CAS NO: | 315694-89-4 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
200mg | 电议 |
生物活性 | TC-DAPK 6 is a potent, ATP-competitive, and highly selectiveDAPKinhibitor (IC50=69 and 225 nM againstDAPK1andDAPK3, respectively, with 10 μM ATP). | ||||||||||||||||
IC50& Target | IC50: 69 nM (DAPK1), 225 nM (DAPK3)[1] | ||||||||||||||||
体外研究 (In Vitro) | TC-DAPK 6 is found to be the most potent Death-associated protein kinase (DAPK) inhibitor with enzyme selectivity. When assayed with 10 μM ATP, the IC50values for DAPK1 and DAPK3 are 69 and 225 nM, respectively. TC-DAPK 6 also inhibits p70S6K (1 μM< IC50< 10 μM)[1]. | ||||||||||||||||
分子量 | 276.29 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C17H12N2O2 | ||||||||||||||||
CAS 号 | 315694-89-4 | ||||||||||||||||
运输条件 | Room temperature in continental US; may vary elsewhere. | ||||||||||||||||
储存方式 |
| ||||||||||||||||
溶解性数据 | In Vitro: DMSO : 18.67 mg/mL(67.57 mM;Need ultrasonic and warming) 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
*以上所有助溶剂都可在本网站选购。 |