JHU37160,99.83%
产品编号:Bellancom-131881| CAS NO:2369979-68-8| 分子式:C19H20ClFN4| 分子量:358.84
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JHU37160
产品介绍 | JHU37160 是一种有效和可透过血脑屏障的 DREADD 激动剂,对 hM3Dq 和 hM4Di DREADDs 的 EC50 值分别为 18.5 nM 和 0.2 nM。JHU37160 在小鼠脑组织中表现出来自 DREADDs 的选择性 [3H]Clozapine 置换作用,而不来自其他 Clozapine 结合部位。 | ||||||||||||||||
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生物活性 | JHU37160 is a potent and brain-penetrant DREADD agonist, with EC50s of 18.5 nM and 0.2 nM for hM3Dq and hM4Di DREADDs in HEK-293 cells, respectively. JHU37160 exhibits selective [3H]Clozapine displacement from DREADDs and not from other Clozapine-binding sites in mice brain tissue. | ||||||||||||||||
体外研究 |
JHU37160 displays high DREADD affinity, with Kis of 1.9 nM and 3.6 nM for hM3Dq and hM4Di expressed in mouse brain sections. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
JHU37160 (0.1 mg/kg; i.p.) exhibits high DREADD occupancy in mice and rats. 西域 has not independently confirmed the accuracy of these methods. They are for reference only. | ||||||||||||||||
体内研究 |
JHU37160 (0.1 mg/kg; i.p.) exhibits high DREADD occupancy in mice and rats. 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 : 50 mg/mL (139.34 mM; Need ultrasonic) 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。 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 |