Triphenylethylene
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File:Triphenylethylene.svg | |
Systematic (IUPAC) name | |
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1,2-Diphenylethenylbenzene
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Identifiers | |
CAS Number | 58-72-0 |
PubChem | CID: 6025 |
ChemSpider | 5803 |
Chemical data | |
Formula | C20H16 |
Molecular mass | 256.34104 g/mol |
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Triphenylethylene (TPE) is a simple aromatic hydrocarbon that possesses weak estrogenic properties.[1][2]
TPE is the parent compound of a group of non-steroidal selective estrogen receptor modulators (SERMs) that includes tamoxifen, clomiphene, chlorotrianisene, DBE, broparestrol, toremifene, droloxifene, idoxifene, ospemifene, fispemifene, and miproxifene, among others.[1][2][3]
TPE and its SERM derivatives were derived from structural modification of diethylstilbestrol.[4]
See also
- Benzothiophene – parent compound for another group of non-steroidal SERMs that includes raloxifene
- Ethamoxytriphetol (MER-25) – a drug related to the TPEs and the first antiestrogen to be discovered
- Stilbestrol – parent compound of a group of non-steroidal estrogens that includes diethylstilbestrol
- Phenanthrene – parent compound of steroidal estrogens like estradiol
- Chrysene – parent compound of a group of non-steroidal weak estrogens that includes 2,8-DHHHC and tetrahydrochrysene
- Doisynolic acid – parent compound of a group of non-steroidal estrogens that includes doisynoestrol
References
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- Polycyclic aromatic hydrocarbons
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