Chine Fabricant de poudre de stéroïdes anabolisants
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Stéroïdes anti-œstrogènes

» Stéroïdes bruts » Stéroïdes anti-œstrogènes

  • Caractéristiques
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  • COA

Alias: Faslodex
CAS: 129453-61-8
MF: C32H47F5O3S
MW: 606.77
Essai: 99% min.
Grade : Qualité pharmaceutique
Stockage: Ombres, conservation confinée

Fulvestrant also called Faslodex or AstraZeneca,is is a drug treatment of hormone receptor-positive metastatic breast cancer in postmenopausal women with disease progression following anti-estrogen therapy. It works by blocking the actions of estrogen in the body. Fulvestrant is a complete estrogen receptor antagonist with no agonist effects, which in addition, accelerates the proteasomal degradation of the estrogen receptor. The drug has poor oral bioavailability, and is administered monthly via intramuscular injection.Certain types of breast cancer use estrogen to grow and multiply in the body.do not use fulvestrant if you are allergic to any ingredient in fulvestrant ,and Contact your doctor or health care provider right away if any of these apply to you.

Many breast cancers are stimulated to grow by the female sex hormones oestrogen and progesterone. These breast cancers are called hormone sensitive or hormone receptor positive. Drugs that block the effects of these hormones can slow or stop the growth of the breast cancer cells. Fulvestrant stops oestrogen getting to the cancer cells by blocking oestrogen receptors and reducing the number of receptors the cancer cell has.

Fulvestrant Acetate (Faslodex, AstraZeneca) 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 by down-regulating the estrogen receptor.

Fulvestrant Acetate 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. The dosing schedule for fulvestrant remains under investigation in an attempt to optimize its effectiveness.

Test Item Spécification Résultats
Apparence A white powder Poudre blanche
Identification The retention time of the major peak in the chromatogram of the assay preparation is same as that of the standard preparation obtained in the assay Se conformer
Any Individual impurity Pas plus que 0.10% 0.18%
Total impurities Pas plus que 1.0% 0.44%
Ratio of isomers Fulvestran A 50.0%-60.0% 51.70%
Fulvestran B 40.0%-50.0% 47.86%
Pureté >99.0% 99.56%

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