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BAY-60-7550

    
10mM in DMSO

Bay 60-7550

源叶(MedMol)
V53636 一键复制产品信息
439083-90-6
C27H32N4O4
476.57
Bay 60-7550
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V53636-1ml
10mM in DMSO

¥1040.00

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: Bay 60-7550 is a potent and selective PDE2 inhibitor with a Ki of 3.8 nM.
靶点: Ki: 3.8±0.2 nM (PDE2);PDE
体内研究: The PDE2 inhibitors Bay 60-7550 (1 mg/kg) reverses restraint stress-induced alterations in behavior, resulting in increased percentages of open-arm entries and open-arm time compared with the vehicle + restraint stress condition. In nonstressed mice, Bay 60-7550 produces a dose-dependent increase in percentages of open-arm entries and open-arm time compared with the vehicle-treated group; significant increases are observed at a dose of 3 mg/kg. In nonstressed mice, Bay 60-7550 increases, in a dose-dependent manner, the number of head-dips and time spent head-dipping, compared with vehicle-treated mice; significant increases are observed at doses of 1 and 3 mg/kg
参考文献: 1. Masood A, et al. Anxiolytic effects of phosphodiesterase-2 inhibitors associated with increased cGMP signaling. J Pharmacol Exp Ther. 2009 Nov;331(2):690-9. 2. Bubb KJ, et al. Inhibition of phosphodiesterase 2 augments cGMP and cAMP signaling to ameliorate pulmonary hypertension. Circulation. 2014 Aug 5;130(6):496-507.
溶解性: Soluble  in  DMSO
保存条件: -80℃(运输条件:冰袋低温运输)
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.098 ml 10.492 ml 20.983 ml
5 mM 0.42 ml 2.098 ml 4.197 ml
10 mM 0.21 ml 1.049 ml 2.098 ml
50 mM 0.042 ml 0.21 ml 0.42 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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