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| CAS_number = 129453-61-8 | | CAS_number = 129453-61-8 | ||
| ATC_prefix = L02 | | ATC_prefix = L02 | ||
| ChEMBL_Ref = {{ebicite|correct|EBI}} | |||
| ChEMBL = 1358 | |||
| ATC_suffix = BA03 | | ATC_suffix = BA03 | ||
| ATC_supplemental = | | ATC_supplemental = |
Revision as of 17:18, 1 February 2011
Pharmaceutical compoundClinical data | |
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Routes of administration | Intramuscular injection |
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Pharmacokinetic data | |
Protein binding | 99% |
Elimination half-life | 40 days |
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ECHA InfoCard | 100.170.955 |
Chemical and physical data | |
Formula | C32H47F5O3S |
Molar mass | 606.772 g/mol g·mol |
3D model (JSmol) | |
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Fulvestrant, also known as ICI 182,780, is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It is an estrogen receptor antagonist with no agonist effects, which works both by down-regulating and by degrading the estrogen receptor. It is administered as a once-monthly injection.
Fulvestrant is marketed by AstraZeneca with the brand name Faslodex.
Clinical uses
Fulvestrant is a Selective Estrogen Receptor Down-Regulator (SERD). Fulvestrant is indicated for the treatment of hormone receptor positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy.
External links
References
- S. Kansra, S. Yamagata, L. Sneade, L. Foster & N. Ben-Jonathan (2005). "Differential effects of estrogen receptor antagonists on pituitary lactotroph proliferation and prolactin release". Mol Cell Endocrinol. 239 (1–2): 27–36. doi:10.1016/j.mce.2005.04.008. PMID 15950373.
{{cite journal}}
: CS1 maint: multiple names: authors list (link)
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