上海金畔生物科技有限公司为生命科学和医药研发人员提供生物活性分子抑制剂、激动剂、特异性抑制剂、化合物库、重组蛋白,专注于信号通路和疾病研究领域。
Almonertinib (Synonyms: 阿美替尼; HS-10296) 纯度: 99.84%
Almonertinib (HS-10296) 是一种口服、不可逆的第三代 EGFR 酪氨酸激酶抑制剂,对 EGFR 致敏和 T790M 耐药突变具有高选择性。Almonertinib 对 T790M、T790M/L858R 和 T790M/Del19 表现出较强的抑制活性 (IC50 分别为 0.37、0.29 和 0.21 nM),对野生型的抑制作用较弱 (3.39 nM)。Almonertinib 用于非小细胞肺癌的研究。
Almonertinib Chemical Structure
CAS No. : 1899921-05-1
规格 | 价格 | 是否有货 | 数量 |
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10 mM * 1 mL in DMSO | ¥2890 | In-stock | |
5 mg | ¥2500 | In-stock | |
10 mg | ¥4000 | In-stock | |
25 mg | ¥7500 | In-stock | |
50 mg | ¥10500 | In-stock | |
100 mg | ¥14500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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Almonertinib 相关产品
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生物活性 |
Almonertinib (HS-10296) is an orally available, irreversible, third-generation EGFR tyrosine kinase inhibitor with high selectivity for EGFR-sensitizing and T790M resistance mutations. Almonertinib shows great inhibitory activity against T790M, T790M/L858R and T790M/Del19 (IC50: 0.37, 0.29 and 0.21 nM, respectively), and is less effective against wild type (3.39 nM). Almonertinib is used for the research of the non-small cell lung cancer[1][2]. |
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IC50 & Target[1] |
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体外研究 (In Vitro) |
HS-10296 is an orally available inhibitor of the epidermal growth factor receptor (EGFR) mutant form T790M, with potential antineoplastic activity, which canbe used to treat NSCLC[2]. Additionaly, HS-10296 could also inhibit other EGFR sensitive mutations, including G719X, del19, L858R and L861Q[3]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. |
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Clinical Trial |
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分子量 |
525.64 |
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Formula |
C30H35N7O2 |
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CAS 号 |
1899921-05-1 |
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中文名称 |
阿美替尼 |
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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 : ≥ 83.33 mg/mL (158.53 mM) * “≥” means soluble, but saturation unknown. 配制储备液
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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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参考文献 |
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