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.
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.
Risk Level
Medium RiskDifficulty
Intermediate| CAS Number | 89778-26-7 |
| Molecular Formula | C26H28ClNO |
| Class | Other |
| Category | SERMs & 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
Related compounds
Finasteride
OtherFinasteride is a selective type II 5-alpha reductase inhibitor approved for male pattern hair loss (1 mg, Propecia) and benign prostatic hyperplasia (5 mg, Proscar). It reduces scalp DHT levels by approximately 60-70% and is one of only two FDA-approved oral medications for androgenetic alopecia. It has decades of clinical data supporting its efficacy.
Tamoxifen
OtherTamoxifen is a selective estrogen receptor modulator (SERM) that has been the gold standard for breast cancer treatment and prevention since the 1970s. It is one of the most widely used compounds in post-cycle therapy (PCT) for restoring endogenous testosterone production after anabolic steroid use.
Clomiphene Citrate
OtherClomiphene citrate is a SERM originally developed for female ovulation induction and widely adopted in PCT protocols and off-label male hypogonadism treatment. It is a racemic mixture of two geometric isomers, enclomiphene (trans) and zuclomiphene (cis), with differing estrogenic properties.
Anastrozole
OtherAnastrozole is a potent, selective non-steroidal aromatase inhibitor that reduces estradiol levels by approximately 80-85%. It is widely used in breast cancer treatment and is the most commonly employed AI during anabolic steroid cycles to manage estrogen-related side effects.
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.