CAS NO: | 2243882-74-6 |
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 |
生物活性 | WEE1-IN-5 is a potentWEE1inhibitor with anIC50value of 0.8 nM. WEE1-IN-5 inhibits phospho-CDC2. WEE1-IN-5 abrogates the G2 check point, increasing sensitivity to DNA damaging agents incancercells. WEE1-IN-5 can be used for researching anticancer[1]. | ||||||||||||||||
IC50& Target | IC50: 0.8 nM (WEE1), 188 nM (CDC2)[1] | ||||||||||||||||
体外研究 (In Vitro) | WEE1-IN-5 exhibits an EC50of 188 nM in pCDC2 and an IC50shift for CYP3A4/5[1]. | ||||||||||||||||
体内研究 (In Vivo) | WEE1-IN-5 (5mg/kg for PO; 1 mg/kg for IV; single dosage) exhibits a CL of 14 mL/min/kg, an AUCint1324 h·ng/mL and bioavailability of 35% in SD rats[1]. | ||||||||||||||||
分子量 | 511.45 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H28Cl2N6O | ||||||||||||||||
CAS 号 | 2243882-74-6 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 20 mg/mL(39.10 mM;ultrasonic and warming and heat to 60℃) 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。 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
|