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Benzestrol

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Benzestrol
Clinical data
Trade namesChemestrogen, Ocestrol, Octestrol, Octoestrol, Octofollin
Drug classNonsteroidal estrogen
Identifiers
  • 4,4'-(3-ethylhexane-2,4-diyl)diphenol
CAS Number
PubChemCID
ChemSpider
UNII
ChEBI
ChEMBL
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(CC)C(C)C2=CC=C(C=C2)O
  • InChI=InChI=1S/C20H26O2/c1-4-19(14(3)15-6-10-17(21)11-7-15)20(5-2)16-8-12-18(22)13-9-16/h6-14,19-22H,4-5H2,1-3H3
  • Key:DUTFBSAKKUNBAL-UHFFFAOYSA-N

Benzestrol (INNTooltip International Nonproprietary Name,BANTooltip British Approved Name) (brand namesChemestrogen,Ocestrol,Octestrol,Octoestrol,Octofollin) is asyntheticnonsteroidal estrogen of thestilbestrol group which was formerly used medically but has since been discontinued.[1][2][3] The stilbestrol estrogens, the best-known of which isdiethylstilbestrol (DES) were used extensively in the mid-1900s and were finally banned by the FDA due to them causing tumors in the children of women who used them.[4]

Medical uses

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Benzestrol and other stilbestrol were used as synthetic estrogens in order to prevent premature births.[4] Based on the idea that premature births happened because the mother did not produce enough estrogen on her own, doctors prescribed benzestrol to mothers in order to increase their estrogen levels.

Studies have been done in the past on normal, mature and castrate female rats. Benzestrol produced the same type of estrus in the castrate rat when injected at 0.8 to 1.0 micrograms as when the rat was injected with 2.0 to 2.5 micrograms of estrone.[5] This is significant because less benzestrol could be used to produce the same effect as estrone in increasing estrogen production. It has been used in the past as a nonsteroidal estrogen antagonist.

Pharmacology

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Pharmacodynamics

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Benzestrol is described as a very potent estrogen.[6] It is reported to have about 130% of therelative binding affinity ofestradiol for theestrogen receptors.[7]

Chemistry

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Benzestrol is usually grouped with the stilbestrol estrogens. However, benzestrol is technically not a stilbestrol derivative because its central chain is elongated by one carbon. In any case, it is a very close analogue of the stilbestrol estrogens.[8]

History

[edit]

Benzestrol is a drug in the stilbestrol family of estrogens. These drugs were first produced in the late 1930s. Benzestrol itself was reported in 1946.[1] In 1953, experiments began on benzestrol and other stilbestrols to see if they actually helped stop premature births. This study in 1953 found that benzestrol did not in fact help stop premature births.[4] A study in 1971 found that benzestrol was the cause of a rare vaginal cancer in girls and women whose mothers had been on benzestrol while pregnant.[4]

See also

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References

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  1. ^abElks J (14 November 2014).The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. pp. 133–.ISBN 978-1-4757-2085-3.
  2. ^Morton IK, Hall JM (6 December 2012).Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. pp. 47–.ISBN 978-94-011-4439-1.
  3. ^"Benzestrol".Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 106–.ISBN 978-3-88763-075-1.
  4. ^abcd"DES History". U.S. Centers for Disease Control and Prevention. Archived fromthe original on 15 June 2019. Retrieved17 December 2012.
  5. ^Stebbins RB, Blanchard EW (1945). "The Effects of a New Synthetic Estrogen, Benzestrol Upon the Hematopoietic System in the Rat".Endocrinology.36 (5): 305.doi:10.1210/endo-36-5-305.
  6. ^Agarwal OP (2006)."Sex hormones".Natural Products. Krishna Prakashan Media. pp. 288–.ISBN 978-81-87224-85-3.
  7. ^Fink BE, Mortensen DS, Stauffer SR, Aron ZD, Katzenellenbogen JA (April 1999)."Novel structural templates for estrogen-receptor ligands and prospects for combinatorial synthesis of estrogens".Chemistry & Biology.6 (4):205–219.doi:10.1016/S1074-5521(99)80037-4.PMID 10099132.
  8. ^Sevringhaus EL (1944). "Therapy of the Patient in the Menopause: Endocrine Methods".The Journal of Clinical Endocrinology & Metabolism.4 (12):597–604.doi:10.1210/jcem-4-12-597.ISSN 0021-972X.
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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