CAS NO: | 1835667-12-3 |
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 | Rezivertinib (BPI-7711) is an orally active, highly selective and irreversible third-generationEGFRtyrosine kinase inhibitor (TKI). Rezivertinib exhibits high potency against the common activationEGFRand the resistance T790M mutations. Rezivertinib has excellent central nervous system (CNS) penetration and has antitumor activity[1][2]. | ||||||||||||||||
IC50& Target[1] |
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体外研究 (In Vitro) | Rezivertinib (BPI-7711) selectively inhibits cellular proliferation of EGFR mutations in cell lines: GI5013.3 nM (PC9, del19), 6.8 nM (HCC827, L858R), 22 nM (NCI-H1975, del19/T790M) and >1000 nM (A431, EGFR WT)[1]. | ||||||||||||||||
体内研究 (In Vivo) | Rezivertinib (BPI-7711; 6.25-25 mg/kg/day; orally; 14 days) shows significant tumor regression[2]. | ||||||||||||||||
Clinical Trial | |||||||||||||||||
分子量 | 486.57 | ||||||||||||||||
性状 | Solid | ||||||||||||||||
Formula | C27H30N6O3 | ||||||||||||||||
CAS 号 | 1835667-12-3 | ||||||||||||||||
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 : 125 mg/mL(256.90 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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