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。
E7090 succinate
E7090 succinate 是具有口服活性的、选择性的、有效的 FGFR1/2/3 抑制剂,其对 FGFR1/2/3/4 的 IC50 值分别为 0.71 nM、0.50 nM、1.2 nM 和120 nM。
![E7090 succinate Chemical Structure E7090 succinate](http://www.fluoroprobe.com/wp-content/uploads/2022/05/hy-101466a.gif)
E7090 succinate Chemical Structure
CAS No. : 1879965-80-6
规格 | 价格 | 是否有货 | |
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5 mg | ¥8500 | 询问价格 & 货期 | |
10 mg | ¥14500 | 询问价格 & 货期 |
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生物活性 |
E7090 succinate is an orally available, selective and potent inhibitor of FGFR1, FGFR2 and FGFR3 tyrosine kinase activities, with IC50 values of 0.71 nM, 0.50 nM, 1.2 nM, and 120 nM for FGFR1/2/3/4, respectively[1]. |
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IC50 & Target[2] |
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体外研究 (In Vitro) |
E7090 also inhibited the growth of SNU-16, human gastric cancer cell line harboring FGFR2 amplification with an IC50 value of 3 nM[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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体内研究 (In Vivo) |
Pharmacodynamics analysis reveals that E7090 inhibits phosphorylation of FGFRs in SNU-16 xenograft tumors in a dose-dependent manner. Overall, the in vitro and in vivo studies confirm that E7090 is a potent and selective FGFRs inhibitor, showing promising antitumor activities with wider therapeutic windows in preclinical cancer models harboring FGFRs gene abnormalities[1]. E7090 (6.25-50 mg/kg, orally, once daily) treatment prolongs survival in a 4T1 mouse lung metastasis model[2. Shanghai Jinpan Biotech Co Ltd has not independently confirmed the accuracy of these methods. They are for reference only.
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Clinical Trial |
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分子量 |
764.82 |
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Formula |
C36H43N5O10 |
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CAS 号 |
1879965-80-6 |
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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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