketed.[1]
In 1969, along with a variety of other progestogens including progesterone, chlormadinone acetate, megestrol acetate, medroxyprogesterone acetate, ethynerone, and chloroethynyl norgestrel, anagestone acetate was found to induce the development of mammary gland tumors in Beagle dogs after extensive treatment (2–7 years) with very high doses (10–25 times the recommended human dose), though notably not with 1–2 times the human dosage.[4][5][6] In contrast, the non-halogenated 19-nortestosterone derivatives norgestrel, norethisterone, noretynodrel, and etynodiol diacetate were not found to produce such nodules.[6] Because of these findings, anagestone acetate was withdrawn from the U.S. market in 1969, and this was followed by its subsequent discontinuation worldwide by the manufacturer.[4][6][7] The findings also led to the virtual disappearance of most 17α-hydroxyprogesterone derivatives as hormonal contraceptives from the market (though medroxyprogesterone acetate has continued to be used).[4][5] According to Hughes et al., "It is still doubtful how much relevance these findings have for humans as the dog mammary gland seems to be the only one which can be directly maintained by progestogens."[6][8] Subsequent research revealed species differences between dogs and humans and established that there is no similar risk in humans.[9]
See also
- Algestone acetophenide
- Cyproterone acetate
- Delmadinone acetate
- Hydroxyprogesterone acetate
- Hydroxyprogesterone caproate
- Hydroxyprogesterone heptanoate
- Melengestrol acetate
References
- 1 2 J. Elks (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 85–. ISBN 978-1-4757-2085-3.
- ↑ William Andrew Publishing (22 October 2013). Pharmaceutical Manufacturing Encyclopedia, 3rd Edition. Elsevier. pp. 322–. ISBN 978-0-8155-1856-3.
- ↑ A. Labhart (6 December 2012). Clinical Endocrinology: Theory and Practice. Springer Science & Business Media. pp. 571–. ISBN 978-3-642-96158-8.
- 1 2 3 4 Christian Streffer; H. Bolt; D. Follesdal; P. Hall; J.G. Hengstler; P. Jacob; D Oughton; K. Prieß; E. Rehbinder; E. Swaton (11 November 2013). Low Dose Exposures in the Environment: Dose-Effect Relations and Risk Evaluation. Springer Science & Business Media. pp. 135–. ISBN 978-3-662-08422-9.
- 1 2 V. H. T. James; J. R. Pasqualini (22 October 2013). Hormonal Steroids: Proceedings of the Fifth International Congress on Hormonal Steroids. Elsevier Science. pp. 7–. ISBN 978-1-4831-5895-2.
- 1 2 3 4 C.H. Lingeman (6 December 2012). Carcinogenic Hormones. Springer Science & Business Media. pp. 149–. ISBN 978-3-642-81267-5.
- ↑ Consolidated List of Products Whose Consumption And/or Sale Have Been Banned, Withdrawn, Severely Restricted Or Not Approved by Governments. United Nations Publications. 1983. pp. 25–. ISBN 978-92-1-130230-1.
- ↑ A. Hughes; S. H. Hasan; G. W. Oertel; H. E. Voss; F. Bahner; F. Neumann; H. Steinbeck, K.-J. Gräf, J. Brotherton, H. J. Horn, R. K. Wagner (27 November 2013). Androgens II and Antiandrogens / Androgene II und Antiandrogene. Springer Science & Business Media. pp. 531–. ISBN 978-3-642-80859-3.
- ↑ Benno Clemens Runnebaum; Thomas Rabe; Ludwig Kiesel (6 December 2012). Female Contraception: Update and Trends. Springer Science & Business Media. pp. 134–135. ISBN 978-3-642-73790-9.
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