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Methestrol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Methestrol
Clinical data
Trade namesMeprane
Other namesMethoestrol; Metestrol; Promethestrol; Promethoestrol; Dimethylhexestrol
Drug classNonsteroidal estrogen
Identifiers
  • 4-[4-(4-hydroxy-3-methylphenyl)hexan-3-yl]-2-methylphenol
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC20H26O2
Molar mass298.426 g·mol−1
3D model (JSmol)
  • CCC(C1=CC(=C(C=C1)O)C)C(CC)C2=CC(=C(C=C2)O)C
  • InChI=1S/C20H26O2/c1-5-17(15-7-9-19(21)13(3)11-15)18(6-2)16-8-10-20(22)14(4)12-16/h7-12,17-18,21-22H,5-6H2,1-4H3
  • Key:PYWBJEDBESDHNP-UHFFFAOYSA-N

Methestrol (INNTooltip International Nonproprietary Name; brand nameMeprane) ormethoestrol, also known aspromethestrol orpromethoestrol (BANTooltip British Approved Name) or asdimethylhexestrol, is asyntheticnonsteroidal estrogen of thestilbestrol group related todiethylstilbestrol which is no longer marketed.[1][2][3][4][5][6][7]

A related drug ismethestrol dipropionate (or promethestrol dipropionate) (brand nameMeprane Dipropionate).[8][9][10][11][12][13]

See also

[edit]

References

[edit]
  1. ^Ganellin CR, Triggle DJ (21 November 1996).Dictionary of Pharmacological Agents. CRC Press. pp. 608–.ISBN 978-0-412-46630-4.
  2. ^Brucker MC, King TL (8 September 2015).Pharmacology for Women's Health. Jones & Bartlett Learning. pp. 640–.ISBN 978-1-284-10811-8.
  3. ^Sturgis SH (April 1947). "Preliminary clinical report on a new synthetic estrogen, meprane".American Journal of Obstetrics and Gynecology.53 (4):678–681.doi:10.1016/0002-9378(47)90289-5.PMID 20291241.
  4. ^Coulton D (August 1947). "Meprane an effective estrogen for inhibition and suppression of lactation".American Journal of Obstetrics and Gynecology.54 (2):289–295.doi:10.1016/s0002-9378(16)39536-9.PMID 20257315.
  5. ^Coulton D, Sewall CW (September 1948). "Meprane in the treatment of the menopausal syndrome; an evaluation of estrogenic efficiency and toxicity".American Journal of Obstetrics and Gynecology.56 (3):541–548.doi:10.1016/0002-9378(48)90643-7.PMID 18877188.
  6. ^Lin HA (August 1947). "A clinical study of a new synthetic estrogen".American Journal of Obstetrics and Gynecology.54 (2):296–300.doi:10.1016/s0002-9378(16)39537-0.PMID 20257316.
  7. ^Jones GF (November 1949)."Physiology and management of the climacteric".California Medicine.71 (5):345–348.PMC 1520053.PMID 15390574.
  8. ^Ganellin CR, Triggle DJ (21 November 1996).Dictionary of Pharmacological Agents. Taylor & Francis. pp. 1298–.ISBN 978-0-412-46630-4.
  9. ^Thomas JA, Keenan EJ (6 December 2012)."Estrogens and Antiestrogenic Drug".Principles of Endocrine Pharmacology. Springer Science & Business Media. pp. 150–.ISBN 978-1-4684-5036-1.
  10. ^"Female Reprodiction – Ovary".Essential of Endocrinology and Reproductive Physiology. Allied Publishers. 1985. pp. 85–. GGKEY:HLNJ1BHUKW2.
  11. ^Modell W (21 November 2013).Drugs in Current Use 1958. Springer. pp. 114–.ISBN 978-3-662-40303-7.
  12. ^Dubin (6 December 2012).Emergency Psychiatry for the House Officer. Springer Science & Business Media. pp. 155–.ISBN 978-94-011-6690-4.
  13. ^Forsberg JG (22 October 2013)."Induction of Conditions Leading to Cancer in the Genital Tract by Estrogen During the Differentiation Phase of the Genital Epithelium". In Raspé G (ed.).Hormones and Embryonic Development: Advances in The Biosciences. Elsevier Science. pp. 141–.ISBN 978-1-4831-5171-7.
Estrogens
ERTooltip Estrogen receptor agonists
Progonadotropins
Antiestrogens
ERTooltip Estrogen receptor antagonists
(incl.SERMsTooltip selective estrogen receptor modulators/SERDsTooltip selective estrogen receptor downregulators)
Aromatase inhibitors
Antigonadotropins
Others
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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