CAS NO: | 1801333-55-0 |
包装 | 价格(元) |
10 mM * 1 mL in DMSO | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
100mg | 电议 |
生物活性 | PF-06952229 is a potent, selective and orally activeTGFbR1inhibitor. PF-06952229 specifically binds to TGFbR1 and prevents TGFbR1-mediated signal transduction. PF-06952229 is a promisingantineoplastic agentfor the study solid tumors, especifically metastatic breastcancer[1]. | ||||||||||||||||
IC50& Target | IC50: transforming growth factor-beta receptor 1 (TGFbR1)[1] | ||||||||||||||||
体内研究 (In Vivo) | PF-06952229 (oral gavage; 30 mg/kg; twice daily; 21 days) combines with Palbociclib 21 days results in an improved inhibition of pSMAD2 in the MCF7 ER+ xenograft breast cancer tumor model. This combination also leads to a significant increase in survival relative to PF-06952229 monotherapy[1].
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Clinical Trial | |||||||||||||||||
分子量 | 458.91 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C23H24ClFN4O3 | ||||||||||||||||
CAS 号 | 1801333-55-0 | ||||||||||||||||
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 : 50 mg/mL(108.95 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。 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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