CAS NO: | 2616821-91-9 |
包装 | 价格(元) |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | PERK-IN-5 is a highly potent, selectively and orally bioavailablePERKinhibitor (IC50s of 2 and 9 nM forPERKand p-eIF2α, respectively). PERK-IN-5 can significantly inhibit tumor growth in the 786-O renal cell carcinoma xenograft tumor model[1]. | ||||||||||||||||
IC50& Target | IC50: 2 nM (PERK), 9 nM (p-eIF2α)[1] | ||||||||||||||||
体外研究 (In Vitro) | PERK-IN-5 (compound 28) (10-48 μM) is relatively stable in both human and dog hepatocytes and is characterized with long half-lives[1]. | ||||||||||||||||
体内研究 (In Vivo) | PERK-IN-5 (3-100 mg/kg; p.o.; 0.25-24 hours) has robust pharmacokinetics in CD1 mice, with Cmaxof 3353 ng/mL, AUC0-lastof 5153 h*ng/mL, and bioavailability of 70%[1].
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分子量 | 468.50 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C25H26F2N4O3 | ||||||||||||||||
CAS 号 | 2616821-91-9 | ||||||||||||||||
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 : 250 mg/mL(533.62 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。 |