分子式:C16H16ClF3N4O2, 分子量:388.77,Rociletinib (CO-1686, AVL-301) is an irreversible, mutant-selective EGFR inhibitor with Ki of 21.5 nM and 303.3 nM for EGFRL858R/T790M and EGFRWT in cell-free assays, respectively. Phase 2.
货号 | 规格 | 数量 | 价格 |
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Q-0022412 | 100mg |
1
|
询价 |
Q-0022412 | 250mg |
1
|
询价 |
Q-0022412 | 500mg |
1
|
询价 |
Q-0022412 | 1g |
1
|
询价 |
Q-0022412 | 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: C13H19N3O2 ,分子量: 249.30886,Rociletinib (CO-1686, AVL-301) is an irreversible, mutant-selective EGFR inhibitor with Ki of 21.5 nM and 303.3 nM for EGFRL858R/T790M and EGFRWT in cell-free assays, respectively. Phase 2.
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分子式:C4H8O2 , 分子量:88.10512,Afatinib (BIBW2992) irreversibly inhibits EGFR/HER2 including EGFR(wt), EGFR(L858R), EGFR(L858R/T790M) and HER2 with IC50 of 0.5 nM, 0.4 nM, 10 nM and 14 nM in cell-free assays, respectively;