中国女人和老外的毛片_少妇激情作爱视频_成人无码区免费AⅤ片在线观看_国产freeXXXX性播放_欧美人与性囗牲恔配的起源

首頁(yè) > 產(chǎn)品目錄 > 信號(hào)通路 > Membrane Transporter/Ion Channel > ATP Synthase > 噁拉戈利

噁拉戈利

ChemLeader 98+%

Elagolix (NBI-56418)

產(chǎn)品編號(hào):CL2564 CAS No.:834153-87-6 MDLNo: 分子式:C32H30F5N3O5 分子量:631.59
規(guī)格 庫(kù)存 目錄價(jià) 會(huì)員專享價(jià) 數(shù)量
1 mg 3-5days ¥320.00 登錄后可見
- +
5 mg 3-5days ¥860.00 登錄后可見
- +
10 mg 3-5days ¥1350.00 登錄后可見
- +

化學(xué)品安全說明書(MSDS)

下載MSDS
  • 基本信息
  • 相關(guān)文檔
  • 產(chǎn)品詳情
  • 相關(guān)文獻(xiàn)
基本信息
英文名稱 Elagolix (NBI-56418)
中文名稱噁拉戈利
CAS號(hào)834153-87-6
分子式C32H30F5N3O5
分子量631.59
外觀White to off-white powder
儲(chǔ)存條件Dry, dark and at 0 - 4 ℃ for short term (days to weeks) or -20 ℃ for long term (months to years).
產(chǎn)品詳情

Elagolix (formerly NBI56418; ABT620; NBI-56418; ABT-620; trade name: Orilissa) is a potent, specific, orally bioavailable, non-peptide antagonist of the gonadotropin-releasing hormone receptor (GnRHR) used for pain management. It inhibits GnRHR with a Kd of 54 pM. Elagolix was given FDA approval on July 23, 2018, to treat endometriosis-related moderate to severe pain. A short-acting GnRH antagonist, elagolix suppresses ovarian estrogen production in a dose-dependent manner, resulting in partial suppression at lower doses and complete suppression at higher doses. Because Elagolix is non-peptide and readily absorbed through the mouth, it is considered the leader of a new class of GnRH inhibitors known as second-generation inhibitors.

相關(guān)文獻(xiàn)
抱歉,暫時(shí)沒有相關(guān)文獻(xiàn)
相關(guān)產(chǎn)品
抱歉,暫時(shí)沒有相關(guān)產(chǎn)品
在線客服
小德
021-58180488
小立
021-58180488
在線服務(wù)時(shí)間: 工作日 9:00-18:00