生物活性 | |||
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靶点 |
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描述 | Olmutinib (HM61713; BI-1482694) is an orally administered, irreversible inhibitor of the EGFR tyrosine kinase, specifically designed to bind to a cysteine residue close to the kinase domain. It is primarily used in the treatment of non-small cell lung cancer (NSCLC)[1].[2]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
2.06mL 0.41mL 0.21mL |
10.28mL 2.06mL 1.03mL |
20.55mL 4.11mL 2.06mL |
参考文献 |
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[1]Kim ES, et al. Olmutinib: First Global Approval. Drugs. 2016 Jul;76(11):1153-7. |