Furostilbestrol

Last updated
Furostilbestrol
Furostilbestrol.svg
Identifiers
  • 4-[(3E)-4-[4-(furan-2-carbonyloxy)phenyl]hex-3-en-3-yl]phenyl furan-2-carboxylate
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
ECHA InfoCard 100.008.151 OOjs UI icon edit-ltr-progressive.svg
Chemical and physical data
Formula C28H24O6
Molar mass 456.494 g·mol−1
3D model (JSmol)
  • CCC(=C(CC)C1=CC=C(C=C1)OC(=O)C2=CC=CO2)C3=CC=C(C=C3)OC(=O)C4=CC=CO4
  • InChI=1S/C28H24O6/c1-3-23(19-9-13-21(14-10-19)33-27(29)25-7-5-17-31-25)24(4-2)20-11-15-22(16-12-20)34-28(30)26-8-6-18-32-26/h5-18H,3-4H2,1-2H3/b24-23+
  • Key:VUDMUAVGKIZQRY-WCWDXBQESA-N

Furostilbestrol (INN), also known as diethylstilbestrol di(2-furoate) [1] or simply as diethylstilbestrol difuroate, is a synthetic, nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol, that was never marketed. [2] [3] It is an ester of diethylstilbestrol and was described in the literature in 1952. [2]

See also

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<span class="mw-page-title-main">Bifluranol</span> Mixture of two compounds

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<span class="mw-page-title-main">Mestilbol</span> Chemical compound

Mestilbol, also known as diethylstilbestrol monomethyl ether, is a synthetic nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol. It was developed by Wallace & Tiernan Company, patented in 1940, and introduced for medical use in the 1940s, but is now no longer marketed. Mestilbol was available both as oral tablets and in oil for intramuscular injection. The drug is gradually demethylated in the body into diethylstilbestrol and hence is a prodrug of diethylstilbestrol. Mestilbol is a highly active estrogen, although somewhat less so than diethylstilbestrol, but is longer-lasting in comparison.

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Terfluranol is a synthetic, nonsteroidal estrogen of the stilbestrol group related to diethylstilbestrol that was developed for the treatment of breast cancer but was never marketed. It was described in the medical literature in 1974.

<span class="mw-page-title-main">Pentafluranol</span> Chemical compound

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<span class="mw-page-title-main">Diethylstilbestrol diacetate</span> Chemical compound

Diethylstilbestrol diacetate (DESDA) is a synthetic, nonsteroidal estrogen of the stilbestrol group and an ester of diethylstilbestrol (DES) that was introduced for clinical use in the 1940s and was formerly marketed but is now no longer available.

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ICI-85966, also known as diethylstilbestrol (DES) bis(di carbamate), is a synthetic, nonsteroidal estrogen and cytostatic antineoplastic agent of the stilbestrol group and a nitrogen mustard ester of diethylstilbestrol (DES) which was developed for the treatment of breast cancer and prostate cancer but was never marketed.

<span class="mw-page-title-main">Triphenylchloroethylene</span> Synthetic form of estrogen

Triphenylchloroethylene, or triphenylchlorethylene, also known as chlorotriphenylethylene or as phenylstilbene chloride, is a synthetic nonsteroidal estrogen of the triphenylethylene group that was marketed in the 1940s for the treatment of menopausal symptoms, vaginal atrophy, lactation suppression, and all other estrogen-indicated conditions.

References

  1. Marler EE (1976). Pharmacological and Chemical Synonyms: A Collection of Names of Drugs, Pesticides and Other Compounds Drawn from the Medical Literature of the World. Excerpta Medica. p. 150. ISBN   978-90-219-0298-2.
  2. 1 2 Elks J (14 November 2014). The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. p. 587. ISBN   978-1-4757-2085-3.
  3. World Health Organization (2013), The use of stems in the selection of International Nonproprietary Names (INN) for pharmaceutical substances (PDF), p. 95, archived from the original (PDF) on August 8, 2016