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Toremifene (CAS 89778-26-7)

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Alternate Names:
Farestone, Chlortamoxifen
Application:
Toremifene is an analog of chlorinated tamoxifen and an antiproliferative agent
CAS Number:
89778-26-7
Purity:
≥98%
Molecular Weight:
405.96
Molecular Formula:
C26H28ClNO
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Toremifene is a chlorinated tamoxifen analogue which competes with estradiol for estrogen receptors and has growth inhibitory effects on MCF-7 breast cancer cells. Toremifene causes growth inhibition of estrogen-sensitive breast cancer cells by inducing some cells to undergo apoptosis and by inhibiting other cells from entering mitosis. Toremifene, also recognized by the name Fareston, is categorized as a type of organic compound referred to as stilbenes. These compounds are characterized by the presence of a 1,2-diphenylethylene structure. Stilbenes (C6-C2-C6) emerge from the fundamental phenylpropene (C6-C3) framework. When hydroxyl groups are introduced to a phenyl ring, they give rise to stilbenoids. Toremifene is solid in form, exhibiting near-insolubility in water and possessing a relatively neutral nature. This compound has been identified in various biofluids, including urine and blood. Inside the cell, toremifene predominantly resides in the cytoplasm and membrane, a deduction drawn from its logarithm of the partition coefficient (logP). The biosynthesis of toremifene can occur through the transformation of stilbene.


Toremifene (CAS 89778-26-7) References

  1. Clinical pharmacokinetics of toremifene.  |  Taras, TL., et al. 2000. Clin Pharmacokinet. 39: 327-34. PMID: 11108432
  2. Toremifene: an evaluation of its safety profile.  |  Harvey, HA., et al. 2006. Breast. 15: 142-57. PMID: 16289904
  3. Toremifene--a promising therapy for the prevention of prostate cancer and complications of androgen deprivation therapy.  |  Taneja, SS., et al. 2006. Expert Opin Investig Drugs. 15: 293-305. PMID: 16503765
  4. Review of the pharmacological properties of toremifene.  |  Kangas, L. 1990. J Steroid Biochem. 36: 191-5. PMID: 2142231
  5. Introduction to toremifene.  |  Kangas, L. 1990. Breast Cancer Res Treat. 16 Suppl: S3-7. PMID: 2149282
  6. Toremifene is an effective and safe alternative to tamoxifen in adjuvant endocrine therapy for breast cancer: results of four randomized trials.  |  Zhou, WB., et al. 2011. Breast Cancer Res Treat. 128: 625-31. PMID: 21553116
  7. Toremifene versus tamoxifen for advanced breast cancer.  |  Mao, C., et al. 2012. Cochrane Database Syst Rev. 2012: CD008926. PMID: 22786516
  8. FDA-approved selective estrogen receptor modulators inhibit Ebola virus infection.  |  Johansen, LM., et al. 2013. Sci Transl Med. 5: 190ra79. PMID: 23785035
  9. Toremifene for breast cancer: a review of 20 years of data.  |  Vogel, CL., et al. 2014. Clin Breast Cancer. 14: 1-9. PMID: 24439786
  10. Apoptosis in toremifene-induced growth inhibition of human breast cancer cells in vivo and in vitro.  |  Wärri, AM., et al. 1993. J Natl Cancer Inst. 85: 1412-8. PMID: 8350365
  11. Toremifene.  |  . 1996. IARC Monogr Eval Carcinog Risks Hum. 66: 367-87. PMID: 9097128
  12. Toremifene. A review of its pharmacological properties and clinical efficacy in the management of advanced breast cancer.  |  Wiseman, LR. and Goa, KL. 1997. Drugs. 54: 141-60. PMID: 9211086
  13. Toremifene in postmenopausal breast cancer. Efficacy, safety and cost.  |  Mäenpää, JU. and Ala-Fossi, SL. 1997. Drugs Aging. 11: 261-70. PMID: 9342556

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Toremifene, 500 mg

sc-205868
500 mg
$85.00

Toremifene, 1 g

sc-205868A
1 g
$129.00