分子式:C20H16N5O3F ,分子量:393.37114,Osimertinib (AZD9291) is an oral, irreversible, and mutant-selective EGFR inhibitor with IC50 of 12.92, 11.44 and 493.8 nM for Exon 19 deletion EGFR, L858R/T790M EGFR, and WT EGFR in LoVo cells, respectively. Phase 4.
| 货号 | 规格 | 数量 | 价格 | 
|---|---|---|---|
| Q-0022315 | 100mg | 
                                                     
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| Q-0022315 | 250mg | 
                                                     
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| Q-0022315 | 500mg | 
                                                     
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| Q-0022315 | 1g | 
                                                     
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| Q-0022315 | 5g | 
                                                     
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											| 参数信息 | |
|---|---|
| 外观状态: | 固体或粉末 | 
| 质量指标: | 95%+ | 
| 溶解条件: | 有机溶剂/水 | 
| CAS号: | N/A | 
| 分子量: | N/A | 
| 储存条件: | -20℃避光保存 | 
| 储存时间: | 1年 | 
| 运输条件: | 室温2周 | 
| 生产厂家: | 西安齐岳生物科技有限公司 | 
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西安齐岳生物科技有限公司提供 CEP-40783,CAS:1437321-24-8 外观N/A 分子量N/A 仅供科研使用!
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西安齐岳生物科技有限公司提供 CEP-40125;RXDX-107,CAS:1456608-94-8 外观N/A 分子量N/A 仅供科研使用!
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分子式:C25H31N7O , 分子量:445.55994,Osimertinib (AZD9291) is an oral, irreversible, and mutant-selective EGFR inhibitor with IC50 of 12.92, 11.44 and 493.8 nM for Exon 19 deletion EGFR, L858R/T790M EGFR, and WT EGFR in LoVo cells, respectively. Phase 3.
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分子式:C18H17N3O2,分子量:307.34648,纯度: > 98%,溶解性: (R.T.: 25℃): DMSO,Orteronel(TAK-700) was selected as a candidate for clinical evaluation. orteronel (TAK-700) is currently in phase III clinical trials for the treatment of castration-resistant prostate cancer.
 




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