Methestrol
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| Identifiers | |
|---|---|
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| Synonyms | Metestrol |
| CAS Number | 130-73-4 |
| PubChem (CID) | 71620 |
| ChemSpider | 64688 |
| Chemical and physical data | |
| Formula | C20H26O2 |
| Molar mass | 298.41924 g/mol |
| 3D model (Jmol) | Interactive image |
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Methestrol (INN) or methoestrol, also known as promethestrol or promethoestrol (BAN) or as dimethylhexestrol, is a synthetic, non-steroidal estrogen of the stilbestrol group related to diethylstilbestrol that was never marketed.[1][2]
A related drug is methestrol dipropionate (or promethestrol dipropionate) (brand name Meprane Dipropionate).[3][4][5][6][7][8]
See also
References
- ↑ C.R. Ganellin; David J. Triggle (21 November 1996). Dictionary of Pharmacological Agents. CRC Press. pp. 608–. ISBN 978-0-412-46630-4.
- ↑ Mary C. Brucker; Tekoa L. King (8 September 2015). Pharmacology for Women’s Health. Jones & Bartlett Learning. pp. 640–. ISBN 978-1-284-10811-8.
- ↑ C.R. Ganellin; David J. Triggle (21 November 1996). Dictionary of Pharmacological Agents. Taylor & Francis. pp. 1298–. ISBN 978-0-412-46630-4.
- ↑ John A. Thomas; Edward J. Keenan (6 December 2012). Principles of Endocrine Pharmacology. Springer Science & Business Media. pp. 150–. ISBN 978-1-4684-5036-1.
- ↑ Essential of Endocrinology and Reproductive Physiology. Allied Publishers. pp. 85–. GGKEY:HLNJ1BHUKW2.
- ↑ Walter Modell (21 November 2013). Drugs in Current Use 1958. Springer. pp. 114–. ISBN 978-3-662-40303-7.
- ↑ Dubin (6 December 2012). Emergency Psychiatry for the House Officer. Springer Science & Business Media. pp. 155–. ISBN 978-94-011-6690-4.
- ↑ G. Raspé (22 October 2013). Hormones and Embryonic Development: Advances in The Biosciences. Elsevier Science. pp. 141–. ISBN 978-1-4831-5171-7.
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