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IPSU

    
≥98%

IPSU

源叶(MedMol)
S83032 一键复制产品信息
1373765-19-5
C23H27N5O2
405.4928
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S83032-5mg
≥98%

¥520.00

货期:3-5天 - - - -
S83032-10mg
≥98%

¥710.00

货期:3-5天 - - - -
S83032-25mg
≥98%

¥1260.00

货期:3-5天 - - - -
S83032-50mg
≥98%

¥1830.00

货期:3-5天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: IPSU is a selective, orally available and brain penetrant OX2R antagonist with a pKi of 7.85.
靶点: pKi: 7.85 (OX2R), 6.29 (OX1R);OXReceptor
体外研究: Orexin receptor antagonists represent attractive targets for the development of drugs for the treatment of insomnia. IPSU binds rapidly and reaches equilibrium very quickly in binding and/or functional assays
体内研究: IPSU has low blood clearance, shows high maximal blood exposure and AUC after oral dosing. It exhibits an acceptable absolute oral bioavailability and a brain/blood concentration ratio that indicated favorable brain penetration. IPSU increases sleep when dosed during the mouse active phase (lights off); IPSU induces sleep primarily by increasing NREM sleep. IPSU shows a fast onset of action, with a clear increase in total sleep time during the first hour afterdosing. The effect lasts 4-5 h, after which time the total sleep time per hour is the same as on vehicle day
参考文献: 1. Betschart C, et al. Identification of a novel series of orexin receptor antagonists with a distinct effect on sleeparchitecture for the treatment of insomnia. J Med Chem. 2013 Oct 10;56(19):7590-607. 2. Callander GE, et al. Kinetic properties of 'dual' orexin receptor antagonists at OX1R and OX2R orexin receptors. Front Neurosci. 2013 Dec 3;7:230. 3. Hoyer D, et al. Distinct effects of IPSU and suvorexant on mouse sleep architecture. Front Neurosci. 2013 Dec 10;7:235.
溶解性: soluble  in  DMSO
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.466 ml 12.331 ml 24.661 ml
5 mM 0.493 ml 2.466 ml 4.932 ml
10 mM 0.247 ml 1.233 ml 2.466 ml
50 mM 0.049 ml 0.247 ml 0.493 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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