Nome del prodotto: Goserelin
Sinonimi: SALE ACETATO DI GOSERELIN;(D-BE(TBU)6,AZAGLY10)-SALE ACETATO DELL'ORmone CHE RILASCIA GONADOTROPINA;(D-BE(TBU)6,AZAGLY10)-SALE ACETATO LHRH;(D-BE(TBU)6,AZAGLY10)-SALE ACETATO FATTORE DI RILASCIO ORMONALE LUTEINIZZANTE;(D-BE(TBU)6,AZAGLY10)-SALE ACETATO DELL'ORmone luteinizzante;PYR-HIS-TRP-SER-TYR-D-SER(TBU)-SALE ACETATO LEU-ARG-PRO-AZAGLY-NH2;2-(amminocarbonile)idrazide;decapeptidei
CAS: 65807-02-5
MF: C61H88N18O16
MW: 1329.46
Goserelin is an analog of luteinizing hormone-releasing hormone (LHRH) useful in the treatment of malignancies responsive to hormonal manipulation. Administered parenterally in a biodegradable depot, goserelin is reportedly as effective as orchidectomy and oophorectomy in patients with advanced prostate carcinoma and pre-menopausal breast cancer.
1. Gonadorelina è un altro nome per l'ormone di rilascio delle gonadotropine (GnRH). È un decapeptide sintetico preparato utilizzando la sintesi peptidica in fase solida. GnRH is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary.
2. Il GnRH è disponibile come gonadorelina cloridrato )e gonadorelina diacetato tetraidrato per uso iniettabile. Studies have described it being used via an infusion pump system to induce ovulation in patients with hypothalamic hypogonadism. Viene utilizzato anche in medicina veterinaria come trattamento per i bovini affetti da malattia cistica dell'ovaio.
3. Gonadorelin is responsible for the release of follicle stimulating hormone and leutinizing hormone from the anterior pitutitary. In the pituitary GnRH stimulates synthesis and release of FSH and LH, a process that is controlled by the frequency and amplitude of GnRH pulses, as well as the feedback of androgens and estrogens.
Uomini
Palliative treatment of advanced carcinoma of the prostate; in combination with flutamide for management of locally confined stage T2b to T4 (stage B2 to C) carcinoma of the prostate.
Donne (3.6 mg only)
Palliative treatment of advanced breast cancer in pre- and perimenopausal women; treatment of endometriosis; as an endometrial thinning agent prior to endometrial ablation for dysfunctional uterine bleeding.