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S86365

TAK-385

源叶(MedMol) 98%
  • 英文名:
  • TAK-385
  • 别名:
  • Relugolix
  • CAS号:
  • 737789-87-6
  • 分子式:
  • C29H27F2N7O5S
  • 分子量:
  • 623.63
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S86365-1mg 98% ¥320.00元 >10 0 0 0 EA 加入购物车
源叶(MedMol) S86365-5mg 98% ¥432.00元 >10 0 0 0 EA 加入购物车
源叶(MedMol) S86365-10mg 98% ¥768.00元 >10 0 0 0 EA 加入购物车
源叶(MedMol) S86365-25mg 98% ¥1560.00元 >10 0 0 0 EA 加入购物车
源叶(MedMol) S86365-100mg 98% ¥3600.00元 >10 0 0 0 EA 加入购物车
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相关产品

  • 产品描述: Relugolix (TAK-385) is a potent, orally active, nonpeptidic gonadotropin-releasing hormone (GnRH) antagonist. Relugolix possesses high affinity and potent antagonistic activity for human receptor (binding IC50=0.33 nM) and monkey receptor (IC50=0.32 nM) compared with TAK-013 (HY-100209). Relugolix is used for the study of sex-hormone-dependent diseases, such as including endometriosis, uterine fibroids and prostate cancer et al
  • 靶点: IC50: 0.33 nM (human GnRH) IC50: 0.32 nM (monkey GnRH)
  • 体内研究: Relugolix (oral administration; 1-3 mg/kg; single dose for pharmacokinetic study) exhibits a good pharmacokinetic profile and obvious suppressive effects of circulating LH levels in monkeys at a dose of 1 mg/kg. The pharmacokinetic profile exhibits with 16.0 ng/mL, 2.7 h, and 90.1 ng for Cmax, Tmax, and AUCo, respectively in male cynomolgus monkeys Relugolix (oral administration; 3, 10 or 30 mg/kg; twice daily; 4 weeks) significantly decreases the testis weight, and reduces the ventral prostate weight at 3 mg/kg and decreases it to castrate levels at 10 mg/kg in male hGNRHR-knock-in mice. Relugolix (oral administration; 30, 100 or 200 mg/kg; twice daily; 4 weeks) induces constant diestrous phases in all mice within the first week at 100 mg/kg, and significantly decreases the weights of ovaries and uteri at this dose after 4 weeks in female hGNRHR-knock-in mice
  • 参考文献:
    1. Kazuhiro Miwa, et al. Discovery of 1-{4-[1-(2,6-Difluorobenzyl)-5-[(dimethylamino)methyl]-3-(6-methoxypyridazin-3-yl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl]phenyl}-3-methoxyurea (TAK-385) as a Potent, Orally Active, Non-Peptide Antagonis 2. Daisuke Nakata, et al. Suppression of the hypothalamic-pituitary-gonadal axis by TAK-385 (relugolix), a novel, investigational, orally active, small molecule gonadotropin-releasing hormone (GnRH) antagonist: studies in human GnRH receptor knock-in mice. E
  • 溶解性: Soluble  in  DMSO
  • 保存条件: 2-8℃
  • 配置溶液浓度参考:
    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
    50 mM 0.032 ml 0.16 ml 0.321 ml
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质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子量 (g/mol)


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