Triphenyliodoethylene

Chemical compound
Triphenyliodoethylene
Clinical data
Other namesTPIE; Iodotriphenylethylene; Phenylstilbene iodide; Triphenylvinyl iodide
Drug classNonsteroidal estrogen
Identifiers
  • (1-iodo-2,2-diphenylethenyl)benzene
PubChem CID
  • 12139089
CompTox Dashboard (EPA)
  • DTXSID201337054 Edit this at Wikidata
Chemical and physical data
FormulaC20H15I
Molar mass382.244 g·mol−1
3D model (JSmol)
  • Interactive image
  • C1=CC=C(C=C1)C(=C(C2=CC=CC=C2)I)C3=CC=CC=C3
InChI
  • InChI=1S/C20H15I/c21-20(18-14-8-3-9-15-18)19(16-10-4-1-5-11-16)17-12-6-2-7-13-17/h1-15H
  • Key:DVJCEGLTPUEWNX-UHFFFAOYSA-N

Triphenyliodoethylene (TPIE), also known as iodotriphenylethylene or as phenylstilbene iodide, as well as triphenylvinyl iodide, is a synthetic nonsteroidal estrogen of the triphenylethylene group that is related to triphenylchloroethylene and triphenylbromoethylene and was never marketed.[1][2][3]

See also

  • Broparestrol
  • Chlorotrianisene
  • Estrobin

References

  1. ^ Tadros W (1947). "Synthetic oestrogens related to triphenylethylene". Proceedings of the XIth International Congress of Pure and Applied Chemistry: Chemistry in relation to medicine and theropeutics [sic], chemistry in relation to fuel, power and transport. Hepworth. p. 149. In fact the cestrogenic activity of either triphenylbromoethylene or triphenyliodoethylene (J. 3d. Robson, A. Schonberg and H. A. Fahim)(3) (Table 1) compares with that of triphenylchloroethylene. A True Oestrogen and A Pro-oestrogen.
  2. ^ Burton TF (1952). British Abstracts. Bureau of Abstracts. p. 549. Roughly quantitative data are reported for the antagonism between oestrogens (oestradiol, stilboestrol, doisynolic acid, allenolic acid, and triphenyliodoethylene) and progesterone, methyltestosterone, and testosterone propionate given [...]
  3. ^ Egyptian Veterinary Medical Association (1966). Annual Veterinary Congress, Proceedings. L'Institut Francais d'Archéologie Orientale. p. 392. But the synthetic oestrogens tested e.g. stilboesterol, triphenyliodoethylene, diosynolic acid and allenolic acid produce constant inhibition of the uterine motility.


  • v
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Estrogen receptor modulators
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
  • Coregulator-binding modulators: ERX-11
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
See also
Receptor/signaling modulators
Estrogens and antiestrogens
Androgen receptor modulators
Progesterone receptor modulators
List of estrogens


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