CAS NO: | 2664214-60-0 |
包装 | 价格(元) |
1mg | 电议 |
5mg | 电议 |
10mg | 电议 |
50mg | 电议 |
生物活性 |
BI-4020 is a fourth-generation, orally active, and non-covalentEGFRtyrosine kinase inhibitor. BI-4020 inhibits not only the triple mutantEGFRdel19 T790M C797S variant (IC50=0.2 nM in BaF3 cell lines) but also the double mutantEGFRdel19 T790M and primary mutantEGFRdel19 (IC50=1 nM). BI-4020 also shows activity againstEGFRwt (IC50=190 nM). BI-4020 shows high kinome selectivity and good DMPK properties[1]. |
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IC50& Target[1] |
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体外研究 (In Vitro) |
BI-4020 inhibits p-EGFR del19 T790M C797S with an IC50of 0.6 nM[1].
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体内研究 (In Vivo) |
BI-4020 leads to tumor regressions in the human PC-9 (EGFR del19 T790M C797S) triple mutant NSCLC xenograft model in mice[1].
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分子量 |
542.68 |
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性状 |
Solid |
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Formula |
C30H38N8O2 |
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CAS 号 |
2664214-60-0 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
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溶解性数据 |
In Vitro:
DMSO : 250 mg/mL(460.68 mM;Need ultrasonic) 1M HCl : 100 mg/mL(184.27 mM;ultrasonic and adjust pH to 1 with HCl)
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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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