Nome: Triptorelina
Sinônimos em inglês: pglu-his-trp-ser-Tyr-d-trp-leu-arg-pro-gly-NH2; PYROGLU-HIS-TRP-SER-TYR-D-TRP-LEU-ARG-PRO-GLYNH2
CAS não. : 57773-63-4
Fórmula molecular: C64H82N18O13
Peso molecular: 1311.47
EINECS não. : 637-328-4
Triptorelina, um decapeptídeo (pGlu-His-Trp-Ser-Tyr-D-Trp-Leu-Arg-PRO-Gly-NH2), é um agonista do hormônio liberador de gonadotrofina (Agonista de GnRH) usado como sais de acetato ou pamoato. Ao causar estimulação constante da hipófise, diminui a secreção hipofisária de gonadotrofinas, hormônio luteinizante (ES) e hormônio folículo estimulante (FSH). Como outros agonistas do GnRH, triptorelina pode ser usada no tratamento de cânceres responsivos a hormônios, como câncer de próstata ou câncer de mama, puberdade precoce, condições dependentes de estrogênio (como endometriose ou miomas uterinos), e na reprodução assistida. Triptorelin is marketed under the brand names Decapeptyl (Ipsen) and Diphereline and Gonapeptyl (Ferring Pharmaceuticals).
Triptorelin is a synthetic agonist analog of gonadotropin releasing hormone (GnRH). Animal studies comparing triptorelin to native GnRH found that triptorelin had 13 fold higher releasing activity for luteinizing hormone, and 21-fold higher releasing activity for follicle-stimulating hormone.
Triptorelin is a man-made form of a hormone that regulates many processes in the body. The Trelstar brand of triptorelin is used in men to treat the symptoms of prostate cancer. Trelstar treats only the symptoms of prostate cancer and does not treat the cancer itself.
Clinically, it is mainly used for the treatment of endometriosis, hormone-dependent prostate cancer, câncer de mama, children's true precocious puberty, and can also be used for assisted fertility technology. The main adverse reactions of triprorelin are as follows: urinary disorders, breast swelling and pain, bone pain, etc., may also occur in the early treatment of men, ondas de calor, hypolibido and impotence. Atrophy of breasts and testicles in rare male female and sleep disorder. A small amount of vaginal bleeding may occur in girls during the first week of treatment and may be corrected by short-term additional therapy. Hot flashes, bleeding or bleeding spots, vaginal dryness, headache and weakness may occur during treatment in women, and abdominal and/or pelvic pain may occur when gonadotropins are used in combination. Slight loss of trabecular matrix may occur as estrogen concentration decreases to postmenopausal levels. It usually returns to normal six to nine months after treatment stops. Patients with endometriosis may have irreversible amenorrhea after medication.
| Impureza Única (HPLC) |
1.0%máx. |
| Composição de aminoácidos |
±10% do teórico |
| Conteúdo Peptídico (N%) |
≥80,0% |
| Conteúdo de água(Carlos Fischer) |
≤6,0% |
| Conteúdo de acetato (HPIC) |
≤15,0% |
| EM(ESI) |
Consistente |
| Balanço de Massa |
95.0~105,0% |
| Rotação Específica (20/D) |
-65.0~-75.0°(c=0,5 1%HAc) |