Molecular Formula | C29H27F2N7O5S |
Molar Mass | 623.63 |
Density | 1.442±0.06 g/cm3(Predicted) |
Melting Point | 228 °C (decomp)(Solv: ethyl acetate (141-78-6); tetrahydrofuran (109-99-9)) |
Storage Condition | 2-8℃ |
Use | Relugolix, chemical name is N-(4-(1-(2, 6-difluorobenzyl)-5-((dimethylamino) methyl))-3-(6-methoxy-3-pyridazinyl)-2, 4-dioxo-1, 2,3, 4-tetrahydrothieno [2,3-d] pyrimidin-6-yl) phenyl)-N'-methoxyurea. It is a new drug jointly developed by Myovant company and Wutian Pharmaceutical (Takeda), is a small molecule gonadotropin releasing hormone (GnRH) receptor antagonist, has the potential for uterine fibroids, endometriosis, prostate cancer and other indications. |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.604 ml | 8.018 ml | 16.035 ml |
5 mM | 0.321 ml | 1.604 ml | 3.207 ml |
10 mM | 0.16 ml | 0.802 ml | 1.604 ml |
5 mM | 0.032 ml | 0.16 ml | 0.321 ml |
currently, relugoli has been evaluated in nearly 1600 study participants in Phase 1, Phase 2, and phase 3 clinical trials. Relugolix, when taken orally once daily, can rapidly reduce estrogen and progesterone levels in women. The safety and efficacy of Relugolix was compared with that of leuprorelin in the treatment of uterine fibrosis in menorrhagia through a series of phase III clinical studies conducted in Japan, as well as the safety and effectiveness of the above two drugs in the treatment of pain symptoms associated with uterine fibrosis, the safety and effectiveness of relugolix for uterine fibroids were finally confirmed. In addition, a phase II clinical study of endometriosis and prostate cancer in relugolix has been conducted by Wutian Pharmaceutical, which confirmed that relugolix can significantly reduce the pain caused by endometriosis, it also reduces serum testosterone to castrate levels and significantly reduces prostate-specific antigen (PSA).