生物活性分子抑制剂 特异性抑制剂 激动剂 化合物库 重组蛋白 MI-773 纯度: 98.05%
MI-773 是一种有效的 MDM2-p53 蛋白质相互作用 (PPI) 抑制剂,对 MDM2 具体高结合亲和力 (Kd=8.2 nM)。MI-773 具有抗肿瘤活性。
MI-773 Chemical Structure
CAS No. : 1303607-07-9
规格 | 价格 | 是否有货 | 数量 |
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Free Sample (0.1-0.5 mg) | Apply now | ||
10 mM * 1 mL in DMSO | ¥1980 | In-stock | |
5 mg | ¥1600 | In-stock | |
10 mg | ¥2650 | In-stock | |
50 mg | ¥10600 | In-stock | |
100 mg | ¥17500 | In-stock | |
200 mg | 询价 | ||
500 mg | 询价 |
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生物活性 |
MI-773 is a potent MDM2-p53 protein‐protein interaction (PPI) inhibitor with high binding affinity against MDM2 (Kd=8.2 nM). MI-773 has antitumor activity[1][2]. |
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体外研究 (In Vitro) |
SAR405838 (MI-77301), an analog of MI-773, displays 10 times higher binding affinity against MDM2 than MI-773 (Kd=62 vs 8.2 nM). The antitumor activity of MI-77301 is more pronounced in a set of wild type p53 xenograft models than MI-773, including SJSA-1 osteosarcoma, human prostate, melanoma, colorectal tumor, LNCAP human prostate tumor and human acute lymphoblastic leukemia[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. |
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分子量 |
562.50 |
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Formula |
C29H34Cl2FN3O3 |
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CAS 号 |
1303607-07-9 |
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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, stored under nitrogen *In solvent : -80°C, 6 months; -20°C, 1 month (stored under nitrogen) |
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溶解性数据 |
In Vitro:
DMSO : ≥ 53 mg/mL (94.22 mM) * “≥” means soluble, but saturation unknown. 配制储备液
*
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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Cell Assay |
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. |
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Animal Administration |
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. |
参考文献 |
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