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OtherIntermediateMedium Risk

Toremifene

Also known as: Fareston

Toremifene is a chlorinated derivative of tamoxifen approved for metastatic breast cancer in postmenopausal women. It shares a similar mechanism to tamoxifen but may have a lower risk of endometrial cancer and is occasionally used as an alternative in PCT protocols.

Evidence70/100 — Moderate

Risk Level

Medium Risk

Difficulty

Intermediate
CAS Number89778-26-7
Molecular FormulaC26H28ClNO
ClassOther
CategorySERMs & AIs

Mechanism of Action

Toremifene binds to estrogen receptors and exerts tissue-selective effects as an antagonist in breast tissue and a partial agonist in bone and lipid metabolism. It blocks estrogen-mediated negative feedback in the hypothalamus similarly to tamoxifen, supporting HPT axis recovery. The chlorine substitution provides slightly different receptor binding kinetics compared to tamoxifen.

Dosing Research

Breast cancer: 60 mg/day orally. PCT use (off-label): 60-120 mg/day for 4-6 weeks. Half-life is approximately 5 days. Primarily metabolized by CYP3A4 to active metabolites including N-desmethyltoremifene.

Side Effects & Risks

Hot flashes, sweating, and nausea are common. Risk of QT prolongation at higher doses requires caution. Thromboembolic risk similar to tamoxifen. Elevated liver enzymes reported. Lower incidence of endometrial changes compared to tamoxifen in some studies.

Research Studies

Disclaimer

CompoundIQ publishes research summaries for informational and educational purposes only. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. Always consult a licensed healthcare provider. Many compounds listed are research chemicals not approved for human use.

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