分子式: C7H7N2O3F ,分子量: 186.14048,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.
货号 | 规格 | 数量 | 价格 |
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Q-0022343 | 100mg |
1
|
询价 |
Q-0022343 | 250mg |
1
|
询价 |
Q-0022343 | 500mg |
1
|
询价 |
Q-0022343 | 1g |
1
|
询价 |
Q-0022343 | 5g |
1
|
询价 |
参数信息 | |
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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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32487-58-4 3-methoxyfuran-2-carbaldehyde 中间体分子
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32487-58-4 3-methoxyfuran-2-carbaldehyde 中间体分子
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分子式:C25H29N7O3 , 分子量:475.54286,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: C6H9N3O2S.C6H6O3S, 分子量: 345.3946,Omarigliptin(MK-3102) is a potent, selective and long-acting DPP-4 inhibitor with IC50 of 1.6 nM; highly selective over all proteases tested (IC50 > 67 μM).IC50 value: 1.6 Nm.