Name | (E)-4-Hydroxy-N-desmethyl Tamoxifen |
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Synonyms |
4-[(E)-1-[4-[2-(methylamino)ethoxy]phenyl]-2-phenylbut-1-enyl]phenol
Endoxifen (E-isomer) |
Description | Endoxifen E-isomer is the E-isomer of (Z)-Endoxifen. (Z)-Endoxifen, an active metabolite generated via actions of CYP3A4/5 and CYP2D6, is a more potent selective estrogen receptor modulator (SERM) than Tamoxifen. |
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Related Catalog | |
In Vitro | Endoxifen exists as the potently anti-estrogenic (Z)-isomer and the lesser known (E)-isomer. It is assumed that (E)-Endoxifen, structurally related to (E)-4-OH-tamoxifen, have similar pharmacological properties. The (E)-isomer is an impurity in (Z)-Endoxifen drug substance and increases under certain storage conditions. (E)-Endoxifen is identified as the primary degradant[1]. |
References |
Molecular Formula | C25H27NO2 |
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Molecular Weight | 373.48700 |
Exact Mass | 373.20400 |
PSA | 41.49000 |
LogP | 5.75040 |
Storage condition | 2-8℃ |
~% 114828-90-9 |
Literature: Fauq, Abdul H.; Maharvi, Ghulam M.; Sinha, Dola Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 10 p. 3036 - 3038 |
Precursor 1 | |
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DownStream 0 |