JZP-361,99.72%
产品编号:Bellancom-121422| CAS NO:1680193-80-9| 分子式:C22H20ClN5O| 分子量:405.88
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JZP-361
产品介绍 | JZP-361是一种有效的、可逆的、选择性的人重组 MAGL (hMAGL) 抑制剂,IC50 为 46 nM。JZP-361 还具有抗组胺能活性,可用于哮喘的研究。 | ||||||||||||||||
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生物活性 | JZP-361 is a potent, reversible and selective inhibitor of human recombinant MAGL (hMAGL) with an IC50 of 46 nM. JZP-361 also shows antihistaminergic activities and can be used for asthma research. | ||||||||||||||||
体外研究 |
JZP-361 has almost 150-fold higher selectivity over human recombinant fatty acid amide hydrolase (hFAAH, IC50 = 7.24 μM) and 35-fold higher selectivity over human α/β-hydrolase-6 (hABHD6, IC50 = 1.79 μM). 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 | |||||||||||||||||
体内研究 | |||||||||||||||||
性状 | Solid | ||||||||||||||||
溶解性数据 |
In Vitro:
DMSO : 125 mg/mL (307.97 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 |