TAK-915,99.74%
产品编号:Bellancom-103493| CAS NO:1476727-50-0| 分子式:C19H18F4N4O5| 分子量:458.36
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TAK-915
产品介绍 | TAK-915 是一种有效的,选择性的,可透过血脑屏障和口服活性的 PDE2A抑制剂,IC50 为 0.61 nM。TAK-915 对 PDE2A的选择性是 PDE1A 的 4100 倍以上。TAK-915 可用于神经精神疾病和神经退行性疾病的研究。 | ||||||||||||||||
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生物活性 | TAK-915 is a potent, selective, brain-penetrant and orally active phosphodiesterase 2A (PDE2A) inhibitor with an IC50 of 0.61 nM. TAK-915 is >4100-fold more selectivity for PDE2A than PDE1A. TAK-915 has the potential for neuropsychiatric and neurodegenerative disorders treatment. | ||||||||||||||||
体外研究 | |||||||||||||||||
体内研究 |
TAK-915 (3 mg/kg; oral administration; daily; for 4 days; male F344 rats) treatment significantly reduces escape latency in aged rats in the Morris water maze task. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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体内研究 |
TAK-915 (3 mg/kg; oral administration; daily; for 4 days; male F344 rats) treatment significantly reduces escape latency in aged rats in the Morris water maze task. 西域 has not independently confirmed the accuracy of these methods. They are for reference only.
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性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 7.5 mg/mL (16.36 mM; ultrasonic and warming and heat to 60°C) 配制储备液
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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。 | ||||||||||||||||
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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