CAS NO: | 2244987-03-7 |
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 |
生物活性 | CDK12-IN-2 is a potent, selective and nanomolarCDK12inhibitor (IC50=52 nM) with good physicochemical properties. CDK12-IN-2 is also a strongCDK13 inhibitordue toCDK13is the closest homologue ofCDK12. CDK12-IN-2 shows excellent kinase selectivity forCDK12overCDK2, 9, 8, and 7. CDK12-IN-2 inhibits the phosphorylation of Ser2 in the C-terminal domain of RNA polymerase II. CDK12-IN-2 can be used an excellent chemical probe for functional studies ofCDK12[1]. | ||||||||||||||||
IC50& Target[1] |
| ||||||||||||||||
体外研究 (In Vitro) | CDK12-IN-2 inhibits the phosphorylation of the CTD Ser2 in SK-BR-3 cells at low submicromolar concentrations, it inhibits C-terminal domain ser2 phosphorylation with an IC50of 185 nM. And CDK12-IN-2 exhibits a growth inhibition with an IC50of 0.8 μM in SK-BR-3 cells[1].CDK12-IN-2 exhibits time dependency for CDK12 inhibition, the IC50value for CDK12-IN-2 are 0.0078 μM, 0.042 μM, 0.057 μM,and 0.059 μM, for 0h, 1h, 2h and 5h respectively[1]. | ||||||||||||||||
分子量 | 532.64 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C32H32N6O2 | ||||||||||||||||
CAS 号 | 2244987-03-7 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 50 mg/mL(93.87 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
|