CAS NO: | 59831-65-1 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
25mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
500mg | 电议 |
生物活性 | Halopemide is a potentphospholipaseD (PLD)inhibitor, withIC50s of 220 and 310 nM for human PLD1 and PLD2, respectively. Halopemid is adopamine receptorsantagonist, and acts a psychotropic agent[1][2]. | ||||||||||||||||
IC50& Target[1][2] |
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体外研究 (In Vitro) | Halopemide (1-2 μM; 21 day) affects calcification in transdifferentiated MOVAS cells[3]. | ||||||||||||||||
体内研究 (In Vivo) | Halopemide (10 mg/kg; p.o.) induces dyskinesias in the majority of monkeys tested[2]. | ||||||||||||||||
分子量 | 416.88 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C21H22ClFN4O2 | ||||||||||||||||
CAS 号 | 59831-65-1 | ||||||||||||||||
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 : 41.67 mg/mL(99.96 mM;Need ultrasonic) 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。 |