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。
FGFR1 inhibitor-2
FGFR1 inhibitor-2 是一个 FGFR1 抑制剂(IC50 为 4.55 μM 在 MDA-MB-231细胞中)。FGFR1 inhibitor-2 可用于转移性三阴性乳腺癌的研究。
![FGFR1 inhibitor-2 Chemical Structure FGFR1 inhibitor-2](http://www.fluoroprobe.com/wp-content/uploads/2022/05/hy-139376.gif)
FGFR1 inhibitor-2 Chemical Structure
CAS No. : 2410612-08-5
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生物活性 |
FGFR1 inhibitor-2 is a FGFR1 inhibitor (IC50 is 4.55 μM in MDA-MB-231 cells). FGFR1 inhibitor-2 can be used for the research of metastatic triple-negative breast cancer[1]. |
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IC50 & Target[1] |
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体外研究 (In Vitro) |
FGFR1 inhibitor-2 (3 and 6 μM; 48 hours; MDA-MB-231) reduces the expression of FGFR1[1]. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only. Western Blot Analysis[1]
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分子量 |
507.45 |
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Formula |
C25H22F5N3O3 |
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CAS 号 |
2410612-08-5 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
Please store the product under the recommended conditions in the Certificate of Analysis. |
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参考文献 |
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