Mardepodect PF-2545920,99.69%
产品编号:Bellancom-50098| CAS NO:898562-94-2| 分子式:C25H20N4O| 分子量:392.45
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Mardepodect PF-2545920
产品介绍 | Mardepodect (PF-2545920) 是一种有效的,口服活性的,选择性的 PDE10A 抑制剂,IC50 为 0.37 nM,比作用于其他 PDE 选择性高 1000 多倍。Mardepodect 可穿过血脑屏障。 | ||||||||||||||||
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生物活性 | Mardepodect (PF-2545920) is a potent, orally active and selective PDE10A inhibitor with an IC50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect can cross the blood-brain barrier. | ||||||||||||||||
体外研究 | |||||||||||||||||
体内研究 |
In the conditioned avoidance response assay (CAR), Mardepodect (PF-2545920) is active with an ED50 of 1 mg/kg. Administration of Mardepodect (PF-2545920) to mice causes a dose dependent increase in striatal cGMP. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
In the conditioned avoidance response assay (CAR), Mardepodect (PF-2545920) is active with an ED50 of 1 mg/kg. Administration of Mardepodect (PF-2545920) to mice causes a dose dependent increase in striatal cGMP. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : ≥ 45 mg/mL (114.66 mM) * "≥" means soluble, but saturation unknown. 配制储备液
*
请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂:
——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用;
以下溶剂前显示的百
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运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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参考文献 |
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海关编码 | 2933990090 |
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~57% ![]() 898562-94-2 |
文献:Pfizer Inc Patent: US2006/154931 A1, 2006 ; Location in patent: Page/Page column 24-25 ; |
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