CAS NO: | 1396337-04-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Auglurant (VU0424238) is a novel and selectivemGlu5antagonist with anIC50value of 11 nM (rat) and anIC50value of 14 nM (human). Auglurant (VU0424238) has an acceptable CNS penetration[1]. | ||||||||||||||||
IC50& Target |
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体外研究 (In Vitro) | Auglurant (VU0424238) with an IC50value of 14 nM in HEK293A cells. It also binding a known allosteric site with Kivalue of 4.4 nM in HEK293A cells. | ||||||||||||||||
体内研究 (In Vivo) | Auglurant (VU0424238) had a clearance of 19.3 mL/min/kg in rats and demonstrates 50% mGlu5 PET ligand occupancy at an oral dose of 0.8 mg/kg in rats. Plus, it also had a clearance of 15.5 mL/min/kg in cynomolgus monkeys and demonstrates 50% mGlu5 PET ligand occupancy at an oral dose of 0.06 mg/kg in baboons[1]. | ||||||||||||||||
分子量 | 325.30 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C16H12FN5O2 | ||||||||||||||||
CAS 号 | 1396337-04-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
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溶解性数据 | In Vitro: DMSO : 22.73 mg/mL(69.87 mM;Need ultrasonic) 配制储备液
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以下溶剂前显示的百
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