Structure via PubChem · Public domain (PubChem)
diethylstilbestrol
Sign in to saveAlso 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- Diethylstilbestrol.Report on carcinogens : carcinogen profiles · 2004
- Diethylstilbestrol metabolic transformation in relation to organ specific tumor manifestation.Archives of toxicology. Supplement. = Archiv fur Toxikologie. Supplement · 1979
- Diethylstilboestrol--a long-term legacy.Maturitas · 2012
- [Administration of diethylstilbestrol during pregnancy, a public health problem].Revue d'epidemiologie et de sante publique · 1983
- [Estrogen therapy--high-dose intravenous diethylstilbestrol diphosphate therapy for advanced or hormone refractory prostate cancer].Nihon rinsho. Japanese journal of clinical medicine · 2002
via PubMed
~35 min read
Encyclopedic overview
27 sectionsContents
- 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.