| 常用名 | 恶拉戈利 | CAS号 | 834153-87-6 |
|---|---|---|---|
| 价格 | ¥需询单/1kg ¥需询单/1g ¥需询单/1mg | 纯度 | 98.0% |
| 备货期 | 需询单 | 库存 | 询单 |
| 产品详情(用途,包装等)
用途: Elagolix is a highly potent, selective, orally-active, short-duration, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) (KD = 54 pM).Target: GnRHin vitro: Elagolix is a short-acting, nonpeptide, GnRH antagonist, administered orally, that unlike injectable depot GnRH agonists and antagonists, produces a dose-dependent suppression of ovarian estrogen production, that is, from partial suppression at lower doses to full suppression at higher doses. Elagolix is regarded as the frontrunner of a new class of GnRH inhibitors that have been denoted as second-generation, due to their non-peptide nature and oral bioavailability. 物理化学性质: CAS号:834153-87-6 常用中文名:恶拉戈利 常用英文名:elagolix 分子式:C32H30F5N3O5 分子量:631.590 密度:1.4±0.1 g/cm3 沸点:728.6±70.0 °C at 760 mmHg 熔点:N/A 闪点:394.5±35.7 °C 储存条件:2-8℃ |