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Usmarapride

    
10mM in DMSO

源叶(MedMol)
V57170 一键复制产品信息
1428862-33-2
C23H31N5O6
473.53
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
V57170-1ml
10mM in DMSO

¥3360.00

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: Usmarapride (SUVN-D4010) is a potent, selective, orally active and brain penetrant 5-HT4 receptor partial agonist (EC50=44 nM). Usmarapride (SUVN-D4010) can be used for the research of cognitive deficits associated with Alzheimer's disease.
靶点: 5-HT4 Receptor:44 nM (EC50)
体外研究: Usmarapride (SUVN-D4010) (1-3 mg/kg; p.o.; Male Wistar rats 10-12 weeks old) attenuates the long-term memory deficits in object recognition test (ORT)[1].
Usmarapride (1, 3, and 10 mg/kg; p.o.) significantly reverses the scopolamine-induced amnesia[1].
Usmarapride shows a statistically significant effect at 3.0 mg/kg on both exploration time and recognition index[1].
Usmarapride (SUVN-D4010) shows good oral exposures, good bioavailability, and good brain exposures in rats[1].
Pharmacokinetic of Usmarapride in Rats[1]
(3.0 mg/kg for p.o. dosing; 1.0 mg/kg for i.v.)
体内研究: Usmarapride (SUVN-D4010) (1-3 mg/kg; p.o.; Male Wistar rats 10-12 weeks old) attenuates the long-term memory deficits in object recognition test (ORT).
Usmarapride (1, 3, and 10 mg/kg; p.o.) significantly reverses the scopolamine-induced amnesia.
Usmarapride shows a statistically significant effect at 3.0 mg/kg on both exploration time and recognition index.
Usmarapride (SUVN-D4010) shows good oral exposures, good bioavailability, and good brain exposures in rats.
Pharmacokinetic of Usmarapride in Rats
(3.0 mg/kg for p.o. dosing; 1.0 mg/kg for i.v.)
保存条件: -80°C 12个月; -20°C 6个月, 干燥
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.112 ml 10.559 ml 21.118 ml
5 mM 0.422 ml 2.112 ml 4.224 ml
10 mM 0.211 ml 1.056 ml 2.112 ml
50 mM 0.042 ml 0.211 ml 0.422 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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