Triphenyliodoethylene

Triphenyliodoethylene
Clinical data
Other names	Iodotriphenylethylene; Phenylstilbene iodide; Triphenylvinyl iodide
Drug class	Nonsteroidal estrogen
Identifiers
	IUPAC name (1-iodo-2,2-diphenylethenyl)benzene;
PubChem CID	12139089;
Chemical and physical data
Formula	C20H15I
Molar mass	382.244 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES 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, 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]

References

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. 1947. 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.
Tom F. Burton (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 [...]
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.

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