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diethylstilbestrol

Structure via PubChem · Public domain (PubChem)

EntityQ423989· pop 28· linked from 1,148 articles

diethylstilbestrol

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Also known as stilboestrol, trans-Diethylstilboesterol, trans-Diethylstilbestrol, trans-Diethylstilbesterol, DES, (e)-4,4'-(1,2-Diethyl-1,2-ethenediyl)bisphenol, Distilbene, 4,4'-dihydroxy-α,β-diethylstilbene

Diethylstilbestrol (DES), also known as stilbestrol or stilboestrol, is a nonsteroidal estrogen medication. Its use now rare; in the past, it was widely used for a variety of indications, including pregnancy support for those with a history of recurrent miscarriage, hormone therapy for menopausal symptoms and estrogen deficiency, treatment of prostate cancer and breast cancer, and other uses. By 2007, it was only used in the treatment of prostate cancer and breast cancer. In 2011, Hoover and colleagues reported adverse reproductive health outcomes linked to DES, including infertility, miscarri

Key facts

Drug.Verifiedfields
verified
Drug.Watchedfields
verified
Drug.verifiedrevid
464188812
Drug.IUPAC_name
4,4'-[(3E)-Hex-3-ene-3,4-diyl]diphenol
Drug.image
Diethylstilbestrol.svg
Drug.image_class
skin-invert-image
Drug.width
250px
Drug.image2
Diethylstilbestrol molecule ball.png
Drug.image_class2
bg-transparent
Drug.width2
250px
Drug.pregnancy_category
X
Drug.routes_of_administration
By mouth, vaginal, topical, intravenous, intramuscular injection (as an ester)
Drug.class
Nonsteroidal estrogen
Drug.bioavailability
Well-absorbed
Drug.protein_bound
>95%
Drug.metabolism
Hydroxylation, oxidation, glucuronidation
Drug.metabolites
• (Z,Z)-Dienestrol• Paroxypropione• Glucuronides
Drug.elimination_half life
24 hours

via Wikipedia infobox

Chemical data

Formula
C18H20O2
Molecular weight
268.3 g/mol
IUPAC name
4-[(E)-4-(4-hydroxyphenyl)hex-3-en-3-yl]phenol
SMILES
CC/C(=C(/CC)\C1=CC=C(C=C1)O)/C2=CC=C(C=C2)O
InChIKey
RGLYKWWBQGJZGM-ISLYRVAYSA-N
XLogP
5.1
Polar surface area
40.5 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Research

10,770 papers

via PubMed

~35 min read

Encyclopedic overview

27 sections
Contents
  • Medical uses
  • Side effects
  • Breast changes and feminization
  • Blood clots and cardiovascular issues
  • Other long-term effects
  • Overdose
  • Pharmacology
  • Pharmacodynamics
  • Estrogenic activity
  • Antigonadotropic effects
  • Other activities
  • Pharmacokinetics
  • Chemistry
  • History
  • Synthesis
  • Clinical use
  • Trials
  • Regulations
  • Medical ethics
  • Lawsuits
  • Society and culture
  • Veterinary use
  • Canine incontinence
  • Livestock growth promotion
  • References
  • Further reading
  • External links

Diethylstilbestrol (DES), also known as stilbestrol or stilboestrol, is a nonsteroidal estrogen medication. Its use now rare; in the past, it was widely used for a variety of indications, including pregnancy support for those with a history of recurrent miscarriage, hormone therapy for menopausal symptoms and estrogen deficiency, treatment of prostate cancer and breast cancer, and other uses. By 2007, it was only used in the treatment of prostate cancer and breast cancer. In 2011, Hoover and colleagues reported adverse reproductive health outcomes linked to DES, including infertility, miscarriage, ectopic pregnancy, preeclampsia, preterm birth, stillbirth, infant death, menopause prior to age 45, breast cancer, cervical cancer, and vaginal cancer. While most commonly taken by mouth, DES was available for use by other routes as well, such as vaginally, topically, and by injection.

DES is an estrogen, or an agonist of the estrogen receptors, the biological target of estrogens like estradiol. It is a synthetic and nonsteroidal estrogen of the stilbestrol group, and differs from the natural estrogen estradiol. Compared to estradiol, DES has greatly improved bioavailability when taken by mouth, is more resistant to metabolism, and shows relatively increased effects in certain parts of the body like the liver and uterus. These differences result in DES having an increased risk of blood clots, cardiovascular issues, and certain other adverse effects.

Excerpted from Wikipedia’s “diethylstilbestrol” article, available under the CC BY-SA 4.0 licence.

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