Chemistry:Trioxifene

From HandWiki
Short description: Chemical compound
Trioxifene
Trioxifene.svg
Clinical data
Other namesLY-133,314
Routes of
administration
Oral
ATC code
  • none
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
Chemical and physical data
FormulaC30H31NO3
Molar mass453.582 g·mol−1

Trioxifene (INN; developmental code LY-133,314), or as the salt trioxifene mesylate (USAN), is a selective estrogen receptor modulator (SERM) with competitive binding activity against estradiol for the ERα and antagonistic activity against ERα-mediated gene expression, that was under preclinical and clinical development by Eli Lilly and Company for breast cancer and prostate cancer,[1] but was abandoned.[2]:11[3][4] Its affinity for the rat estrogen receptor was reported to be 20% relative to estradiol.[5][6]

References

  1. "The selective estrogen receptor modulator trioxifene (LY133314) inhibits metastasis and extends survival in the PAIII rat prostatic carcinoma model". Cancer Research 63 (18): 6056–62. September 2003. PMID 14522935. 
  2. "Tamoxifen: Pioneering Medicine in Breast Cancer.". Milestones in Drug Therapy. Springer Science & Business Media. 2013. ISBN 978-3-03-480664-0. 
  3. The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014. pp. 1252–. ISBN 978-1-4757-2085-3. https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA1252. 
  4. Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer Science & Business Media. 6 December 2012. pp. 281–. ISBN 978-94-011-4439-1. https://books.google.com/books?id=tsjrCAAAQBAJ&pg=PA281. 
  5. "The biological evaluation of novel antioestrogens for the treatment of breast cancer". Crit Rev Oncol Hematol 15 (3): 243–69. December 1993. doi:10.1016/1040-8428(93)90044-5. PMID 8142059. 
  6. "Endocrine Disruptors: Effects on Sex Steroid Hormone Receptors and Sex Development". Drug Toxicity in Embryonic Development II: Advances in Understanding Mechanisms of Birth Defects: Mechanistics Understanding of Human Development Toxicants. Springer Science & Business Media. 6 December 2012. pp. 437–. ISBN 978-3-642-60447-8. https://books.google.com/books?id=vcHsCAAAQBAJ&pg=PA437.