CAS NO: | 1914078-41-3 |
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 | eCF506 is a highly potent and orally bioavailable inhibitor of the non-receptor tyrosine kinaseSrcwith anIC50of less than 0.5 nM. | ||||||||||||||||
IC50& Target | IC50: less than 0.5 nM (Src)[1] | ||||||||||||||||
体外研究 (In Vitro) | eCF506 induces a very potent antiproliferative effect in both MCF7 and MDA-MB-231 cells. eCF506 inhibits phosphorylation of SRC and FAK at low nanomolar levels, with complete inhibition observed at 100 nM. eCF506 significantly reduces cell motility at 10 nM as early as 6 h into the study, with equivalent efficacy to dasatinib. eCF506 exclusively inhibits SFK, with subnanomolar IC50values against SRC and YES (IC50=0.5, 2.1 nM). It is important to highlight that eCF506 displays a vast difference in activity (>950-fold difference) between ABL and its primary target SRC[1]. | ||||||||||||||||
体内研究 (In Vivo) | eCF506 shows a moderate oral bioavailability (25.3%). A significant reduction of phospho-SRCY416is observed in the xenograft sections from mice treated with eCF506 relative to the untreated animal controls[1]. | ||||||||||||||||
分子量 | 510.63 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C26H38N8O3 | ||||||||||||||||
CAS 号 | 1914078-41-3 | ||||||||||||||||
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 : 62.5 mg/mL(122.40 mM;Need ultrasonic) H2O :< 0.1 mg/mL(insoluble) 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
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