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。
BTYNB 纯度: ≥98.0%
BTYNB 是 IMP1 结合 c-Myc mRNA 的有效选择性抑制剂, IC50 为 5 μM。BTYNB 对 IMP1 阳性的癌细胞株表现出选择性和有效性。BTYNB 可用于癌症研究。
BTYNB Chemical Structure
CAS No. : 304456-62-0
规格 | 价格 | 是否有货 | 数量 |
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5 mg | ¥1000 | In-stock | |
10 mg | ¥1700 | In-stock | |
25 mg | ¥3500 | In-stock | |
50 mg | ¥5500 | In-stock | |
100 mg | ¥8500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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BTYNB 相关产品
•相关化合物库:
- Bioactive Compound Library Plus
- Apoptosis Compound Library
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- Glutamine Metabolism Compound Library
- Transcription Factor Targeted Library
- Targeted Diversity Library
生物活性 |
BTYNB is a potent and selective inhibitor of IMP1 binding to c-Myc mRNA (IC50=5 μM). BTYNB exhibits selectivity and effectiveness against IMP1-postive cancer cell lines. BTYNB can be used for cancer research[1]. |
IC50 & Target |
IC50: 5 μM (IMP1 c-Myc mRNA internation)[1] |
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体外研究 (In Vitro) |
The oncofetal mRNA-binding protein, IMP1 binds to and stabilizes c-Myc, β-TrCP1, and other oncogenic mRNAs, it leads to increased expression of the proteins encoded by its target mRNAs[1].BTYNB (10 uM; 0.5-1 hour) enhances the degradation rate of c-Myc mRNA in SK-MEL2 cells[1].BTYNB (10-40 uM; 72 hours) degrades c-Myc expression in a dose-dependent manner in SK-MEL2 cells[1].BTYNB (10-40 uM; 72 hours) decreases IMP1 expression in a dose-dependent manner in SK-MEL2 cells[1].BTYNB (1-40 μM; 72 hours) decreases levels of CDC34, CALM1, β-TRCP1, and Col5A1 mRNAs expression in T47D/(A1-2) cells in the presence of hormone[1].BTYNB elicits a robust dose-dependent inhibition of cell proliferation in IMP1-positive cells with IC50 of 2.3 μM, 3.6 μM, and 4.5 μM in ES-2, IGROV-1, and SK-MEL2 cells, respectively. BTYNB has no effects on IMP1-negative cells and demonstrates no inhibition of cell proliferation at all concentrations tested, including 50 μM[1]. 上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only. RT-PCR[1]
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分子量 |
309.18 |
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Formula |
C12H9BrN2OS |
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CAS 号 |
304456-62-0 |
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运输条件 |
Room temperature in continental US; may vary elsewhere. |
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储存方式 |
4°C, protect from light *In solvent : -80°C, 6 months; -20°C, 1 month (protect from light) |
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溶解性数据 |
In Vitro:
DMSO : 62.5 mg/mL (202.15 mM; Need ultrasonic) 配制储备液
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请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效。 In Vivo:
请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液,再依次添加助溶剂: ——为保证实验结果的可靠性,澄清的储备液可以根据储存条件,适当保存;体内实验的工作液,建议您现用现配,当天使用; 以下溶剂前显示的百
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参考文献 |
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